Variant #0000301552 (NC_000002.11:g.190718917C>T, NC_000002.11(NM_000534.4):c.967-48C>T (PMS1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.190718917C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PMS1_000064
Frequency 1/10994
Freq. EA 1/7538
Freq. AA 0/3456
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:22:05 +02:00 (CEST)
Date last edited 2013-05-04 00:13:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PMS1 NM_000534.4 ?/? c.967-48C>T r.(=) p.(=)