Variant #0000980720 (NC_000013.10:g.79176510_79176512dup, NM_006237.3:c.324_326dup (POU4F1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79176510_79176512dup
DNA change (hg38) -
Published as POU4F1(NM_006237.4):c.324_326dup (p.(His108dup))
ISCN -
DB-ID POU4F1_000007
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POU4F1 NM_006237.3 -?/. - c.324_326dup r.(?) p.(His108dup)
RNF219 NM_024546.3 -?/. - c.*13229_*13231dup r.(=) p.(=)
POU4F1-AS1 NR_047001.1 -?/. - n.385-2926_385-2924dup r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.