Variant #0000001963 (NC_000002.12:g.47403500T>C, NC_000002.12(NM_000251.2):c.211+98T>C (MSH2))

Individual ID 00000420
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.47403500T>C
Published as -
Reference dbSNP
DB-ID MSH2_000006 See all 3 reported entries
dbSNP ID rs3815865
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-02-16 11:04:39 +08:00 (CST)
Date last edited 2021-08-01 12:50:22 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MSH2 NM_000251.2 +/. - c.211+98T>C - r.(=) p.(=) - benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000440 DNA PCR MSH2 2 Nur Aisyah Athirah