17-73493828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493828
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493828
    reference: chr 17
allele count: 1
allele frequency: 8.528930131004366e-6
allele num: 117248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.225-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3408-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3438-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.167-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1095-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4177-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4013-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2361-34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.34-34G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3582
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

17-73493834-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493834
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493834
    reference: chr 17
allele count: 1
allele frequency: 8.493723138600575e-6
allele num: 117734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.34-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2361-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3408-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4177-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1095-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3438-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.225-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.167-28A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4013-28A>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7315
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

17-73493837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493837
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493837
    reference: chr 17
allele count: 1
allele frequency: 8.478887569950822e-6
allele num: 117940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4013-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.225-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.34-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3408-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3438-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4177-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1095-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.167-25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2361-25C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

17-73493838-CTCTACCTGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493838
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493829
    reference: chr 17
allele count: 1
allele frequency: 8.468978133098461e-6
allele num: 118078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7377
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: CTCTACCTGA
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-73493840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493840
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493840
    reference: chr 17
allele count: 3
allele frequency: 2.537083706848435e-5
allele num: 118246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4013-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2361-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.225-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4177-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.34-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3438-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.167-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3408-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1095-22C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24780
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

17-73493855-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493855
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493855
    reference: chr 17
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1095-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.34-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4177-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2361-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.225-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.167-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3408-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3438-7T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4013-7T>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6345
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.75e1
  variant carriers: 0
hgvs: c.3408-7T>C
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

17-73493867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493867
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493867
    reference: chr 17
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3413C>T
  hgvsp: ENSP00000313885.7:p.Ser1138Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.230C>T
  hgvsp: ENSP00000464437.1:p.Ser77Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2366C>T
  hgvsp: ENSP00000463929.1:p.Ser789Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4018C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1100C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4182C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3443C>T
  hgvsp: ENSP00000364397.5:p.Ser1148Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.172C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.39C>T
  hgvsp: ENSP00000463046.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4037
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6365
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1138Phe
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

17-73493871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493871
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493871
    reference: chr 17
allele count: 22
allele frequency: 1.82769793137825e-4
allele num: 120370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.43G>A
  hgvsp: ENST00000584694.1:c.43G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.234G>A
  hgvsp: ENST00000577247.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3447G>A
  hgvsp: ENST00000375248.5:c.3447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4186G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3417G>A
  hgvsp: ENST00000314256.7:c.3417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2370G>A
  hgvsp: ENST00000579208.1:c.2370G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1104G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4022G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.176G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2674
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7861
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu1139Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

17-73493874-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493874
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493874
    reference: chr 17
allele count: 17811
allele frequency: 1.47644942553509e-1
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.179G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3450G>C
  hgvsp: ENST00000375248.5:c.3450G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2373G>C
  hgvsp: ENST00000579208.1:c.2373G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.237G>C
  hgvsp: ENST00000577247.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.46G>C
  hgvsp: ENST00000584694.1:c.46G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3420G>C
  hgvsp: ENST00000314256.7:c.3420G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1107G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4025G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4189G>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 1466
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 3.25e1
  variant carriers: 1057
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 748
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 1734
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 1459
genotype depth: GenotypeDepth
  all individuals: 19732
  bin: 2.25e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 1592
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.25e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.75e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 2.75e1
  variant carriers: 706
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 969
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 1276
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 8.25e1
  variant carriers: 428
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.75e1
  variant carriers: 337
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 6.25e1
  variant carriers: 1171
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.75e1
  variant carriers: 1694
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 19610
  bin: 9.75e1
  variant carriers: 15499
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 8.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 62
hgvs: p.Leu1140Leu
num of homozygotes: 1880
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

17-73493874-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493874
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493874
    reference: chr 17
allele count: 10
allele frequency: 8.28953694646617e-5
allele num: 120634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1107G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3450G>T
  hgvsp: ENST00000375248.5:c.3450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4025G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4189G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.237G>T
  hgvsp: ENST00000577247.1:c.237G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3420G>T
  hgvsp: ENST00000314256.7:c.3420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.179G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.46G>T
  hgvsp: ENST00000584694.1:c.46G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2373G>T
  hgvsp: ENST00000579208.1:c.2373G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu1140Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

17-73493875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493875
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493875
    reference: chr 17
allele count: 3
allele frequency: 2.485460058656858e-5
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.180G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2374G>A
  hgvsp: ENSP00000463929.1:p.Gly792Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3451G>A
  hgvsp: ENSP00000364397.5:p.Gly1151Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1108G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.47G>A
  hgvsp: ENSP00000463046.1:p.Gly17Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4190G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3421G>A
  hgvsp: ENSP00000313885.7:p.Gly1141Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4026G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.238G>A
  hgvsp: ENSP00000464437.1:p.Gly80Arg
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6107
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly1141Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

17-73493880-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493880
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493881
    reference: chr 17
allele count: 15
allele frequency: 1.244008027998474e-4
allele num: 120578
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.59dupC
  hgvsp: ENSP00000463046.1:p.His21ProfsTer2
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4202dupC
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2386dupC
  hgvsp: ENSP00000463929.1:p.His796ProfsTer2
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3433dupC
  hgvsp: ENSP00000313885.7:p.His1145ProfsTer2
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.192dupC
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1120dupC
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4038dupC
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.250dupC
  hgvsp: ENSP00000464437.1:p.His84ProfsTer2
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3463dupC
  hgvsp: ENSP00000364397.5:p.His1155ProfsTer2
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 9581
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21038
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 3
hgvs: p.His1145ProfsTer2
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

17-73493882-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493882
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493882
    reference: chr 17
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3458C>G
  hgvsp: ENSP00000364397.5:p.Pro1153Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4197C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.54C>G
  hgvsp: ENSP00000463046.1:p.Pro19Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2381C>G
  hgvsp: ENSP00000463929.1:p.Pro794Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.187C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.245C>G
  hgvsp: ENSP00000464437.1:p.Pro82Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3428C>G
  hgvsp: ENSP00000313885.7:p.Pro1143Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4033C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1115C>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33031
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro1143Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-73493892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493892
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493892
    reference: chr 17
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1125C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.197C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4043C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3438C>T
  hgvsp: ENST00000314256.7:c.3438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.9C>T
  hgvsp: ENST00000577245.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4207C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2391C>T
  hgvsp: ENST00000579208.1:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3468C>T
  hgvsp: ENST00000375248.5:c.3468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.64C>T
  hgvsp: ENST00000584694.1:c.64C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.255C>T
  hgvsp: ENST00000577247.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8288
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser1146Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-73493894-CCAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493894
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493891
    reference: chr 17
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1131_1133delCAT
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2397_2399delCAT
  hgvsp: ENSP00000463929.1:p.Ile799del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.261_263delCAT
  hgvsp: ENSP00000464437.1:p.Ile87del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3474_3476delCAT
  hgvsp: ENSP00000364397.5:p.Ile1158del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.15_17delCAT
  hgvsp: ENSP00000462084.1:p.Ile5del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4213_4215delCAT
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3444_3446delCAT
  hgvsp: ENSP00000313885.7:p.Ile1148del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.70_72delCAT
  hgvsp: ENSP00000463046.1:p.Ile24del
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.203_205delCAT
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4049_4051delCAT
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33398
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile1148del
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: CCAT
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-73493904-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493904
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493904
    reference: chr 17
allele count: 1
allele frequency: 8.266102367411717e-6
allele num: 120976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3480T>C
  hgvsp: ENST00000375248.5:c.3480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.267T>C
  hgvsp: ENST00000577247.1:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.209T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3450T>C
  hgvsp: ENST00000314256.7:c.3450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4219T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.21T>C
  hgvsp: ENST00000577245.1:c.21T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.76T>C
  hgvsp: ENST00000584694.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1137T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2403T>C
  hgvsp: ENST00000579208.1:c.2403T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4055T>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1150Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

17-73493905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493905
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493905
    reference: chr 17
allele count: 2
allele frequency: 1.653083827880912e-5
allele num: 120986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4220A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2404A>G
  hgvsp: ENSP00000463929.1:p.Met802Val
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.22A>G
  hgvsp: ENSP00000462084.1:p.Met8Val
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3451A>G
  hgvsp: ENSP00000313885.7:p.Met1151Val
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.77A>G
  hgvsp: ENSP00000463046.1:p.Met27Val
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.210A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1138A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.268A>G
  hgvsp: ENSP00000464437.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4056A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3481A>G
  hgvsp: ENSP00000364397.5:p.Met1161Val
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met1151Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

17-73493905-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493905
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493905
    reference: chr 17
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1138A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.77A>T
  hgvsp: ENSP00000463046.1:p.Met27Leu
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4056A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4220A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.268A>T
  hgvsp: ENSP00000464437.1:p.Met90Leu
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2404A>T
  hgvsp: ENSP00000463929.1:p.Met802Leu
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3451A>T
  hgvsp: ENSP00000313885.7:p.Met1151Leu
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.210A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3481A>T
  hgvsp: ENSP00000364397.5:p.Met1161Leu
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.22A>T
  hgvsp: ENSP00000462084.1:p.Met8Leu
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met1151Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-73493912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493912
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493912
    reference: chr 17
allele count: 3
allele frequency: 2.480240748702007e-5
allele num: 120956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.275C>T
  hgvsp: ENSP00000464437.1:p.Thr92Met
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4227C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.217C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2411C>T
  hgvsp: ENSP00000463929.1:p.Thr804Met
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3488C>T
  hgvsp: ENSP00000364397.5:p.Thr1163Met
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3458C>T
  hgvsp: ENSP00000313885.7:p.Thr1153Met
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1145C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.84C>T
  hgvsp: ENSP00000463046.1:p.Thr29Met
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4063C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.29C>T
  hgvsp: ENSP00000462084.1:p.Thr10Met
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr1153Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

17-73493913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493913
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493913
    reference: chr 17
allele count: 7
allele frequency: 5.787132723755353e-5
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.30G>A
  hgvsp: ENST00000577245.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.85G>A
  hgvsp: ENST00000584694.1:c.85G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1146G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3459G>A
  hgvsp: ENST00000314256.7:c.3459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3489G>A
  hgvsp: ENST00000375248.5:c.3489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2412G>A
  hgvsp: ENST00000579208.1:c.2412G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.276G>A
  hgvsp: ENST00000577247.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4228G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4064G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.218G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr1153Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-73493913-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493913
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493913
    reference: chr 17
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3489G>T
  hgvsp: ENST00000375248.5:c.3489G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.85G>T
  hgvsp: ENST00000584694.1:c.85G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3459G>T
  hgvsp: ENST00000314256.7:c.3459G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.30G>T
  hgvsp: ENST00000577245.1:c.30G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4064G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2412G>T
  hgvsp: ENST00000579208.1:c.2412G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.218G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.276G>T
  hgvsp: ENST00000577247.1:c.276G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4228G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1146G>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr1153Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

17-73493916-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493916
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493917
    reference: chr 17
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.93dupA
  hgvsp: ENSP00000463046.1:p.Asn32LysfsTer12
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.284dupA
  hgvsp: ENSP00000464437.1:p.Asn95LysfsTer41
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4236dupA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1154dupA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.226dupA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3467dupA
  hgvsp: ENSP00000313885.7:p.Asn1156LysfsTer41
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2420dupA
  hgvsp: ENSP00000463929.1:p.Asn807LysfsTer41
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3497dupA
  hgvsp: ENSP00000364397.5:p.Asn1166LysfsTer41
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.38dupA
  hgvsp: ENSP00000462084.1:p.Asn13LysfsTer41
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4072dupA
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3895
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn1156LysfsTer41
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-73493931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493931
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493931
    reference: chr 17
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2430C>T
  hgvsp: ENST00000579208.1:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3507C>T
  hgvsp: ENST00000375248.5:c.3507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.236C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.294C>T
  hgvsp: ENST00000577247.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.103C>T
  hgvsp: ENST00000584694.1:c.103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3477C>T
  hgvsp: ENST00000314256.7:c.3477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.48C>T
  hgvsp: ENST00000577245.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1164C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4082C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4246C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3885
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser1159Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

17-73493937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493937
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493937
    reference: chr 17
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.54C>T
  hgvsp: ENST00000577245.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3513C>T
  hgvsp: ENST00000375248.5:c.3513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3483C>T
  hgvsp: ENST00000314256.7:c.3483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.242C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1170C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4252C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.109C>T
  hgvsp: ENST00000584694.1:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.300C>T
  hgvsp: ENST00000577247.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2436C>T
  hgvsp: ENST00000579208.1:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4088C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro1161Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-73493939-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493939
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493939
    reference: chr 17
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.56A>C
  hgvsp: ENSP00000462084.1:p.Lys19Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.244A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4254A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.302A>C
  hgvsp: ENSP00000464437.1:p.Lys101Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.111A>C
  hgvsp: ENSP00000463046.1:p.Lys38Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1172A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3515A>C
  hgvsp: ENSP00000364397.5:p.Lys1172Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3485A>C
  hgvsp: ENSP00000313885.7:p.Lys1162Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2438A>C
  hgvsp: ENSP00000463929.1:p.Lys813Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4090A>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys1162Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

17-73493955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493955
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493955
    reference: chr 17
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+12A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+12A>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3819
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

17-73493966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493966
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493966
    reference: chr 17
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+23G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+23G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

17-73493968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493968
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493968
    reference: chr 17
allele count: 2
allele frequency: 1.664502813009754e-5
allele num: 120156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+25C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+25C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-73493974-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493974
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493974
    reference: chr 17
allele count: 1
allele frequency: 8.330695279828055e-6
allele num: 120038
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+31A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

17-73493975-G-GTGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493975
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493978
    reference: chr 17
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: GTGA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+33_4258+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+33_60+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+33_2442+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+33_4094+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+33_3519+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+33_115+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+33_248+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+33_1176+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+33_306+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+33_3489+35dupTGA
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

17-73493977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493977
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493977
    reference: chr 17
allele count: 3
allele frequency: 2.50075022506752e-5
allele num: 119964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+34G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+34G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-73493979-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493979
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493979
    reference: chr 17
allele count: 1
allele frequency: 8.340561820244212e-6
allele num: 119896
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+36G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+36G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16273
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6032
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

17-73493987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493987
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493987
    reference: chr 17
allele count: 2
allele frequency: 1.67369619066747e-5
allele num: 119496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+44G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+44G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6030
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-73493993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73493993
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73493993
    reference: chr 17
allele count: 1
allele frequency: 8.40039649871474e-6
allele num: 119042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2442+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3519+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.248+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.115+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4094+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.306+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3489+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4258+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.60+50G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1176+50G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4869
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

17-73494207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494207
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494207
    reference: chr 17
allele count: 1
allele frequency: 8.311584686736373e-6
allele num: 120314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-49C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-136C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

17-73494208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494208
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494208
    reference: chr 17
allele count: 12
allele frequency: 9.977218684004855e-5
allele num: 120274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-135C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-48C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-48C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-73494209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494209
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494209
    reference: chr 17
allele count: 2
allele frequency: 1.661930165694438e-5
allele num: 120342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-134G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-47G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-47G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

17-73494213-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494213
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494213
    reference: chr 17
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-130G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-43G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-43G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

17-73494218-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494218
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494218
    reference: chr 17
allele count: 1
allele frequency: 8.303716743614441e-6
allele num: 120428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-38G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-125G>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3817
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-73494224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494224
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494224
    reference: chr 17
allele count: 15
allele frequency: 1.245536826372166e-4
allele num: 120430
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-119C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-32C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25801
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

17-73494225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494225
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494225
    reference: chr 17
allele count: 5
allele frequency: 4.149997510001494e-5
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-118G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-31G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-31G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-73494227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494227
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494227
    reference: chr 17
allele count: 8
allele frequency: 6.635700066357e-5
allele num: 120560
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-116C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-29C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-29C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

17-73494228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494228
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494228
    reference: chr 17
allele count: 49
allele frequency: 4.064636007697923e-4
allele num: 120552
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-115C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-28C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-28C>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9605
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9912
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-73494232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494232
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494232
    reference: chr 17
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-111G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-24G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-24G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10226
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

17-73494232-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494232
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494232
    reference: chr 17
allele count: 2
allele frequency: 1.657687525901368e-5
allele num: 120650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-111G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-24G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-24G>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

17-73494251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494251
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494251
    reference: chr 17
allele count: 2
allele frequency: 1.653575857792476e-5
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-92C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3490-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3520-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2443-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4259-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4095-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.307-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1177-5C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.249-5C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10705
  bin: 6.25e1
  variant carriers: 0
hgvs: c.3490-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-73494287-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494287
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494287
    reference: chr 17
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3551T>G
  hgvsp: ENSP00000364397.5:p.Leu1184Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2474T>G
  hgvsp: ENSP00000463929.1:p.Leu825Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.92T>G
  hgvsp: ENSP00000462084.1:p.Leu31Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.338T>G
  hgvsp: ENSP00000464437.1:p.Leu113Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4126T>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3521T>G
  hgvsp: ENSP00000313885.7:p.Leu1174Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4290T>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1208T>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-56T>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.280T>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25804
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu1174Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

17-73494304-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494304
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494304
    reference: chr 17
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.109A>T
  hgvsp: ENSP00000462084.1:p.Ile37Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4307A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3538A>T
  hgvsp: ENSP00000313885.7:p.Ile1180Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.355A>T
  hgvsp: ENSP00000464437.1:p.Ile119Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2491A>T
  hgvsp: ENSP00000463929.1:p.Ile831Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-39A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3568A>T
  hgvsp: ENSP00000364397.5:p.Ile1190Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.297A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1225A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.7A>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4143A>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1180Phe
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-73494309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494309
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494309
    reference: chr 17
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.12C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4312C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.114C>T
  hgvsp: ENST00000577245.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3573C>T
  hgvsp: ENST00000375248.5:c.3573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.302C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4148C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3543C>T
  hgvsp: ENST00000314256.7:c.3543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2496C>T
  hgvsp: ENST00000579208.1:c.2496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-34C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1230C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.360C>T
  hgvsp: ENST00000577247.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1181Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

17-73494311-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494311
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494311
    reference: chr 17
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3545C>G
  hgvsp: ENSP00000313885.7:p.Ser1182Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2498C>G
  hgvsp: ENSP00000463929.1:p.Ser833Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3575C>G
  hgvsp: ENSP00000364397.5:p.Ser1192Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1232C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4314C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.14C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.116C>G
  hgvsp: ENSP00000462084.1:p.Ser39Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.304C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-32C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4150C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.362C>G
  hgvsp: ENSP00000464437.1:p.Ser121Cys
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1182Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

17-73494311-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494311
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494311
    reference: chr 17
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.362C>T
  hgvsp: ENSP00000464437.1:p.Ser121Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.304C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3545C>T
  hgvsp: ENSP00000313885.7:p.Ser1182Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2498C>T
  hgvsp: ENSP00000463929.1:p.Ser833Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.116C>T
  hgvsp: ENSP00000462084.1:p.Ser39Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-32C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3575C>T
  hgvsp: ENSP00000364397.5:p.Ser1192Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4314C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.14C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1232C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4150C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1182Phe
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-73494320-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494320
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494320
    reference: chr 17
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2507T>C
  hgvsp: ENSP00000463929.1:p.Ile836Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3584T>C
  hgvsp: ENSP00000364397.5:p.Ile1195Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.125T>C
  hgvsp: ENSP00000462084.1:p.Ile42Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.313T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3554T>C
  hgvsp: ENSP00000313885.7:p.Ile1185Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.371T>C
  hgvsp: ENSP00000464437.1:p.Ile124Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1241T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4159T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4323T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-23T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.23T>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1185Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

17-73494321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494321
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494321
    reference: chr 17
allele count: 2
allele frequency: 1.65174589541145e-5
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.314C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-22C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3555C>T
  hgvsp: ENST00000314256.7:c.3555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4324C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3585C>T
  hgvsp: ENST00000375248.5:c.3585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.126C>T
  hgvsp: ENST00000577245.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2508C>T
  hgvsp: ENST00000579208.1:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4160C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.372C>T
  hgvsp: ENST00000577247.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.24C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1242C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile1185Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

17-73494334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494334
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494334
    reference: chr 17
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.37A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4173A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1255A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3598A>G
  hgvsp: ENSP00000364397.5:p.Thr1200Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2521A>G
  hgvsp: ENSP00000463929.1:p.Thr841Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.385A>G
  hgvsp: ENSP00000464437.1:p.Thr129Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4337A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3568A>G
  hgvsp: ENSP00000313885.7:p.Thr1190Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.327A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-9A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.139A>G
  hgvsp: ENSP00000462084.1:p.Thr47Ala
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1190Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

17-73494339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494339
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494339
    reference: chr 17
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2526G>A
  hgvsp: ENST00000579208.1:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.332G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.42G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4342G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1260G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3603G>A
  hgvsp: ENST00000375248.5:c.3603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116-4G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.144G>A
  hgvsp: ENST00000577245.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3573G>A
  hgvsp: ENST00000314256.7:c.3573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4178G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.390G>A
  hgvsp: ENST00000577247.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.116-4G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/17-73494343-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494343
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494343
    reference: chr 17
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.148A>C
  hgvsp: ENSP00000462084.1:p.Ser50Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1264A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4182A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3577A>C
  hgvsp: ENSP00000313885.7:p.Ser1193Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.336A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3607A>C
  hgvsp: ENSP00000364397.5:p.Ser1203Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4346A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2530A>C
  hgvsp: ENSP00000463929.1:p.Ser844Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.116A>C
  hgvsp: ENSP00000463046.1:p.Ser40Arg
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.46A>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.394A>C
  hgvsp: ENSP00000464437.1:p.Ser132Arg
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1193Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

17-73494361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494361
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494361
    reference: chr 17
allele count: 3
allele frequency: 2.480445818795165e-5
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.64C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1282C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3625C>T
  hgvsp: ENSP00000364397.5:p.Arg1209Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4200C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.412C>T
  hgvsp: ENSP00000464437.1:p.Arg138Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.134C>T
  hgvsp: ENSP00000463046.1:p.Arg46Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.166C>T
  hgvsp: ENSP00000462084.1:p.Arg56Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.354C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3595C>T
  hgvsp: ENSP00000313885.7:p.Arg1199Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2548C>T
  hgvsp: ENSP00000463929.1:p.Arg850Trp
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4364C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1199Trp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

17-73494362-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494362
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494362
    reference: chr 17
allele count: 2
allele frequency: 1.653630545863443e-5
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2549G>A
  hgvsp: ENSP00000463929.1:p.Arg850Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.413G>A
  hgvsp: ENSP00000464437.1:p.Arg138Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4201G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1283G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.135G>A
  hgvsp: ENSP00000463046.1:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3596G>A
  hgvsp: ENSP00000313885.7:p.Arg1199Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3626G>A
  hgvsp: ENSP00000364397.5:p.Arg1209Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.167G>A
  hgvsp: ENSP00000462084.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.355G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4365G>A
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.65G>A
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1199Gln
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

17-73494367-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494367
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494367
    reference: chr 17
allele count: 24
allele frequency: 1.98455355813915e-4
allele num: 120934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4370C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3631C>T
  hgvsp: ENSP00000364397.5:p.Arg1211Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1288C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.140C>T
  hgvsp: ENSP00000463046.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.172C>T
  hgvsp: ENSP00000462084.1:p.Arg58Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2554C>T
  hgvsp: ENSP00000463929.1:p.Arg852Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.360C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3601C>T
  hgvsp: ENSP00000313885.7:p.Arg1201Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4206C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.418C>T
  hgvsp: ENSP00000464437.1:p.Arg140Cys
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.70C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9850
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg1201Cys
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

17-73494369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494369
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494369
    reference: chr 17
allele count: 1
allele frequency: 8.269930532583527e-6
allele num: 120920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1290C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.174C>T
  hgvsp: ENST00000577245.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4208C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.142C>T
  hgvsp: ENST00000584694.1:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4372C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3633C>T
  hgvsp: ENST00000375248.5:c.3633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2556C>T
  hgvsp: ENST00000579208.1:c.2556C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.72C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.362C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3603C>T
  hgvsp: ENST00000314256.7:c.3603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.420C>T
  hgvsp: ENST00000577247.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1201Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

17-73494371-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494371
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494371
    reference: chr 17
allele count: 5
allele frequency: 4.135854550267176e-5
allele num: 120894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.422A>G
  hgvsp: ENSP00000464437.1:p.Asn141Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.74A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.176A>G
  hgvsp: ENSP00000462084.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3605A>G
  hgvsp: ENSP00000313885.7:p.Asn1202Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1292A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4210A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.364A>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2558A>G
  hgvsp: ENSP00000463929.1:p.Asn853Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3635A>G
  hgvsp: ENSP00000364397.5:p.Asn1212Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.144A>G
  hgvsp: ENSP00000463046.1:p.Asn49Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4374A>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn1202Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

17-73494372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494372
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494372
    reference: chr 17
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.177C>T
  hgvsp: ENST00000577245.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2559C>T
  hgvsp: ENST00000579208.1:c.2559C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.145C>T
  hgvsp: ENST00000584694.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.365C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4211C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.75C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3636C>T
  hgvsp: ENST00000375248.5:c.3636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4375C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1293C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3606C>T
  hgvsp: ENST00000314256.7:c.3606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.423C>T
  hgvsp: ENST00000577247.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn1202Asn
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-73494387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494387
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494387
    reference: chr 17
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.160C>T
  hgvsp: ENST00000584694.1:c.160C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2574C>T
  hgvsp: ENST00000579208.1:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.438C>T
  hgvsp: ENST00000577247.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4226C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1308C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3651C>T
  hgvsp: ENST00000375248.5:c.3651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.192C>T
  hgvsp: ENST00000577245.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4390C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3621C>T
  hgvsp: ENST00000314256.7:c.3621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.380C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.90C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1207Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

17-73494390-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494390
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494390
    reference: chr 17
allele count: 10
allele frequency: 8.278693953241937e-5
allele num: 120792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.383C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3654C>T
  hgvsp: ENST00000375248.5:c.3654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.93C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.163C>T
  hgvsp: ENST00000584694.1:c.163C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.441C>T
  hgvsp: ENST00000577247.1:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4393C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.195C>T
  hgvsp: ENST00000577245.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3624C>T
  hgvsp: ENST00000314256.7:c.3624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4229C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2577C>T
  hgvsp: ENST00000579208.1:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1311C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1208Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

17-73494391-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494391
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494391
    reference: chr 17
allele count: 97
allele frequency: 8.03192898781134e-4
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3625G>T
  hgvsp: ENSP00000313885.7:p.Val1209Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.384G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.442G>T
  hgvsp: ENSP00000464437.1:p.Val148Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.164G>T
  hgvsp: ENSP00000463046.1:p.Val56Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.196G>T
  hgvsp: ENSP00000462084.1:p.Val66Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4394G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.94G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3655G>T
  hgvsp: ENSP00000364397.5:p.Val1219Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2578G>T
  hgvsp: ENSP00000463929.1:p.Val860Phe
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4230G>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1312G>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9156
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1209Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum

17-73494395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494395
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494395
    reference: chr 17
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.168T>C
  hgvsp: ENSP00000463046.1:p.Met57Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4234T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3629T>C
  hgvsp: ENSP00000313885.7:p.Met1210Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1316T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3659T>C
  hgvsp: ENSP00000364397.5:p.Met1220Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2582T>C
  hgvsp: ENSP00000463929.1:p.Met861Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.446T>C
  hgvsp: ENSP00000464437.1:p.Met149Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4398T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.388T>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.200T>C
  hgvsp: ENSP00000462084.1:p.Met67Thr
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.98T>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1210Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

17-73494400-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494400
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494400
    reference: chr 17
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3664C>G
  hgvsp: ENSP00000364397.5:p.Pro1222Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.451C>G
  hgvsp: ENSP00000464437.1:p.Pro151Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3634C>G
  hgvsp: ENSP00000313885.7:p.Pro1212Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.393C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2587C>G
  hgvsp: ENSP00000463929.1:p.Pro863Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.173C>G
  hgvsp: ENSP00000463046.1:p.Pro59Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4403C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.205C>G
  hgvsp: ENSP00000462084.1:p.Pro69Ala
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.103C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4239C>G
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1321C>G
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1212Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-73494400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494400
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494400
    reference: chr 17
allele count: 97
allele frequency: 8.032195025007452e-4
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3664C>T
  hgvsp: ENSP00000364397.5:p.Pro1222Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4403C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3634C>T
  hgvsp: ENSP00000313885.7:p.Pro1212Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2587C>T
  hgvsp: ENSP00000463929.1:p.Pro863Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.451C>T
  hgvsp: ENSP00000464437.1:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.393C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.205C>T
  hgvsp: ENSP00000462084.1:p.Pro69Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4239C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.173C>T
  hgvsp: ENSP00000463046.1:p.Pro59Ser
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.103C>T
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1321C>T
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Pro1212Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-73494409-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73494409
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73494409
    reference: chr 17
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581085
  gene symbol: KIAA0195
  hgvsc: ENST00000581085.1:n.4243+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000462084
  ensembl transcript: ENST00000577245
  gene symbol: KIAA0195
  hgvsc: ENST00000577245.1:c.209+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463046
  ensembl transcript: ENST00000584694
  gene symbol: KIAA0195
  hgvsc: ENST00000584694.1:c.177+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000579898
  gene symbol: KIAA0195
  hgvsc: ENST00000579898.1:n.1325+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000585105
  gene symbol: KIAA0195
  hgvsc: ENST00000585105.1:n.4407+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000463929
  ensembl transcript: ENST00000579208
  gene symbol: KIAA0195
  hgvsc: ENST00000579208.1:c.2591+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000464437
  ensembl transcript: ENST00000577247
  gene symbol: KIAA0195
  hgvsc: ENST00000577247.1:c.455+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000313885
  ensembl transcript: ENST00000314256
  gene symbol: KIAA0195
  hgvsc: ENST00000314256.7:c.3638+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl protein: ENSP00000364397
  ensembl transcript: ENST00000375248
  gene symbol: KIAA0195
  hgvsc: ENST00000375248.5:c.3668+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000577194
  gene symbol: KIAA0195
  hgvsc: ENST00000577194.1:n.107+5G>C
  variant of: http://identifiers.org/hgnc/28983
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177728
  ensembl transcript: ENST00000581453
  gene symbol: KIAA0195
  hgvsc: ENST00000581453.1:n.397+5G>C
  variant of: http://identifiers.org/hgnc/28983
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
hgvs: c.3638+5G>C
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24356
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550916591705698e-5
allele num: 64478
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15690
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.604164e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.989e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

QD
type: SiteQuality
SIO_000300: 1.064e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3010
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544735541275334e-5
allele num: 64736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.542e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.636505e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 954
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7322
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15798
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

DP
type: SiteQuality
SIO_000300: 1.651464e6

MQ
type: SiteQuality
SIO_000300: 5.929e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.486e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.746e1

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6304
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64956
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 3.73e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 1.656611e6

FS
type: SiteQuality
SIO_000300: 3.991e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 28600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.75e1
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: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 916
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15850
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.611978846390358e-5
allele num: 65048
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.975e0

QD
type: SiteQuality
SIO_000300: 1.65e1

VQSLOD
type: SiteQuality
SIO_000300: -2.999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 3.633e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

DP
type: SiteQuality
SIO_000300: 1.663109e6

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3204
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GenotypeQuality
all individuals: 1153
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.211180124223603e-5
allele num: 16100
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.65e0

DP
type: SiteQuality
SIO_000300: 1.703446e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.035e0

GenotypeQuality
all individuals: 32399
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3242
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
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: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513592056668887e-5
allele num: 66068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.304e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 1.717714e6

VQSLOD
type: SiteQuality
SIO_000300: -2.765e0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 2.998e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 3247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6387
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variant carriers: 22

GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1520
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 22
allele frequency: 2.548656163113994e-3
allele num: 8632
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

QD
type: SiteQuality
SIO_000300: 1.16e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.309e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

DP
type: SiteQuality
SIO_000300: 1.721832e6

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 2773
bin: 7.75e1
variant carriers: 58

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 96
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variant carriers: 23

GenotypeQuality
all individuals: 16
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variant carriers: 2

GenotypeQuality
all individuals: 2305
bin: 7.25e1
variant carriers: 39

GenotypeQuality
all individuals: 359
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variant carriers: 7

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 9

GenotypeQuality
all individuals: 25455
bin: 6.25e1
variant carriers: 29

GenotypeQuality
all individuals: 5796
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variant carriers: 29

GenotypeQuality
all individuals: 105
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variant carriers: 12

GenotypeQuality
all individuals: 1074
bin: 9.25e1
variant carriers: 63

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 10

GenotypeQuality
all individuals: 83
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variant carriers: 19

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 12

African
type: Population
allele count: 363
allele frequency: 3.529068636982306e-2
allele num: 10286
num of homozygotes: 10

East Asian
type: Population
allele count: 9
allele frequency: 1.042390548992356e-3
allele num: 8634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1566
allele frequency: 2.369137670196672e-1
allele num: 6610
num of homozygotes: 199

European (Non-Finnish)
type: Population
allele count: 14253
allele frequency: 2.149449555119891e-1
allele num: 66310
num of homozygotes: 1607

South Asian
type: Population
allele count: 774
allele frequency: 4.722968025384428e-2
allele num: 16388
num of homozygotes: 26

Latino
type: Population
allele count: 716
allele frequency: 6.222840257257083e-2
allele num: 11506
num of homozygotes: 23

Other
type: Population
allele count: 130
allele frequency: 1.444444444444444e-1
allele num: 900
num of homozygotes: 15

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.35e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.58e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

DP
type: SiteQuality
SIO_000300: 2.178571e6

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 359
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GenotypeQuality
all individuals: 1811
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GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 25455
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GenotypeQuality
all individuals: 19610
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2773
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 803
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variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.508068164681044e-4
allele num: 66310
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: 11506
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

QD
type: SiteQuality
SIO_000300: 1.58e1

VQSLOD
type: SiteQuality
SIO_000300: 6.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.35e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

DP
type: SiteQuality
SIO_000300: 2.178571e6

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 107
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GenotypeQuality
all individuals: 1546
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 3972
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8237
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GenotypeQuality
all individuals: 3195
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GenotypeQuality
all individuals: 2643
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.520659413519785e-5
allele num: 66362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.442e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.772e-1

QD
type: SiteQuality
SIO_000300: 2.183e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.779868e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2604
bin: 8.25e1
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GenotypeQuality
all individuals: 6077
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GenotypeQuality
all individuals: 3181
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GenotypeQuality
all individuals: 28
bin: 1.25e1
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GenotypeQuality
all individuals: 32776
bin: 6.25e1
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GenotypeQuality
all individuals: 344
bin: 2.25e1
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 93
bin: 4.25e1
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GenotypeQuality
all individuals: 8207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
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GenotypeQuality
all individuals: 3943
bin: 7.75e1
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GenotypeQuality
all individuals: 1100
bin: 8.75e1
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GenotypeQuality
all individuals: 1537
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.917152858809801e-4
allele num: 10284
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.812196079615815e-4
allele num: 66218
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 3.0e-1

FS
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.783173e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.82e-1

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 3194
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 1099
bin: 8.75e1
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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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bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505888022166672e-5
allele num: 66406
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.716e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: -1.772e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.557e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.782e1

DP
type: SiteQuality
SIO_000300: 1.783103e6

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 5.031e0

VQSLOD
type: SiteQuality
SIO_000300: -1.417e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.573e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

InbreedingCoeff
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SIO_000300: 1.1e-3

DP
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SIO_000300: 1.783324e6

FS
type: SiteQuality
SIO_000300: 2.945e0

MQRankSum
type: SiteQuality
SIO_000300: -4.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

QD
type: SiteQuality
SIO_000300: 2.747e1

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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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.351e0

QD
type: SiteQuality
SIO_000300: 7.97e0

FS
type: SiteQuality
SIO_000300: 2.369e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.271e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: -1.372e0

DP
type: SiteQuality
SIO_000300: 1.783646e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008785654110001e-5
allele num: 66472
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.783687e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
type: Population
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South Asian
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allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
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VQSLOD
type: SiteQuality
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QD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
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SIO_000300: -9.0e-2

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

South Asian
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allele num: 16464
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African
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allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504709741490866e-5
allele num: 66458
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Other
type: Population
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BaseQRankSum
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SIO_000300: -1.2e-2

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
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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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variant carriers: 0

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

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

African
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Other
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South Asian
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East Asian
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allele count: 7
allele frequency: 8.103727714748784e-4
allele num: 8638
num of homozygotes: 0

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

QD
type: SiteQuality
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MQRankSum
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DP
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MQ
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.504619180885318e-5
allele num: 66462
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Other
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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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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Latino
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allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.157675387821255e-4
allele num: 8638
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South Asian
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allele frequency: 0.0e0
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QD
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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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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allele frequency: 1.506024096385542e-5
allele num: 66400
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South Asian
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

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

MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 9.695559433779329e-5
allele num: 10314
num of homozygotes: 0

ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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VQSLOD
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QD
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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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East Asian
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allele count: 0
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num of homozygotes: 0

African
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South Asian
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Latino
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num of homozygotes: 0

European (Finnish)
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.511670093118878e-5
allele num: 66152
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 259
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65954
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: 898
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: 10234
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.739730816290858e-5
allele num: 11442
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.427e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

FS
type: SiteQuality
SIO_000300: 2.151e0

DP
type: SiteQuality
SIO_000300: 1.709745e6

MQRankSum
type: SiteQuality
SIO_000300: -1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65936
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
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

QD
type: SiteQuality
SIO_000300: 2.105e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.706114e6

MQ
type: SiteQuality
SIO_000300: 5.74e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.930832356389214e-4
allele num: 10236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65900
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.694314e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 2.914e1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.777e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-5
allele num: 65860
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 3.833e0

QD
type: SiteQuality
SIO_000300: 8.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.316e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

DP
type: SiteQuality
SIO_000300: 1.684881e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-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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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046829773620548e-5
allele num: 65642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.686e0

DP
type: SiteQuality
SIO_000300: 1.657069e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

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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bin: 1.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65404
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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: 16094
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

FS
type: SiteQuality
SIO_000300: 6.146e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.647677e6

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.195019204559534e-5
allele num: 16142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
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: 5.794e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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ClippingRankSum
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SIO_000300: -8.05e-1

BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.1e-3

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
allele frequency: 3.863987635239567e-4
allele num: 10352
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05909764880322e-4
allele num: 66094
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
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SIO_000300: 2.387e0

VQSLOD
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SIO_000300: 2.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ClippingRankSum
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SIO_000300: -2.4e-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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
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: 11558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025077895755816e-5
allele num: 66114
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

DP
type: SiteQuality
SIO_000300: 2.39362e6

FS
type: SiteQuality
SIO_000300: 2.991e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

QD
type: SiteQuality
SIO_000300: 1.064e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 1

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4269
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

FS
type: SiteQuality
SIO_000300: 2.412e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

DP
type: SiteQuality
SIO_000300: 2.397938e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.171315724512466e-5
allele num: 16204
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e0

DP
type: SiteQuality
SIO_000300: 2.40232e6

FS
type: SiteQuality
SIO_000300: 1.0897e1

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: -3.746e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.534736078360239e-5
allele num: 66156
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 12
allele frequency: 1.038062283737024e-3
allele num: 11560
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 2.282e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.409121e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.816e0

QD
type: SiteQuality
SIO_000300: 1.194e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
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
all individuals: 13
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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: 25800
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.827186715582159e-4
allele num: 10358
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 6.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.409938e6

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

GenotypeQuality
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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: 10362
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.057369867979819e-4
allele num: 66202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
type: SiteQuality
SIO_000300: 2.41244e6

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.59e-2

QD
type: SiteQuality
SIO_000300: 1.065e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 49

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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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: 100
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GenotypeQuality
all individuals: 4216
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.552870090634441e-5
allele num: 66200
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.595155709342561e-4
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.237136465324385e-3
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 38
allele frequency: 2.334152334152334e-3
allele num: 16280
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

FS
type: SiteQuality
SIO_000300: 5.739e0

DP
type: SiteQuality
SIO_000300: 2.413851e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.57e0

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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bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.316e0

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

QD
type: SiteQuality
SIO_000300: 9.19e0

DP
type: SiteQuality
SIO_000300: 2.417214e6

GenotypeQuality
all individuals: 88
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
all individuals: 10226
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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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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European (Non-Finnish)
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allele frequency: 3.019141356198297e-5
allele num: 66244
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Other
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East Asian
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InbreedingCoeff
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FS
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 1.39e-1

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

European (Non-Finnish)
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allele frequency: 1.506387081224391e-5
allele num: 66384
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele num: 11566
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South Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

Other
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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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DP
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

European (Non-Finnish)
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allele num: 66488
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African
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East Asian
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European (Finnish)
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Latino
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South Asian
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Other
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507295309296997e-5
allele num: 66344
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQRankSum
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FS
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SIO_000300: 1.029e1

VQSLOD
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BaseQRankSum
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SIO_000300: -4.603e0

InbreedingCoeff
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SIO_000300: 1.2e-3

DP
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SIO_000300: 2.428111e6

MQ
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SIO_000300: 5.866e1

QD
type: SiteQuality
SIO_000300: 1.149e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 4
allele frequency: 3.461405330564209e-4
allele num: 11556
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 7.991e0

VQSLOD
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SIO_000300: 8.29e-1

MQRankSum
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SIO_000300: 5.31e-1

DP
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SIO_000300: 2.428123e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

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

Other
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allele num: 900
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

QD
type: SiteQuality
SIO_000300: 8.4e0

FS
type: SiteQuality
SIO_000300: 3.439e0

DP
type: SiteQuality
SIO_000300: 2.425517e6

VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.358572593062223e-4
allele num: 66246
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.955e1

ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 72
allele frequency: 1.087087812537746e-3
allele num: 66232
num of homozygotes: 0

African
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East Asian
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South Asian
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allele frequency: 8.479709267110841e-4
allele num: 16510
num of homozygotes: 0

Latino
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allele frequency: 7.789510126363164e-4
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num of homozygotes: 0

Other
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allele num: 898
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
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Latino
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African
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Other
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East Asian
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 2.424324e6

QD
type: SiteQuality
SIO_000300: 1.745e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25785
bin: 9.75e1
variant carriers: 97

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4324
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 9
allele frequency: 7.790858725761773e-4
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 72
allele frequency: 1.087120640193266e-3
allele num: 66230
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
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: 10334
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.481764206955047e-4
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

DP
type: SiteQuality
SIO_000300: 2.424324e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 5.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.745e1