ClinVar Miner

Submissions for variant NM_005188.3(CBL):c.1076_1087del (p.Asp359_Lys362del) (rs397507490)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000033351 SCV000057256 pathogenic Rasopathy 2012-05-13 criteria provided, single submitter clinical testing This mutation is denoted c.1076_1087delACCATATCAAAG at the cDNA level and p.Asp359_Lys362del at the protein level. The c.1076_1087del12 mutation in exon 7 of the CBL gene (NM_005188.2) has not been published as a mutation or as a benign polymorphism to our knowledge. This in-frame deletion is predicted to result in the loss of four amino acids from the highly conserved linker region of the CBL protein. According to the Catalogue of Somatic Mutations in Cancer (COSMIC) database, other adjacent in-frame deletions have been reported in association with acute and chronic myelomonocytic leukemia. The variant is found in NOONAN panel(s).

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