10-34648953-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648953
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648953
    reference: chr 10
allele count: 2
allele frequency: 1.681096074640666e-5
allele num: 118970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+46A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+46A>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

10-34648959-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648959
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648959
    reference: chr 10
allele count: 1
allele frequency: 8.403078888104602e-6
allele num: 119004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+40A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+40A>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

10-34648968-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648968
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648968
    reference: chr 10
allele count: 1
allele frequency: 8.379981899239097e-6
allele num: 119332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+31A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+31A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

10-34648969-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648969
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648969
    reference: chr 10
allele count: 1
allele frequency: 8.37436773523599e-6
allele num: 119412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+30T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+30T>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

10-34648970-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648970
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648970
    reference: chr 10
allele count: 1
allele frequency: 8.368621018628551e-6
allele num: 119494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+29C>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+29C>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

10-34648971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648971
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648971
    reference: chr 10
allele count: 4
allele frequency: 3.345600535296086e-5
allele num: 119560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+28C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+28C>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13776
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

10-34648974-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648974
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648974
    reference: chr 10
allele count: 1
allele frequency: 8.342510094437214e-6
allele num: 119868
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+25A>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+25A>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

10-34648976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648976
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648976
    reference: chr 10
allele count: 2
allele frequency: 1.666361167119361e-5
allele num: 120022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+23G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+23G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17927
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

10-34648977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648977
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648977
    reference: chr 10
allele count: 2
allele frequency: 1.663561352142667e-5
allele num: 120224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+22C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+22C>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

10-34648988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34648988
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34648988
    reference: chr 10
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1896+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1725+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.210+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1857+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1857+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1896+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1047+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1896+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1896+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1896+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1857+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1725+11A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1725+11A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

10-34649003-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649003
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649003
    reference: chr 10
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1853C>G
  hgvsp: ENSP00000363908.1:p.Ser618Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1892C>G
  hgvsp: ENSP00000363921.3:p.Ser631Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1721C>G
  hgvsp: ENSP00000440857.1:p.Ser574Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1043C>G
  hgvsp: ENSP00000444429.1:p.Ser348Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1892C>G
  hgvsp: ENSP00000363905.1:p.Ser631Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1892C>G
  hgvsp: ENSP00000341844.5:p.Ser631Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1892C>G
  hgvsp: ENSP00000363920.3:p.Ser631Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1721C>G
  hgvsp: ENSP00000363926.3:p.Ser574Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1892C>G
  hgvsp: ENSP00000340591.4:p.Ser631Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1853C>G
  hgvsp: ENSP00000311986.6:p.Ser618Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.206C>G
  hgvsp: ENSP00000363900.1:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1853C>G
  hgvsp: ENSP00000443147.1:p.Ser618Cys
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1721C>G
  hgvsp: ENSP00000363922.3:p.Ser574Cys
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser631Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

10-34649014-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649014
    reference: chr 10
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.195A>T
  hgvsp: ENST00000374768.1:c.195A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1032A>T
  hgvsp: ENST00000544292.1:c.1032A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1881A>T
  hgvsp: ENST00000374788.3:c.1881A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1842A>T
  hgvsp: ENST00000350537.4:c.1842A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1881A>T
  hgvsp: ENST00000346874.4:c.1881A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1881A>T
  hgvsp: ENST00000340077.5:c.1881A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1842A>T
  hgvsp: ENST00000374776.1:c.1842A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1710A>T
  hgvsp: ENST00000374790.3:c.1710A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1842A>T
  hgvsp: ENST00000545693.1:c.1842A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1710A>T
  hgvsp: ENST00000374794.3:c.1710A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1710A>T
  hgvsp: ENST00000545260.1:c.1710A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1881A>T
  hgvsp: ENST00000374789.3:c.1881A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1881A>T
  hgvsp: ENST00000374773.1:c.1881A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly627Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-34649031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649031
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649031
    reference: chr 10
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1693A>G
  hgvsp: ENSP00000363926.3:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1864A>G
  hgvsp: ENSP00000363921.3:p.Lys622Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1015A>G
  hgvsp: ENSP00000444429.1:p.Lys339Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1864A>G
  hgvsp: ENSP00000363920.3:p.Lys622Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1864A>G
  hgvsp: ENSP00000363905.1:p.Lys622Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1825A>G
  hgvsp: ENSP00000311986.6:p.Lys609Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1693A>G
  hgvsp: ENSP00000363922.3:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1693A>G
  hgvsp: ENSP00000440857.1:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.178A>G
  hgvsp: ENSP00000363900.1:p.Lys60Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1825A>G
  hgvsp: ENSP00000443147.1:p.Lys609Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1864A>G
  hgvsp: ENSP00000340591.4:p.Lys622Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1825A>G
  hgvsp: ENSP00000363908.1:p.Lys609Glu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1864A>G
  hgvsp: ENSP00000341844.5:p.Lys622Glu
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys622Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

10-34649032-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649032
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649032
    reference: chr 10
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1824C>A
  hgvsp: ENST00000374776.1:c.1824C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1824C>A
  hgvsp: ENST00000545693.1:c.1824C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1692C>A
  hgvsp: ENST00000545260.1:c.1692C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1863C>A
  hgvsp: ENST00000340077.5:c.1863C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1863C>A
  hgvsp: ENST00000374773.1:c.1863C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1863C>A
  hgvsp: ENST00000346874.4:c.1863C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1014C>A
  hgvsp: ENST00000544292.1:c.1014C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1863C>A
  hgvsp: ENST00000374788.3:c.1863C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1692C>A
  hgvsp: ENST00000374794.3:c.1692C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1824C>A
  hgvsp: ENST00000350537.4:c.1824C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1863C>A
  hgvsp: ENST00000374789.3:c.1863C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.177C>A
  hgvsp: ENST00000374768.1:c.177C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1692C>A
  hgvsp: ENST00000374790.3:c.1692C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18638
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val621Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-34649034-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649034
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649035
    reference: chr 10
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: CA
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1860dupT
  hgvsp: ENSP00000363921.3:p.Val621CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1860dupT
  hgvsp: ENSP00000363905.1:p.Val621CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.174dupT
  hgvsp: ENSP00000363900.1:p.Val59CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1860dupT
  hgvsp: ENSP00000341844.5:p.Val621CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1860dupT
  hgvsp: ENSP00000363920.3:p.Val621CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1860dupT
  hgvsp: ENSP00000340591.4:p.Val621CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1689dupT
  hgvsp: ENSP00000440857.1:p.Val564CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1689dupT
  hgvsp: ENSP00000363922.3:p.Val564CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1821dupT
  hgvsp: ENSP00000311986.6:p.Val608CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1821dupT
  hgvsp: ENSP00000443147.1:p.Val608CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1821dupT
  hgvsp: ENSP00000363908.1:p.Val608CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1011dupT
  hgvsp: ENSP00000444429.1:p.Val338CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1689dupT
  hgvsp: ENSP00000363926.3:p.Val564CysfsTer6
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val621CysfsTer6
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

10-34649034-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649034
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649034
    reference: chr 10
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1690G>C
  hgvsp: ENSP00000363922.3:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1861G>C
  hgvsp: ENSP00000341844.5:p.Val621Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1822G>C
  hgvsp: ENSP00000311986.6:p.Val608Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1861G>C
  hgvsp: ENSP00000363905.1:p.Val621Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1861G>C
  hgvsp: ENSP00000363920.3:p.Val621Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1861G>C
  hgvsp: ENSP00000340591.4:p.Val621Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1690G>C
  hgvsp: ENSP00000440857.1:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1822G>C
  hgvsp: ENSP00000443147.1:p.Val608Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.175G>C
  hgvsp: ENSP00000363900.1:p.Val59Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1861G>C
  hgvsp: ENSP00000363921.3:p.Val621Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1012G>C
  hgvsp: ENSP00000444429.1:p.Val338Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1822G>C
  hgvsp: ENSP00000363908.1:p.Val608Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1690G>C
  hgvsp: ENSP00000363926.3:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val621Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/10-34649035-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649035
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649035
    reference: chr 10
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1860T>G
  hgvsp: ENSP00000363921.3:p.Phe620Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1689T>G
  hgvsp: ENSP00000440857.1:p.Phe563Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1011T>G
  hgvsp: ENSP00000444429.1:p.Phe337Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1860T>G
  hgvsp: ENSP00000340591.4:p.Phe620Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1860T>G
  hgvsp: ENSP00000363920.3:p.Phe620Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1860T>G
  hgvsp: ENSP00000341844.5:p.Phe620Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1821T>G
  hgvsp: ENSP00000443147.1:p.Phe607Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.174T>G
  hgvsp: ENSP00000363900.1:p.Phe58Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1821T>G
  hgvsp: ENSP00000311986.6:p.Phe607Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1689T>G
  hgvsp: ENSP00000363922.3:p.Phe563Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1821T>G
  hgvsp: ENSP00000363908.1:p.Phe607Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1860T>G
  hgvsp: ENSP00000363905.1:p.Phe620Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1689T>G
  hgvsp: ENSP00000363926.3:p.Phe563Leu
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe620Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

10-34649035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649035
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649035
    reference: chr 10
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1860T>C
  hgvsp: ENST00000346874.4:c.1860T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1689T>C
  hgvsp: ENST00000545260.1:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1689T>C
  hgvsp: ENST00000374790.3:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1860T>C
  hgvsp: ENST00000340077.5:c.1860T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.174T>C
  hgvsp: ENST00000374768.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1689T>C
  hgvsp: ENST00000374794.3:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1860T>C
  hgvsp: ENST00000374773.1:c.1860T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1821T>C
  hgvsp: ENST00000374776.1:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1821T>C
  hgvsp: ENST00000545693.1:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1821T>C
  hgvsp: ENST00000350537.4:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1860T>C
  hgvsp: ENST00000374788.3:c.1860T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1011T>C
  hgvsp: ENST00000544292.1:c.1011T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1860T>C
  hgvsp: ENST00000374789.3:c.1860T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe620Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

10-34649046-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649046
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649046
    reference: chr 10
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1849T>C
  hgvsp: ENST00000374788.3:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1810T>C
  hgvsp: ENST00000545693.1:c.1810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.1000T>C
  hgvsp: ENST00000544292.1:c.1000T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1678T>C
  hgvsp: ENST00000374790.3:c.1678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.163T>C
  hgvsp: ENST00000374768.1:c.163T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1810T>C
  hgvsp: ENST00000350537.4:c.1810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1678T>C
  hgvsp: ENST00000545260.1:c.1678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1849T>C
  hgvsp: ENST00000374789.3:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1849T>C
  hgvsp: ENST00000346874.4:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1849T>C
  hgvsp: ENST00000374773.1:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1849T>C
  hgvsp: ENST00000340077.5:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1810T>C
  hgvsp: ENST00000374776.1:c.1810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1678T>C
  hgvsp: ENST00000374794.3:c.1678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu617Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

10-34649048-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649048
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649048
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.161A>G
  hgvsp: ENSP00000363900.1:p.Asp54Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.998A>G
  hgvsp: ENSP00000444429.1:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1847A>G
  hgvsp: ENSP00000341844.5:p.Asp616Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1808A>G
  hgvsp: ENSP00000363908.1:p.Asp603Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1847A>G
  hgvsp: ENSP00000363920.3:p.Asp616Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1808A>G
  hgvsp: ENSP00000443147.1:p.Asp603Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1676A>G
  hgvsp: ENSP00000363926.3:p.Asp559Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1847A>G
  hgvsp: ENSP00000363905.1:p.Asp616Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1676A>G
  hgvsp: ENSP00000363922.3:p.Asp559Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1847A>G
  hgvsp: ENSP00000340591.4:p.Asp616Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1847A>G
  hgvsp: ENSP00000363921.3:p.Asp616Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1808A>G
  hgvsp: ENSP00000311986.6:p.Asp603Gly
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1676A>G
  hgvsp: ENSP00000440857.1:p.Asp559Gly
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp616Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

10-34649052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649052
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649052
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1843G>A
  hgvsp: ENSP00000340591.4:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1672G>A
  hgvsp: ENSP00000440857.1:p.Ala558Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1843G>A
  hgvsp: ENSP00000363905.1:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.157G>A
  hgvsp: ENSP00000363900.1:p.Ala53Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1804G>A
  hgvsp: ENSP00000363908.1:p.Ala602Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1843G>A
  hgvsp: ENSP00000363920.3:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1804G>A
  hgvsp: ENSP00000311986.6:p.Ala602Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1672G>A
  hgvsp: ENSP00000363922.3:p.Ala558Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1843G>A
  hgvsp: ENSP00000341844.5:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.994G>A
  hgvsp: ENSP00000444429.1:p.Ala332Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1672G>A
  hgvsp: ENSP00000363926.3:p.Ala558Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1804G>A
  hgvsp: ENSP00000443147.1:p.Ala602Thr
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1843G>A
  hgvsp: ENSP00000363921.3:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala615Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

10-34649053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649053
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649053
    reference: chr 10
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1842C>T
  hgvsp: ENST00000374789.3:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.156C>T
  hgvsp: ENST00000374768.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1803C>T
  hgvsp: ENST00000545693.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1803C>T
  hgvsp: ENST00000350537.4:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.993C>T
  hgvsp: ENST00000544292.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1842C>T
  hgvsp: ENST00000346874.4:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1842C>T
  hgvsp: ENST00000340077.5:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1842C>T
  hgvsp: ENST00000374788.3:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1803C>T
  hgvsp: ENST00000374776.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1842C>T
  hgvsp: ENST00000374773.1:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1671C>T
  hgvsp: ENST00000374794.3:c.1671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1671C>T
  hgvsp: ENST00000374790.3:c.1671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1671C>T
  hgvsp: ENST00000545260.1:c.1671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His614His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

10-34649065-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649065
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649065
    reference: chr 10
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1659A>T
  hgvsp: ENST00000374790.3:c.1659A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1791A>T
  hgvsp: ENST00000374776.1:c.1791A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.981A>T
  hgvsp: ENST00000544292.1:c.981A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1830A>T
  hgvsp: ENST00000374789.3:c.1830A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1659A>T
  hgvsp: ENST00000374794.3:c.1659A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1830A>T
  hgvsp: ENST00000346874.4:c.1830A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1830A>T
  hgvsp: ENST00000374788.3:c.1830A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1830A>T
  hgvsp: ENST00000374773.1:c.1830A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1791A>T
  hgvsp: ENST00000350537.4:c.1791A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.144A>T
  hgvsp: ENST00000374768.1:c.144A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1791A>T
  hgvsp: ENST00000545693.1:c.1791A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1830A>T
  hgvsp: ENST00000340077.5:c.1830A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1659A>T
  hgvsp: ENST00000545260.1:c.1659A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser610Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

10-34649069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649069
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649069
    reference: chr 10
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1655G>A
  hgvsp: ENSP00000363926.3:p.Arg552Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1826G>A
  hgvsp: ENSP00000363905.1:p.Arg609Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1826G>A
  hgvsp: ENSP00000363921.3:p.Arg609Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1826G>A
  hgvsp: ENSP00000363920.3:p.Arg609Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1826G>A
  hgvsp: ENSP00000340591.4:p.Arg609Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1787G>A
  hgvsp: ENSP00000311986.6:p.Arg596Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1826G>A
  hgvsp: ENSP00000341844.5:p.Arg609Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.977G>A
  hgvsp: ENSP00000444429.1:p.Arg326Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1787G>A
  hgvsp: ENSP00000443147.1:p.Arg596Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1655G>A
  hgvsp: ENSP00000440857.1:p.Arg552Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.140G>A
  hgvsp: ENSP00000363900.1:p.Arg47Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1787G>A
  hgvsp: ENSP00000363908.1:p.Arg596Gln
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1655G>A
  hgvsp: ENSP00000363922.3:p.Arg552Gln
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg609Gln
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

10-34649070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649070
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649070
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1654C>T
  hgvsp: ENSP00000440857.1:p.Arg552Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.139C>T
  hgvsp: ENSP00000363900.1:p.Arg47Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1654C>T
  hgvsp: ENSP00000363926.3:p.Arg552Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1825C>T
  hgvsp: ENSP00000341844.5:p.Arg609Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1786C>T
  hgvsp: ENSP00000443147.1:p.Arg596Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.976C>T
  hgvsp: ENSP00000444429.1:p.Arg326Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1786C>T
  hgvsp: ENSP00000363908.1:p.Arg596Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1825C>T
  hgvsp: ENSP00000340591.4:p.Arg609Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1825C>T
  hgvsp: ENSP00000363920.3:p.Arg609Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1786C>T
  hgvsp: ENSP00000311986.6:p.Arg596Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1654C>T
  hgvsp: ENSP00000363922.3:p.Arg552Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1825C>T
  hgvsp: ENSP00000363905.1:p.Arg609Trp
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1825C>T
  hgvsp: ENSP00000363921.3:p.Arg609Trp
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg609Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

10-34649078-TTGACAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649078
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649072
    reference: chr 10
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.962_967delGTGTCA
  hgvsp: ENSP00000444429.1:p.Ser321_Val322del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1640_1645delGTGTCA
  hgvsp: ENSP00000363922.3:p.Ser547_Val548del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.125_130delGTGTCA
  hgvsp: ENSP00000363900.1:p.Ser42_Val43del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1811_1816delGTGTCA
  hgvsp: ENSP00000363921.3:p.Ser604_Val605del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1772_1777delGTGTCA
  hgvsp: ENSP00000363908.1:p.Ser591_Val592del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1811_1816delGTGTCA
  hgvsp: ENSP00000363905.1:p.Ser604_Val605del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1772_1777delGTGTCA
  hgvsp: ENSP00000311986.6:p.Ser591_Val592del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1811_1816delGTGTCA
  hgvsp: ENSP00000340591.4:p.Ser604_Val605del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1811_1816delGTGTCA
  hgvsp: ENSP00000341844.5:p.Ser604_Val605del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1811_1816delGTGTCA
  hgvsp: ENSP00000363920.3:p.Ser604_Val605del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1772_1777delGTGTCA
  hgvsp: ENSP00000443147.1:p.Ser591_Val592del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1640_1645delGTGTCA
  hgvsp: ENSP00000440857.1:p.Ser547_Val548del
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1640_1645delGTGTCA
  hgvsp: ENSP00000363926.3:p.Ser547_Val548del
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser604_Val605del
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TTGACAC
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff

10-34649082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649082
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649082
    reference: chr 10
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1813G>A
  hgvsp: ENSP00000341844.5:p.Val605Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.964G>A
  hgvsp: ENSP00000444429.1:p.Val322Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1774G>A
  hgvsp: ENSP00000363908.1:p.Val592Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1642G>A
  hgvsp: ENSP00000363922.3:p.Val548Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1774G>A
  hgvsp: ENSP00000443147.1:p.Val592Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1813G>A
  hgvsp: ENSP00000340591.4:p.Val605Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1813G>A
  hgvsp: ENSP00000363905.1:p.Val605Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1813G>A
  hgvsp: ENSP00000363921.3:p.Val605Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1813G>A
  hgvsp: ENSP00000363920.3:p.Val605Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1642G>A
  hgvsp: ENSP00000363926.3:p.Val548Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.127G>A
  hgvsp: ENSP00000363900.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1774G>A
  hgvsp: ENSP00000311986.6:p.Val592Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1642G>A
  hgvsp: ENSP00000440857.1:p.Val548Ile
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val605Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-34649100-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649100
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649100
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1624G>T
  hgvsp: ENSP00000363926.3:p.Ala542Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1756G>T
  hgvsp: ENSP00000311986.6:p.Ala586Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1756G>T
  hgvsp: ENSP00000363908.1:p.Ala586Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1795G>T
  hgvsp: ENSP00000363920.3:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.109G>T
  hgvsp: ENSP00000363900.1:p.Ala37Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1624G>T
  hgvsp: ENSP00000363922.3:p.Ala542Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1624G>T
  hgvsp: ENSP00000440857.1:p.Ala542Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1795G>T
  hgvsp: ENSP00000340591.4:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1795G>T
  hgvsp: ENSP00000363905.1:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1756G>T
  hgvsp: ENSP00000443147.1:p.Ala586Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1795G>T
  hgvsp: ENSP00000363921.3:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1795G>T
  hgvsp: ENSP00000341844.5:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.946G>T
  hgvsp: ENSP00000444429.1:p.Ala316Ser
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala599Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-34649119-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649119
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649119
    reference: chr 10
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1776A>G
  hgvsp: ENST00000374773.1:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1737A>G
  hgvsp: ENST00000374776.1:c.1737A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1605A>G
  hgvsp: ENST00000374790.3:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1605A>G
  hgvsp: ENST00000545260.1:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1776A>G
  hgvsp: ENST00000346874.4:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1776A>G
  hgvsp: ENST00000340077.5:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1737A>G
  hgvsp: ENST00000350537.4:c.1737A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1776A>G
  hgvsp: ENST00000374789.3:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1737A>G
  hgvsp: ENST00000545693.1:c.1737A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1776A>G
  hgvsp: ENST00000374788.3:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.927A>G
  hgvsp: ENST00000544292.1:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1605A>G
  hgvsp: ENST00000374794.3:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.90A>G
  hgvsp: ENST00000374768.1:c.90A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro592Pro
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

10-34649130-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649130
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649130
    reference: chr 10
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1765T>C
  hgvsp: ENSP00000363920.3:p.Phe589Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1765T>C
  hgvsp: ENSP00000363921.3:p.Phe589Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.916T>C
  hgvsp: ENSP00000444429.1:p.Phe306Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1726T>C
  hgvsp: ENSP00000443147.1:p.Phe576Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1765T>C
  hgvsp: ENSP00000340591.4:p.Phe589Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1726T>C
  hgvsp: ENSP00000363908.1:p.Phe576Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1765T>C
  hgvsp: ENSP00000341844.5:p.Phe589Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1765T>C
  hgvsp: ENSP00000363905.1:p.Phe589Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1594T>C
  hgvsp: ENSP00000363926.3:p.Phe532Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1594T>C
  hgvsp: ENSP00000440857.1:p.Phe532Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1594T>C
  hgvsp: ENSP00000363922.3:p.Phe532Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.79T>C
  hgvsp: ENSP00000363900.1:p.Phe27Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1726T>C
  hgvsp: ENSP00000311986.6:p.Phe576Leu
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe589Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS

10-34649134-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649134
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649134
    reference: chr 10
allele count: 81
allele frequency: 6.672597864768683e-4
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1590G>C
  hgvsp: ENST00000374790.3:c.1590G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.912G>C
  hgvsp: ENST00000544292.1:c.912G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1722G>C
  hgvsp: ENST00000374776.1:c.1722G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1590G>C
  hgvsp: ENST00000374794.3:c.1590G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1722G>C
  hgvsp: ENST00000545693.1:c.1722G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1761G>C
  hgvsp: ENST00000374788.3:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1761G>C
  hgvsp: ENST00000374773.1:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1761G>C
  hgvsp: ENST00000374789.3:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1761G>C
  hgvsp: ENST00000346874.4:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1590G>C
  hgvsp: ENST00000545260.1:c.1590G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.75G>C
  hgvsp: ENST00000374768.1:c.75G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1722G>C
  hgvsp: ENST00000350537.4:c.1722G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1761G>C
  hgvsp: ENST00000340077.5:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu587Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

10-34649143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649143
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649143
    reference: chr 10
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.903G>A
  hgvsp: ENST00000544292.1:c.903G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1752G>A
  hgvsp: ENST00000340077.5:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1581G>A
  hgvsp: ENST00000374794.3:c.1581G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1752G>A
  hgvsp: ENST00000374788.3:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1752G>A
  hgvsp: ENST00000374773.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1713G>A
  hgvsp: ENST00000545693.1:c.1713G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1713G>A
  hgvsp: ENST00000374776.1:c.1713G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1581G>A
  hgvsp: ENST00000374790.3:c.1581G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1752G>A
  hgvsp: ENST00000374789.3:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1752G>A
  hgvsp: ENST00000346874.4:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1581G>A
  hgvsp: ENST00000545260.1:c.1581G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1713G>A
  hgvsp: ENST00000350537.4:c.1713G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.66G>A
  hgvsp: ENST00000374768.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg584Arg
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

10-34649146-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649146
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649146
    reference: chr 10
allele count: 2210
allele frequency: 1.821058356268231e-2
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1710C>G
  hgvsp: ENST00000374776.1:c.1710C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1749C>G
  hgvsp: ENST00000374788.3:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1749C>G
  hgvsp: ENST00000374773.1:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1749C>G
  hgvsp: ENST00000340077.5:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1749C>G
  hgvsp: ENST00000346874.4:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1578C>G
  hgvsp: ENST00000374790.3:c.1578C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1578C>G
  hgvsp: ENST00000545260.1:c.1578C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1710C>G
  hgvsp: ENST00000350537.4:c.1710C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1710C>G
  hgvsp: ENST00000545693.1:c.1710C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.900C>G
  hgvsp: ENST00000544292.1:c.900C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1578C>G
  hgvsp: ENST00000374794.3:c.1578C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.63C>G
  hgvsp: ENST00000374768.1:c.63C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1749C>G
  hgvsp: ENST00000374789.3:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 1105
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 5.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13764
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
hgvs: p.Thr583Thr
num of homozygotes: 33
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

10-34649148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649148
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649148
    reference: chr 10
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1576A>G
  hgvsp: ENSP00000440857.1:p.Thr526Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1708A>G
  hgvsp: ENSP00000311986.6:p.Thr570Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1576A>G
  hgvsp: ENSP00000363922.3:p.Thr526Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1708A>G
  hgvsp: ENSP00000363908.1:p.Thr570Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.898A>G
  hgvsp: ENSP00000444429.1:p.Thr300Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1576A>G
  hgvsp: ENSP00000363926.3:p.Thr526Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1747A>G
  hgvsp: ENSP00000340591.4:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1747A>G
  hgvsp: ENSP00000363921.3:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1708A>G
  hgvsp: ENSP00000443147.1:p.Thr570Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1747A>G
  hgvsp: ENSP00000363905.1:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1747A>G
  hgvsp: ENSP00000363920.3:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.61A>G
  hgvsp: ENSP00000363900.1:p.Thr21Ala
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1747A>G
  hgvsp: ENSP00000341844.5:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr583Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-34649151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649151
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649151
    reference: chr 10
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.58G>A
  hgvsp: ENSP00000363900.1:p.Gly20Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1744G>A
  hgvsp: ENSP00000340591.4:p.Gly582Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1744G>A
  hgvsp: ENSP00000363905.1:p.Gly582Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1573G>A
  hgvsp: ENSP00000363922.3:p.Gly525Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1744G>A
  hgvsp: ENSP00000363920.3:p.Gly582Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1705G>A
  hgvsp: ENSP00000363908.1:p.Gly569Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1573G>A
  hgvsp: ENSP00000363926.3:p.Gly525Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1705G>A
  hgvsp: ENSP00000311986.6:p.Gly569Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1744G>A
  hgvsp: ENSP00000363921.3:p.Gly582Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.895G>A
  hgvsp: ENSP00000444429.1:p.Gly299Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1705G>A
  hgvsp: ENSP00000443147.1:p.Gly569Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1744G>A
  hgvsp: ENSP00000341844.5:p.Gly582Ser
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1573G>A
  hgvsp: ENSP00000440857.1:p.Gly525Ser
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly582Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

10-34649159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649159
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649159
    reference: chr 10
allele count: 5
allele frequency: 4.121196135966503e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1736C>T
  hgvsp: ENSP00000341844.5:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1697C>T
  hgvsp: ENSP00000311986.6:p.Thr566Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1736C>T
  hgvsp: ENSP00000363920.3:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1565C>T
  hgvsp: ENSP00000363922.3:p.Thr522Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1736C>T
  hgvsp: ENSP00000340591.4:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1565C>T
  hgvsp: ENSP00000440857.1:p.Thr522Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1736C>T
  hgvsp: ENSP00000363905.1:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1565C>T
  hgvsp: ENSP00000363926.3:p.Thr522Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1736C>T
  hgvsp: ENSP00000363921.3:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1697C>T
  hgvsp: ENSP00000363908.1:p.Thr566Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1697C>T
  hgvsp: ENSP00000443147.1:p.Thr566Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.50C>T
  hgvsp: ENSP00000363900.1:p.Thr17Ile
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.887C>T
  hgvsp: ENSP00000444429.1:p.Thr296Ile
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr579Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

10-34649166-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649166
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649166
    reference: chr 10
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1729G>C
  hgvsp: ENSP00000363905.1:p.Val577Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1729G>C
  hgvsp: ENSP00000363920.3:p.Val577Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1729G>C
  hgvsp: ENSP00000340591.4:p.Val577Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1690G>C
  hgvsp: ENSP00000311986.6:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1558G>C
  hgvsp: ENSP00000440857.1:p.Val520Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1729G>C
  hgvsp: ENSP00000363921.3:p.Val577Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1690G>C
  hgvsp: ENSP00000363908.1:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1558G>C
  hgvsp: ENSP00000363922.3:p.Val520Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.880G>C
  hgvsp: ENSP00000444429.1:p.Val294Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1729G>C
  hgvsp: ENSP00000341844.5:p.Val577Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.43G>C
  hgvsp: ENSP00000363900.1:p.Val15Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1690G>C
  hgvsp: ENSP00000443147.1:p.Val564Leu
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1558G>C
  hgvsp: ENSP00000363926.3:p.Val520Leu
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val577Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

10-34649171-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649171
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649171
    reference: chr 10
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1553A>T
  hgvsp: ENSP00000363922.3:p.Asp518Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.875A>T
  hgvsp: ENSP00000444429.1:p.Asp292Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1685A>T
  hgvsp: ENSP00000311986.6:p.Asp562Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1724A>T
  hgvsp: ENSP00000363921.3:p.Asp575Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1685A>T
  hgvsp: ENSP00000363908.1:p.Asp562Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1724A>T
  hgvsp: ENSP00000340591.4:p.Asp575Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1553A>T
  hgvsp: ENSP00000363926.3:p.Asp518Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1685A>T
  hgvsp: ENSP00000443147.1:p.Asp562Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.38A>T
  hgvsp: ENSP00000363900.1:p.Asp13Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1724A>T
  hgvsp: ENSP00000363920.3:p.Asp575Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1724A>T
  hgvsp: ENSP00000363905.1:p.Asp575Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1724A>T
  hgvsp: ENSP00000341844.5:p.Asp575Val
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1553A>T
  hgvsp: ENSP00000440857.1:p.Asp518Val
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp575Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-34649172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649172
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649172
    reference: chr 10
allele count: 48
allele frequency: 3.958305845098298e-4
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1552G>A
  hgvsp: ENSP00000363922.3:p.Asp518Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1684G>A
  hgvsp: ENSP00000443147.1:p.Asp562Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1723G>A
  hgvsp: ENSP00000363921.3:p.Asp575Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.874G>A
  hgvsp: ENSP00000444429.1:p.Asp292Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1723G>A
  hgvsp: ENSP00000363920.3:p.Asp575Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1684G>A
  hgvsp: ENSP00000311986.6:p.Asp562Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1552G>A
  hgvsp: ENSP00000363926.3:p.Asp518Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1723G>A
  hgvsp: ENSP00000341844.5:p.Asp575Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1684G>A
  hgvsp: ENSP00000363908.1:p.Asp562Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1723G>A
  hgvsp: ENSP00000340591.4:p.Asp575Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1723G>A
  hgvsp: ENSP00000363905.1:p.Asp575Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1552G>A
  hgvsp: ENSP00000440857.1:p.Asp518Asn
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.37G>A
  hgvsp: ENSP00000363900.1:p.Asp13Asn
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6982
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Asp575Asn
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

10-34649173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649173
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649173
    reference: chr 10
allele count: 45
allele frequency: 3.710911729779654e-4
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1722G>A
  hgvsp: ENST00000340077.5:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.36G>A
  hgvsp: ENST00000374768.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1683G>A
  hgvsp: ENST00000545693.1:c.1683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1722G>A
  hgvsp: ENST00000374789.3:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.873G>A
  hgvsp: ENST00000544292.1:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1551G>A
  hgvsp: ENST00000545260.1:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1722G>A
  hgvsp: ENST00000346874.4:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1722G>A
  hgvsp: ENST00000374788.3:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1551G>A
  hgvsp: ENST00000374790.3:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1722G>A
  hgvsp: ENST00000374773.1:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1683G>A
  hgvsp: ENST00000374776.1:c.1683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1551G>A
  hgvsp: ENST00000374794.3:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1683G>A
  hgvsp: ENST00000350537.4:c.1683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19283
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu574Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

10-34649192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649192
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649192
    reference: chr 10
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-5A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-5A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1708-5A>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

10-34649194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649194
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649194
    reference: chr 10
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-7C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-7C>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1708-7C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-34649202-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649202
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649202
    reference: chr 10
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-15T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-15T>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14233
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-34649210-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649210
    reference: chr 10
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-23T>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-23T>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

10-34649210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649210
    reference: chr 10
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-23T>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

10-34649214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649214
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649214
    reference: chr 10
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-27G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

10-34649219-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649219
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649219
    reference: chr 10
allele count: 1
allele frequency: 8.318913882603488e-6
allele num: 120208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-32A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-32A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS

10-34649219-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649219
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649219
    reference: chr 10
allele count: 1
allele frequency: 8.318913882603488e-6
allele num: 120208
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-32A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-32A>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13264
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

10-34649220-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649220
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649220
    reference: chr 10
allele count: 1
allele frequency: 8.317806760713336e-6
allele num: 120224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-33T>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-33T>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

10-34649221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649221
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649221
    reference: chr 10
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-34C>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-34C>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

10-34649221-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649221
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649221
    reference: chr 10
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-34C>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-34649223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649223
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649223
    reference: chr 10
allele count: 2
allele frequency: 1.666083537428567e-5
allele num: 120042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-36G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-36G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-34649226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649226
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649226
    reference: chr 10
allele count: 1
allele frequency: 8.337085021593051e-6
allele num: 119946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-39T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-39T>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS

10-34649228-GTTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649228
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649224
    reference: chr 10
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-45_1708-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-45_1708-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-45_1537-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-45_1708-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-45_1537-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-45_1669-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-45_859-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-45_1708-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-45_1708-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-45_1669-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-45_1537-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-45_22-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-45_1669-42delGAAA
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13830
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: GTTTC
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-34649232-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34649232
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34649232
    reference: chr 10
allele count: 2
allele frequency: 1.674901599531028e-5
allele num: 119410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1708-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1708-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.22-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1669-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1669-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1537-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1669-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1708-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.859-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1708-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1708-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1537-45G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1537-45G>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

10-34661378-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661378
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661378
    reference: chr 10
allele count: 3
allele frequency: 2.476882430647292e-5
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+48T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2424T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2424T>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

10-34661379-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661379
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661379
    reference: chr 10
allele count: 2
allele frequency: 1.651364026686043e-5
allele num: 121112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+47A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2423A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2423A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

10-34661379-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661379
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661379
    reference: chr 10
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2423A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+47A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2423A>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-34661381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661381
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661381
    reference: chr 10
allele count: 3
allele frequency: 2.476473501733531e-5
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+45A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+45A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2421A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+45A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+45A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+45A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+45A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-34661382-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661382
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661382
    reference: chr 10
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+44T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+44T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+44T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+44T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+44T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2420T>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+44T>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

10-34661383-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661383
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661383
    reference: chr 10
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+43A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2419A>C
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2419A>C
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-34661392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661392
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661392
    reference: chr 10
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+34G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+34G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+34G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+34G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2410G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+34G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+34G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9422
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-34661414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661414
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661414
    reference: chr 10
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+12G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+12G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+12G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+12G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+12G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2388G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+12G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

10-34661420-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661420
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661420
    reference: chr 10
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+6A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2382A>G
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2382A>G
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9258
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1707+6A>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/10-34661425-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661425
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661425
    reference: chr 10
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2377G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707+1G>T
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2377G>T
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1707+1G>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-34661426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34661426
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 34661426
    reference: chr 10
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363900
  ensembl transcript: ENST00000374768
  gene symbol: PARD3
  hgvsc: ENST00000374768.1:c.21G>A
  hgvsp: ENST00000374768.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363921
  ensembl transcript: ENST00000374789
  gene symbol: PARD3
  hgvsc: ENST00000374789.3:c.1707G>A
  hgvsp: ENST00000374789.3:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000443147
  ensembl transcript: ENST00000545693
  gene symbol: PARD3
  hgvsc: ENST00000545693.1:c.1668+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363926
  ensembl transcript: ENST00000374794
  gene symbol: PARD3
  hgvsc: ENST00000374794.3:c.1536+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363920
  ensembl transcript: ENST00000374788
  gene symbol: PARD3
  hgvsc: ENST00000374788.3:c.1707G>A
  hgvsp: ENST00000374788.3:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000440857
  ensembl transcript: ENST00000545260
  gene symbol: PARD3
  hgvsc: ENST00000545260.1:c.1536+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000341844
  ensembl transcript: ENST00000340077
  gene symbol: PARD3
  hgvsc: ENST00000340077.5:c.1707G>A
  hgvsp: ENST00000340077.5:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363908
  ensembl transcript: ENST00000374776
  gene symbol: PARD3
  hgvsc: ENST00000374776.1:c.1668+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363922
  ensembl transcript: ENST00000374790
  gene symbol: PARD3
  hgvsc: ENST00000374790.3:c.1536+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000340591
  ensembl transcript: ENST00000346874
  gene symbol: PARD3
  hgvsc: ENST00000346874.4:c.1707G>A
  hgvsp: ENST00000346874.4:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000311986
  ensembl transcript: ENST00000350537
  gene symbol: PARD3
  hgvsc: ENST00000350537.4:c.1668+2376G>A
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000363905
  ensembl transcript: ENST00000374773
  gene symbol: PARD3
  hgvsc: ENST00000374773.1:c.1707G>A
  hgvsp: ENST00000374773.1:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148498
  ensembl protein: ENSP00000444429
  ensembl transcript: ENST00000544292
  gene symbol: PARD3
  hgvsc: ENST00000544292.1:c.858+2376G>A
  variant of: http://identifiers.org/hgnc/16051
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1707G>A
num of homozygotes: 0
population: African
reference allele: C

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10257
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.335470085470086e-4
allele num: 14976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66036
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

FS
type: SiteQuality
SIO_000300: 2.091e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.45e1

VQSLOD
type: SiteQuality
SIO_000300: -1.931e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.974762e6

GenotypeDepth
all individuals: 465
bin: 6.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10251
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66056
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.669334400426837e-5
allele num: 14994
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.980372e6

QD
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SIO_000300: 1.97e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: 4.57e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

FS
type: SiteQuality
SIO_000300: 2.994e0

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

ClippingRankSum
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SIO_000300: 1.56e0

MQRankSum
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SIO_000300: 1.15e-1

MQ
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SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.513e1

ReadPosRankSum
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SIO_000300: -7.44e-1

FS
type: SiteQuality
SIO_000300: 1.479e0

VQSLOD
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SIO_000300: 5.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.997947e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511395925276585e-5
allele num: 66164
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.81e1

VQSLOD
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SIO_000300: 1.12e-1

DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

FS
type: SiteQuality
SIO_000300: 1.655e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 7855
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

Other
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15294
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.602e0

ClippingRankSum
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SIO_000300: 1.77e0

BaseQRankSum
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SIO_000300: -7.34e-1

QD
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ReadPosRankSum
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SIO_000300: -1.035e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

DP
type: SiteQuality
SIO_000300: 2.002509e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 896
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.042843762274526e-5
allele num: 66194
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50934283213089e-5
allele num: 66254
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 frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

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

Other
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 15642
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.014772384684956e-5
allele num: 66340
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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East Asian
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

African
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allele num: 10388
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Other
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South Asian
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allele num: 16430
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
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Latino
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East Asian
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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East Asian
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allele num: 8654
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Other
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Latino
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European (Non-Finnish)
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South Asian
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MQ
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BaseQRankSum
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QD
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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VQSLOD
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FS
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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South Asian
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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East Asian
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DP
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InbreedingCoeff
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QD
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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South Asian
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East Asian
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DP
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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African
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MQ
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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South Asian
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 549
bin: 9.75e1
variant carriers: 4

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

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

GenotypeDepth
all individuals: 461
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13943
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8118
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3417
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4336
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1554
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10254
bin: 9.75e1
variant carriers: 6

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e0

DP
type: SiteQuality
SIO_000300: 2.037153e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

GenotypeDepth
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3844
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1314
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27651
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10247
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8122
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.851e0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

DP
type: SiteQuality
SIO_000300: 2.03682e6

QD
type: SiteQuality
SIO_000300: 2.68e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: -2.784e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 671
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2094
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8124
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27644
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4338
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10247
bin: 9.75e1
variant carriers: 3

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

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

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

GenotypeQuality
all individuals: 2328
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1554
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3034
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
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: -1.68e0

FS
type: SiteQuality
SIO_000300: 2.833e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.037063e6

GenotypeDepth
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 897
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13948
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8123
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27643
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3034
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4339
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10246
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.251e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

FS
type: SiteQuality
SIO_000300: 5.929e0

DP
type: SiteQuality
SIO_000300: 2.036891e6

GenotypeDepth
all individuals: 2094
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 671
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 895
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4339
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 10245
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 5.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.775e0

MQ
type: SiteQuality
SIO_000300: 5.209e1

QD
type: SiteQuality
SIO_000300: 7.91e0

DP
type: SiteQuality
SIO_000300: 2.036888e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeDepth
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 144
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27637
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variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.037116e6

FS
type: SiteQuality
SIO_000300: 3.329e0

QD
type: SiteQuality
SIO_000300: 1.235e1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2094
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 895
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18677
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 365
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variant carriers: 0

GenotypeQuality
all individuals: 3417
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variant carriers: 0

GenotypeQuality
all individuals: 4
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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: 5
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4340
bin: 7.75e1
variant carriers: 0

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

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

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

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

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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.727e0

DP
type: SiteQuality
SIO_000300: 2.036823e6

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.445e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.654e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 671
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variant carriers: 0

GenotypeDepth
all individuals: 13953
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variant carriers: 0

GenotypeDepth
all individuals: 365
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variant carriers: 0

GenotypeDepth
all individuals: 461
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variant carriers: 0

GenotypeDepth
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 27643
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GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 3417
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GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 5.486e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.059e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

DP
type: SiteQuality
SIO_000300: 2.036828e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeDepth
all individuals: 3843
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variant carriers: 0

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

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 1555
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GenotypeQuality
all individuals: 8119
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GenotypeQuality
all individuals: 27633
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 0
bin: 2.5e0
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
all individuals: 3028
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2325
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GenotypeQuality
all individuals: 3420
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GenotypeQuality
all individuals: 10247
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variant carriers: 4

GenotypeQuality
all individuals: 4338
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

DP
type: SiteQuality
SIO_000300: 2.036961e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

QD
type: SiteQuality
SIO_000300: 1.252e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

FS
type: SiteQuality
SIO_000300: 1.168e0

GenotypeDepth
all individuals: 463
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variant carriers: 4

GenotypeDepth
all individuals: 2092
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variant carriers: 3

GenotypeDepth
all individuals: 7012
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variant carriers: 1

GenotypeDepth
all individuals: 216
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variant carriers: 5

GenotypeDepth
all individuals: 147
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variant carriers: 4

GenotypeDepth
all individuals: 295
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variant carriers: 4

GenotypeQuality
all individuals: 8114
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1553
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 10269
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variant carriers: 81

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3026
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3413
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GenotypeQuality
all individuals: 4335
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variant carriers: 0

GenotypeQuality
all individuals: 2321
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variant carriers: 0

GenotypeQuality
all individuals: 27627
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 72
allele frequency: 6.923076923076923e-3
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.183137525915688e-4
allele num: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

DP
type: SiteQuality
SIO_000300: 2.040985e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeDepth
all individuals: 892
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7017
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variant carriers: 0

GenotypeDepth
all individuals: 211
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variant carriers: 0

GenotypeDepth
all individuals: 145
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variant carriers: 0

GenotypeDepth
all individuals: 291
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variant carriers: 0

GenotypeDepth
all individuals: 461
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 3421
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variant carriers: 0

GenotypeQuality
all individuals: 8122
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variant carriers: 0

GenotypeQuality
all individuals: 1553
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 27652
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10201
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3026
bin: 7.25e1
variant carriers: 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: 16506
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.395e-1

FS
type: SiteQuality
SIO_000300: 5.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.178e1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

DP
type: SiteQuality
SIO_000300: 2.035566e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.071e0

GenotypeDepth
all individuals: 320
bin: 8.25e1
variant carriers: 128

GenotypeDepth
all individuals: 648
bin: 6.25e1
variant carriers: 94

GenotypeDepth
all individuals: 807
bin: 5.75e1
variant carriers: 60

GenotypeDepth
all individuals: 276
bin: 8.75e1
variant carriers: 148

GenotypeDepth
all individuals: 9793
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 18516
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 3337
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variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 1486
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GenotypeQuality
all individuals: 27394
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variant carriers: 0

GenotypeQuality
all individuals: 2219
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 4256
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GenotypeQuality
all individuals: 10870
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variant carriers: 2174

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 8052
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2983
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GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 25
allele frequency: 2.753303964757709e-2
allele num: 908
num of homozygotes: 1

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

African
type: Population
allele count: 45
allele frequency: 4.329420819703675e-3
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 135
allele frequency: 1.166407465007776e-2
allele num: 11574
num of homozygotes: 1

South Asian
type: Population
allele count: 48
allele frequency: 2.908033442384587e-3
allele num: 16506
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 79
allele frequency: 1.194436044753553e-2
allele num: 6614
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1877
allele frequency: 2.813755471607603e-2
allele num: 66708
num of homozygotes: 29

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

FS
type: SiteQuality
SIO_000300: 5.54e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.828e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 2.156287e6

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 201
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 779
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variant carriers: 0

GenotypeDepth
all individuals: 6991
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variant carriers: 0

GenotypeDepth
all individuals: 19307
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variant carriers: 0

GenotypeDepth
all individuals: 99
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variant carriers: 1

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 3451
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 4419
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 8392
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 1539
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GenotypeQuality
all individuals: 2292
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 9034
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GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 3085
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GenotypeQuality
all individuals: 28399
bin: 6.25e1
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: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 3.415e0

DP
type: SiteQuality
SIO_000300: 2.006807e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

GenotypeDepth
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variant carriers: 0

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

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

African
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
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
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DP
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SIO_000300: 2.006642e6

BaseQRankSum
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SIO_000300: -1.247e0

QD
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FS
type: SiteQuality
SIO_000300: 3.298e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Other
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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
allele num: 6614
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.887947631882942e-4
allele num: 10388
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQRankSum
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SIO_000300: 4.11e-1

FS
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SIO_000300: 4.394e0

ClippingRankSum
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SIO_000300: 6.900000000000001e-2

DP
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SIO_000300: 2.006648e6

BaseQRankSum
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SIO_000300: -3.61e0

VQSLOD
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SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.046e1

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
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: 1
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allele num: 11564
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.988e0

BaseQRankSum
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SIO_000300: 8.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

VQSLOD
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MQ
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SIO_000300: 5.982e1

ClippingRankSum
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SIO_000300: -2.63e-1

ReadPosRankSum
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DP
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SIO_000300: 2.005595e6

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

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

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

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

Other
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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SIO_000300: -9.77e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 5

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

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

East Asian
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allele frequency: 5.546568061012249e-3
allele num: 8654
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Latino
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num of homozygotes: 0

South Asian
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African
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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QD
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MQ
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 2.06e-2

MQRankSum
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SIO_000300: 2.02e-1

GenotypeDepth
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variant carriers: 0

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

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

Other
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 44
allele frequency: 6.600660066006601e-4
allele num: 66660
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66278
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

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

East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

European (Non-Finnish)
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African
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South Asian
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East Asian
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European (Finnish)
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Other
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FS
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15886
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.038405444822557e-5
allele num: 65824
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.82916e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.747e0

InbreedingCoeff
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SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 5.905e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.505451596431682e-5
allele num: 66586
num of homozygotes: 0

DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.09e-2

QD
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BaseQRankSum
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SIO_000300: 2.46e-1

FS
type: SiteQuality
SIO_000300: 1.747e0

ReadPosRankSum
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SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

East Asian
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allele num: 8644
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
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

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

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

DP
type: SiteQuality
SIO_000300: 2.698881e6

ReadPosRankSum
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SIO_000300: 4.94e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 4.0e-4

MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.49e-1

VQSLOD
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FS
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SIO_000300: 5.797e0

QD
type: SiteQuality
SIO_000300: 1.417e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

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: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.49e-1

VQSLOD
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InbreedingCoeff
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QD
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DP
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SIO_000300: 2.698881e6

MQRankSum
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SIO_000300: 7.09e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 4.94e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7262
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

African
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num of homozygotes: 0

East Asian
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South Asian
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num of homozygotes: 0

Latino
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allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

European (Finnish)
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Other
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MQRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
type: SiteQuality
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GenotypeDepth
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variant carriers: 1

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

African
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allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
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SIO_000300: 2.701266e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.184e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

MQ
type: SiteQuality
SIO_000300: 5.82e1

VQSLOD
type: SiteQuality
SIO_000300: -4.444e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
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SIO_000300: -2.823e0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
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: 10392
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 2.70396e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.265e0

FS
type: SiteQuality
SIO_000300: 1.026e0

QD
type: SiteQuality
SIO_000300: 9.75e0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.407e0

MQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

ReadPosRankSum
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SIO_000300: -2.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.704178e6

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

GenotypeDepth
all individuals: 9257
bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

ClippingRankSum
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SIO_000300: -6.99e-1

FS
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SIO_000300: 5.097e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
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SIO_000300: -2.135e0

ReadPosRankSum
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SIO_000300: 6.17e-1

DP
type: SiteQuality
SIO_000300: 2.704328e6

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeDepth
all individuals: 367
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2460
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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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: 7258
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4701
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GenotypeQuality
all individuals: 5321
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 3
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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
all individuals: 20619
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GenotypeQuality
all individuals: 2256
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0