19-18328909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328909
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328909
    reference: chr 19
allele count: 1
allele frequency: 8.449656943928076e-6
allele num: 118348
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+792G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+50C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+50C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

19-18328913-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328913
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328913
    reference: chr 19
allele count: 6
allele frequency: 5.070822487407458e-5
allele num: 118324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+796G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+46C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+46C>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

19-18328917-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328917
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328917
    reference: chr 19
allele count: 3
allele frequency: 2.532072923700203e-5
allele num: 118480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+800G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+42C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+42C>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8761
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

19-18328923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328923
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328923
    reference: chr 19
allele count: 2
allele frequency: 1.685658418178141e-5
allele num: 118648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+806C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+36G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+36G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-18328926-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328926
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328926
    reference: chr 19
allele count: 1
allele frequency: 8.421903687109433e-6
allele num: 118738
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+809C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+33G>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

19-18328928-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328925
    reference: chr 19
allele count: 7
allele frequency: 5.888786068814672e-5
allele num: 118870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+28_637+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+28_*488+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+28_1330+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+814_570+816delCCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+28_1234+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+28_2325+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+28_1330+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+28_475+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+28_1012+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+28_1330+30delGAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+28_640+30delGAG
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5267
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: TCTC
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

19-18328930-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328930
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328930
    reference: chr 19
allele count: 5
allele frequency: 4.205497426235575e-5
allele num: 118892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+813T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+29A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+29A>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

19-18328935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328935
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328935
    reference: chr 19
allele count: 1
allele frequency: 8.398703240219711e-6
allele num: 119066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+818C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+24G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+24G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35188
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-18328938-C-CCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328938
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328940
    reference: chr 19
allele count: 1
allele frequency: 8.383072899201931e-6
allele num: 119288
alternate allele: CCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+19_1330+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+19_637+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+19_640+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+823_570+824dupAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+19_1234+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+19_1330+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+19_1012+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+19_2325+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+19_*488+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+19_1330+20dupTG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+19_475+20dupTG
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-18328941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328941
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328941
    reference: chr 19
allele count: 1
allele frequency: 8.367640660039494e-6
allele num: 119508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+824C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+18G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+18G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP

19-18328948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328948
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328948
    reference: chr 19
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+831C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+11G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+11G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

19-18328950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328950
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328950
    reference: chr 19
allele count: 1
allele frequency: 8.317530026283395e-6
allele num: 120228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+833C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+9G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+9G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

19-18328950-CCTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328950
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328947
    reference: chr 19
allele count: 77
allele frequency: 6.404498120238214e-4
allele num: 120228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+836_570+838delACT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.637+6_637+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*488+6_*488+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1330+6_1330+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1012+6_1012+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.475+6_475+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1234+6_1234+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2325+6_2325+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1330+6_1330+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.640+6_640+8delTAG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1330+6_1330+8delTAG
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: c.1330+6_1330+8delTAG
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: CCTA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

19-18328959-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328958
    reference: chr 19
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1329delC
  hgvsp: ENSP00000469696.1:p.Asn444ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*487delC
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1011delC
  hgvsp: ENSP00000402091.1:p.Asn338ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1329delC
  hgvsp: ENSP00000470210.1:p.Asn444ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2324delC
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.636delC
  hgvsp: ENSP00000439470.1:p.Asn213ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.639delC
  hgvsp: ENSP00000476923.1:p.Asn214ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1329delC
  hgvsp: ENSP00000347689.2:p.Asn444ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.474delC
  hgvsp: ENSP00000474591.3:p.Asn159ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+844delG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1233delC
  hgvsp: ENSP00000262805.10:p.Asn412ThrfsTer43
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn444ThrfsTer43
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: TG
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-18328961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328961
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328961
    reference: chr 19
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1328C>T
  hgvsp: ENSP00000347689.2:p.Thr443Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1328C>T
  hgvsp: ENSP00000470210.1:p.Thr443Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.473C>T
  hgvsp: ENSP00000474591.3:p.Thr158Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1232C>T
  hgvsp: ENSP00000262805.10:p.Thr411Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1010C>T
  hgvsp: ENSP00000402091.1:p.Thr337Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2323C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*486C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.638C>T
  hgvsp: ENSP00000476923.1:p.Thr213Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1328C>T
  hgvsp: ENSP00000469696.1:p.Thr443Ile
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+844G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.635C>T
  hgvsp: ENSP00000439470.1:p.Thr212Ile
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr443Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

19-18328963-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328963
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328963
    reference: chr 19
allele count: 8
allele frequency: 6.611460967587313e-5
allele num: 121002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*484C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1326C>G
  hgvsp: ENSP00000347689.2:p.Asn442Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.471C>G
  hgvsp: ENSP00000474591.3:p.Asn157Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+846G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1326C>G
  hgvsp: ENSP00000469696.1:p.Asn442Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1230C>G
  hgvsp: ENSP00000262805.10:p.Asn410Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.633C>G
  hgvsp: ENSP00000439470.1:p.Asn211Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.636C>G
  hgvsp: ENSP00000476923.1:p.Asn212Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1326C>G
  hgvsp: ENSP00000470210.1:p.Asn442Lys
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2321C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.1008C>G
  hgvsp: ENSP00000402091.1:p.Asn336Lys
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn442Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

19-18328980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18328980
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18328980
    reference: chr 19
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1309A>G
  hgvsp: ENSP00000469696.1:p.Asn437Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1309A>G
  hgvsp: ENSP00000347689.2:p.Asn437Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1309A>G
  hgvsp: ENSP00000470210.1:p.Asn437Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.991A>G
  hgvsp: ENSP00000402091.1:p.Asn331Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1213A>G
  hgvsp: ENSP00000262805.10:p.Asn405Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.616A>G
  hgvsp: ENSP00000439470.1:p.Asn206Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.619A>G
  hgvsp: ENSP00000476923.1:p.Asn207Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2304A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.454A>G
  hgvsp: ENSP00000474591.3:p.Asn152Asp
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*467A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+863T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn437Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-18329000-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329000
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329000
    reference: chr 19
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*447T>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.971T>C
  hgvsp: ENSP00000402091.1:p.Val324Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+883A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.596T>C
  hgvsp: ENSP00000439470.1:p.Val199Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.434T>C
  hgvsp: ENSP00000474591.3:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2284T>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1289T>C
  hgvsp: ENSP00000469696.1:p.Val430Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1289T>C
  hgvsp: ENSP00000470210.1:p.Val430Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1289T>C
  hgvsp: ENSP00000347689.2:p.Val430Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1193T>C
  hgvsp: ENSP00000262805.10:p.Val398Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.599T>C
  hgvsp: ENSP00000476923.1:p.Val200Ala
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val430Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

19-18329001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329001
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329001
    reference: chr 19
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.433G>A
  hgvsp: ENSP00000474591.3:p.Val145Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+884C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2283G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1288G>A
  hgvsp: ENSP00000470210.1:p.Val430Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1192G>A
  hgvsp: ENSP00000262805.10:p.Val398Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.598G>A
  hgvsp: ENSP00000476923.1:p.Val200Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1288G>A
  hgvsp: ENSP00000469696.1:p.Val430Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1288G>A
  hgvsp: ENSP00000347689.2:p.Val430Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.970G>A
  hgvsp: ENSP00000402091.1:p.Val324Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.595G>A
  hgvsp: ENSP00000439470.1:p.Val199Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*446G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val430Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

19-18329002-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329002
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329002
    reference: chr 19
allele count: 8
allele frequency: 6.592175088170342e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*445C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1287C>T
  hgvsp: ENST00000594617.3:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+885G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.594C>T
  hgvsp: ENST00000539010.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.432C>T
  hgvsp: ENST00000598111.2:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1191C>T
  hgvsp: ENST00000262805.12:c.1191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1287C>T
  hgvsp: ENST00000355502.3:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2282C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.969C>T
  hgvsp: ENST00000447275.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.597C>T
  hgvsp: ENST00000597297.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1287C>T
  hgvsp: ENST00000594465.3:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp429Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

19-18329005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329005
    reference: chr 19
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1284C>T
  hgvsp: ENST00000355502.3:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1188C>T
  hgvsp: ENST00000262805.12:c.1188C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1284C>T
  hgvsp: ENST00000594465.3:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2279C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*442C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1284C>T
  hgvsp: ENST00000594617.3:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.591C>T
  hgvsp: ENST00000539010.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.429C>T
  hgvsp: ENST00000598111.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.594C>T
  hgvsp: ENST00000597297.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.966C>T
  hgvsp: ENST00000447275.3:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+888G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His428His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum

19-18329007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329007
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329007
    reference: chr 19
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.589C>T
  hgvsp: ENSP00000439470.1:p.His197Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1282C>T
  hgvsp: ENSP00000469696.1:p.His428Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.592C>T
  hgvsp: ENSP00000476923.1:p.His198Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1186C>T
  hgvsp: ENSP00000262805.10:p.His396Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1282C>T
  hgvsp: ENSP00000347689.2:p.His428Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+890G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*440C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.964C>T
  hgvsp: ENSP00000402091.1:p.His322Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2277C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1282C>T
  hgvsp: ENSP00000470210.1:p.His428Tyr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.427C>T
  hgvsp: ENSP00000474591.3:p.His143Tyr
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His428Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-18329012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329012
    reference: chr 19
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1277C>T
  hgvsp: ENSP00000470210.1:p.Ala426Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2272C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1181C>T
  hgvsp: ENSP00000262805.10:p.Ala394Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1277C>T
  hgvsp: ENSP00000347689.2:p.Ala426Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*435C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1277C>T
  hgvsp: ENSP00000469696.1:p.Ala426Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.584C>T
  hgvsp: ENSP00000439470.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.422C>T
  hgvsp: ENSP00000474591.3:p.Ala141Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+895G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.587C>T
  hgvsp: ENSP00000476923.1:p.Ala196Val
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.959C>T
  hgvsp: ENSP00000402091.1:p.Ala320Val
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala426Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

19-18329013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329013
    reference: chr 19
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2271G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.421G>A
  hgvsp: ENSP00000474591.3:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1180G>A
  hgvsp: ENSP00000262805.10:p.Ala394Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*434G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.958G>A
  hgvsp: ENSP00000402091.1:p.Ala320Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+896C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1276G>A
  hgvsp: ENSP00000470210.1:p.Ala426Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.583G>A
  hgvsp: ENSP00000439470.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1276G>A
  hgvsp: ENSP00000469696.1:p.Ala426Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.586G>A
  hgvsp: ENSP00000476923.1:p.Ala196Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1276G>A
  hgvsp: ENSP00000347689.2:p.Ala426Thr
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala426Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

19-18329014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329014
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329014
    reference: chr 19
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1275C>T
  hgvsp: ENST00000355502.3:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.585C>T
  hgvsp: ENST00000597297.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1275C>T
  hgvsp: ENST00000594617.3:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.420C>T
  hgvsp: ENST00000598111.2:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1275C>T
  hgvsp: ENST00000594465.3:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1179C>T
  hgvsp: ENST00000262805.12:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*433C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+897G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.957C>T
  hgvsp: ENST00000447275.3:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.582C>T
  hgvsp: ENST00000539010.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2270C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser425Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-18329039-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329038
    reference: chr 19
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1153delG
  hgvsp: ENSP00000262805.10:p.Glu385LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*407delG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.556delG
  hgvsp: ENSP00000439470.1:p.Glu186LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.559delG
  hgvsp: ENSP00000476923.1:p.Glu187LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+924delC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1249delG
  hgvsp: ENSP00000470210.1:p.Glu417LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.931delG
  hgvsp: ENSP00000402091.1:p.Glu311LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1249delG
  hgvsp: ENSP00000347689.2:p.Glu417LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2244delG
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.394delG
  hgvsp: ENSP00000474591.3:p.Glu132LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1249delG
  hgvsp: ENSP00000469696.1:p.Glu417LysfsTer24
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu417LysfsTer24
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: TC
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

19-18329055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329055
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329055
    reference: chr 19
allele count: 6
allele frequency: 4.944538756942956e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.916G>A
  hgvsp: ENSP00000402091.1:p.Val306Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2229G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1234G>A
  hgvsp: ENSP00000469696.1:p.Val412Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.541G>A
  hgvsp: ENSP00000439470.1:p.Val181Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1234G>A
  hgvsp: ENSP00000347689.2:p.Val412Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.379G>A
  hgvsp: ENSP00000474591.3:p.Val127Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*392G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.544G>A
  hgvsp: ENSP00000476923.1:p.Val182Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1234G>A
  hgvsp: ENSP00000470210.1:p.Val412Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1138G>A
  hgvsp: ENSP00000262805.10:p.Val380Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+938C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val412Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-18329068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329068
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329068
    reference: chr 19
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+951C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-10G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-10G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

19-18329072-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329072
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329072
    reference: chr 19
allele count: 100
allele frequency: 8.244023083264633e-4
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+955G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-14C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-14C>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-18329079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329079
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329079
    reference: chr 19
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+962G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-21C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-21C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

19-18329081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329081
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329081
    reference: chr 19
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+964C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-23G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-23G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

19-18329082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329082
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329082
    reference: chr 19
allele count: 10
allele frequency: 8.246334504312833e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+965G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-24C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-24C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

19-18329087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329087
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329087
    reference: chr 19
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+970G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-29C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-29C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

19-18329088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329088
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329088
    reference: chr 19
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-30C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+971G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-18329088-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329088
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329088
    reference: chr 19
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+971G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-30C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-30C>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-18329091-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329091
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329091
    reference: chr 19
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+974C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-33G>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-33G>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-18329091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329091
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329091
    reference: chr 19
allele count: 3
allele frequency: 2.475942095967516e-5
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+974C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-33G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-33G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
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: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-18329092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329092
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329092
    reference: chr 19
allele count: 9
allele frequency: 7.432733759476735e-5
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.538-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2226-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1231-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*389-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1135-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1231-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.913-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+975G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.541-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-34C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1231-34C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8635
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-18329101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329101
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329101
    reference: chr 19
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+984G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+43C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+43C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-18329101-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329101
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329101
    reference: chr 19
allele count: 5
allele frequency: 4.124936063491016e-5
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+984G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+43C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+43C>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7529
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3228
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-18329104-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329104
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329104
    reference: chr 19
allele count: 4
allele frequency: 3.300656830709311e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+987C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-46G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+40G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+40G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-18329113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329113
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329113
    reference: chr 19
allele count: 4
allele frequency: 3.300711303285858e-5
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-55G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+996C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+31G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+31G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

19-18329114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329114
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329114
    reference: chr 19
allele count: 11
allele frequency: 9.079203671299811e-5
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-56C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+997G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+30C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+30C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-18329119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329119
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329119
    reference: chr 19
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1002C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-61G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+25G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+25G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-18329121-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329121
    reference: chr 19
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-63A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1004T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+23A>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+23A>C
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-18329123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329123
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329123
    reference: chr 19
allele count: 3
allele frequency: 2.474675817467912e-5
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1006C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+21G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-65G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ

19-18329124-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329124
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329124
    reference: chr 19
allele count: 64
allele frequency: 5.278785879247773e-4
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1007C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+20G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-66G>C
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+20G>C
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-18329128-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329128
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329128
    reference: chr 19
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1011A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-70T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+16T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+16T>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-18329136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329136
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329136
    reference: chr 19
allele count: 5
allele frequency: 4.123371268349002e-5
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-78G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1019C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+8G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+8G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1230+8G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

19-18329137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329137
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329137
    reference: chr 19
allele count: 71
allele frequency: 5.855476932719745e-4
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-79C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+7C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1020G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+7C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.1230+7C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-18329137-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329137
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329137
    reference: chr 19
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1230+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1230+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.540+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1134+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-79C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1020G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*388+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1230+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.537+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.912+7C>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2225+7C>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1230+7C>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

19-18329147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329147
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329147
    reference: chr 19
allele count: 7
allele frequency: 5.771672630728385e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1227C>T
  hgvsp: ENST00000594617.3:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2222C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1227C>T
  hgvsp: ENST00000355502.3:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-89C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.537C>T
  hgvsp: ENST00000597297.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1227C>T
  hgvsp: ENST00000594465.3:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*385C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1030G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1131C>T
  hgvsp: ENST00000262805.12:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.534C>T
  hgvsp: ENST00000539010.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.909C>T
  hgvsp: ENST00000447275.3:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu409Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-18329148-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329148
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329148
    reference: chr 19
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1226T>G
  hgvsp: ENSP00000347689.2:p.Leu409Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1130T>G
  hgvsp: ENSP00000262805.10:p.Leu377Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.908T>G
  hgvsp: ENSP00000402091.1:p.Leu303Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*384T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1031A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-90T>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.533T>G
  hgvsp: ENSP00000439470.1:p.Leu178Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1226T>G
  hgvsp: ENSP00000469696.1:p.Leu409Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1226T>G
  hgvsp: ENSP00000470210.1:p.Leu409Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.536T>G
  hgvsp: ENSP00000476923.1:p.Leu179Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2221T>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu409Arg
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

19-18329153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329153
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329153
    reference: chr 19
allele count: 4
allele frequency: 3.297500494625074e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1221C>T
  hgvsp: ENST00000355502.3:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2216C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.531C>T
  hgvsp: ENST00000597297.1:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1125C>T
  hgvsp: ENST00000262805.12:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1036G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-95C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.903C>T
  hgvsp: ENST00000447275.3:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.528C>T
  hgvsp: ENST00000539010.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1221C>T
  hgvsp: ENST00000594465.3:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*379C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1221C>T
  hgvsp: ENST00000594617.3:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro407Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP

19-18329154-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329154
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329154
    reference: chr 19
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.527C>G
  hgvsp: ENSP00000439470.1:p.Pro176Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1124C>G
  hgvsp: ENSP00000262805.10:p.Pro375Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1037G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.530C>G
  hgvsp: ENSP00000476923.1:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2215C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.902C>G
  hgvsp: ENSP00000402091.1:p.Pro301Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1220C>G
  hgvsp: ENSP00000469696.1:p.Pro407Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1220C>G
  hgvsp: ENSP00000470210.1:p.Pro407Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-96C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1220C>G
  hgvsp: ENSP00000347689.2:p.Pro407Arg
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*378C>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro407Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

19-18329155-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329155
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329155
    reference: chr 19
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-97C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1219C>G
  hgvsp: ENSP00000469696.1:p.Pro407Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.529C>G
  hgvsp: ENSP00000476923.1:p.Pro177Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*377C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2214C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1219C>G
  hgvsp: ENSP00000347689.2:p.Pro407Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1123C>G
  hgvsp: ENSP00000262805.10:p.Pro375Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.526C>G
  hgvsp: ENSP00000439470.1:p.Pro176Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.901C>G
  hgvsp: ENSP00000402091.1:p.Pro301Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1219C>G
  hgvsp: ENSP00000470210.1:p.Pro407Ala
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1038G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro407Ala
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: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

19-18329157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329157
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329157
    reference: chr 19
allele count: 3
allele frequency: 2.472758444470088e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1217C>T
  hgvsp: ENSP00000470210.1:p.Thr406Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1121C>T
  hgvsp: ENSP00000262805.10:p.Thr374Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1040G>A
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1217C>T
  hgvsp: ENSP00000347689.2:p.Thr406Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1217C>T
  hgvsp: ENSP00000469696.1:p.Thr406Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-99C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2212C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*375C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.899C>T
  hgvsp: ENSP00000402091.1:p.Thr300Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.527C>T
  hgvsp: ENSP00000476923.1:p.Thr176Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.524C>T
  hgvsp: ENSP00000439470.1:p.Thr175Met
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr406Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-18329169-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329169
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329169
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1205T>A
  hgvsp: ENSP00000470210.1:p.Val402Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.515T>A
  hgvsp: ENSP00000476923.1:p.Val172Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-111T>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2200T>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1109T>A
  hgvsp: ENSP00000262805.10:p.Val370Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.887T>A
  hgvsp: ENSP00000402091.1:p.Val296Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1205T>A
  hgvsp: ENSP00000347689.2:p.Val402Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*363T>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.512T>A
  hgvsp: ENSP00000439470.1:p.Val171Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1205T>A
  hgvsp: ENSP00000469696.1:p.Val402Glu
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1052A>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val402Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-18329174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329174
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329174
    reference: chr 19
allele count: 3
allele frequency: 2.471861971227527e-5
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1057C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2195G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.507G>A
  hgvsp: ENST00000539010.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1200G>A
  hgvsp: ENST00000594465.3:c.1200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.510G>A
  hgvsp: ENST00000597297.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1200G>A
  hgvsp: ENST00000594617.3:c.1200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*358G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1104G>A
  hgvsp: ENST00000262805.12:c.1104G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.882G>A
  hgvsp: ENST00000447275.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1200G>A
  hgvsp: ENST00000355502.3:c.1200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-116G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr400Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

19-18329175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329175
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329175
    reference: chr 19
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.506C>T
  hgvsp: ENSP00000439470.1:p.Thr169Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2194C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1058G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1103C>T
  hgvsp: ENSP00000262805.10:p.Thr368Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1199C>T
  hgvsp: ENSP00000347689.2:p.Thr400Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1199C>T
  hgvsp: ENSP00000469696.1:p.Thr400Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1199C>T
  hgvsp: ENSP00000470210.1:p.Thr400Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.509C>T
  hgvsp: ENSP00000476923.1:p.Thr170Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.881C>T
  hgvsp: ENSP00000402091.1:p.Thr294Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-117C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr400Met
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-18329188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329188
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329188
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1090G>A
  hgvsp: ENSP00000262805.10:p.Val364Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1186G>A
  hgvsp: ENSP00000347689.2:p.Val396Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*344G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-130G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.493G>A
  hgvsp: ENSP00000439470.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.868G>A
  hgvsp: ENSP00000402091.1:p.Val290Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1186G>A
  hgvsp: ENSP00000469696.1:p.Val396Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1186G>A
  hgvsp: ENSP00000470210.1:p.Val396Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2181G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.496G>A
  hgvsp: ENSP00000476923.1:p.Val166Met
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1071C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val396Met
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

19-18329189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329189
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329189
    reference: chr 19
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.492C>T
  hgvsp: ENST00000539010.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1185C>T
  hgvsp: ENST00000594465.3:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.867C>T
  hgvsp: ENST00000447275.3:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1089C>T
  hgvsp: ENST00000262805.12:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1072G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-131C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1185C>T
  hgvsp: ENST00000594617.3:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.495C>T
  hgvsp: ENST00000597297.1:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1185C>T
  hgvsp: ENST00000355502.3:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*343C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2180C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp395Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

19-18329191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329191
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329191
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1074C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.493G>A
  hgvsp: ENSP00000476923.1:p.Asp165Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2178G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1087G>A
  hgvsp: ENSP00000262805.10:p.Asp363Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1183G>A
  hgvsp: ENSP00000470210.1:p.Asp395Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*341G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.490G>A
  hgvsp: ENSP00000439470.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.865G>A
  hgvsp: ENSP00000402091.1:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1183G>A
  hgvsp: ENSP00000469696.1:p.Asp395Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1183G>A
  hgvsp: ENSP00000347689.2:p.Asp395Asn
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-133G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp395Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

19-18329192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329192
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329192
    reference: chr 19
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-134C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1075G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*340C>T
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.492C>T
  hgvsp: ENST00000597297.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1182C>T
  hgvsp: ENST00000594617.3:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.864C>T
  hgvsp: ENST00000447275.3:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1086C>T
  hgvsp: ENST00000262805.12:c.1086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1182C>T
  hgvsp: ENST00000594465.3:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.489C>T
  hgvsp: ENST00000539010.1:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1182C>T
  hgvsp: ENST00000355502.3:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2177C>T
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala394Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-18329194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329194
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329194
    reference: chr 19
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.862G>A
  hgvsp: ENSP00000402091.1:p.Ala288Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.487G>A
  hgvsp: ENSP00000439470.1:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1077C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.490G>A
  hgvsp: ENSP00000476923.1:p.Ala164Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1180G>A
  hgvsp: ENSP00000469696.1:p.Ala394Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*338G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1180G>A
  hgvsp: ENSP00000470210.1:p.Ala394Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1180G>A
  hgvsp: ENSP00000347689.2:p.Ala394Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2175G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1084G>A
  hgvsp: ENSP00000262805.10:p.Ala362Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-136G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala394Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

19-18329197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329197
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329197
    reference: chr 19
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1177G>A
  hgvsp: ENSP00000470210.1:p.Ala393Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*335G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1081G>A
  hgvsp: ENSP00000262805.10:p.Ala361Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1177G>A
  hgvsp: ENSP00000469696.1:p.Ala393Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2172G>A
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1177G>A
  hgvsp: ENSP00000347689.2:p.Ala393Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.487G>A
  hgvsp: ENSP00000476923.1:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1080C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.484G>A
  hgvsp: ENSP00000439470.1:p.Ala162Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.859G>A
  hgvsp: ENSP00000402091.1:p.Ala287Thr
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-139G>A
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala393Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

19-18329208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329208
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.848A>G
  hgvsp: ENSP00000402091.1:p.Asn283Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1070A>G
  hgvsp: ENSP00000262805.10:p.Asn357Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1166A>G
  hgvsp: ENSP00000469696.1:p.Asn389Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2161A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-150A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*324A>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.476A>G
  hgvsp: ENSP00000476923.1:p.Asn159Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1166A>G
  hgvsp: ENSP00000470210.1:p.Asn389Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1091T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.473A>G
  hgvsp: ENSP00000439470.1:p.Asn158Ser
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1166A>G
  hgvsp: ENSP00000347689.2:p.Asn389Ser
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn389Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-18329213-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18329213
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 18329213
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000470210
  ensembl transcript: ENST00000594465
  gene symbol: PDE4C
  hgvsc: ENST00000594465.3:c.1161C>G
  hgvsp: ENSP00000470210.1:p.Tyr387Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268650
  ensembl transcript: ENST00000594805
  gene symbol: AC068499.10
  hgvsc: ENST00000594805.3:n.570+1096G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105650
  ensembl transcript: ENST00000597360
  gene symbol: PDE4C
  hgvsc: ENST00000597360.1:n.2156C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000469696
  ensembl transcript: ENST00000594617
  gene symbol: PDE4C
  hgvsc: ENST00000594617.3:c.1161C>G
  hgvsp: ENSP00000469696.1:p.Tyr387Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000402091
  ensembl transcript: ENST00000447275
  gene symbol: PDE4C
  hgvsc: ENST00000447275.3:c.843C>G
  hgvsp: ENSP00000402091.1:p.Tyr281Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000347689
  ensembl transcript: ENST00000355502
  gene symbol: PDE4C
  hgvsc: ENST00000355502.3:c.1161C>G
  hgvsp: ENSP00000347689.2:p.Tyr387Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000439470
  ensembl transcript: ENST00000539010
  gene symbol: PDE4C
  hgvsc: ENST00000539010.1:c.468C>G
  hgvsp: ENSP00000439470.1:p.Tyr156Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000262805
  ensembl transcript: ENST00000262805
  gene symbol: PDE4C
  hgvsc: ENST00000262805.12:c.1065C>G
  hgvsp: ENSP00000262805.10:p.Tyr355Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000476923
  ensembl transcript: ENST00000597297
  gene symbol: PDE4C
  hgvsc: ENST00000597297.1:c.471C>G
  hgvsp: ENSP00000476923.1:p.Tyr157Ter
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000473713
  ensembl transcript: ENST00000599188
  gene symbol: PDE4C
  hgvsc: ENST00000599188.1:c.*319C>G
  variant of: http://identifiers.org/hgnc/8782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105650
  ensembl protein: ENSP00000474591
  ensembl transcript: ENST00000598111
  gene symbol: PDE4C
  hgvsc: ENST00000598111.2:c.376-155C>G
  variant of: http://identifiers.org/hgnc/8782
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr387Ter
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35127
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65922
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

FS
type: SiteQuality
SIO_000300: 5.828e0

DP
type: SiteQuality
SIO_000300: 2.529733e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.867e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.482e0

VQSLOD
type: SiteQuality
SIO_000300: -1.082e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
all individuals: 334
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 229
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2839
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35145
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 413
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.198405822214521e-4
allele num: 11542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14364
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.082e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.67e0

DP
type: SiteQuality
SIO_000300: 2.531899e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4347
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35158
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 3
allele frequency: 2.892402622445044e-4
allele num: 10372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65978
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.15e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.536273e6

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

FS
type: SiteQuality
SIO_000300: 7.466e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

GenotypeQuality
all individuals: 911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3323
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35175
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4743
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514279657167086e-5
allele num: 66038
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.541759e6

MQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e0

FS
type: SiteQuality
SIO_000300: 5.408e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.197e1

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5057
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35180
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14642
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.009e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.366e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.77e-1

FS
type: SiteQuality
SIO_000300: 1.063e0

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

DP
type: SiteQuality
SIO_000300: 2.54496e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2801
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35186
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

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

East Asian
type: Population
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: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.059450296646083e-4
allele num: 66072
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.723e1

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

FS
type: SiteQuality
SIO_000300: 5.57e0

QD
type: SiteQuality
SIO_000300: 1.602e1

DP
type: SiteQuality
SIO_000300: 2.546985e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.384323812102342e-4
allele num: 14774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.386e1

BaseQRankSum
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SIO_000300: -1.454e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
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SIO_000300: -1.26e-1

FS
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SIO_000300: 1.158e1

DP
type: SiteQuality
SIO_000300: 2.549083e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: -1.204e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.148e1

VQSLOD
type: SiteQuality
SIO_000300: -1.391e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

DP
type: SiteQuality
SIO_000300: 2.556579e6

MQ
type: SiteQuality
SIO_000300: 5.755e1

FS
type: SiteQuality
SIO_000300: 4.058e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 35193
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511167528032158e-5
allele num: 66174
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.89e-1

DP
type: SiteQuality
SIO_000300: 2.561597e6

FS
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -1.054e0

QD
type: SiteQuality
SIO_000300: 1.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.78e-1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 263
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 117
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509707418702255e-5
allele num: 66238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15186
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.447e0

VQSLOD
type: SiteQuality
SIO_000300: -7.22e-2

QD
type: SiteQuality
SIO_000300: 1.224e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e0

FS
type: SiteQuality
SIO_000300: 5.537e0

DP
type: SiteQuality
SIO_000300: 2.566385e6

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66380
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15580
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.54e0

BaseQRankSum
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SIO_000300: -1.54e0

ReadPosRankSum
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SIO_000300: -7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.93e-1

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.472e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66424
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.683e1

GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 77

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 74
allele frequency: 4.714576962283384e-3
allele num: 15696
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.580921e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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SIO_000300: 1.02e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

South Asian
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num of homozygotes: 0

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

East Asian
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BaseQRankSum
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SIO_000300: 1.01e-1

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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DP
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SIO_000300: 2.590846e6

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

East Asian
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South Asian
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African
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Latino
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Other
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ClippingRankSum
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MQ
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QD
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BaseQRankSum
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VQSLOD
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DP
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

African
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allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66690
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European (Finnish)
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South Asian
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Other
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African
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East Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

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

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

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

Other
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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SIO_000300: 2.59838e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.29e-1

GenotypeDepth
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variant carriers: 0

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

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

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

Other
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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SIO_000300: -8.82e-1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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South Asian
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African
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Other
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MQ
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SIO_000300: 5.965e1

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

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

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

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

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

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

Other
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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 frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

Latino
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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VQSLOD
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DP
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MQ
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SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQRankSum
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SIO_000300: -2.93e-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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 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 frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Finnish)
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African
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Latino
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VQSLOD
type: SiteQuality
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

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

East Asian
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999850007499625e-5
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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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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SIO_000300: -6.6e-2

MQ
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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SIO_000300: 7.69e-1

BaseQRankSum
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SIO_000300: -4.803e0

ReadPosRankSum
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SIO_000300: 1.04e-1

FS
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SIO_000300: 2.387e0

DP
type: SiteQuality
SIO_000300: 2.597167e6

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 99
allele frequency: 5.996365838885524e-3
allele num: 16510
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
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African
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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
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.0e-1

DP
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BaseQRankSum
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SIO_000300: -3.376e0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66606
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DP
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SIO_000300: 2.594027e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.034e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

DP
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SIO_000300: 2.592936e6

MQRankSum
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SIO_000300: -1.041e0

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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QD
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SIO_000300: 1.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

FS
type: SiteQuality
SIO_000300: 5.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 8
allele frequency: 1.200732446792543e-4
allele num: 66626
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

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
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num of homozygotes: 0

African
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allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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VQSLOD
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
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allele num: 66624
num of homozygotes: 0

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

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

Latino
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European (Finnish)
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Other
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African
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South Asian
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East Asian
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MQRankSum
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VQSLOD
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.979e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 2.589196e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 1.194e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.506e0

VQSLOD
type: SiteQuality
SIO_000300: -1.401e0

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
all individuals: 3176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.506e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.401e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.979e0

FS
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 2.589196e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.242424242424243e-4
allele num: 16500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 2.422e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

DP
type: SiteQuality
SIO_000300: 2.589641e6

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.236e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

FS
type: SiteQuality
SIO_000300: 1.998e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.65e-1

DP
type: SiteQuality
SIO_000300: 2.586961e6

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.810467577448528e-4
allele num: 10394
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

FS
type: SiteQuality
SIO_000300: 1.998e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.236e0

QD
type: SiteQuality
SIO_000300: 1.408e1

DP
type: SiteQuality
SIO_000300: 2.586961e6

GenotypeQuality
all individuals: 11
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
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: 3
allele frequency: 3.468208092485549e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.587383e6

FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.2e-3

ClippingRankSum
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SIO_000300: -6.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818402230573403e-4
allele num: 16498
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
allele num: 906
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QD
type: SiteQuality
SIO_000300: 1.419e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

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

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: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

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

African
type: Population
allele count: 9
allele frequency: 8.665511265164644e-4
allele num: 10386
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 2.590707e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.768e0

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35475
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.79e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.639e0

FS
type: SiteQuality
SIO_000300: 2.335e0

VQSLOD
type: SiteQuality
SIO_000300: -2.794e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

QD
type: SiteQuality
SIO_000300: 2.587e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 2.599498e6

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 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: 66596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

FS
type: SiteQuality
SIO_000300: 1.708e0

DP
type: SiteQuality
SIO_000300: 2.600002e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.357e0

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.81e-1

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 3190
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3343
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504639778972342e-5
allele num: 66598
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 2.444e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.528e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

QD
type: SiteQuality
SIO_000300: 1.222e1

DP
type: SiteQuality
SIO_000300: 2.600629e6

MQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
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GenotypeQuality
all individuals: 7380
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 35523
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 64
allele frequency: 3.878317779663071e-3
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 5.37e-1

DP
type: SiteQuality
SIO_000300: 2.603003e6

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.861e0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2205
bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.847e0

VQSLOD
type: SiteQuality
SIO_000300: -1.682e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 5.825e1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.602521e6

QD
type: SiteQuality
SIO_000300: 1.264e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

GenotypeDepth
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

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

GenotypeQuality
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GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQRankSum
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SIO_000300: 3.23e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 1.8e0

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

DP
type: SiteQuality
SIO_000300: 2.603796e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 32

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 71

GenotypeQuality
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GenotypeQuality
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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: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.271845836868258e-4
allele num: 16502
num of homozygotes: 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: 6612
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.655588579663155e-4
allele num: 66618
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.185825410544512e-4
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
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SIO_000300: -4.55e-1

BaseQRankSum
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SIO_000300: 1.42e0

MQRankSum
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SIO_000300: -1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

DP
type: SiteQuality
SIO_000300: 2.607318e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3049
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 6612
num of homozygotes: 0

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

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

DP
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SIO_000300: 2.607318e6

QD
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BaseQRankSum
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SIO_000300: 1.42e0

VQSLOD
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FS
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SIO_000300: 5.47e-1

InbreedingCoeff
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SIO_000300: -5.0e-4

MQRankSum
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SIO_000300: -1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
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

South Asian
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allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.001290554938624e-5
allele num: 66638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
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SIO_000300: 1.02e0

MQRankSum
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DP
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SIO_000300: 2.609315e6

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 4.5e0

MQ
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SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

QD
type: SiteQuality
SIO_000300: 1.41e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 2
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allele num: 66642
num of homozygotes: 0

African
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.57e-1

FS
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SIO_000300: 1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 3.27e0

DP
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SIO_000300: 2.609616e6

InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
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SIO_000300: -9.15e-1

QD
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SIO_000300: 1.292e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 22
bin: 3.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.500585076059888e-5
allele num: 66658
num of homozygotes: 0

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

East Asian
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allele count: 0
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BaseQRankSum
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SIO_000300: 1.73e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -8.49e-1

ReadPosRankSum
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MQ
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.569e0

DP
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SIO_000300: 2.610514e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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Other
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MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
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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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BaseQRankSum
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DP
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QD
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SIO_000300: 1.278e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

African
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East Asian
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allele frequency: 1.15606936416185e-4
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Other
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South Asian
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European (Finnish)
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 4.53e-1

InbreedingCoeff
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BaseQRankSum
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FS
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QD
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SIO_000300: 1.332e1

VQSLOD
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SIO_000300: 7.43e-1

ReadPosRankSum
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SIO_000300: -5.629999999999999e-1

MQ
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SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

DP
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SIO_000300: 2.612112e6

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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SIO_000300: 2.612688e6

QD
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SIO_000300: 1.349e1

InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
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VQSLOD
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FS
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SIO_000300: 3.404e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
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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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66708
num of homozygotes: 0

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

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

FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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SIO_000300: 1.11e0

QD
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SIO_000300: 1.517e1

DP
type: SiteQuality
SIO_000300: 2.612752e6

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66722
num of homozygotes: 0

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

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

MQRankSum
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FS
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MQ
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SIO_000300: 5.986e1

DP
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.273e0

ClippingRankSum
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SIO_000300: 2.39e-1

VQSLOD
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ReadPosRankSum
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QD
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SIO_000300: 1.296e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

Other
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South Asian
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East Asian
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
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allele num: 906
num of homozygotes: 0

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

African
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.997332374186974e-5
allele num: 66726
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European (Finnish)
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South Asian
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

East Asian
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African
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allele frequency: 9.611687812379854e-5
allele num: 10404
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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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FS
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.613911e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

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

GenotypeQuality
all individuals: 2224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3087
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35580
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2217
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 7479
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.074e0

MQRankSum
type: SiteQuality
SIO_000300: -1.046e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 2.614236e6

GenotypeQuality
all individuals: 3392
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2225
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7466
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3086
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 35583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.383e0

QD
type: SiteQuality
SIO_000300: 1.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.177e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 2.614496e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.736e0

GenotypeQuality
all individuals: 35584
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0