ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3246G>T (p.Pro1082=) (rs3136351)

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Total submissions: 17
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757474 SCV000885716 benign not provided 2018-06-27 criteria provided, single submitter clinical testing
Ambry Genetics RCV000126832 SCV000212729 likely benign Hereditary cancer-predisposing syndrome 2017-09-28 criteria provided, single submitter clinical testing
Color RCV000126832 SCV000537401 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000614249 SCV000744296 benign Hereditary nonpolyposis colorectal cancer type 5 2015-09-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000035323 SCV000592629 benign not specified 2017-02-07 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000614249 SCV000734218 likely benign Hereditary nonpolyposis colorectal cancer type 5 no assertion criteria provided clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000035323 SCV000110154 benign not specified 2013-02-22 criteria provided, single submitter clinical testing
GeneDx RCV000035323 SCV000170360 benign not specified 2013-11-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam RCV000614249 SCV000745653 likely benign Hereditary nonpolyposis colorectal cancer type 5 2015-05-13 no assertion criteria provided clinical testing
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074825 SCV000108036 benign Lynch syndrome I 2018-06-13 reviewed by expert panel curation Multifactorial likelihood analysis posterior probability < 0.001 (0.00065)
Invitae RCV000524161 SCV000252628 benign Hereditary nonpolyposis colon cancer 2018-01-23 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000035323 SCV000058971 likely benign not specified 2011-08-02 criteria provided, single submitter clinical testing Pro1082Pro in exon 5 of MSH6: This variant has been reported in individuals wit h hereditary breast and colorectal cancer, and hereditary breast cancer (3 of 27 2 chromosomes, ~1%) and was absent from 332 control chromosomes (Wasielewski 201 0). It has also been reported in dbSNP with a frequency of about 1% (rs3136351) and as a polymorphism without frequency information in individuals with HNPCC, H NPCC-related tumors, and CRC (Wijnen 1999, Woods 2005, Kets 2006, Perez-Caborner o 2009). This variant is not expected to have clinical significance because it d oes not alter an amino acid residue and is not located near a splice junction.
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000035323 SCV000257246 benign not specified no assertion criteria provided research
PreventionGenetics RCV000035323 SCV000302875 benign not specified criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000035323 SCV000601566 likely benign not specified 2017-04-07 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000757474 SCV000888267 benign not provided 2018-04-14 criteria provided, single submitter clinical testing
True Health Diagnostics RCV000126832 SCV000788048 likely benign Hereditary cancer-predisposing syndrome 2017-11-10 no assertion criteria provided clinical testing

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