Variant #0000879787 (NC_000002.11:g.47639552G>C, NC_000002.11(NM_000251.2):c.646-1G>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47639552G>C
DNA change (hg38) g.47412413G>C
Published as -
ISCN -
DB-ID MSH2_001845 See all 6 reported entries
Variant remarks data from in-vitro expression mini-gene splicing assay
Reference PubMed: Meulemans 2022
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-09-29 09:45:35 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +/. 3i c.646-1G>C r.[645_646ins[646-27_646-3;gg]|0.53,645_646ins[646-24_646-3;gg]|0.47] p.[0?,Glu215_Ile216insPheLysLeuPheLeuSerLysTrp]


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