Variant #0000345992 (NC_000002.11:g.47643457G>A, NM_000251.2:c.965G>A (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.47643457G>A
DNA change (hg38) g.47416318G>A
Published as MSH2(NM_000251.2):c.965G>A (p.G322D, p.(Gly322Asp), p.Gly322Asp), MSH2(NM_000251.3):c.965G>A (p.G322D)
ISCN -
DB-ID MSH2_001563 See all 149 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) 0.01364 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.965G>A r.(?) p.(Gly322Asp)


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