Variant #0000801391 (NC_000003.11:g.87311353C>G, NM_000306.2:c.472G>C (POU1F1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.87311353C>G
DNA change (hg38) -
Published as POU1F1(NM_000306.2):c.472G>C (p.(Ala158Pro)), POU1F1(NM_001122757.3):c.550G>C (p.A184P)
ISCN -
DB-ID POU1F1_000001 See all 2 reported entries
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) 2.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POU1F1 NM_000306.2 +/. - c.472G>C r.(?) p.(Ala158Pro)


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