Variant #0000371708 (NC_000002.11:g.(47630542_47635539)_(47643569_47656880)inv, NC_000002.11(NM_000251.2):c.(211+1_212-1)_(1076+1_1077-1)inv (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(47630542_47635539)_(47643569_47656880)inv
DNA change (hg38) -
Published as -
ISCN -
DB-ID MSH2_001579 See all 3 reported entries
Variant remarks Insight class: 5
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_6i c.(211+1_212-1)_(1076+1_1077-1)inv r.212_1076del p.Gly71Aspfs*2


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