15-69721603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69721603
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69721603
    reference: chr 15
allele count: 1
allele frequency: 1.26237123813371e-5
allele num: 79216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1072+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*128+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1072+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.481+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.523+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1072+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.523+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1072+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*605+51A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.686+51A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10264
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/15-69727773-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727773
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727773
    reference: chr 15
allele count: 264
allele frequency: 2.489626556016597e-3
allele num: 106040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-49C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-49C>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16491
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 1.75e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4910
  bin: 9.75e1
  variant carriers: 259
num of homozygotes: 2
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

15-69727776-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727776
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727776
    reference: chr 15
allele count: 14
allele frequency: 1.317175974710221e-4
allele num: 106288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-46C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-46C>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6571
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16401
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6784
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7329
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

15-69727778-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727778
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727778
    reference: chr 15
allele count: 1
allele frequency: 9.385617479773995e-6
allele num: 106546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-44A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-44A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14677
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

15-69727781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727781
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727781
    reference: chr 15
allele count: 1
allele frequency: 9.375410174195122e-6
allele num: 106662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-41C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-41C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

15-69727799-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727799
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727799
    reference: chr 15
allele count: 5
allele frequency: 4.493412657044773e-5
allele num: 111274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-23G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-23G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31985
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4759
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

15-69727801-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727801
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727800
    reference: chr 15
allele count: 1
allele frequency: 8.888572850743085e-6
allele num: 112504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-20delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-20delT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: CT
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

15-69727807-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727807
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727808
    reference: chr 15
allele count: 960
allele frequency: 8.329284375650725e-3
allele num: 115256
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-8dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-8dupT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 36032
  bin: 2.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 2.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 3.25e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34825
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 33
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-69727807-A-ATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727807
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727809
    reference: chr 15
allele count: 4
allele frequency: 3.470535156521136e-5
allele num: 115256
alternate allele: ATT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-9_1073-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-9_*129-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-9_*606-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-9_482-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-9_687-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-9_524-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-9_1073-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-9_1073-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-9_524-8dupTT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-9_1073-8dupTT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

15-69727819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727819
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727819
    reference: chr 15
allele count: 7
allele frequency: 5.885221368398043e-5
allele num: 118942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*606-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*129-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.482-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.524-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1073-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1073-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1073-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.524-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.687-3C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1073-3C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9956
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38321
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1073-3C>T
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

15-69727846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727846
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727846
    reference: chr 15
allele count: 2
allele frequency: 1.65218253312626e-5
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.548C>T
  hgvsp: ENSP00000442969.1:p.Thr183Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1097C>T
  hgvsp: ENSP00000453386.1:p.Thr366Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*630C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1097C>T
  hgvsp: ENSP00000378790.2:p.Thr366Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*153C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1097C>T
  hgvsp: ENSP00000260363.4:p.Thr366Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.506C>T
  hgvsp: ENSP00000452901.1:p.Thr169Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.548C>T
  hgvsp: ENSP00000453102.1:p.Thr183Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.711C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1097C>T
  hgvsp: ENSP00000304978.6:p.Thr366Met
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr366Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

15-69727847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727847
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727847
    reference: chr 15
allele count: 19
allele frequency: 1.569210439378923e-4
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1098G>A
  hgvsp: ENST00000559279.1:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.507G>A
  hgvsp: ENST00000559283.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1098G>A
  hgvsp: ENST00000260363.4:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1098G>A
  hgvsp: ENST00000395392.2:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.549G>A
  hgvsp: ENST00000558585.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.549G>A
  hgvsp: ENST00000537891.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.712G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*631G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1098G>A
  hgvsp: ENST00000352331.4:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr366Thr
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

15-69727852-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727852
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727852
    reference: chr 15
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*159G>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.717G>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.554G>C
  hgvsp: ENSP00000453102.1:p.Arg185Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1103G>C
  hgvsp: ENSP00000260363.4:p.Arg368Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*636G>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1103G>C
  hgvsp: ENSP00000304978.6:p.Arg368Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1103G>C
  hgvsp: ENSP00000453386.1:p.Arg368Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.554G>C
  hgvsp: ENSP00000442969.1:p.Arg185Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1103G>C
  hgvsp: ENSP00000378790.2:p.Arg368Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.512G>C
  hgvsp: ENSP00000452901.1:p.Arg171Thr
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg368Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

15-69727863-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727863
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727863
    reference: chr 15
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1114G>A
  hgvsp: ENSP00000378790.2:p.Asp372Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*170G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.728G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1114G>A
  hgvsp: ENSP00000453386.1:p.Asp372Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1114G>A
  hgvsp: ENSP00000260363.4:p.Asp372Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.523G>A
  hgvsp: ENSP00000452901.1:p.Asp175Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.565G>A
  hgvsp: ENSP00000442969.1:p.Asp189Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*647G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1114G>A
  hgvsp: ENSP00000304978.6:p.Asp372Asn
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.565G>A
  hgvsp: ENSP00000453102.1:p.Asp189Asn
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp372Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

15-69727866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727866
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727866
    reference: chr 15
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.568G>A
  hgvsp: ENSP00000442969.1:p.Val190Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1117G>A
  hgvsp: ENSP00000378790.2:p.Val373Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.731G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1117G>A
  hgvsp: ENSP00000260363.4:p.Val373Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*173G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.568G>A
  hgvsp: ENSP00000453102.1:p.Val190Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.526G>A
  hgvsp: ENSP00000452901.1:p.Val176Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1117G>A
  hgvsp: ENSP00000453386.1:p.Val373Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1117G>A
  hgvsp: ENSP00000304978.6:p.Val373Ile
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val373Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

15-69727871-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727871
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727869
    reference: chr 15
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*184_*185delGA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.742_743delGA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1128_1129delGA
  hgvsp: ENSP00000304978.6:p.Asn377ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1128_1129delGA
  hgvsp: ENSP00000378790.2:p.Asn377ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1128_1129delGA
  hgvsp: ENSP00000453386.1:p.Asn377ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.579_580delGA
  hgvsp: ENSP00000442969.1:p.Asn194ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1128_1129delGA
  hgvsp: ENSP00000260363.4:p.Asn377ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.537_538delGA
  hgvsp: ENSP00000452901.1:p.Asn180ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.579_580delGA
  hgvsp: ENSP00000453102.1:p.Asn194ProfsTer6
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*661_*662delGA
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn377ProfsTer6
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: AAG
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

15-69727877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727877
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727877
    reference: chr 15
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1128G>A
  hgvsp: ENST00000559279.1:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*661G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.579G>A
  hgvsp: ENST00000558585.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.537G>A
  hgvsp: ENST00000559283.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1128G>A
  hgvsp: ENST00000395392.2:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1128G>A
  hgvsp: ENST00000352331.4:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.579G>A
  hgvsp: ENST00000537891.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*184G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1128G>A
  hgvsp: ENST00000260363.4:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.742G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu376Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

15-69727883-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727883
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727883
    reference: chr 15
allele count: 7
allele frequency: 5.770530723954297e-5
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1134A>G
  hgvsp: ENST00000395392.2:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1134A>G
  hgvsp: ENST00000559279.1:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1134A>G
  hgvsp: ENST00000260363.4:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*190A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.585A>G
  hgvsp: ENST00000537891.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*667A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.543A>G
  hgvsp: ENST00000559283.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.585A>G
  hgvsp: ENST00000558585.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1134A>G
  hgvsp: ENST00000352331.4:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.748A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln378Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

15-69727886-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727886
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727886
    reference: chr 15
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*670G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1137G>T
  hgvsp: ENSP00000378790.2:p.Met379Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.588G>T
  hgvsp: ENSP00000453102.1:p.Met196Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1137G>T
  hgvsp: ENSP00000453386.1:p.Met379Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1137G>T
  hgvsp: ENSP00000260363.4:p.Met379Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.588G>T
  hgvsp: ENSP00000442969.1:p.Met196Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1137G>T
  hgvsp: ENSP00000304978.6:p.Met379Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*193G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.751G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.546G>T
  hgvsp: ENSP00000452901.1:p.Met182Ile
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met379Ile
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

15-69727898-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727898
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727898
    reference: chr 15
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1149C>G
  hgvsp: ENSP00000453386.1:p.Asn383Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*682C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1149C>G
  hgvsp: ENSP00000378790.2:p.Asn383Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1149C>G
  hgvsp: ENSP00000304978.6:p.Asn383Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.558C>G
  hgvsp: ENSP00000452901.1:p.Asn186Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1149C>G
  hgvsp: ENSP00000260363.4:p.Asn383Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.600C>G
  hgvsp: ENSP00000442969.1:p.Asn200Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.600C>G
  hgvsp: ENSP00000453102.1:p.Asn200Lys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*205C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.763C>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn383Lys
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: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

15-69727905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727905
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727905
    reference: chr 15
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+4A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+4A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39034
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1152+4A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-69727908-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727908
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727908
    reference: chr 15
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+7A>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+7A>C
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1152+7A>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

15-69727909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727909
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727909
    reference: chr 15
allele count: 15
allele frequency: 1.236501525018548e-4
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+8G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+8G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1152+8G>A
num of homozygotes: 1
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-69727913-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727913
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727913
    reference: chr 15
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+12C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+12C>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

15-69727914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727914
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727914
    reference: chr 15
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+13C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+13C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-69727915-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727915
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727915
    reference: chr 15
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+14T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+14T>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-69727924-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727924
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727924
    reference: chr 15
allele count: 14
allele frequency: 1.154049063571617e-4
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+23C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+23C>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38060
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38564
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS

15-69727929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727929
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727929
    reference: chr 15
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+28G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+28G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38558
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5224
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

15-69727929-GTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727929
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727927
    reference: chr 15
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+31_766+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+31_1152+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+31_561+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+31_1152+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+31_1152+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+31_603+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+31_*685+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+31_1152+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+31_603+32delTA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+31_*208+32delTA
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 37976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: GTA
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

15-69727934-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727934
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727933
    reference: chr 15
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+36delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+36delT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: GT
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/15-69727938-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727938
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727938
    reference: chr 15
allele count: 9
allele frequency: 7.418397626112759e-5
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+37C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+37C>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

15-69727941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727941
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727941
    reference: chr 15
allele count: 3
allele frequency: 2.472839974282464e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+40T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+40T>C
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5232
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

15-69727945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727945
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727945
    reference: chr 15
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.561+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.766+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1152+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*685+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.603+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1152+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*208+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.603+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1152+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1152+44G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

15-69727949-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727949
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727950
    reference: chr 15
allele count: 3
allele frequency: 2.491115023084333e-5
allele num: 120428
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-34dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-34dupT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

15-69727949-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727949
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727949
    reference: chr 15
allele count: 1
allele frequency: 8.303716743614441e-6
allele num: 120428
alternate allele: T
canonical: false
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5208
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 9.656237929702588e-5
  allele num: 10356
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 896
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11494
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6594
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

15-69727949-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727949
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727948
    reference: chr 15
allele count: 6
allele frequency: 4.982230046168665e-5
allele num: 120428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-34delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-34delT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: AT
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

15-69727959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727959
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727959
    reference: chr 15
allele count: 271
allele frequency: 2.233688305693845e-3
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-32C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 35646
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 11836
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2494
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 3
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

15-69727960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727960
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727960
    reference: chr 15
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-31G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-31G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD

15-69727968-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727968
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727968
    reference: chr 15
allele count: 9
allele frequency: 7.416074754033521e-5
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-23T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-23T>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

15-69727969-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727969
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727969
    reference: chr 15
allele count: 4
allele frequency: 3.296087544085171e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-22T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-22T>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-69727988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727988
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727988
    reference: chr 15
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153-3T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604-3T>C
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1153-3T>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

15-69727991-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69727991
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69727991
    reference: chr 15
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1153A>G
  hgvsp: ENSP00000304978.6:p.Met385Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1153A>G
  hgvsp: ENSP00000453386.1:p.Met385Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.604A>G
  hgvsp: ENSP00000453102.1:p.Met202Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*686A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1153A>G
  hgvsp: ENSP00000260363.4:p.Met385Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.604A>G
  hgvsp: ENSP00000442969.1:p.Met202Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.767A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1153A>G
  hgvsp: ENSP00000378790.2:p.Met385Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.562A>G
  hgvsp: ENSP00000452901.1:p.Met188Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*209A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met385Val
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-69728005-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728005
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728005
    reference: chr 15
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.576A>G
  hgvsp: ENST00000559283.1:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1167A>G
  hgvsp: ENST00000559279.1:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.618A>G
  hgvsp: ENST00000537891.1:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*223A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*700A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1167A>G
  hgvsp: ENST00000352331.4:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1167A>G
  hgvsp: ENST00000260363.4:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.618A>G
  hgvsp: ENST00000558585.1:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1167A>G
  hgvsp: ENST00000395392.2:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.781A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg389Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

15-69728022-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728022
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728022
    reference: chr 15
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1184A>G
  hgvsp: ENSP00000304978.6:p.His395Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.593A>G
  hgvsp: ENSP00000452901.1:p.His198Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1184A>G
  hgvsp: ENSP00000453386.1:p.His395Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.635A>G
  hgvsp: ENSP00000442969.1:p.His212Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1184A>G
  hgvsp: ENSP00000378790.2:p.His395Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.635A>G
  hgvsp: ENSP00000453102.1:p.His212Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*240A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1184A>G
  hgvsp: ENSP00000260363.4:p.His395Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.798A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*717A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37627
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His395Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-69728024-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728024
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728024
    reference: chr 15
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1186C>G
  hgvsp: ENSP00000378790.2:p.Leu396Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1186C>G
  hgvsp: ENSP00000304978.6:p.Leu396Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.800C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*242C>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.637C>G
  hgvsp: ENSP00000442969.1:p.Leu213Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1186C>G
  hgvsp: ENSP00000453386.1:p.Leu396Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.637C>G
  hgvsp: ENSP00000453102.1:p.Leu213Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.595C>G
  hgvsp: ENSP00000452901.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1186C>G
  hgvsp: ENSP00000260363.4:p.Leu396Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*719C>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu396Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

15-69728024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728024
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728024
    reference: chr 15
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*719C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1186C>T
  hgvsp: ENST00000352331.4:c.1186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1186C>T
  hgvsp: ENST00000395392.2:c.1186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*242C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1186C>T
  hgvsp: ENST00000260363.4:c.1186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.637C>T
  hgvsp: ENST00000537891.1:c.637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.800C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.637C>T
  hgvsp: ENST00000558585.1:c.637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.595C>T
  hgvsp: ENST00000559283.1:c.595C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1186C>T
  hgvsp: ENST00000559279.1:c.1186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37627
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu396Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

15-69728034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728034
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728034
    reference: chr 15
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1196A>G
  hgvsp: ENSP00000453386.1:p.Asn399Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*252A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.605A>G
  hgvsp: ENSP00000452901.1:p.Asn202Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1196A>G
  hgvsp: ENSP00000260363.4:p.Asn399Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.647A>G
  hgvsp: ENSP00000453102.1:p.Asn216Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.647A>G
  hgvsp: ENSP00000442969.1:p.Asn216Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*729A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1196A>G
  hgvsp: ENSP00000304978.6:p.Asn399Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1196A>G
  hgvsp: ENSP00000378790.2:p.Asn399Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.810A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn399Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-69728047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728047
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728047
    reference: chr 15
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.823G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1209G>A
  hgvsp: ENST00000395392.2:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.618G>A
  hgvsp: ENST00000559283.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1209G>A
  hgvsp: ENST00000260363.4:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.660G>A
  hgvsp: ENST00000537891.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*742G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1209G>A
  hgvsp: ENST00000352331.4:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*265G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1209G>A
  hgvsp: ENST00000559279.1:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.660G>A
  hgvsp: ENST00000558585.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly403Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

15-69728055-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728055
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728055
    reference: chr 15
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1217A>T
  hgvsp: ENSP00000304978.6:p.Lys406Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*273A>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.668A>T
  hgvsp: ENSP00000453102.1:p.Lys223Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.668A>T
  hgvsp: ENSP00000442969.1:p.Lys223Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1217A>T
  hgvsp: ENSP00000378790.2:p.Lys406Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1217A>T
  hgvsp: ENSP00000260363.4:p.Lys406Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*750A>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.626A>T
  hgvsp: ENSP00000452901.1:p.Lys209Ile
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.831A>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1217A>T
  hgvsp: ENSP00000453386.1:p.Lys406Ile
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys406Ile
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

15-69728060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728060
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728060
    reference: chr 15
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*755C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1222C>T
  hgvsp: ENSP00000260363.4:p.Arg408Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.673C>T
  hgvsp: ENSP00000453102.1:p.Arg225Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.836C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1222C>T
  hgvsp: ENSP00000453386.1:p.Arg408Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.631C>T
  hgvsp: ENSP00000452901.1:p.Arg211Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.673C>T
  hgvsp: ENSP00000442969.1:p.Arg225Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1222C>T
  hgvsp: ENSP00000378790.2:p.Arg408Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1222C>T
  hgvsp: ENSP00000304978.6:p.Arg408Trp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*278C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg408Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

15-69728061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728061
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728061
    reference: chr 15
allele count: 142
allele frequency: 1.169744797930705e-3
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.674G>A
  hgvsp: ENSP00000453102.1:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*756G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.632G>A
  hgvsp: ENSP00000452901.1:p.Arg211Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1223G>A
  hgvsp: ENSP00000378790.2:p.Arg408Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1223G>A
  hgvsp: ENSP00000304978.6:p.Arg408Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.674G>A
  hgvsp: ENSP00000442969.1:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1223G>A
  hgvsp: ENSP00000260363.4:p.Arg408Gln
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.837G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*279G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1223G>A
  hgvsp: ENSP00000453386.1:p.Arg408Gln
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2517
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg408Gln
num of homozygotes: 3
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

15-69728068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728068
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728068
    reference: chr 15
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*286C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.681C>T
  hgvsp: ENST00000537891.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.681C>T
  hgvsp: ENST00000558585.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1230C>T
  hgvsp: ENST00000395392.2:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1230C>T
  hgvsp: ENST00000260363.4:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1230C>T
  hgvsp: ENST00000559279.1:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.844C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1230C>T
  hgvsp: ENST00000352331.4:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.639C>T
  hgvsp: ENST00000559283.1:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile410Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

15-69728069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728069
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728069
    reference: chr 15
allele count: 70
allele frequency: 5.766252594813667e-4
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.640G>A
  hgvsp: ENSP00000452901.1:p.Val214Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1231G>A
  hgvsp: ENSP00000260363.4:p.Val411Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*764G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.682G>A
  hgvsp: ENSP00000453102.1:p.Val228Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.845G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1231G>A
  hgvsp: ENSP00000378790.2:p.Val411Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*287G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.682G>A
  hgvsp: ENSP00000442969.1:p.Val228Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1231G>A
  hgvsp: ENSP00000304978.6:p.Val411Met
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1231G>A
  hgvsp: ENSP00000453386.1:p.Val411Met
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 5924
  bin: 9.75e1
  variant carriers: 69
hgvs: p.Val411Met
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/15-69728081-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728081
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728081
    reference: chr 15
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.694C>A
  hgvsp: ENSP00000442969.1:p.Pro232Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1243C>A
  hgvsp: ENSP00000453386.1:p.Pro415Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1243C>A
  hgvsp: ENSP00000260363.4:p.Pro415Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*299C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1243C>A
  hgvsp: ENSP00000304978.6:p.Pro415Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.652C>A
  hgvsp: ENSP00000452901.1:p.Pro218Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.694C>A
  hgvsp: ENSP00000453102.1:p.Pro232Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1243C>A
  hgvsp: ENSP00000378790.2:p.Pro415Thr
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.857C>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*776C>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro415Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

15-69728085-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728085
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728085
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.656A>G
  hgvsp: ENSP00000452901.1:p.Lys219Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*303A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.698A>G
  hgvsp: ENSP00000453102.1:p.Lys233Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1247A>G
  hgvsp: ENSP00000453386.1:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1247A>G
  hgvsp: ENSP00000378790.2:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1247A>G
  hgvsp: ENSP00000260363.4:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.698A>G
  hgvsp: ENSP00000442969.1:p.Lys233Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1247A>G
  hgvsp: ENSP00000304978.6:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*780A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.861A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys416Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum

15-69728096-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728096
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728096
    reference: chr 15
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.872T>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1258T>G
  hgvsp: ENSP00000260363.4:p.Tyr420Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*314T>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.709T>G
  hgvsp: ENSP00000442969.1:p.Tyr237Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*791T>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1258T>G
  hgvsp: ENSP00000378790.2:p.Tyr420Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.667T>G
  hgvsp: ENSP00000452901.1:p.Tyr223Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.709T>G
  hgvsp: ENSP00000453102.1:p.Tyr237Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1258T>G
  hgvsp: ENSP00000304978.6:p.Tyr420Asp
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1258T>G
  hgvsp: ENSP00000453386.1:p.Tyr420Asp
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr420Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

15-69728097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728097
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728097
    reference: chr 15
allele count: 11
allele frequency: 9.06409136604097e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*315A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.873A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1259A>G
  hgvsp: ENSP00000304978.6:p.Tyr420Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.710A>G
  hgvsp: ENSP00000442969.1:p.Tyr237Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1259A>G
  hgvsp: ENSP00000260363.4:p.Tyr420Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1259A>G
  hgvsp: ENSP00000453386.1:p.Tyr420Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.668A>G
  hgvsp: ENSP00000452901.1:p.Tyr223Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1259A>G
  hgvsp: ENSP00000378790.2:p.Tyr420Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.710A>G
  hgvsp: ENSP00000453102.1:p.Tyr237Cys
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*792A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr420Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

15-69728109-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728109
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728109
    reference: chr 15
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1271T>C
  hgvsp: ENSP00000304978.6:p.Leu424Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*804T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1271T>C
  hgvsp: ENSP00000453386.1:p.Leu424Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1271T>C
  hgvsp: ENSP00000378790.2:p.Leu424Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*327T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.722T>C
  hgvsp: ENSP00000442969.1:p.Leu241Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.885T>C
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.680T>C
  hgvsp: ENSP00000452901.1:p.Leu227Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.722T>C
  hgvsp: ENSP00000453102.1:p.Leu241Ser
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1271T>C
  hgvsp: ENSP00000260363.4:p.Leu424Ser
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu424Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

15-69728120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728120
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728120
    reference: chr 15
allele count: 5
allele frequency: 4.126774513040608e-5
allele num: 121160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.691A>G
  hgvsp: ENSP00000452901.1:p.Ile231Val
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+10A>G
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+10A>G
  variant of: http://identifiers.org/hgnc/6392
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile231Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

15-69728131-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728131
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728131
    reference: chr 15
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.692+10C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+21C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+21C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6861
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

15-69728153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728153
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728153
    reference: chr 15
allele count: 6
allele frequency: 4.970178926441352e-5
allele num: 120720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.692+32C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+43C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+43C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6700
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

15-69728154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728154
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728154
    reference: chr 15
allele count: 3
allele frequency: 2.484513201046808e-5
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.692+33G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+44G>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+44G>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34579
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-69728167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728167
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728167
    reference: chr 15
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.692+46C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+57C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+57C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

15-69728171-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728171
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728171
    reference: chr 15
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.886+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1272+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.692+50G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.723+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1272+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.723+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*805+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1272+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*328+61G>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1272+61G>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3224
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

15-69728429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728429
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728429
    reference: chr 15
allele count: 1
allele frequency: 8.457804015765346e-6
allele num: 118234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*329-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.887-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.724-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.724-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1273-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1273-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.693-59C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1273-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1273-48C>T
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*806-48C>T
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3251
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-69728441-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728441
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728440
    reference: chr 15
allele count: 1
allele frequency: 8.426729586247577e-6
allele num: 118670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1273-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.724-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*329-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*806-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.724-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.693-46delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.887-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1273-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1273-35delA
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1273-35delA
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: TA
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-69728442-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728442
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728443
    reference: chr 15
allele count: 14
allele frequency: 1.255672951010817e-4
allele num: 111494
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.887-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1273-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*806-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1273-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1273-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.693-37dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.724-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1273-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*329-26dupT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.724-26dupT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15123
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD

15-69728442-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728442
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728441
    reference: chr 15
allele count: 149
allele frequency: 1.336394783575798e-3
allele num: 111494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1273-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*806-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.693-37delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1273-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.724-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1273-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.887-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1273-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.724-26delT
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*329-26delT
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 15123
  bin: 2.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 2.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 7.5e0
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 1.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 2.75e1
  variant carriers: 30
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: AT
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

15-69728451-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69728451
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 69728451
    reference: chr 15
allele count: 1
allele frequency: 8.359666282122017e-6
allele num: 119622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000442969
  ensembl transcript: ENST00000537891
  gene symbol: KIF23
  hgvsc: ENST00000537891.1:c.724-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453629
  ensembl transcript: ENST00000561089
  gene symbol: KIF23
  hgvsc: ENST00000561089.1:c.*806-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000378790
  ensembl transcript: ENST00000395392
  gene symbol: KIF23
  hgvsc: ENST00000395392.2:c.1273-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000304978
  ensembl transcript: ENST00000352331
  gene symbol: KIF23
  hgvsc: ENST00000352331.4:c.1273-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl transcript: ENST00000559456
  gene symbol: KIF23
  hgvsc: ENST00000559456.1:n.887-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000260363
  ensembl transcript: ENST00000260363
  gene symbol: KIF23
  hgvsc: ENST00000260363.4:c.1273-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453102
  ensembl transcript: ENST00000558585
  gene symbol: KIF23
  hgvsc: ENST00000558585.1:c.724-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000452901
  ensembl transcript: ENST00000559283
  gene symbol: KIF23
  hgvsc: ENST00000559283.1:c.693-37T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453386
  ensembl transcript: ENST00000559279
  gene symbol: KIF23
  hgvsc: ENST00000559279.1:c.1273-26T>A
  variant of: http://identifiers.org/hgnc/6392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137807
  ensembl protein: ENSP00000453576
  ensembl transcript: ENST00000558346
  gene symbol: KIF23
  hgvsc: ENST00000558346.1:c.*329-26T>A
  variant of: http://identifiers.org/hgnc/6392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17095
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2176
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 12294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5317
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5204
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4206
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7007
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2676
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.344809037116729e-4
allele num: 7436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42828
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

DP
type: SiteQuality
SIO_000300: 9.20157e5

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 7.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.249e-1

GenotypeQuality
all individuals: 6827
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7937
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 504
bin: 7.5e0
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1204
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3652
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 948
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 529
bin: 9.25e1
variant carriers: 5

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

African
type: Population
allele count: 252
allele frequency: 2.734375e-2
allele num: 9216
num of homozygotes: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.356116083536751e-4
allele num: 14748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57536
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 9.881422924901185e-4
allele num: 10120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.363e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

QD
type: SiteQuality
SIO_000300: 1.398e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.28051e6

GenotypeQuality
all individuals: 1224
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5621
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 468
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4705
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3563
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 10
allele frequency: 9.858044164037854e-4
allele num: 10144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.938902959442112e-5
allele num: 57646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.513e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.291325e6

GenotypeQuality
all individuals: 6464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3377
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4868
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6731
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 478
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variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 543
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variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.082251082251082e-4
allele num: 9240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14868
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

DP
type: SiteQuality
SIO_000300: 1.301929e6

VQSLOD
type: SiteQuality
SIO_000300: 9.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

GenotypeQuality
all individuals: 6867
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
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variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
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variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6635
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14886
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.358326541700625e-4
allele num: 7362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.392e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.320674e6

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
all individuals: 640
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30948
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
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variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5167
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4928
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.603488674824265e-4
allele num: 15364
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.649729444371123e-5
allele num: 60616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 1.510525e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

GenotypeQuality
all individuals: 4593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5189
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32823
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628452318916102e-5
allele num: 61408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.002e0

DP
type: SiteQuality
SIO_000300: 1.534936e6

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.711e1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1447
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 821
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 562
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variant carriers: 2

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 5562
bin: 9.75e1
variant carriers: 892

GenotypeQuality
all individuals: 3083
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 7.25e1
variant carriers: 5

GenotypeQuality
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bin: 7.75e1
variant carriers: 3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5568
bin: 6.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 445
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1331
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.25e1
variant carriers: 2

South Asian
type: Population
allele count: 3
allele frequency: 1.904761904761905e-4
allele num: 15750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

African
type: Population
allele count: 852
allele frequency: 8.511488511488512e-2
allele num: 10010
num of homozygotes: 32

Latino
type: Population
allele count: 73
allele frequency: 6.608727141046533e-3
allele num: 11046
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.83371298405467e-3
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.972289309775009e-4
allele num: 62936
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.2306177701206e-4
allele num: 8126
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

DP
type: SiteQuality
SIO_000300: 1.603974e6

FS
type: SiteQuality
SIO_000300: 7.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 1.197e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.569999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

GenotypeQuality
all individuals: 1701
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 940
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5562
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15750
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.996003996003996e-4
allele num: 10010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

DP
type: SiteQuality
SIO_000300: 1.603974e6

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.569999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 1.197e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
all individuals: 391
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 206
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GenotypeQuality
all individuals: 316
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 901
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.676953784738216e-5
allele num: 65130
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.999e0

QD
type: SiteQuality
SIO_000300: 1.1e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.151e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

DP
type: SiteQuality
SIO_000300: 1.651954e6

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6806
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variant carriers: 0

GenotypeQuality
all individuals: 39324
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variant carriers: 0

GenotypeQuality
all individuals: 797
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 183
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5176
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008061605101673e-5
allele num: 66488
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.443e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.687287e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.438e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

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

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

GenotypeQuality
all individuals: 2041
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variant carriers: 0

GenotypeQuality
all individuals: 39322
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 166
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5194
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 2891
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 798
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variant carriers: 0

GenotypeQuality
all individuals: 6816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.152772721757068e-3
allele num: 16482
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.68822e6

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.95e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 807
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 2320
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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
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 39357
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variant carriers: 0

GenotypeQuality
all individuals: 2049
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

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

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

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

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: 11554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.489e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

QD
type: SiteQuality
SIO_000300: 6.55e0

DP
type: SiteQuality
SIO_000300: 1.689321e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.829e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2924
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GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 810
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 4.75e1
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GenotypeQuality
all individuals: 21
bin: 3.25e1
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GenotypeQuality
all individuals: 6876
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variant carriers: 0

GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.239e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.013e1

DP
type: SiteQuality
SIO_000300: 1.691355e6

GenotypeQuality
all individuals: 24
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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
all individuals: 809
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GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.55e-1

DP
type: SiteQuality
SIO_000300: 1.691634e6

ReadPosRankSum
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SIO_000300: -6.42e-1

VQSLOD
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MQ
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ClippingRankSum
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SIO_000300: 2.55e-1

MQRankSum
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SIO_000300: 1.9e0

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

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

South Asian
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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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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

East Asian
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Other
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DP
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: -1.006e0

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

Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
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allele frequency: 1.156604210039325e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 906
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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
allele num: 6614
num of homozygotes: 0

South Asian
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DP
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.04e-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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

African
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allele frequency: 6.73076923076923e-4
allele num: 10400
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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MQRankSum
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SIO_000300: -2.53e-1

ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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QD
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ClippingRankSum
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SIO_000300: -1.87e-1

BaseQRankSum
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VQSLOD
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SIO_000300: 2.04e0

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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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Latino
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num of homozygotes: 0

East Asian
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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FS
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VQSLOD
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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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variant carriers: 0

Latino
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num of homozygotes: 0

European (Finnish)
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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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East Asian
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MQRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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VQSLOD
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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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East Asian
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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 frequency: 2.249820014398848e-4
allele num: 66672
num of homozygotes: 1

Other
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allele frequency: 0.0e0
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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ClippingRankSum
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DP
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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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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

African
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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QD
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MQ
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InbreedingCoeff
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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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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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South Asian
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African
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allele num: 10404
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Other
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European (Non-Finnish)
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MQRankSum
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SIO_000300: -1.4e-2

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

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 8.481764206955047e-4
allele num: 16506
num of homozygotes: 0

Latino
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Other
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num of homozygotes: 0

European (Finnish)
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MQRankSum
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MQ
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.25e-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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African
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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QD
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InbreedingCoeff
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FS
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MQRankSum
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DP
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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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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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European (Finnish)
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Other
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MQ
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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Latino
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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South Asian
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6929
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.451902108068815e-4
allele num: 16508
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.05e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.758e0

VQSLOD
type: SiteQuality
SIO_000300: 9.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.343e1

GenotypeQuality
all individuals: 2389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

DP
type: SiteQuality
SIO_000300: 1.699523e6

FS
type: SiteQuality
SIO_000300: 7.248e0

VQSLOD
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SIO_000300: 4.25e-1

MQRankSum
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SIO_000300: -4.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.494e1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

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

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
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.061e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.700288e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.887e0

FS
type: SiteQuality
SIO_000300: 6.053e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.68e-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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2045
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.155361319709468e-5
allele num: 16246
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509753004408479e-5
allele num: 66236
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.287e0

QD
type: SiteQuality
SIO_000300: 3.86e0

DP
type: SiteQuality
SIO_000300: 1.742651e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16246
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 3.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 1.742651e6

FS
type: SiteQuality
SIO_000300: 1.287e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 183
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variant carriers: 2

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 455
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variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.84660839591284e-4
allele num: 16246
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019506008816958e-5
allele num: 66236
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 1.287e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.742651e6

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

QD
type: SiteQuality
SIO_000300: 3.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-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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variant carriers: 268

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.499745043342632e-4
allele num: 66678
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 16
allele frequency: 1.382886776145203e-3
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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African
type: Population
allele count: 243
allele frequency: 2.335191235825485e-2
allele num: 10406
num of homozygotes: 3

Other
type: Population
allele count: 2
allele frequency: 2.212389380530973e-3
allele num: 904
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QD
type: SiteQuality
SIO_000300: 1.386e1

BaseQRankSum
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SIO_000300: -2.29e-1

MQRankSum
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SIO_000300: 3.45e-1

DP
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SIO_000300: 1.746048e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.81e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
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SIO_000300: 6.889999999999999e-1

GenotypeQuality
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variant carriers: 3

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: 4.85e-1

BaseQRankSum
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1112
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.726888333653661e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.740416e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

QD
type: SiteQuality
SIO_000300: 1.372e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

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

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5782
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1111
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37322
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.740355e6

FS
type: SiteQuality
SIO_000300: 4.039e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.338e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

FS
type: SiteQuality
SIO_000300: 1.045e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

DP
type: SiteQuality
SIO_000300: 1.741503e6

VQSLOD
type: SiteQuality
SIO_000300: -1.147e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.33e-1

QD
type: SiteQuality
SIO_000300: 1.61e1

GenotypeDepth
all individuals: 1270
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5784
bin: 9.75e1
variant carriers: 2

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998231043684226e-5
allele num: 66706
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

FS
type: SiteQuality
SIO_000300: 2.526e0

DP
type: SiteQuality
SIO_000300: 1.742085e6

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

QD
type: SiteQuality
SIO_000300: 1.649e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.014e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37554
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5791
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 1.912e0

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.345e0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

DP
type: SiteQuality
SIO_000300: 1.743208e6

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeQuality
all individuals: 2304
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 3261
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2519
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5791
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1117
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

FS
type: SiteQuality
SIO_000300: 3.716e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.744042e6

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2518
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

QD
type: SiteQuality
SIO_000300: 1.584e1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

DP
type: SiteQuality
SIO_000300: 1.744193e6

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

QD
type: SiteQuality
SIO_000300: 1.584e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 5.35e-1

DP
type: SiteQuality
SIO_000300: 1.744193e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.76e-1

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5794
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7049
bin: 6.75e1
variant carriers: 0

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

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

African
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European (Non-Finnish)
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South Asian
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East Asian
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QD
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MQ
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DP
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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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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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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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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South Asian
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Other
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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East Asian
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Latino
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European (Finnish)
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Other
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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East Asian
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European (Finnish)
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Other
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ReadPosRankSum
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DP
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MQ
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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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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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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South Asian
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FS
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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Other
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FS
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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Other
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South Asian
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ClippingRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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European (Non-Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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ClippingRankSum
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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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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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African
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European (Finnish)
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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Other
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FS
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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allele num: 66692
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Latino
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East Asian
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South Asian
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Other
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QD
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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Latino
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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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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European (Non-Finnish)
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African
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Other
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Latino
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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FS
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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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African
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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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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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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Latino
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European (Finnish)
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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SIO_000300: 5.498e0

DP
type: SiteQuality
SIO_000300: 1.715393e6

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.178942165101334e-5
allele num: 16184
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.474e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.492e0

FS
type: SiteQuality
SIO_000300: 3.662e0

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.708472e6

MQ
type: SiteQuality
SIO_000300: 5.849e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.41e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.168e0

VQSLOD
type: SiteQuality
SIO_000300: 8.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

FS
type: SiteQuality
SIO_000300: 1.904e0

DP
type: SiteQuality
SIO_000300: 1.710618e6

GenotypeQuality
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3111
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variant carriers: 0

GenotypeQuality
all individuals: 3354
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.203473945409429e-5
allele num: 16120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
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: 11358
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.498e1

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.78979e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.087e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.922e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 3507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 809
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variant carriers: 0

GenotypeQuality
all individuals: 6666
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GenotypeQuality
all individuals: 2277
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4323
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variant carriers: 0

GenotypeQuality
all individuals: 17517
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533224985434363e-5
allele num: 65222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
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: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.77e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.852689e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

FS
type: SiteQuality
SIO_000300: 1.315e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 3080
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1731
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2862
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variant carriers: 1

GenotypeQuality
all individuals: 1964
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1629
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variant carriers: 2

GenotypeQuality
all individuals: 1564
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.214075010535188e-4
allele num: 14238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.300474673255738e-4
allele num: 61516
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 1.921818e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.775e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

FS
type: SiteQuality
SIO_000300: 3.12e0

QD
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeQuality
all individuals: 1731
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2134
bin: 3.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3080
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 1.75e1
variant carriers: 20

GenotypeQuality
all individuals: 2862
bin: 7.25e1
variant carriers: 4

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 2050
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GenotypeQuality
all individuals: 2159
bin: 2.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1964
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variant carriers: 16

GenotypeQuality
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bin: 3.25e1
variant carriers: 28

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 4

GenotypeQuality
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bin: 5.25e1
variant carriers: 10

GenotypeQuality
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bin: 7.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1564
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1629
bin: 4.25e1
variant carriers: 12

Latino
type: Population
allele count: 12
allele frequency: 1.120448179271709e-3
allele num: 10710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 35
allele frequency: 2.458210422812193e-3
allele num: 14238
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.249063202598052e-3
allele num: 8006
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.10494721589733e-4
allele num: 9662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 89
allele frequency: 1.446778073997009e-3
allele num: 61516
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 3.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 1.921818e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.775e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

GenotypeQuality
all individuals: 701
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 485
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 17595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 9.25e1
variant carriers: 0