ClinVar Miner

Submissions for variant NM_022455.4(NSD1):c.4765+1G>A (rs1057520671)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000435432 SCV000516834 pathogenic not provided 2015-04-30 criteria provided, single submitter clinical testing The IVS12+1 G>A variant has not been published as a pathogenic variant, nor has it been reported as a benignpolymorphism to our knowledge. This change in the NSD1 gene destroys the canonical splice donor site inintron 12. It is predicted to cause abnormal gene splicing, either leading to an abnormal message that issubject to nonsense-mediated mRNA decay, or to an abnormal protein product if the message is used forprotein translation. The IVS12+1 G>A variant was not observed in approximately 6500 individuals ofEuropean and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not acommon benign variant in these populations. Although this variant has not been previously reported to ourknowledge, we consider it to be pathogenic.

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