14-96986562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986562
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986562
    reference: chr 14
allele count: 2
allele frequency: 1.67596829067994e-5
allele num: 119334
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.179G>A
  hgvsp: ENSP00000216277.8:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.179G>A
  hgvsp: ENSP00000451267.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.328G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.179G>A
  hgvsp: ENSP00000450437.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.179G>A
  hgvsp: ENSP00000451600.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.179G>A
  hgvsp: ENSP00000376716.2:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.179G>A
  hgvsp: ENSP00000450812.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.360G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-572G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.582G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5085G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27916
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg60His
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-96986565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986565
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986565
    reference: chr 14
allele count: 1
allele frequency: 8.438676140487081e-6
allele num: 118502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182G>A
  hgvsp: ENSP00000376716.2:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182G>A
  hgvsp: ENSP00000451600.1:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182G>A
  hgvsp: ENSP00000216277.8:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5082G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182G>A
  hgvsp: ENSP00000450437.1:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182G>A
  hgvsp: ENSP00000450812.1:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182G>A
  hgvsp: ENSP00000451267.1:p.Ser61Asn
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg61Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-96986568-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986568
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986568
    reference: chr 14
allele count: 1
allele frequency: 8.502967535669949e-6
allele num: 117606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5079A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+3A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+3A>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.182+3A>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

14-96986570-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986570
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986570
    reference: chr 14
allele count: 4
allele frequency: 3.420206580477461e-5
allele num: 116952
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+5A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5077A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+5A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.182+5A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-96986583-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986583
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986584
    reference: chr 14
allele count: 3
allele frequency: 2.675322822287223e-5
allele num: 112136
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5057dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+25dupT
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22551
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/14-96986592-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986592
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986592
    reference: chr 14
allele count: 2
allele frequency: 1.833920187793427e-5
allele num: 109056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+27A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5055A>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16218
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-96986594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986594
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986594
    reference: chr 14
allele count: 1
allele frequency: 9.225773119787439e-6
allele num: 108392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5053T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+29T>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14852
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

14-96986595-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986595
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986595
    reference: chr 14
allele count: 1
allele frequency: 9.259087794670468e-6
allele num: 108002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5052C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+30C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+30C>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

14-96986595-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986595
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986595
    reference: chr 14
allele count: 7
allele frequency: 6.481361456269329e-5
allele num: 108002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5052C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+30C>T
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14874
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18093
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-96986596-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986596
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986596
    reference: chr 14
allele count: 1
allele frequency: 9.286085729143452e-6
allele num: 107688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5051G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+31G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18597
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4517
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-96986601-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986601
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986599
    reference: chr 14
allele count: 1
allele frequency: 9.423471984017792e-6
allele num: 106118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+39_-569+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+39_363+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+39_331+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+39_585+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5043_220-5042delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+39_182+40delTT
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: CTT
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/14-96986609-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986609
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986609
    reference: chr 14
allele count: 1
allele frequency: 9.791442279447762e-6
allele num: 102130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5038A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+44A>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+44A>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5233
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

14-96986610-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96986610
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96986610
    reference: chr 14
allele count: 5
allele frequency: 4.955106732999029e-5
allele num: 100906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.363+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-5037A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.331+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-569+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.585+45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.182+45A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15814
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17830
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

14-96987256-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987256
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987256
    reference: chr 14
allele count: 1
allele frequency: 9.734065335046528e-6
allele num: 102732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-45A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4391A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-87A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-87A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13345
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-96987263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987263
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987263
    reference: chr 14
allele count: 1
allele frequency: 9.702332440718748e-6
allele num: 103068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-38G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-80G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4384G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-80G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

14-96987265-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987265
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987265
    reference: chr 14
allele count: 2
allele frequency: 1.93345062933818e-5
allele num: 103442
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4382A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-78A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-78A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20594
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

14-96987268-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987268
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987268
    reference: chr 14
allele count: 1
allele frequency: 9.623157165402826e-6
allele num: 103916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4379A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-33A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-75A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-75A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-96987269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987269
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987269
    reference: chr 14
allele count: 2
allele frequency: 1.927859497599815e-5
allele num: 103742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4378C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-74C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-32C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-74C>T
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

14-96987270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987270
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987270
    reference: chr 14
allele count: 1
allele frequency: 9.584603293269692e-6
allele num: 104334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-31G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-73G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4377G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-73G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2820
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-96987275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987275
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987275
    reference: chr 14
allele count: 1
allele frequency: 9.405568096313017e-6
allele num: 106320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-26T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4372T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-68T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-68T>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff

14-96987298-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987298
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987298
    reference: chr 14
allele count: 1
allele frequency: 8.580892069539549e-6
allele num: 116538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-45C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4349C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.183-3C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-45C>G
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: c.183-3C>G
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

14-96987303-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987303
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987303
    reference: chr 14
allele count: 6636
allele frequency: 5.606718599503202e-2
allele num: 118358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4344A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.185A>T
  hgvsp: ENSP00000451267.1:p.Asn62Ile
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-40A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-40A>T
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 2.75e1
  variant carriers: 509
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 587
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 3.75e1
  variant carriers: 914
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.25e1
  variant carriers: 912
genotype depth: GenotypeDepth
  all individuals: 35963
  bin: 2.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 787
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 277
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 3.25e1
  variant carriers: 756
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
hgvs: p.Asn62Ile
num of homozygotes: 201
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

14-96987308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987308
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987308
    reference: chr 14
allele count: 1
allele frequency: 8.381105635455429e-6
allele num: 119316
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.190C>T
  hgvsp: ENST00000556619.1:c.190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4339C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-35C>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-35C>T
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu64Leu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

14-96987310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987310
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987310
    reference: chr 14
allele count: 1
allele frequency: 8.359246999030327e-6
allele num: 119628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.192G>A
  hgvsp: ENST00000556619.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4337G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-33G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-33G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36504
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu64Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

14-96987317-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987317
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987317
    reference: chr 14
allele count: 3
allele frequency: 2.495840266222962e-5
allele num: 120200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4330T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.199T>G
  hgvsp: ENSP00000451267.1:p.Leu67Val
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-26T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-26T>G
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35815
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu67Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

14-96987321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987321
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987321
    reference: chr 14
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4326T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.203T>C
  hgvsp: ENSP00000451267.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-22T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-22T>C
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile68Thr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-96987324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987324
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987324
    reference: chr 14
allele count: 2
allele frequency: 1.659503144758459e-5
allele num: 120518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4323A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.206A>G
  hgvsp: ENSP00000451267.1:p.Asp69Gly
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-19A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-19A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp69Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-96987324-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987324
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987324
    reference: chr 14
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4323A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.206A>T
  hgvsp: ENSP00000451267.1:p.Asp69Val
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-19A>T
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-19A>T
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp69Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

14-96987326-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987326
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987326
    reference: chr 14
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.208A>G
  hgvsp: ENSP00000451267.1:p.Asn70Asp
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-17A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4321A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn70Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

14-96987327-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987327
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987328
    reference: chr 14
allele count: 3
allele frequency: 2.488016055996948e-5
allele num: 120578
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.211dupT
  hgvsp: ENSP00000451267.1:p.Cys71LeufsTer14
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4318dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586-14dupT
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183-14dupT
  variant of: http://identifiers.org/hgnc/14981
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys71LeufsTer14
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-96987343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987343
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987343
    reference: chr 14
allele count: 13
allele frequency: 1.076141123491333e-4
allele num: 120802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.364G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-568G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4304G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.183G>A
  hgvsp: ENST00000216277.8:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.225G>A
  hgvsp: ENST00000556619.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.332G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.183G>A
  hgvsp: ENST00000557320.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.183G>A
  hgvsp: ENST00000557471.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.183G>A
  hgvsp: ENST00000392990.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.183G>A
  hgvsp: ENST00000553689.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.586G>A
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.183G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

14-96987373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987373
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987373
    reference: chr 14
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.213G>A
  hgvsp: ENST00000553689.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.213G>A
  hgvsp: ENST00000557471.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.255G>A
  hgvsp: ENST00000556619.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.21G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.213G>A
  hgvsp: ENST00000392990.2:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.616G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.362G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.394G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4274G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.213G>A
  hgvsp: ENST00000557320.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-538G>A
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.213G>A
  hgvsp: ENST00000216277.8:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu71Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

14-96987376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987376
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987376
    reference: chr 14
allele count: 2
allele frequency: 1.652537471287161e-5
allele num: 121026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4271A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.216A>G
  hgvsp: ENST00000557471.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.216A>G
  hgvsp: ENST00000216277.8:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.216A>G
  hgvsp: ENST00000557320.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.24A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.216A>G
  hgvsp: ENST00000392990.2:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-535A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000556248
  gene symbol: PAPOLA
  hgvsc: ENST00000556248.1:n.619A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.365A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.258A>G
  hgvsp: ENST00000556619.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.216A>G
  hgvsp: ENST00000553689.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.397A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val72Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

14-96987421-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987421
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987421
    reference: chr 14
allele count: 7
allele frequency: 5.784263497992034e-5
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4226T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+12T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+12T>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-96987422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987422
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987422
    reference: chr 14
allele count: 34
allele frequency: 2.809313701188174e-4
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+13T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4225T>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36645
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

14-96987430-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987430
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987430
    reference: chr 14
allele count: 11
allele frequency: 9.090758830432555e-5
allele num: 121002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4217A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+21A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+21A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

14-96987437-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987437
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987437
    reference: chr 14
allele count: 27033
allele frequency: 2.2347601805466e-1
allele num: 120966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4210A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+28A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+28A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 9.75e1
  variant carriers: 4962
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 8.25e1
  variant carriers: 1532
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 5.75e1
  variant carriers: 1853
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.25e1
  variant carriers: 1505
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 1944
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 1737
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 2.75e1
  variant carriers: 269
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 689
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.75e1
  variant carriers: 1267
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.25e1
  variant carriers: 467
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 6.75e1
  variant carriers: 2029
genotype depth: GenotypeDepth
  all individuals: 24764
  bin: 2.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 923
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 8.75e1
  variant carriers: 1237
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 9.25e1
  variant carriers: 1058
genotype quality: GenotypeQuality
num of homozygotes: 3304
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

14-96987441-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987441
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987441
    reference: chr 14
allele count: 29
allele frequency: 2.397605701341006e-4
allele num: 120954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4206T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+32T>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+32T>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-96987444-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987444
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987444
    reference: chr 14
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4203T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+35T>C
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+35T>C
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-96987445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987445
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987445
    reference: chr 14
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4202A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+36A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+36A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

14-96987460-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96987460
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96987460
    reference: chr 14
allele count: 1
allele frequency: 8.278968109414843e-6
allele num: 120788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.249+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.291+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.57+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.249+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.398+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.430+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.249+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.249+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.249+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-4187C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.10+51C>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-502+51C>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-96991598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96991598
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 96991598
    reference: chr 14
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451600
  ensembl transcript: ENST00000553689
  gene symbol: PAPOLA
  hgvsc: ENST00000553689.1:c.250-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450812
  ensembl transcript: ENST00000557471
  gene symbol: PAPOLA
  hgvsc: ENST00000557471.1:c.250-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554130
  gene symbol: PAPOLA
  hgvsc: ENST00000554130.1:n.431-2169A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450534
  ensembl transcript: ENST00000555626
  gene symbol: PAPOLA
  hgvsc: ENST00000555626.1:c.-501-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000376716
  ensembl transcript: ENST00000392990
  gene symbol: PAPOLA
  hgvsc: ENST00000392990.2:c.250-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000450437
  ensembl transcript: ENST00000557320
  gene symbol: PAPOLA
  hgvsc: ENST00000557320.1:c.250-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000557406
  gene symbol: PAPOLA
  hgvsc: ENST00000557406.1:n.58-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000555224
  gene symbol: PAPOLA
  hgvsc: ENST00000555224.1:n.11-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000452578
  ensembl transcript: ENST00000553357
  gene symbol: PAPOLA
  hgvsc: ENST00000553357.1:c.220-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000451267
  ensembl transcript: ENST00000556619
  gene symbol: PAPOLA
  hgvsc: ENST00000556619.1:c.292-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl protein: ENSP00000216277
  ensembl transcript: ENST00000216277
  gene symbol: PAPOLA
  hgvsc: ENST00000216277.8:c.250-49A>G
  variant of: http://identifiers.org/hgnc/14981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090060
  ensembl transcript: ENST00000554887
  gene symbol: PAPOLA
  hgvsc: ENST00000554887.1:n.399-49A>G
  variant of: http://identifiers.org/hgnc/14981
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30910
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

15-101152674-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101152674
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101152674
    reference: chr 15
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.211+42A>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+42A>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.211+42A>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183475
  ensembl transcript: ENST00000561192
  gene symbol: ASB7
  hgvsc: ENST00000561192.1:n.586A>G
  variant of: http://identifiers.org/hgnc/17182
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12085
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

15-101152679-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101152679
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101152679
    reference: chr 15
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.211+47T>C
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.211+47T>C
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183475
  ensembl transcript: ENST00000561192
  gene symbol: ASB7
  hgvsc: ENST00000561192.1:n.591T>C
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+47T>C
  variant of: http://identifiers.org/hgnc/17182
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3632
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7096
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32272
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

15-101152681-ATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101152681
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101152679
    reference: chr 15
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183475
  ensembl transcript: ENST00000561192
  gene symbol: ASB7
  hgvsc: ENST00000561192.1:n.595_596delGT
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.211+51_211+52delGT
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+51_211+52delGT
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.211+51_211+52delGT
  variant of: http://identifiers.org/hgnc/17182
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3633
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2872
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: ATG
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

15-101169601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169601
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169601
    reference: chr 15
allele count: 1
allele frequency: 8.932718762282489e-6
allele num: 111948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+16969C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-41C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-41C>T
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37024
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

15-101169604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169604
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169604
    reference: chr 15
allele count: 1
allele frequency: 8.922835320151331e-6
allele num: 112072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+16972G>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-38G>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-38G>A
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

15-101169618-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169618
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169618
    reference: chr 15
allele count: 1
allele frequency: 8.865091044485026e-6
allele num: 112802
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-24C>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-24C>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+16986C>G
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

15-101169618-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169618
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169618
    reference: chr 15
allele count: 1
allele frequency: 8.865091044485026e-6
allele num: 112802
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-24C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+16986C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-24C>T
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8365
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

15-101169629-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169629
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169629
    reference: chr 15
allele count: 1
allele frequency: 8.789199831247363e-6
allele num: 113776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-13G>C
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+16997G>C
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-13G>C
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 565
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

15-101169638-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169638
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169638
    reference: chr 15
allele count: 10
allele frequency: 8.671823511047904e-5
allele num: 115316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.212-4C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17006C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.212-4C>T
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26283
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39829
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8465
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2914
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
hgvs: c.212-4C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

15-101169643-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169643
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169643
    reference: chr 15
allele count: 265
allele frequency: 2.271441551094578e-3
allele num: 116666
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.213T>C
  hgvsp: ENST00000332783.7:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.213T>C
  hgvsp: ENST00000343276.4:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17011T>C
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26403
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 13926
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 8538
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40719
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
hgvs: c.213T>C
num of homozygotes: 3
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

15-101169651-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169651
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169651
    reference: chr 15
allele count: 1
allele frequency: 8.47314014573801e-6
allele num: 118020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17019C>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.221C>G
  hgvsp: ENSP00000328327.7:p.Thr74Arg
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.221C>G
  hgvsp: ENSP00000339819.4:p.Thr74Arg
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41568
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr74Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

15-101169653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169653
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169653
    reference: chr 15
allele count: 1
allele frequency: 8.447230153232754e-6
allele num: 118382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17021G>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.223G>A
  hgvsp: ENSP00000328327.7:p.Val75Ile
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.223G>A
  hgvsp: ENSP00000339819.4:p.Val75Ile
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41903
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val75Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/15-101169667-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169667
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169667
    reference: chr 15
allele count: 1
allele frequency: 8.339866228545694e-6
allele num: 119906
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.237C>A
  hgvsp: ENST00000332783.7:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17035C>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.237C>A
  hgvsp: ENST00000343276.4:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 777
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42734
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile79Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

15-101169667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169667
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169667
    reference: chr 15
allele count: 2
allele frequency: 1.667973245709139e-5
allele num: 119906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.237C>T
  hgvsp: ENST00000343276.4:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17035C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.237C>T
  hgvsp: ENST00000332783.7:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42734
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile79Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

15-101169679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169679
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169679
    reference: chr 15
allele count: 4
allele frequency: 3.313617310336829e-5
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17047G>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.249G>A
  hgvsp: ENST00000332783.7:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.249G>A
  hgvsp: ENST00000343276.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27573
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43461
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr83Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

15-101169688-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169688
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169688
    reference: chr 15
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.258C>T
  hgvsp: ENST00000332783.7:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17056C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.258C>T
  hgvsp: ENST00000343276.4:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43605
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His86His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

15-101169694-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169694
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169694
    reference: chr 15
allele count: 3344
allele frequency: 2.763773410251748e-2
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.264A>G
  hgvsp: ENST00000343276.4:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17062A>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.264A>G
  hgvsp: ENST00000332783.7:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 288
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 721
genotype depth: GenotypeDepth
  all individuals: 27369
  bin: 2.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 222
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 303
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 3.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8641
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4187
  bin: 9.75e1
  variant carriers: 3273
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Ala88Ala
num of homozygotes: 68
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

15-101169696-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169696
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169696
    reference: chr 15
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17064C>G
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.266C>G
  hgvsp: ENSP00000339819.4:p.Ala89Gly
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.266C>G
  hgvsp: ENSP00000328327.7:p.Ala89Gly
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala89Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD

15-101169715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169715
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169715
    reference: chr 15
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.285C>T
  hgvsp: ENST00000332783.7:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.285C>T
  hgvsp: ENST00000343276.4:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17083C>T
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg95Arg
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

15-101169727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169727
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169727
    reference: chr 15
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.297G>A
  hgvsp: ENST00000332783.7:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.297G>A
  hgvsp: ENST00000343276.4:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17095G>A
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 589
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9206
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 45921
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu99Leu
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-101169752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169752
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169752
    reference: chr 15
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17120G>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.322G>A
  hgvsp: ENSP00000339819.4:p.Asp108Asn
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.322G>A
  hgvsp: ENSP00000328327.7:p.Asp108Asn
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1708
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45875
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp108Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

15-101169757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169757
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169757
    reference: chr 15
allele count: 4
allele frequency: 3.299676631690094e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.327C>T
  hgvsp: ENST00000343276.4:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17125C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.327C>T
  hgvsp: ENST00000332783.7:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14611
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile109Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

15-101169773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169773
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169773
    reference: chr 15
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.343A>G
  hgvsp: ENSP00000339819.4:p.Asn115Asp
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.343A>G
  hgvsp: ENSP00000328327.7:p.Asn115Asp
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17141A>G
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9187
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn115Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

15-101169778-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169778
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169778
    reference: chr 15
allele count: 10
allele frequency: 8.253004093490031e-5
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.348C>T
  hgvsp: ENST00000332783.7:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.348C>T
  hgvsp: ENST00000343276.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17146C>T
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 9177
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp116Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-101169788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169788
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169788
    reference: chr 15
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17156C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.358C>T
  hgvsp: ENSP00000328327.7:p.Pro120Ser
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.358C>T
  hgvsp: ENSP00000339819.4:p.Pro120Ser
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9169
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro120Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-101169790-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169790
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169790
    reference: chr 15
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17158C>A
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.360C>A
  hgvsp: ENST00000343276.4:c.360C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.360C>A
  hgvsp: ENST00000332783.7:c.360C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9168
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro120Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

15-101169790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169790
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169790
    reference: chr 15
allele count: 6
allele frequency: 4.952292911618079e-5
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.360C>T
  hgvsp: ENST00000332783.7:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17158C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.360C>T
  hgvsp: ENST00000343276.4:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9168
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro120Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

15-101169793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169793
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169793
    reference: chr 15
allele count: 3
allele frequency: 2.475982965237199e-5
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17161C>T
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.363C>T
  hgvsp: ENST00000332783.7:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.363C>T
  hgvsp: ENST00000343276.4:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9162
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu121Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-101169796-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101169796
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101169796
    reference: chr 15
allele count: 44
allele frequency: 3.631561571475734e-4
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000328327
  ensembl transcript: ENST00000332783
  gene symbol: ASB7
  hgvsc: ENST00000332783.7:c.366T>C
  hgvsp: ENST00000332783.7:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000339819
  ensembl transcript: ENST00000343276
  gene symbol: ASB7
  hgvsc: ENST00000343276.4:c.366T>C
  hgvsp: ENST00000343276.4:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183475
  ensembl protein: ENSP00000453626
  ensembl transcript: ENST00000558747
  gene symbol: ASB7
  hgvsc: ENST00000558747.1:c.211+17164T>C
  variant of: http://identifiers.org/hgnc/17182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His122His
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046180090166931e-5
allele num: 65656
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

FS
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.268e1

DP
type: SiteQuality
SIO_000300: 1.72187e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

GenotypeDepth
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 471
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
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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: 0

GenotypeQuality
all individuals: 1910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534683855125844e-5
allele num: 65160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15944
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
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SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ReadPosRankSum
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SIO_000300: 3.5e-2

DP
type: SiteQuality
SIO_000300: 1.702314e6

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.852e1

VQSLOD
type: SiteQuality
SIO_000300: -1.992e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.111e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15784
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64640
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
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SIO_000300: 5.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

ClippingRankSum
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SIO_000300: -7.17e-1

FS
type: SiteQuality
SIO_000300: 1.786e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.674824e6

QD
type: SiteQuality
SIO_000300: 1.321e1

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

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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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
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.55574224462491e-5
allele num: 64278
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.06873977086743e-4
allele num: 9776
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 frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.26e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 1.655365e6

FS
type: SiteQuality
SIO_000300: 4.576e0

QD
type: SiteQuality
SIO_000300: 1.21e1

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

GenotypeQuality
all individuals: 2095
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 32241
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variant carriers: 0

GenotypeQuality
all individuals: 5828
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623007757977083e-5
allele num: 61614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.963786303334529e-5
allele num: 11156
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.085e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.039e1

MQ
type: SiteQuality
SIO_000300: 6.033e1

DP
type: SiteQuality
SIO_000300: 1.483492e6

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4142
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.340571237681643e-5
allele num: 59870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

QD
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DP
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ClippingRankSum
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SIO_000300: 2.24e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 8.664999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -3.511e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.931e1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.67993817827504e-5
allele num: 59526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

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

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

South Asian
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FS
type: SiteQuality
SIO_000300: 3.565e0

BaseQRankSum
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MQRankSum
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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SIO_000300: 9.58e-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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variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.117437722419929e-5
allele num: 14050
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

QD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
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VQSLOD
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FS
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DP
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SIO_000300: 1.252204e6

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 625
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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.423487544483986e-4
allele num: 14050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 2.252252252252252e-4
allele num: 8880
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 59306
num of homozygotes: 0

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

Latino
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allele count: 3
allele frequency: 2.765486725663717e-4
allele num: 10848
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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SIO_000300: -1.06e-1

FS
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BaseQRankSum
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MQ
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ClippingRankSum
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SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10844
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.691532189857573e-5
allele num: 59118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 8840
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -6.5e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.146263182026593e-4
allele num: 8724
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58224
num of homozygotes: 0

MQRankSum
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InbreedingCoeff
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SIO_000300: -2.1e-3

BaseQRankSum
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SIO_000300: 3.76e-1

VQSLOD
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SIO_000300: 1.6e0

ReadPosRankSum
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FS
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QD
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MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
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SIO_000300: 1.156131e6

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.787437886533443e-5
allele num: 55946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.473e0

QD
type: SiteQuality
SIO_000300: 1.679e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

MQRankSum
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SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 1.074961e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12650
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 7.058159232072275e-4
allele num: 7084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55264
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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SIO_000300: -5.92e-1

ReadPosRankSum
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DP
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FS
type: SiteQuality
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QD
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SIO_000300: 1.38e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
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)
type: Population
allele count: 1
allele frequency: 1.805510417795111e-5
allele num: 55386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8710
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6256
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
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DP
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FS
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

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

African
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.585257421482863e-5
allele num: 55784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
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Other
type: Population
allele count: 0
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allele num: 800
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MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.783739431343869e-5
allele num: 56062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.53e-1

FS
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MQRankSum
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SIO_000300: -1.164e0

VQSLOD
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SIO_000300: -9.320000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.276043e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.573087504912996e-5
allele num: 55974
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.534e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.621e0

DP
type: SiteQuality
SIO_000300: 1.288472e6

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7278
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56286
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.582779360557138e-4
allele num: 6318
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.601e0

MQRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.6e0

DP
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SIO_000300: 1.311097e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

QD
type: SiteQuality
SIO_000300: 1.818e1

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: 2362
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.612e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 1.149e1

DP
type: SiteQuality
SIO_000300: 1.369047e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

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: 711
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562109472631842e-5
allele num: 64016
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
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SIO_000300: 1.541883e6

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.271e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 848
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variant carriers: 11

African
type: Population
allele count: 161
allele frequency: 1.657742998352554e-2
allele num: 9712
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3756
allele frequency: 5.764626435017497e-2
allele num: 65156
num of homozygotes: 102

East Asian
type: Population
allele count: 431
allele frequency: 5.172827652424388e-2
allele num: 8332
num of homozygotes: 7

Latino
type: Population
allele count: 899
allele frequency: 7.885964912280702e-2
allele num: 11400
num of homozygotes: 37

European (Finnish)
type: Population
allele count: 462
allele frequency: 7.010622154779969e-2
allele num: 6590
num of homozygotes: 17

South Asian
type: Population
allele count: 879
allele frequency: 5.399926280869886e-2
allele num: 16278
num of homozygotes: 32

Other
type: Population
allele count: 48
allele frequency: 5.393258426966292e-2
allele num: 890
num of homozygotes: 5

DP
type: SiteQuality
SIO_000300: 1.716344e6

FS
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.996e0

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65698
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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ReadPosRankSum
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FS
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MQ
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QD
type: SiteQuality
SIO_000300: 1.511e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51804960986125e-5
allele num: 65874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -5.0e-4

QD
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SIO_000300: 1.875e1

BaseQRankSum
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SIO_000300: -2.501e0

ClippingRankSum
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SIO_000300: -8.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQ
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SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.738103e6

VQSLOD
type: SiteQuality
SIO_000300: -5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.531448250860975e-5
allele num: 66204
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

QD
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
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SIO_000300: -4.29e0

VQSLOD
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MQRankSum
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SIO_000300: -2.64e-1

DP
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SIO_000300: 1.745168e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
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SIO_000300: -1.436e0

FS
type: SiteQuality
SIO_000300: 1.1657e1

InbreedingCoeff
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SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
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SIO_000300: 1.747761e6

VQSLOD
type: SiteQuality
SIO_000300: -2.406e0

BaseQRankSum
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SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01313727853441e-5
allele num: 66376
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.98e-1

DP
type: SiteQuality
SIO_000300: 1.749412e6

InbreedingCoeff
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SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

FS
type: SiteQuality
SIO_000300: 6.166e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

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 (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

InbreedingCoeff
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SIO_000300: 2.8e-3

FS
type: SiteQuality
SIO_000300: 6.166e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 9.99e-1

ClippingRankSum
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SIO_000300: -9.46e-1

MQRankSum
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VQSLOD
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QD
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DP
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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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bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9964
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

DP
type: SiteQuality
SIO_000300: 1.75005e6

BaseQRankSum
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FS
type: SiteQuality
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MQ
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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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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African
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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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.517528008673654e-5
allele num: 66408
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

MQRankSum
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SIO_000300: 1.17e-1

ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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VQSLOD
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 4

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10032
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European (Non-Finnish)
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allele count: 12
allele frequency: 1.803534928459781e-4
allele num: 66536
num of homozygotes: 0

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

African
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allele frequency: 0.0e0
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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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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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SIO_000300: -1.778e0

GenotypeDepth
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variant carriers: 0

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

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

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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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

QD
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BaseQRankSum
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MQ
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ClippingRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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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

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

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

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

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

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

African
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allele count: 34
allele frequency: 3.328764440963384e-3
allele num: 10214
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
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InbreedingCoeff
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SIO_000300: 3.7e-3

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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SIO_000300: 2.83e0

VQSLOD
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FS
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SIO_000300: 0.0e0

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: 10

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

Latino
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allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

South Asian
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allele num: 16508
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European (Finnish)
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num of homozygotes: 0

Other
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allele frequency: 1.103752759381898e-3
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num of homozygotes: 0

African
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BaseQRankSum
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QD
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 1933

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16

European (Non-Finnish)
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allele count: 14668
allele frequency: 2.205913315487112e-1
allele num: 66494
num of homozygotes: 1624

South Asian
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allele frequency: 2.340038778477945e-1
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Other
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European (Finnish)
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allele frequency: 2.136377381312368e-1
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African
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East Asian
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allele frequency: 1.230608937253994e-1
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Latino
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allele frequency: 1.577036140411551e-1
allele num: 11566
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BaseQRankSum
type: SiteQuality
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MQ
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DP
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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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

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

European (Non-Finnish)
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African
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allele num: 10218
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South Asian
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Latino
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European (Finnish)
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Other
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FS
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QD
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DP
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1997
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504257047444267e-5
allele num: 66478
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.778e0

VQSLOD
type: SiteQuality
SIO_000300: -3.177e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
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MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 2.200851e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.79431929480901e-5
allele num: 10210
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

MQRankSum
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SIO_000300: -1.57e-1

FS
type: SiteQuality
SIO_000300: 8.654999999999999e0

BaseQRankSum
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SIO_000300: 4.03e0

ReadPosRankSum
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SIO_000300: 7.77e-1

DP
type: SiteQuality
SIO_000300: 2.20019e6

QD
type: SiteQuality
SIO_000300: 1.614e1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1967
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GenotypeQuality
all individuals: 2025
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.197289e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.85e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 874
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.872e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.74e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.014e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.785465e6

QD
type: SiteQuality
SIO_000300: 9.84e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

FS
type: SiteQuality
SIO_000300: 4.058e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.176e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 1.691e1

DP
type: SiteQuality
SIO_000300: 1.561237e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
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allele num: 16498
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.558419e6

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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num of homozygotes: 0

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

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

FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 1

European (Non-Finnish)
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allele num: 64112
num of homozygotes: 0

African
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East Asian
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South Asian
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European (Finnish)
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allele num: 6608
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Latino
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Other
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
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DP
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ClippingRankSum
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MQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.55860349127182e-5
allele num: 64160
num of homozygotes: 0

Latino
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African
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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QD
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

East Asian
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South Asian
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African
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Other
type: Population
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.554001554001554e-5
allele num: 64350
num of homozygotes: 0

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

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

African
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European (Non-Finnish)
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allele frequency: 1.554001554001554e-5
allele num: 64350
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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DP
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BaseQRankSum
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MQRankSum
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FS
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

GenotypeQuality
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variant carriers: 1

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
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European (Non-Finnish)
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allele frequency: 1.548083472660846e-5
allele num: 64596
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South Asian
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QD
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ReadPosRankSum
type: SiteQuality
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FS
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

Latino
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East Asian
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South Asian
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African
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allele frequency: 0.0e0
allele num: 9826
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European (Non-Finnish)
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allele count: 9
allele frequency: 1.385041551246538e-4
allele num: 64980
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European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
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Other
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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FS
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DP
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VQSLOD
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SIO_000300: 3.24e0

GenotypeQuality
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variant carriers: 257

GenotypeQuality
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Latino
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allele frequency: 1.127297953520638e-3
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East Asian
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allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
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African
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allele count: 244
allele frequency: 2.465144473631036e-2
allele num: 9898
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Other
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allele count: 3
allele frequency: 3.529411764705882e-3
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South Asian
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allele count: 1
allele frequency: 7.240081088908195e-5
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.592211609110948e-5
allele num: 65328
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.705411e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
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SIO_000300: 1.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

QD
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SIO_000300: 1.23e1

GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8642
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65670
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Latino
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allele num: 11558
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African
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Other
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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FS
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ClippingRankSum
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 1.0e-4

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Latino
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allele frequency: 0.0e0
allele num: 11556
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East Asian
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South Asian
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allele count: 1
allele frequency: 6.685385746757588e-5
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.154e1

DP
type: SiteQuality
SIO_000300: 1.711694e6

GenotypeQuality
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variant carriers: 0

Other
type: Population
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allele num: 890
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Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

InbreedingCoeff
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SIO_000300: 5.5e-3

DP
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SIO_000300: 1.728761e6

MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
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European (Finnish)
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allele count: 0
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African
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East Asian
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South Asian
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Other
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Latino
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.967e1

BaseQRankSum
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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East Asian
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allele num: 8652
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European (Finnish)
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allele count: 0
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Latino
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South Asian
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African
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Other
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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QD
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 3.946174780768068e-2
allele num: 6614
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East Asian
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Other
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allele frequency: 3.436807095343681e-2
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Latino
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allele frequency: 1.408572416176979e-2
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South Asian
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allele frequency: 1.515702679762338e-2
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African
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allele frequency: 6.858710562414266e-3
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European (Non-Finnish)
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allele frequency: 3.860023439612946e-2
allele num: 66554
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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FS
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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European (Non-Finnish)
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allele num: 66554
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African
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South Asian
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Latino
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East Asian
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Other
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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DP
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MQ
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VQSLOD
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GenotypeQuality
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variant carriers: 0

African
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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Latino
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QD
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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Latino
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Other
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South Asian
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.221e0

DP
type: SiteQuality
SIO_000300: 1.703787e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.06e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.525e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.246e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.702607e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

MQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 1482
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 3.231e0

QD
type: SiteQuality
SIO_000300: 1.205e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

DP
type: SiteQuality
SIO_000300: 1.702579e6

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 1708
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.795e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.34e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.700735e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.739e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.55e-1

GenotypeQuality
all individuals: 45664
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

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

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

African
type: Population
allele count: 7
allele frequency: 6.767208043310132e-4
allele num: 10344
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.212e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

DP
type: SiteQuality
SIO_000300: 1.701008e6

FS
type: SiteQuality
SIO_000300: 5.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.46e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.652e-1

FS
type: SiteQuality
SIO_000300: 2.987e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

DP
type: SiteQuality
SIO_000300: 1.699921e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

QD
type: SiteQuality
SIO_000300: 7.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.283e0

GenotypeQuality
all individuals: 1706
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

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

African
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allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.258e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.7002e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

FS
type: SiteQuality
SIO_000300: 2.452e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
all individuals: 1706
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.00792697573865e-5
allele num: 66608
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

FS
type: SiteQuality
SIO_000300: 2.452e0

DP
type: SiteQuality
SIO_000300: 1.7002e6

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.935e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

African
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allele frequency: 2.901353965183752e-4
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.109e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.886e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

DP
type: SiteQuality
SIO_000300: 1.699226e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

QD
type: SiteQuality
SIO_000300: 1.331e1