ClinVar Miner

Submissions for variant NM_182643.3(DLC1):c.2725A>G (p.Ile909Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004242721 SCV003760848 uncertain significance not specified 2021-09-22 criteria provided, single submitter clinical testing The c.2725A>G (p.I909V) alteration is located in exon 9 (coding exon 8) of the DLC1 gene. This alteration results from a A to G substitution at nucleotide position 2725, causing the isoleucine (I) at amino acid position 909 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Fulgent Genetics, Fulgent Genetics RCV005047400 SCV005677833 uncertain significance Colorectal cancer 2024-05-30 criteria provided, single submitter clinical testing

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