ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.537+1G>C

dbSNP: rs863224450
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000255096 SCV000322570 likely pathogenic not provided 2016-05-24 criteria provided, single submitter clinical testing This variant is denoted PMS2 c.537+1G>C or IVS5+1G>C and consists of a G>C nucleotide substitution at the +1 position of intron 5 of the PMS2 gene. This variant destroys a canonical splice donor site and is predicted to cause abnormal gene splicing, leading to either an abnormal message that is subject to nonsense-mediated mRNA decay or to an abnormal protein product. This variant has not, to our knowledge, been published in the literature. Based on the currently available information, we consider PMS2 c.537+1G>C to be a likely pathogenic variant.

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