Variant #0000371369 (NC_000002.11:g.47703501T>A, NC_000002.11(NM_000251.2):c.2006-5T>A (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.47703501T>A
DNA change (hg38) g.47476362T>A
Published as -
ISCN -
DB-ID MSH2_001081 See all 5 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 2018-11-09 17:29:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/? 12i c.2006-5T>A r.[2005_2006ins2006-3_2006-1; 2006_2210del] p.[Thr668_Gly669insVal; Pro670Leufs*7]


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.