14-24651977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24651977
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24651977
    reference: chr 14
allele count: 3
allele frequency: 2.484101748807631e-5
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2183+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2585+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.268+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2472+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2475+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1975+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3099+21C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2472+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.389C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2626+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.862+21C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2635+21C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32450
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-24651978-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24651978
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24651978
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2626+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2635+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.268+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2472+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.388A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.862+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3099+20A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2472+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1975+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2183+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2475+20A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2585+20A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

14-24651989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24651989
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24651989
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1975+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.862+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2472+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.268+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2472+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.377C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2475+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2635+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2626+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3099+9C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2183+9C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2585+9C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

14-24651997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24651997
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24651997
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2472+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2585+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2635+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2183+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.369G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2626+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.268+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3099+1G>A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2475+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2472+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1975+1G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.862+1G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2472+1G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

14-24652013-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652013
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652013
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2611G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.253G>C
  hgvsp: ENSP00000453818.1:p.Glu85Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2457G>C
  hgvsp: ENSP00000453825.1:p.Glu819Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2620G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2168G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2457G>C
  hgvsp: ENSP00000346453.6:p.Glu819Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2460G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.353G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.847G>C
  hgvsp: ENSP00000453708.1:p.Glu283Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1960G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2570G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3084G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu819Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-24652015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652015
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652015
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.845G>A
  hgvsp: ENSP00000453708.1:p.Glu283Lys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2618G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2455G>A
  hgvsp: ENSP00000453825.1:p.Glu819Lys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2568G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.251G>A
  hgvsp: ENSP00000453818.1:p.Glu85Lys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.351G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1958G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3082G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2166G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2458G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2455G>A
  hgvsp: ENSP00000346453.6:p.Glu819Lys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2609G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu819Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-24652016-TTCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652016
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652013
    reference: chr 14
allele count: 10
allele frequency: 8.280339162692104e-5
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.347_349delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3078_*3080delGGA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2162_*2164delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2454_2456delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2451_2453delGGA
  hgvsp: ENSP00000346453.6:p.Glu820del
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.841_843delGGA
  hgvsp: ENSP00000453708.1:p.Glu284del
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1954_*1956delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2451_2453delGGA
  hgvsp: ENSP00000453825.1:p.Glu820del
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2605_2607delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.247_249delGGA
  hgvsp: ENSP00000453818.1:p.Glu86del
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2564_2566delGGA
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2614_2616delGGA
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu820del
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: TTCC
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

14-24652019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652019
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652019
    reference: chr 14
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2454G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1954G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2451G>A
  hgvsp: ENST00000354464.6:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.841G>A
  hgvsp: ENST00000561462.1:c.841G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2614G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2564G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2451G>A
  hgvsp: ENST00000560155.1:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2162G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.347G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.247G>A
  hgvsp: ENST00000558233.1:c.247G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2605G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3078G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32444
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu817Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

14-24652022-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652022
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652022
    reference: chr 14
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2451G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1951G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.244G>C
  hgvsp: ENSP00000453818.1:p.Glu82Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3075G>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2159G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.838G>C
  hgvsp: ENSP00000453708.1:p.Glu280Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2448G>C
  hgvsp: ENSP00000453825.1:p.Glu816Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2448G>C
  hgvsp: ENSP00000346453.6:p.Glu816Asp
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2561G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2602G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.344G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2611G>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32444
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu816Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

14-24652028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652028
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652028
    reference: chr 14
allele count: 170
allele frequency: 1.407680969809384e-3
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.238C>T
  hgvsp: ENST00000558233.1:c.238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1945C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.338C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.832C>T
  hgvsp: ENST00000561462.1:c.832C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2555C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2445C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2442C>T
  hgvsp: ENST00000354464.6:c.2442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2153C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3069C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2442C>T
  hgvsp: ENST00000560155.1:c.2442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.696C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2596C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2605C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp814Asp
num of homozygotes: 2
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-24652032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652032
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652032
    reference: chr 14
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2438C>T
  hgvsp: ENSP00000453825.1:p.Thr813Ile
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.334C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.828C>T
  hgvsp: ENSP00000453708.1:p.Thr277Ile
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.234C>T
  hgvsp: ENSP00000453818.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2551C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2149C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2438C>T
  hgvsp: ENSP00000346453.6:p.Thr813Ile
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3065C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2441C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.692C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2592C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2601C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1941C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr813Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-24652042-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652042
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652042
    reference: chr 14
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.224T>G
  hgvsp: ENSP00000453818.1:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.818T>G
  hgvsp: ENSP00000453708.1:p.Cys274Gly
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2139T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1931T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2428T>G
  hgvsp: ENSP00000346453.6:p.Cys810Gly
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.682T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3055T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2591T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2582T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2431T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2428T>G
  hgvsp: ENSP00000453825.1:p.Cys810Gly
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2541T>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.324T>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys810Gly
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-24652052-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652052
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652052
    reference: chr 14
allele count: 3
allele frequency: 2.484142887898912e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-4G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-4G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-4G>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32381
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.2422-4G>T
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

14-24652053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652053
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652053
    reference: chr 14
allele count: 7
allele frequency: 5.79652539706199e-5
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-5T>C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-5T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-5T>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2422-5T>C
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

14-24652055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652055
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652055
    reference: chr 14
allele count: 25
allele frequency: 2.070187641807854e-4
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-7C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-7C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-7C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32378
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2422-7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-24652059-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652059
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652059
    reference: chr 14
allele count: 15
allele frequency: 1.24209201417641e-4
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-11A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-11A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-11A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

14-24652066-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652066
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652066
    reference: chr 14
allele count: 3
allele frequency: 2.484184028352821e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-18T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-18T>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-18T>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-24652077-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652077
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652077
    reference: chr 14
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-29G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-29G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-29G>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

14-24652077-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652077
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652077
    reference: chr 14
allele count: 2
allele frequency: 1.656479318855704e-5
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-29G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-29G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-29G>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/14-24652083-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652083
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652083
    reference: chr 14
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-35G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-35G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-35G>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

14-24652083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652083
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652083
    reference: chr 14
allele count: 4
allele frequency: 3.312355084465055e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-35G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-35G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-35G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32362
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

14-24652084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652084
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652084
    reference: chr 14
allele count: 5
allele frequency: 4.140581006326808e-5
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-36C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-36C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-36C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32361
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

14-24652086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652086
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652086
    reference: chr 14
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-38G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-38G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-38G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-24652087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652087
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652087
    reference: chr 14
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-39G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-39G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-39G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

14-24652097-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652097
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652097
    reference: chr 14
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-49A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-49A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

14-24652100-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652100
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652100
    reference: chr 14
allele count: 2
allele frequency: 1.952095574599332e-5
allele num: 102454
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-52A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-52A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-52A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-24652100-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652100
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652100
    reference: chr 14
allele count: 1
allele frequency: 9.760477872996661e-6
allele num: 102454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.676-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2576-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.318-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.812-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2133-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2585-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1925-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2535-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.218-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2422-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2425-52A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3049-52A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2422-52A>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

14-24652131-CCAACCGAGGCCCAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652131
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652117
    reference: chr 14
allele count: 19
allele frequency: 1.577863406856232e-4
allele num: 120416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30431
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9088
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CCAACCGAGGCCCAG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-24652134-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652134
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652134
    reference: chr 14
allele count: 2
allele frequency: 1.661792076575379e-5
allele num: 120352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+48T>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+48T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+48T>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-24652136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652136
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652136
    reference: chr 14
allele count: 204
allele frequency: 1.695309643320148e-3
allele num: 120332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+46G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+46G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+46G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30337
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 14263
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

14-24652140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652140
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652140
    reference: chr 14
allele count: 2
allele frequency: 1.661957786272229e-5
allele num: 120340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+42C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+42C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+42C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

14-24652150-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652150
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652150
    reference: chr 14
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+32A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+32A>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+32A>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

14-24652157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652157
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652157
    reference: chr 14
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+25G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+25G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+25G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

14-24652159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652159
    reference: chr 14
allele count: 11
allele frequency: 9.157966598398188e-5
allele num: 120114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+23G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+23G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+23G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

14-24652160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652160
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652160
    reference: chr 14
allele count: 10
allele frequency: 8.3236224404861e-5
allele num: 120140
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+22C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+22C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+22C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

14-24652164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652164
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652164
    reference: chr 14
allele count: 1
allele frequency: 8.326117364950376e-6
allele num: 120104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+18G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+18G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+18G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ

14-24652169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652169
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652169
    reference: chr 14
allele count: 2
allele frequency: 1.664918502239315e-5
allele num: 120126
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+13G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+13G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

14-24652171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652171
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652171
    reference: chr 14
allele count: 3
allele frequency: 2.497959999333877e-5
allele num: 120098
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+11C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+11C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+11C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

14-24652171-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652171
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652170
    reference: chr 14
allele count: 6
allele frequency: 4.995919998667755e-5
allele num: 120098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+10delG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+10delG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+10delG
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30226
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: GC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-24652175-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652175
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652175
    reference: chr 14
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2534+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2584+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2424+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.675+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2132+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2575+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1924+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3048+7A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.217+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2421+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.317+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.811+7A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2421+7A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2421+7A>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

14-24652202-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652202
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652202
    reference: chr 14
allele count: 1
allele frequency: 8.334722453742291e-6
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2404A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2514A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.655A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.197A>C
  hgvsp: ENSP00000453818.1:p.Lys67Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1904A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3028A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.791A>C
  hgvsp: ENSP00000453708.1:p.Lys265Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2401A>C
  hgvsp: ENSP00000346453.6:p.Lys801Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2555A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2112A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2564A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.297A>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2401A>C
  hgvsp: ENSP00000453825.1:p.Lys801Gln
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10373
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys801Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-24652208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652208
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652208
    reference: chr 14
allele count: 2
allele frequency: 1.667361400583577e-5
allele num: 119950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.191G>A
  hgvsp: ENSP00000453818.1:p.Val65Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.291G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.785G>A
  hgvsp: ENSP00000453708.1:p.Val263Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2398G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3022G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.649G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2395G>A
  hgvsp: ENSP00000346453.6:p.Val799Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2395G>A
  hgvsp: ENSP00000453825.1:p.Val799Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2106G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2558G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1898G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2549G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2508G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val799Met
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

14-24652209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652209
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652209
    reference: chr 14
allele count: 2
allele frequency: 1.66716681671168e-5
allele num: 119964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2507C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.784C>T
  hgvsp: ENST00000561462.1:c.784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.290C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1897C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2394C>T
  hgvsp: ENST00000560155.1:c.2394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2397C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2394C>T
  hgvsp: ENST00000354464.6:c.2394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3021C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.190C>T
  hgvsp: ENST00000558233.1:c.190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2557C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.648C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2548C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2105C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly798Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/14-24652210-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652210
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652208
    reference: chr 14
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.781_782delTG
  hgvsp: ENSP00000453708.1:p.Cys261TrpfsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2391_2392delTG
  hgvsp: ENSP00000346453.6:p.Cys797TrpfsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2102_*2103delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3018_*3019delTG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.645_646delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2391_2392delTG
  hgvsp: ENSP00000453825.1:p.Cys797TrpfsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2554_2555delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1894_*1895delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2394_2395delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.187_188delTG
  hgvsp: ENSP00000453818.1:p.Cys63TrpfsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.287_288delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2545_2546delTG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2504_2505delTG
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys797TrpfsTer17
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: CCA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

14-24652223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652223
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652223
    reference: chr 14
allele count: 1
allele frequency: 8.343206127250579e-6
allele num: 119858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2380G>A
  hgvsp: ENSP00000453825.1:p.Ala794Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2493G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2543G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.176G>A
  hgvsp: ENSP00000453818.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1883G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2534G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.634G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.276G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.770G>A
  hgvsp: ENSP00000453708.1:p.Ala258Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3007G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2091G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2380G>A
  hgvsp: ENSP00000346453.6:p.Ala794Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2383G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala794Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

14-24652224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652224
    reference: chr 14
allele count: 1
allele frequency: 8.34278849362611e-6
allele num: 119864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2533C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.275C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2492C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2382C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3006C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2379C>T
  hgvsp: ENST00000354464.6:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1882C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.769C>T
  hgvsp: ENST00000561462.1:c.769C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2090C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.175C>T
  hgvsp: ENST00000558233.1:c.175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.633C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2542C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2379C>T
  hgvsp: ENST00000560155.1:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu793Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24652228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652228
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652228
    reference: chr 14
allele count: 8
allele frequency: 6.67411943336726e-5
allele num: 119866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.765G>A
  hgvsp: ENSP00000453708.1:p.Arg256His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.271G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2378G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.629G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2488G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2086G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1878G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2375G>A
  hgvsp: ENSP00000453825.1:p.Arg792His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3002G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.171G>A
  hgvsp: ENSP00000453818.1:p.Arg58His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2375G>A
  hgvsp: ENSP00000346453.6:p.Arg792His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2529G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2538G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30304
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg792His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

14-24652229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652229
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652229
    reference: chr 14
allele count: 2
allele frequency: 1.669003271246412e-5
allele num: 119832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2528C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.764C>T
  hgvsp: ENSP00000453708.1:p.Arg256Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.170C>T
  hgvsp: ENSP00000453818.1:p.Arg58Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2537C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.270C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2085C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2374C>T
  hgvsp: ENSP00000453825.1:p.Arg792Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2377C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*3001C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1877C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2374C>T
  hgvsp: ENSP00000346453.6:p.Arg792Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2487C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.628C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg792Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

14-24652234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652234
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652234
    reference: chr 14
allele count: 1
allele frequency: 8.342927700188551e-6
allele num: 119862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2369C>T
  hgvsp: ENSP00000453825.1:p.Pro790Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.165C>T
  hgvsp: ENSP00000453818.1:p.Pro56Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2482C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1872C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.623C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.759C>T
  hgvsp: ENSP00000453708.1:p.Pro254Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2369C>T
  hgvsp: ENSP00000346453.6:p.Pro790Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2372C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2996C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2523C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2080C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.265C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2532C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro790Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

14-24652239-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652239
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652239
    reference: chr 14
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.618G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2364G>A
  hgvsp: ENST00000354464.6:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2991G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2367G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2527G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.260G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2518G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2075G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2364G>A
  hgvsp: ENST00000560155.1:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.160G>A
  hgvsp: ENST00000558233.1:c.160G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.754G>A
  hgvsp: ENST00000561462.1:c.754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1867G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2477G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys788Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

14-24652244-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652244
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652244
    reference: chr 14
allele count: 1
allele frequency: 8.341675008341675e-6
allele num: 119880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.749C>A
  hgvsp: ENSP00000453708.1:p.Leu251Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2522C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2070C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1862C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2472C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2359C>A
  hgvsp: ENSP00000346453.6:p.Leu787Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.255C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.155C>A
  hgvsp: ENSP00000453818.1:p.Leu53Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2513C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2359C>A
  hgvsp: ENSP00000453825.1:p.Leu787Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.613C>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2986C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2362C>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu787Met
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

14-24652247-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652247
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652247
    reference: chr 14
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.746A>G
  hgvsp: ENSP00000453708.1:p.Thr250Ala
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2510A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2359A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.610A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.152A>G
  hgvsp: ENSP00000453818.1:p.Thr52Ala
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2356A>G
  hgvsp: ENSP00000346453.6:p.Thr786Ala
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2983A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2519A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2356A>G
  hgvsp: ENSP00000453825.1:p.Thr786Ala
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2067A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2469A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.252A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1859A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr786Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

14-24652257-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652257
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652257
    reference: chr 14
allele count: 1
allele frequency: 8.340283569641367e-6
allele num: 119900
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2973T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2509T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.242T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.142T>A
  hgvsp: ENSP00000453818.1:p.Cys48Ter
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2459T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1849T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.736T>A
  hgvsp: ENSP00000453708.1:p.Cys246Ter
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2346T>A
  hgvsp: ENSP00000346453.6:p.Cys782Ter
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2346T>A
  hgvsp: ENSP00000453825.1:p.Cys782Ter
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2057T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2500T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2349T>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.600T>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys782Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

14-24652264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652264
    reference: chr 14
allele count: 2
allele frequency: 1.668223675430402e-5
allele num: 119888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2493G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2452G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2966G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.729G>A
  hgvsp: ENSP00000453708.1:p.Arg244His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2339G>A
  hgvsp: ENSP00000453825.1:p.Arg780His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2502G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2050G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1842G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.135G>A
  hgvsp: ENSP00000453818.1:p.Arg46His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2339G>A
  hgvsp: ENSP00000346453.6:p.Arg780His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.593G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2342G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.235G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg780His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

14-24652265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652265
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652265
    reference: chr 14
allele count: 6
allele frequency: 5.004253615573237e-5
allele num: 119898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1841C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.728C>T
  hgvsp: ENSP00000453708.1:p.Arg244Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2049C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2341C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2338C>T
  hgvsp: ENSP00000453825.1:p.Arg780Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2338C>T
  hgvsp: ENSP00000346453.6:p.Arg780Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2965C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2492C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.134C>T
  hgvsp: ENSP00000453818.1:p.Arg46Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2451C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.592C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2501C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.234C>T
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13598
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg780Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

14-24652273-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652273
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652271
    reference: chr 14
allele count: 2
allele frequency: 1.667583837777444e-5
allele num: 119934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2331_2332delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1831_*1832delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.718_719delAG
  hgvsp: ENSP00000453708.1:p.Val242AlafsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.124_125delAG
  hgvsp: ENSP00000453818.1:p.Val44AlafsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2955_*2956delAG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2039_*2040delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2328_2329delAG
  hgvsp: ENSP00000453825.1:p.Val778AlafsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2482_2483delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.224_225delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2328_2329delAG
  hgvsp: ENSP00000346453.6:p.Val778AlafsTer17
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2441_2442delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.582_583delAG
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2491_2492delAG
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val778AlafsTer17
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: CCT
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

14-24652275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652275
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652275
    reference: chr 14
allele count: 3
allele frequency: 2.501459184524306e-5
allele num: 119930
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2328A>G
  hgvsp: ENST00000354464.6:c.2328A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1831A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2441A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2039A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2491A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.124A>G
  hgvsp: ENST00000558233.1:c.124A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2482A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2331A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.718A>G
  hgvsp: ENST00000561462.1:c.718A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2328A>G
  hgvsp: ENST00000560155.1:c.2328A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.224A>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2955A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.582A>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr776Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

14-24652280-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652280
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652280
    reference: chr 14
allele count: 1
allele frequency: 8.33541718763024e-6
allele num: 119970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.577C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2323C>G
  hgvsp: ENSP00000346453.6:p.Leu775Val
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.119C>G
  hgvsp: ENSP00000453818.1:p.Leu41Val
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2034C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2486C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2323C>G
  hgvsp: ENSP00000453825.1:p.Leu775Val
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.713C>G
  hgvsp: ENSP00000453708.1:p.Leu239Val
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2436C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.219C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2950C>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1826C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2326C>G
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2477C>G
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30524
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu775Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

14-24652292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652292
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652292
    reference: chr 14
allele count: 1
allele frequency: 8.333333333333334e-6
allele num: 120000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2314G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.565G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2474G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2465G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2311G>A
  hgvsp: ENSP00000453825.1:p.Val771Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2022G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.701G>A
  hgvsp: ENSP00000453708.1:p.Val235Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1814G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2938G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.107G>A
  hgvsp: ENSP00000453818.1:p.Val37Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2311G>A
  hgvsp: ENSP00000346453.6:p.Val771Met
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2424G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.207G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val771Met
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

14-24652293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652293
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652293
    reference: chr 14
allele count: 181
allele frequency: 1.508207649362553e-3
allele num: 120010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.564C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.206C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2423C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2021C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2313C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.700C>T
  hgvsp: ENST00000561462.1:c.700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.106C>T
  hgvsp: ENST00000558233.1:c.106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2310C>T
  hgvsp: ENST00000560155.1:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2937C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2473C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2464C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1813C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2310C>T
  hgvsp: ENST00000354464.6:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30565
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13586
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ala770Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

14-24652295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652295
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652295
    reference: chr 14
allele count: 2
allele frequency: 1.666444474070124e-5
allele num: 120016
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2935G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2308G>A
  hgvsp: ENSP00000346453.6:p.Ala770Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2421G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.204G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.104G>A
  hgvsp: ENSP00000453818.1:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2019G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2311G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.562G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1811G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.698G>A
  hgvsp: ENSP00000453708.1:p.Ala234Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2308G>A
  hgvsp: ENSP00000453825.1:p.Ala770Thr
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2462G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2471G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala770Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-24652301-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652301
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652301
    reference: chr 14
allele count: 1
allele frequency: 8.332222370350619e-6
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2305G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2302G>T
  hgvsp: ENSP00000453825.1:p.Val768Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2302G>T
  hgvsp: ENSP00000346453.6:p.Val768Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.198G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.98G>T
  hgvsp: ENSP00000453818.1:p.Val34Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2456G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.692G>T
  hgvsp: ENSP00000453708.1:p.Val232Leu
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2013G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.556G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2465G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1805G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2415G>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2929G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val768Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

14-24652302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652302
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652302
    reference: chr 14
allele count: 1
allele frequency: 8.332500083325001e-6
allele num: 120012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1804G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2304G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.197G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.97G>A
  hgvsp: ENST00000558233.1:c.97G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2455G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.691G>A
  hgvsp: ENST00000561462.1:c.691G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2464G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2414G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2301G>A
  hgvsp: ENST00000354464.6:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.555G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2301G>A
  hgvsp: ENST00000560155.1:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2012G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2928G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val767Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

14-24652309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652309
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652309
    reference: chr 14
allele count: 7
allele frequency: 5.832458464563649e-5
allele num: 120018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1797G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2448G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2297G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.90G>A
  hgvsp: ENSP00000453818.1:p.Arg31His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2294G>A
  hgvsp: ENSP00000346453.6:p.Arg765His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.684G>A
  hgvsp: ENSP00000453708.1:p.Arg229His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2005G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2294G>A
  hgvsp: ENSP00000453825.1:p.Arg765His
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2457G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.548G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2921G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2407G>A
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.190G>A
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13639
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10770
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg765His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

14-24652310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652310
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652310
    reference: chr 14
allele count: 8
allele frequency: 6.665000416562526e-5
allele num: 120030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.89C>T
  hgvsp: ENSP00000453818.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2004C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.547C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.683C>T
  hgvsp: ENSP00000453708.1:p.Arg229Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2296C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.189C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2293C>T
  hgvsp: ENSP00000346453.6:p.Arg765Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2293C>T
  hgvsp: ENSP00000453825.1:p.Arg765Cys
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1796C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2456C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2406C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2447C>T
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2920C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg765Cys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-24652313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24652313
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24652313
    reference: chr 14
allele count: 1
allele frequency: 8.330556481172942e-6
allele num: 120040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453825
  ensembl transcript: ENST00000560155
  gene symbol: IPO4
  hgvsc: ENST00000560155.1:c.2290G>C
  hgvsp: ENSP00000453825.1:p.Glu764Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000259522
  ensembl protein: ENSP00000454374
  ensembl transcript: ENST00000561419
  gene symbol: RP11-468E2.2
  hgvsc: ENST00000561419.1:c.*2917G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000346453
  ensembl transcript: ENST00000354464
  gene symbol: IPO4
  hgvsc: ENST00000354464.6:c.2290G>C
  hgvsp: ENSP00000346453.6:p.Glu764Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561090
  gene symbol: IPO4
  hgvsc: ENST00000561090.1:n.2453G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000452798
  ensembl transcript: ENST00000558046
  gene symbol: IPO4
  hgvsc: ENST00000558046.1:c.*1793G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453818
  ensembl transcript: ENST00000558233
  gene symbol: IPO4
  hgvsc: ENST00000558233.1:c.86G>C
  hgvsp: ENSP00000453818.1:p.Glu30Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561379
  gene symbol: IPO4
  hgvsc: ENST00000561379.1:n.186G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453708
  ensembl transcript: ENST00000561462
  gene symbol: IPO4
  hgvsc: ENST00000561462.1:c.680G>C
  hgvsp: ENSP00000453708.1:p.Glu228Gln
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560935
  gene symbol: IPO4
  hgvsc: ENST00000560935.1:n.544G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196497
  ensembl protein: ENSP00000453108
  ensembl transcript: ENST00000558780
  gene symbol: IPO4
  hgvsc: ENST00000558780.1:c.*2001G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000560798
  gene symbol: IPO4
  hgvsc: ENST00000560798.1:n.2403G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000559588
  gene symbol: IPO4
  hgvsc: ENST00000559588.1:n.2444G>C
  variant of: http://identifiers.org/hgnc/19426
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196497
  ensembl transcript: ENST00000561199
  gene symbol: IPO4
  hgvsc: ENST00000561199.1:n.2293G>C
  variant of: http://identifiers.org/hgnc/19426
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu764Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

GenotypeDepth
all individuals: 2726
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31693
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10567
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3487
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6781
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 5.878955e6

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

FS
type: SiteQuality
SIO_000300: 4.164e0

MQRankSum
type: SiteQuality
SIO_000300: -1.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.219e0

QD
type: SiteQuality
SIO_000300: 1.207e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeDepth
all individuals: 32448
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3636
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6781
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31693
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 3488
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

DP
type: SiteQuality
SIO_000300: 5.878072e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 4.02e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

GenotypeDepth
all individuals: 2103
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10569
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6781
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2586
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e0

VQSLOD
type: SiteQuality
SIO_000300: -2.455e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.145e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 5.877997e6

GenotypeDepth
all individuals: 32447
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1616
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31693
bin: 9.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.014e1

BaseQRankSum
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SIO_000300: -5.947e0

MQRankSum
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SIO_000300: 1.19e0

ClippingRankSum
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SIO_000300: 5.6e-2

InbreedingCoeff
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SIO_000300: 2.0e-3

FS
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SIO_000300: 3.297e0

DP
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SIO_000300: 5.877699e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeDepth
all individuals: 3398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3484
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 2.694e0

MQRankSum
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SIO_000300: 1.26e0

ReadPosRankSum
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SIO_000300: 1.36e-1

QD
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SIO_000300: 1.288e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

DP
type: SiteQuality
SIO_000300: 5.87744e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.84e-1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.605e1

VQSLOD
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SIO_000300: 4.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1

DP
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SIO_000300: 5.877224e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e0

GenotypeDepth
all individuals: 3092
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 9

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31692
bin: 9.75e1
variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.04887770086008e-4
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.877197e6

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

QD
type: SiteQuality
SIO_000300: 1.686e1

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeDepth
all individuals: 3398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2207
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2013
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6781
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

VQSLOD
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SIO_000300: -1.381e0

MQRankSum
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -3.411e0

ClippingRankSum
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SIO_000300: -3.784e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.15e1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -4.461e0

VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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SIO_000300: -6.0e-1

InbreedingCoeff
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DP
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 157

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 168

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 9.502418797512094e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 153
allele frequency: 1.560905937563762e-2
allele num: 9802
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.492208103572285e-5
allele num: 66736
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.52e-2

FS
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ClippingRankSum
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SIO_000300: -4.85e-1

VQSLOD
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MQRankSum
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SIO_000300: 3.88e-1

ReadPosRankSum
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SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 5.878399e6

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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South Asian
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MQRankSum
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DP
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MQ
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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African
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allele num: 9802
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East Asian
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
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FS
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 16512
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European (Finnish)
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Other
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European (Non-Finnish)
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ReadPosRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 3.596475454055026e-4
allele num: 66732
num of homozygotes: 0

East Asian
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African
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South Asian
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Latino
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European (Finnish)
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Other
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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Other
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African
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East Asian
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Latino
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South Asian
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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South Asian
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allele num: 16512
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Other
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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SIO_000300: 3.65e0

ReadPosRankSum
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SIO_000300: 3.61e-1

ClippingRankSum
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SIO_000300: -2.86e-1

FS
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SIO_000300: 3.692e0

InbreedingCoeff
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SIO_000300: 6.7e-3

QD
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DP
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SIO_000300: 5.843486e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.969e1

BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 5.1e-3

QD
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GenotypeDepth
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variant carriers: 0

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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bin: 9.75e1
variant carriers: 2

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

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

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

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

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 5.1e-3

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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MQRankSum
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SIO_000300: 3.62e-1

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 5.841693e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.019991840065279e-4
allele num: 9804
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 5.42e0

ClippingRankSum
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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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SIO_000300: 1.458e1

FS
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SIO_000300: 4.198e0

MQ
type: SiteQuality
SIO_000300: 6.033e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

European (Finnish)
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allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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Other
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African
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East Asian
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MQ
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BaseQRankSum
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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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InbreedingCoeff
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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 num: 16512
num of homozygotes: 0

African
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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: 66726
num of homozygotes: 0

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

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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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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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bin: 8.75e1
variant carriers: 0

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

African
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Latino
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South Asian
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allele num: 16406
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East Asian
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Other
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European (Finnish)
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
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allele num: 61236
num of homozygotes: 0

African
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Latino
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European (Finnish)
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East Asian
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Other
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VQSLOD
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SIO_000300: 5.86e-1

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

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
allele num: 6064
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.633026324384349e-5
allele num: 61236
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -4.97e-1

ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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SIO_000300: 5.86e-1

FS
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SIO_000300: 7.93e-1

DP
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SIO_000300: 5.714857e6

GenotypeDepth
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variant carriers: 2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 1.944330740892345e-3
allele num: 9772
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16486
num of homozygotes: 0

European (Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.009781790820166e-5
allele num: 66450
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African
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Latino
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Other
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FS
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QD
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.808466913275791e-2
allele num: 9732
num of homozygotes: 0

European (Finnish)
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South Asian
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East Asian
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Latino
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allele num: 11560
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European (Non-Finnish)
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allele num: 66438
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Other
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 3.010325416177489e-5
allele num: 66438
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.509115054931788e-5
allele num: 66264
num of homozygotes: 0

East Asian
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allele num: 8616
num of homozygotes: 0

Other
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Latino
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African
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South Asian
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allele frequency: 1.216397031991242e-4
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European (Finnish)
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allele frequency: 1.515151515151515e-4
allele num: 6600
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66258
num of homozygotes: 0

East Asian
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European (Finnish)
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African
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Latino
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Other
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South Asian
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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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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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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MQ
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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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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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DP
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FS
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MQ
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BaseQRankSum
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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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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
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MQRankSum
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InbreedingCoeff
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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 (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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Other
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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FS
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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QD
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MQ
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SIO_000300: 6.026e1

DP
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SIO_000300: 1.699425e6

GenotypeDepth
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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 count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16496
num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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ReadPosRankSum
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DP
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QD
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.96e1

ClippingRankSum
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SIO_000300: 9.02e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Other
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allele frequency: 0.0e0
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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 frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.973e1

DP
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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: 3.61e-1

InbreedingCoeff
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SIO_000300: 0.0e0

FS
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SIO_000300: 8.7e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: 8.05e-1

ClippingRankSum
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SIO_000300: -3.3e-2

GenotypeDepth
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.24345295829292e-4
allele num: 16496
num of homozygotes: 0

Other
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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: 66040
num of homozygotes: 0

Latino
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
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East Asian
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BaseQRankSum
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SIO_000300: -2.083e0

InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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MQRankSum
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SIO_000300: 2.31e-1

ClippingRankSum
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SIO_000300: -4.0e-2

QD
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SIO_000300: 1.142e1

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.029017992366875e-5
allele num: 66028
num of homozygotes: 0

European (Finnish)
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Latino
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Other
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African
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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Latino
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allele num: 11560
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South Asian
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 66052
num of homozygotes: 0

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

Latino
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allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.513912859175826e-5
allele num: 66054
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.513592056668887e-5
allele num: 66068
num of homozygotes: 0

FS
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SIO_000300: 3.86e0

MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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SIO_000300: -9.63e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027734043841589e-5
allele num: 66056
num of homozygotes: 0

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

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

Other
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South Asian
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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SIO_000300: 2.68e-1

MQ
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SIO_000300: 5.97e1

ReadPosRankSum
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SIO_000300: 2.93e-1

DP
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SIO_000300: 1.701093e6

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

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 9.082102203923468e-5
allele num: 66064
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European (Finnish)
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East Asian
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African
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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: 2
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Other
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African
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Latino
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European (Finnish)
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East Asian
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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MQ
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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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allele frequency: 1.030502885408079e-4
allele num: 9704
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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South Asian
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
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allele frequency: 1.118568232662192e-3
allele num: 894
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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ClippingRankSum
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FS
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 6

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 frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

African
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allele count: 5
allele frequency: 5.14827018121911e-4
allele num: 9712
num of homozygotes: 0

European (Non-Finnish)
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allele count: 157
allele frequency: 2.374255209751081e-3
allele num: 66126
num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 16
allele frequency: 2.424242424242424e-3
allele num: 6600
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.09e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.024437454633438e-5
allele num: 66128
num of homozygotes: 0

East Asian
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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Other
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 1.512401693889897e-5
allele num: 66120
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

FS
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 1.699473e6

QD
type: SiteQuality
SIO_000300: 1.235e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeDepth
all individuals: 78
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2950
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40077
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 9.75e1
variant carriers: 8

Latino
type: Population
allele count: 4
allele frequency: 3.458412588621823e-4
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.536381781890764e-5
allele num: 66132
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.117e0

DP
type: SiteQuality
SIO_000300: 1.699877e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeDepth
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10801
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11064
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447535e-5
allele num: 66140
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.96e1