ClinVar Miner

Submissions for variant NM_005340.7(HINT1):c.284G>A (p.Arg95Gln) (rs373197800)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000644 SCV001157667 uncertain significance Autosomal recessive axonal neuropathy with neuromyotonia 2018-08-13 criteria provided, single submitter clinical testing The HINT1 p.Arg95Gln variant (rs373197800), to our knowledge, has not been reported in the medical literature or gene specific databases. This variant is found in the general population with an overall allele frequency of 0.0004% (1/275,000 alleles) in the Genome Aggregation Database. The arginine at codon 95 is moderately conserved, and computational analyses (SIFT: tolerated, PolyPhen-2: probably damaging) predict conflicting effects of this variant on protein structure/function. However, a nearby variant, p.Gly93Asp, has been observed in trans with a pathogenic variant, p.Gln62Ter, in two siblings with neuromytonia (Hahn 1991 and Zimon 2012), suggesting this region of HINT1 is critical for protein function. However, based on the available information, the clinical significance of the p.Arg95Gln variant is uncertain. Zimon M et al. Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia. Nat Genet. 2012 Oct;44(10):1080-3. Hahn AF et al. Neuromyotonia in hereditary motor neuropathy. J Neurol Neurosurg Psychiatry. 1991 Mar;54(3):230-5.

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