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31 records found for search term Fam20b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597748894CV3665460single nucleotide variantNM_014864.4(FAM20B):c.17G>A (p.Arg6Gln)not specified [RCV004923223]uncertain significance1179043864179043864Humanname
156103112CV2352340single nucleotide variantNM_014864.4(FAM20B):c.104G>A (p.Arg35Gln)not specified [RCV004200811]uncertain significance1179043951179043951Humanname
156043852CV2381581single nucleotide variantNM_014864.4(FAM20B):c.118G>A (p.Ala40Thr)not specified [RCV004232059]uncertain significance1179043965179043965Humanname
401881716CV2767842single nucleotide variantNM_014864.4(FAM20B):c.265C>T (p.His89Tyr)not specified [RCV004345959]uncertain significance1179044112179044112Humanname
401880210CV2769986single nucleotide variantNM_014864.4(FAM20B):c.233C>T (p.Pro78Leu)not specified [RCV004353820]uncertain significance1179044080179044080Humanname
405745329CV3256286single nucleotide variantNM_014864.4(FAM20B):c.128G>A (p.Arg43Gln)not specified [RCV004381184]uncertain significance1179043975179043975Humanname
405745336CV3256287single nucleotide variantNM_014864.4(FAM20B):c.187C>T (p.Pro63Ser)not specified [RCV004381185]uncertain significance1179044034179044034Humanname
407508628CV3435665single nucleotide variantNM_014864.4(FAM20B):c.101A>G (p.Asn34Ser)not specified [RCV004625470]uncertain significance1179043948179043948Humanname
598226284CV3962195single nucleotide variantNM_014864.4(FAM20B):c.146G>A (p.Arg49Gln)not specified [RCV005341583]uncertain significance1179043993179043993Humanname
598226290CV3962196single nucleotide variantNM_014864.4(FAM20B):c.229T>C (p.Tyr77His)not specified [RCV005341584]uncertain significance1179044076179044076Humanname
155925967CV2208081single nucleotide variantNM_014864.4(FAM20B):c.838G>C (p.Val280Leu)not specified [RCV004086768]uncertain significance1179064396179064396Humanname
156250338CV2286704single nucleotide variantNM_014864.4(FAM20B):c.497T>C (p.Val166Ala)not specified [RCV004142529]uncertain significance1179054561179054561Humanname
156268667CV2293041single nucleotide variantNM_014864.4(FAM20B):c.878A>G (p.Tyr293Cys)not specified [RCV004148794]uncertain significance1179064436179064436Humanname
329396679CV2458930single nucleotide variantNM_014864.4(FAM20B):c.301G>A (p.Val101Met)not specified [RCV004272427]uncertain significance1179044148179044148Humanname
329377906CV2460821single nucleotide variantNM_014864.4(FAM20B):c.509T>C (p.Val170Ala)not specified [RCV004271137]uncertain significance1179054573179054573Humanname
329401951CV2467696single nucleotide variantNM_014864.4(FAM20B):c.682G>T (p.Val228Leu)not specified [RCV004281315]uncertain significance1179064034179064034Humanname
401871972CV2754244single nucleotide variantNM_014864.4(FAM20B):c.392A>G (p.His131Arg)not specified [RCV004334430]uncertain significance1179050293179050293Humanname
407508619CV3435663single nucleotide variantNM_014864.4(FAM20B):c.910A>G (p.Met304Val)not specified [RCV004625468]uncertain significance1179064468179064468Humanname
407508623CV3435664single nucleotide variantNM_014864.4(FAM20B):c.835G>A (p.Ala279Thr)not specified [RCV004625469]uncertain significance1179064393179064393Humanname
408367564CV3509622single nucleotide variantNM_014864.4(FAM20B):c.339A>G (p.Ile113Met)FAM20B-related condition [RCV004759013]likely benign1179044186179044186Humanname , trait
597748867CV3665454single nucleotide variantNM_014864.4(FAM20B):c.811C>T (p.Arg271Cys)not specified [RCV004923217]uncertain significance1179064369179064369Humanname
597748871CV3665455single nucleotide variantNM_014864.4(FAM20B):c.518G>A (p.Arg173Gln)not specified [RCV004923218]uncertain significance1179054582179054582Humanname
597748876CV3665456single nucleotide variantNM_014864.4(FAM20B):c.564C>G (p.Phe188Leu)not specified [RCV004923219]uncertain significance1179054628179054628Humanname
597748899CV3665461single nucleotide variantNM_014864.4(FAM20B):c.410C>A (p.Pro137Gln)not specified [RCV004923224]uncertain significance1179050311179050311Humanname
597748903CV3665462single nucleotide variantNM_014864.4(FAM20B):c.958G>T (p.Asp320Tyr)not specified [RCV004923225]uncertain significance1179066819179066819Humanname
598226275CV3962194single nucleotide variantNM_014864.4(FAM20B):c.808C>T (p.Pro270Ser)not specified [RCV005341582]uncertain significance1179064366179064366Humanname
156345839CV2377780single nucleotide variantNM_014864.4(FAM20B):c.1171G>A (p.Asp391Asn)not specified [RCV004230361]uncertain significance1179072085179072085Humanname
405745322CV3256285single nucleotide variantNM_014864.4(FAM20B):c.1013C>T (p.Thr338Ile)not specified [RCV004381183]uncertain significance1179071927179071927Humanname
597748862CV3665453single nucleotide variantNM_014864.4(FAM20B):c.1123G>A (p.Val375Met)not specified [RCV004923216]uncertain significance1179072037179072037Humanname
597748884CV3665458single nucleotide variantNM_014864.4(FAM20B):c.1119C>G (p.Asp373Glu)not specified [RCV004923221]uncertain significance1179072033179072033Humanname
597748889CV3665459single nucleotide variantNM_014864.4(FAM20B):c.1091C>T (p.Ser364Phe)not specified [RCV004923222]uncertain significance1179072005179072005Humanname