Pank1 Variant Search Result - Rat Genome Database

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20 records found for search term Pank1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15159404	CV701466	single nucleotide variant	NM_148977.3(PANK1):c.-81G>A	not provided [RCV000947268]	benign	10	89644972	89644972	Human		name
156293836	CV2233582	single nucleotide variant	NM_148977.3(PANK1):c.-315C>T	not specified [RCV004100055]	uncertain significance	10	89645206	89645206	Human		name
156246773	CV2396839	single nucleotide variant	NM_148977.3(PANK1):c.-198G>T	not specified [RCV004233969]	uncertain significance	10	89645089	89645089	Human		name
155976307	CV2236019	single nucleotide variant	NM_148977.3(PANK1):c.52G>T (p.Ala18Ser)	not specified [RCV004113886]	uncertain significance	10	89644840	89644840	Human		name
156246834	CV2221826	single nucleotide variant	NM_148977.3(PANK1):c.613G>A (p.Gly205Arg)	not specified [RCV004102855]	uncertain significance	10	89611728	89611728	Human		name
156305433	CV2252612	single nucleotide variant	NM_148977.3(PANK1):c.409C>T (p.Arg137Trp)	not specified [RCV004118488]	uncertain significance	10	89611932	89611932	Human		name
156368378	CV2266993	single nucleotide variant	NM_148977.3(PANK1):c.518T>C (p.Ile173Thr)	not specified [RCV004131639]	uncertain significance	10	89611823	89611823	Human		name
329394250	CV2472403	single nucleotide variant	NM_148977.3(PANK1):c.665A>G (p.His222Arg)	not specified [RCV004285277]	uncertain significance	10	89599486	89599486	Human		name
405758655	CV3364036	single nucleotide variant	NM_148977.3(PANK1):c.488T>C (p.Met163Thr)	not specified [RCV004500237]	uncertain significance	10	89611853	89611853	Human		name
405758663	CV3364037	single nucleotide variant	NM_148977.3(PANK1):c.518T>G (p.Ile173Ser)	not specified [RCV004500238]	uncertain significance	10	89611823	89611823	Human		name
407479420	CV3466413	single nucleotide variant	NM_148977.3(PANK1):c.370G>A (p.Glu124Lys)	not specified [RCV004664129]	uncertain significance	10	89611971	89611971	Human		name
597657770	CV3571171	single nucleotide variant	NM_148977.3(PANK1):c.393G>T (p.Glu131Asp)	not specified [RCV004827673]	uncertain significance	10	89611948	89611948	Human		name
598259084	CV4005771	single nucleotide variant	NM_148977.3(PANK1):c.401A>G (p.Lys134Arg)	not specified [RCV005386412]	uncertain significance	10	89611940	89611940	Human		name
156153125	CV2374820	single nucleotide variant	NM_148977.3(PANK1):c.1132G>A (p.Ala378Thr)	not specified [RCV004227855]	uncertain significance	10	89593265	89593265	Human		name
401783629	CV2723782	single nucleotide variant	NM_148977.3(PANK1):c.1069G>A (p.Ala357Thr)	not specified [RCV004325939]	uncertain significance	10	89593820	89593820	Human		name
401907575	CV2809455	single nucleotide variant	NM_148977.3(PANK1):c.1027G>A (p.Gly343Arg)	not provided [RCV003422716]	uncertain significance	10	89593862	89593862	Human		name
407517948	CV3466412	single nucleotide variant	NM_148977.3(PANK1):c.1255A>T (p.Met419Leu)	not specified [RCV004650834]	uncertain significance	10	89588723	89588723	Human		name
597716951	CV3571170	single nucleotide variant	NM_148977.3(PANK1):c.1216G>A (p.Val406Met)	not specified [RCV004841483]	uncertain significance	10	89588762	89588762	Human		name
597716963	CV3571172	single nucleotide variant	NM_148977.3(PANK1):c.1109A>G (p.Asp370Gly)	not specified [RCV004841484]	uncertain significance	10	89593288	89593288	Human		name
597716975	CV3571173	single nucleotide variant	NM_148977.3(PANK1):c.1091T>A (p.Met364Lys)	not specified [RCV004841485]	uncertain significance	10	89593306	89593306	Human		name

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