22-32134705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134705
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134705
    reference: chr 22
allele count: 1
allele frequency: 4.518344478583047e-5
allele num: 22132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.142G>A
  hgvsp: ENSP00000388314.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.142G>A
  hgvsp: ENSP00000331845.6:p.Val48Ile
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11274G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.142G>A
  hgvsp: ENSP00000411129.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.142G>A
  hgvsp: ENSP00000380630.2:p.Val48Ile
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val48Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

22-32134730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134730
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134730
    reference: chr 22
allele count: 2
allele frequency: 9.025270758122743e-5
allele num: 22160
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.117C>T
  hgvsp: ENST00000327423.6:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.117C>T
  hgvsp: ENST00000434485.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.117C>T
  hgvsp: ENST00000412743.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11249C>T
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.117C>T
  hgvsp: ENST00000397493.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7323
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp39Asp
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

22-32134738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134738
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134738
    reference: chr 22
allele count: 1
allele frequency: 4.504098729844158e-5
allele num: 22202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.109C>T
  hgvsp: ENSP00000411129.1:p.His37Tyr
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.109C>T
  hgvsp: ENSP00000388314.1:p.His37Tyr
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.109C>T
  hgvsp: ENSP00000380630.2:p.His37Tyr
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.109C>T
  hgvsp: ENSP00000331845.6:p.His37Tyr
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11241C>T
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His37Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

22-32134753-CACTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134753
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134749
    reference: chr 22
allele count: 1
allele frequency: 4.496807266840543e-5
allele num: 22238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.90_93delAAGT
  hgvsp: ENSP00000380630.2:p.Val32ProfsTer12
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11222_80+11225delAAGT
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.90_93delAAGT
  hgvsp: ENSP00000331845.6:p.Val32ProfsTer12
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.90_93delAAGT
  hgvsp: ENSP00000388314.1:p.Val32ProfsTer12
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.90_93delAAGT
  hgvsp: ENSP00000411129.1:p.Val32ProfsTer12
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val32ProfsTer12
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: CACTT
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/22-32134758-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134758
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134758
    reference: chr 22
allele count: 2
allele frequency: 8.988764044943821e-5
allele num: 22250
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.89T>G
  hgvsp: ENSP00000331845.6:p.Val30Gly
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.89T>G
  hgvsp: ENSP00000380630.2:p.Val30Gly
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.89T>G
  hgvsp: ENSP00000388314.1:p.Val30Gly
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.89T>G
  hgvsp: ENSP00000411129.1:p.Val30Gly
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11221T>G
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val30Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

22-32134781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134781
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134781
    reference: chr 22
allele count: 1
allele frequency: 4.473072105922347e-5
allele num: 22356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.66G>A
  hgvsp: ENST00000412743.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.66G>A
  hgvsp: ENST00000397493.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.66G>A
  hgvsp: ENST00000434485.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.66G>A
  hgvsp: ENST00000327423.6:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11198G>A
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln22Gln
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

22-32134789-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134789
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134789
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 22396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.58G>A
  hgvsp: ENSP00000411129.1:p.Val20Met
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11190G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.58G>A
  hgvsp: ENSP00000388314.1:p.Val20Met
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.58G>A
  hgvsp: ENSP00000380630.2:p.Val20Met
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.58G>A
  hgvsp: ENSP00000331845.6:p.Val20Met
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val20Met
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

22-32134812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134812
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134812
    reference: chr 22
allele count: 1
allele frequency: 4.534736078360239e-5
allele num: 22052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.35C>T
  hgvsp: ENSP00000380630.2:p.Pro12Leu
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.35C>T
  hgvsp: ENSP00000411129.1:p.Pro12Leu
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.35C>T
  hgvsp: ENSP00000331845.6:p.Pro12Leu
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11167C>T
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.35C>T
  hgvsp: ENSP00000388314.1:p.Pro12Leu
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro12Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS

22-32134824-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134824
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134824
    reference: chr 22
allele count: 1
allele frequency: 4.610844706750277e-5
allele num: 21688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.23C>G
  hgvsp: ENSP00000388314.1:p.Thr8Ser
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.23C>G
  hgvsp: ENSP00000331845.6:p.Thr8Ser
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.23C>G
  hgvsp: ENSP00000380630.2:p.Thr8Ser
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11155C>G
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.23C>G
  hgvsp: ENSP00000411129.1:p.Thr8Ser
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr8Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

22-32134833-CCAGATGACAGCATTAGGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134833
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134815
    reference: chr 22
allele count: 2
allele frequency: 9.589566551591868e-5
allele num: 20856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: coding sequence
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5444
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: CCAGATGACAGCATTAGGA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-32134871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32134871
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32134871
    reference: chr 22
allele count: 9
allele frequency: 5.277973258268825e-4
allele num: 17052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000388314
  ensembl transcript: ENST00000434485
  gene symbol: PRR14L
  hgvsc: ENST00000434485.1:c.-25G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000411129
  ensembl transcript: ENST00000412743
  gene symbol: PRR14L
  hgvsc: ENST00000412743.1:c.-25G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000331845
  ensembl transcript: ENST00000327423
  gene symbol: PRR14L
  hgvsc: ENST00000327423.6:c.-25G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183530
  ensembl transcript: ENST00000461722
  gene symbol: PRR14L
  hgvsc: ENST00000461722.1:n.80+11108G>A
  variant of: http://identifiers.org/hgnc/28738
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183530
  ensembl protein: ENSP00000380630
  ensembl transcript: ENST00000397493
  gene symbol: PRR14L
  hgvsc: ENST00000397493.2:c.-25G>A
  variant of: http://identifiers.org/hgnc/28738
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

22-32150857-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150857
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150857
    reference: chr 22
allele count: 1
allele frequency: 8.291873963515755e-6
allele num: 120600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-51A>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.37A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-51A>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

22-32150861-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150861
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150861
    reference: chr 22
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-47C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.41C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-47C>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

22-32150866-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150866
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150866
    reference: chr 22
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-42C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.46C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-42C>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

22-32150871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150871
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150871
    reference: chr 22
allele count: 2
allele frequency: 1.657550140891762e-5
allele num: 120660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-37C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.51C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-37C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7590
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9525
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/22-32150874-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150874
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150874
    reference: chr 22
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-34A>C
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.54A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

22-32150875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150875
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150875
    reference: chr 22
allele count: 2
allele frequency: 1.657247974014352e-5
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-33G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.55G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-33G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

22-32150880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150880
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150880
    reference: chr 22
allele count: 3
allele frequency: 2.485665992774998e-5
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-28G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.60G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9594
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7609
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

22-32150886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150886
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150886
    reference: chr 22
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-22C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.66C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-32150890-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150890
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150889
    reference: chr 22
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.73delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-15delG
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: AG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

22-32150894-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150894
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150894
    reference: chr 22
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-14A>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.74A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

22-32150898-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150898
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150898
    reference: chr 22
allele count: 4
allele frequency: 3.312794010468429e-5
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-10A>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.78A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/22-32150900-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150900
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150900
    reference: chr 22
allele count: 6
allele frequency: 4.968944099378882e-5
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-8A>C
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.80A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

22-32150902-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150902
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150902
    reference: chr 22
allele count: 6
allele frequency: 4.969026402093616e-5
allele num: 120748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.-6T>C
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.82T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

22-32150912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150912
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150912
    reference: chr 22
allele count: 4
allele frequency: 3.312245371137094e-5
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.5G>A
  hgvsp: ENSP00000416314.1:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000371545.2:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000371539.2:p.Arg2Lys
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.92G>A
  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.5G>A
  hgvsp: ENSP00000440210.1:p.Arg2Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.5G>A
  hgvsp: ENSP00000405351.1:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000383107.1:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000266091.3:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000383105.1:p.Arg2Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.5G>A
  hgvsp: ENSP00000441358.1:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000371546.3:p.Arg2Lys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.5G>A
  hgvsp: ENSP00000383101.3:p.Arg2Lys
  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.5G>A
  hgvsp: ENSP00000383108.2:p.Arg2Lys
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2Lys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32150921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150921
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150921
    reference: chr 22
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.14A>G
  hgvsp: ENSP00000405351.1:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000383105.1:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000371539.2:p.Lys5Arg
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.101A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.14A>G
  hgvsp: ENSP00000441358.1:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000371546.3:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000440210.1:p.Lys5Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.14A>G
  hgvsp: ENSP00000383101.3:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000383108.2:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000383107.1:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000371545.2:p.Lys5Arg
  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.14A>G
  hgvsp: ENSP00000266091.3:p.Lys5Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.14A>G
  hgvsp: ENSP00000416314.1:p.Lys5Arg
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys5Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

22-32150927-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150927
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150927
    reference: chr 22
allele count: 7
allele frequency: 5.796333405097461e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.20A>G
  hgvsp: ENSP00000440210.1:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000383105.1:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000383108.2:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000383107.1:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.20A>G
  hgvsp: ENSP00000441358.1:p.Tyr7Cys
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.107A>G
  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.20A>G
  hgvsp: ENSP00000371539.2:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.20A>G
  hgvsp: ENSP00000405351.1:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000266091.3:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000371546.3:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.20A>G
  hgvsp: ENSP00000383101.3:p.Tyr7Cys
  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.20A>G
  hgvsp: ENSP00000371545.2:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.20A>G
  hgvsp: ENSP00000416314.1:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr7Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

22-32150928-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150928
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150928
    reference: chr 22
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.21C>G
  hgvsp: ENSP00000383107.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.21C>G
  hgvsp: ENSP00000371539.2:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.21C>G
  hgvsp: ENSP00000266091.3:p.Tyr7Ter
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.108C>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.21C>G
  hgvsp: ENSP00000383101.3:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371546
  ensembl transcript: ENST00000382112
  gene symbol: DEPDC5
  hgvsc: ENST00000382112.3:c.21C>G
  hgvsp: ENSP00000371546.3:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.21C>G
  hgvsp: ENSP00000383105.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.21C>G
  hgvsp: ENSP00000371545.2:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.21C>G
  hgvsp: ENSP00000405351.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.21C>G
  hgvsp: ENSP00000441358.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.21C>G
  hgvsp: ENSP00000416314.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.21C>G
  hgvsp: ENSP00000383108.2:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.21C>G
  hgvsp: ENSP00000440210.1:p.Tyr7Ter
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr7Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

22-32150934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150934
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150934
    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: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.27C>T
  hgvsp: ENST00000400248.2:c.27C>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: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.27C>T
  hgvsp: ENST00000456178.1:c.27C>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.27C>T
  hgvsp: ENST00000400249.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.27C>T
  hgvsp: ENST00000400242.3:c.27C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.114C>T
  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.27C>T
  hgvsp: ENST00000535622.1:c.27C>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.27C>T
  hgvsp: ENST00000266091.3:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.27C>T
  hgvsp: ENST00000437411.1:c.27C>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.27C>T
  hgvsp: ENST00000382105.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.27C>T
  hgvsp: ENST00000536766.1:c.27C>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.27C>T
  hgvsp: ENST00000382112.3:c.27C>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.27C>T
  hgvsp: ENST00000382111.2:c.27C>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.27C>T
  hgvsp: ENST00000400246.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu9Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

22-32150935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150935
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150935
    reference: chr 22
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.28G>A
  hgvsp: ENSP00000266091.3:p.Val10Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.28G>A
  hgvsp: ENSP00000441358.1:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000440210.1:p.Val10Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.28G>A
  hgvsp: ENSP00000383101.3:p.Val10Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.28G>A
  hgvsp: ENSP00000416314.1:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000371539.2:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000371545.2:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000383107.1:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000383105.1:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000371546.3:p.Val10Ile
  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.28G>A
  hgvsp: ENSP00000383108.2:p.Val10Ile
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.28G>A
  hgvsp: ENSP00000405351.1:p.Val10Ile
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.115G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val10Ile
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

22-32150949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150949
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150949
    reference: chr 22
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383107
  ensembl transcript: ENST00000400248
  gene symbol: DEPDC5
  hgvsc: ENST00000400248.2:c.42G>A
  hgvsp: ENST00000400248.2:c.42G>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.42G>A
  hgvsp: ENST00000400249.2:c.42G>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.42G>A
  hgvsp: ENST00000535622.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.42G>A
  hgvsp: ENST00000400242.3:c.42G>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.42G>A
  hgvsp: ENST00000382111.2:c.42G>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.42G>A
  hgvsp: ENST00000400246.1:c.42G>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.42G>A
  hgvsp: ENST00000266091.3:c.42G>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.42G>A
  hgvsp: ENST00000382112.3:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.42G>A
  hgvsp: ENST00000536766.1:c.42G>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: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.42G>A
  hgvsp: ENST00000456178.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.42G>A
  hgvsp: ENST00000437411.1:c.42G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.129G>A
  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.42G>A
  hgvsp: ENST00000382105.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys14Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

22-32150951-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150951
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150951
    reference: chr 22
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.44G>C
  hgvsp: ENSP00000371545.2:p.Gly15Ala
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.44G>C
  hgvsp: ENSP00000441358.1:p.Gly15Ala
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.131G>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.44G>C
  hgvsp: ENSP00000266091.3:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000383105.1:p.Gly15Ala
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.44G>C
  hgvsp: ENSP00000416314.1:p.Gly15Ala
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.44G>C
  hgvsp: ENSP00000405351.1:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000371539.2:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000371546.3:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000383107.1:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000383108.2:p.Gly15Ala
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.44G>C
  hgvsp: ENSP00000383101.3:p.Gly15Ala
  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.44G>C
  hgvsp: ENSP00000440210.1:p.Gly15Ala
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly15Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

22-32150952-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150952
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150952
    reference: chr 22
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.45C>T
  hgvsp: ENST00000456178.1:c.45C>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.45C>T
  hgvsp: ENST00000382111.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.45C>T
  hgvsp: ENST00000400242.3:c.45C>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.45C>T
  hgvsp: ENST00000400249.2:c.45C>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.45C>T
  hgvsp: ENST00000266091.3:c.45C>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.45C>T
  hgvsp: ENST00000382112.3:c.45C>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.45C>T
  hgvsp: ENST00000382105.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.45C>T
  hgvsp: ENST00000536766.1:c.45C>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.45C>T
  hgvsp: ENST00000400246.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.45C>T
  hgvsp: ENST00000437411.1:c.45C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.132C>T
  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.45C>T
  hgvsp: ENST00000400248.2:c.45C>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.45C>T
  hgvsp: ENST00000535622.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly15Gly
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

22-32150968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150968
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150968
    reference: chr 22
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
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.58+3C>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.58+3C>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.58+3C>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: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+3C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+3C>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.58+3C>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.58+3C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+3C>T
  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.58+3C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+3C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.148C>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.58+3C>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.58+3C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.58+3C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-32150972-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150972
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150972
    reference: chr 22
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+7A>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.58+7A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+7A>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: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+7A>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.152A>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.58+7A>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.58+7A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+7A>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.58+7A>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.58+7A>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.58+7A>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.58+7A>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.58+7A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.58+7A>G
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-32150974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150974
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150974
    reference: chr 22
allele count: 4
allele frequency: 3.312958637711408e-5
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+9C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+9C>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.58+9C>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.58+9C>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.58+9C>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.58+9C>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.58+9C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+9C>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.58+9C>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.154C>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.58+9C>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.58+9C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+9C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

22-32150975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150975
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150975
    reference: chr 22
allele count: 2
allele frequency: 1.656534199148542e-5
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.58+10G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+10G>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.58+10G>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.58+10G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+10G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.155G>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.58+10G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+10G>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.58+10G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+10G>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.58+10G>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.58+10G>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.58+10G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

22-32150976-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150976
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150976
    reference: chr 22
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100150
  ensembl transcript: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.156A>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.58+11A>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.58+11A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+11A>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.58+11A>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.58+11A>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.58+11A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+11A>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.58+11A>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.58+11A>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.58+11A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+11A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+11A>T
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-32150977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150977
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150977
    reference: chr 22
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.58+12T>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.58+12T>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.58+12T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+12T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+12T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+12T>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.58+12T>C
  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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.157T>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.58+12T>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.58+12T>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.58+12T>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.58+12T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+12T>C
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

22-32150980-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150980
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150980
    reference: chr 22
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.58+15G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+15G>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.58+15G>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.58+15G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.160G>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.58+15G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+15G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+15G>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.58+15G>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.58+15G>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.58+15G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+15G>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.58+15G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-32150987-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150987
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150987
    reference: chr 22
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
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.58+22G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+22G>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.58+22G>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.58+22G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.167G>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.58+22G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+22G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+22G>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.58+22G>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.58+22G>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.58+22G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+22G>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.58+22G>T
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32150997-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32150997
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32150997
    reference: chr 22
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+32A>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.58+32A>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.58+32A>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.58+32A>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.58+32A>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.58+32A>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.58+32A>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.177A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+32A>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.58+32A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+32A>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.58+32A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+32A>T
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

22-32151003-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32151003
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32151003
    reference: chr 22
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.58+38G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.183G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+38G>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.58+38G>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.58+38G>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.58+38G>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.58+38G>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.58+38G>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.58+38G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+38G>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.58+38G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+38G>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+38G>T
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

22-32151006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32151006
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32151006
    reference: chr 22
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.58+41G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.186G>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.58+41G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+41G>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.58+41G>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.58+41G>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.58+41G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+41G>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.58+41G>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.58+41G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+41G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+41G>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.58+41G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-32151008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32151008
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32151008
    reference: chr 22
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.58+43G>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.58+43G>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.58+43G>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.58+43G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.58+43G>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.58+43G>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.58+43G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.58+43G>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: ENST00000469969
  gene symbol: DEPDC5
  hgvsc: ENST00000469969.1:n.188G>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.58+43G>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.58+43G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.58+43G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.58+43G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

22-32154473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154473
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154473
    reference: chr 22
allele count: 3
allele frequency: 2.553452267465614e-5
allele num: 117488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371539
  ensembl transcript: ENST00000382105
  gene symbol: DEPDC5
  hgvsc: ENST00000382105.2:c.59-59G>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.59-59G>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.59-59G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-40G>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.59-59G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-59G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-59G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-59G>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.59-59G>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.59-59G>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.59-59G>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.59-59G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

22-32154475-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154475
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154475
    reference: chr 22
allele count: 404
allele frequency: 3.434322826345676e-3
allele num: 117636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-57A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-57A>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.59-57A>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.59-57A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-38A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-57A>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.59-57A>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.59-57A>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.59-57A>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.59-57A>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.59-57A>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.59-57A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 1.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 3.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 2.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20683
  bin: 2.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 5
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

22-32154480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154480
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154480
    reference: chr 22
allele count: 1
allele frequency: 8.483922965979469e-6
allele num: 117870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-33C>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.59-52C>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.59-52C>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.59-52C>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.59-52C>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.59-52C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-52C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-52C>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.59-52C>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-52C>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.59-52C>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.59-52C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

22-32154480-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154480
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154478
    reference: chr 22
allele count: 1
allele frequency: 8.483922965979469e-6
allele num: 117870
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.59-51_59-50delAG
  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.59-51_59-50delAG
  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.59-51_59-50delAG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-51_59-50delAG
  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.59-51_59-50delAG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-51_59-50delAG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-51_59-50delAG
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-32_59-31delAG
  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.59-51_59-50delAG
  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.59-51_59-50delAG
  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.59-51_59-50delAG
  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.59-51_59-50delAG
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23546
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: CAG
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

22-32154482-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154482
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154482
    reference: chr 22
allele count: 178
allele frequency: 1.508244505075497e-3
allele num: 118018
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.59-50G>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.59-50G>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.59-50G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-50G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-50G>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.59-50G>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.59-50G>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.59-50G>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.59-50G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-50G>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-31G>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.59-50G>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12012
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 24221
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 3.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

22-32154484-GTACCTAATGAGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154484
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154472
    reference: chr 22
allele count: 1
allele frequency: 8.462957634434082e-6
allele num: 118162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  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
  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
  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
  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
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  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
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  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
  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
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6948
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: GTACCTAATGAGT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

22-32154484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154484
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154484
    reference: chr 22
allele count: 1
allele frequency: 8.462957634434082e-6
allele num: 118162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-29G>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.59-48G>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.59-48G>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.59-48G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-48G>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.59-48G>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.59-48G>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.59-48G>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.59-48G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-48G>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.59-48G>A
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-48G>A
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-32154485-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154485
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154485
    reference: chr 22
allele count: 1
allele frequency: 8.45594452900389e-6
allele num: 118260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.59-47T>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.59-47T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-28T>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.59-47T>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.59-47T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-47T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-47T>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.59-47T>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.59-47T>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.59-47T>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.59-47T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-47T>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25019
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

22-32154494-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154494
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154494
    reference: chr 22
allele count: 1
allele frequency: 8.381527114240214e-6
allele num: 119310
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.59-38A>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.59-38A>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.59-38A>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.59-38A>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.59-38A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-38A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-38A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-19A>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.59-38A>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.59-38A>T
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-38A>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.59-38A>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32154502-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154502
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154502
    reference: chr 22
allele count: 265
allele frequency: 2.210691404164442e-3
allele num: 119872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000266091
  ensembl transcript: ENST00000266091
  gene symbol: DEPDC5
  hgvsc: ENST00000266091.3:c.59-30T>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.59-30T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.59-11T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.59-30T>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.59-30T>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.59-30T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.59-30T>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.59-30T>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.59-30T>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.59-30T>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.59-30T>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.59-30T>C
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 27069
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13721
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

22-32154539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154539
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154539
    reference: chr 22
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.66G>A
  hgvsp: ENST00000400246.1:c.66G>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.66G>A
  hgvsp: ENST00000382112.3:c.66G>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.66G>A
  hgvsp: ENST00000382111.2:c.66G>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.66G>A
  hgvsp: ENST00000400249.2:c.66G>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.66G>A
  hgvsp: ENST00000535622.1:c.66G>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.66G>A
  hgvsp: ENST00000266091.3:c.66G>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.66G>A
  hgvsp: ENST00000382105.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.66G>A
  hgvsp: ENST00000437411.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*4G>A
  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.66G>A
  hgvsp: ENST00000400248.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.66G>A
  hgvsp: ENST00000536766.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.66G>A
  hgvsp: ENST00000400242.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu22Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

22-32154542-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154542
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154542
    reference: chr 22
allele count: 3
allele frequency: 2.484718978283556e-5
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*7A>G
  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.69A>G
  hgvsp: ENST00000400248.2:c.69A>G(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.69A>G
  hgvsp: ENST00000382105.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.69A>G
  hgvsp: ENST00000536766.1:c.69A>G(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.69A>G
  hgvsp: ENST00000400249.2:c.69A>G(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.69A>G
  hgvsp: ENST00000266091.3:c.69A>G(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.69A>G
  hgvsp: ENST00000535622.1:c.69A>G(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.69A>G
  hgvsp: ENST00000400246.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.69A>G
  hgvsp: ENST00000400242.3:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.69A>G
  hgvsp: ENST00000437411.1:c.69A>G(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.69A>G
  hgvsp: ENST00000382112.3:c.69A>G(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.69A>G
  hgvsp: ENST00000382111.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu23Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

22-32154544-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154544
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154544
    reference: chr 22
allele count: 41
allele frequency: 3.395557616815464e-4
allele num: 120746
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.71T>G
  hgvsp: ENSP00000383105.1:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000371539.2:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000371546.3:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000266091.3:p.Val24Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.71T>G
  hgvsp: ENSP00000416314.1:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000371545.2:p.Val24Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.71T>G
  hgvsp: ENSP00000383101.3:p.Val24Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*9T>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.71T>G
  hgvsp: ENSP00000383107.1:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000383108.2:p.Val24Gly
  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.71T>G
  hgvsp: ENSP00000440210.1:p.Val24Gly
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.71T>G
  hgvsp: ENSP00000441358.1:p.Val24Gly
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val24Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

22-32154549-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154549
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154549
    reference: chr 22
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000440210
  ensembl transcript: ENST00000535622
  gene symbol: DEPDC5
  hgvsc: ENST00000535622.1:c.76A>G
  hgvsp: ENSP00000440210.1:p.Asn26Asp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.76A>G
  hgvsp: ENSP00000383101.3:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000371545.2:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000371546.3:p.Asn26Asp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.76A>G
  hgvsp: ENSP00000416314.1:p.Asn26Asp
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.76A>G
  hgvsp: ENSP00000441358.1:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000266091.3:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000371539.2:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000383105.1:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000383108.2:p.Asn26Asp
  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.76A>G
  hgvsp: ENSP00000383107.1:p.Asn26Asp
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn26Asp
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

22-32154563-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154563
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154563
    reference: chr 22
allele count: 8
allele frequency: 6.624819887709302e-5
allele num: 120758
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.90C>G
  hgvsp: ENSP00000371539.2:p.Phe30Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*28C>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.90C>G
  hgvsp: ENSP00000440210.1:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000371545.2:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000383108.2:p.Phe30Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.90C>G
  hgvsp: ENSP00000441358.1:p.Phe30Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.90C>G
  hgvsp: ENSP00000416314.1:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000383105.1:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000266091.3:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000383107.1:p.Phe30Leu
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.90C>G
  hgvsp: ENSP00000383101.3:p.Phe30Leu
  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.90C>G
  hgvsp: ENSP00000371546.3:p.Phe30Leu
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Phe30Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-32154563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154563
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154563
    reference: chr 22
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.90C>T
  hgvsp: ENST00000382111.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.90C>T
  hgvsp: ENST00000400242.3:c.90C>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.90C>T
  hgvsp: ENST00000382105.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.90C>T
  hgvsp: ENST00000536766.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.90C>T
  hgvsp: ENST00000437411.1:c.90C>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.90C>T
  hgvsp: ENST00000266091.3:c.90C>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.90C>T
  hgvsp: ENST00000382112.3:c.90C>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.90C>T
  hgvsp: ENST00000400248.2:c.90C>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.90C>T
  hgvsp: ENST00000535622.1:c.90C>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.90C>T
  hgvsp: ENST00000400246.1:c.90C>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.90C>T
  hgvsp: ENST00000400249.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*28C>T
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe30Phe
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

22-32154568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154568
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154568
    reference: chr 22
allele count: 3
allele frequency: 2.484307457890989e-5
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.95A>G
  hgvsp: ENSP00000441358.1:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000383107.1:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000371545.2:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000266091.3:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000383105.1:p.His32Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.95A>G
  hgvsp: ENSP00000383101.3:p.His32Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.95A>G
  hgvsp: ENSP00000416314.1:p.His32Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*33A>G
  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.95A>G
  hgvsp: ENSP00000371539.2:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000383108.2:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000371546.3:p.His32Arg
  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.95A>G
  hgvsp: ENSP00000440210.1:p.His32Arg
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His32Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-32154575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154575
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154575
    reference: chr 22
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.102G>A
  hgvsp: ENST00000437411.1:c.102G>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.102G>A
  hgvsp: ENST00000382112.3:c.102G>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.102G>A
  hgvsp: ENST00000400246.1:c.102G>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.102G>A
  hgvsp: ENST00000535622.1:c.102G>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.102G>A
  hgvsp: ENST00000266091.3:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.102G>A
  hgvsp: ENST00000536766.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*40G>A
  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.102G>A
  hgvsp: ENST00000382105.2:c.102G>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.102G>A
  hgvsp: ENST00000382111.2:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.102G>A
  hgvsp: ENST00000400242.3:c.102G>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.102G>A
  hgvsp: ENST00000400249.2:c.102G>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.102G>A
  hgvsp: ENST00000400248.2:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys34Lys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

22-32154579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154579
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154579
    reference: chr 22
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383105
  ensembl transcript: ENST00000400246
  gene symbol: DEPDC5
  hgvsc: ENST00000400246.1:c.106G>A
  hgvsp: ENSP00000383105.1:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000266091.3:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000371539.2:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*44G>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.106G>A
  hgvsp: ENSP00000383107.1:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000371545.2:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.106G>A
  hgvsp: ENSP00000416314.1:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000440210.1:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.106G>A
  hgvsp: ENSP00000383101.3:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000383108.2:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.106G>A
  hgvsp: ENSP00000441358.1:p.Gly36Arg
  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.106G>A
  hgvsp: ENSP00000371546.3:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly36Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-32154585-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154585
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154585
    reference: chr 22
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.112A>G
  hgvsp: ENSP00000441358.1:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000440210.1:p.Ile38Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.112A>G
  hgvsp: ENSP00000416314.1:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000371546.3:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000371545.2:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000383107.1:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000266091.3:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000371539.2:p.Ile38Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.112A>G
  hgvsp: ENSP00000383101.3:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000383108.2:p.Ile38Val
  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.112A>G
  hgvsp: ENSP00000383105.1:p.Ile38Val
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile38Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-32154587-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154587
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154587
    reference: chr 22
allele count: 4
allele frequency: 3.312355084465055e-5
allele num: 120760
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.114T>G
  hgvsp: ENSP00000371539.2:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000371545.2:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000383105.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.114T>G
  hgvsp: ENSP00000416314.1:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000383107.1:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000266091.3:p.Ile38Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.114T>G
  hgvsp: ENSP00000383101.3:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000383108.2:p.Ile38Met
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*52T>G
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.114T>G
  hgvsp: ENSP00000441358.1:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000371546.3:p.Ile38Met
  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.114T>G
  hgvsp: ENSP00000440210.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile38Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

22-32154600-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154600
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154600
    reference: chr 22
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000371545
  ensembl transcript: ENST00000382111
  gene symbol: DEPDC5
  hgvsc: ENST00000382111.2:c.127C>T
  hgvsp: ENSP00000371545.2:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000383107.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.127C>T
  hgvsp: ENSP00000383101.3:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000371539.2:p.His43Tyr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*65C>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.127C>T
  hgvsp: ENSP00000371546.3:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000383108.2:p.His43Tyr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.127C>T
  hgvsp: ENSP00000416314.1:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000266091.3:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000440210.1:p.His43Tyr
  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.127C>T
  hgvsp: ENSP00000383105.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.127C>T
  hgvsp: ENSP00000441358.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His43Tyr
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/22-32154601-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32154601
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32154601
    reference: chr 22
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383108
  ensembl transcript: ENST00000400249
  gene symbol: DEPDC5
  hgvsc: ENST00000400249.2:c.128A>C
  hgvsp: ENSP00000383108.2:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000371539.2:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000383107.1:p.His43Pro
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000416314
  ensembl transcript: ENST00000437411
  gene symbol: DEPDC5
  hgvsc: ENST00000437411.1:c.128A>C
  hgvsp: ENSP00000416314.1:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000371546.3:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000383105.1:p.His43Pro
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000383101
  ensembl transcript: ENST00000400242
  gene symbol: DEPDC5
  hgvsc: ENST00000400242.3:c.128A>C
  hgvsp: ENSP00000383101.3:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000266091.3:p.His43Pro
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000405351
  ensembl transcript: ENST00000456178
  gene symbol: DEPDC5
  hgvsc: ENST00000456178.1:c.*66A>C
  variant of: http://identifiers.org/hgnc/18423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100150
  ensembl protein: ENSP00000441358
  ensembl transcript: ENST00000536766
  gene symbol: DEPDC5
  hgvsc: ENST00000536766.1:c.128A>C
  hgvsp: ENSP00000441358.1:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000371545.2:p.His43Pro
  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.128A>C
  hgvsp: ENSP00000440210.1:p.His43Pro
  variant of: http://identifiers.org/hgnc/18423
canonical: true
consequence: missense
filter: PASS
hgvs: p.His43Pro
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.098177026136613e-4
allele num: 9106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.57907e5

FS
type: SiteQuality
SIO_000300: 9.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.46e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.527167045741723e-4
allele num: 7914
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.641e0

FS
type: SiteQuality
SIO_000300: 4.0168e1

DP
type: SiteQuality
SIO_000300: 3.58471e5

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.092896174863388e-4
allele num: 9150
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.68e1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.526e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.205e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 7.451e0

DP
type: SiteQuality
SIO_000300: 3.58557e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-1

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.089561996077577e-4
allele num: 9178
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.118e0

MQ
type: SiteQuality
SIO_000300: 5.812e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

DP
type: SiteQuality
SIO_000300: 3.59066e5

MQRankSum
type: SiteQuality
SIO_000300: -6.43e-1

QD
type: SiteQuality
SIO_000300: 1.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

GenotypeQuality
all individuals: 861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1823
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 150
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.527805864509606e-4
allele num: 7912
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2226
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

DP
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SIO_000300: 3.59286e5

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 1.344e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 246
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 frequency: 1.075037626316921e-4
allele num: 9302
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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.58952e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

ClippingRankSum
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SIO_000300: -2.539e0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

African
type: Population
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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: 588
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1660
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
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FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.401e-1

ReadPosRankSum
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SIO_000300: -1.159e0

DP
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SIO_000300: 3.58466e5

InbreedingCoeff
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SIO_000300: -6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 7.79e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1684
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.294330830960394e-4
allele num: 7726
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2256
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9234
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.195e0

MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -6.0e-3

QD
type: SiteQuality
SIO_000300: 1.511e1

FS
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SIO_000300: 0.0e0

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2224
num of homozygotes: 0

South Asian
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allele frequency: 1.330849081714134e-4
allele num: 7514
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

QD
type: SiteQuality
SIO_000300: 5.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

DP
type: SiteQuality
SIO_000300: 3.43932e5

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2200
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.837684449489217e-4
allele num: 7048
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.004e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 2.82e0

MQRankSum
type: SiteQuality
SIO_000300: -2.233e0

MQ
type: SiteQuality
SIO_000300: 5.348e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 3.31643e5

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1682
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.438553226469379e-3
allele num: 4866
num of homozygotes: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.316135825217162e-4
allele num: 7598
num of homozygotes: 0

Latino
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allele frequency: 3.496503496503497e-3
allele num: 286
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.70286e5

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
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SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

InbreedingCoeff
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SIO_000300: -5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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African
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allele count: 0
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Other
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

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

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

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

European (Non-Finnish)
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allele num: 66634
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66656
num of homozygotes: 0

African
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South Asian
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Other
type: Population
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Latino
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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QD
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.428e0

MQ
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SIO_000300: 5.922e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
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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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele num: 11554
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 9.299999999999999e-3

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8624
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

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

Other
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FS
type: SiteQuality
SIO_000300: 1.1366e1

ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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SIO_000300: 2.946606e6

QD
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SIO_000300: 1.756e1

MQRankSum
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SIO_000300: -1.233e0

ReadPosRankSum
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SIO_000300: 1.95e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

African
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Other
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South Asian
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Latino
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allele num: 11560
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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QD
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DP
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ClippingRankSum
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MQ
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SIO_000300: 5.968e1

MQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

South Asian
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African
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66690
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
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SIO_000300: 1.11e-2

BaseQRankSum
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SIO_000300: 2.61e0

MQRankSum
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SIO_000300: 2.23e0

ReadPosRankSum
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SIO_000300: 2.27e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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QD
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VQSLOD
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SIO_000300: -1.419e0

DP
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SIO_000300: 2.951383e6

MQ
type: SiteQuality
SIO_000300: 5.898e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.32e1

FS
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InbreedingCoeff
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MQRankSum
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SIO_000300: -2.94e-1

BaseQRankSum
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MQ
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SIO_000300: 5.962e1

ClippingRankSum
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SIO_000300: -9.409999999999999e-1

VQSLOD
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SIO_000300: 1.12e0

ReadPosRankSum
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SIO_000300: 7.03e-1

DP
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SIO_000300: 2.951412e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.25e1
variant carriers: 0

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

East Asian
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allele count: 6
allele frequency: 6.955715279387897e-4
allele num: 8626
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
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SIO_000300: 2.9e-3

ClippingRankSum
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DP
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SIO_000300: 2.951791e6

ReadPosRankSum
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FS
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SIO_000300: 1.271e0

BaseQRankSum
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SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
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SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30372
bin: 9.75e1
variant carriers: 6

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
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: 11570
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: 900
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.253e1

ClippingRankSum
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BaseQRankSum
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SIO_000300: 2.0e0

InbreedingCoeff
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SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 1.251e0

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.951669e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.019991840065279e-4
allele num: 9804
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: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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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: 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 frequency: 0.0e0
allele num: 900
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6
allele frequency: 6.955715279387897e-4
allele num: 8626
num of homozygotes: 0

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

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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QD
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MQRankSum
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SIO_000300: -6.879999999999999e-1

BaseQRankSum
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FS
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SIO_000300: 7.729e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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SIO_000300: 2.951962e6

VQSLOD
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GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

South Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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SIO_000300: 5.963e1

VQSLOD
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SIO_000300: 1.66e0

BaseQRankSum
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SIO_000300: -7.04e-1

DP
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SIO_000300: 2.952223e6

FS
type: SiteQuality
SIO_000300: 1.111e0

InbreedingCoeff
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SIO_000300: 1.0e-3

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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bin: 9.25e1
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: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 900
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

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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FS
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SIO_000300: 6.794e0

ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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BaseQRankSum
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QD
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SIO_000300: 1.42e1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 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
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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Other
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allele num: 900
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East Asian
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South Asian
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African
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allele frequency: 1.020199959192002e-4
allele num: 9802
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Latino
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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FS
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Latino
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num of homozygotes: 0

European (Finnish)
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South Asian
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African
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: -1.633e0

FS
type: SiteQuality
SIO_000300: 8.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.841e1

InbreedingCoeff
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SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-3

QD
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SIO_000300: 1.248e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 7.75e1
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Other
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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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
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SIO_000300: 2.425e0

ReadPosRankSum
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SIO_000300: 4.57e-1

VQSLOD
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QD
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MQRankSum
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SIO_000300: 1.13e-1

BaseQRankSum
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SIO_000300: 3.25e0

DP
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SIO_000300: 2.951544e6

ClippingRankSum
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SIO_000300: -6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995563283170454e-5
allele num: 66716
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 1.179e0

InbreedingCoeff
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SIO_000300: 2.9e-3

MQRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.89e0

DP
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SIO_000300: 2.951678e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

VQSLOD
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SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.384e1

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

InbreedingCoeff
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FS
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.32e-1

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.951341e6

QD
type: SiteQuality
SIO_000300: 1.282e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66716
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11568
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

African
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allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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FS
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.058403004967891e-5
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num of homozygotes: 0

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

Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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FS
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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East Asian
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African
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European (Non-Finnish)
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allele num: 66712
num of homozygotes: 0

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

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: 66710
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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num of homozygotes: 0

Other
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African
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num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
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SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 2.949495e6

MQRankSum
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SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
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SIO_000300: -6.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.77e-1

ClippingRankSum
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SIO_000300: 1.48e0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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: 900
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

DP
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SIO_000300: 2.943808e6

ReadPosRankSum
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SIO_000300: 1.82e0

MQ
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SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -3.31e-1

BaseQRankSum
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SIO_000300: 1.92e0

VQSLOD
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SIO_000300: 1.04e0

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

Other
type: Population
allele count: 0
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: 11568
num of homozygotes: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.308e0

BaseQRankSum
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SIO_000300: -1.589e0

VQSLOD
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InbreedingCoeff
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SIO_000300: 8.800000000000001e-3

MQRankSum
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SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
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SIO_000300: 2.939564e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
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

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

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

DP
type: SiteQuality
SIO_000300: 2.935918e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

VQSLOD
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SIO_000300: -1.02e0

BaseQRankSum
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SIO_000300: -4.665e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
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SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 1.914e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

QD
type: SiteQuality
SIO_000300: 1.857e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 275
bin: 5.25e1
variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.271e0

BaseQRankSum
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SIO_000300: -6.159e0

MQ
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QD
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ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 2.933652e6

ClippingRankSum
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SIO_000300: -1.299e0

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

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: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.606596646397641e-5
allele num: 65124
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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Other
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East Asian
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Latino
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VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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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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variant carriers: 391

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 185
allele frequency: 2.838816597102872e-3
allele num: 65168
num of homozygotes: 0

Other
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allele frequency: 7.882882882882882e-3
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Latino
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allele frequency: 6.319971108703503e-4
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num of homozygotes: 0

East Asian
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South Asian
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allele count: 203
allele frequency: 1.267640814287498e-2
allele num: 16014
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European (Finnish)
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allele count: 2
allele frequency: 3.048780487804878e-4
allele num: 6560
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QD
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ClippingRankSum
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VQSLOD
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FS
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16038
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.531018433461939e-5
allele num: 65316
num of homozygotes: 0

African
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East Asian
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Other
type: Population
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 1.451e0

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ReadPosRankSum
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SIO_000300: 1.2e0

BaseQRankSum
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SIO_000300: -2.171e0

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.247e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

DP
type: SiteQuality
SIO_000300: 1.80465e6

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65316
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.007386056566384e-5
allele num: 11102
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 3.7e-3

VQSLOD
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MQRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.451e0

DP
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SIO_000300: 1.80465e6

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65398
num of homozygotes: 0

Latino
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allele frequency: 2.693481774106662e-4
allele num: 11138
num of homozygotes: 0

African
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allele count: 173
allele frequency: 1.794233561501763e-2
allele num: 9642
num of homozygotes: 1

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

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

Other
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allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 2.42e-1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.18e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 7.2e-3

BaseQRankSum
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SIO_000300: -1.929e0

DP
type: SiteQuality
SIO_000300: 1.817274e6

QD
type: SiteQuality
SIO_000300: 1.533e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.97021887334051e-5
allele num: 11148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65482
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.794e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ClippingRankSum
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QD
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DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16060
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.527137228551358e-5
allele num: 65482
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 3.5e-3

BaseQRankSum
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MQRankSum
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DP
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MQ
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SIO_000300: 5.747e1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
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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: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52597204419215e-5
allele num: 65532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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

MQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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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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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
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
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

East Asian
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allele num: 8528
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QD
type: SiteQuality
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -5.75e-1

GenotypeDepth
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variant carriers: 42

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10005
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variant carriers: 264

South Asian
type: Population
allele count: 12
allele frequency: 7.364674113170492e-4
allele num: 16294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.815980629539952e-3
allele num: 6608
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.232142857142857e-3
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.580611169652266e-3
allele num: 11388
num of homozygotes: 1

African
type: Population
allele count: 8
allele frequency: 8.200082000820008e-4
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 213
allele frequency: 3.210345451257009e-3
allele num: 66348
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
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QD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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DP
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SIO_000300: 1.891417e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7507
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14212
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28304
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9846
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 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: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 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: 9800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-2

DP
type: SiteQuality
SIO_000300: 1.902963e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.474e0

QD
type: SiteQuality
SIO_000300: 8.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

GenotypeDepth
all individuals: 27496
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28311
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9847
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

QD
type: SiteQuality
SIO_000300: 1.453e1

DP
type: SiteQuality
SIO_000300: 1.903224e6

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeDepth
all individuals: 14207
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 359
bin: 6.75e1
variant carriers: 5

GenotypeDepth
all individuals: 254
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 243
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4513
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9887
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3210
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.362490913496486e-3
allele num: 16508
num of homozygotes: 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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

FS
type: SiteQuality
SIO_000300: 1.988e0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.905269e6

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

GenotypeDepth
all individuals: 425
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1780
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 717
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28313
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9860
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.522e0

MQ
type: SiteQuality
SIO_000300: 5.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 5.246e0

DP
type: SiteQuality
SIO_000300: 1.90368e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

GenotypeDepth
all individuals: 239
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 425
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14228
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 201
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4516
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9867
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 8.75e1
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: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 1.90436e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.52e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.116e0

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

GenotypeDepth
all individuals: 252
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3255
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14228
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 201
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4516
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9867
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3390
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 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
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

DP
type: SiteQuality
SIO_000300: 1.90436e6

FS
type: SiteQuality
SIO_000300: 1.116e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 1.52e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

GenotypeDepth
all individuals: 14229
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1143
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9865
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
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: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e0

FS
type: SiteQuality
SIO_000300: 9.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.903987e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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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
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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: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.15e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

MQRankSum
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SIO_000300: 1.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.513e0

FS
type: SiteQuality
SIO_000300: 2.881e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.983e0

QD
type: SiteQuality
SIO_000300: 1.208e1

DP
type: SiteQuality
SIO_000300: 1.903944e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 0

GenotypeQuality
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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: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

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

East Asian
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allele 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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.154e0

FS
type: SiteQuality
SIO_000300: 3.201e0

VQSLOD
type: SiteQuality
SIO_000300: -2.942e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

QD
type: SiteQuality
SIO_000300: 2.007e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

DP
type: SiteQuality
SIO_000300: 1.903966e6

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.75e1
variant carriers: 1

GenotypeDepth
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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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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: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.868e0

QD
type: SiteQuality
SIO_000300: 1.319e1

ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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SIO_000300: 1.903961e6

BaseQRankSum
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SIO_000300: 5.649999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.452e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
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South Asian
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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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num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.09e-1

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

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

European (Finnish)
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Other
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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QD
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InbreedingCoeff
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SIO_000300: 1.38e-2