Variant #0000074729 (NC_000007.13:g.6026827G>C, NM_000535.6:c.1569C>G (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6026827G>C
DNA change (hg38) g.5987196G>C
Published as -
ISCN -
DB-ID PMS2_000250 See all 14 reported entries
Variant remarks Insight class: 2
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00578 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2015-07-20 15:58:19 +02:00 (CEST)
Date last edited 2019-02-22 12:22:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 -?/-? 11 c.1569C>G r.1569c>g p.=


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.