Variant #0000282600 (NC_000002.11:g.47635667G>A, NM_000251.2:c.339G>A (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47635667G>A
DNA change (hg38) g.47408528G>A
Published as MSH2(NM_000251.2):c.339G>A (p.K113=, p.(Lys113=), p.Lys113=), MSH2(NM_000251.3):c.339G>A (p.K113=)
ISCN -
DB-ID MSH2_000096 See all 37 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) 0.00291 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +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.339G>A r.(?) p.(Lys113=)


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