Cstf2t Variant Search Result - Rat Genome Database

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64 records found for search term Cstf2t

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405689115	CV3246007	single nucleotide variant	NM_015235.3(CSTF2T):c.242A>C (p.Glu81Ala)	not specified [RCV004372767]	uncertain significance	10	51699308	51699308	Human		name
155915901	CV2274450	single nucleotide variant	NM_015235.3(CSTF2T):c.689A>T (p.Asn230Ile)	not specified [RCV004136813]	uncertain significance	10	51698861	51698861	Human		name
156007808	CV2288376	single nucleotide variant	NM_015235.3(CSTF2T):c.977C>T (p.Pro326Leu)	not specified [RCV004151931]	uncertain significance	10	51698573	51698573	Human		name
156072567	CV2365395	single nucleotide variant	NM_015235.3(CSTF2T):c.842C>T (p.Thr281Ile)	not specified [RCV004209476]	uncertain significance	10	51698708	51698708	Human		name
156191566	CV2385251	single nucleotide variant	NM_015235.3(CSTF2T):c.904C>T (p.Arg302Trp)	not specified [RCV004228495]	uncertain significance	10	51698646	51698646	Human		name
156101210	CV2386772	single nucleotide variant	NM_015235.3(CSTF2T):c.417G>C (p.Gln139His)	not specified [RCV004233438]	uncertain significance	10	51699133	51699133	Human		name
329355029	CV2449225	single nucleotide variant	NM_015235.3(CSTF2T):c.842C>G (p.Thr281Ser)	not specified [RCV004257365]	uncertain significance	10	51698708	51698708	Human		name
401750252	CV2695993	single nucleotide variant	NM_015235.3(CSTF2T):c.742A>G (p.Lys248Glu)	not specified [RCV004308254]	uncertain significance	10	51698808	51698808	Human		name
401762970	CV2707400	single nucleotide variant	NM_015235.3(CSTF2T):c.805C>T (p.Pro269Ser)	not specified [RCV004312788]	uncertain significance	10	51698745	51698745	Human		name
405689110	CV3246008	single nucleotide variant	NM_015235.3(CSTF2T):c.365A>G (p.Glu122Gly)	not specified [RCV004372768]	uncertain significance	10	51699185	51699185	Human		name
405689104	CV3246009	single nucleotide variant	NM_015235.3(CSTF2T):c.425A>C (p.Glu142Ala)	not specified [RCV004372769]	uncertain significance	10	51699125	51699125	Human		name
405689098	CV3246010	single nucleotide variant	NM_015235.3(CSTF2T):c.434A>G (p.Lys145Arg)	not specified [RCV004372770]	uncertain significance	10	51699116	51699116	Human		name
405688923	CV3246011	single nucleotide variant	NM_015235.3(CSTF2T):c.595C>T (p.Pro199Ser)	not specified [RCV004372771]	uncertain significance	10	51698955	51698955	Human		name
405688792	CV3246012	single nucleotide variant	NM_015235.3(CSTF2T):c.844C>T (p.Pro282Ser)	not specified [RCV004372772]	uncertain significance	10	51698706	51698706	Human		name
405688678	CV3246013	single nucleotide variant	NM_015235.3(CSTF2T):c.940A>G (p.Ile314Val)	not specified [RCV004372773]	uncertain significance	10	51698610	51698610	Human		name
407478345	CV3426147	single nucleotide variant	NM_015235.3(CSTF2T):c.682C>A (p.Leu228Met)	not specified [RCV004615755]	uncertain significance	10	51698868	51698868	Human		name
407478350	CV3426148	single nucleotide variant	NM_015235.3(CSTF2T):c.649C>T (p.Pro217Ser)	not specified [RCV004615756]	uncertain significance	10	51698901	51698901	Human		name
407478355	CV3426149	single nucleotide variant	NM_015235.3(CSTF2T):c.889C>T (p.Pro297Ser)	not specified [RCV004615757]	uncertain significance	10	51698661	51698661	Human		name
407478360	CV3426150	single nucleotide variant	NM_015235.3(CSTF2T):c.529G>A (p.Val177Ile)	not specified [RCV004615758]	uncertain significance	10	51699021	51699021	Human		name
407478366	CV3426151	single nucleotide variant	NM_015235.3(CSTF2T):c.376G>A (p.Glu126Lys)	not specified [RCV004615759]	uncertain significance	10	51699174	51699174	Human		name
407478371	CV3426152	single nucleotide variant	NM_015235.3(CSTF2T):c.341C>T (p.Pro114Leu)	not specified [RCV004615760]	uncertain significance	10	51699209	51699209	Human		name
597805285	CV3651364	single nucleotide variant	NM_015235.3(CSTF2T):c.721C>G (p.His241Asp)	not specified [RCV004908422]	uncertain significance	10	51698829	51698829	Human		name
597805287	CV3651365	single nucleotide variant	NM_015235.3(CSTF2T):c.862C>A (p.Pro288Thr)	not specified [RCV004908423]	uncertain significance	10	51698688	51698688	Human		name
598219675	CV3959520	single nucleotide variant	NM_015235.3(CSTF2T):c.641G>A (p.Gly214Asp)	not specified [RCV005317426]	uncertain significance	10	51698909	51698909	Human		name
598160270	CV3959527	single nucleotide variant	NM_015235.3(CSTF2T):c.588T>A (p.His196Gln)	not specified [RCV005328736]	uncertain significance	10	51698962	51698962	Human		name
598219717	CV3959528	single nucleotide variant	NM_015235.3(CSTF2T):c.856A>G (p.Met286Val)	not specified [RCV005317433]	uncertain significance	10	51698694	51698694	Human		name
156370479	CV2204222	single nucleotide variant	NM_015235.3(CSTF2T):c.1520G>T (p.Gly507Val)	not specified [RCV004077018]	uncertain significance	10	51698030	51698030	Human		name
156336413	CV2270726	single nucleotide variant	NM_015235.3(CSTF2T):c.1393C>G (p.Pro465Ala)	not specified [RCV004131791]	uncertain significance	10	51698157	51698157	Human		name
155923512	CV2280314	single nucleotide variant	NM_015235.3(CSTF2T):c.1574G>C (p.Gly525Ala)	not specified [RCV004140512]	uncertain significance	10	51697976	51697976	Human		name
156135966	CV2284777	single nucleotide variant	NM_015235.3(CSTF2T):c.1474C>T (p.Pro492Ser)	not specified [RCV004142958]	uncertain significance	10	51698076	51698076	Human		name
156176193	CV2327085	single nucleotide variant	NM_015235.3(CSTF2T):c.1243T>C (p.Ser415Pro)	not specified [RCV004178667]	uncertain significance	10	51698307	51698307	Human		name
156211198	CV2370326	single nucleotide variant	NM_015235.3(CSTF2T):c.1250C>T (p.Ala417Val)	not specified [RCV004213236]	uncertain significance	10	51698300	51698300	Human		name
329372158	CV2455072	single nucleotide variant	NM_015235.3(CSTF2T):c.1528G>C (p.Gly510Arg)	not specified [RCV004272321]	uncertain significance	10	51698022	51698022	Human		name
329396940	CV2468345	single nucleotide variant	NM_015235.3(CSTF2T):c.1234G>A (p.Gly412Ser)	not specified [RCV004275889]	likely benign	10	51698316	51698316	Human		name
401723343	CV2674919	single nucleotide variant	NM_015235.3(CSTF2T):c.1714C>G (p.Gln572Glu)	not specified [RCV004296232]	uncertain significance	10	51697836	51697836	Human		name
401760602	CV2706012	single nucleotide variant	NM_015235.3(CSTF2T):c.1822C>A (p.Gln608Lys)	not specified [RCV004320922]	uncertain significance	10	51697728	51697728	Human		name
401752146	CV2723134	single nucleotide variant	NM_015235.3(CSTF2T):c.1648G>C (p.Gly550Arg)	not specified [RCV004329386]	uncertain significance	10	51697902	51697902	Human		name
401718129	CV2725437	single nucleotide variant	NM_015235.3(CSTF2T):c.1237A>G (p.Arg413Gly)	not specified [RCV004320073]	uncertain significance	10	51698313	51698313	Human		name
401878719	CV2777014	single nucleotide variant	NM_015235.3(CSTF2T):c.1117C>A (p.Arg373Ser)	not specified [RCV004351814]	uncertain significance	10	51698433	51698433	Human		name
405689186	CV3245994	single nucleotide variant	NM_015235.3(CSTF2T):c.1123C>T (p.Pro375Ser)	not specified [RCV004372754]	uncertain significance	10	51698427	51698427	Human		name
405689181	CV3245995	single nucleotide variant	NM_015235.3(CSTF2T):c.1291C>T (p.Arg431Cys)	not specified [RCV004372755]	uncertain significance	10	51698259	51698259	Human		name
405689175	CV3245996	single nucleotide variant	NM_015235.3(CSTF2T):c.1322G>C (p.Cys441Ser)	not specified [RCV004372756]	uncertain significance	10	51698228	51698228	Human		name
405689171	CV3245997	single nucleotide variant	NM_015235.3(CSTF2T):c.1343T>G (p.Met448Arg)	not specified [RCV004372757]	uncertain significance	10	51698207	51698207	Human		name
405689164	CV3245998	single nucleotide variant	NM_015235.3(CSTF2T):c.1457G>A (p.Gly486Asp)	not specified [RCV004372758]	uncertain significance	10	51698093	51698093	Human		name
405689160	CV3245999	single nucleotide variant	NM_015235.3(CSTF2T):c.1622G>T (p.Gly541Val)	not specified [RCV004372759]	likely benign	10	51697928	51697928	Human		name
405689153	CV3246000	single nucleotide variant	NM_015235.3(CSTF2T):c.1624G>A (p.Gly542Ser)	not specified [RCV004372760]	uncertain significance	10	51697926	51697926	Human		name
405689146	CV3246001	single nucleotide variant	NM_015235.3(CSTF2T):c.1640G>T (p.Gly547Val)	not specified [RCV004372761]	uncertain significance	10	51697910	51697910	Human		name
405689141	CV3246002	single nucleotide variant	NM_015235.3(CSTF2T):c.1716G>C (p.Gln572His)	not specified [RCV004372762]	uncertain significance	10	51697834	51697834	Human		name
405689130	CV3246004	single nucleotide variant	NM_015235.3(CSTF2T):c.1717G>C (p.Asp573His)	not specified [RCV004372764]	uncertain significance	10	51697833	51697833	Human		name
405689125	CV3246005	single nucleotide variant	NM_015235.3(CSTF2T):c.1721A>G (p.Gln574Arg)	not specified [RCV004372765]	uncertain significance	10	51697829	51697829	Human		name
405689121	CV3246006	single nucleotide variant	NM_015235.3(CSTF2T):c.1779G>T (p.Met593Ile)	not specified [RCV004372766]	uncertain significance	10	51697771	51697771	Human		name
407478376	CV3426153	single nucleotide variant	NM_015235.3(CSTF2T):c.1036A>C (p.Thr346Pro)	not specified [RCV004615761]	uncertain significance	10	51698514	51698514	Human		name
597805279	CV3651361	single nucleotide variant	NM_015235.3(CSTF2T):c.1777A>G (p.Met593Val)	not specified [RCV004908419]	uncertain significance	10	51697773	51697773	Human		name
597805281	CV3651362	single nucleotide variant	NM_015235.3(CSTF2T):c.1189G>A (p.Gly397Ser)	not specified [RCV004908420]	uncertain significance	10	51698361	51698361	Human		name
597805283	CV3651363	single nucleotide variant	NM_015235.3(CSTF2T):c.1150C>A (p.Pro384Thr)	not specified [RCV004908421]	uncertain significance	10	51698400	51698400	Human		name
597805289	CV3651366	single nucleotide variant	NM_015235.3(CSTF2T):c.1084C>A (p.Pro362Thr)	not specified [RCV004908424]	uncertain significance	10	51698466	51698466	Human		name
597805290	CV3651367	single nucleotide variant	NM_015235.3(CSTF2T):c.1261C>G (p.Arg421Gly)	not specified [RCV004908425]	uncertain significance	10	51698289	51698289	Human		name
597805292	CV3651368	single nucleotide variant	NM_015235.3(CSTF2T):c.1432C>T (p.Pro478Ser)	not specified [RCV004908426]	uncertain significance	10	51698118	51698118	Human		name
598219681	CV3959521	single nucleotide variant	NM_015235.3(CSTF2T):c.1117C>T (p.Arg373Cys)	not specified [RCV005317427]	uncertain significance	10	51698433	51698433	Human		name
598219687	CV3959522	single nucleotide variant	NM_015235.3(CSTF2T):c.1118G>A (p.Arg373His)	not specified [RCV005317428]	uncertain significance	10	51698432	51698432	Human		name
598219694	CV3959523	single nucleotide variant	NM_015235.3(CSTF2T):c.1602A>T (p.Gln534His)	not specified [RCV005317429]	uncertain significance	10	51697948	51697948	Human		name
598219698	CV3959524	single nucleotide variant	NM_015235.3(CSTF2T):c.1216C>A (p.Pro406Thr)	not specified [RCV005317430]	uncertain significance	10	51698334	51698334	Human		name
598219711	CV3959526	single nucleotide variant	NM_015235.3(CSTF2T):c.1357A>G (p.Met453Val)	not specified [RCV005317432]	uncertain significance	10	51698193	51698193	Human		name
15198664	CV701374	deletion	NM_015235.3(CSTF2T):c.720_722del (p.Gln240del)	not provided [RCV000956824]	likely benign	10	51698828	51698830	Human		name

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