Variant #0000426347 (NC_000002.11:g.47698108T>C, NM_000251.2:c.1666T>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47698108T>C
DNA change (hg38) g.47470969T>C
Published as L556L
ISCN -
DB-ID MSH2_000564 See all 45 reported entries
Variant remarks {GR:383}
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) 0.00434 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 22:00:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 -/. 11 c.1666T>C r.1666u>c p.=


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