Tbc1d21 Variant Search Result - Rat Genome Database

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28 records found for search term Tbc1d21

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597760984	CV3609432	single nucleotide variant	NM_153356.3(TBC1D21):c.5C>T (p.Thr2Ile)	not specified [RCV004869327]	uncertain significance	15	73873714	73873714	Human		name
156087317	CV2388122	single nucleotide variant	NM_153356.3(TBC1D21):c.92A>G (p.Glu31Gly)	not specified [RCV004241240]	uncertain significance	15	73881430	73881430	Human		name
598196125	CV3916654	single nucleotide variant	NM_153356.3(TBC1D21):c.753C>T (p.Phe251=)	not specified [RCV005289369]	likely benign	15	73886588	73886588	Human		name
155931871	CV2371046	single nucleotide variant	NM_153356.3(TBC1D21):c.136C>T (p.Arg46Trp)	not specified [RCV004220807]	uncertain significance	15	73881474	73881474	Human		name
156088810	CV2391995	single nucleotide variant	NM_153356.3(TBC1D21):c.254C>T (p.Thr85Met)	not specified [RCV004235854]	uncertain significance	15	73881729	73881729	Human		name
401725261	CV2726081	single nucleotide variant	NM_153356.3(TBC1D21):c.184G>A (p.Val62Met)	not specified [RCV004324434]	uncertain significance	15	73881659	73881659	Human		name
401867791	CV2777348	single nucleotide variant	NM_153356.3(TBC1D21):c.188G>C (p.Arg63Thr)	not specified [RCV004354359]	uncertain significance	15	73881663	73881663	Human		name
407512278	CV3475485	single nucleotide variant	NM_153356.3(TBC1D21):c.212C>T (p.Thr71Met)	not specified [RCV004673415]	uncertain significance	15	73881687	73881687	Human		name
407512281	CV3475486	single nucleotide variant	NM_153356.3(TBC1D21):c.197C>T (p.Ala66Val)	not specified [RCV004673416]	uncertain significance	15	73881672	73881672	Human		name
407512288	CV3475488	single nucleotide variant	NM_153356.3(TBC1D21):c.137G>A (p.Arg46Gln)	not specified [RCV004673418]	uncertain significance	15	73881475	73881475	Human		name
597760975	CV3609429	single nucleotide variant	NM_153356.3(TBC1D21):c.167G>A (p.Arg56Lys)	not specified [RCV004869325]	uncertain significance	15	73881505	73881505	Human		name
8635560	CV90782	single nucleotide variant	NM_153356.2(TBC1D21):c.241G>A (p.Asp81Asn)	Malignant melanoma [RCV000070880]	not provided	15	73881716	73881716	Human		name
156329754	CV2216484	single nucleotide variant	NM_153356.3(TBC1D21):c.412G>A (p.Val138Ile)	not specified [RCV004097286]	uncertain significance	15	73884825	73884825	Human		name
156065179	CV2240275	single nucleotide variant	NM_153356.3(TBC1D21):c.899G>A (p.Cys300Tyr)	not specified [RCV004112837]	uncertain significance	15	73888434	73888434	Human		name
156194302	CV2251709	single nucleotide variant	NM_153356.3(TBC1D21):c.865G>A (p.Glu289Lys)	not specified [RCV004119719]	uncertain significance	15	73887707	73887707	Human		name
156266678	CV2299481	single nucleotide variant	NM_153356.3(TBC1D21):c.736C>T (p.Arg246Cys)	not specified [RCV004154555]	uncertain significance	15	73886571	73886571	Human		name
156207559	CV2307973	single nucleotide variant	NM_153356.3(TBC1D21):c.460G>A (p.Val154Ile)	not specified [RCV004170409]	uncertain significance	15	73884873	73884873	Human		name
155900919	CV2345696	single nucleotide variant	NM_153356.3(TBC1D21):c.913G>A (p.Asp305Asn)	not specified [RCV004205637]	uncertain significance	15	73888448	73888448	Human		name
155982710	CV2351723	single nucleotide variant	NM_153356.3(TBC1D21):c.371G>A (p.Arg124His)	not specified [RCV004195427]	likely benign	15	73884784	73884784	Human		name
155991397	CV2372161	single nucleotide variant	NM_153356.3(TBC1D21):c.943G>A (p.Ala315Thr)	not specified [RCV004223683]	uncertain significance	15	73888478	73888478	Human		name
401731261	CV2701277	single nucleotide variant	NM_153356.3(TBC1D21):c.877G>A (p.Gly293Arg)	not specified [RCV004311663]	uncertain significance	15	73887719	73887719	Human		name
401783975	CV2720915	single nucleotide variant	NM_153356.3(TBC1D21):c.337C>T (p.Arg113Trp)	not specified [RCV004328256]	uncertain significance	15	73884215	73884215	Human		name
401880640	CV2792919	single nucleotide variant	NM_153356.3(TBC1D21):c.740C>G (p.Ala247Gly)	not specified [RCV004365650]	uncertain significance	15	73886575	73886575	Human		name
405790495	CV3335132	single nucleotide variant	NM_153356.3(TBC1D21):c.302A>G (p.Tyr101Cys)	not specified [RCV004473894]	uncertain significance	15	73884180	73884180	Human		name
407512284	CV3475487	single nucleotide variant	NM_153356.3(TBC1D21):c.893T>C (p.Leu298Pro)	not specified [RCV004673417]	uncertain significance	15	73887735	73887735	Human		name
597760979	CV3609430	single nucleotide variant	NM_153356.3(TBC1D21):c.833T>C (p.Met278Thr)	not specified [RCV004869326]	uncertain significance	15	73887675	73887675	Human		name
598196120	CV3916652	single nucleotide variant	NM_153356.3(TBC1D21):c.824C>T (p.Ala275Val)	not specified [RCV005289368]	uncertain significance	15	73887666	73887666	Human		name
598265333	CV3916653	single nucleotide variant	NM_153356.3(TBC1D21):c.736C>A (p.Arg246Ser)	not specified [RCV005280981]	uncertain significance	15	73886571	73886571	Human		name

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