Variant #0000000645 (NC_000007.13:g.6017376T>C, NM_000535.5:c.2288A>G (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.6017376T>C
Reference -
DB-ID PMS2_000008
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2024-09-09 15:32:22 +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 ?/? . c.2288A>G r.(?) p.(Glu763Gly)