7-50611583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611583
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611583
    reference: chr 7
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.201G>A
  hgvsp: ENST00000426377.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.201G>A
  hgvsp: ENST00000380984.4:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.201G>A
  hgvsp: ENST00000357936.5:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.201G>A
  hgvsp: ENST00000444124.2:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.201G>A
  hgvsp: ENST00000431062.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.98G>A
  hgvsp: ENST00000430300.1:c.98G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.201G>A
  hgvsp: ENST00000444733.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 9.25e1
  variant carriers: 0
hgvs: c.201G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

7-50611584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611584
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611584
    reference: chr 7
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.200G>A
  hgvsp: ENSP00000399184.1:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.200G>A
  hgvsp: ENSP00000403644.2:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.97G>A
  hgvsp: ENSP00000389422.1:p.Gly33Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.200G>A
  hgvsp: ENSP00000395069.1:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.200G>A
  hgvsp: ENSP00000393724.1:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.200G>A
  hgvsp: ENSP00000370371.4:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.200G>A
  hgvsp: ENSP00000350616.5:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48898
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly67Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

7-50611588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611588
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611588
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.196C>T
  hgvsp: ENSP00000350616.5:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.196C>T
  hgvsp: ENSP00000403644.2:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.196C>T
  hgvsp: ENSP00000393724.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.196C>T
  hgvsp: ENSP00000395069.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.93C>T
  hgvsp: ENSP00000389422.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.196C>T
  hgvsp: ENSP00000370371.4:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.196C>T
  hgvsp: ENSP00000399184.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro66Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

7-50611597-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611597
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611597
    reference: chr 7
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.187A>G
  hgvsp: ENSP00000399184.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.187A>G
  hgvsp: ENSP00000395069.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.84A>G
  hgvsp: ENSP00000389422.1:p.Ile29Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.187A>G
  hgvsp: ENSP00000370371.4:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.187A>G
  hgvsp: ENSP00000403644.2:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.187A>G
  hgvsp: ENSP00000393724.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.187A>G
  hgvsp: ENSP00000350616.5:p.Ile63Val
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48902
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile63Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-50611598-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611598
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611598
    reference: chr 7
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.186G>C
  hgvsp: ENSP00000395069.1:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.186G>C
  hgvsp: ENSP00000370371.4:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.83G>C
  hgvsp: ENSP00000389422.1:p.Lys28Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.186G>C
  hgvsp: ENSP00000350616.5:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.186G>C
  hgvsp: ENSP00000403644.2:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.186G>C
  hgvsp: ENSP00000393724.1:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.186G>C
  hgvsp: ENSP00000399184.1:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys62Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-50611601-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611601
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611601
    reference: chr 7
allele count: 176
allele frequency: 1.449633473354748e-3
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.183G>T
  hgvsp: ENSP00000403644.2:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.183G>T
  hgvsp: ENSP00000399184.1:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.80G>T
  hgvsp: ENSP00000389422.1:p.Glu27Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.183G>T
  hgvsp: ENSP00000350616.5:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.183G>T
  hgvsp: ENSP00000395069.1:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.183G>T
  hgvsp: ENSP00000370371.4:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.183G>T
  hgvsp: ENSP00000393724.1:p.Glu61Asp
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6572
  bin: 9.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu61Asp
num of homozygotes: 3
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-50611605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611605
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611605
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.179T>C
  hgvsp: ENSP00000393724.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.179T>C
  hgvsp: ENSP00000350616.5:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.179T>C
  hgvsp: ENSP00000395069.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.76T>C
  hgvsp: ENSP00000389422.1:p.Val26Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.179T>C
  hgvsp: ENSP00000399184.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.179T>C
  hgvsp: ENSP00000370371.4:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.179T>C
  hgvsp: ENSP00000403644.2:p.Val60Ala
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val60Ala
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

7-50611606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611606
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611606
    reference: chr 7
allele count: 8
allele frequency: 6.589243060703402e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.178G>A
  hgvsp: ENSP00000350616.5:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.75G>A
  hgvsp: ENSP00000389422.1:p.Val26Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.178G>A
  hgvsp: ENSP00000393724.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.178G>A
  hgvsp: ENSP00000370371.4:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.178G>A
  hgvsp: ENSP00000395069.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.178G>A
  hgvsp: ENSP00000399184.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.178G>A
  hgvsp: ENSP00000403644.2:p.Val60Ile
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6571
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val60Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff

7-50611607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611607
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611607
    reference: chr 7
allele count: 6
allele frequency: 4.941932295527551e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.177C>T
  hgvsp: ENST00000444733.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.177C>T
  hgvsp: ENST00000426377.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.177C>T
  hgvsp: ENST00000444124.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.74C>T
  hgvsp: ENST00000430300.1:c.74C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.177C>T
  hgvsp: ENST00000380984.4:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.177C>T
  hgvsp: ENST00000431062.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.177C>T
  hgvsp: ENST00000357936.5:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp59Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-50611610-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611610
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611610
    reference: chr 7
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.71C>T
  hgvsp: ENST00000430300.1:c.71C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.174C>T
  hgvsp: ENST00000380984.4:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.174C>T
  hgvsp: ENST00000444124.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.174C>T
  hgvsp: ENST00000444733.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.174C>T
  hgvsp: ENST00000431062.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.174C>T
  hgvsp: ENST00000357936.5:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.174C>T
  hgvsp: ENST00000426377.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48942
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn58Asn
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

7-50611610-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611610
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611610
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.174C>G
  hgvsp: ENSP00000370371.4:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.174C>G
  hgvsp: ENSP00000350616.5:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.174C>G
  hgvsp: ENSP00000395069.1:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.71C>G
  hgvsp: ENSP00000389422.1:p.Asn24Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.174C>G
  hgvsp: ENSP00000393724.1:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.174C>G
  hgvsp: ENSP00000403644.2:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.174C>G
  hgvsp: ENSP00000399184.1:p.Asn58Lys
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn58Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-50611624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611624
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611624
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.160G>A
  hgvsp: ENSP00000370371.4:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.160G>A
  hgvsp: ENSP00000399184.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.160G>A
  hgvsp: ENSP00000350616.5:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.57G>A
  hgvsp: ENSP00000389422.1:p.Glu20Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.160G>A
  hgvsp: ENSP00000393724.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.160G>A
  hgvsp: ENSP00000403644.2:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.160G>A
  hgvsp: ENSP00000395069.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu54Lys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-50611628-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611628
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611628
    reference: chr 7
allele count: 11
allele frequency: 9.060209208467177e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.156G>A
  hgvsp: ENST00000426377.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.53G>A
  hgvsp: ENST00000430300.1:c.53G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.156G>A
  hgvsp: ENST00000444124.2:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.156G>A
  hgvsp: ENST00000431062.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.156G>A
  hgvsp: ENST00000357936.5:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.156G>A
  hgvsp: ENST00000444733.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.156G>A
  hgvsp: ENST00000380984.4:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr52Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

7-50611629-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611629
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611629
    reference: chr 7
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.155C>T
  hgvsp: ENSP00000395069.1:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.52C>T
  hgvsp: ENSP00000389422.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.155C>T
  hgvsp: ENSP00000350616.5:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.155C>T
  hgvsp: ENSP00000403644.2:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.155C>T
  hgvsp: ENSP00000370371.4:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.155C>T
  hgvsp: ENSP00000393724.1:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.155C>T
  hgvsp: ENSP00000399184.1:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr52Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

7-50611631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611631
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611631
    reference: chr 7
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.153C>T
  hgvsp: ENST00000431062.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.153C>T
  hgvsp: ENST00000426377.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.153C>T
  hgvsp: ENST00000380984.4:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.153C>T
  hgvsp: ENST00000444733.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.50C>T
  hgvsp: ENST00000430300.1:c.50C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.153C>T
  hgvsp: ENST00000357936.5:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.153C>T
  hgvsp: ENST00000444124.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp51Asp
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

7-50611632-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611632
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.152A>T
  hgvsp: ENSP00000393724.1:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.152A>T
  hgvsp: ENSP00000403644.2:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.152A>T
  hgvsp: ENSP00000399184.1:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.49A>T
  hgvsp: ENSP00000389422.1:p.Asp17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.152A>T
  hgvsp: ENSP00000370371.4:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.152A>T
  hgvsp: ENSP00000395069.1:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.152A>T
  hgvsp: ENSP00000350616.5:p.Asp51Val
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48947
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp51Val
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-50611636-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611636
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611636
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.148C>T
  hgvsp: ENSP00000395069.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.148C>T
  hgvsp: ENSP00000370371.4:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.148C>T
  hgvsp: ENSP00000350616.5:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.148C>T
  hgvsp: ENSP00000403644.2:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.45C>T
  hgvsp: ENSP00000389422.1:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.148C>T
  hgvsp: ENSP00000393724.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.148C>T
  hgvsp: ENSP00000399184.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro50Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

7-50611637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611637
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611637
    reference: chr 7
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.147G>A
  hgvsp: ENST00000380984.4:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.147G>A
  hgvsp: ENST00000426377.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.147G>A
  hgvsp: ENST00000431062.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.44G>A
  hgvsp: ENST00000430300.1:c.44G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.147G>A
  hgvsp: ENST00000444124.2:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.147G>A
  hgvsp: ENST00000444733.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.147G>A
  hgvsp: ENST00000357936.5:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu49Glu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-50611644-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611644
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611644
    reference: chr 7
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.140C>A
  hgvsp: ENSP00000370371.4:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.140C>A
  hgvsp: ENSP00000399184.1:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.140C>A
  hgvsp: ENSP00000393724.1:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.140C>A
  hgvsp: ENSP00000403644.2:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.37C>A
  hgvsp: ENSP00000389422.1:p.Pro13His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.140C>A
  hgvsp: ENSP00000395069.1:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.140C>A
  hgvsp: ENSP00000350616.5:p.Pro47His
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro47His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

7-50611649-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611649
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611649
    reference: chr 7
allele count: 27
allele frequency: 2.223869532987398e-4
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.135T>C
  hgvsp: ENST00000380984.4:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.135T>C
  hgvsp: ENST00000444733.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.135T>C
  hgvsp: ENST00000431062.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.135T>C
  hgvsp: ENST00000426377.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.135T>C
  hgvsp: ENST00000444124.2:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.32T>C
  hgvsp: ENST00000430300.1:c.32T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.135T>C
  hgvsp: ENST00000357936.5:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala45Ala
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: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

7-50611651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611651
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611651
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.30G>A
  hgvsp: ENSP00000389422.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.133G>A
  hgvsp: ENSP00000403644.2:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.133G>A
  hgvsp: ENSP00000350616.5:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.133G>A
  hgvsp: ENSP00000393724.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.133G>A
  hgvsp: ENSP00000370371.4:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.133G>A
  hgvsp: ENSP00000399184.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.133G>A
  hgvsp: ENSP00000395069.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala45Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

7-50611652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611652
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611652
    reference: chr 7
allele count: 8
allele frequency: 6.589243060703402e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.132C>T
  hgvsp: ENST00000357936.5:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.132C>T
  hgvsp: ENST00000444733.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.132C>T
  hgvsp: ENST00000426377.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.132C>T
  hgvsp: ENST00000380984.4:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.132C>T
  hgvsp: ENST00000444124.2:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.29C>T
  hgvsp: ENST00000430300.1:c.29C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.132C>T
  hgvsp: ENST00000431062.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala44Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

7-50611655-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611655
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611654
    reference: chr 7
allele count: 4
allele frequency: 3.295435821387378e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.128delC
  hgvsp: ENSP00000403644.2:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.25delC
  hgvsp: ENSP00000389422.1:p.Pro9LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.128delC
  hgvsp: ENSP00000370371.4:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.128delC
  hgvsp: ENSP00000393724.1:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.128delC
  hgvsp: ENSP00000399184.1:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.128delC
  hgvsp: ENSP00000350616.5:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.128delC
  hgvsp: ENSP00000395069.1:p.Pro43LeufsTer21
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48944
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro43LeufsTer21
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: AG
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

7-50611663-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611663
    reference: chr 7
allele count: 13
allele frequency: 1.070769636267791e-4
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.18C>A
  hgvsp: ENSP00000389422.1:p.Leu7Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.121C>A
  hgvsp: ENSP00000403644.2:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.121C>A
  hgvsp: ENSP00000370371.4:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.121C>A
  hgvsp: ENSP00000399184.1:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.121C>A
  hgvsp: ENSP00000350616.5:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.121C>A
  hgvsp: ENSP00000395069.1:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.121C>A
  hgvsp: ENSP00000393724.1:p.Leu41Met
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu41Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

7-50611664-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611664
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611664
    reference: chr 7
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.120G>A
  hgvsp: ENST00000444733.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.17G>A
  hgvsp: ENST00000430300.1:c.17G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.120G>A
  hgvsp: ENST00000380984.4:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.120G>A
  hgvsp: ENST00000357936.5:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.120G>A
  hgvsp: ENST00000426377.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.120G>A
  hgvsp: ENST00000431062.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.120G>A
  hgvsp: ENST00000444124.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro40Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

7-50611665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611665
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611665
    reference: chr 7
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.119C>T
  hgvsp: ENSP00000403644.2:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.119C>T
  hgvsp: ENSP00000370371.4:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.119C>T
  hgvsp: ENSP00000393724.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.16C>T
  hgvsp: ENSP00000389422.1:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.119C>T
  hgvsp: ENSP00000399184.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.119C>T
  hgvsp: ENSP00000350616.5:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.119C>T
  hgvsp: ENSP00000395069.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6661
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro40Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

7-50611668-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611668
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611668
    reference: chr 7
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.116G>A
  hgvsp: ENSP00000393724.1:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.13G>A
  hgvsp: ENSP00000389422.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.116G>A
  hgvsp: ENSP00000399184.1:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.116G>A
  hgvsp: ENSP00000350616.5:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.116G>A
  hgvsp: ENSP00000395069.1:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.116G>A
  hgvsp: ENSP00000370371.4:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.116G>A
  hgvsp: ENSP00000403644.2:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg39Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

7-50611669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611669
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611669
    reference: chr 7
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.115C>T
  hgvsp: ENSP00000395069.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.12C>T
  hgvsp: ENSP00000389422.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.115C>T
  hgvsp: ENSP00000393724.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.115C>T
  hgvsp: ENSP00000370371.4:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.115C>T
  hgvsp: ENSP00000403644.2:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.115C>T
  hgvsp: ENSP00000350616.5:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.115C>T
  hgvsp: ENSP00000399184.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6666
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg39Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

7-50611669-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611669
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611669
    reference: chr 7
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.115C>A
  hgvsp: ENST00000444733.1:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.115C>A
  hgvsp: ENST00000444124.2:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.115C>A
  hgvsp: ENST00000357936.5:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.12C>A
  hgvsp: ENST00000430300.1:c.12C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.115C>A
  hgvsp: ENST00000426377.1:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.115C>A
  hgvsp: ENST00000380984.4:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.115C>A
  hgvsp: ENST00000431062.1:c.115C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6666
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg39Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

7-50611676-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611676
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611676
    reference: chr 7
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.108G>A
  hgvsp: ENST00000426377.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.5G>A
  hgvsp: ENST00000430300.1:c.5G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.108G>A
  hgvsp: ENST00000444124.2:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.108G>A
  hgvsp: ENST00000357936.5:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.108G>A
  hgvsp: ENST00000431062.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.108G>A
  hgvsp: ENST00000380984.4:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.108G>A
  hgvsp: ENST00000444733.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6673
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly36Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-50611678-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611678
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611678
    reference: chr 7
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.106G>A
  hgvsp: ENSP00000350616.5:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.106G>A
  hgvsp: ENSP00000399184.1:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.106G>A
  hgvsp: ENSP00000370371.4:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.106G>A
  hgvsp: ENSP00000403644.2:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.106G>A
  hgvsp: ENSP00000395069.1:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.3G>A
  hgvsp: ENSP00000389422.1:p.Gly2Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.106G>A
  hgvsp: ENSP00000393724.1:p.Gly36Arg
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly36Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-50611679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611679
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611679
    reference: chr 7
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000389422
  ensembl transcript: ENST00000430300
  gene symbol: DDC
  hgvsc: ENST00000430300.1:c.2C>T
  hgvsp: ENST00000430300.1:c.2C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.105C>T
  hgvsp: ENST00000357936.5:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.105C>T
  hgvsp: ENST00000426377.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.105C>T
  hgvsp: ENST00000444733.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.105C>T
  hgvsp: ENST00000444124.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.105C>T
  hgvsp: ENST00000431062.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.105C>T
  hgvsp: ENST00000380984.4:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro35Pro
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-50611681-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611681
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611681
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.103C>G
  hgvsp: ENSP00000399184.1:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.103C>G
  hgvsp: ENSP00000395069.1:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.103C>G
  hgvsp: ENSP00000370371.4:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.103C>G
  hgvsp: ENSP00000350616.5:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.103C>G
  hgvsp: ENSP00000403644.2:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.103C>G
  hgvsp: ENSP00000393724.1:p.Pro35Ala
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro35Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-50611687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611687
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611687
    reference: chr 7
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.97G>A
  hgvsp: ENSP00000370371.4:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.97G>A
  hgvsp: ENSP00000393724.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.97G>A
  hgvsp: ENSP00000399184.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.97G>A
  hgvsp: ENSP00000395069.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.97G>A
  hgvsp: ENSP00000403644.2:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.97G>A
  hgvsp: ENSP00000350616.5:p.Val33Met
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48983
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val33Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-50611688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611688
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611688
    reference: chr 7
allele count: 534
allele frequency: 4.39831974301952e-3
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.96C>T
  hgvsp: ENST00000444124.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.96C>T
  hgvsp: ENST00000431062.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.96C>T
  hgvsp: ENST00000444733.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.96C>T
  hgvsp: ENST00000357936.5:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.96C>T
  hgvsp: ENST00000380984.4:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.96C>T
  hgvsp: ENST00000426377.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 9.75e1
  variant carriers: 510
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp32Asp
num of homozygotes: 4
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

7-50611694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611694
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611694
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.90C>T
  hgvsp: ENST00000444124.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.90C>T
  hgvsp: ENST00000420203.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.90C>T
  hgvsp: ENST00000426377.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.90C>T
  hgvsp: ENST00000444733.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.90C>T
  hgvsp: ENST00000357936.5:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.90C>T
  hgvsp: ENST00000380984.4:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.90C>T
  hgvsp: ENST00000431062.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr30Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-50611697-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611697
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611697
    reference: chr 7
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.87C>G
  hgvsp: ENST00000444733.1:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.87C>G
  hgvsp: ENST00000426377.1:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.87C>G
  hgvsp: ENST00000357936.5:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.87C>G
  hgvsp: ENST00000431062.1:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.87C>G
  hgvsp: ENST00000380984.4:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.87C>G
  hgvsp: ENST00000444124.2:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.87C>G
  hgvsp: ENST00000420203.1:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49081
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val29Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

7-50611699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611699
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611699
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.85G>A
  hgvsp: ENSP00000370371.4:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.85G>A
  hgvsp: ENSP00000399184.1:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.85G>A
  hgvsp: ENSP00000393724.1:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.85G>A
  hgvsp: ENSP00000408626.1:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.85G>A
  hgvsp: ENSP00000350616.5:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.85G>A
  hgvsp: ENSP00000403644.2:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.85G>A
  hgvsp: ENSP00000395069.1:p.Val29Ile
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49081
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val29Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

7-50611702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611702
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611702
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.82C>T
  hgvsp: ENSP00000403644.2:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.82C>T
  hgvsp: ENSP00000408626.1:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.82C>T
  hgvsp: ENSP00000370371.4:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.82C>T
  hgvsp: ENSP00000399184.1:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.82C>T
  hgvsp: ENSP00000393724.1:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.82C>T
  hgvsp: ENSP00000350616.5:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.82C>T
  hgvsp: ENSP00000395069.1:p.Gln28Ter
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln28Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

7-50611704-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611704
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611704
    reference: chr 7
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.80G>A
  hgvsp: ENSP00000370371.4:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.80G>A
  hgvsp: ENSP00000393724.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.80G>A
  hgvsp: ENSP00000395069.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.80G>A
  hgvsp: ENSP00000350616.5:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.80G>A
  hgvsp: ENSP00000403644.2:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.80G>A
  hgvsp: ENSP00000399184.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.80G>A
  hgvsp: ENSP00000408626.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49082
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg27His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-50611705-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611705
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611705
    reference: chr 7
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.79C>T
  hgvsp: ENSP00000393724.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.79C>T
  hgvsp: ENSP00000395069.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.79C>T
  hgvsp: ENSP00000403644.2:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.79C>T
  hgvsp: ENSP00000350616.5:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.79C>T
  hgvsp: ENSP00000370371.4:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.79C>T
  hgvsp: ENSP00000408626.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.79C>T
  hgvsp: ENSP00000399184.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7083
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg27Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-50611711-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611711
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611711
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.73G>A
  hgvsp: ENSP00000350616.5:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.73G>A
  hgvsp: ENSP00000408626.1:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.73G>A
  hgvsp: ENSP00000403644.2:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.73G>A
  hgvsp: ENSP00000393724.1:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.73G>A
  hgvsp: ENSP00000399184.1:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.73G>A
  hgvsp: ENSP00000370371.4:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.73G>A
  hgvsp: ENSP00000395069.1:p.Glu25Lys
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu25Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-50611735-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611735
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611735
    reference: chr 7
allele count: 121191
allele frequency: 9.981797515896287e-1
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.49A>G
  hgvsp: ENSP00000395069.1:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.49A>G
  hgvsp: ENSP00000408626.1:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.49A>G
  hgvsp: ENSP00000350616.5:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.49A>G
  hgvsp: ENSP00000370371.4:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.49A>G
  hgvsp: ENSP00000393724.1:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.49A>G
  hgvsp: ENSP00000399184.1:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.49A>G
  hgvsp: ENSP00000403644.2:p.Met17Val
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 59084
  bin: 9.75e1
  variant carriers: 59084
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 78
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 60546
  bin: 9.75e1
  variant carriers: 60543
hgvs: p.Met17Val
num of homozygotes: 60489
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

7-50611736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611736
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611736
    reference: chr 7
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.48C>T
  hgvsp: ENST00000380984.4:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.48C>T
  hgvsp: ENST00000444124.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.48C>T
  hgvsp: ENST00000420203.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.48C>T
  hgvsp: ENST00000431062.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.48C>T
  hgvsp: ENST00000426377.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.48C>T
  hgvsp: ENST00000444733.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.48C>T
  hgvsp: ENST00000357936.5:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr16Tyr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-50611736-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611736
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611736
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.48C>G
  hgvsp: ENSP00000350616.5:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.48C>G
  hgvsp: ENSP00000370371.4:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.48C>G
  hgvsp: ENSP00000395069.1:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.48C>G
  hgvsp: ENSP00000393724.1:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.48C>G
  hgvsp: ENSP00000399184.1:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.48C>G
  hgvsp: ENSP00000403644.2:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.48C>G
  hgvsp: ENSP00000408626.1:p.Tyr16Ter
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr16Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

7-50611741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611741
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611741
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.43G>A
  hgvsp: ENSP00000350616.5:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.43G>A
  hgvsp: ENSP00000403644.2:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.43G>A
  hgvsp: ENSP00000393724.1:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.43G>A
  hgvsp: ENSP00000399184.1:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.43G>A
  hgvsp: ENSP00000370371.4:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.43G>A
  hgvsp: ENSP00000408626.1:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.43G>A
  hgvsp: ENSP00000395069.1:p.Asp15Asn
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43379
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp15Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

7-50611744-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611744
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611744
    reference: chr 7
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.40G>A
  hgvsp: ENSP00000393724.1:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.40G>A
  hgvsp: ENSP00000395069.1:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.40G>A
  hgvsp: ENSP00000403644.2:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.40G>A
  hgvsp: ENSP00000350616.5:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.40G>A
  hgvsp: ENSP00000408626.1:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.40G>A
  hgvsp: ENSP00000370371.4:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.40G>A
  hgvsp: ENSP00000399184.1:p.Val14Met
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2541
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43379
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val14Met
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

7-50611751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611751
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611751
    reference: chr 7
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.33G>A
  hgvsp: ENST00000426377.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.33G>A
  hgvsp: ENST00000380984.4:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.33G>A
  hgvsp: ENST00000431062.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.33G>A
  hgvsp: ENST00000444124.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.33G>A
  hgvsp: ENST00000357936.5:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.33G>A
  hgvsp: ENST00000420203.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.33G>A
  hgvsp: ENST00000444733.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys11Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

7-50611764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611764
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611764
    reference: chr 7
allele count: 9
allele frequency: 7.417174880501072e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.20G>A
  hgvsp: ENSP00000393724.1:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.20G>A
  hgvsp: ENSP00000395069.1:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.20G>A
  hgvsp: ENSP00000370371.4:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.20G>A
  hgvsp: ENSP00000403644.2:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.20G>A
  hgvsp: ENSP00000350616.5:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.20G>A
  hgvsp: ENSP00000408626.1:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.20G>A
  hgvsp: ENSP00000399184.1:p.Arg7Gln
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg7Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

7-50611765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611765
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611765
    reference: chr 7
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.19C>T
  hgvsp: ENSP00000399184.1:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.19C>T
  hgvsp: ENSP00000393724.1:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.19C>T
  hgvsp: ENSP00000403644.2:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.19C>T
  hgvsp: ENSP00000370371.4:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.19C>T
  hgvsp: ENSP00000350616.5:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.19C>T
  hgvsp: ENSP00000408626.1:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.19C>T
  hgvsp: ENSP00000395069.1:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2340
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg7Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

7-50611773-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611773
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611773
    reference: chr 7
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.11G>C
  hgvsp: ENSP00000350616.5:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.11G>C
  hgvsp: ENSP00000395069.1:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.11G>C
  hgvsp: ENSP00000370371.4:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.11G>C
  hgvsp: ENSP00000393724.1:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.11G>C
  hgvsp: ENSP00000408626.1:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.11G>C
  hgvsp: ENSP00000403644.2:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.11G>C
  hgvsp: ENSP00000399184.1:p.Ser4Thr
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser4Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

7-50611774-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611774
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611774
    reference: chr 7
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.10A>C
  hgvsp: ENSP00000350616.5:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.10A>C
  hgvsp: ENSP00000393724.1:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.10A>C
  hgvsp: ENSP00000399184.1:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.10A>C
  hgvsp: ENSP00000408626.1:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.10A>C
  hgvsp: ENSP00000370371.4:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.10A>C
  hgvsp: ENSP00000403644.2:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.10A>C
  hgvsp: ENSP00000395069.1:p.Ser4Arg
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser4Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-50611775-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611775
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611775
    reference: chr 7
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.9A>C
  hgvsp: ENST00000431062.1:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.9A>C
  hgvsp: ENST00000380984.4:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.9A>C
  hgvsp: ENST00000444124.2:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.9A>C
  hgvsp: ENST00000357936.5:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.9A>C
  hgvsp: ENST00000444733.1:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.9A>C
  hgvsp: ENST00000426377.1:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.9A>C
  hgvsp: ENST00000420203.1:c.9A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala3Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

7-50611777-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611777
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611777
    reference: chr 7
allele count: 3
allele frequency: 2.473818751546137e-5
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.7G>A
  hgvsp: ENSP00000370371.4:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.7G>A
  hgvsp: ENSP00000399184.1:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.7G>A
  hgvsp: ENSP00000350616.5:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.7G>A
  hgvsp: ENSP00000393724.1:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.7G>A
  hgvsp: ENSP00000403644.2:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.7G>A
  hgvsp: ENSP00000408626.1:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.7G>A
  hgvsp: ENSP00000395069.1:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala3Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

7-50611778-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611778
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611778
    reference: chr 7
allele count: 7
allele frequency: 5.772910206505245e-5
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.6C>T
  hgvsp: ENST00000444733.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.6C>T
  hgvsp: ENST00000444124.2:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.6C>T
  hgvsp: ENST00000426377.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.6C>T
  hgvsp: ENST00000380984.4:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.6C>T
  hgvsp: ENST00000357936.5:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.6C>T
  hgvsp: ENST00000431062.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.6C>T
  hgvsp: ENST00000420203.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn2Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

7-50611779-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611779
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611779
    reference: chr 7
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.5A>T
  hgvsp: ENSP00000393724.1:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.5A>T
  hgvsp: ENSP00000350616.5:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.5A>T
  hgvsp: ENSP00000399184.1:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.5A>T
  hgvsp: ENSP00000370371.4:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.5A>T
  hgvsp: ENSP00000395069.1:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.5A>T
  hgvsp: ENSP00000403644.2:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.5A>T
  hgvsp: ENSP00000408626.1:p.Asn2Ile
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4220
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn2Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

7-50611783-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611783
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611783
    reference: chr 7
allele count: 3
allele frequency: 2.474390062849507e-5
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.1A>G
  hgvsp: ENSP00000395069.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.1A>G
  hgvsp: ENSP00000350616.5:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.1A>G
  hgvsp: ENSP00000399184.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.1A>G
  hgvsp: ENSP00000370371.4:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.1A>G
  hgvsp: ENSP00000403644.2:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.1A>G
  hgvsp: ENSP00000393724.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.1A>G
  hgvsp: ENSP00000408626.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

7-50611792-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611792
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611792
    reference: chr 7
allele count: 2
allele frequency: 1.650955077512341e-5
allele num: 121142
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000399184
  ensembl transcript: ENST00000431062
  gene symbol: DDC
  hgvsc: ENST00000431062.1:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.-9C>G
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43364
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-50611819-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611819
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611819
    reference: chr 7
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.-28-8T>C
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
hgvs: c.-28-8T>C
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: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

7-50611821-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611821
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611821
    reference: chr 7
allele count: 1
allele frequency: 8.269930532583527e-6
allele num: 120920
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.-28-10C>T
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2521
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

7-50611828-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50611828
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50611828
    reference: chr 7
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000403644
  ensembl transcript: ENST00000444124
  gene symbol: DDC
  hgvsc: ENST00000444124.2:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000395069
  ensembl transcript: ENST00000426377
  gene symbol: DDC
  hgvsc: ENST00000426377.1:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000393724
  ensembl transcript: ENST00000444733
  gene symbol: DDC
  hgvsc: ENST00000444733.1:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000370371
  ensembl transcript: ENST00000380984
  gene symbol: DDC
  hgvsc: ENST00000380984.4:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000350616
  ensembl transcript: ENST00000357936
  gene symbol: DDC
  hgvsc: ENST00000357936.5:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132437
  ensembl protein: ENSP00000408626
  ensembl transcript: ENST00000420203
  gene symbol: DDC
  hgvsc: ENST00000420203.1:c.-28-17T>C
  variant of: http://identifiers.org/hgnc/2719
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/7-50660602-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660602
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660602
    reference: chr 7
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.598G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

7-50660608-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660608
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660608
    reference: chr 7
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.592A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

7-50660611-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660611
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660611
    reference: chr 7
allele count: 3
allele frequency: 2.484389751064147e-5
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.589A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*38A>G
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/7-50660612-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660612
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660612
    reference: chr 7
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.588G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-50660627-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660627
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660627
    reference: chr 7
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.573A>G
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

7-50660628-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660628
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660628
    reference: chr 7
allele count: 3
allele frequency: 2.484225170169424e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.572G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*21G>A
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

7-50660632-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660632
    reference: chr 7
allele count: 6
allele frequency: 4.968203497615263e-5
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.568G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

7-50660633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660633
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660633
    reference: chr 7
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.567C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-50660638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660638
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660638
    reference: chr 7
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.562C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

7-50660640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50660640
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 50660640
    reference: chr 7
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385366
  ensembl transcript: ENST00000406641
  gene symbol: GRB10
  hgvsc: ENST00000406641.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000406716
  ensembl transcript: ENST00000439599
  gene symbol: GRB10
  hgvsc: ENST00000439599.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385046
  ensembl transcript: ENST00000407526
  gene symbol: GRB10
  hgvsc: ENST00000407526.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385544
  ensembl transcript: ENST00000403097
  gene symbol: GRB10
  hgvsc: ENST00000403097.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000338543
  ensembl transcript: ENST00000335866
  gene symbol: GRB10
  hgvsc: ENST00000335866.3:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385770
  ensembl transcript: ENST00000401949
  gene symbol: GRB10
  hgvsc: ENST00000401949.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385748
  ensembl transcript: ENST00000402497
  gene symbol: GRB10
  hgvsc: ENST00000402497.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000349818
  ensembl transcript: ENST00000357271
  gene symbol: GRB10
  hgvsc: ENST00000357271.5:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381790
  ensembl transcript: ENST00000398810
  gene symbol: GRB10
  hgvsc: ENST00000398810.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000385189
  ensembl transcript: ENST00000402578
  gene symbol: GRB10
  hgvsc: ENST00000402578.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106070
  ensembl protein: ENSP00000381793
  ensembl transcript: ENST00000398812
  gene symbol: GRB10
  hgvsc: ENST00000398812.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/4564
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106070
  ensembl transcript: ENST00000461886
  gene symbol: GRB10
  hgvsc: ENST00000461886.1:n.560G>A
  variant of: http://identifiers.org/hgnc/4564
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
reference allele: C

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 48899
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
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: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.844e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 9.85e-1

DP
type: SiteQuality
SIO_000300: 3.499472e6

VQSLOD
type: SiteQuality
SIO_000300: -2.831e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.178e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.156e1

GenotypeQuality
all individuals: 2274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 906
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 6.01e0

DP
type: SiteQuality
SIO_000300: 3.499518e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.536e0

FS
type: SiteQuality
SIO_000300: 1.344e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.468e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.146e0

VQSLOD
type: SiteQuality
SIO_000300: -2.118e0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48900
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.353e0

MQRankSum
type: SiteQuality
SIO_000300: -4.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.201000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.05e1

DP
type: SiteQuality
SIO_000300: 3.499814e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.375e0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1918
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1444
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2019
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1037
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.034e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

QD
type: SiteQuality
SIO_000300: 1.559e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

VQSLOD
type: SiteQuality
SIO_000300: 5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

DP
type: SiteQuality
SIO_000300: 3.500132e6

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

GenotypeQuality
all individuals: 1037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48902
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2276
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 7.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.197e0

MQRankSum
type: SiteQuality
SIO_000300: -7.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 3.500268e6

FS
type: SiteQuality
SIO_000300: 4.584e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.629e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
all individuals: 1706
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1911
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48943
bin: 9.75e1
variant carriers: 173

GenotypeQuality
all individuals: 2014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 170
allele frequency: 1.633672881030175e-2
allele num: 10406
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.513008e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.86e0

FS
type: SiteQuality
SIO_000300: 1.324e0

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1706
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48941
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e0

QD
type: SiteQuality
SIO_000300: 1.669e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.075e0

VQSLOD
type: SiteQuality
SIO_000300: -2.144e0

FS
type: SiteQuality
SIO_000300: 1.887e0

DP
type: SiteQuality
SIO_000300: 3.512812e6

GenotypeQuality
all individuals: 1379
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 1034
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48941
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2271
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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European (Non-Finnish)
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allele count: 6
allele frequency: 8.990110878034162e-5
allele num: 66740
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 frequency: 0.0e0
allele num: 906
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -5.98e-1

MQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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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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bin: 1.75e1
variant carriers: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
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 frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 2.882952142994427e-4
allele num: 10406
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

South Asian
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allele num: 16512
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ClippingRankSum
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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
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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

MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 66740
num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.321e0

InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
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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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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QD
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.94e-1

BaseQRankSum
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MQ
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SIO_000300: 5.959e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

Other
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allele num: 906
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South Asian
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allele num: 16512
num of homozygotes: 0

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 5.993407252022775e-5
allele num: 66740
num of homozygotes: 0

African
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FS
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BaseQRankSum
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VQSLOD
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QD
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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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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 1.921968095329617e-4
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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Other
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QD
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VQSLOD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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East Asian
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African
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European (Non-Finnish)
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allele num: 66740
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South Asian
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66740
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Other
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DP
type: SiteQuality
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
type: Population
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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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.693e0

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.312e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
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SIO_000300: 1.238e1

FS
type: SiteQuality
SIO_000300: 4.618e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.269e0

QD
type: SiteQuality
SIO_000300: 1.442e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1442
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.7e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.453e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 3.517789e6

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: 27

GenotypeQuality
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GenotypeQuality
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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: 906
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 2.332008982553118e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.521932e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.461e0

QD
type: SiteQuality
SIO_000300: 1.316e1

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 1.977e0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1376
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GenotypeQuality
all individuals: 1033
bin: 7.25e1
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: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.522205e6

MQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

FS
type: SiteQuality
SIO_000300: 5.304e0

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.305e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.4e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 48959
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.169e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.523102e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995563283170454e-5
allele num: 66716
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Other
type: Population
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BaseQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.04887770086008e-4
allele num: 66738
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Other
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South Asian
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Latino
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allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

East Asian
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African
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-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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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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African
type: Population
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allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
type: Population
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European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

European (Finnish)
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East Asian
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Latino
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South Asian
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Other
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allele num: 908
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

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Latino
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East Asian
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allele frequency: 0.0e0
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African
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele num: 66738
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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Other
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MQ
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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African
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allele num: 10404
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Other
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

QD
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MQ
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: 1.3e0

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.51e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.45e-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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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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African
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

DP
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VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.194e0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

African
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Latino
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East Asian
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num of homozygotes: 0

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

African
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allele num: 10406
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South Asian
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
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MQ
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DP
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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Other
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South Asian
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Latino
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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African
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East Asian
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Other
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South Asian
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European (Finnish)
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 6.650544135429262e-3
allele num: 11578
num of homozygotes: 0

European (Finnish)
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Other
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African
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allele frequency: 5.382545174932718e-3
allele num: 10404
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European (Non-Finnish)
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allele count: 217
allele frequency: 3.251423434222355e-3
allele num: 66740
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East Asian
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South Asian
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allele frequency: 1.065891472868217e-2
allele num: 16512
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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FS
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 8.25e1
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: 908
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 4.84e-1

DP
type: SiteQuality
SIO_000300: 3.609681e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 1675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 1985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e-1

DP
type: SiteQuality
SIO_000300: 3.610363e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.05e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 1673
bin: 7.75e1
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GenotypeQuality
all individuals: 1881
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 3.610446e6

QD
type: SiteQuality
SIO_000300: 1.332e1

FS
type: SiteQuality
SIO_000300: 1.115e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.675e0

VQSLOD
type: SiteQuality
SIO_000300: 9.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

GenotypeQuality
all individuals: 1366
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.106e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 3.610708e6

VQSLOD
type: SiteQuality
SIO_000300: -5.063e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.374e0

QD
type: SiteQuality
SIO_000300: 1.557e1

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

GenotypeQuality
all individuals: 1023
bin: 7.25e1
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: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1987
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 6.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.205e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.361e0

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

DP
type: SiteQuality
SIO_000300: 3.611213e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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
all individuals: 1430
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

FS
type: SiteQuality
SIO_000300: 1.108e0

QD
type: SiteQuality
SIO_000300: 1.3e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 3.611506e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-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
all individuals: 1881
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.32e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 3.611724e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 36

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 32

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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bin: 6.25e1
variant carriers: 13

South Asian
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allele count: 16511
allele frequency: 9.999394379844961e-1
allele num: 16512
num of homozygotes: 8255

East Asian
type: Population
allele count: 8653
allele frequency: 9.998844464987289e-1
allele num: 8654
num of homozygotes: 4326

European (Finnish)
type: Population
allele count: 6614
allele frequency: 1.0e0
allele num: 6614
num of homozygotes: 3307

Other
type: Population
allele count: 908
allele frequency: 1.0e0
allele num: 908
num of homozygotes: 454

Latino
type: Population
allele count: 11568
allele frequency: 9.991362929694247e-1
allele num: 11578
num of homozygotes: 5779

European (Non-Finnish)
type: Population
allele count: 66738
allele frequency: 9.999700329637399e-1
allele num: 66740
num of homozygotes: 33368

African
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allele count: 10199
allele frequency: 9.801076302133385e-1
allele num: 10406
num of homozygotes: 5000

DP
type: SiteQuality
SIO_000300: 1.4587651e7

FS
type: SiteQuality
SIO_000300: 1.379e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 3.295e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.25e-2

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43382
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variant carriers: 4

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

South Asian
type: Population
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.485107e6

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e0

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-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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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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allele num: 66732
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Latino
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Other
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Other
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South Asian
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Latino
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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South Asian
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8646
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Latino
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European (Finnish)
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African
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Other
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South Asian
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European (Non-Finnish)
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66698
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South Asian
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East Asian
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Other
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African
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Latino
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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European (Non-Finnish)
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Latino
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African
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FS
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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FS
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VQSLOD
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DP
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MQRankSum
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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DP
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

QD
type: SiteQuality
SIO_000300: 1.506e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

DP
type: SiteQuality
SIO_000300: 3.478781e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-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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variant carriers: 7

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

South Asian
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allele count: 6
allele frequency: 3.63460140537921e-4
allele num: 16508
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: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 2.667e0

QD
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MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.178e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -1.842e0

QD
type: SiteQuality
SIO_000300: 1.727e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.469e0

DP
type: SiteQuality
SIO_000300: 3.477425e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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)
type: Population
allele count: 2
allele frequency: 3.001290554938624e-5
allele num: 66638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

DP
type: SiteQuality
SIO_000300: 3.476769e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.189e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.622e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-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
all individuals: 2244
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

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

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

East Asian
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allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.474223e6

VQSLOD
type: SiteQuality
SIO_000300: -1.892e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -6.865e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.076e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 3.183e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.461304e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

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

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

ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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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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Other
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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MQ
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SIO_000300: 5.948e1

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

Latino
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allele num: 11574
num of homozygotes: 0

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

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

African
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Other
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East Asian
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -8.01e-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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variant carriers: 0

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

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

East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66730
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Other
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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SIO_000300: 4.5e-3

VQSLOD
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6612
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Latino
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allele num: 11574
num of homozygotes: 0

East Asian
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BaseQRankSum
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SIO_000300: -6.499e0

QD
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MQ
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MQRankSum
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ClippingRankSum
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DP
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 1.56e0

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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ReadPosRankSum
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SIO_000300: -2.37e-1

DP
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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SIO_000300: 1.705e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

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

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

European (Non-Finnish)
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num of homozygotes: 0

African
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allele num: 9804
num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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Latino
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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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

African
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allele frequency: 1.019991840065279e-4
allele num: 9804
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

African
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Other
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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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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

QD
type: SiteQuality
SIO_000300: 1.488e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 3.248561e6

FS
type: SiteQuality
SIO_000300: 8.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.277e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeDepth
all individuals: 1240
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3158
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1646
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5892
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38359
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 3245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3029
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

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