Variant #0000886011 (NC_000003.11:g.87325586A>G, NM_000306.2:c.27T>C (POU1F1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.87325586A>G
DNA change (hg38) -
Published as POU1F1(NM_000306.4):c.27T>C (p.A9=), POU1F1(NM_001122757.2):c.27T>C (p.A9=)
ISCN -
DB-ID POU1F1_000009 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) 0.00022 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POU1F1 NM_000306.2 -/. - c.27T>C r.(?) p.(Ala9=)


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