http://identifiers.org/exac.variant/16-15714351-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714351
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714351
    reference: chr 16
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1239T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2677T>G
  hgvsp: ENSP00000379654.3:p.Cys893Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2677T>G
  hgvsp: ENSP00000449329.1:p.Cys893Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2182T>G
  hgvsp: ENSP00000439819.2:p.Cys728Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2677T>G
  hgvsp: ENSP00000450309.1:p.Cys893Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2668T>G
  hgvsp: ENSP00000473601.1:p.Cys890Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2668T>G
  hgvsp: ENSP00000449376.1:p.Cys890Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4396A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.434T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys893Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

16-15714374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714374
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714374
    reference: chr 16
allele count: 2
allele frequency: 1.664946222237022e-5
allele num: 120124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2654C>G
  hgvsp: ENSP00000449329.1:p.Ser885Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2645C>G
  hgvsp: ENSP00000449376.1:p.Ser882Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2654C>G
  hgvsp: ENSP00000450309.1:p.Ser885Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1216C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2654C>G
  hgvsp: ENSP00000379654.3:p.Ser885Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4373G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2159C>G
  hgvsp: ENSP00000439819.2:p.Ser720Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.411C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2645C>G
  hgvsp: ENSP00000473601.1:p.Ser882Cys
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3594
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser885Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum

16-15714378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714378
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714378
    reference: chr 16
allele count: 2
allele frequency: 1.66730580055688e-5
allele num: 119954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2641A>G
  hgvsp: ENSP00000449376.1:p.Met881Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2641A>G
  hgvsp: ENSP00000473601.1:p.Met881Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2650A>G
  hgvsp: ENSP00000379654.3:p.Met884Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4369T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2650A>G
  hgvsp: ENSP00000450309.1:p.Met884Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2155A>G
  hgvsp: ENSP00000439819.2:p.Met719Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1212A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2650A>G
  hgvsp: ENSP00000449329.1:p.Met884Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.407A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met884Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

16-15714386-GCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714386
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714384
    reference: chr 16
allele count: 1
allele frequency: 8.38335401227323e-6
allele num: 119284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145_2146delTG
  hgvsp: ENSP00000439819.2:p.Ala716ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640_2641delTG
  hgvsp: ENSP00000450309.1:p.Ala881ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631_2632delTG
  hgvsp: ENSP00000473601.1:p.Ala878ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640_2641delTG
  hgvsp: ENSP00000379654.3:p.Ala881ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1202_1646+1203delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397_398delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631_2632delTG
  hgvsp: ENSP00000449376.1:p.Ala878ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640_2641delTG
  hgvsp: ENSP00000449329.1:p.Ala881ArgfsTer18
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4359_*13-4358delAC
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala881ArgfsTer18
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: GCA
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

16-15714393-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714393
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714393
    reference: chr 16
allele count: 1
allele frequency: 8.445945945945946e-6
allele num: 118400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-5T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4354A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1197T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-5T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
hgvs: c.2640-5T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-15714394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714394
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714394
    reference: chr 16
allele count: 1
allele frequency: 8.453799983092399e-6
allele num: 118290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1196T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-6T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4353A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-6T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: c.2640-6T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

16-15714402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714402
    reference: chr 16
allele count: 2
allele frequency: 1.712035610340695e-5
allele num: 116820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4345G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1188C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-14C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-14C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

16-15714404-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714404
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714404
    reference: chr 16
allele count: 4
allele frequency: 3.427709604442312e-5
allele num: 116696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1186A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4343T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-16A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-16A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16218
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4195
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15714408-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714408
    reference: chr 16
allele count: 2
allele frequency: 1.722860637803008e-5
allele num: 116086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1182A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-20A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4339T>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-20A>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14727
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7539
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-15714412-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714412
    reference: chr 16
allele count: 1
allele frequency: 8.651417102121328e-6
allele num: 115588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4335G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1178C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-24C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4887
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8447
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26077
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

16-15714423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714423
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714423
    reference: chr 16
allele count: 3
allele frequency: 2.627798605514873e-5
allele num: 114164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1167A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-35A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4324T>C
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12909
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15603
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11784
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5890
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

16-15714430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714430
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714430
    reference: chr 16
allele count: 1
allele frequency: 8.92889031751134e-6
allele num: 111996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1160G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4317C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-42G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-42G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7504
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-15714432-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15714432
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15714432
    reference: chr 16
allele count: 6
allele frequency: 5.430453985953225e-5
allele num: 110488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-4315T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2640-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2631-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.397-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2145-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2640-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+1158A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2640-44A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2631-44A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11840
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7821
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-15715539-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715539
    reference: chr 16
allele count: 2
allele frequency: 1.703925845147219e-5
allele num: 117376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3208T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.379A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+51A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

16-15715543-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715543
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715543
    reference: chr 16
allele count: 2
allele frequency: 1.701837985023826e-5
allele num: 117520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3204T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.375A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+47A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+47A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14468
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

16-15715567-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715567
    reference: chr 16
allele count: 1
allele frequency: 8.434405627435435e-6
allele num: 118562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.351A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3180T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+23A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+23A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-15715568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715568
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715568
    reference: chr 16
allele count: 1
allele frequency: 8.427581789681268e-6
allele num: 118658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.350T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3179A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+22T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+22T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19580
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

16-15715570-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715570
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715570
    reference: chr 16
allele count: 1
allele frequency: 8.418075291265404e-6
allele num: 118792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3177A>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+20T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.348T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+20T>A
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

16-15715573-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715573
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715573
    reference: chr 16
allele count: 9
allele frequency: 7.558959887119532e-5
allele num: 119064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.345C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3174G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+17C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33218
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-15715574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715574
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715574
    reference: chr 16
allele count: 1
allele frequency: 8.393768466290626e-6
allele num: 119136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2639+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.344G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3173C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2639+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2630+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.396+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2144+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2639+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1646+16G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2630+16G>T
  variant of: http://identifiers.org/hgnc/29562
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19873
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6627
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7849
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

16-15715601-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715601
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715601
    reference: chr 16
allele count: 3
allele frequency: 2.490287877278613e-5
allele num: 120468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.317C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.385C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1635C>G
  hgvsp: ENST00000344181.3:c.1635C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2619C>G
  hgvsp: ENST00000548025.1:c.2619C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2133C>G
  hgvsp: ENST00000540441.2:c.2133C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2619C>G
  hgvsp: ENST00000602337.1:c.2619C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3146G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2628C>G
  hgvsp: ENST00000552553.1:c.2628C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2628C>G
  hgvsp: ENST00000396368.3:c.2628C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2628C>G
  hgvsp: ENST00000551742.1:c.2628C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu876Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-15715613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715613
    reference: chr 16
allele count: 3
allele frequency: 2.487438435898711e-5
allele num: 120606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.373C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2616C>T
  hgvsp: ENST00000551742.1:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2121C>T
  hgvsp: ENST00000540441.2:c.2121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2616C>T
  hgvsp: ENST00000552553.1:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2607C>T
  hgvsp: ENST00000602337.1:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2607C>T
  hgvsp: ENST00000548025.1:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2616C>T
  hgvsp: ENST00000396368.3:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3134G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1623C>T
  hgvsp: ENST00000344181.3:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.305C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2715
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34658
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala872Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-15715622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715622
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715622
    reference: chr 16
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2598C>T
  hgvsp: ENST00000602337.1:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.364C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2607C>T
  hgvsp: ENST00000396368.3:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3125G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2607C>T
  hgvsp: ENST00000551742.1:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.296C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1614C>T
  hgvsp: ENST00000344181.3:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2112C>T
  hgvsp: ENST00000540441.2:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2607C>T
  hgvsp: ENST00000552553.1:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2598C>T
  hgvsp: ENST00000548025.1:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr869Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15715624-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715624
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715624
    reference: chr 16
allele count: 82
allele frequency: 6.794941911533171e-4
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2110A>T
  hgvsp: ENSP00000439819.2:p.Thr704Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1612A>T
  hgvsp: ENSP00000341939.3:p.Thr538Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2596A>T
  hgvsp: ENSP00000473601.1:p.Thr866Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2605A>T
  hgvsp: ENSP00000449329.1:p.Thr869Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.294A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2605A>T
  hgvsp: ENSP00000450309.1:p.Thr869Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3123T>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2605A>T
  hgvsp: ENSP00000379654.3:p.Thr869Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2596A>T
  hgvsp: ENSP00000449376.1:p.Thr866Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.362A>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20662
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9348
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 20899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8041
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr869Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

16-15715631-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715631
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715631
    reference: chr 16
allele count: 3
allele frequency: 2.48541887592789e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2103A>C
  hgvsp: ENST00000540441.2:c.2103A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2598A>C
  hgvsp: ENST00000551742.1:c.2598A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1605A>C
  hgvsp: ENST00000344181.3:c.1605A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2589A>C
  hgvsp: ENST00000602337.1:c.2589A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2589A>C
  hgvsp: ENST00000548025.1:c.2589A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.355A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.287A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3116T>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2598A>C
  hgvsp: ENST00000396368.3:c.2598A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2598A>C
  hgvsp: ENST00000552553.1:c.2598A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6628
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser866Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-15715636-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715636
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715636
    reference: chr 16
allele count: 989
allele frequency: 8.192647326827814e-3
allele num: 120718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.282G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2584G>C
  hgvsp: ENSP00000449376.1:p.Val862Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2593G>C
  hgvsp: ENSP00000450309.1:p.Val865Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1600G>C
  hgvsp: ENSP00000341939.3:p.Val534Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2593G>C
  hgvsp: ENSP00000379654.3:p.Val865Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2098G>C
  hgvsp: ENSP00000439819.2:p.Val700Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2593G>C
  hgvsp: ENSP00000449329.1:p.Val865Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.350G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2584G>C
  hgvsp: ENSP00000473601.1:p.Val862Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3111C>G
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 20282
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 20750
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val865Leu
num of homozygotes: 13
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

16-15715639-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715639
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715639
    reference: chr 16
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2590C>G
  hgvsp: ENSP00000379654.3:p.Leu864Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3108G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2590C>G
  hgvsp: ENSP00000450309.1:p.Leu864Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2590C>G
  hgvsp: ENSP00000449329.1:p.Leu864Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1597C>G
  hgvsp: ENSP00000341939.3:p.Leu533Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2581C>G
  hgvsp: ENSP00000449376.1:p.Leu861Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.347C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2581C>G
  hgvsp: ENSP00000473601.1:p.Leu861Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.279C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2095C>G
  hgvsp: ENSP00000439819.2:p.Leu699Val
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu864Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15715662-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715662
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715662
    reference: chr 16
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1574A>G
  hgvsp: ENSP00000341939.3:p.Tyr525Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2567A>G
  hgvsp: ENSP00000450309.1:p.Tyr856Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2558A>G
  hgvsp: ENSP00000473601.1:p.Tyr853Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2567A>G
  hgvsp: ENSP00000449329.1:p.Tyr856Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.256A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2567A>G
  hgvsp: ENSP00000379654.3:p.Tyr856Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2558A>G
  hgvsp: ENSP00000449376.1:p.Tyr853Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2072A>G
  hgvsp: ENSP00000439819.2:p.Tyr691Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3085T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.324A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr856Cys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

16-15715670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715670
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715670
    reference: chr 16
allele count: 3
allele frequency: 2.484430899695243e-5
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2550C>T
  hgvsp: ENST00000548025.1:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1566C>T
  hgvsp: ENST00000344181.3:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2559C>T
  hgvsp: ENST00000552553.1:c.2559C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.316C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2559C>T
  hgvsp: ENST00000551742.1:c.2559C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2559C>T
  hgvsp: ENST00000396368.3:c.2559C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2064C>T
  hgvsp: ENST00000540441.2:c.2064C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3077G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2550C>T
  hgvsp: ENST00000602337.1:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.248C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8061
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu853Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

16-15715677-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715677
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715677
    reference: chr 16
allele count: 2
allele frequency: 1.656232402530723e-5
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.309A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1559A>G
  hgvsp: ENSP00000341939.3:p.Asn520Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2057A>G
  hgvsp: ENSP00000439819.2:p.Asn686Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2552A>G
  hgvsp: ENSP00000449329.1:p.Asn851Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2552A>G
  hgvsp: ENSP00000379654.3:p.Asn851Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.241A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2543A>G
  hgvsp: ENSP00000473601.1:p.Asn848Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2552A>G
  hgvsp: ENSP00000450309.1:p.Asn851Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3070T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2543A>G
  hgvsp: ENSP00000449376.1:p.Asn848Ser
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn851Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15715682-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715682
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715682
    reference: chr 16
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3065T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2547A>G
  hgvsp: ENST00000396368.3:c.2547A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1554A>G
  hgvsp: ENST00000344181.3:c.1554A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2052A>G
  hgvsp: ENST00000540441.2:c.2052A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2547A>G
  hgvsp: ENST00000551742.1:c.2547A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2538A>G
  hgvsp: ENST00000548025.1:c.2538A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2538A>G
  hgvsp: ENST00000602337.1:c.2538A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2547A>G
  hgvsp: ENST00000552553.1:c.2547A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.236A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.304A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala849Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-15715687-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715687
    reference: chr 16
allele count: 3
allele frequency: 2.484430899695243e-5
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2542G>T
  hgvsp: ENSP00000379654.3:p.Gly848Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2047G>T
  hgvsp: ENSP00000439819.2:p.Gly683Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1549G>T
  hgvsp: ENSP00000341939.3:p.Gly517Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2533G>T
  hgvsp: ENSP00000473601.1:p.Gly845Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2542G>T
  hgvsp: ENSP00000450309.1:p.Gly848Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3060C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2533G>T
  hgvsp: ENSP00000449376.1:p.Gly845Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2542G>T
  hgvsp: ENSP00000449329.1:p.Gly848Cys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.231G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.299G>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly848Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-15715687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715687
    reference: chr 16
allele count: 10
allele frequency: 8.281436332317477e-5
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.231G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2542G>A
  hgvsp: ENSP00000379654.3:p.Gly848Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3060C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.299G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1549G>A
  hgvsp: ENSP00000341939.3:p.Gly517Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2533G>A
  hgvsp: ENSP00000473601.1:p.Gly845Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2047G>A
  hgvsp: ENSP00000439819.2:p.Gly683Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2542G>A
  hgvsp: ENSP00000450309.1:p.Gly848Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2542G>A
  hgvsp: ENSP00000449329.1:p.Gly848Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2533G>A
  hgvsp: ENSP00000449376.1:p.Gly845Ser
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly848Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-15715688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715688
    reference: chr 16
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2541C>T
  hgvsp: ENST00000552553.1:c.2541C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.230C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2541C>T
  hgvsp: ENST00000551742.1:c.2541C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1548C>T
  hgvsp: ENST00000344181.3:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2532C>T
  hgvsp: ENST00000548025.1:c.2532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2541C>T
  hgvsp: ENST00000396368.3:c.2541C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2532C>T
  hgvsp: ENST00000602337.1:c.2532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3059G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.298C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2046C>T
  hgvsp: ENST00000540441.2:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile847Ile
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/16-15715691-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715691
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715691
    reference: chr 16
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2538G>T
  hgvsp: ENST00000396368.3:c.2538G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2529G>T
  hgvsp: ENST00000602337.1:c.2529G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.295G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2538G>T
  hgvsp: ENST00000552553.1:c.2538G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2043G>T
  hgvsp: ENST00000540441.2:c.2043G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2529G>T
  hgvsp: ENST00000548025.1:c.2529G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1545G>T
  hgvsp: ENST00000344181.3:c.1545G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3056C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2538G>T
  hgvsp: ENST00000551742.1:c.2538G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.227G>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala846Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-15715699-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715699
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715699
    reference: chr 16
allele count: 7
allele frequency: 5.797005432622234e-5
allele num: 120752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2530C>G
  hgvsp: ENSP00000449329.1:p.Gln844Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1537C>G
  hgvsp: ENSP00000341939.3:p.Gln513Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3048G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.287C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2530C>G
  hgvsp: ENSP00000450309.1:p.Gln844Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2530C>G
  hgvsp: ENSP00000379654.3:p.Gln844Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2521C>G
  hgvsp: ENSP00000449376.1:p.Gln841Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.2035C>G
  hgvsp: ENSP00000439819.2:p.Gln679Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2521C>G
  hgvsp: ENSP00000473601.1:p.Gln841Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.219C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln844Glu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-15715743-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715743
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715743
    reference: chr 16
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.175A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2486A>G
  hgvsp: ENSP00000450309.1:p.His829Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1991A>G
  hgvsp: ENSP00000439819.2:p.His664Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2477A>G
  hgvsp: ENSP00000473601.1:p.His826Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2477A>G
  hgvsp: ENSP00000449376.1:p.His826Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1493A>G
  hgvsp: ENSP00000341939.3:p.His498Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.243A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2486A>G
  hgvsp: ENSP00000379654.3:p.His829Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2486A>G
  hgvsp: ENSP00000449329.1:p.His829Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3004T>C
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His829Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

16-15715744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715744
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715744
    reference: chr 16
allele count: 3
allele frequency: 2.485665992774998e-5
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2476C>T
  hgvsp: ENSP00000473601.1:p.His826Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1990C>T
  hgvsp: ENSP00000439819.2:p.His664Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2476C>T
  hgvsp: ENSP00000449376.1:p.His826Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1492C>T
  hgvsp: ENSP00000341939.3:p.His498Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.242C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3003G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2485C>T
  hgvsp: ENSP00000379654.3:p.His829Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2485C>T
  hgvsp: ENSP00000449329.1:p.His829Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2485C>T
  hgvsp: ENSP00000450309.1:p.His829Tyr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.174C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His829Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

16-15715747-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715747
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715747
    reference: chr 16
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2473C>T
  hgvsp: ENSP00000449376.1:p.Pro825Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.171C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2482C>T
  hgvsp: ENSP00000449329.1:p.Pro828Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2482C>T
  hgvsp: ENSP00000379654.3:p.Pro828Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.239C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2482C>T
  hgvsp: ENSP00000450309.1:p.Pro828Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2473C>T
  hgvsp: ENSP00000473601.1:p.Pro825Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-3000G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1489C>T
  hgvsp: ENSP00000341939.3:p.Pro497Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1987C>T
  hgvsp: ENSP00000439819.2:p.Pro663Ser
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6520
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro828Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

16-15715748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715748
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715748
    reference: chr 16
allele count: 4
allele frequency: 3.314770617873243e-5
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2472C>T
  hgvsp: ENST00000602337.1:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2481C>T
  hgvsp: ENST00000552553.1:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1488C>T
  hgvsp: ENST00000344181.3:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2472C>T
  hgvsp: ENST00000548025.1:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2481C>T
  hgvsp: ENST00000396368.3:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2999G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2481C>T
  hgvsp: ENST00000551742.1:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.170C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1986C>T
  hgvsp: ENST00000540441.2:c.1986C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.238C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6523
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Ser827Ser
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: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-15715753-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715753
    reference: chr 16
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2994G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1483C>T
  hgvsp: ENSP00000341939.3:p.Leu495Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2476C>T
  hgvsp: ENSP00000450309.1:p.Leu826Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2476C>T
  hgvsp: ENSP00000449329.1:p.Leu826Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1981C>T
  hgvsp: ENSP00000439819.2:p.Leu661Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.165C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2467C>T
  hgvsp: ENSP00000449376.1:p.Leu823Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.233C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2476C>T
  hgvsp: ENSP00000379654.3:p.Leu826Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2467C>T
  hgvsp: ENSP00000473601.1:p.Leu823Phe
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu826Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-15715757-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715757
    reference: chr 16
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.161T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2463T>C
  hgvsp: ENST00000548025.1:c.2463T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2990A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2472T>C
  hgvsp: ENST00000396368.3:c.2472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1479T>C
  hgvsp: ENST00000344181.3:c.1479T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.229T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1977T>C
  hgvsp: ENST00000540441.2:c.1977T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2463T>C
  hgvsp: ENST00000602337.1:c.2463T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2472T>C
  hgvsp: ENST00000552553.1:c.2472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2472T>C
  hgvsp: ENST00000551742.1:c.2472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val824Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

16-15715785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715785
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715785
    reference: chr 16
allele count: 3
allele frequency: 2.505177366557552e-5
allele num: 119752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2962G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-17C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-17C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6511
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

16-15715785-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715785
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715785
    reference: chr 16
allele count: 1
allele frequency: 8.350591221858508e-6
allele num: 119752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2962G>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-17C>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-17C>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-15715792-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715792
    reference: chr 16
allele count: 3
allele frequency: 2.514163118903154e-5
allele num: 119324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2955A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-24T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-24T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

16-15715795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715795
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715795
    reference: chr 16
allele count: 3
allele frequency: 2.520203632453502e-5
allele num: 119038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2952C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-27G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-27G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

16-15715796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715796
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715796
    reference: chr 16
allele count: 203
allele frequency: 1.705337791293536e-3
allele num: 119038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2951G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-28C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-28C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15150
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 18524
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

16-15715801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715801
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715801
    reference: chr 16
allele count: 1
allele frequency: 8.416233230655287e-6
allele num: 118818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2946G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-33C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-33C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

16-15715802-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715802
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715802
    reference: chr 16
allele count: 1
allele frequency: 8.418075291265404e-6
allele num: 118792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2945T>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-34A>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-34A>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3115
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-15715804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715804
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715804
    reference: chr 16
allele count: 8379
allele frequency: 7.081643002028398e-2
allele num: 118320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2943C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-36G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-36G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 452
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 1020
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 1.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 12610
  bin: 2.25e1
  variant carriers: 985
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 1.75e1
  variant carriers: 517
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.5e0
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 16025
  bin: 2.75e1
  variant carriers: 1286
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 3.25e1
  variant carriers: 1323
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 9.75e1
  variant carriers: 294
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 756
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 4.75e1
  variant carriers: 15
num of homozygotes: 488
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

16-15715805-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715805
    reference: chr 16
allele count: 2
allele frequency: 1.692505585268431e-5
allele num: 118168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2942G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-37C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17197
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-15715806-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715806
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715806
    reference: chr 16
allele count: 10
allele frequency: 8.451370812345763e-5
allele num: 118324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2941C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-38G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-38G>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6427
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

16-15715815-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715815
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715815
    reference: chr 16
allele count: 1
allele frequency: 8.551978927923921e-6
allele num: 116932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2932C>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-47G>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-47G>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5061
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-15715815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715815
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715815
    reference: chr 16
allele count: 1
allele frequency: 8.551978927923921e-6
allele num: 116932
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2932C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-47G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-47G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4860
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5061
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-15715818-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715818
    reference: chr 16
allele count: 1
allele frequency: 8.591655783902673e-6
allele num: 116392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2929T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-50A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-50A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3230
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-15715819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15715819
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15715819
    reference: chr 16
allele count: 1
allele frequency: 8.64528399757932e-6
allele num: 115670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2452-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.218-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2452-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2461-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-2928C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2461-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1966-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.150-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1468-51G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2461-51G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8010
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

16-15716757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716757
    reference: chr 16
allele count: 1
allele frequency: 8.9391068044481e-6
allele num: 111868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1990T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+34A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+34A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-15716758-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716758
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716758
    reference: chr 16
allele count: 1
allele frequency: 8.921561630147741e-6
allele num: 112088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1989A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+33T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+33T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5730
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-15716766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716766
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716766
    reference: chr 16
allele count: 15
allele frequency: 1.330211769713738e-4
allele num: 112764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+25C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1981G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+25C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23658
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19090
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 9.75e1
  variant carriers: 13
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15716770-GCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716770
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716768
    reference: chr 16
allele count: 1
allele frequency: 8.82861885086697e-6
allele num: 113268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+19_1965+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1974_*13-1973delCA
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+19_2451+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+19_2460+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+19_2460+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+19_2451+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+19_149+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+19_217+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+19_1467+20delTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+19_2460+20delTG
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19453
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: GCA
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

16-15716777-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716777
    reference: chr 16
allele count: 2
allele frequency: 1.747304782373189e-5
allele num: 114462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1970A>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+14T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+14T>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-15716778-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716778
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716778
    reference: chr 16
allele count: 1
allele frequency: 8.72493761669604e-6
allele num: 114614
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2460+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.149+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2460+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2460+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1969G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2451+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1467+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1965+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2451+13C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.217+13C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24752
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-15716800-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716800
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716800
    reference: chr 16
allele count: 1
allele frequency: 8.45337120443633e-6
allele num: 118296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2451G>A
  hgvsp: ENST00000552553.1:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.140G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2442G>A
  hgvsp: ENST00000548025.1:c.2442G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2442G>A
  hgvsp: ENST00000602337.1:c.2442G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1458G>A
  hgvsp: ENST00000344181.3:c.1458G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.208G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1956G>A
  hgvsp: ENST00000540441.2:c.1956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2451G>A
  hgvsp: ENST00000396368.3:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1947C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2451G>A
  hgvsp: ENST00000551742.1:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20824
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6195
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg817Arg
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-15716803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716803
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716803
    reference: chr 16
allele count: 1
allele frequency: 8.417933565668301e-6
allele num: 118794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.137C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2448C>T
  hgvsp: ENST00000396368.3:c.2448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1944G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2448C>T
  hgvsp: ENST00000551742.1:c.2448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2439C>T
  hgvsp: ENST00000548025.1:c.2439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2439C>T
  hgvsp: ENST00000602337.1:c.2439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1455C>T
  hgvsp: ENST00000344181.3:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2448C>T
  hgvsp: ENST00000552553.1:c.2448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.205C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1953C>T
  hgvsp: ENST00000540441.2:c.1953C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala816Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-15716805-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716805
    reference: chr 16
allele count: 10
allele frequency: 8.405904307185368e-5
allele num: 118964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1453G>T
  hgvsp: ENSP00000341939.3:p.Ala485Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1942C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1951G>T
  hgvsp: ENSP00000439819.2:p.Ala651Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.203G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2437G>T
  hgvsp: ENSP00000473601.1:p.Ala813Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2446G>T
  hgvsp: ENSP00000379654.3:p.Ala816Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2437G>T
  hgvsp: ENSP00000449376.1:p.Ala813Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2446G>T
  hgvsp: ENSP00000449329.1:p.Ala816Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.135G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2446G>T
  hgvsp: ENSP00000450309.1:p.Ala816Ser
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26803
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala816Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-15716812-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716812
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716812
    reference: chr 16
allele count: 1
allele frequency: 8.367640660039494e-6
allele num: 119508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1935T>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1446A>T
  hgvsp: ENSP00000341939.3:p.Glu482Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.196A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2430A>T
  hgvsp: ENSP00000473601.1:p.Glu810Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2439A>T
  hgvsp: ENSP00000450309.1:p.Glu813Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2439A>T
  hgvsp: ENSP00000379654.3:p.Glu813Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2430A>T
  hgvsp: ENSP00000449376.1:p.Glu810Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.128A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1944A>T
  hgvsp: ENSP00000439819.2:p.Glu648Asp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2439A>T
  hgvsp: ENSP00000449329.1:p.Glu813Asp
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu813Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

16-15716814-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716814
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716814
    reference: chr 16
allele count: 9
allele frequency: 7.522944982195697e-5
allele num: 119634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1942G>A
  hgvsp: ENSP00000439819.2:p.Glu648Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2437G>A
  hgvsp: ENSP00000450309.1:p.Glu813Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2428G>A
  hgvsp: ENSP00000473601.1:p.Glu810Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2428G>A
  hgvsp: ENSP00000449376.1:p.Glu810Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2437G>A
  hgvsp: ENSP00000449329.1:p.Glu813Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2437G>A
  hgvsp: ENSP00000379654.3:p.Glu813Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1444G>A
  hgvsp: ENSP00000341939.3:p.Glu482Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.126G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.194G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1933C>T
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48508
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu813Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-15716818-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716818
    reference: chr 16
allele count: 1
allele frequency: 8.344598541364175e-6
allele num: 119838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2424G>T
  hgvsp: ENST00000548025.1:c.2424G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2433G>T
  hgvsp: ENST00000551742.1:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2433G>T
  hgvsp: ENST00000396368.3:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1440G>T
  hgvsp: ENST00000344181.3:c.1440G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2424G>T
  hgvsp: ENST00000602337.1:c.2424G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.190G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.122G>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2433G>T
  hgvsp: ENST00000552553.1:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1929C>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1938G>T
  hgvsp: ENST00000540441.2:c.1938G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu811Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

16-15716818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15716818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15716818
    reference: chr 16
allele count: 14
allele frequency: 1.168243795790985e-4
allele num: 119838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.2424G>A
  hgvsp: ENST00000602337.1:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.1938G>A
  hgvsp: ENST00000540441.2:c.1938G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.2433G>A
  hgvsp: ENST00000551742.1:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.2433G>A
  hgvsp: ENST00000396368.3:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.2433G>A
  hgvsp: ENST00000552553.1:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.2424G>A
  hgvsp: ENST00000548025.1:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.1440G>A
  hgvsp: ENST00000344181.3:c.1440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551678
  gene symbol: KIAA0430
  hgvsc: ENST00000551678.1:n.122G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*13-1929C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000546864
  gene symbol: KIAA0430
  hgvsc: ENST00000546864.2:n.190G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu811Leu
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46832
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.621195e6

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

QD
type: SiteQuality
SIO_000300: 9.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5387
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01559060341968e-5
allele num: 66322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.35e-1

QD
type: SiteQuality
SIO_000300: 1.017e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 1.616673e6

FS
type: SiteQuality
SIO_000300: 7.784e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45939
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
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: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.219363492257042e-4
allele num: 16402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.131e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
type: SiteQuality
SIO_000300: 1.613488e6

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-1

GenotypeQuality
all individuals: 1588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44377
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65786
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027960526315789e-4
allele num: 9728
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.291e0

FS
type: SiteQuality
SIO_000300: 2.791e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

QD
type: SiteQuality
SIO_000300: 1.701e1

DP
type: SiteQuality
SIO_000300: 1.598091e6

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 6.084e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2786
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532332209623046e-5
allele num: 65260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: -1.208e0

FS
type: SiteQuality
SIO_000300: 2.949e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.414e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

DP
type: SiteQuality
SIO_000300: 1.572743e6

GenotypeQuality
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bin: 7.25e1
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533648242439114e-5
allele num: 65204
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.619e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.567812e6

MQRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.295e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.111484489249821e-5
allele num: 64278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16006
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

QD
type: SiteQuality
SIO_000300: 1.065e1

FS
type: SiteQuality
SIO_000300: 2.253e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.005e0

DP
type: SiteQuality
SIO_000300: 1.497687e6

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15990
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.693965517241379e-4
allele num: 11136
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.192179303767287e-4
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64194
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.484307e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.381e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.23e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.256281407035176e-4
allele num: 15920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63822
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.437955e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

FS
type: SiteQuality
SIO_000300: 4.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 9.08e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574406448768814e-5
allele num: 63516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.354e0

DP
type: SiteQuality
SIO_000300: 1.398549e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.83e0

VQSLOD
type: SiteQuality
SIO_000300: -9.349e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

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

Latino
type: Population
allele count: 2
allele frequency: 1.847063169560399e-4
allele num: 10828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596169193934557e-5
allele num: 62650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.299505e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.473e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7992
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.631321370309951e-5
allele num: 61300
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0

DP
type: SiteQuality
SIO_000300: 1.252939e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.204e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 918
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.655848456749238e-5
allele num: 60392
num of homozygotes: 0

Other
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

Latino
type: Population
allele count: 4
allele frequency: 3.858024691358024e-4
allele num: 10368
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.076658053402239e-4
allele num: 9288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15366
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.506e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

DP
type: SiteQuality
SIO_000300: 1.235918e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

GenotypeQuality
all individuals: 1653
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.050454517723141e-5
allele num: 65564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.483e1

FS
type: SiteQuality
SIO_000300: 6.475e0

DP
type: SiteQuality
SIO_000300: 1.69474e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524111443028714e-5
allele num: 65612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.835269993164729e-5
allele num: 14630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.66e-1

DP
type: SiteQuality
SIO_000300: 1.704156e6

QD
type: SiteQuality
SIO_000300: 1.534e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

GenotypeQuality
all individuals: 2672
bin: 7.25e1
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
all individuals: 99
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GenotypeQuality
all individuals: 6631
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515656734062869e-5
allele num: 65978
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: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.89e-2

QD
type: SiteQuality
SIO_000300: 1.13e1

FS
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.767735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

GenotypeQuality
all individuals: 7795
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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
all individuals: 2678
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GenotypeQuality
all individuals: 2256
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514738404677512e-5
allele num: 66018
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

QD
type: SiteQuality
SIO_000300: 1.517e1

FS
type: SiteQuality
SIO_000300: 2.169e0

DP
type: SiteQuality
SIO_000300: 1.769749e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
all individuals: 1340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
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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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variant carriers: 0

GenotypeQuality
all individuals: 257
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variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514187941007238e-5
allele num: 66042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15366
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.937e1

QD
type: SiteQuality
SIO_000300: 1.113e1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

FS
type: SiteQuality
SIO_000300: 1.202e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

DP
type: SiteQuality
SIO_000300: 1.773045e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3313
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.023122570083896e-4
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.058521094813247e-4
allele num: 66130
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15522
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

FS
type: SiteQuality
SIO_000300: 1.342e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.957e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

DP
type: SiteQuality
SIO_000300: 1.779333e6

QD
type: SiteQuality
SIO_000300: 1.248e1

GenotypeQuality
all individuals: 96
bin: 4.75e1
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
all individuals: 2271
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66160
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.769e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.077e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.019e1

FS
type: SiteQuality
SIO_000300: 3.849e0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.781039e6

GenotypeQuality
all individuals: 3344
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 54
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 37
bin: 4.25e1
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GenotypeQuality
all individuals: 6632
bin: 9.75e1
variant carriers: 3

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

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.183e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 3.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

DP
type: SiteQuality
SIO_000300: 1.802958e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6631
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8026
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.820388349514563e-4
allele num: 16480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 2.621e0

MQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

DP
type: SiteQuality
SIO_000300: 1.805957e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

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

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2704
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2281
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6630
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8050
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 1.807709e6

VQSLOD
type: SiteQuality
SIO_000300: -6.868e-1

FS
type: SiteQuality
SIO_000300: 9.87e-1

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 34828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 9.75e1
variant carriers: 82

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

GenotypeQuality
all individuals: 2273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

African
type: Population
allele count: 76
allele frequency: 7.761437908496732e-3
allele num: 9792
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.323763403666552e-4
allele num: 11564
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

FS
type: SiteQuality
SIO_000300: 1.807e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.367e1

DP
type: SiteQuality
SIO_000300: 1.810959e6

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34905
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497885993583016e-5
allele num: 66698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
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: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.808451e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

FS
type: SiteQuality
SIO_000300: 2.608e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 8.65e0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1292
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7399
bin: 9.75e1
variant carriers: 976

GenotypeQuality
all individuals: 7904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 64
allele frequency: 9.679370840895343e-3
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 419
allele frequency: 2.537855844942459e-2
allele num: 16510
num of homozygotes: 9

European (Non-Finnish)
type: Population
allele count: 281
allele frequency: 4.212640921084193e-3
allele num: 66704
num of homozygotes: 0

East Asian
type: Population
allele count: 176
allele frequency: 2.04034314862045e-2
allele num: 8626
num of homozygotes: 4

Other
type: Population
allele count: 7
allele frequency: 7.777777777777778e-3
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 2.33442849731973e-3
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 1.530612244897959e-3
allele num: 9800
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.39e-1

DP
type: SiteQuality
SIO_000300: 1.850146e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35134
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 7.75e1
variant carriers: 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: 900
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.788e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

FS
type: SiteQuality
SIO_000300: 3.644e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.809546e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.273e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8063
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6523
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 970
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35181
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 3331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2239
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.810171e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.52e-1

FS
type: SiteQuality
SIO_000300: 7.022e0

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

QD
type: SiteQuality
SIO_000300: 1.545e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeQuality
all individuals: 6524
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 35196
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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QD
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66730
num of homozygotes: 0

Latino
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allele num: 11570
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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DP
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66730
num of homozygotes: 0

African
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Latino
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allele num: 11570
num of homozygotes: 0

European (Finnish)
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South Asian
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allele num: 16512
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East Asian
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Other
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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BaseQRankSum
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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QD
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ClippingRankSum
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FS
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MQ
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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MQ
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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DP
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.927e1

DP
type: SiteQuality
SIO_000300: 1.809619e6

FS
type: SiteQuality
SIO_000300: 3.051e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.184e1

VQSLOD
type: SiteQuality
SIO_000300: 8.41e-1

GenotypeQuality
all individuals: 8053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6523
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817741153659719e-4
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 1.809586e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.908e1

FS
type: SiteQuality
SIO_000300: 7.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

GenotypeQuality
all individuals: 2232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

DP
type: SiteQuality
SIO_000300: 1.809266e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.346e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

GenotypeQuality
all individuals: 1320
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99970001499925e-5
allele num: 66670
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.809299e6

FS
type: SiteQuality
SIO_000300: 6.112e0

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.368e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 3321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2687
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6520
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 8036
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.229e1

FS
type: SiteQuality
SIO_000300: 5.806e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.883e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.957e0

VQSLOD
type: SiteQuality
SIO_000300: -1.131e0

DP
type: SiteQuality
SIO_000300: 1.808429e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.18e-1

GenotypeQuality
all individuals: 1317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6520
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2685
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.11e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 1.807797e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 2.189e0

VQSLOD
type: SiteQuality
SIO_000300: -1.517e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

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

GenotypeQuality
all individuals: 1380
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7698
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variant carriers: 0

GenotypeQuality
all individuals: 548
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508341126429153e-5
allele num: 66298
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16114
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.724e0

QD
type: SiteQuality
SIO_000300: 1.073e1

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.781166e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

FS
type: SiteQuality
SIO_000300: 3.206e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508341126429153e-5
allele num: 66298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
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: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16114
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.781166e6

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.206e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.724e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2542
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6508
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.539814170273297e-5
allele num: 66082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.93e0

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-2

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.747261e6

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

GenotypeQuality
all individuals: 590
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6507
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6940
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.033244358165494e-5
allele num: 65936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.271951831409934e-5
allele num: 15944
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.501e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

DP
type: SiteQuality
SIO_000300: 1.715275e6

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1285
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variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 9.75e1
variant carriers: 203

Other
type: Population
allele count: 3
allele frequency: 3.393665158371041e-3
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 113
allele frequency: 1.716803403220905e-2
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 87
allele frequency: 1.31950131950132e-3
allele num: 65934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.715932e6

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.05e0

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.323e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

GenotypeQuality
all individuals: 728
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
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GenotypeQuality
all individuals: 151
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GenotypeQuality
all individuals: 1288
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2421
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3307
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variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6491
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 450
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variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2169
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518741267237713e-5
allele num: 65844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

FS
type: SiteQuality
SIO_000300: 1.4981e1

VQSLOD
type: SiteQuality
SIO_000300: -1.62e0

DP
type: SiteQuality
SIO_000300: 1.686516e6

MQRankSum
type: SiteQuality
SIO_000300: 2.35e0

QD
type: SiteQuality
SIO_000300: 8.32e0

GenotypeQuality
all individuals: 1605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
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variant carriers: 0

GenotypeQuality
all individuals: 2163
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variant carriers: 0

GenotypeQuality
all individuals: 149
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GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 23498
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variant carriers: 0

GenotypeQuality
all individuals: 2859
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variant carriers: 0

GenotypeQuality
all individuals: 917
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variant carriers: 0

GenotypeQuality
all individuals: 6628
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 6490
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.312334301224592e-5
allele num: 15842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65848
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e0

DP
type: SiteQuality
SIO_000300: 1.682121e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

VQSLOD
type: SiteQuality
SIO_000300: -2.242e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.142e1

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 611
bin: 5.25e1
variant carriers: 17

GenotypeQuality
all individuals: 609
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 19963
bin: 6.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1649
bin: 8.25e1
variant carriers: 33

GenotypeQuality
all individuals: 725
bin: 8.75e1
variant carriers: 27

GenotypeQuality
all individuals: 2477
bin: 7.75e1
variant carriers: 33

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1965
bin: 7.25e1
variant carriers: 26

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3065
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3362
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2802
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1076
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 5392
bin: 6.75e1
variant carriers: 38

GenotypeQuality
all individuals: 12487
bin: 9.75e1
variant carriers: 7620

European (Non-Finnish)
type: Population
allele count: 4312
allele frequency: 6.573771991340671e-2
allele num: 65594
num of homozygotes: 155

African
type: Population
allele count: 2272
allele frequency: 2.336487042369395e-1
allele num: 9724
num of homozygotes: 279

European (Finnish)
type: Population
allele count: 284
allele frequency: 4.334554334554334e-2
allele num: 6552
num of homozygotes: 10

East Asian
type: Population
allele count: 267
allele frequency: 3.165757647616789e-2
allele num: 8434
num of homozygotes: 9

Other
type: Population
allele count: 66
allele frequency: 7.5e-2
allele num: 880
num of homozygotes: 4

South Asian
type: Population
allele count: 765
allele frequency: 4.858376730598247e-2
allele num: 15746
num of homozygotes: 24

Latino
type: Population
allele count: 413
allele frequency: 3.625987708516242e-2
allele num: 11390
num of homozygotes: 7

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.37e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: 6.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.642e1

DP
type: SiteQuality
SIO_000300: 1.713179e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeQuality
all individuals: 6102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1849
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 4.75e1
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GenotypeQuality
all individuals: 3131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.5e0
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GenotypeQuality
all individuals: 1161
bin: 9.25e1
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GenotypeQuality
all individuals: 575
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GenotypeQuality
all individuals: 832
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GenotypeQuality
all individuals: 1921
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 6086
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3450
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GenotypeQuality
all individuals: 3814
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.188495364868077e-4
allele num: 8414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5253668507276e-5
allele num: 65558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.509e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

QD
type: SiteQuality
SIO_000300: 1.13e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.649917e6

GenotypeQuality
all individuals: 23005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.75e1
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GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 1160
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GenotypeQuality
all individuals: 186
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GenotypeQuality
all individuals: 2208
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GenotypeQuality
all individuals: 2803
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variant carriers: 0

GenotypeQuality
all individuals: 3883
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GenotypeQuality
all individuals: 3594
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GenotypeQuality
all individuals: 6085
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variant carriers: 9

GenotypeQuality
all individuals: 3286
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 444
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GenotypeQuality
all individuals: 1916
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65636
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.18595825426945e-3
allele num: 8432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.641686e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.125e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.231e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 12711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6072
bin: 9.75e1
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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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9666
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.53907716932927e-5
allele num: 64974
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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SIO_000300: 5.954e1

BaseQRankSum
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SIO_000300: -2.751e0

DP
type: SiteQuality
SIO_000300: 1.574075e6

QD
type: SiteQuality
SIO_000300: 1.37e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53907716932927e-5
allele num: 64974
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.751e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.37e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-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: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544496957340994e-5
allele num: 64746
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11234
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

MQRankSum
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.169e0

QD
type: SiteQuality
SIO_000300: 1.062e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55265037418874e-5
allele num: 64406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.561934e6

QD
type: SiteQuality
SIO_000300: 9.94e0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.45e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 4.594e0

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
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DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9586
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

European (Finnish)
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: 1.55918672820257e-5
allele num: 64136
num of homozygotes: 0

South Asian
type: Population
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num of homozygotes: 0

Other
type: Population
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allele num: 820
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.44888e6

MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.842e0

VQSLOD
type: SiteQuality
SIO_000300: -1.792e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 2.095e1

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

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

European (Non-Finnish)
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allele count: 11
allele frequency: 1.708180632337412e-4
allele num: 64396
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.486142583231654e-4
allele num: 11474
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Other
type: Population
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allele frequency: 0.0e0
allele num: 832
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DP
type: SiteQuality
SIO_000300: 1.476799e6

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.764e0

BaseQRankSum
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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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 8.544087491455913e-5
allele num: 11704
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 frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64596
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Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.079007328037441e-5
allele num: 64956
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.708e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.506445e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e-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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bin: 7.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.007687379884689e-5
allele num: 12488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
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SIO_000300: 2.05e-1

ClippingRankSum
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SIO_000300: -5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.317e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.552e1

DP
type: SiteQuality
SIO_000300: 1.508516e6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65948
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.690753378830456e-5
allele num: 14946
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.217e0

DP
type: SiteQuality
SIO_000300: 1.553246e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.658e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.966e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.199e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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: 0
allele frequency: 0.0e0
allele num: 15290
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513179796023364e-5
allele num: 66086
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: -1.8e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

QD
type: SiteQuality
SIO_000300: 1.571e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.257e0

FS
type: SiteQuality
SIO_000300: 1.065e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.55835e6

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.656509695290858e-4
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15382
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.561383e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

FS
type: SiteQuality
SIO_000300: 5.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.91e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.378e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

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

African
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

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.68e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.89e-1

BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.452e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 5.944e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.055043106046904e-4
allele num: 66348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9784
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VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.569417e6

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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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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Other
type: Population
allele count: 0
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African
type: Population
allele count: 0
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Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.09e0

MQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0