22-32239115-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239115
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239115
    reference: chr 22
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2316C>G
  hgvsp: ENSP00000371539.2:p.Asp772Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2550C>G
  hgvsp: ENSP00000371545.2:p.Asp850Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.606C>G
  hgvsp: ENSP00000402173.1:p.Asp202Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2523C>G
  hgvsp: ENSP00000371546.3:p.Asp841Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2550C>G
  hgvsp: ENSP00000383105.1:p.Asp850Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2523C>G
  hgvsp: ENSP00000383107.1:p.Asp841Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.742C>G
  hgvsp: ENSP00000410544.1:p.Asp248Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2316C>G
  hgvsp: ENSP00000440210.1:p.Asp772Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.504C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.468C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2550C>G
  hgvsp: ENSP00000266091.3:p.Asp850Glu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2523C>G
  hgvsp: ENSP00000383108.2:p.Asp841Glu
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp841Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-32239118-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239118
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239118
    reference: chr 22
allele count: 13
allele frequency: 1.077014846235419e-4
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2526G>C
  hgvsp: ENSP00000371546.3:p.Gln842His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2526G>C
  hgvsp: ENSP00000383107.1:p.Gln842His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.609G>C
  hgvsp: ENSP00000402173.1:p.Gln203His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2319G>C
  hgvsp: ENSP00000440210.1:p.Gln773His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2553G>C
  hgvsp: ENSP00000266091.3:p.Gln851His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2526G>C
  hgvsp: ENSP00000383108.2:p.Gln842His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2319G>C
  hgvsp: ENSP00000371539.2:p.Gln773His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.745G>C
  hgvsp: ENSP00000410544.1:p.Gln249His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.507G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2553G>C
  hgvsp: ENSP00000383105.1:p.Gln851His
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.471G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2553G>C
  hgvsp: ENSP00000371545.2:p.Gln851His
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln842His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32239124-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239124
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239124
    reference: chr 22
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.513G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2325G>T
  hgvsp: ENSP00000371539.2:p.Trp775Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2532G>T
  hgvsp: ENSP00000383108.2:p.Trp844Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.615G>T
  hgvsp: ENSP00000402173.1:p.Trp205Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2325G>T
  hgvsp: ENSP00000440210.1:p.Trp775Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2559G>T
  hgvsp: ENSP00000383105.1:p.Trp853Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.751G>T
  hgvsp: ENSP00000410544.1:p.Trp251Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2559G>T
  hgvsp: ENSP00000371545.2:p.Trp853Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2559G>T
  hgvsp: ENSP00000266091.3:p.Trp853Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2532G>T
  hgvsp: ENSP00000371546.3:p.Trp844Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.477G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2532G>T
  hgvsp: ENSP00000383107.1:p.Trp844Cys
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp844Cys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

22-32239131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239131
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239131
    reference: chr 22
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2566A>G
  hgvsp: ENSP00000383105.1:p.Met856Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2539A>G
  hgvsp: ENSP00000371546.3:p.Met847Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.622A>G
  hgvsp: ENSP00000402173.1:p.Met208Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2539A>G
  hgvsp: ENSP00000383108.2:p.Met847Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.758A>G
  hgvsp: ENSP00000410544.1:p.Met254Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2332A>G
  hgvsp: ENSP00000371539.2:p.Met778Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2566A>G
  hgvsp: ENSP00000266091.3:p.Met856Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2566A>G
  hgvsp: ENSP00000371545.2:p.Met856Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2539A>G
  hgvsp: ENSP00000383107.1:p.Met847Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.520A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2332A>G
  hgvsp: ENSP00000440210.1:p.Met778Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.484A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met847Val
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

22-32239138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239138
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239138
    reference: chr 22
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.765G>A
  hgvsp: ENSP00000410544.1:p.Arg256Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2573G>A
  hgvsp: ENSP00000383105.1:p.Arg858Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2546G>A
  hgvsp: ENSP00000371546.3:p.Arg849Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2546G>A
  hgvsp: ENSP00000383108.2:p.Arg849Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.527G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.491G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2546G>A
  hgvsp: ENSP00000383107.1:p.Arg849Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2573G>A
  hgvsp: ENSP00000266091.3:p.Arg858Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2339G>A
  hgvsp: ENSP00000371539.2:p.Arg780Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.629G>A
  hgvsp: ENSP00000402173.1:p.Arg210Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2339G>A
  hgvsp: ENSP00000440210.1:p.Arg780Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2573G>A
  hgvsp: ENSP00000371545.2:p.Arg858Lys
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg849Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-32239141-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239141
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239141
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2342C>A
  hgvsp: ENSP00000440210.1:p.Thr781Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.768C>A
  hgvsp: ENSP00000410544.1:p.Thr257Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.530C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2576C>A
  hgvsp: ENSP00000266091.3:p.Thr859Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2549C>A
  hgvsp: ENSP00000383107.1:p.Thr850Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.494C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2549C>A
  hgvsp: ENSP00000371546.3:p.Thr850Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.632C>A
  hgvsp: ENSP00000402173.1:p.Thr211Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2549C>A
  hgvsp: ENSP00000383108.2:p.Thr850Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2576C>A
  hgvsp: ENSP00000383105.1:p.Thr859Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2342C>A
  hgvsp: ENSP00000371539.2:p.Thr781Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2576C>A
  hgvsp: ENSP00000371545.2:p.Thr859Lys
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr850Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

22-32239141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239141
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239141
    reference: chr 22
allele count: 14
allele frequency: 1.159573939403979e-4
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2342C>T
  hgvsp: ENSP00000371539.2:p.Thr781Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.494C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2549C>T
  hgvsp: ENSP00000383108.2:p.Thr850Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2576C>T
  hgvsp: ENSP00000266091.3:p.Thr859Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.632C>T
  hgvsp: ENSP00000402173.1:p.Thr211Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2549C>T
  hgvsp: ENSP00000383107.1:p.Thr850Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2549C>T
  hgvsp: ENSP00000371546.3:p.Thr850Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.768C>T
  hgvsp: ENSP00000410544.1:p.Thr257Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.530C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2342C>T
  hgvsp: ENSP00000440210.1:p.Thr781Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2576C>T
  hgvsp: ENSP00000371545.2:p.Thr859Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2576C>T
  hgvsp: ENSP00000383105.1:p.Thr859Met
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Thr850Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

22-32239142-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239142
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239142
    reference: chr 22
allele count: 2
allele frequency: 1.656589083077942e-5
allele num: 120730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.495G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.633G>T
  hgvsp: ENST00000448753.1:c.633G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2577G>T
  hgvsp: ENST00000400246.1:c.2577G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2343G>T
  hgvsp: ENST00000382105.2:c.2343G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.531G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.769G>T
  hgvsp: ENST00000433147.1:c.769G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2550G>T
  hgvsp: ENST00000400248.2:c.2550G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2550G>T
  hgvsp: ENST00000382112.3:c.2550G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2550G>T
  hgvsp: ENST00000400249.2:c.2550G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2343G>T
  hgvsp: ENST00000535622.1:c.2343G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2577G>T
  hgvsp: ENST00000266091.3:c.2577G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2577G>T
  hgvsp: ENST00000382111.2:c.2577G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr850Thr
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/22-32239150-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239150
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239150
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2351A>C
  hgvsp: ENSP00000371539.2:p.Lys784Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2585A>C
  hgvsp: ENSP00000371545.2:p.Lys862Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2558A>C
  hgvsp: ENSP00000383108.2:p.Lys853Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.503A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.641A>C
  hgvsp: ENSP00000402173.1:p.Lys214Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.777A>C
  hgvsp: ENSP00000410544.1:p.Lys260Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2351A>C
  hgvsp: ENSP00000440210.1:p.Lys784Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.539A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2585A>C
  hgvsp: ENSP00000266091.3:p.Lys862Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2585A>C
  hgvsp: ENSP00000383105.1:p.Lys862Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2558A>C
  hgvsp: ENSP00000383107.1:p.Lys853Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2558A>C
  hgvsp: ENSP00000371546.3:p.Lys853Thr
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys853Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

22-32239155-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239155
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239155
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.782A>T
  hgvsp: ENSP00000410544.1:p.Thr262Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2590A>T
  hgvsp: ENSP00000266091.3:p.Thr864Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2356A>T
  hgvsp: ENSP00000440210.1:p.Thr786Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2563A>T
  hgvsp: ENSP00000383108.2:p.Thr855Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2590A>T
  hgvsp: ENSP00000371545.2:p.Thr864Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2356A>T
  hgvsp: ENSP00000371539.2:p.Thr786Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.646A>T
  hgvsp: ENSP00000402173.1:p.Thr216Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2563A>T
  hgvsp: ENSP00000383107.1:p.Thr855Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.508A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.544A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2563A>T
  hgvsp: ENSP00000371546.3:p.Thr855Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2590A>T
  hgvsp: ENSP00000383105.1:p.Thr864Ser
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr855Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

22-32239156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239156
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239156
    reference: chr 22
allele count: 8
allele frequency: 6.625917275422816e-5
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2357C>T
  hgvsp: ENSP00000371539.2:p.Thr786Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2357C>T
  hgvsp: ENSP00000440210.1:p.Thr786Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2564C>T
  hgvsp: ENSP00000383108.2:p.Thr855Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.545C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2591C>T
  hgvsp: ENSP00000383105.1:p.Thr864Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.783C>T
  hgvsp: ENSP00000410544.1:p.Thr262Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.647C>T
  hgvsp: ENSP00000402173.1:p.Thr216Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2564C>T
  hgvsp: ENSP00000383107.1:p.Thr855Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2591C>T
  hgvsp: ENSP00000266091.3:p.Thr864Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2564C>T
  hgvsp: ENSP00000371546.3:p.Thr855Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.509C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2591C>T
  hgvsp: ENSP00000371545.2:p.Thr864Met
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr855Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-32239157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239157
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239157
    reference: chr 22
allele count: 20
allele frequency: 1.656506758547575e-4
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.546G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.648G>A
  hgvsp: ENST00000448753.1:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.784G>A
  hgvsp: ENST00000433147.1:c.784G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2565G>A
  hgvsp: ENST00000400248.2:c.2565G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2565G>A
  hgvsp: ENST00000400249.2:c.2565G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2592G>A
  hgvsp: ENST00000382111.2:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2358G>A
  hgvsp: ENST00000382105.2:c.2358G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2592G>A
  hgvsp: ENST00000266091.3:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2592G>A
  hgvsp: ENST00000400246.1:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2565G>A
  hgvsp: ENST00000382112.3:c.2565G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.510G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2358G>A
  hgvsp: ENST00000535622.1:c.2358G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Thr855Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

22-32239165-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239165
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239165
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2573A>G
  hgvsp: ENSP00000383108.2:p.Asp858Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2600A>G
  hgvsp: ENSP00000383105.1:p.Asp867Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2366A>G
  hgvsp: ENSP00000371539.2:p.Asp789Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2600A>G
  hgvsp: ENSP00000266091.3:p.Asp867Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.554A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2573A>G
  hgvsp: ENSP00000383107.1:p.Asp858Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.656A>G
  hgvsp: ENSP00000402173.1:p.Asp219Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2573A>G
  hgvsp: ENSP00000371546.3:p.Asp858Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2366A>G
  hgvsp: ENSP00000440210.1:p.Asp789Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.518A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2600A>G
  hgvsp: ENSP00000371545.2:p.Asp867Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.792A>G
  hgvsp: ENSP00000410544.1:p.Asp265Gly
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp858Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

22-32239173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239173
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239173
    reference: chr 22
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2581A>G
  hgvsp: ENSP00000383107.1:p.Ile861Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2374A>G
  hgvsp: ENSP00000371539.2:p.Ile792Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.526A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.800A>G
  hgvsp: ENSP00000410544.1:p.Ile268Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2581A>G
  hgvsp: ENSP00000383108.2:p.Ile861Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2608A>G
  hgvsp: ENSP00000266091.3:p.Ile870Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2608A>G
  hgvsp: ENSP00000371545.2:p.Ile870Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2608A>G
  hgvsp: ENSP00000383105.1:p.Ile870Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.664A>G
  hgvsp: ENSP00000402173.1:p.Ile222Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2581A>G
  hgvsp: ENSP00000371546.3:p.Ile861Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2374A>G
  hgvsp: ENSP00000440210.1:p.Ile792Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.562A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile861Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

22-32239179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239179
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239179
    reference: chr 22
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2380G>A
  hgvsp: ENSP00000371539.2:p.Val794Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.568G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2587G>A
  hgvsp: ENSP00000383108.2:p.Val863Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2614G>A
  hgvsp: ENSP00000371545.2:p.Val872Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2587G>A
  hgvsp: ENSP00000383107.1:p.Val863Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.670G>A
  hgvsp: ENSP00000402173.1:p.Val224Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2614G>A
  hgvsp: ENSP00000266091.3:p.Val872Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2587G>A
  hgvsp: ENSP00000371546.3:p.Val863Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2614G>A
  hgvsp: ENSP00000383105.1:p.Val872Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2380G>A
  hgvsp: ENSP00000440210.1:p.Val794Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.532G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.806G>A
  hgvsp: ENSP00000410544.1:p.Val270Met
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val863Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

22-32239184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239184
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239184
    reference: chr 22
allele count: 3
allele frequency: 2.486737400530504e-5
allele num: 120640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.675G>A
  hgvsp: ENST00000448753.1:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2592G>A
  hgvsp: ENST00000400248.2:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2385G>A
  hgvsp: ENST00000535622.1:c.2385G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.811G>A
  hgvsp: ENST00000433147.1:c.811G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.537G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2592G>A
  hgvsp: ENST00000400249.2:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2619G>A
  hgvsp: ENST00000266091.3:c.2619G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2385G>A
  hgvsp: ENST00000382105.2:c.2385G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2619G>A
  hgvsp: ENST00000382111.2:c.2619G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2619G>A
  hgvsp: ENST00000400246.1:c.2619G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2592G>A
  hgvsp: ENST00000382112.3:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.573G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr864Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32239187-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239187
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239187
    reference: chr 22
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.576A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2388A>T
  hgvsp: ENST00000382105.2:c.2388A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.814A>T
  hgvsp: ENST00000433147.1:c.814A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2595A>T
  hgvsp: ENST00000400248.2:c.2595A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.678A>T
  hgvsp: ENST00000448753.1:c.678A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2622A>T
  hgvsp: ENST00000266091.3:c.2622A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2622A>T
  hgvsp: ENST00000400246.1:c.2622A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2595A>T
  hgvsp: ENST00000382112.3:c.2595A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2595A>T
  hgvsp: ENST00000400249.2:c.2595A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.540A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2622A>T
  hgvsp: ENST00000382111.2:c.2622A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2388A>T
  hgvsp: ENST00000535622.1:c.2388A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg865Arg
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

22-32239211-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239211
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239211
    reference: chr 22
allele count: 2
allele frequency: 1.666472244904761e-5
allele num: 120014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2399+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2606+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2606+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.689+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2633+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.551+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2633+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2606+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2633+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2399+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.825+13A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.587+13A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-32239222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239222
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239222
    reference: chr 22
allele count: 2
allele frequency: 1.670369318656355e-5
allele num: 119734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2633+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2606+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2606+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2606+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2633+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.689+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.587+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2633+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.551+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.825+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2399+24C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2399+24C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13323
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

22-32239225-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239225
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239225
    reference: chr 22
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2606+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.689+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2399+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.551+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2606+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2633+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.587+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.825+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2606+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2633+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2399+27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2633+27C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

22-32239226-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239226
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239226
    reference: chr 22
allele count: 1
allele frequency: 8.354777261638205e-6
allele num: 119692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2399+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2399+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2633+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2633+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.825+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2606+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.551+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2606+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2606+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.587+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.689+28A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2633+28A>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

22-32239235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239235
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239235
    reference: chr 22
allele count: 2
allele frequency: 1.675771692864564e-5
allele num: 119348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2633+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2399+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2606+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2399+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2606+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.587+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2633+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2633+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2606+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.551+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.825+37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.689+37C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

22-32239581-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239581
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239581
    reference: chr 22
allele count: 2
allele frequency: 1.684267259528742e-5
allele num: 118746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-50A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-50A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-32239588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239588
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239588
    reference: chr 22
allele count: 1
allele frequency: 8.410428931875526e-6
allele num: 118900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-43C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-43C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

22-32239591-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239591
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239591
    reference: chr 22
allele count: 1
allele frequency: 8.399126490844953e-6
allele num: 119060
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-40T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-40T>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

22-32239593-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239593
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239593
    reference: chr 22
allele count: 1
allele frequency: 8.396446623788812e-6
allele num: 119098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-38A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-32239608-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239608
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239608
    reference: chr 22
allele count: 1
allele frequency: 8.365960579593749e-6
allele num: 119532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-23G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-23G>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-32239610-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239610
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239610
    reference: chr 22
allele count: 47
allele frequency: 3.928714725157149e-4
allele num: 119632
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-21G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-21G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26333
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32239614-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239614
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239613
    reference: chr 22
allele count: 2
allele frequency: 1.668474180362059e-5
allele num: 119870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.826-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2400-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2634-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2607-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.690-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2634-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000490731
  gene symbol: DEPDC5
  hgvsc: ENST00000490731.1:n.588-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2400-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2634-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.552-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2607-16delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2607-16delG
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: TG
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

22-32239647-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239647
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239647
    reference: chr 22
allele count: 2
allele frequency: 1.657357840131263e-5
allele num: 120674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2650G>T
  hgvsp: ENSP00000266091.3:p.Ala884Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.706G>T
  hgvsp: ENSP00000402173.1:p.Ala236Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2416G>T
  hgvsp: ENSP00000440210.1:p.Ala806Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2416G>T
  hgvsp: ENSP00000371539.2:p.Ala806Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000471914
  gene symbol: DEPDC5
  hgvsc: ENST00000471914.1:n.568G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2650G>T
  hgvsp: ENSP00000383105.1:p.Ala884Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2623G>T
  hgvsp: ENSP00000371546.3:p.Ala875Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2623G>T
  hgvsp: ENSP00000383107.1:p.Ala875Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2623G>T
  hgvsp: ENSP00000383108.2:p.Ala875Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.842G>T
  hgvsp: ENSP00000410544.1:p.Ala282Ser
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2650G>T
  hgvsp: ENSP00000371545.2:p.Ala884Ser
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala875Ser
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-32239656-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239656
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239656
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2632C>A
  hgvsp: ENSP00000371546.3:p.His878Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2659C>A
  hgvsp: ENSP00000266091.3:p.His887Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.715C>A
  hgvsp: ENSP00000402173.1:p.His239Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2632C>A
  hgvsp: ENSP00000383107.1:p.His878Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2659C>A
  hgvsp: ENSP00000383105.1:p.His887Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2425C>A
  hgvsp: ENSP00000440210.1:p.His809Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2632C>A
  hgvsp: ENSP00000383108.2:p.His878Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.851C>A
  hgvsp: ENSP00000410544.1:p.His285Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2659C>A
  hgvsp: ENSP00000371545.2:p.His887Asn
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2425C>A
  hgvsp: ENSP00000371539.2:p.His809Asn
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His878Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

22-32239669-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239669
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239669
    reference: chr 22
allele count: 22
allele frequency: 1.821885817447041e-4
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2672G>C
  hgvsp: ENSP00000383105.1:p.Ser891Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2645G>C
  hgvsp: ENSP00000371546.3:p.Ser882Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2438G>C
  hgvsp: ENSP00000371539.2:p.Ser813Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2645G>C
  hgvsp: ENSP00000383107.1:p.Ser882Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2672G>C
  hgvsp: ENSP00000371545.2:p.Ser891Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2645G>C
  hgvsp: ENSP00000383108.2:p.Ser882Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2672G>C
  hgvsp: ENSP00000266091.3:p.Ser891Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.864G>C
  hgvsp: ENSP00000410544.1:p.Ser289Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2438G>C
  hgvsp: ENSP00000440210.1:p.Ser813Thr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.728G>C
  hgvsp: ENSP00000402173.1:p.Ser243Thr
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33800
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser882Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

22-32239687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239687
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239687
    reference: chr 22
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2456C>T
  hgvsp: ENSP00000440210.1:p.Ser819Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2690C>T
  hgvsp: ENSP00000383105.1:p.Ser897Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2690C>T
  hgvsp: ENSP00000371545.2:p.Ser897Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.746C>T
  hgvsp: ENSP00000402173.1:p.Ser249Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.882C>T
  hgvsp: ENSP00000410544.1:p.Ser295Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2663C>T
  hgvsp: ENSP00000383108.2:p.Ser888Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2663C>T
  hgvsp: ENSP00000383107.1:p.Ser888Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2663C>T
  hgvsp: ENSP00000371546.3:p.Ser888Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2690C>T
  hgvsp: ENSP00000266091.3:p.Ser897Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2456C>T
  hgvsp: ENSP00000371539.2:p.Ser819Leu
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10331
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser888Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-32239688-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239688
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239688
    reference: chr 22
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.747A>C
  hgvsp: ENST00000448753.1:c.747A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2691A>C
  hgvsp: ENST00000266091.3:c.2691A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2691A>C
  hgvsp: ENST00000400246.1:c.2691A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2664A>C
  hgvsp: ENST00000400249.2:c.2664A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.883A>C
  hgvsp: ENST00000433147.1:c.883A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2457A>C
  hgvsp: ENST00000382105.2:c.2457A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2457A>C
  hgvsp: ENST00000535622.1:c.2457A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2664A>C
  hgvsp: ENST00000382112.3:c.2664A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2664A>C
  hgvsp: ENST00000400248.2:c.2664A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2691A>C
  hgvsp: ENST00000382111.2:c.2691A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser888Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

22-32239696-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239696
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239696
    reference: chr 22
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2699A>G
  hgvsp: ENSP00000266091.3:p.Glu900Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2699A>G
  hgvsp: ENSP00000383105.1:p.Glu900Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.755A>G
  hgvsp: ENSP00000402173.1:p.Glu252Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2672A>G
  hgvsp: ENSP00000383107.1:p.Glu891Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2672A>G
  hgvsp: ENSP00000383108.2:p.Glu891Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2699A>G
  hgvsp: ENSP00000371545.2:p.Glu900Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2465A>G
  hgvsp: ENSP00000440210.1:p.Glu822Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2672A>G
  hgvsp: ENSP00000371546.3:p.Glu891Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.891A>G
  hgvsp: ENSP00000410544.1:p.Glu298Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2465A>G
  hgvsp: ENSP00000371539.2:p.Glu822Gly
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33825
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu891Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

22-32239700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239700
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239700
    reference: chr 22
allele count: 6
allele frequency: 4.968203497615263e-5
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.759C>T
  hgvsp: ENST00000448753.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2676C>T
  hgvsp: ENST00000400249.2:c.2676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2676C>T
  hgvsp: ENST00000400248.2:c.2676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2469C>T
  hgvsp: ENST00000535622.1:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2703C>T
  hgvsp: ENST00000266091.3:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2469C>T
  hgvsp: ENST00000382105.2:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.895C>T
  hgvsp: ENST00000433147.1:c.895C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2676C>T
  hgvsp: ENST00000382112.3:c.2676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2703C>T
  hgvsp: ENST00000400246.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2703C>T
  hgvsp: ENST00000382111.2:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe892Phe
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

22-32239701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239701
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239701
    reference: chr 22
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2704G>A
  hgvsp: ENSP00000371545.2:p.Val902Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2704G>A
  hgvsp: ENSP00000266091.3:p.Val902Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.896G>A
  hgvsp: ENSP00000410544.1:p.Val300Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2470G>A
  hgvsp: ENSP00000371539.2:p.Val824Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2704G>A
  hgvsp: ENSP00000383105.1:p.Val902Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2470G>A
  hgvsp: ENSP00000440210.1:p.Val824Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2677G>A
  hgvsp: ENSP00000371546.3:p.Val893Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2677G>A
  hgvsp: ENSP00000383107.1:p.Val893Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2677G>A
  hgvsp: ENSP00000383108.2:p.Val893Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.760G>A
  hgvsp: ENSP00000402173.1:p.Val254Ile
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val893Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

22-32239709-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239709
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239709
    reference: chr 22
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2478C>T
  hgvsp: ENST00000382105.2:c.2478C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2685C>T
  hgvsp: ENST00000400249.2:c.2685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2685C>T
  hgvsp: ENST00000382112.3:c.2685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2478C>T
  hgvsp: ENST00000535622.1:c.2478C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2712C>T
  hgvsp: ENST00000382111.2:c.2712C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2712C>T
  hgvsp: ENST00000266091.3:c.2712C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2712C>T
  hgvsp: ENST00000400246.1:c.2712C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.904C>T
  hgvsp: ENST00000433147.1:c.904C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2685C>T
  hgvsp: ENST00000400248.2:c.2685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.768C>T
  hgvsp: ENST00000448753.1:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys895Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

22-32239724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239724
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239724
    reference: chr 22
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2700C>T
  hgvsp: ENST00000400249.2:c.2700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2727C>T
  hgvsp: ENST00000266091.3:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2700C>T
  hgvsp: ENST00000382112.3:c.2700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2727C>T
  hgvsp: ENST00000400246.1:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2700C>T
  hgvsp: ENST00000400248.2:c.2700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2493C>T
  hgvsp: ENST00000535622.1:c.2493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2727C>T
  hgvsp: ENST00000382111.2:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2493C>T
  hgvsp: ENST00000382105.2:c.2493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.919C>T
  hgvsp: ENST00000433147.1:c.919C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.783C>T
  hgvsp: ENST00000448753.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser900Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

22-32239727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239727
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239727
    reference: chr 22
allele count: 4
allele frequency: 3.312245371137094e-5
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2703C>T
  hgvsp: ENST00000400249.2:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2703C>T
  hgvsp: ENST00000382112.3:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2730C>T
  hgvsp: ENST00000266091.3:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2703C>T
  hgvsp: ENST00000400248.2:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2730C>T
  hgvsp: ENST00000400246.1:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.922C>T
  hgvsp: ENST00000433147.1:c.922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2730C>T
  hgvsp: ENST00000382111.2:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2496C>T
  hgvsp: ENST00000382105.2:c.2496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.786C>T
  hgvsp: ENST00000448753.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2496C>T
  hgvsp: ENST00000535622.1:c.2496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His901His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-32239731-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239731
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239731
    reference: chr 22
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2707C>T
  hgvsp: ENSP00000371546.3:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2500C>T
  hgvsp: ENSP00000440210.1:p.Arg834Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2734C>T
  hgvsp: ENSP00000371545.2:p.Arg912Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2734C>T
  hgvsp: ENSP00000266091.3:p.Arg912Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2500C>T
  hgvsp: ENSP00000371539.2:p.Arg834Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2707C>T
  hgvsp: ENSP00000383107.1:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2707C>T
  hgvsp: ENSP00000383108.2:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2734C>T
  hgvsp: ENSP00000383105.1:p.Arg912Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.926C>T
  hgvsp: ENSP00000410544.1:p.Arg310Trp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.790C>T
  hgvsp: ENSP00000402173.1:p.Arg264Trp
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg903Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

22-32239732-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239732
    reference: chr 22
allele count: 2
allele frequency: 1.656177542232527e-5
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2708G>A
  hgvsp: ENSP00000371546.3:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2735G>A
  hgvsp: ENSP00000371545.2:p.Arg912Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2708G>A
  hgvsp: ENSP00000383107.1:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2735G>A
  hgvsp: ENSP00000383105.1:p.Arg912Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.791G>A
  hgvsp: ENSP00000402173.1:p.Arg264Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2735G>A
  hgvsp: ENSP00000266091.3:p.Arg912Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2708G>A
  hgvsp: ENSP00000383108.2:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.927G>A
  hgvsp: ENSP00000410544.1:p.Arg310Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2501G>A
  hgvsp: ENSP00000440210.1:p.Arg834Gln
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2501G>A
  hgvsp: ENSP00000371539.2:p.Arg834Gln
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg903Gln
num of homozygotes: 1
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

22-32239734-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239734
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239734
    reference: chr 22
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2710C>T
  hgvsp: ENST00000400249.2:c.2710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2737C>T
  hgvsp: ENST00000400246.1:c.2737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2503C>T
  hgvsp: ENST00000382105.2:c.2503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.793C>T
  hgvsp: ENST00000448753.1:c.793C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2737C>T
  hgvsp: ENST00000266091.3:c.2737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2710C>T
  hgvsp: ENST00000382112.3:c.2710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2737C>T
  hgvsp: ENST00000382111.2:c.2737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2710C>T
  hgvsp: ENST00000400248.2:c.2710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2503C>T
  hgvsp: ENST00000535622.1:c.2503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.929C>T
  hgvsp: ENST00000433147.1:c.929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27185
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu904Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

22-32239738-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239738
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239738
    reference: chr 22
allele count: 6
allele frequency: 4.979170470199664e-5
allele num: 120502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2741A>G
  hgvsp: ENSP00000383105.1:p.Glu914Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2741A>G
  hgvsp: ENSP00000266091.3:p.Glu914Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.797A>G
  hgvsp: ENSP00000402173.1:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.933A>G
  hgvsp: ENSP00000410544.1:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2714A>G
  hgvsp: ENSP00000383108.2:p.Glu905Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2714A>G
  hgvsp: ENSP00000383107.1:p.Glu905Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2741A>G
  hgvsp: ENSP00000371545.2:p.Glu914Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2507A>G
  hgvsp: ENSP00000371539.2:p.Glu836Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2714A>G
  hgvsp: ENSP00000371546.3:p.Glu905Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2507A>G
  hgvsp: ENSP00000440210.1:p.Glu836Gly
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Glu905Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

22-32239739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239739
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239739
    reference: chr 22
allele count: 1385
allele frequency: 1.146959935074614e-2
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2508G>A
  hgvsp: ENST00000382105.2:c.2508G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2742G>A
  hgvsp: ENST00000400246.1:c.2742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2715G>A
  hgvsp: ENST00000382112.3:c.2715G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.798G>A
  hgvsp: ENST00000448753.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2508G>A
  hgvsp: ENST00000535622.1:c.2508G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2742G>A
  hgvsp: ENST00000382111.2:c.2742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2715G>A
  hgvsp: ENST00000400248.2:c.2715G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2715G>A
  hgvsp: ENST00000400249.2:c.2715G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2742G>A
  hgvsp: ENST00000266091.3:c.2742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.934G>A
  hgvsp: ENST00000433147.1:c.934G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 9.75e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27189
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 10805
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 12824
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 33764
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu905Glu
num of homozygotes: 12
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

22-32239741-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239741
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239741
    reference: chr 22
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2717A>G
  hgvsp: ENSP00000383107.1:p.Glu906Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2744A>G
  hgvsp: ENSP00000383105.1:p.Glu915Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2744A>G
  hgvsp: ENSP00000371545.2:p.Glu915Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2510A>G
  hgvsp: ENSP00000440210.1:p.Glu837Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2717A>G
  hgvsp: ENSP00000383108.2:p.Glu906Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2717A>G
  hgvsp: ENSP00000371546.3:p.Glu906Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.800A>G
  hgvsp: ENSP00000402173.1:p.Glu267Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.936A>G
  hgvsp: ENSP00000410544.1:p.Glu313Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2744A>G
  hgvsp: ENSP00000266091.3:p.Glu915Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2510A>G
  hgvsp: ENSP00000371539.2:p.Glu837Gly
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 27881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu906Gly
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

22-32239742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239742
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239742
    reference: chr 22
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2745G>A
  hgvsp: ENST00000382111.2:c.2745G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2718G>A
  hgvsp: ENST00000400249.2:c.2718G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2718G>A
  hgvsp: ENST00000400248.2:c.2718G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2511G>A
  hgvsp: ENST00000535622.1:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.937G>A
  hgvsp: ENST00000433147.1:c.937G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2745G>A
  hgvsp: ENST00000266091.3:c.2745G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2745G>A
  hgvsp: ENST00000400246.1:c.2745G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2511G>A
  hgvsp: ENST00000382105.2:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2718G>A
  hgvsp: ENST00000382112.3:c.2718G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.801G>A
  hgvsp: ENST00000448753.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu906Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

22-32239775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239775
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239775
    reference: chr 22
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2778T>C
  hgvsp: ENST00000266091.3:c.2778T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.970T>C
  hgvsp: ENST00000433147.1:c.970T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2778T>C
  hgvsp: ENST00000382111.2:c.2778T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2751T>C
  hgvsp: ENST00000400248.2:c.2751T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2544T>C
  hgvsp: ENST00000535622.1:c.2544T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2751T>C
  hgvsp: ENST00000382112.3:c.2751T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2544T>C
  hgvsp: ENST00000382105.2:c.2544T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2751T>C
  hgvsp: ENST00000400249.2:c.2751T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.834T>C
  hgvsp: ENST00000448753.1:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2778T>C
  hgvsp: ENST00000400246.1:c.2778T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys917Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-32239781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239781
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239781
    reference: chr 22
allele count: 15
allele frequency: 1.244008027998474e-4
allele num: 120578
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2757C>T
  hgvsp: ENST00000382112.3:c.2757C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2757C>T
  hgvsp: ENST00000400248.2:c.2757C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2757C>T
  hgvsp: ENST00000400249.2:c.2757C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2550C>T
  hgvsp: ENST00000382105.2:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2784C>T
  hgvsp: ENST00000400246.1:c.2784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2550C>T
  hgvsp: ENST00000535622.1:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2784C>T
  hgvsp: ENST00000382111.2:c.2784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.976C>T
  hgvsp: ENST00000433147.1:c.976C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2784C>T
  hgvsp: ENST00000266091.3:c.2784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.840C>T
  hgvsp: ENST00000448753.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27715
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala919Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

22-32239806-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239806
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239806
    reference: chr 22
allele count: 58
allele frequency: 4.834139023170529e-4
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+8A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+8A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26353
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2774+8A>G
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

22-32239816-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239816
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239816
    reference: chr 22
allele count: 4
allele frequency: 3.342413556829387e-5
allele num: 119674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+18G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+18G>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25080
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-32239823-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239823
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239823
    reference: chr 22
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+25C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23412
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

22-32239825-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239825
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239825
    reference: chr 22
allele count: 1
allele frequency: 8.376612497905846e-6
allele num: 119380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+27T>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+27T>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23456
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

22-32239829-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239829
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239829
    reference: chr 22
allele count: 2
allele frequency: 1.676614579840386e-5
allele num: 119288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+31T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+31T>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21895
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

22-32239832-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239832
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239832
    reference: chr 22
allele count: 1
allele frequency: 8.393627557957998e-6
allele num: 119138
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+34A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+34A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

22-32239838-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32239838
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32239838
    reference: chr 22
allele count: 1
allele frequency: 8.426445556735258e-6
allele num: 118674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.993+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.857+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2567+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2774+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2567+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2801+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2801+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2801+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2774+40G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2774+40G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

22-32240955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240955
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240955
    reference: chr 22
allele count: 86
allele frequency: 7.218640881009939e-4
allele num: 119136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-49A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-49A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15819
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22297
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/22-32240963-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240963
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240963
    reference: chr 22
allele count: 1
allele frequency: 8.371142995864656e-6
allele num: 119458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-41C>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-41C>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

22-32240969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240969
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240969
    reference: chr 22
allele count: 1
allele frequency: 8.352125615969264e-6
allele num: 119730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-35C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-35C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40225
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

22-32240973-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240973
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240973
    reference: chr 22
allele count: 2
allele frequency: 1.668808303990121e-5
allele num: 119846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-31C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-31C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6119
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

22-32240977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240977
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240977
    reference: chr 22
allele count: 8
allele frequency: 6.664889362836577e-5
allele num: 120032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-27C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-27C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20403
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

22-32240979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240979
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240979
    reference: chr 22
allele count: 6
allele frequency: 4.99542086420781e-5
allele num: 120110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-25C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-25C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

22-32240980-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240980
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240980
    reference: chr 22
allele count: 1
allele frequency: 8.324315325064513e-6
allele num: 120130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-24C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-24C>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7408
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

22-32240994-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240994
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240994
    reference: chr 22
allele count: 3
allele frequency: 2.491321895397698e-5
allele num: 120418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-10G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-10G>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-32240999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32240999
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32240999
    reference: chr 22
allele count: 2
allele frequency: 1.659695943703114e-5
allele num: 120504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-5C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-5C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2775-5C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-32241000-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32241000
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32241000
    reference: chr 22
allele count: 7
allele frequency: 5.808357396528262e-5
allele num: 120516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.994-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2802-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2802-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2775-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2568-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2568-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2775-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2802-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.858-4T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2775-4T>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
hgvs: c.2775-4T>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/22-32241034-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32241034
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32241034
    reference: chr 22
allele count: 2
allele frequency: 1.657138122462507e-5
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2805C>A
  hgvsp: ENST00000382112.3:c.2805C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.1024C>A
  hgvsp: ENST00000433147.1:c.1024C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2832C>A
  hgvsp: ENST00000400246.1:c.2832C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2832C>A
  hgvsp: ENST00000382111.2:c.2832C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2598C>A
  hgvsp: ENST00000382105.2:c.2598C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.888C>A
  hgvsp: ENST00000448753.1:c.888C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2832C>A
  hgvsp: ENST00000266091.3:c.2832C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2805C>A
  hgvsp: ENST00000400249.2:c.2805C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2805C>A
  hgvsp: ENST00000400248.2:c.2805C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2598C>A
  hgvsp: ENST00000535622.1:c.2598C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7482
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr935Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-32241036-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32241036
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32241036
    reference: chr 22
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.2807G>T
  hgvsp: ENSP00000383107.1:p.Arg936Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.2600G>T
  hgvsp: ENSP00000440210.1:p.Arg867Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000402173
  ensembl transcript: ENST00000448753
  gene symbol: DEPDC5
  hgvsc: ENST00000448753.1:c.890G>T
  hgvsp: ENSP00000402173.1:p.Arg297Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.2807G>T
  hgvsp: ENSP00000371546.3:p.Arg936Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000410544
  ensembl transcript: ENST00000433147
  gene symbol: DEPDC5
  hgvsc: ENST00000433147.1:c.1026G>T
  hgvsp: ENSP00000410544.1:p.Arg343Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.2834G>T
  hgvsp: ENSP00000371545.2:p.Arg945Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.2834G>T
  hgvsp: ENSP00000266091.3:p.Arg945Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.2807G>T
  hgvsp: ENSP00000383108.2:p.Arg936Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.2600G>T
  hgvsp: ENSP00000371539.2:p.Arg867Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.2834G>T
  hgvsp: ENSP00000383105.1:p.Arg945Leu
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg936Leu
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8043
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7569
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.6084e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.286e0

DP
type: SiteQuality
SIO_000300: 1.729537e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.979e0

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeDepth
all individuals: 213
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 279
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7383
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8057
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4449
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648977633867002e-4
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.115e0

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.730574e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

GenotypeDepth
all individuals: 3054
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8058
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7567
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
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East Asian
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European (Non-Finnish)
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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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 (Finnish)
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African
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Latino
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East Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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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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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.798453330136083e-4
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African
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South Asian
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Latino
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European (Finnish)
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East Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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FS
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DP
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ClippingRankSum
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MQRankSum
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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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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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MQ
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QD
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African
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European (Non-Finnish)
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MQ
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QD
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498845888665727e-5
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num of homozygotes: 0

ReadPosRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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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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allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

South Asian
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Latino
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allele num: 11574
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African
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East Asian
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DP
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 20

European (Non-Finnish)
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allele count: 5
allele frequency: 7.494229443328637e-5
allele num: 66718
num of homozygotes: 0

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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South Asian
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Other
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num of homozygotes: 0

Latino
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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SIO_000300: 5.28e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

Latino
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South Asian
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East Asian
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African
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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ClippingRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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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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South Asian
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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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QD
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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QD
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FS
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele frequency: 1.500285054160291e-5
allele num: 66654
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Other
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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African
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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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)
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num of homozygotes: 0

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

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

African
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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South Asian
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FS
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MQRankSum
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DP
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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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ReadPosRankSum
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QD
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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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East Asian
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African
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South Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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DP
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MQRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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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: 1.509844184080203e-5
allele num: 66232
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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508932882665379e-5
allele num: 66272
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: 1.07e-2

FS
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MQ
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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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508841813024323e-5
allele num: 66276
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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VQSLOD
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DP
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BaseQRankSum
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 1.27e-2

ClippingRankSum
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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: 8.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.385696040868455e-5
allele num: 15660
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

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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East Asian
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FS
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SIO_000300: 2.398e0

InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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QD
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 47

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15724
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 5.451171421943865e-3
allele num: 8622
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Latino
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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 frequency: 0.0e0
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num of homozygotes: 0

MQ
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SIO_000300: 5.97e1

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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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: 2
allele frequency: 3.008423586040914e-5
allele num: 66480
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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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
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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South Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
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allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

BaseQRankSum
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SIO_000300: -2.89e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 2.311e0

DP
type: SiteQuality
SIO_000300: 1.879193e6

QD
type: SiteQuality
SIO_000300: 1.083e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 21
allele frequency: 3.147293327738145e-4
allele num: 66724
num of homozygotes: 0

MQ
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SIO_000300: 5.957e1

MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: -1.738e0

DP
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ClippingRankSum
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SIO_000300: -5.52e-1

QD
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VQSLOD
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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ClippingRankSum
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SIO_000300: -4.66e-1

DP
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.094e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.87928e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.303e1

DP
type: SiteQuality
SIO_000300: 1.879311e6

FS
type: SiteQuality
SIO_000300: 9.105e0

InbreedingCoeff
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.83e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
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allele frequency: 3.028100775193798e-4
allele num: 16512
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 frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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MQRankSum
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SIO_000300: 3.17e-1

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

Latino
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

South Asian
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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East Asian
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Finnish)
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QD
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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 count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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East Asian
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allele frequency: 1.159554730983302e-4
allele num: 8624
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DP
type: SiteQuality
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.2e-3

BaseQRankSum
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SIO_000300: -1.933e0

VQSLOD
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MQRankSum
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SIO_000300: 1.06e0

ReadPosRankSum
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SIO_000300: 1.2e0

QD
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 3.060599877576005e-4
allele num: 9802
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 (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

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

FS
type: SiteQuality
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QD
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MQ
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.32e0

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
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allele frequency: 1.160092807424594e-4
allele num: 8620
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South Asian
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MQRankSum
type: SiteQuality
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FS
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ReadPosRankSum
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DP
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.5e-3

VQSLOD
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SIO_000300: 1.3e-1

ClippingRankSum
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SIO_000300: 9.31e-1

BaseQRankSum
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SIO_000300: 3.32e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 3.079e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.878701e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.52e-2

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
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DP
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QD
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ClippingRankSum
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MQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.011421701232342e-5
allele num: 66540
num of homozygotes: 0

African
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allele frequency: 1.023960679909891e-4
allele num: 9766
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.803e1

ClippingRankSum
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SIO_000300: 3.28e0

FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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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: 0

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

Latino
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allele count: 60
allele frequency: 5.184929139301763e-3
allele num: 11572
num of homozygotes: 0

South Asian
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allele count: 190
allele frequency: 1.150817686250757e-2
allele num: 16510
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African
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allele frequency: 1.326259946949602e-3
allele num: 9802
num of homozygotes: 0

European (Finnish)
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allele count: 57
allele frequency: 8.618082854550952e-3
allele num: 6614
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: 11
allele frequency: 1.222222222222222e-2
allele num: 900
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European (Non-Finnish)
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allele count: 1054
allele frequency: 1.579310138152177e-2
allele num: 66738
num of homozygotes: 10

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1024
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.05e0

DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.788e0

FS
type: SiteQuality
SIO_000300: 6.0826e1

MQ
type: SiteQuality
SIO_000300: 5.721e1

MQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

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

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

GenotypeQuality
all individuals: 4473
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 1.839967e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 1.0345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.567e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.886e0

QD
type: SiteQuality
SIO_000300: 1.61e1

GenotypeQuality
all individuals: 1018
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

FS
type: SiteQuality
SIO_000300: 5.797e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

DP
type: SiteQuality
SIO_000300: 1.835241e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 34224
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variant carriers: 0

GenotypeQuality
all individuals: 4451
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variant carriers: 15

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.250495108923963e-4
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.87e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.832548e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
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variant carriers: 0

GenotypeQuality
all individuals: 977
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 576
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32199
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variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 1955
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variant carriers: 0

GenotypeQuality
all individuals: 525
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variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

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

African
type: Population
allele count: 56
allele frequency: 5.757762697923093e-3
allele num: 9726
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.79011e6

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.445e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 15
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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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variant carriers: 0

GenotypeQuality
all individuals: 1863
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GenotypeQuality
all individuals: 30671
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.548211036992117e-4
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.75774e6

FS
type: SiteQuality
SIO_000300: 2.0992e1

VQSLOD
type: SiteQuality
SIO_000300: -3.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.121e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.937e0

GenotypeQuality
all individuals: 2756
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variant carriers: 0

GenotypeQuality
all individuals: 75
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513958699206686e-5
allele num: 66052
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16186
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.459e0

DP
type: SiteQuality
SIO_000300: 1.714996e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.355e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

QD
type: SiteQuality
SIO_000300: 7.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-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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GenotypeQuality
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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: 937
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.175889328063241e-5
allele num: 16192
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.178e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

FS
type: SiteQuality
SIO_000300: 6.495e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.029e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

DP
type: SiteQuality
SIO_000300: 1.713139e6

GenotypeQuality
all individuals: 70
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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
all individuals: 8687
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GenotypeQuality
all individuals: 3258
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029843963035904e-5
allele num: 66010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.680994e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.254e1

MQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23631
bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.032844453625284e-4
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

DP
type: SiteQuality
SIO_000300: 1.64221e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.668e0

QD
type: SiteQuality
SIO_000300: 1.051e1

FS
type: SiteQuality
SIO_000300: 3.973e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 129
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034126163391934e-4
allele num: 9670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.509e0

FS
type: SiteQuality
SIO_000300: 6.627e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 2.753e1

DP
type: SiteQuality
SIO_000300: 1.581487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

GenotypeQuality
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 86

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1102
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variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087909411907951e-5
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 83
allele frequency: 9.769303201506591e-3
allele num: 8496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514417252241338e-5
allele num: 66032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.768853034023149e-5
allele num: 11404
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

DP
type: SiteQuality
SIO_000300: 1.742368e6

GenotypeQuality
all individuals: 655
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7096
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GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.770098e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.267e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.332e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: -5.921999999999999e-1

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 573
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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
all individuals: 631
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GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.454e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-1

DP
type: SiteQuality
SIO_000300: 1.786758e6

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7310
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 334
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 495
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 255
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GenotypeQuality
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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: 41072
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variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009962977455377e-5
allele num: 66446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.49e-1

FS
type: SiteQuality
SIO_000300: 7.91e0

DP
type: SiteQuality
SIO_000300: 1.795167e6

QD
type: SiteQuality
SIO_000300: 1.545e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.415e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 73
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1531
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.241910071506484e-4
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.199e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 6.882e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 1.800103e6

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e-1

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

GenotypeQuality
all individuals: 327
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GenotypeQuality
all individuals: 1539
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GenotypeQuality
all individuals: 146
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 7412
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GenotypeQuality
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GenotypeQuality
all individuals: 361
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GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 41730
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GenotypeQuality
all individuals: 6117
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1361
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GenotypeQuality
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GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.014693951140358e-5
allele num: 66558
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

FS
type: SiteQuality
SIO_000300: 2.954e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.235e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.835e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 1.801318e6

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

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.802189e6

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6111
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1354
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999670036296008e-5
allele num: 66674
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

DP
type: SiteQuality
SIO_000300: 1.807847e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.626e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
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variant carriers: 0

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

GenotypeQuality
all individuals: 7485
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6108
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

DP
type: SiteQuality
SIO_000300: 1.809195e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

FS
type: SiteQuality
SIO_000300: 6.299e0

QD
type: SiteQuality
SIO_000300: 1.173e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.62e-1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 42362
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
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GenotypeQuality
all individuals: 6111
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.675e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

QD
type: SiteQuality
SIO_000300: 1.132e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 1.194e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.80944e6

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
all individuals: 1563
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GenotypeQuality
all individuals: 6107
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

FS
type: SiteQuality
SIO_000300: 1.546e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

DP
type: SiteQuality
SIO_000300: 1.81185e6

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

GenotypeQuality
all individuals: 48
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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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
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GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

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