ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3084A>T (p.Ser1028=) (rs786201843)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000164336 SCV000214968 likely benign Hereditary cancer-predisposing syndrome 2018-05-04 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000197176 SCV000253104 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Counsyl RCV000411527 SCV000489456 likely benign Hereditary nonpolyposis colorectal cancer type 5 2016-10-11 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000507785 SCV000604278 likely benign not specified 2017-01-19 criteria provided, single submitter clinical testing
Color RCV000164336 SCV000908407 likely benign Hereditary cancer-predisposing syndrome 2017-11-23 criteria provided, single submitter clinical testing

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