Variant #0000520731 (NC_000003.11:g.87299075A>C, NM_014043.3:c.372A>C (CHMP2B))

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.87299075A>C
DNA change (hg38) g.87249925A>C
Published as CHMP2B(NM_014043.3):c.372A>C (p.T124=), CHMP2B(NM_014043.4):c.372A>C (p.T124=)
ISCN -
DB-ID CHMP2B_000012 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) 0.09375 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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.372A>C r.(?) p.(Thr124=)


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