Variant #0000074703 (NC_000007.13:g.6027012T>G, NM_000535.6:c.1384A>C (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.6027012T>G
DNA change (hg38) g.5987381T>G
Published as -
ISCN -
DB-ID PMS2_000214 See all 4 reported entries
Variant remarks Insight class: 3
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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.1384A>C r.(?) p.(Ile462Leu)


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