Variant #0000323622 (NC_000014.8:g.24653972G>A, NC_000014.8(NM_024658.3):c.1523-3C>T (IPO4))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.24653972G>A
DNA change (hg38) g.24184766G>A
Published as IPO4(NM_024658.3):c.1523-3C>T (p.?)
ISCN -
DB-ID IPO4_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00122 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-05 13:45:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REC8 NM_005132.2 ?/. - c.*4671G>A r.(=) p.(=)
TM9SF1 NM_006405.5 ?/. - c.*4649C>T r.(=) p.(=)
IPO4 NM_024658.3 ?/. - c.1523-3C>T r.spl? p.?


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