Variant #0000355606 (NC_000003.11:g.(?_37034841)_(37042545_37045891)del, MLH1(NM_000249.3):c.(?_-198)_(306+1_307-1)del)

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method InSiGHT
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_37034841)_(37042545_37045891)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID MLH1_000946 See all 6 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     
MLH1 NM_000249.3 +/+ _1_3i c.(?_-198)_(306+1_307-1)del r.0? p.0?