Variant #0000800692 (NC_000002.11:g.47698179A>G, NM_000251.2:c.1737A>G (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47698179A>G
DNA change (hg38) -
Published as MSH2(NM_000251.2):c.1737A>G (p.K579=, p.(Lys579=), p.Lys579=, p.=), MSH2(NM_000251.3):c.1737A>G (p.K579=)
ISCN -
DB-ID MSH2_000218 See all 35 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00214 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 -/. - c.1737A>G r.(?) p.(Lys579=)


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