ClinVar Miner

Submissions for variant NM_022041.4(GAN):c.890C>T (p.Pro297Leu)

dbSNP: rs771785420
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de genetique medicale, Pr. Levy, Hopital de La Timone Enfants, APHM RCV000735275 SCV000851993 likely pathogenic Giant axonal neuropathy 1 2018-11-07 no assertion criteria provided clinical testing The chr16:g.[81391453C>T] (GRCh37,NC_000016.9) variant (inherited from the mother) have been found in compound heterozygote state with the chr16:g.[(81367334_81379355)_(81401689_81410823)del] (GRCh37,NC_000016.9) variant (inherited from the father) in a patient with a consistent phenotype with Giant axonal neuropathy-1 (OMIM #256850). These variants (a SNV and a CNV) have been found with a targeted sequencing panel focusing on already reported gene associated with neuropathy and an arrayCGH. The SNV have been confirmed by PCR sequencing. No functional test have been performed. These variants are not currently reported in any public database.

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