ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.2556C>T (p.Leu852=)

dbSNP: rs1580945275
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000870030 SCV001011500 likely benign not provided 2018-08-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249198 SCV005899827 benign Hereditary diffuse gastric adenocarcinoma 2024-10-15 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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