Variant #0000520729 (NC_000003.11:g.87295041A>G, NM_014043.3:c.304A>G (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.87295041A>G
DNA change (hg38) g.87245891A>G
Published as CHMP2B(NM_014043.3):c.304A>G (p.M102V), CHMP2B(NM_014043.4):c.304A>G (p.M102V)
ISCN -
DB-ID CHMP2B_000016 See all 3 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHMP2B NM_014043.3 ?/. - c.304A>G r.(?) p.(Met102Val)


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