All variants in the MLH1 gene


MLH1 variants classified by the InSiGHT consortium: criteria used for classification are available here. We encourage submission of relevant unpublished information to assist in the classification of variants via LOVD or this template which can be emailed to the curator.
Information The variants shown are described using the NM_000249.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/+ 1 c.9del r.(?) p.Phe3Leufs*14 InSiGHT pathogenic g.37035047del g.36993556del - - MLH1_000966 Insight class: 5 InSiGHT - - SUMMARY record - - - 0 - InSiGHT - John-Paul Plazzer
?/. 1 c.9del r.(?) p.(Phe3Leufs*14) - VUS g.37035047del g.36993556del - - MLH1_000966 - PubMed: Bisgaard 2002 - - Germline - - - 0 - Michael Woods
+/. 1 c.9del r.(?) p.(Phe3Leufs*14) - pathogenic g.37035047del g.36993556del - - MLH1_000966 - PubMed: Nilbert 2008 - - Germline - - - 0 - Michael Woods
+/. 1 c.9del r.(?) p.Phe3Leufs*14 - pathogenic g.37035047del g.36993556del 9delC - MLH1_000966 - {PMID:Bisgaard Hum Mutat. 2002 Jul;20(1):20-7.:12112654}; {PMID:Nilbert Fam Cancer. 2009;8(1):75-83.:18566915} - - Germline - - - 0 - Thomas Hansen
+/. 1 c.9del r.(?) p.(Phe3Leufs*14) - pathogenic g.37035047del g.36993556del 9delC - MLH1_000966 ICCON data, Royal Prince Alfred/Liverpool, NSW - - - Germline - - - 0 - InSiGHT - John-Paul Plazzer
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