14-23417179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417179
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417179
    reference: chr 14
allele count: 4
allele frequency: 3.449465332873405e-5
allele num: 115960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.135C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.471C>T
  hgvsp: ENST00000555986.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.846C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.606C>T
  hgvsp: ENST00000555040.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.606C>T
  hgvsp: ENST00000541587.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.234C>T
  hgvsp: ENST00000490506.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.648C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.606C>T
  hgvsp: ENST00000206474.7:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.471C>T
  hgvsp: ENST00000342454.8:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-239C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6361G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-239C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.94C>T
  hgvsp: ENST00000555074.1:c.94C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.471C>T
  hgvsp: ENST00000555367.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.487C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.806C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7160G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.265C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-239C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-239C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu32Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

14-23417188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417188
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417188
    reference: chr 14
allele count: 1
allele frequency: 8.938307799567386e-6
allele num: 111878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-248G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.837G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-248G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.797G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.126G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.478G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.597G>A
  hgvsp: ENST00000541587.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.597G>A
  hgvsp: ENST00000206474.7:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.462G>A
  hgvsp: ENST00000342454.8:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.462G>A
  hgvsp: ENST00000555367.1:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.597G>A
  hgvsp: ENST00000555040.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.225G>A
  hgvsp: ENST00000490506.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.462G>A
  hgvsp: ENST00000555986.1:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-248G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6352C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-248G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.256G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-248G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.85G>A
  hgvsp: ENST00000555074.1:c.85G>A(p.%3D)
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7151C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val29Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-23417194-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417194
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417194
    reference: chr 14
allele count: 1
allele frequency: 9.220158955540394e-6
allele num: 108458
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.79A>G
  hgvsp: ENST00000555074.1:c.79A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.591A>G
  hgvsp: ENST00000555040.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.219A>G
  hgvsp: ENST00000490506.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.456A>G
  hgvsp: ENST00000555367.1:c.456A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.456A>G
  hgvsp: ENST00000342454.8:c.456A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.120A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.456A>G
  hgvsp: ENST00000555986.1:c.456A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-254A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.591A>G
  hgvsp: ENST00000206474.7:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.591A>G
  hgvsp: ENST00000541587.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.472A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-254A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.831A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.250A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7145T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.791A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-254A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-254A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-254A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.633A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala27Ala
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

14-23417194-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417194
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417194
    reference: chr 14
allele count: 1
allele frequency: 9.220158955540394e-6
allele num: 108458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-254A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-254A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.591A>C
  hgvsp: ENST00000206474.7:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.633A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.120A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.79A>C
  hgvsp: ENST00000555074.1:c.79A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.791A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.219A>C
  hgvsp: ENST00000490506.1:c.219A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.456A>C
  hgvsp: ENST00000555986.1:c.456A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.456A>C
  hgvsp: ENST00000342454.8:c.456A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-254A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.591A>C
  hgvsp: ENST00000541587.1:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-254A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.831A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.472A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.250A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6346T>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7145T>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.456A>C
  hgvsp: ENST00000555367.1:c.456A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.591A>C
  hgvsp: ENST00000555040.1:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala27Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

14-23417201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417201
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417201
    reference: chr 14
allele count: 4
allele frequency: 3.971248163297724e-5
allele num: 100724
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.465A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.584A>G
  hgvsp: ENSP00000206474.7:p.Lys195Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-261A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.626A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.784A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.243A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.113A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-261A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-261A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7138T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.584A>G
  hgvsp: ENSP00000452165.1:p.Lys195Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.449A>G
  hgvsp: ENSP00000451018.1:p.Lys150Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.449A>G
  hgvsp: ENSP00000452239.1:p.Lys150Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.584A>G
  hgvsp: ENSP00000441026.1:p.Lys195Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-261A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6339T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.212A>G
  hgvsp: ENSP00000452260.1:p.Lys71Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.449A>G
  hgvsp: ENSP00000342776.8:p.Lys150Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.72A>G
  hgvsp: ENSP00000450856.2:p.Lys25Arg
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-261A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys25Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

14-23417205-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417205
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417204
    reference: chr 14
allele count: 1
allele frequency: 1.005854070691424e-5
allele num: 99418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.579delC
  hgvsp: ENSP00000452165.1:p.Val194Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.460delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.207delC
  hgvsp: ENSP00000452260.1:p.Val70Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7132delG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.779delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.621delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.108delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-266delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.67delC
  hgvsp: ENSP00000450856.2:p.Val24Ter
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.819delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-266delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.579delC
  hgvsp: ENSP00000206474.7:p.Val194Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.444delC
  hgvsp: ENSP00000452239.1:p.Val149Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.444delC
  hgvsp: ENSP00000451018.1:p.Val149Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.444delC
  hgvsp: ENSP00000342776.8:p.Val149Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6333delG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-266delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.579delC
  hgvsp: ENSP00000441026.1:p.Val194Ter
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-266delC
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-266delC
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val24Ter
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: CG
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

14-23417206-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417206
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417206
    reference: chr 14
allele count: 5
allele frequency: 5.072434362699347e-5
allele num: 98572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.108C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-266C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.579C>T
  hgvsp: ENST00000555040.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.67C>T
  hgvsp: ENST00000555074.1:c.67C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.444C>T
  hgvsp: ENST00000555986.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.460C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-266C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.444C>T
  hgvsp: ENST00000342454.8:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.444C>T
  hgvsp: ENST00000555367.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.819C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.207C>T
  hgvsp: ENST00000490506.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.579C>T
  hgvsp: ENST00000541587.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.238C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.579C>T
  hgvsp: ENST00000206474.7:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7133G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.621C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6334G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-266C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-266C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr23Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

14-23417216-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417216
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417216
    reference: chr 14
allele count: 8
allele frequency: 8.813096261043911e-5
allele num: 90774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.569A>C
  hgvsp: ENSP00000452165.1:p.Asp190Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.769A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.434A>C
  hgvsp: ENSP00000452239.1:p.Asp145Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.98A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6324T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.197A>C
  hgvsp: ENSP00000452260.1:p.Asp66Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.228A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.450A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.57A>C
  hgvsp: ENSP00000450856.2:p.Asp20Ala
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.434A>C
  hgvsp: ENSP00000342776.8:p.Asp145Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-276A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-276A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.434A>C
  hgvsp: ENSP00000451018.1:p.Asp145Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.569A>C
  hgvsp: ENSP00000441026.1:p.Asp190Ala
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.809A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-276A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-276A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-276A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7123T>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.569A>C
  hgvsp: ENSP00000206474.7:p.Asp190Ala
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp20Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-23417218-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417218
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417218
    reference: chr 14
allele count: 1
allele frequency: 1.142622089170228e-5
allele num: 87518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.567T>G
  hgvsp: ENST00000541587.1:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.567T>G
  hgvsp: ENST00000555040.1:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.609T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.432T>G
  hgvsp: ENST00000342454.8:c.432T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.432T>G
  hgvsp: ENST00000555986.1:c.432T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.807T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.195T>G
  hgvsp: ENST00000490506.1:c.195T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.96T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-278T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.567T>G
  hgvsp: ENST00000206474.7:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.226T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6322A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-278T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.55T>G
  hgvsp: ENST00000555074.1:c.55T>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.432T>G
  hgvsp: ENST00000555367.1:c.432T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.767T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-278T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7121A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-278T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.448T>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala19Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-23417236-C-CAGAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417236
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417240
    reference: chr 14
allele count: 5
allele frequency: 6.814402922015973e-5
allele num: 73374
alternate allele: CAGAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6303_195-6300dupAGAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-300_450-297dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-18_428-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.74_77dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-18_563-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.204_207dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.785_788dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.587_590dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.426_429dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-300_331-297dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-18_51-15dupCTCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-18_563-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-18_563-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-18_428-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-300_428-297dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-300_331-297dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-300_311-297dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.745_748dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-18_428-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7102_159-7099dupAGAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-18_191-15dupCTCT
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

14-23417236-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417236
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417236
    reference: chr 14
allele count: 1183
allele frequency: 1.612287731348979e-2
allele num: 73374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6304C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-296G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-296G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.591G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.430G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.208G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-296G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.78G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7103C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.789G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-296G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.749G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-14G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-14G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-296G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-14G>C
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 80
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

14-23417255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417255
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417255
    reference: chr 14
allele count: 2
allele frequency: 3.695764653706852e-5
allele num: 54116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.59G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-315G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-315G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7084C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-315G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-13G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.189G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.783-13G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-315G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-315G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.585-13G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6285C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-33G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-33G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.743-13G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

14-23417258-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417258
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417258
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 50994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.56A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6282T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-318A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.585-16A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-16A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.186A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7081T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-36A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.783-16A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-318A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-318A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.743-16A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-36A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-318A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-318A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-36A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-23417269-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417269
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417269
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 39438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-329T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.783-27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.175T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.585-27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.743-27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-329T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-329T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6271A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-329T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-329T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7070A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-47T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-47T>C
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-23417271-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23417271
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23417271
    reference: chr 14
allele count: 1
allele frequency: 2.646903123345685e-5
allele num: 37780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554063
  gene symbol: HAUS4
  hgvsc: ENST00000554063.1:n.43G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.743-29G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-29G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.428-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-7068C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-6269C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000556421
  gene symbol: HAUS4
  hgvsc: ENST00000556421.1:n.173G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.311-331G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.191-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.331-331G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.331-331G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.428-331G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.428-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.563-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.563-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.783-29G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-49G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.585-29G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.428-49G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.450-331G>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.563-49G>T
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

14-23419474-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419474
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419474
    reference: chr 14
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.427+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2232G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4865C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.562+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.742+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.310+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+2063G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.584+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.427+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-4066C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+2063G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.562+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.190+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.449+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.427+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.427+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.782+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.562+49G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2252G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

14-23419480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419480
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419480
    reference: chr 14
allele count: 2
allele frequency: 1.658402295228776e-5
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.562+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.742+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.562+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.562+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.427+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+2057G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-4060C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.427+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.310+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+2057G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.427+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.449+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4859C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.427+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.782+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2238G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.190+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.584+43G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2258G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-23419505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419505
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419505
    reference: chr 14
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.427+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.449+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.584+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.782+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.742+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.562+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.190+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+2032G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.562+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2263G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2283G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+2032G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.310+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.562+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.427+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-4035C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.427+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4834C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.427+18G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

14-23419516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419516
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419516
    reference: chr 14
allele count: 5
allele frequency: 4.126433935792688e-5
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2294G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.562+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+2021G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.449+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.562+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.310+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.584+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.427+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.562+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+2021G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4823C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.427+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.742+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.427+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-4024C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.190+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.782+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2274G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.427+7G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.562+7G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

14-23419537-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419537
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419537
    reference: chr 14
allele count: 383
allele frequency: 3.157408781388601e-3
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.548A>G
  hgvsp: ENSP00000452165.1:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4802T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.548A>G
  hgvsp: ENSP00000452261.1:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2295A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.413A>G
  hgvsp: ENSP00000342776.8:p.Tyr138Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.413A>G
  hgvsp: ENSP00000451018.1:p.Tyr138Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.296A>G
  hgvsp: ENSP00000450542.1:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-4003T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.413A>G
  hgvsp: ENSP00000452239.1:p.Tyr138Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.176A>G
  hgvsp: ENSP00000452260.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.570A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.435A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.548A>G
  hgvsp: ENSP00000206474.7:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.768A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.728A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+2000A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.413A>G
  hgvsp: ENSP00000452595.1:p.Tyr138Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+2000A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.548A>G
  hgvsp: ENSP00000441026.1:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2315A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr183Cys
num of homozygotes: 8
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-23419547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419547
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419547
    reference: chr 14
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4792G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2305C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.403C>T
  hgvsp: ENSP00000451018.1:p.Leu135Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.286C>T
  hgvsp: ENSP00000450542.1:p.Leu96Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.538C>T
  hgvsp: ENSP00000206474.7:p.Leu180Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.718C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.403C>T
  hgvsp: ENSP00000342776.8:p.Leu135Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.538C>T
  hgvsp: ENSP00000452165.1:p.Leu180Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.758C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.403C>T
  hgvsp: ENSP00000452239.1:p.Leu135Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.538C>T
  hgvsp: ENSP00000441026.1:p.Leu180Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.166C>T
  hgvsp: ENSP00000452260.1:p.Leu56Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3993G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.538C>T
  hgvsp: ENSP00000452261.1:p.Leu180Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1990C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.403C>T
  hgvsp: ENSP00000452595.1:p.Leu135Phe
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1990C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.560C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2325C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.425C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu180Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

14-23419564-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419564
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419564
    reference: chr 14
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.386A>C
  hgvsp: ENSP00000342776.8:p.Lys129Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.521A>C
  hgvsp: ENSP00000452165.1:p.Lys174Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1973A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.741A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.701A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.521A>C
  hgvsp: ENSP00000452261.1:p.Lys174Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.386A>C
  hgvsp: ENSP00000452239.1:p.Lys129Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.521A>C
  hgvsp: ENSP00000441026.1:p.Lys174Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.386A>C
  hgvsp: ENSP00000451018.1:p.Lys129Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.521A>C
  hgvsp: ENSP00000206474.7:p.Lys174Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3976T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.543A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.149A>C
  hgvsp: ENSP00000452260.1:p.Lys50Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.269A>C
  hgvsp: ENSP00000450542.1:p.Lys90Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.408A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2342A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1973A>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4775T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.386A>C
  hgvsp: ENSP00000452595.1:p.Lys129Thr
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2322A>C
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys174Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

14-23419588-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419588
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419588
    reference: chr 14
allele count: 2
allele frequency: 1.649647800194658e-5
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.362A>G
  hgvsp: ENSP00000452595.1:p.Gln121Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.125A>G
  hgvsp: ENSP00000452260.1:p.Gln42Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.362A>G
  hgvsp: ENSP00000452239.1:p.Gln121Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.519A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.497A>G
  hgvsp: ENSP00000452165.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.677A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.497A>G
  hgvsp: ENSP00000206474.7:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2366A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.362A>G
  hgvsp: ENSP00000342776.8:p.Gln121Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.362A>G
  hgvsp: ENSP00000451018.1:p.Gln121Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.717A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.245A>G
  hgvsp: ENSP00000450542.1:p.Gln82Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3952T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4751T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.497A>G
  hgvsp: ENSP00000441026.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.497A>G
  hgvsp: ENSP00000452261.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1949A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.384A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2346A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1949A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln166Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

14-23419597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419597
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419597
    reference: chr 14
allele count: 3
allele frequency: 2.475451769948015e-5
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.488G>A
  hgvsp: ENSP00000452165.1:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.668G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.236G>A
  hgvsp: ENSP00000450542.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.353G>A
  hgvsp: ENSP00000451018.1:p.Arg118Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3943C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.353G>A
  hgvsp: ENSP00000452239.1:p.Arg118Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4742C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.488G>A
  hgvsp: ENSP00000452261.1:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.488G>A
  hgvsp: ENSP00000206474.7:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.353G>A
  hgvsp: ENSP00000452595.1:p.Arg118Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1940G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.510G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.488G>A
  hgvsp: ENSP00000441026.1:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.116G>A
  hgvsp: ENSP00000452260.1:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.353G>A
  hgvsp: ENSP00000342776.8:p.Arg118Gln
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1940G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2375G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.375G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.708G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2355G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg163Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

14-23419598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419598
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419598
    reference: chr 14
allele count: 31
allele frequency: 2.55822013896912e-4
allele num: 121178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.352C>T
  hgvsp: ENSP00000451018.1:p.Arg118Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1939C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.487C>T
  hgvsp: ENSP00000452261.1:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.235C>T
  hgvsp: ENSP00000450542.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.487C>T
  hgvsp: ENSP00000452165.1:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4741G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.352C>T
  hgvsp: ENSP00000342776.8:p.Arg118Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.352C>T
  hgvsp: ENSP00000452595.1:p.Arg118Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.352C>T
  hgvsp: ENSP00000452239.1:p.Arg118Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.487C>T
  hgvsp: ENSP00000441026.1:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3942G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.509C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.115C>T
  hgvsp: ENSP00000452260.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.667C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.487C>T
  hgvsp: ENSP00000206474.7:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2376C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.707C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1939C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.374C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2356C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg163Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

14-23419603-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419603
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419603
    reference: chr 14
allele count: 132
allele frequency: 1.09002625972353e-3
allele num: 121098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.110G>A
  hgvsp: ENSP00000452260.1:p.Arg37Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2381G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.347G>A
  hgvsp: ENSP00000451018.1:p.Arg116Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3937C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4736C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.482G>A
  hgvsp: ENSP00000452165.1:p.Arg161Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.482G>A
  hgvsp: ENSP00000452261.1:p.Arg161Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.230G>A
  hgvsp: ENSP00000450542.1:p.Arg77Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.347G>A
  hgvsp: ENSP00000452239.1:p.Arg116Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.482G>A
  hgvsp: ENSP00000441026.1:p.Arg161Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.482G>A
  hgvsp: ENSP00000206474.7:p.Arg161Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1934G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.702G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.347G>A
  hgvsp: ENSP00000342776.8:p.Arg116Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.347G>A
  hgvsp: ENSP00000452595.1:p.Arg116Lys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2361G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1934G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.662G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.504G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.369G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg161Lys
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: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

14-23419605-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419605
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419605
    reference: chr 14
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1932G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4734C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.480G>A
  hgvsp: ENSP00000206474.7:p.Met160Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.367G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.228G>A
  hgvsp: ENSP00000450542.1:p.Met76Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.480G>A
  hgvsp: ENSP00000452165.1:p.Met160Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.660G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.480G>A
  hgvsp: ENSP00000452058.1:p.Met160Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.345G>A
  hgvsp: ENSP00000451018.1:p.Met115Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.345G>A
  hgvsp: ENSP00000452239.1:p.Met115Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2363G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.345G>A
  hgvsp: ENSP00000342776.8:p.Met115Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1932G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.108G>A
  hgvsp: ENSP00000452260.1:p.Met36Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.502G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.345G>A
  hgvsp: ENSP00000452595.1:p.Met115Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3935C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2383G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.480G>A
  hgvsp: ENSP00000452261.1:p.Met160Ile
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.700G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met160Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

14-23419608-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419608
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419608
    reference: chr 14
allele count: 5
allele frequency: 4.130661070997802e-5
allele num: 121046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.477G>C
  hgvsp: ENSP00000441026.1:p.Trp159Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.477G>C
  hgvsp: ENSP00000206474.7:p.Trp159Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.477G>C
  hgvsp: ENSP00000452165.1:p.Trp159Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.105G>C
  hgvsp: ENSP00000452260.1:p.Trp35Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4731C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.499G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.657G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.477G>C
  hgvsp: ENSP00000452058.1:p.Trp159Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1929G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.477G>C
  hgvsp: ENSP00000452261.1:p.Trp159Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.342G>C
  hgvsp: ENSP00000342776.8:p.Trp114Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.364G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.697G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2366G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.342G>C
  hgvsp: ENSP00000451018.1:p.Trp114Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.342G>C
  hgvsp: ENSP00000452239.1:p.Trp114Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.225G>C
  hgvsp: ENSP00000450542.1:p.Trp75Cys
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1929G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2386G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.342G>C
  hgvsp: ENSP00000452595.1:p.Trp114Cys
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Trp159Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

14-23419621-TAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419621
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419619
    reference: chr 14
allele count: 2
allele frequency: 1.658869977771142e-5
allele num: 120564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-4_466-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-4_94-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-4_331-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-4_466-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-4_466-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-4_466-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-4_488-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-4_686-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-4_214-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-4_646-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4716_159-4715delCA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-4_331-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3917_195-3916delCA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-4_331-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-4_466-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-4_331-3delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1914_330+1915delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2381_424-2380delGT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2401_51-2400delGT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-4_353-3delGT
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.466-4_466-3delGT
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: TAC
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

14-23419625-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419625
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419625
    reference: chr 14
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1912C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4714G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3915G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2383C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1912C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-6C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.466-6C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-23419629-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419629
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419629
    reference: chr 14
allele count: 4
allele frequency: 3.332278111931222e-5
allele num: 120038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2387A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3911T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2407A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1908A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4710T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-10A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1908A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-10A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-23419640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419640
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419640
    reference: chr 14
allele count: 1
allele frequency: 8.424599831508003e-6
allele num: 118700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4699G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2418C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1897C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1897C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2398C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-21C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3900G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-21C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

14-23419649-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419649
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419649
    reference: chr 14
allele count: 1
allele frequency: 8.486514927779759e-6
allele num: 117834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2407G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1888G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3891C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4690C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1888G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2427G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-30G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-30G>C
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum

14-23419649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419649
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419649
    reference: chr 14
allele count: 13
allele frequency: 1.103246940611368e-4
allele num: 117834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1888G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2407G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4690C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1888G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2427G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3891C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-30G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-30G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-23419650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419650
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419650
    reference: chr 14
allele count: 5
allele frequency: 4.25032727520019e-5
allele num: 117638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1887C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1887C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2408C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2428C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4689G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3890G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-31C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-31C>T
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

14-23419653-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419653
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419653
    reference: chr 14
allele count: 1
allele frequency: 8.511797351128664e-6
allele num: 117484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1884A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2411A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3887T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2431A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4686T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-34A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1884A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

14-23419657-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419657
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419657
    reference: chr 14
allele count: 1
allele frequency: 8.580597552813579e-6
allele num: 116542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4682C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1880G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2435G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1880G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3883C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-38G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2415G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-38G>C
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-23419660-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419660
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419660
    reference: chr 14
allele count: 1
allele frequency: 8.607481623026734e-6
allele num: 116178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2418A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3880T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1877A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2438A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1877A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4679T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-41A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-41A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

14-23419662-A-AAAACTAGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419662
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419670
    reference: chr 14
allele count: 1
allele frequency: 8.626192571122958e-6
allele num: 115926
alternate allele: AAAACTAGG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

14-23419664-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23419664
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23419664
    reference: chr 14
allele count: 1
allele frequency: 8.687493484379887e-6
allele num: 115108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.466-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.466-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.466-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.94-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.331-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.331-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.353-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.214-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.646-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-3876A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+1873T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-4675A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-2422T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.686-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.488-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.331-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+1873T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.466-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.331-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.466-45T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-2442T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

14-23420687-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420687
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420687
    reference: chr 14
allele count: 1
allele frequency: 1.259509295178599e-5
allele num: 79396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3465A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2853T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3652T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3445A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+850A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+77A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+77A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/14-23420690-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420690
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420691
    reference: chr 14
allele count: 16
allele frequency: 2.183644502674965e-4
allele num: 73272
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3641dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3469dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3449dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+846dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2842dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+73dupT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+846dupT
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23420690-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420690
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420689
    reference: chr 14
allele count: 15
allele frequency: 2.047166721257779e-4
allele num: 73272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3449delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3469delT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3641delA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2842delA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+73delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+846delT
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CA
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/14-23420691-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420691
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420691
    reference: chr 14
allele count: 26
allele frequency: 3.488902605941869e-4
allele num: 74522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3449T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3469T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3648A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2849A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+73T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+846T>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

14-23420696-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420696
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420696
    reference: chr 14
allele count: 1
allele frequency: 1.213444970270598e-5
allele num: 82410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3454T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3643A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2844A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3474T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+68T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+841T>C
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23420698-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420698
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420697
    reference: chr 14
allele count: 5
allele frequency: 6.06060606060606e-5
allele num: 82500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3457delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3640delC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3477delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2841delC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+65delG
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+838delG
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: AC
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-23420699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420699
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420699
    reference: chr 14
allele count: 2
allele frequency: 2.437716347325825e-5
allele num: 82044
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3477G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2841C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3640C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3457G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+65G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+838G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

14-23420709-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420709
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420709
    reference: chr 14
allele count: 20
allele frequency: 2.236836218852056e-4
allele num: 89412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3467T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.*22T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3630A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+828T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+55T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3487T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2831A>G
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
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: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

14-23420712-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420712
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420712
    reference: chr 14
allele count: 1
allele frequency: 1.074344649763644e-5
allele num: 93080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.*19A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3470A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3627T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3490A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+825A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2828T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+52A>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+825A>T
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

14-23420712-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420712
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420712
    reference: chr 14
allele count: 2
allele frequency: 2.148689299527288e-5
allele num: 93080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3470A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2828T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3490A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3627T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+52A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+825A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+52A>G
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

14-23420714-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420714
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420714
    reference: chr 14
allele count: 3
allele frequency: 3.146369090070059e-5
allele num: 95348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3472C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3625G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2826G>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3492C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+823C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+50C>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+50C>A
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-23420723-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420723
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420723
    reference: chr 14
allele count: 1
allele frequency: 9.453582907922103e-6
allele num: 105780
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.*8T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2817A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3481T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3616A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+41T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3501T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+814T>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+41T>G
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

14-23420737-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420737
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420737
    reference: chr 14
allele count: 1
allele frequency: 8.608222574202878e-6
allele num: 116168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.437T>C
  hgvsp: ENST00000553420.1:c.437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3495T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+800T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3602A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+27T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2803A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3515T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+27T>C
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn146Asn
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-23420746-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420746
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420746
    reference: chr 14
allele count: 1
allele frequency: 8.426161546369167e-6
allele num: 118678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3504G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3524G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.428G>A
  hgvsp: ENST00000553420.1:c.428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3593C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+18G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2794C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+791G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+18G>A
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu143Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

14-23420748-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420748
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420748
    reference: chr 14
allele count: 5
allele frequency: 4.198646356414692e-5
allele num: 119086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.426T>C
  hgvsp: ENST00000553420.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3506T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3591A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3526T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+789T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+16T>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+16T>C
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu143Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

14-23420752-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420752
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420752
    reference: chr 14
allele count: 1
allele frequency: 8.362182864214875e-6
allele num: 119586
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3510G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2788C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.422G>C
  hgvsp: ENSP00000450612.1:p.Glu141Asp
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3530G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+12G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+785G>C
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+12G>C
  variant of: http://identifiers.org/hgnc/20163
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu141Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-23420757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420757
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420757
    reference: chr 14
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3535G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.417G>A
  hgvsp: ENSP00000450612.1:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3582C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+780G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3515G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+7G>A
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2783C>T
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly140Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

14-23420758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420758
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420758
    reference: chr 14
allele count: 3
allele frequency: 2.496463343596572e-5
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3581G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.465+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.465+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.213+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.465+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.465+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.416C>T
  hgvsp: ENST00000553420.1:c.416C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.685+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3536C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.465+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.645+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3516C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+779C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.93+6C>T
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2782G>A
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.465+6C>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

14-23420770-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420770
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420770
    reference: chr 14
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.679C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.459C>G
  hgvsp: ENST00000554516.1:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.459C>G
  hgvsp: ENST00000206474.7:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.459C>G
  hgvsp: ENST00000541587.1:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000342776
  ensembl transcript: ENST00000342454
  gene symbol: HAUS4
  hgvsc: ENST00000342454.8:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.207C>G
  hgvsp: ENST00000553859.1:c.207C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3569G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.87C>G
  hgvsp: ENST00000490506.1:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.459C>G
  hgvsp: ENST00000555040.1:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.404C>G
  hgvsp: ENST00000553420.1:c.404C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3548C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000553794
  gene symbol: HAUS4
  hgvsc: ENST00000553794.1:n.424-3528C>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.459C>G
  hgvsp: ENST00000557591.1:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+767C>G
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu153Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

14-23420782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23420782
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23420782
    reference: chr 14
allele count: 477
allele frequency: 3.945539968237163e-3
allele num: 120896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452261
  ensembl transcript: ENST00000554516
  gene symbol: HAUS4
  hgvsc: ENST00000554516.1:c.447A>G
  hgvsp: ENST00000554516.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554651
  gene symbol: HAUS4
  hgvsc: ENST00000554651.1:n.627A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554446
  gene symbol: HAUS4
  hgvsc: ENST00000554446.1:n.352+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548819
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548819.1:n.195-2758T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000206474
  ensembl transcript: ENST00000206474
  gene symbol: HAUS4
  hgvsc: ENST00000206474.7:c.447A>G
  hgvsp: ENST00000206474.7:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000441026
  ensembl transcript: ENST00000541587
  gene symbol: HAUS4
  hgvsc: ENST00000541587.1:c.447A>G
  hgvsp: ENST00000541587.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452260
  ensembl transcript: ENST00000490506
  gene symbol: HAUS4
  hgvsc: ENST00000490506.1:c.75A>G
  hgvsp: ENST00000490506.1:c.75A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554349
  gene symbol: HAUS4
  hgvsc: ENST00000554349.1:n.487+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000380556
  ensembl transcript: ENST00000397409
  gene symbol: HAUS4
  hgvsc: ENST00000397409.4:c.330+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000343473
  ensembl transcript: ENST00000347758
  gene symbol: HAUS4
  hgvsc: ENST00000347758.2:c.330+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450542
  ensembl transcript: ENST00000553859
  gene symbol: HAUS4
  hgvsc: ENST00000553859.1:c.195A>G
  hgvsp: ENST00000553859.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259132
  ensembl protein: ENSP00000450856
  ensembl transcript: ENST00000555074
  gene symbol: RP11-298I3.5
  hgvsc: ENST00000555074.1:c.51-3560A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000450612
  ensembl transcript: ENST00000553420
  gene symbol: HAUS4
  hgvsc: ENST00000553420.1:c.392A>G
  hgvsp: ENST00000553420.1:c.392A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452595
  ensembl transcript: ENST00000556915
  gene symbol: HAUS4
  hgvsc: ENST00000556915.1:c.330+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000092036
  ensembl transcript: ENST00000554373
  gene symbol: HAUS4
  hgvsc: ENST00000554373.1:n.667A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257285
  ensembl transcript: ENST00000548322
  gene symbol: RP11-298I3.1
  hgvsc: ENST00000548322.1:n.159-3557T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452165
  ensembl transcript: ENST00000555040
  gene symbol: HAUS4
  hgvsc: ENST00000555040.1:c.447A>G
  hgvsp: ENST00000555040.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000451018
  ensembl transcript: ENST00000555986
  gene symbol: HAUS4
  hgvsc: ENST00000555986.1:c.330+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452239
  ensembl transcript: ENST00000555367
  gene symbol: HAUS4
  hgvsc: ENST00000555367.1:c.330+755A>G
  variant of: http://identifiers.org/hgnc/20163
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000092036
  ensembl protein: ENSP00000452058
  ensembl transcript: ENST00000557591
  gene symbol: HAUS4
  hgvsc: ENST00000557591.1:c.447A>G
  hgvsp: ENST00000557591.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20163
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Glu149Glu
num of homozygotes: 2
reference allele: T

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.331-239C>T
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15512
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28525
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1124
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2562
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2614
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8304
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1554
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.208313194780087e-4
allele num: 8276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.695717505634861e-5
allele num: 63888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
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: 862
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 1.049e1

DP
type: SiteQuality
SIO_000300: 1.539979e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.817e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000554349
gene symbol: HAUS4
hgvsc: ENST00000554349.1:n.639G>A
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 944
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7106
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4700
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4584
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1607
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25859
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14852
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8110
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1308
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 837
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 342
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.032204789430223e-4
allele num: 9688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.395e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.456167e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.396e0

FS
type: SiteQuality
SIO_000300: 2.127e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.033e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.639e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.152e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000257285
ensembl transcript: ENST00000548819
gene symbol: RP11-298I3.1
hgvsc: ENST00000548819.1:n.195-6346T>C

GenotypeDepth
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6582
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14536
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6270
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23452
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5968
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.301066874837367e-4
allele num: 7686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

FS
type: SiteQuality
SIO_000300: 3.511e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.235e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.383292e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.331-254A>C
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23452
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6270
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6582
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14536
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5968
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5345
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14748
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.033057851239669e-4
allele num: 9680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60012
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

DP
type: SiteQuality
SIO_000300: 1.383292e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

FS
type: SiteQuality
SIO_000300: 3.511e0

VQSLOD
type: SiteQuality
SIO_000300: -3.235e-1

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000554373
gene symbol: HAUS4
hgvsc: ENST00000554373.1:n.824A>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 13101
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2936
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 663
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4288
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17954
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10774
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9841
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3973
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17908
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.157683773530885e-5
allele num: 55884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7144
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.261e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.234914e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000556421
gene symbol: HAUS4
hgvsc: ENST00000556421.1:n.238delC
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 3805
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11323
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10341
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 13455
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2925
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17092
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 378
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.811594202898551e-5
allele num: 55200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13450
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.211379e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.331-266C>T
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 10702
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 286
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2921
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 11834
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16624
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13304
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3559
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.440092165898618e-4
allele num: 6944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.305936073059361e-5
allele num: 54750
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.465e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

FS
type: SiteQuality
SIO_000300: 3.955e0

DP
type: SiteQuality
SIO_000300: 1.19518e6

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000554349
gene symbol: HAUS4
hgvsc: ENST00000554349.1:n.611A>C
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 647
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2582
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3336
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16759
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14308
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11858
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9818
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 26871
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.633453119895459e-4
allele num: 12244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.575795776867318e-4
allele num: 6346
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.872680291284943e-4
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7418
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

FS
type: SiteQuality
SIO_000300: 8.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.551e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

DP
type: SiteQuality
SIO_000300: 1.047954e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.331-278T>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 18656
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3610
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9893
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2294
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8310
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15645
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 918
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 452
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.054316118164263e-5
allele num: 48678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4934
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 5.119e0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 9.8949e5

QD
type: SiteQuality
SIO_000300: 1.612e1

GenotypeDepth
all individuals: 49
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3408
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19858
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3488
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 24004
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 470
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3072
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1314
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4150
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3766
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3813
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6409
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.729475100942127e-4
allele num: 7430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.89473e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.668e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.290000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 51
bin: 6.25e1
variant carriers: 20

GenotypeDepth
all individuals: 19858
bin: 7.5e0
variant carriers: 122

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 7

GenotypeDepth
all individuals: 3072
bin: 1.75e1
variant carriers: 302

GenotypeDepth
all individuals: 4150
bin: 2.75e1
variant carriers: 91

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 25

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 8

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1058

Other
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allele count: 7
allele frequency: 1.198630136986301e-2
allele num: 584
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 45
allele frequency: 1.102346773798442e-3
allele num: 40822
num of homozygotes: 0

Latino
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allele frequency: 8.730447435431065e-3
allele num: 5498
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African
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allele count: 1080
allele frequency: 1.453566621803499e-1
allele num: 7430
num of homozygotes: 77

South Asian
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allele frequency: 3.058727569331158e-4
allele num: 9808
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InbreedingCoeff
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QD
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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SIO_000300: -6.0e-1

GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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Other
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allele count: 0
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African
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 6.503219093451258e-5
allele num: 30754
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South Asian
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ClippingRankSum
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SIO_000300: 7.31e-1

FS
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.96e-1

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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East Asian
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FS
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SIO_000300: 0.0e0

DP
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.64e0

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

European (Finnish)
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num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQ
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QD
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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

East Asian
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allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

Other
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allele count: 0
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num of homozygotes: 0

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

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

South Asian
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MQRankSum
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SIO_000300: 5.27e-1

FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 1.771309e6

MQ
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SIO_000300: 5.958e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

African
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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 num: 66638
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East Asian
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Other
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South Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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BaseQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
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African
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allele num: 10376
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European (Finnish)
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East Asian
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Latino
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Other
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DP
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InbreedingCoeff
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MQRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 131

GenotypeQuality
all individuals: 437
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 42664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 528
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7775
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 131
allele frequency: 1.137350234415697e-2
allele num: 11518
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: -2.066e0

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 1.771895e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
SIO_000300: 2.892e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000441026
ensembl transcript: ENST00000541587
gene symbol: HAUS4
hgvsc: ENST00000541587.1:c.480G>A
hgvsp: ENSP00000441026.1:p.Met160Ile
variant of: http://identifiers.org/hgnc/20163

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

GenotypeDepth
all individuals: 25396
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2175
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19459
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8897
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 561
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 385
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3725
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
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: 10366
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.15e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

VQSLOD
type: SiteQuality
SIO_000300: -2.358e0

DP
type: SiteQuality
SIO_000300: 1.769006e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.783e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.479e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000257285
ensembl transcript: ENST00000548819
gene symbol: RP11-298I3.1
hgvsc: ENST00000548819.1:n.195-3932C>G

GenotypeDepth
all individuals: 950
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25394
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2172
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19366
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8897
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 214
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.78168362627197e-4
allele num: 8648
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.7613e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.768128e6

VQSLOD
type: SiteQuality
SIO_000300: -2.472e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.330+1914_330+1915delGT
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 1027
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18519
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 25248
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 558
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8865
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2165
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7580
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1852
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 434
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41894
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.321801718133271e-4
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

DP
type: SiteQuality
SIO_000300: 1.756087e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.01e-1

QD
type: SiteQuality
SIO_000300: 1.774e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000259132
ensembl protein: ENSP00000450856
ensembl transcript: ENST00000555074
gene symbol: RP11-298I3.5
hgvsc: ENST00000555074.1:c.51-2403C>T

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

GenotypeDepth
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25053
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8821
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 554
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 728
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 198
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1542
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 946
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2163
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17974
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1823
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41104
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
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: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

DP
type: SiteQuality
SIO_000300: 1.74699e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.325e0

QD
type: SiteQuality
SIO_000300: 1.082e1

GenotypeDepth
all individuals: 17479
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 558
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2161
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 666
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24904
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8779
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1999
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 198
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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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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European (Non-Finnish)
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
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European (Finnish)
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allele count: 0
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African
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East Asian
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Latino
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Other
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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DP
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FS
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64910
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Latino
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South Asian
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European (Finnish)
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East Asian
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African
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Other
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MQRankSum
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BaseQRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Finnish)
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African
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Latino
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South Asian
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European (Non-Finnish)
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Other
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 892
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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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East Asian
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South Asian
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MQ
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 9.18105031215571e-5
allele num: 10892
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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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European (Non-Finnish)
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South Asian
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MQRankSum
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QD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15942
num of homozygotes: 0

African
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Other
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East Asian
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allele count: 0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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VQSLOD
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ClippingRankSum
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MQ
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QD
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 63904
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South Asian
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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African
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 1.569530187297269e-4
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East Asian
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Latino
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Other
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European (Finnish)
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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ReadPosRankSum
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QD
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VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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Other
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East Asian
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QD
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 4916
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5656
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 806
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5355
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5922
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.494768310911809e-4
allele num: 6690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.627765064836003e-5
allele num: 13110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.87096330905593e-5
allele num: 43662
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.17354e5

MQ
type: SiteQuality
SIO_000300: 6.051e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 1.012e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 3.937e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

GenotypeDepth
all individuals: 1753
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18032
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4710
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 10516
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17167
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2553
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16238
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7990
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12239
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 542
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5394
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 2.838489923360772e-4
allele num: 7046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43436
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 4.367e0

DP
type: SiteQuality
SIO_000300: 9.26939e5

QD
type: SiteQuality
SIO_000300: 5.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.633e0

VQSLOD
type: SiteQuality
SIO_000300: -1.669e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452261
ensembl transcript: ENST00000554516
gene symbol: HAUS4
hgvsc: ENST00000554516.1:c.465+55T>C
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1744
bin: 1.75e1
variant carriers: 6

GenotypeDepth
all individuals: 363
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23263
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 753
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5100
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15219
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10238
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2712
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24757
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 931
bin: 9.75e1
variant carriers: 19

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47844
num of homozygotes: 0

East Asian
type: Population
allele count: 20
allele frequency: 3.08641975308642e-3
allele num: 6480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 1.070468e6

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 1.993e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000451018
ensembl transcript: ENST00000555986
gene symbol: HAUS4
hgvsc: ENST00000555986.1:c.330+825A>T
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 2767
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5458
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13498
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1249
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7620
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27864
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29066
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13582
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.998321410015587e-5
allele num: 50042
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: -6.18e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 1.127088e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 7.927e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.252e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452595
ensembl transcript: ENST00000556915
gene symbol: HAUS4
hgvsc: ENST00000556915.1:c.330+825A>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 5458
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7620
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27864
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1249
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2767
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13498
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13582
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29066
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6764
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.319609395618897e-4
allele num: 7578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.76678445229682e-4
allele num: 5660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13834
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

FS
type: SiteQuality
SIO_000300: 7.927e0

DP
type: SiteQuality
SIO_000300: 1.127088e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000343473
ensembl transcript: ENST00000347758
gene symbol: HAUS4
hgvsc: ENST00000347758.2:c.330+823C>A
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 6016
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6466
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2894
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1314
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 365
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12336
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29507
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 926
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 488
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.449695563931574e-4
allele num: 6898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.886513797123979e-5
allele num: 51460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.160793e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.96e-1

QD
type: SiteQuality
SIO_000300: 7.38e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000554446
gene symbol: HAUS4
hgvsc: ENST00000554446.1:n.352+814T>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 54
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 711
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 793
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36944
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3007
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3184
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7533
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7322
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38219
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.731721677691961e-5
allele num: 57746
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.277073e6

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

VQSLOD
type: SiteQuality
SIO_000300: -6.217e-1

FS
type: SiteQuality
SIO_000300: 6.133e0

QD
type: SiteQuality
SIO_000300: 1.626e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000342776
ensembl transcript: ENST00000342454
gene symbol: HAUS4
hgvsc: ENST00000342454.8:c.330+800T>C
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 770
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42472
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2534
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3745
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9022
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 384
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 843
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1004
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15808
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.539408866995074e-4
allele num: 6496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.390118e6

VQSLOD
type: SiteQuality
SIO_000300: -2.672e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 3.98e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000451018
ensembl transcript: ENST00000555986
gene symbol: HAUS4
hgvsc: ENST00000555986.1:c.330+791G>A
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 54
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3932
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1331
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 871
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9642
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43373
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528210770829513e-5
allele num: 65436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

MQRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.418604e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.315e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000257285
ensembl transcript: ENST00000548819
gene symbol: RP11-298I3.1
hgvsc: ENST00000548819.1:n.195-2792A>G

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 110
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3952
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1135
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 871
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9750
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43527
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523368472366096e-5
allele num: 65644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.469135802469136e-4
allele num: 16200
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.82e-1

FS
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.731e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.423481e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.11e1

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000257285
ensembl transcript: ENST00000548322
gene symbol: RP11-298I3.1
hgvsc: ENST00000548322.1:n.159-3587C>G

GenotypeDepth
all individuals: 3983
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43647
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9909
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 896
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 228
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 880
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47374
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 991
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 922
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517358582180141e-5
allele num: 65904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
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: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.428381e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452260
ensembl transcript: ENST00000490506
gene symbol: HAUS4
hgvsc: ENST00000490506.1:c.93+7G>A
variant of: http://identifiers.org/hgnc/20163

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452058
ensembl transcript: ENST00000557591
gene symbol: HAUS4
hgvsc: ENST00000557591.1:c.465+7G>A
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10180
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 903
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43591
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4045
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5664
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.173158141717503e-4
allele num: 8524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.218e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

FS
type: SiteQuality
SIO_000300: 5.392e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 1.435594e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452595
ensembl transcript: ENST00000556915
gene symbol: HAUS4
hgvsc: ENST00000556915.1:c.330+779C>T
variant of: http://identifiers.org/hgnc/20163

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000452239
ensembl transcript: ENST00000555367
gene symbol: HAUS4
hgvsc: ENST00000555367.1:c.330+779C>T
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 43504
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 913
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 10264
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4082
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5677
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022791850553171e-5
allele num: 66164
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.16e-1

FS
type: SiteQuality
SIO_000300: 1.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

DP
type: SiteQuality
SIO_000300: 1.437965e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000257285
ensembl transcript: ENST00000548819
gene symbol: RP11-298I3.1
hgvsc: ENST00000548819.1:n.195-2770G>C

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000554651
gene symbol: HAUS4
hgvsc: ENST00000554651.1:n.639C>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10526
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 43513
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 907
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4117
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 8.75e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: -9.325e-1

DP
type: SiteQuality
SIO_000300: 1.443139e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.586e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.297e0

FS
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl protein: ENSP00000342776
ensembl transcript: ENST00000342454
gene symbol: HAUS4
hgvsc: ENST00000342454.8:c.330+755A>G
variant of: http://identifiers.org/hgnc/20163

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000092036
ensembl transcript: ENST00000553794
gene symbol: HAUS4
hgvsc: ENST00000553794.1:n.423+3527A>G
variant of: http://identifiers.org/hgnc/20163

GenotypeDepth
all individuals: 942
bin: 3.75e1
variant carriers: 38

GenotypeDepth
all individuals: 94
bin: 6.25e1
variant carriers: 41

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 5

GenotypeDepth
all individuals: 42
bin: 7.25e1
variant carriers: 18

GenotypeDepth
all individuals: 4149
bin: 3.25e1
variant carriers: 22

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 5.25e1
variant carriers: 62

GenotypeDepth
all individuals: 76
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 254
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 114
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 7

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 57

GenotypeDepth
all individuals: 10683
bin: 2.75e1
variant carriers: 10

GenotypeDepth
all individuals: 43048
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 31
bin: 7.75e1
variant carriers: 19

GenotypeDepth
all individuals: 80
bin: 6.75e1
variant carriers: 33

GenotypeDepth
all individuals: 463
bin: 4.25e1
variant carriers: 54

GenotypeDepth
all individuals: 283
bin: 4.75e1
variant carriers: 54

GenotypeDepth
all individuals: 55
bin: 9.75e1
variant carriers: 39