Variant #0001039748 (NC_000013.10:g.79175845_79175850del, NM_006237.3:c.960_965del (POU4F1))

Chromosome 13
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.79175845_79175850del
DNA change (hg38) -
Published as POU4F1(NM_006237.4):c.960_965del (p.(Asn320_Met322delinsLys))
ISCN -
DB-ID POU4F1_000010
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) Retrieve
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     
POU4F1 NM_006237.3 ?/. - c.960_965del r.(?) p.(Asn320_Met322delinsLys)
RNF219 NM_024546.3 ?/. - c.*13865_*13870del r.(=) p.(=)
POU4F1-AS1 NR_047001.1 ?/. - n.385-3591_385-3586del r.(?) -


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