Variant #0000791696 (NC_000002.11:g.47643490G>A, NM_000251.2:c.998G>A (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.47643490G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MSH2_000539 See all 55 reported entries
Variant remarks RNA DATA pCAS2 minigene splicing assay in HeLa cells 2 independent experiments (Inserm U1245, Rouen, France: No effect on exon 6 splicing
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
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-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2021-07-30 04:59:17 +02:00 (CEST)
Date last edited 2021-11-23 07:20:53 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 -/. - c.998G>A r.(?) p.(Cys333Tyr)


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