Variant #0000408138 (NC_000010.10:g.121429394G>A, NM_004281.3:c.212G>A (BAG3))

Chromosome 10
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.121429394G>A
DNA change (hg38) g.119669882G>A
Published as -
ISCN -
DB-ID BAG3_000003 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35434411
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02006 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-03-11 21:40:57 +01:00 (CET)
Date last edited 2012-11-02 20:40:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAG3 NM_004281.3 ?/. 2 c.212G>A r.(?) p.(Arg71Gln)


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