6-162394319-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394319
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394319
    reference: chr 6
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.287+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.161+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.161+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.734+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.497+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.650+15A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.734+15A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-162394323-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394323
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394323
    reference: chr 6
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.650+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.497+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.161+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.734+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.161+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.734+11A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.287+11A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8140
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-162394323-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394323
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394322
    reference: chr 6
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.650+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.497+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.734+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.161+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.161+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.287+10delT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.734+10delT
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5473
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TA
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-162394336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394336
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394336
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.159C>T
  hgvsp: ENST00000366894.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.285C>T
  hgvsp: ENST00000366896.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.732C>T
  hgvsp: ENST00000366892.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.732C>T
  hgvsp: ENST00000366898.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.648C>T
  hgvsp: ENST00000366897.1:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.495C>T
  hgvsp: ENST00000479615.1:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.159C>T
  hgvsp: ENST00000338468.3:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: c.732C>T
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-162394338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394338
    reference: chr 6
allele count: 4
allele frequency: 3.296902560044838e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.646G>A
  hgvsp: ENSP00000355863.1:p.Val216Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.730G>A
  hgvsp: ENSP00000355865.1:p.Val244Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.283G>A
  hgvsp: ENSP00000355862.1:p.Val95Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.157G>A
  hgvsp: ENSP00000355860.1:p.Val53Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.157G>A
  hgvsp: ENSP00000343589.3:p.Val53Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.493G>A
  hgvsp: ENSP00000434414.1:p.Val165Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.730G>A
  hgvsp: ENSP00000355858.1:p.Val244Ile
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43736
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val244Ile
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-162394341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394341
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394341
    reference: chr 6
allele count: 37
allele frequency: 3.049182489451477e-4
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.727G>A
  hgvsp: ENSP00000355858.1:p.Asp243Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.280G>A
  hgvsp: ENSP00000355862.1:p.Asp94Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.727G>A
  hgvsp: ENSP00000355865.1:p.Asp243Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.490G>A
  hgvsp: ENSP00000434414.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.154G>A
  hgvsp: ENSP00000355860.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.154G>A
  hgvsp: ENSP00000343589.3:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.643G>A
  hgvsp: ENSP00000355863.1:p.Asp215Asn
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5519
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp243Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-162394343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394343
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394343
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.725C>T
  hgvsp: ENSP00000355865.1:p.Thr242Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.641C>T
  hgvsp: ENSP00000355863.1:p.Thr214Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.278C>T
  hgvsp: ENSP00000355862.1:p.Thr93Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.152C>T
  hgvsp: ENSP00000343589.3:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.725C>T
  hgvsp: ENSP00000355858.1:p.Thr242Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.488C>T
  hgvsp: ENSP00000434414.1:p.Thr163Ile
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.152C>T
  hgvsp: ENSP00000355860.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8135
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr242Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-162394348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394348
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394348
    reference: chr 6
allele count: 5
allele frequency: 4.120041530018623e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.636G>A
  hgvsp: ENST00000366897.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.483G>A
  hgvsp: ENST00000479615.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.147G>A
  hgvsp: ENST00000338468.3:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.273G>A
  hgvsp: ENST00000366896.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.720G>A
  hgvsp: ENST00000366898.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.720G>A
  hgvsp: ENST00000366892.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.147G>A
  hgvsp: ENST00000366894.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8137
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr240Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

6-162394349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394349
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394349
    reference: chr 6
allele count: 35
allele frequency: 2.883886490227745e-4
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.146C>T
  hgvsp: ENSP00000355860.1:p.Thr49Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.146C>T
  hgvsp: ENSP00000343589.3:p.Thr49Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.719C>T
  hgvsp: ENSP00000355865.1:p.Thr240Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.272C>T
  hgvsp: ENSP00000355862.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.482C>T
  hgvsp: ENSP00000434414.1:p.Thr161Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.635C>T
  hgvsp: ENSP00000355863.1:p.Thr212Met
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.719C>T
  hgvsp: ENSP00000355858.1:p.Thr240Met
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20272
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8153
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr240Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-162394349-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394349
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394349
    reference: chr 6
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.482C>A
  hgvsp: ENSP00000434414.1:p.Thr161Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.719C>A
  hgvsp: ENSP00000355865.1:p.Thr240Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.272C>A
  hgvsp: ENSP00000355862.1:p.Thr91Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.146C>A
  hgvsp: ENSP00000355860.1:p.Thr49Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.719C>A
  hgvsp: ENSP00000355858.1:p.Thr240Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.146C>A
  hgvsp: ENSP00000343589.3:p.Thr49Lys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.635C>A
  hgvsp: ENSP00000355863.1:p.Thr212Lys
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20272
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43838
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr240Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/6-162394352-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394352
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394352
    reference: chr 6
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.716T>G
  hgvsp: ENSP00000355865.1:p.Ile239Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.479T>G
  hgvsp: ENSP00000434414.1:p.Ile160Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.632T>G
  hgvsp: ENSP00000355863.1:p.Ile211Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.143T>G
  hgvsp: ENSP00000355860.1:p.Ile48Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.143T>G
  hgvsp: ENSP00000343589.3:p.Ile48Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.716T>G
  hgvsp: ENSP00000355858.1:p.Ile239Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.269T>G
  hgvsp: ENSP00000355862.1:p.Ile90Ser
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 8.25e1
  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
hgvs: p.Ile239Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

6-162394354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394354
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394354
    reference: chr 6
allele count: 131
allele frequency: 1.079308583386887e-3
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.630C>T
  hgvsp: ENST00000366897.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.141C>T
  hgvsp: ENST00000338468.3:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.714C>T
  hgvsp: ENST00000366892.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.477C>T
  hgvsp: ENST00000479615.1:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.714C>T
  hgvsp: ENST00000366898.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.141C>T
  hgvsp: ENST00000366894.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.267C>T
  hgvsp: ENST00000366896.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20290
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8218
  bin: 9.75e1
  variant carriers: 131
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys238Cys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

6-162394354-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394354
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394354
    reference: chr 6
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.477C>G
  hgvsp: ENSP00000434414.1:p.Cys159Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.141C>G
  hgvsp: ENSP00000343589.3:p.Cys47Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.141C>G
  hgvsp: ENSP00000355860.1:p.Cys47Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.714C>G
  hgvsp: ENSP00000355865.1:p.Cys238Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.630C>G
  hgvsp: ENSP00000355863.1:p.Cys210Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.714C>G
  hgvsp: ENSP00000355858.1:p.Cys238Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.267C>G
  hgvsp: ENSP00000355862.1:p.Cys89Trp
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys238Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-162394357-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394357
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394356
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.473delC
  hgvsp: ENSP00000434414.1:p.Thr158IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.137delC
  hgvsp: ENSP00000343589.3:p.Thr46IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.710delC
  hgvsp: ENSP00000355865.1:p.Thr237IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.263delC
  hgvsp: ENSP00000355862.1:p.Thr88IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.626delC
  hgvsp: ENSP00000355863.1:p.Thr209IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.137delC
  hgvsp: ENSP00000355860.1:p.Thr46IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.710delC
  hgvsp: ENSP00000355858.1:p.Thr237IlefsTer22
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  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
hgvs: p.Thr237IlefsTer22
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: AG
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-162394367-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394367
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394367
    reference: chr 6
allele count: 17
allele frequency: 1.400421774087255e-4
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.464G>A
  hgvsp: ENSP00000434414.1:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.617G>A
  hgvsp: ENSP00000355863.1:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.254G>A
  hgvsp: ENSP00000355862.1:p.Arg85Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.128G>A
  hgvsp: ENSP00000355860.1:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.701G>A
  hgvsp: ENSP00000355865.1:p.Arg234Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.128G>A
  hgvsp: ENSP00000343589.3:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.701G>A
  hgvsp: ENSP00000355858.1:p.Arg234Gln
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 1
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: 920
  bin: 7.75e1
  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: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg234Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-162394368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394368
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394368
    reference: chr 6
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.463C>T
  hgvsp: ENSP00000434414.1:p.Arg155Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.616C>T
  hgvsp: ENSP00000355863.1:p.Arg206Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.253C>T
  hgvsp: ENSP00000355862.1:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.127C>T
  hgvsp: ENSP00000355860.1:p.Arg43Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.700C>T
  hgvsp: ENSP00000355858.1:p.Arg234Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.700C>T
  hgvsp: ENSP00000355865.1:p.Arg234Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.127C>T
  hgvsp: ENSP00000343589.3:p.Arg43Trp
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg234Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-162394372-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394372
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394372
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.612T>C
  hgvsp: ENST00000366897.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.696T>C
  hgvsp: ENST00000366898.1:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.123T>C
  hgvsp: ENST00000338468.3:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.249T>C
  hgvsp: ENST00000366896.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.696T>C
  hgvsp: ENST00000366892.1:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.123T>C
  hgvsp: ENST00000366894.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.459T>C
  hgvsp: ENST00000479615.1:c.459T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5529
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn232Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

6-162394376-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394376
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.692C>G
  hgvsp: ENSP00000355865.1:p.Thr231Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.608C>G
  hgvsp: ENSP00000355863.1:p.Thr203Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.119C>G
  hgvsp: ENSP00000355860.1:p.Thr40Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.692C>G
  hgvsp: ENSP00000355858.1:p.Thr231Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.119C>G
  hgvsp: ENSP00000343589.3:p.Thr40Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.455C>G
  hgvsp: ENSP00000434414.1:p.Thr152Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.245C>G
  hgvsp: ENSP00000355862.1:p.Thr82Arg
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8092
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44001
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr231Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

6-162394379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394379
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394379
    reference: chr 6
allele count: 31
allele frequency: 2.553878600144994e-4
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.452C>T
  hgvsp: ENSP00000434414.1:p.Ala151Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.242C>T
  hgvsp: ENSP00000355862.1:p.Ala81Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.116C>T
  hgvsp: ENSP00000343589.3:p.Ala39Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.689C>T
  hgvsp: ENSP00000355858.1:p.Ala230Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.605C>T
  hgvsp: ENSP00000355863.1:p.Ala202Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.689C>T
  hgvsp: ENSP00000355865.1:p.Ala230Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.116C>T
  hgvsp: ENSP00000355860.1:p.Ala39Val
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20415
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43977
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8112
  bin: 9.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala230Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-162394381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394381
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394381
    reference: chr 6
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.114C>T
  hgvsp: ENST00000338468.3:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.450C>T
  hgvsp: ENST00000479615.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.687C>T
  hgvsp: ENST00000366892.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.240C>T
  hgvsp: ENST00000366896.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.687C>T
  hgvsp: ENST00000366898.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.603C>T
  hgvsp: ENST00000366897.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.114C>T
  hgvsp: ENST00000366894.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  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: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile229Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

6-162394397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394397
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394397
    reference: chr 6
allele count: 16
allele frequency: 1.318152609118321e-4
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.671T>C
  hgvsp: ENSP00000355865.1:p.Val224Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.671T>C
  hgvsp: ENSP00000355858.1:p.Val224Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.98T>C
  hgvsp: ENSP00000343589.3:p.Val33Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.98T>C
  hgvsp: ENSP00000355860.1:p.Val33Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.434T>C
  hgvsp: ENSP00000434414.1:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.224T>C
  hgvsp: ENSP00000355862.1:p.Val75Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.587T>C
  hgvsp: ENSP00000355863.1:p.Val196Ala
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44008
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val224Ala
num of homozygotes: 1
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

6-162394399-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394399
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394399
    reference: chr 6
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.432A>G
  hgvsp: ENST00000479615.1:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.669A>G
  hgvsp: ENST00000366898.1:c.669A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.669A>G
  hgvsp: ENST00000366892.1:c.669A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.96A>G
  hgvsp: ENST00000338468.3:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.585A>G
  hgvsp: ENST00000366897.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.96A>G
  hgvsp: ENST00000366894.1:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.222A>G
  hgvsp: ENST00000366896.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser223Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

6-162394409-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394409
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394409
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.212A>G
  hgvsp: ENSP00000355862.1:p.Lys71Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.86A>G
  hgvsp: ENSP00000343589.3:p.Lys29Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.575A>G
  hgvsp: ENSP00000355863.1:p.Lys192Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.659A>G
  hgvsp: ENSP00000355865.1:p.Lys220Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.659A>G
  hgvsp: ENSP00000355858.1:p.Lys220Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.422A>G
  hgvsp: ENSP00000434414.1:p.Lys141Arg
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.86A>G
  hgvsp: ENSP00000355860.1:p.Lys29Arg
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys220Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

6-162394415-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394415
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394415
    reference: chr 6
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.206C>G
  hgvsp: ENSP00000355862.1:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.80C>G
  hgvsp: ENSP00000355860.1:p.Ser27Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.416C>G
  hgvsp: ENSP00000434414.1:p.Ser139Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.569C>G
  hgvsp: ENSP00000355863.1:p.Ser190Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.80C>G
  hgvsp: ENSP00000343589.3:p.Ser27Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.653C>G
  hgvsp: ENSP00000355865.1:p.Ser218Cys
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.653C>G
  hgvsp: ENSP00000355858.1:p.Ser218Cys
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser218Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

6-162394423-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394423
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394423
    reference: chr 6
allele count: 2
allele frequency: 1.650982334489021e-5
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.72C>A
  hgvsp: ENSP00000355860.1:p.His24Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.408C>A
  hgvsp: ENSP00000434414.1:p.His136Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.72C>A
  hgvsp: ENSP00000343589.3:p.His24Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.198C>A
  hgvsp: ENSP00000355862.1:p.His66Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.645C>A
  hgvsp: ENSP00000355865.1:p.His215Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.561C>A
  hgvsp: ENSP00000355863.1:p.His187Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.645C>A
  hgvsp: ENSP00000355858.1:p.His215Gln
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His215Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

6-162394429-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394429
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394429
    reference: chr 6
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.402A>G
  hgvsp: ENST00000479615.1:c.402A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.66A>G
  hgvsp: ENST00000338468.3:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.639A>G
  hgvsp: ENST00000366898.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.555A>G
  hgvsp: ENST00000366897.1:c.555A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.66A>G
  hgvsp: ENST00000366894.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.192A>G
  hgvsp: ENST00000366896.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.639A>G
  hgvsp: ENST00000366892.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly213Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

6-162394433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394433
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394433
    reference: chr 6
allele count: 2
allele frequency: 1.661571181709424e-5
allele num: 120368
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.62G>A
  hgvsp: ENSP00000355860.1:p.Cys21Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.188G>A
  hgvsp: ENSP00000355862.1:p.Cys63Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.62G>A
  hgvsp: ENSP00000343589.3:p.Cys21Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.635G>A
  hgvsp: ENSP00000355865.1:p.Cys212Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.398G>A
  hgvsp: ENSP00000434414.1:p.Cys133Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.551G>A
  hgvsp: ENSP00000355863.1:p.Cys184Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.635G>A
  hgvsp: ENSP00000355858.1:p.Cys212Tyr
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys212Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-162394435-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394435
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394435
    reference: chr 6
allele count: 2
allele frequency: 1.6655008160954e-5
allele num: 120084
alternate allele: A
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.633A>T
  hgvsp: ENSP00000355865.1:p.Lys211Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.549A>T
  hgvsp: ENSP00000355863.1:p.Lys183Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.60A>T
  hgvsp: ENSP00000355860.1:p.Lys20Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.60A>T
  hgvsp: ENSP00000343589.3:p.Lys20Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.186A>T
  hgvsp: ENSP00000355862.1:p.Lys62Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.633A>T
  hgvsp: ENSP00000355858.1:p.Lys211Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.396A>T
  hgvsp: ENSP00000434414.1:p.Lys132Asn
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8089
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys211Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-162394449-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394449
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394449
    reference: chr 6
allele count: 2
allele frequency: 1.720755755928004e-5
allele num: 116228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172G>C
  hgvsp: ENSP00000355862.1:p.Glu58Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619G>C
  hgvsp: ENSP00000355858.1:p.Glu207Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382G>C
  hgvsp: ENSP00000434414.1:p.Glu128Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46G>C
  hgvsp: ENSP00000343589.3:p.Glu16Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619G>C
  hgvsp: ENSP00000355865.1:p.Glu207Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46G>C
  hgvsp: ENSP00000355860.1:p.Glu16Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535G>C
  hgvsp: ENSP00000355863.1:p.Glu179Gln
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18878
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8088
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu207Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-162394461-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394461
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394461
    reference: chr 6
allele count: 2
allele frequency: 1.803459034428033e-5
allele num: 110898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-12T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-12T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15076
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8086
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

6-162394469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394469
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394469
    reference: chr 6
allele count: 2
allele frequency: 1.853087243347417e-5
allele num: 107928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-20C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-20C>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19756
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3880
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8085
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

6-162394475-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394475
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394475
    reference: chr 6
allele count: 1
allele frequency: 9.470593806231651e-6
allele num: 105590
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-26T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-26T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8819
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-162394479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394479
    reference: chr 6
allele count: 10
allele frequency: 9.668935643564357e-5
allele num: 103424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-30T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-30T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22169
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6877
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-162394480-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394480
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394480
    reference: chr 6
allele count: 1
allele frequency: 9.712698381864449e-6
allele num: 102958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-31A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-31A>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5444
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

6-162394480-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394480
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394480
    reference: chr 6
allele count: 1
allele frequency: 9.712698381864449e-6
allele num: 102958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-31A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-31A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

6-162394486-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394486
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394486
    reference: chr 6
allele count: 1
allele frequency: 1.013007010008509e-5
allele num: 98716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-37G>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-37G>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4966
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-162394487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394487
    reference: chr 6
allele count: 4
allele frequency: 4.094920251428104e-5
allele num: 97682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-38G>A
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10622
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7738
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5047
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-162394488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394488
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394488
    reference: chr 6
allele count: 3
allele frequency: 3.099173553719008e-5
allele num: 96800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-39C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-39C>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21397
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8077
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-162394492-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394492
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394492
    reference: chr 6
allele count: 2
allele frequency: 2.131787077106739e-5
allele num: 93818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-43C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-43C>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11186
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8074
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5573
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7837
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-162394497-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162394497
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162394497
    reference: chr 6
allele count: 1
allele frequency: 1.104093980479618e-5
allele num: 90572
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.619-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.382-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.46-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.46-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-48A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.619-48A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5442
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2858
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

6-162475094-AAGAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475094
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475089
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+24_45+28delCCTCT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+24_45+28delCCTCT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+24_381+28delCCTCT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+24_618+28delCCTCT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+24_618+28delCCTCT
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 26363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: AAGAGG
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

6-162475095-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475095
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475095
    reference: chr 6
allele count: 6
allele frequency: 4.942909396470763e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+28T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+28T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+28T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+28T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+28T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80646T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80646T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37533
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS

6-162475098-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475098
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475098
    reference: chr 6
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80649C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80649C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+25C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+25C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+25C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+25C>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+25C>A
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8928
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-162475099-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475099
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475099
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+24C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80650C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+24C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+24C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+24C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+24C>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80650C>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37544
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8930
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  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: 21
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

6-162475106-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475106
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+17A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+17A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+17A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80657A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+17A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+17A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80657A>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8717
  bin: 9.75e1
  variant carriers: 1
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: 463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

6-162475110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475110
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475110
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.45+13T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.618+13T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.45+13T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.618+13T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80661T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.381+13T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80661T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  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: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8917
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8714
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-162475124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475124
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475124
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80675C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.44C>T
  hgvsp: ENSP00000355860.1:p.Ala15Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.44C>T
  hgvsp: ENSP00000343589.3:p.Ala15Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.617C>T
  hgvsp: ENSP00000355865.1:p.Ala206Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.617C>T
  hgvsp: ENSP00000355858.1:p.Ala206Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80675C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.380C>T
  hgvsp: ENSP00000434414.1:p.Ala127Val
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala206Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-162475124-GCACTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475124
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475119
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.612_616delTAGTG
  hgvsp: ENSP00000355858.1:p.Ser205ArgfsTer5
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.612_616delTAGTG
  hgvsp: ENSP00000355865.1:p.Ser205ArgfsTer5
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.375_379delTAGTG
  hgvsp: ENSP00000434414.1:p.Ser126ArgfsTer5
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.39_43delTAGTG
  hgvsp: ENSP00000355860.1:p.Ser14ArgfsTer5
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.39_43delTAGTG
  hgvsp: ENSP00000343589.3:p.Ser14ArgfsTer5
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 9.25e1
  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
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8714
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser205ArgfsTer5
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: GCACTA
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

6-162475127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475127
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475127
    reference: chr 6
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80678G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.41G>A
  hgvsp: ENSP00000355860.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.614G>A
  hgvsp: ENSP00000355865.1:p.Ser205Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.614G>A
  hgvsp: ENSP00000355858.1:p.Ser205Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.41G>A
  hgvsp: ENSP00000343589.3:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.377G>A
  hgvsp: ENSP00000434414.1:p.Ser126Asn
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80678G>A
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8909
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser205Asn
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-162475131-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475131
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475131
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80682A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.373A>T
  hgvsp: ENSP00000434414.1:p.Thr125Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80682A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.610A>T
  hgvsp: ENSP00000355858.1:p.Thr204Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.610A>T
  hgvsp: ENSP00000355865.1:p.Thr204Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.37A>T
  hgvsp: ENSP00000343589.3:p.Thr13Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.37A>T
  hgvsp: ENSP00000355860.1:p.Thr13Ser
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  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: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37618
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr204Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-162475145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475145
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475145
    reference: chr 6
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.596C>T
  hgvsp: ENSP00000355865.1:p.Pro199Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.23C>T
  hgvsp: ENSP00000343589.3:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.596C>T
  hgvsp: ENSP00000355858.1:p.Pro199Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80696C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.359C>T
  hgvsp: ENSP00000434414.1:p.Pro120Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.23C>T
  hgvsp: ENSP00000355860.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80696C>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro199Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-162475150-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475150
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475150
    reference: chr 6
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.591A>G
  hgvsp: ENST00000366892.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.18A>G
  hgvsp: ENST00000338468.3:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.354A>G
  hgvsp: ENST00000479615.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.18A>G
  hgvsp: ENST00000366894.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.591A>G
  hgvsp: ENST00000366898.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80701A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80701A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8706
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8887
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln197Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-162475160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475160
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475160
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.8G>A
  hgvsp: ENSP00000343589.3:p.Gly3Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.581G>A
  hgvsp: ENSP00000355865.1:p.Gly194Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.344G>A
  hgvsp: ENSP00000434414.1:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80711G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.8G>A
  hgvsp: ENSP00000355860.1:p.Gly3Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80711G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.581G>A
  hgvsp: ENSP00000355858.1:p.Gly194Asp
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly194Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

6-162475162-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475162
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475162
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80713T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.6T>C
  hgvsp: ENST00000338468.3:c.6T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.579T>C
  hgvsp: ENST00000366892.1:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.579T>C
  hgvsp: ENST00000366898.1:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.6T>C
  hgvsp: ENST00000366894.1:c.6T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80713T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.342T>C
  hgvsp: ENST00000479615.1:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8880
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser193Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

6-162475167-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475167
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475167
    reference: chr 6
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.574A>T
  hgvsp: ENSP00000355858.1:p.Met192Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.1A>T
  hgvsp: ENSP00000355860.1:p.Met1?
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.337A>T
  hgvsp: ENSP00000434414.1:p.Met113Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.574A>T
  hgvsp: ENSP00000355865.1:p.Met192Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.1A>T
  hgvsp: ENSP00000343589.3:p.Met1?
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80718A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80718A>T
  variant of: http://identifiers.org/hgnc/8607
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-162475167-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475167
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475167
    reference: chr 6
allele count: 656
allele frequency: 5.409417003380886e-3
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80718A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.574A>C
  hgvsp: ENSP00000355858.1:p.Met192Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80718A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.337A>C
  hgvsp: ENSP00000434414.1:p.Met113Leu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.1A>C
  hgvsp: ENSP00000343589.3:p.Met1?
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.1A>C
  hgvsp: ENSP00000355860.1:p.Met1?
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.574A>C
  hgvsp: ENSP00000355865.1:p.Met192Leu
  variant of: http://identifiers.org/hgnc/8607
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 9.75e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26327
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 8.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 14231
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37573
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 22
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

6-162475169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475169
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475169
    reference: chr 6
allele count: 3
allele frequency: 2.474226804123711e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.572G>A
  hgvsp: ENSP00000355865.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-2G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.572G>A
  hgvsp: ENSP00000355858.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80720G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-2G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80720G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.335G>A
  hgvsp: ENSP00000434414.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8264
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg191Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

6-162475170-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475170
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475170
    reference: chr 6
allele count: 6
allele frequency: 4.948616861587186e-5
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.571C>T
  hgvsp: ENSP00000355865.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.334C>T
  hgvsp: ENSP00000434414.1:p.Arg112Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.571C>T
  hgvsp: ENSP00000355858.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80721C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-3C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80721C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-3C>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg191Trp
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

6-162475173-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475173
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475173
    reference: chr 6
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.568A>G
  hgvsp: ENSP00000355865.1:p.Asn190Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.568A>G
  hgvsp: ENSP00000355858.1:p.Asn190Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80724A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-6A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.331A>G
  hgvsp: ENSP00000434414.1:p.Asn111Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80724A>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-6A>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37946
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn190Asp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-162475176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475176
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475176
    reference: chr 6
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80727C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.565C>T
  hgvsp: ENSP00000355858.1:p.Pro189Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80727C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-9C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.328C>T
  hgvsp: ENSP00000434414.1:p.Pro110Ser
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.565C>T
  hgvsp: ENSP00000355865.1:p.Pro189Ser
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro189Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

6-162475186-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475186
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475186
    reference: chr 6
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-19T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.318T>A
  hgvsp: ENSP00000434414.1:p.Asp106Glu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80737T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80737T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.555T>A
  hgvsp: ENSP00000355858.1:p.Asp185Glu
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-19T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.555T>A
  hgvsp: ENSP00000355865.1:p.Asp185Glu
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37778
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp185Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-162475186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475186
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475186
    reference: chr 6
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.318T>C
  hgvsp: ENST00000479615.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.555T>C
  hgvsp: ENST00000366892.1:c.555T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80737T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.555T>C
  hgvsp: ENST00000366898.1:c.555T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80737T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8247
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37778
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp185Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-162475187-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475187
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475187
    reference: chr 6
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.554A>C
  hgvsp: ENSP00000355865.1:p.Asp185Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-20A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80738A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-20A>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.317A>C
  hgvsp: ENSP00000434414.1:p.Asp106Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.554A>C
  hgvsp: ENSP00000355858.1:p.Asp185Ala
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80738A>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp185Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-162475188-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475188
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475188
    reference: chr 6
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-21G>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.316G>T
  hgvsp: ENSP00000434414.1:p.Asp106Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80739G>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.553G>T
  hgvsp: ENSP00000355865.1:p.Asp185Tyr
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80739G>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-21G>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.553G>T
  hgvsp: ENSP00000355858.1:p.Asp185Tyr
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp185Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ

6-162475190-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475190
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475190
    reference: chr 6
allele count: 3
allele frequency: 2.480650922802143e-5
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80741A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.314A>T
  hgvsp: ENSP00000434414.1:p.Asp105Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-23A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.551A>T
  hgvsp: ENSP00000355858.1:p.Asp184Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.551A>T
  hgvsp: ENSP00000355865.1:p.Asp184Val
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80741A>T
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8241
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp184Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

6-162475200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475200
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475200
    reference: chr 6
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.541T>C
  hgvsp: ENSP00000355865.1:p.Ser181Pro
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80751T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-33T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-33T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.541T>C
  hgvsp: ENSP00000355858.1:p.Ser181Pro
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.304T>C
  hgvsp: ENSP00000434414.1:p.Ser102Pro
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80751T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser181Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-162475205-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475205
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475205
    reference: chr 6
allele count: 2
allele frequency: 1.673164120668596e-5
allele num: 119534
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.536G>A
  hgvsp: ENSP00000355865.1:p.Gly179Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80756G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-38G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.299G>A
  hgvsp: ENSP00000434414.1:p.Gly100Asp
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80756G>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.536G>A
  hgvsp: ENSP00000355858.1:p.Gly179Asp
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8215
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly179Asp
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

6-162475215-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475215
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475215
    reference: chr 6
allele count: 45
allele frequency: 3.840639082343302e-4
allele num: 117168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80766T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.535-9T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80766T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-39-9T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.535-9T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.298-9T>A
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-39-9T>A
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23498
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-162475217-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475217
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475217
    reference: chr 6
allele count: 1
allele frequency: 8.577800651912849e-6
allele num: 116580
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.535-11T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-39-11T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.535-11T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80768T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.298-11T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80768T>G
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-39-11T>G
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22678
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-162475217-AAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475217
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475214
    reference: chr 6
allele count: 1
allele frequency: 8.577800651912849e-6
allele num: 116580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.535-14_535-12delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-39-14_-39-12delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.535-14_535-12delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80771_535-80769delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80771_172-80769delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-39-14_-39-12delGTT
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.298-14_298-12delGTT
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22678
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8182
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: AAAC
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

6-162475225-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475225
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475225
    reference: chr 6
allele count: 1
allele frequency: 8.863519526333516e-6
allele num: 112822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-39-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80776T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-39-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.535-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.535-19T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80776T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.298-19T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

6-162475227-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 162475227
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 162475227
    reference: chr 6
allele count: 1
allele frequency: 8.881152418337803e-6
allele num: 112598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355863
  ensembl transcript: ENST00000366897
  gene symbol: PARK2
  hgvsc: ENST00000366897.1:c.535-80778T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000434414
  ensembl transcript: ENST00000479615
  gene symbol: PARK2
  hgvsc: ENST00000479615.1:c.298-21T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355865
  ensembl transcript: ENST00000366898
  gene symbol: PARK2
  hgvsc: ENST00000366898.1:c.535-21T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355862
  ensembl transcript: ENST00000366896
  gene symbol: PARK2
  hgvsc: ENST00000366896.1:c.172-80778T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355858
  ensembl transcript: ENST00000366892
  gene symbol: PARK2
  hgvsc: ENST00000366892.1:c.535-21T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000343589
  ensembl transcript: ENST00000338468
  gene symbol: PARK2
  hgvsc: ENST00000338468.3:c.-39-21T>C
  variant of: http://identifiers.org/hgnc/8607
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185345
  ensembl protein: ENSP00000355860
  ensembl transcript: ENST00000366894
  gene symbol: PARK2
  hgvsc: ENST00000366894.1:c.-39-21T>C
  variant of: http://identifiers.org/hgnc/8607
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43331
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.31e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 1.845098e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

GenotypeQuality
all individuals: 507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5473
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.846632e6

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.571e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 2.947e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

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

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8140
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002011347602894e-5
allele num: 66622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

QD
type: SiteQuality
SIO_000300: 1.571e1

FS
type: SiteQuality
SIO_000300: 2.947e0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

DP
type: SiteQuality
SIO_000300: 1.846632e6

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8136
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5512
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 0
allele frequency: 0.0e0
allele num: 66706
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: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.025e1

FS
type: SiteQuality
SIO_000300: 1.624e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.850849e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.916e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.286e0

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e0

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

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8140
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.594258042199931e-4
allele num: 11564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
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: 8648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.095e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.104e0

DP
type: SiteQuality
SIO_000300: 1.851351e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43814
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8149
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495128166691651e-5
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.697587001333818e-3
allele num: 16494
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.231e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.791e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

FS
type: SiteQuality
SIO_000300: 2.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.85385e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 5524
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

FS
type: SiteQuality
SIO_000300: 1.043e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

VQSLOD
type: SiteQuality
SIO_000300: 8.29e-1

DP
type: SiteQuality
SIO_000300: 1.852067e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

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

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

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.424830261881668e-4
allele num: 16496
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 1.824e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

DP
type: SiteQuality
SIO_000300: 1.852642e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43838
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348880429243728e-4
allele num: 66722
num of homozygotes: 0

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

South Asian
type: Population
allele count: 24
allele frequency: 1.454898157129001e-3
allele num: 16496
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.854587e6

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.75e-2

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 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: 16496
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.854587e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.75e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1060
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.069e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.804e0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

MQRankSum
type: SiteQuality
SIO_000300: 9.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

DP
type: SiteQuality
SIO_000300: 1.853134e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 128
allele frequency: 1.230059581010955e-2
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

DP
type: SiteQuality
SIO_000300: 1.861054e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.302e0

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 318
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variant carriers: 0

GenotypeQuality
all individuals: 43849
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.302e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.154e1

DP
type: SiteQuality
SIO_000300: 1.861054e6

FS
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

GenotypeQuality
all individuals: 921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 43966
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.004e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.851004e6

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.74e-1

FS
type: SiteQuality
SIO_000300: 1.497e0

QD
type: SiteQuality
SIO_000300: 1.088e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 239
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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: 8104
bin: 9.75e1
variant carriers: 17

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
all individuals: 5527
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.635482307319437e-4
allele num: 16504
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: 6
allele frequency: 8.990919171636647e-5
allele num: 66734
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.852479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
all individuals: 239
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 8096
bin: 9.75e1
variant carriers: 3

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 1.116e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.851219e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.65e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 920
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 8092
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 495
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 6.059871530723549e-5
allele num: 16502
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: 8650
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.22e-1

FS
type: SiteQuality
SIO_000300: 1.517e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.483e1

DP
type: SiteQuality
SIO_000300: 1.851063e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

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

GenotypeQuality
all individuals: 920
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 5529
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 1.498531439189594e-5
allele num: 66732
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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.387e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.649e0

DP
type: SiteQuality
SIO_000300: 1.850995e6

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 920
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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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: 908
num of homozygotes: 0

South Asian
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allele count: 30
allele frequency: 1.817741153659719e-3
allele num: 16504
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

QD
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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DP
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MQ
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SIO_000300: 5.981e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.597e0

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
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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ReadPosRankSum
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FS
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DP
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MQRankSum
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VQSLOD
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MQ
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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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variant carriers: 15

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

South Asian
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allele count: 16
allele frequency: 9.695794449157678e-4
allele num: 16502
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
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DP
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.13e-2

VQSLOD
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 2

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.211e1

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

Latino
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allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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MQ
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ReadPosRankSum
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SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.850705e6

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-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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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

Other
type: Population
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South Asian
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allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

East Asian
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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DP
type: SiteQuality
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ReadPosRankSum
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66628
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European (Finnish)
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Latino
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South Asian
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Other
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East Asian
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ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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

African
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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Other
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East Asian
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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South Asian
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East Asian
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MQRankSum
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BaseQRankSum
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MQ
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DP
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FS
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VQSLOD
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024437454633438e-5
allele num: 66128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.095e1

DP
type: SiteQuality
SIO_000300: 1.831416e6

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 8.282999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.936e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4740
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.124023742580444e-5
allele num: 64020
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.756632e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.083e0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

FS
type: SiteQuality
SIO_000300: 1.304e0

QD
type: SiteQuality
SIO_000300: 8.26e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 493
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variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.993223041658362e-4
allele num: 10034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.01e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.153e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 1.609756e6

GenotypeQuality
all individuals: 691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 16468
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.331735251032095e-4
allele num: 15018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59302
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.069e0

DP
type: SiteQuality
SIO_000300: 1.507946e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -8.262e-1

FS
type: SiteQuality
SIO_000300: 9.071999999999999e0

QD
type: SiteQuality
SIO_000300: 1.149e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.604e0

GenotypeQuality
all individuals: 2640
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 395
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variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.068376068376068e-4
allele num: 9360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7248
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

QD
type: SiteQuality
SIO_000300: 1.107e1

FS
type: SiteQuality
SIO_000300: 7.544e0

DP
type: SiteQuality
SIO_000300: 1.422026e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-1

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
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variant carriers: 0

GenotypeQuality
all individuals: 18646
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variant carriers: 0

GenotypeQuality
all individuals: 1475
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GenotypeQuality
all individuals: 478
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 8091
bin: 9.75e1
variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 376
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GenotypeQuality
all individuals: 9290
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.11731843575419e-3
allele num: 8950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7076
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

DP
type: SiteQuality
SIO_000300: 1.354831e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8082
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variant carriers: 1

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.123848055742864e-4
allele num: 8898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14558
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.346e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.345468e6

QD
type: SiteQuality
SIO_000300: 1.005e1

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 672
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variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56410
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.420858198351804e-4
allele num: 7038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.87e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 1.345468e6

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.346e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.48544266191325e-4
allele num: 6732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.608e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

DP
type: SiteQuality
SIO_000300: 1.288195e6

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8078
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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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: 219
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variant carriers: 1

GenotypeQuality
all individuals: 452
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.512019230769231e-5
allele num: 53248
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.280561e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

FS
type: SiteQuality
SIO_000300: 4.734e0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-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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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.690224194833277e-5
allele num: 52722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

FS
type: SiteQuality
SIO_000300: 2.185e0

QD
type: SiteQuality
SIO_000300: 1.3e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 1.271269e6

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.310959622443629e-4
allele num: 7628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.965022597759874e-5
allele num: 50890
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13788
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
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SIO_000300: 1.246894e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

FS
type: SiteQuality
SIO_000300: 1.3076e1

QD
type: SiteQuality
SIO_000300: 1.501e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.041316240712011e-5
allele num: 48988
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.761e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

DP
type: SiteQuality
SIO_000300: 1.232485e6

QD
type: SiteQuality
SIO_000300: 1.413e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.121291e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 5.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

FS
type: SiteQuality
SIO_000300: 8.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.131e0

MQ
type: SiteQuality
SIO_000300: 5.208e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.558e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 6
allele frequency: 5.185825410544512e-4
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 16510
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.501e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

DP
type: SiteQuality
SIO_000300: 2.121414e6

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 2.973e0

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: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
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: 11570
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.121361e6

FS
type: SiteQuality
SIO_000300: 2.782e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.539e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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QD
type: SiteQuality
SIO_000300: 1.159e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
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MQRankSum
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ClippingRankSum
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SIO_000300: -8.81e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 5.588e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
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SIO_000300: 4.875e0

ReadPosRankSum
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DP
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
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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: 16510
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

FS
type: SiteQuality
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQRankSum
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SIO_000300: 6.29e-1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

FS
type: SiteQuality
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QD
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.859e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.785e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

DP
type: SiteQuality
SIO_000300: 2.120801e6

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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: 10386
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: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
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: 2.812e0

VQSLOD
type: SiteQuality
SIO_000300: -1.507e0

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.120488e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.886e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e0

QD
type: SiteQuality
SIO_000300: 1.08e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.831e0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 2.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 2.120254e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.69e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
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SIO_000300: 1.221e1

InbreedingCoeff
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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South Asian
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allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.82e-1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.31e-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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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
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: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

South Asian
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East Asian
type: Population
allele count: 0
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allele num: 8652
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

DP
type: SiteQuality
SIO_000300: 2.141328e6

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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bin: 9.75e1
variant carriers: 632

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.299142223022014e-4
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 608
allele frequency: 5.869859046147905e-2
allele num: 10358
num of homozygotes: 22

Latino
type: Population
allele count: 23
allele frequency: 1.988931165686614e-3
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.141328e6

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.87e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
all individuals: 3
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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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bin: 5.25e1
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499370088187654e-5
allele num: 66676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.101085e6

QD
type: SiteQuality
SIO_000300: 1.293e1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

GenotypeQuality
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bin: 2.5e0
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: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.49940004799616e-5
allele num: 66672
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
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SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.100887e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

FS
type: SiteQuality
SIO_000300: 3.884e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 1.933114247052001e-4
allele num: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
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: 66670
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.69e0

DP
type: SiteQuality
SIO_000300: 2.100344e6

QD
type: SiteQuality
SIO_000300: 1.454e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.679e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.449e0

QD
type: SiteQuality
SIO_000300: 1.154e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 2.099805e6

VQSLOD
type: SiteQuality
SIO_000300: 9.61e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 8902
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.053e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 1.2367e1

DP
type: SiteQuality
SIO_000300: 2.096634e6

VQSLOD
type: SiteQuality
SIO_000300: -5.451e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.37e-1

QD
type: SiteQuality
SIO_000300: 1.508e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
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: 16444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.053e0

VQSLOD
type: SiteQuality
SIO_000300: -5.451e-1

FS
type: SiteQuality
SIO_000300: 1.2367e1

DP
type: SiteQuality
SIO_000300: 2.096634e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

QD
type: SiteQuality
SIO_000300: 1.508e1

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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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

QD
type: SiteQuality
SIO_000300: 1.585e1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.096111e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514692517418964e-4
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 5.859e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.095624e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 0
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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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variant carriers: 0

GenotypeQuality
all individuals: 416
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variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508024283224139e-5
allele num: 66548
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

DP
type: SiteQuality
SIO_000300: 2.094627e6

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
all individuals: 146
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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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variant carriers: 0

GenotypeQuality
all individuals: 435
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.128201985537444e-5
allele num: 16318
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

DP
type: SiteQuality
SIO_000300: 2.080824e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.114e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

FS
type: SiteQuality
SIO_000300: 2.3806e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.66e0

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.374e0

GenotypeQuality
all individuals: 36222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65832
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.233806292412091e-4
allele num: 16210
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.857e0

QD
type: SiteQuality
SIO_000300: 1.392e1

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.345e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.057741e6

GenotypeQuality
all individuals: 8207
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7649
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.15473441108545e-3
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 6.829116871022816e-4
allele num: 64430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.717e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

DP
type: SiteQuality
SIO_000300: 1.977164e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5615
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.099181073703367e-5
allele num: 10990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64064
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

DP
type: SiteQuality
SIO_000300: 1.951785e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

FS
type: SiteQuality
SIO_000300: 1.636e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

QD
type: SiteQuality
SIO_000300: 1.853e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

GenotypeQuality
all individuals: 1678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5615
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560939060939061e-5
allele num: 64064
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.951785e6

FS
type: SiteQuality
SIO_000300: 1.636e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.853e1

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8174
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 898
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.494872768704899e-5
allele num: 10532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61870
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 1.732679e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

QD
type: SiteQuality
SIO_000300: 1.713e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0