Variant #0001039931 (NC_000014.8:g.24656660G>A, NM_024658.3:c.534C>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.24656660G>A
DNA change (hg38) -
Published as IPO4(NM_024658.4):c.534C>T (p.(Phe178=))
ISCN -
DB-ID IPO4_000008
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) 1.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REC8 NM_005132.2 ?/. - c.*7359G>A r.(=) p.(=)
TM9SF1 NM_006405.5 ?/. - c.*1961C>T r.(=) p.(=)
IPO4 NM_024658.3 ?/. - c.534C>T r.(?) p.(=)


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