Variant #0000371765 (NC_000002.11:g.(?_47630263)_(47643569_47656880)del, MSH2(NM_000251.2):c.(?_-68)_(1076+1_1077-1)del)

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.(?_47630263)_(47643569_47656880)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID MSH2_001644 See all 11 reported entries
Variant remarks Insight class: 5
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner InSiGHT - John-Paul Plazzer
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +/+ - c.(?_-68)_(1076+1_1077-1)del r.(?) p.?