Slfn5 Variant Search Result - Rat Genome Database

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84 records found for search term Slfn5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15201311	CV778350	single nucleotide variant	NM_144975.4(SLFN5):c.1012+7G>A	not provided [RCV000957585]	benign	17	35259709	35259709	Human		name
156224777	CV2202999	single nucleotide variant	NM_144975.4(SLFN5):c.31T>C (p.Phe11Leu)	not specified [RCV004069254]	uncertain significance	17	35258721	35258721	Human		name
156278009	CV2209988	single nucleotide variant	NM_144975.4(SLFN5):c.96C>A (p.Asp32Glu)	not specified [RCV004076426]	uncertain significance	17	35258786	35258786	Human		name
401935743	CV2811242	single nucleotide variant	NM_144975.4(SLFN5):c.747G>A (p.Thr249=)	not provided [RCV003413204]	likely benign	17	35259437	35259437	Human		name
155966854	CV2312647	single nucleotide variant	NM_144975.4(SLFN5):c.235C>T (p.Pro79Ser)	not specified [RCV004169382]	uncertain significance	17	35258925	35258925	Human		name
329374823	CV2440061	single nucleotide variant	NM_144975.4(SLFN5):c.101G>A (p.Arg34His)	not specified [RCV004260529]	uncertain significance	17	35258791	35258791	Human		name
329394402	CV2460745	single nucleotide variant	NM_144975.4(SLFN5):c.211C>T (p.Arg71Cys)	not specified [RCV004271078]	uncertain significance	17	35258901	35258901	Human		name
401782147	CV2686557	single nucleotide variant	NM_144975.4(SLFN5):c.137C>T (p.Ala46Val)	not specified [RCV004299990]	uncertain significance	17	35258827	35258827	Human		name
401914512	CV2811243	single nucleotide variant	NM_144975.4(SLFN5):c.1446C>T (p.Gly482=)	not provided [RCV003428225]	likely benign	17	35264490	35264490	Human		name
405772977	CV3333049	single nucleotide variant	NM_144975.4(SLFN5):c.134G>A (p.Arg45Gln)	not specified [RCV004457308]	likely benign	17	35258824	35258824	Human		name
407493833	CV3477416	single nucleotide variant	NM_144975.4(SLFN5):c.269A>G (p.Gln90Arg)	not specified [RCV004667482]	uncertain significance	17	35258959	35258959	Human		name
407493840	CV3477418	single nucleotide variant	NM_144975.4(SLFN5):c.106C>T (p.Arg36Trp)	not specified [RCV004667484]	uncertain significance	17	35258796	35258796	Human		name
407493856	CV3477423	single nucleotide variant	NM_144975.4(SLFN5):c.283T>G (p.Phe95Val)	not specified [RCV004667488]	uncertain significance	17	35258973	35258973	Human		name
597777690	CV3603281	single nucleotide variant	NM_144975.4(SLFN5):c.107G>A (p.Arg36Gln)	not specified [RCV004873093]	uncertain significance	17	35258797	35258797	Human		name
597777717	CV3603292	single nucleotide variant	NM_144975.4(SLFN5):c.124A>G (p.Ile42Val)	not specified [RCV004873100]	uncertain significance	17	35258814	35258814	Human		name
598261533	CV3922337	single nucleotide variant	NM_144975.4(SLFN5):c.119A>G (p.Asn40Ser)	not specified [RCV005280000]	uncertain significance	17	35258809	35258809	Human		name
15119112	CV715380	single nucleotide variant	NM_144975.4(SLFN5):c.176A>G (p.Lys59Arg)	not provided [RCV000962493]	benign	17	35258866	35258866	Human		name
8627966	CV83110	single nucleotide variant	NM_144975.3(SLFN5):c.2565C>T (p.Ile855=)	Malignant melanoma [RCV000063190]	not provided	17	35265777	35265777	Human		name
156377772	CV2207547	single nucleotide variant	NM_144975.4(SLFN5):c.317C>T (p.Ala106Val)	not specified [RCV004090340]	uncertain significance	17	35259007	35259007	Human		name
156285915	CV2232891	single nucleotide variant	NM_144975.4(SLFN5):c.704C>T (p.Thr235Ile)	not specified [RCV004101498]	uncertain significance	17	35259394	35259394	Human		name
155915514	CV2239484	single nucleotide variant	NM_144975.4(SLFN5):c.746C>T (p.Thr249Met)	not specified [RCV004114491]	uncertain significance	17	35259436	35259436	Human		name
155988862	CV2259613	single nucleotide variant	NM_144975.4(SLFN5):c.527T>C (p.Phe176Ser)	not specified [RCV004116654]	uncertain significance	17	35259217	35259217	Human		name
156185569	CV2294962	single nucleotide variant	NM_144975.4(SLFN5):c.580C>T (p.His194Tyr)	not specified [RCV004156109]	uncertain significance	17	35259270	35259270	Human		name
156346568	CV2305393	single nucleotide variant	NM_144975.4(SLFN5):c.977G>A (p.Arg326Lys)	not specified [RCV004171293]	likely benign	17	35259667	35259667	Human		name
401744826	CV2697080	single nucleotide variant	NM_144975.4(SLFN5):c.443A>G (p.Asn148Ser)	not specified [RCV004293059]	uncertain significance	17	35259133	35259133	Human		name
401878610	CV2754712	single nucleotide variant	NM_144975.4(SLFN5):c.478G>C (p.Gly160Arg)	not specified [RCV004339380]	uncertain significance	17	35259168	35259168	Human		name
405772997	CV3333053	single nucleotide variant	NM_144975.4(SLFN5):c.307A>T (p.Asn103Tyr)	not specified [RCV004457312]	uncertain significance	17	35258997	35258997	Human		name
405773002	CV3333054	single nucleotide variant	NM_144975.4(SLFN5):c.523T>G (p.Leu175Val)	not specified [RCV004457313]	uncertain significance	17	35259213	35259213	Human		name
405773016	CV3333056	single nucleotide variant	NM_144975.4(SLFN5):c.597G>T (p.Met199Ile)	not specified [RCV004457315]	uncertain significance	17	35259287	35259287	Human		name
405773023	CV3333057	single nucleotide variant	NM_144975.4(SLFN5):c.676T>C (p.Tyr226His)	not specified [RCV004457316]	uncertain significance	17	35259366	35259366	Human		name
405773028	CV3333058	single nucleotide variant	NM_144975.4(SLFN5):c.730G>C (p.Glu244Gln)	not specified [RCV004457317]	uncertain significance	17	35259420	35259420	Human		name
405773034	CV3333059	single nucleotide variant	NM_144975.4(SLFN5):c.836A>G (p.Asn279Ser)	not specified [RCV004457318]	uncertain significance	17	35259526	35259526	Human		name
407493828	CV3477415	single nucleotide variant	NM_144975.4(SLFN5):c.911C>T (p.Ala304Val)	not specified [RCV004667481]	uncertain significance	17	35259601	35259601	Human		name
407452192	CV3477419	single nucleotide variant	NM_144975.4(SLFN5):c.539G>A (p.Arg180Gln)	not specified [RCV004683923]	uncertain significance	17	35259229	35259229	Human		name
407493849	CV3477421	single nucleotide variant	NM_144975.4(SLFN5):c.781A>C (p.Lys261Gln)	not specified [RCV004667486]	uncertain significance	17	35259471	35259471	Human		name
407493860	CV3477425	single nucleotide variant	NM_144975.4(SLFN5):c.604A>G (p.Thr202Ala)	not specified [RCV004667489]	uncertain significance	17	35259294	35259294	Human		name
407493867	CV3477427	single nucleotide variant	NM_144975.4(SLFN5):c.602C>T (p.Ser201Leu)	not specified [RCV004667491]	uncertain significance	17	35259292	35259292	Human		name
597726058	CV3603282	single nucleotide variant	NM_144975.4(SLFN5):c.638C>T (p.Pro213Leu)	not specified [RCV004862511]	uncertain significance	17	35259328	35259328	Human		name
597777694	CV3603283	single nucleotide variant	NM_144975.4(SLFN5):c.955C>T (p.Arg319Cys)	not specified [RCV004873094]	uncertain significance	17	35259645	35259645	Human		name
598261489	CV3922327	single nucleotide variant	NM_144975.4(SLFN5):c.605C>G (p.Thr202Arg)	not specified [RCV005279990]	uncertain significance	17	35259295	35259295	Human		name
598261493	CV3922328	single nucleotide variant	NM_144975.4(SLFN5):c.538C>T (p.Arg180Trp)	not specified [RCV005279991]	uncertain significance	17	35259228	35259228	Human		name
598261510	CV3922332	single nucleotide variant	NM_144975.4(SLFN5):c.997A>G (p.Met333Val)	not specified [RCV005279995]	uncertain significance	17	35259687	35259687	Human		name
598261514	CV3922333	single nucleotide variant	NM_144975.4(SLFN5):c.622G>A (p.Val208Ile)	not specified [RCV005279996]	uncertain significance	17	35259312	35259312	Human		name
598261529	CV3922336	single nucleotide variant	NM_144975.4(SLFN5):c.400C>G (p.Leu134Val)	not specified [RCV005279999]	uncertain significance	17	35259090	35259090	Human		name
15162178	CV704089	single nucleotide variant	NM_144975.4(SLFN5):c.829G>A (p.Val277Ile)	not provided [RCV000947808]	benign	17	35259519	35259519	Human		name
156143222	CV2200076	single nucleotide variant	NM_144975.4(SLFN5):c.1679A>T (p.Gln560Leu)	not specified [RCV004069657]	uncertain significance	17	35264723	35264723	Human		name
155920671	CV2211907	single nucleotide variant	NM_144975.4(SLFN5):c.2344C>T (p.Arg782Trp)	not specified [RCV004087039]	uncertain significance	17	35265556	35265556	Human		name
155987233	CV2259450	single nucleotide variant	NM_144975.4(SLFN5):c.1454C>A (p.Thr485Asn)	not specified [RCV004122658]	uncertain significance	17	35264498	35264498	Human		name
156256023	CV2277550	single nucleotide variant	NM_144975.4(SLFN5):c.2618T>C (p.Leu873Pro)	not specified [RCV004145237]	uncertain significance	17	35265830	35265830	Human		name
156006954	CV2299634	single nucleotide variant	NM_144975.4(SLFN5):c.1571A>G (p.Gln524Arg)	not specified [RCV004154951]	uncertain significance	17	35264615	35264615	Human		name
155902157	CV2301393	single nucleotide variant	NM_144975.4(SLFN5):c.2050G>T (p.Asp684Tyr)	not specified [RCV004162331]	uncertain significance	17	35265262	35265262	Human		name
155970092	CV2338026	single nucleotide variant	NM_144975.4(SLFN5):c.1380T>A (p.Asp460Glu)	not specified [RCV004186066]	uncertain significance	17	35264424	35264424	Human		name
156175780	CV2355717	single nucleotide variant	NM_144975.4(SLFN5):c.1066C>T (p.Pro356Ser)	not specified [RCV004199079]	uncertain significance	17	35261024	35261024	Human		name
156262654	CV2377024	single nucleotide variant	NM_144975.4(SLFN5):c.1069C>T (p.Arg357Cys)	not specified [RCV004229703]	uncertain significance	17	35261027	35261027	Human		name
156212714	CV2378449	single nucleotide variant	NM_144975.4(SLFN5):c.1127G>A (p.Arg376His)	not specified [RCV004226460]	uncertain significance	17	35261085	35261085	Human		name
329367149	CV2442134	single nucleotide variant	NM_144975.4(SLFN5):c.2021A>G (p.Asp674Gly)	not specified [RCV004264327]	uncertain significance	17	35265233	35265233	Human		name
329389757	CV2445364	single nucleotide variant	NM_144975.4(SLFN5):c.2566G>A (p.Val856Met)	not specified [RCV004263979]	uncertain significance	17	35265778	35265778	Human		name
329393568	CV2453438	single nucleotide variant	NM_144975.4(SLFN5):c.2584G>A (p.Gly862Arg)	not specified [RCV004267045]	uncertain significance	17	35265796	35265796	Human		name
401760090	CV2709597	single nucleotide variant	NM_144975.4(SLFN5):c.1185A>C (p.Glu395Asp)	not specified [RCV004318823]	uncertain significance	17	35264229	35264229	Human		name
401862639	CV2762287	single nucleotide variant	NM_144975.4(SLFN5):c.1039C>G (p.Leu347Val)	not specified [RCV004335407]	uncertain significance	17	35260997	35260997	Human		name
401871043	CV2788998	single nucleotide variant	NM_144975.4(SLFN5):c.1351A>G (p.Ile451Val)	not specified [RCV004363310]	uncertain significance	17	35264395	35264395	Human		name
405772970	CV3333048	single nucleotide variant	NM_144975.4(SLFN5):c.1192T>C (p.Ser398Pro)	not specified [RCV004457307]	uncertain significance	17	35264236	35264236	Human		name
405772981	CV3333050	single nucleotide variant	NM_144975.4(SLFN5):c.2189G>A (p.Arg730Gln)	not specified [RCV004457309]	uncertain significance	17	35265401	35265401	Human		name
405772986	CV3333051	single nucleotide variant	NM_144975.4(SLFN5):c.2455C>T (p.Leu819Phe)	not specified [RCV004457310]	uncertain significance	17	35265667	35265667	Human		name
405772992	CV3333052	single nucleotide variant	NM_144975.4(SLFN5):c.2591C>A (p.Ala864Asp)	not specified [RCV004457311]	uncertain significance	17	35265803	35265803	Human		name
407493837	CV3477417	single nucleotide variant	NM_144975.4(SLFN5):c.1070G>A (p.Arg357His)	not specified [RCV004667483]	uncertain significance	17	35261028	35261028	Human		name
407493852	CV3477422	single nucleotide variant	NM_144975.4(SLFN5):c.2248T>G (p.Trp750Gly)	not specified [RCV004667487]	uncertain significance	17	35265460	35265460	Human		name
407452194	CV3477424	single nucleotide variant	NM_144975.4(SLFN5):c.1726G>T (p.Val576Phe)	not specified [RCV004683924]	uncertain significance	17	35264770	35264770	Human		name
407493864	CV3477426	single nucleotide variant	NM_144975.4(SLFN5):c.1895G>A (p.Arg632Gln)	not specified [RCV004667490]	uncertain significance	17	35265107	35265107	Human		name
597777698	CV3603284	single nucleotide variant	NM_144975.4(SLFN5):c.2204C>T (p.Pro735Leu)	not specified [RCV004873095]	uncertain significance	17	35265416	35265416	Human		name
597777702	CV3603285	single nucleotide variant	NM_144975.4(SLFN5):c.1534C>A (p.Gln512Lys)	not specified [RCV004873096]	uncertain significance	17	35264578	35264578	Human		name
597777706	CV3603286	single nucleotide variant	NM_144975.4(SLFN5):c.1951G>A (p.Ala651Thr)	not specified [RCV004873097]	uncertain significance	17	35265163	35265163	Human		name
597726064	CV3603287	single nucleotide variant	NM_144975.4(SLFN5):c.1099T>G (p.Ser367Ala)	not specified [RCV004862512]	uncertain significance	17	35261057	35261057	Human		name
597777710	CV3603288	single nucleotide variant	NM_144975.4(SLFN5):c.1929C>G (p.Ile643Met)	not specified [RCV004873098]	uncertain significance	17	35265141	35265141	Human		name
597777713	CV3603289	single nucleotide variant	NM_144975.4(SLFN5):c.2466G>T (p.Glu822Asp)	not specified [RCV004873099]	uncertain significance	17	35265678	35265678	Human		name
597726070	CV3603290	single nucleotide variant	NM_144975.4(SLFN5):c.1064C>T (p.Thr355Met)	not specified [RCV004862513]	uncertain significance	17	35261022	35261022	Human		name
597726077	CV3603291	single nucleotide variant	NM_144975.4(SLFN5):c.1453A>C (p.Thr485Pro)	not specified [RCV004862514]	uncertain significance	17	35264497	35264497	Human		name
598261484	CV3922326	single nucleotide variant	NM_144975.4(SLFN5):c.1964G>A (p.Arg655His)	not specified [RCV005279989]	uncertain significance	17	35265176	35265176	Human		name
598261497	CV3922329	single nucleotide variant	NM_144975.4(SLFN5):c.1091A>G (p.His364Arg)	not specified [RCV005279992]	uncertain significance	17	35261049	35261049	Human		name
598261500	CV3922330	single nucleotide variant	NM_144975.4(SLFN5):c.2485A>G (p.Ile829Val)	not specified [RCV005279993]	likely benign	17	35265697	35265697	Human		name
598261505	CV3922331	single nucleotide variant	NM_144975.4(SLFN5):c.2464G>A (p.Glu822Lys)	not specified [RCV005279994]	uncertain significance	17	35265676	35265676	Human		name
598261519	CV3922334	single nucleotide variant	NM_144975.4(SLFN5):c.1651G>A (p.Glu551Lys)	not specified [RCV005279997]	uncertain significance	17	35264695	35264695	Human		name
598261524	CV3922335	single nucleotide variant	NM_144975.4(SLFN5):c.2621T>C (p.Leu874Pro)	not specified [RCV005279998]	uncertain significance	17	35265833	35265833	Human		name
15176695	CV727112	single nucleotide variant	NM_144975.4(SLFN5):c.2107T>C (p.Tyr703His)	not provided [RCV000884640]	benign	17	35265319	35265319	Human		name

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