Variant #0000371392 (NC_000002.11:g.47630639T>C, NC_000002.11(NM_000251.2):c.211+98T>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method InSiGHT
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47630639T>C
DNA change (hg38) g.47403500T>C
Published as -
ISCN -
DB-ID MSH2_001106 See all 25 reported entries
Variant remarks Insight class: 1
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2018-07-06 14:04:02 +02:00 (CEST)
Date last edited 2018-11-09 17:29:21 +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 -/- 1i c.211+98T>C r.spl? p.(=)


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