ClinVar Miner

Submissions for variant NM_022455.4(NSD1):c.2108del (p.Leu703fs) (rs886041550)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000310036 SCV000330225 pathogenic not provided 2016-02-12 criteria provided, single submitter clinical testing The c.2108delT pathogenic variant in the NSD1 gene causes a frameshift starting with codon Leucine 703, changes this amino acid to a Proline residue and creates a premature Stop codon at position 10 of the new reading frame, denoted p.Leu703ProfsX10. This pathogenic variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. Although this variant has not been previously reported to our knowledge, other frameshift variants have been reported in the NSD1 gene in association with Sotos syndrome (Stenson et al., 2014).

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