ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.255C>T (p.Asn85=)

dbSNP: rs759463996
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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 RCV001466181 SCV001670181 likely benign Costello syndrome 2023-06-27 criteria provided, single submitter clinical testing
Ambry Genetics RCV002432305 SCV002741157 likely benign Cardiovascular phenotype 2020-11-19 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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