Variant #0000370819 (NC_000002.11:g.47698179A>G, NM_000251.2:c.1737A>G (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47698179A>G
DNA change (hg38) g.47471040A>G
Published as -
ISCN -
DB-ID MSH2_000218 See all 35 reported entries
Variant remarks Insight class: 2
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00214 View details
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 -?/-? 11 c.1737A>G r.1737a>g p.=


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