Variant #0000001957 (NC_000002.12:g.47403411C>G, NC_000002.12(NM_000251.2):c.211+9C>G (MSH2))

Individual ID 00000418
Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.47403411C>G
Published as -
Reference dbSNP
DB-ID MSH2_000007 See all 4 reported entries
dbSNP ID rs2303426
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 10:54:39 +08:00 (CST)
Date last edited 2021-09-05 12:17:25 +08:00 (CST)
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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+9C>G - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000437 DNA PCR MSH2 1 Nur Aisyah Athirah