ClinVar Miner

Submissions for variant NM_003995.4(NPR2):c.613C>T (p.Arg205Ter)

dbSNP: rs1180840764
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001942099 SCV002228763 pathogenic Acromesomelic dysplasia 1, Maroteaux type; Tall stature-scoliosis-macrodactyly of the great toes syndrome 2024-01-08 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg205*) in the NPR2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in NPR2 are known to be pathogenic (PMID: 15146390, 15572448, 16384845). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with acromesomelic dysplasia, Maroteaux type and/or short stature (PMID: 31990356, 32506268). It has also been observed to segregate with disease in related individuals. ClinVar contains an entry for this variant (Variation ID: 1454887). For these reasons, this variant has been classified as Pathogenic.

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