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10 records found for search term Rab13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156188449CV2292547single nucleotide variantNM_002870.5(RAB13):c.16G>T (p.Asp6Tyr)not specified [RCV004150319]uncertain significance1153986221153986221Humanname
407483646CV3461636single nucleotide variantNM_002870.5(RAB13):c.16G>C (p.Asp6His)not specified [RCV004664983]uncertain significance1153986221153986221Humanname
401932986CV2805973single nucleotide variantNM_002870.5(RAB13):c.360G>C (p.Gly120=)not provided [RCV003409059]likely benign1153982773153982773Humanname
156065643CV2196968single nucleotide variantNM_002870.5(RAB13):c.116C>T (p.Ser39Phe)not specified [RCV004071425]uncertain significance1153986121153986121Humanname
405679488CV3308560single nucleotide variantNM_002870.5(RAB13):c.138G>T (p.Lys46Asn)not specified [RCV004443016]uncertain significance1153984768153984768Humanname
597774928CV3588988single nucleotide variantNM_002870.5(RAB13):c.245T>C (p.Met82Thr)not specified [RCV004852110]uncertain significance1153983522153983522Humanname
156346725CV2353709single nucleotide variantNM_002870.5(RAB13):c.572C>T (p.Thr191Ile)not specified [RCV004201722]uncertain significance1153982139153982139Humanname
401895121CV2792702single nucleotide variantNM_002870.5(RAB13):c.521G>A (p.Gly174Glu)not specified [RCV004365479]uncertain significance1153982404153982404Humanname
597774924CV3588987single nucleotide variantNM_002870.5(RAB13):c.373A>G (p.Met125Val)not specified [RCV004852109]uncertain significance1153982760153982760Humanname
598163844CV3898515single nucleotide variantNM_002870.5(RAB13):c.554C>G (p.Pro185Arg)not specified [RCV005261616]uncertain significance1153982157153982157Humanname