Variant #0000426207 (NC_000002.11:g.47698179A>G, NM_000251.2:c.1737A>G (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47698179A>G
DNA change (hg38) g.47471040A>G
Published as K579K
ISCN -
DB-ID MSH2_000218 See all 35 reported entries
Variant remarks {GR:385}
Reference PubMed: Tournier 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00214 View details
Owner Rolf Sijmons
Database submission license No license selected
Created by Rolf Sijmons
Date created 2009-02-06 12:00:00 +01:00 (CET)
Date last edited 2020-07-14 21:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 -?/. 11 c.1737A>G r.1737a>g p.=


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.