Variant #0000000377 (NC_000007.13:g.6017268C>T, NM_000535.5:c.2396G>A (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.6017268C>T
Reference -
DB-ID PMS2_000006
Frequency -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-18 09:29:08 +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     
PMS2 NM_000535.5 ?/? 14 c.2396G>A r.(?) p.(Arg799Gln)