ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.355A>G (p.Thr119Ala)

dbSNP: rs977932120
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV001170063 SCV001251947 likely pathogenic Colorectal cancer, hereditary nonpolyposis, type 2 2020-05-03 criteria provided, single submitter clinical testing

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