Variant #0000874851 (NC_000022.10:g.37637653G>C, NM_002872.4:c.81C>G (RAC2))

Chromosome 22
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.37637653G>C
DNA change (hg38) g.37241613G>C
Published as -
ISCN -
DB-ID RAC2_000017
Variant remarks -
Reference PubMed: Roos 2021, Journal: Roos 2021
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.1526 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 2022-08-13 09:04:04 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAC2 NM_002872.4 -/. - c.81C>G r.(=) p.(Ala27=)


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