Variant #0000370603 (NC_000002.11:g.(?_47630206)_(47643569_47656880)dup, NC_000002.11(NM_000251.2):c.(?_-125)_(1076+1_1077-1)dup (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_47630206)_(47643569_47656880)dup
DNA change (hg38) -
Published as c.(?_-68)_1076+?dup
ISCN -
DB-ID MSH2_000004 See all 4 reported entries
Variant remarks Insight class: 3
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 2020-03-04 02:25:28 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/? _1_6i c.(?_-125)_(1076+1_1077-1)dup r.0? p.0?


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