Variant #0000719628 (NC_000003.11:g.87309149T>C, NM_014043.3:c.*6177T>C (CHMP2B))

Chromosome 3
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.87309149T>C
DNA change (hg38) -
Published as POU1F1(NM_001122757.2):c.849A>G (p.V283=)
ISCN -
DB-ID CHMP2B_000027
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.771A>G r.(?) p.(Val257=)
CHMP2B NM_014043.3 ?/. - c.*6177T>C r.(=) p.(=)


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