Tc2n Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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42 records found for search term Tc2n

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598209063	CV3913144	single nucleotide variant	NM_001128596.3(TC2N):c.22A>T (p.Ser8Cys)	not specified [RCV005291628]	uncertain significance	14	91813748	91813748	Human		name
405791831	CV3331708	single nucleotide variant	NM_001128596.3(TC2N):c.68T>C (p.Phe23Ser)	not specified [RCV004474358]	uncertain significance	14	91812545	91812545	Human		name
156271030	CV2312314	single nucleotide variant	NM_001128596.3(TC2N):c.200C>T (p.Pro67Leu)	not specified [RCV004167022]	uncertain significance	14	91812413	91812413	Human		name
156156185	CV2367960	single nucleotide variant	NM_001128596.3(TC2N):c.122T>C (p.Ile41Thr)	not specified [RCV004223051]	uncertain significance	14	91812491	91812491	Human		name
405791812	CV3331701	single nucleotide variant	NM_001128596.3(TC2N):c.274A>T (p.Thr92Ser)	not specified [RCV004474351]	uncertain significance	14	91812339	91812339	Human		name
597794884	CV3619470	single nucleotide variant	NM_001128596.3(TC2N):c.169T>G (p.Cys57Gly)	not specified [RCV004878007]	uncertain significance	14	91812444	91812444	Human		name
156287204	CV2335002	single nucleotide variant	NM_001128596.3(TC2N):c.428G>A (p.Arg143His)	not specified [RCV004182094]	uncertain significance	14	91802295	91802295	Human		name
155923906	CV2347582	single nucleotide variant	NM_001128596.3(TC2N):c.425G>A (p.Arg142Gln)	not specified [RCV004200520]	uncertain significance	14	91802298	91802298	Human		name
156126261	CV2350270	single nucleotide variant	NM_001128596.3(TC2N):c.947C>T (p.Pro316Leu)	not specified [RCV004202226]	uncertain significance	14	91792467	91792467	Human		name
156142727	CV2386175	single nucleotide variant	NM_001128596.3(TC2N):c.854A>G (p.Asn285Ser)	not specified [RCV004229220]	uncertain significance	14	91797786	91797786	Human		name
329389832	CV2441364	single nucleotide variant	NM_001128596.3(TC2N):c.427C>T (p.Arg143Cys)	not specified [RCV004257171]	uncertain significance	14	91802296	91802296	Human		name
329363057	CV2449717	single nucleotide variant	NM_001128596.3(TC2N):c.364C>G (p.Pro122Ala)	not specified [RCV004268616]	uncertain significance	14	91802359	91802359	Human		name
401752900	CV2682974	single nucleotide variant	NM_001128596.3(TC2N):c.394A>G (p.Met132Val)	not specified [RCV004283763]	uncertain significance	14	91802329	91802329	Human		name
405791815	CV3331702	single nucleotide variant	NM_001128596.3(TC2N):c.359A>G (p.His120Arg)	not specified [RCV004474352]	uncertain significance	14	91802364	91802364	Human		name
405791818	CV3331703	single nucleotide variant	NM_001128596.3(TC2N):c.398A>G (p.Tyr133Cys)	not specified [RCV004474353]	uncertain significance	14	91802325	91802325	Human		name
405791821	CV3331704	single nucleotide variant	NM_001128596.3(TC2N):c.508G>T (p.Gly170Trp)	not specified [RCV004474354]	uncertain significance	14	91800334	91800334	Human		name
405791824	CV3331705	single nucleotide variant	NM_001128596.3(TC2N):c.509G>T (p.Gly170Val)	not specified [RCV004474355]	uncertain significance	14	91800333	91800333	Human		name
405791828	CV3331707	single nucleotide variant	NM_001128596.3(TC2N):c.595T>A (p.Ser199Thr)	not specified [RCV004474357]	uncertain significance	14	91799031	91799031	Human		name
405791834	CV3331709	single nucleotide variant	NM_001128596.3(TC2N):c.701A>C (p.Asn234Thr)	not specified [RCV004474359]	uncertain significance	14	91798336	91798336	Human		name
405791837	CV3331710	single nucleotide variant	NM_001128596.3(TC2N):c.875C>T (p.Thr292Met)	not specified [RCV004474360]	uncertain significance	14	91792539	91792539	Human		name
597762499	CV3619468	single nucleotide variant	NM_001128596.3(TC2N):c.967G>A (p.Glu323Lys)	not specified [RCV004869646]	likely benign	14	91792447	91792447	Human		name
597762509	CV3619471	single nucleotide variant	NM_001128596.3(TC2N):c.970T>C (p.Cys324Arg)	not specified [RCV004869648]	uncertain significance	14	91792444	91792444	Human		name
597762514	CV3619472	single nucleotide variant	NM_001128596.3(TC2N):c.566A>G (p.His189Arg)	not specified [RCV004869649]	uncertain significance	14	91799060	91799060	Human		name
597794887	CV3619473	single nucleotide variant	NM_001128596.3(TC2N):c.848G>T (p.Gly283Val)	not specified [RCV004878008]	uncertain significance	14	91797792	91797792	Human		name
597762518	CV3619474	single nucleotide variant	NM_001128596.3(TC2N):c.518A>G (p.Lys173Arg)	not specified [RCV004869650]	uncertain significance	14	91800324	91800324	Human		name
597762523	CV3619475	single nucleotide variant	NM_001128596.3(TC2N):c.904C>A (p.Leu302Ile)	not specified [RCV004869651]	uncertain significance	14	91792510	91792510	Human		name
598209025	CV3913138	single nucleotide variant	NM_001128596.3(TC2N):c.420G>C (p.Leu140Phe)	not specified [RCV005291622]	uncertain significance	14	91802303	91802303	Human		name
598209030	CV3913139	single nucleotide variant	NM_001128596.3(TC2N):c.976A>G (p.Met326Val)	not specified [RCV005291623]	uncertain significance	14	91792438	91792438	Human		name
598209043	CV3913141	single nucleotide variant	NM_001128596.3(TC2N):c.932T>C (p.Ile311Thr)	not specified [RCV005291625]	uncertain significance	14	91792482	91792482	Human		name
598209050	CV3913142	single nucleotide variant	NM_001128596.3(TC2N):c.773A>G (p.Asp258Gly)	not specified [RCV005291626]	uncertain significance	14	91797867	91797867	Human		name
598209055	CV3913143	single nucleotide variant	NM_001128596.3(TC2N):c.662A>G (p.Glu221Gly)	not specified [RCV005291627]	uncertain significance	14	91798375	91798375	Human		name
156170482	CV2247383	single nucleotide variant	NM_001128596.3(TC2N):c.1259G>T (p.Gly420Val)	not specified [RCV004108720]	uncertain significance	14	91785265	91785265	Human		name
156062474	CV2263211	single nucleotide variant	NM_001128596.3(TC2N):c.1369A>G (p.Ile457Val)	not specified [RCV004131437]	uncertain significance	14	91783204	91783204	Human		name
156047520	CV2390947	single nucleotide variant	NM_001128596.3(TC2N):c.1279C>T (p.Leu427Phe)	not specified [RCV004234956]	uncertain significance	14	91785245	91785245	Human		name
329387046	CV2452812	single nucleotide variant	NM_001128596.3(TC2N):c.1289G>T (p.Ser430Ile)	not specified [RCV004275343]	uncertain significance	14	91785235	91785235	Human		name
401779729	CV2676668	single nucleotide variant	NM_001128596.3(TC2N):c.1039A>G (p.Lys347Glu)	not specified [RCV004290850]	uncertain significance	14	91792375	91792375	Human		name
401744810	CV2697077	single nucleotide variant	NM_001128596.3(TC2N):c.1429C>G (p.Pro477Ala)	not specified [RCV004293057]	uncertain significance	14	91783144	91783144	Human		name
405791801	CV3331697	single nucleotide variant	NM_001128596.3(TC2N):c.1289G>C (p.Ser430Thr)	not specified [RCV004474347]	uncertain significance	14	91785235	91785235	Human		name
405791804	CV3331698	single nucleotide variant	NM_001128596.3(TC2N):c.1417A>G (p.Thr473Ala)	not specified [RCV004474348]	uncertain significance	14	91783156	91783156	Human		name
407530739	CV3485798	single nucleotide variant	NM_001128596.3(TC2N):c.1222C>T (p.Arg408Cys)	not specified [RCV004682065]	uncertain significance	14	91785302	91785302	Human		name
407513085	CV3485799	single nucleotide variant	NM_001128596.3(TC2N):c.1241A>G (p.Asn414Ser)	not specified [RCV004673588]	likely benign	14	91785283	91785283	Human		name
407530742	CV3485800	single nucleotide variant	NM_001128596.3(TC2N):c.1418C>T (p.Thr473Ile)	not specified [RCV004682066]	uncertain significance	14	91783155	91783155	Human		name

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