Variant #0001024607 (NC_000002.11:g.47635557_47635558del, NM_000251.2:c.229_230del (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47635557_47635558del
DNA change (hg38) -
Published as MSH2(NM_000251.2):c.229_230delAG (p.Ser77Cysfs*4)
ISCN -
DB-ID MSH2_000100 See all 11 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) Retrieve
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2025-02-07 18:57:27 +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.229_230del r.(?) p.(Ser77Cysfs*4)


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