Variant #0000000590 (NC_000007.13:g.152346170C>G, NM_005431.2:c.400G>C (XRCC2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.152346170C>G
Reference -
DB-ID XRCC2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-06-03 15:43:54 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XRCC2 NM_005431.1 ?/? - c.400G>C r.(?) p.(Glu134Gln)
XRCC2 NM_005431.2 ?/? - c.400G>C r.(?) p.(Glu134Gln)