ClinVar Miner

Submissions for variant NM_015338.6(ASXL1):c.207G>T (p.Gly69=)

dbSNP: rs748455832
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001870561 SCV002129695 likely benign not provided 2024-10-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001870561 SCV005194929 uncertain significance not provided criteria provided, single submitter not provided
Ambry Genetics RCV004968396 SCV005496491 likely benign Inborn genetic diseases 2024-11-22 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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