Sfmbt2 Variant Search Result - Rat Genome Database

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77 records found for search term Sfmbt2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15097683	CV777875	single nucleotide variant	NM_001387889.1(SFMBT2):c.1487+8C>T	not provided [RCV000958370]	benign	10	7202472	7202472	Human		name
8652264	CV128839	single nucleotide variant	NM_001018039.1(SFMBT2):c.1203+3307A>G	Lung cancer [RCV000109326]	uncertain significance	10	7224548	7224548	Human		name
155927602	CV2285190	single nucleotide variant	NM_001387889.1(SFMBT2):c.26A>G (p.Asn9Ser)	not specified [RCV004145398]	likely benign	10	7381873	7381873	Human		name
156191011	CV2356814	single nucleotide variant	NM_001387889.1(SFMBT2):c.32A>C (p.Gln11Pro)	not specified [RCV004202155]	uncertain significance	10	7381867	7381867	Human		name
597673381	CV3595578	single nucleotide variant	NM_001387889.1(SFMBT2):c.94G>T (p.Asp32Tyr)	not specified [RCV004856542]	uncertain significance	10	7381805	7381805	Human		name
598128470	CV3887674	single nucleotide variant	NM_001387889.1(SFMBT2):c.375C>T (p.Ile125=)	not provided [RCV005243848]	likely benign	10	7367710	7367710	Human		name
155994139	CV2286379	single nucleotide variant	NM_001387889.1(SFMBT2):c.128G>T (p.Gly43Val)	not specified [RCV004139906]	uncertain significance	10	7370348	7370348	Human		name
401776730	CV2703337	single nucleotide variant	NM_001387889.1(SFMBT2):c.296C>T (p.Thr99Met)	not specified [RCV004315688]	uncertain significance	10	7367789	7367789	Human		name
401866052	CV2762506	single nucleotide variant	NM_001387889.1(SFMBT2):c.215G>A (p.Ser72Asn)	not specified [RCV004338042]	uncertain significance	10	7367870	7367870	Human		name
401938101	CV2812984	single nucleotide variant	NM_001387889.1(SFMBT2):c.1104C>T (p.Ser368=)	not provided [RCV003417206]	likely benign	10	7243574	7243574	Human		name
405763674	CV3321462	single nucleotide variant	NM_001387889.1(SFMBT2):c.113G>T (p.Ser38Ile)	not specified [RCV004455754]	uncertain significance	10	7370363	7370363	Human		name
597673371	CV3595579	single nucleotide variant	NM_001387889.1(SFMBT2):c.163G>A (p.Ala55Thr)	not specified [RCV004856543]	uncertain significance	10	7370313	7370313	Human		name
156385521	CV2227949	single nucleotide variant	NM_001387889.1(SFMBT2):c.910A>G (p.Met304Val)	not specified [RCV004096201]	uncertain significance	10	7248610	7248610	Human		name
156021168	CV2264430	single nucleotide variant	NM_001387889.1(SFMBT2):c.746A>G (p.Asn249Ser)	not specified [RCV004138328]	uncertain significance	10	7283930	7283930	Human		name
155917690	CV2332864	single nucleotide variant	NM_001387889.1(SFMBT2):c.361T>A (p.Cys121Ser)	not specified [RCV004192127]	uncertain significance	10	7367724	7367724	Human		name
405763758	CV3321476	single nucleotide variant	NM_001387889.1(SFMBT2):c.673G>A (p.Asp225Asn)	not specified [RCV004455768]	uncertain significance	10	7284003	7284003	Human		name
405763763	CV3321477	single nucleotide variant	NM_001387889.1(SFMBT2):c.934T>C (p.Cys312Arg)	not specified [RCV004455769]	uncertain significance	10	7248586	7248586	Human		name
407489833	CV3484003	single nucleotide variant	NM_001387889.1(SFMBT2):c.737G>T (p.Cys246Phe)	not specified [RCV004666170]	uncertain significance	10	7283939	7283939	Human		name
407489853	CV3484008	single nucleotide variant	NM_001387889.1(SFMBT2):c.352G>A (p.Asp118Asn)	not specified [RCV004666174]	uncertain significance	10	7367733	7367733	Human		name
597673422	CV3595573	single nucleotide variant	NM_001387889.1(SFMBT2):c.962C>T (p.Ser321Leu)	not specified [RCV004856538]	uncertain significance	10	7248558	7248558	Human		name
597673353	CV3595581	single nucleotide variant	NM_001387889.1(SFMBT2):c.958G>A (p.Ala320Thr)	not specified [RCV004856545]	uncertain significance	10	7248562	7248562	Human		name
598198352	CV3921109	single nucleotide variant	NM_001387889.1(SFMBT2):c.949A>G (p.Ile317Val)	not specified [RCV005268238]	uncertain significance	10	7248571	7248571	Human		name
598198414	CV3921117	single nucleotide variant	NM_001387889.1(SFMBT2):c.376G>A (p.Ala126Thr)	not specified [RCV005268246]	uncertain significance	10	7367709	7367709	Human		name
15172699	CV724060	single nucleotide variant	NM_001387889.1(SFMBT2):c.877G>A (p.Ala293Thr)	not provided [RCV000883892]	benign	10	7248643	7248643	Human		name
156381708	CV2212320	single nucleotide variant	NM_001387889.1(SFMBT2):c.2102A>G (p.Gln701Arg)	not specified [RCV004091269]	uncertain significance	10	7172544	7172544	Human		name
156331428	CV2218160	single nucleotide variant	NM_001387889.1(SFMBT2):c.2308G>A (p.Val770Met)	not specified [RCV004086582]	uncertain significance	10	7172002	7172002	Human		name
155941117	CV2232445	single nucleotide variant	NM_001387889.1(SFMBT2):c.2312G>T (p.Arg771Leu)	not specified [RCV004099064]	uncertain significance	10	7171998	7171998	Human		name
155984516	CV2247768	single nucleotide variant	NM_001387889.1(SFMBT2):c.1904G>C (p.Cys635Ser)	not specified [RCV004121238]	uncertain significance	10	7176070	7176070	Human		name
156147887	CV2265235	single nucleotide variant	NM_001387889.1(SFMBT2):c.2650G>C (p.Val884Leu)	not specified [RCV004126345]	uncertain significance	10	7163805	7163805	Human		name
155905913	CV2283235	single nucleotide variant	NM_001387889.1(SFMBT2):c.1171G>A (p.Ala391Thr)	not specified [RCV004145907]	likely benign	10	7227887	7227887	Human		name
156127656	CV2283806	single nucleotide variant	NM_001387889.1(SFMBT2):c.1912A>C (p.Asn638His)	not specified [RCV004142322]	uncertain significance	10	7176062	7176062	Human		name
156296763	CV2297606	single nucleotide variant	NM_001387889.1(SFMBT2):c.2212T>C (p.Ser738Pro)	not specified [RCV004155305]	uncertain significance	10	7172098	7172098	Human		name
156081871	CV2301121	single nucleotide variant	NM_001387889.1(SFMBT2):c.2591A>G (p.Gln864Arg)	not specified [RCV004160038]	uncertain significance	10	7163864	7163864	Human		name
156194432	CV2302085	single nucleotide variant	NM_001387889.1(SFMBT2):c.2404G>A (p.Glu802Lys)	not specified [RCV004158843]	uncertain significance	10	7171906	7171906	Human		name
155968031	CV2339262	single nucleotide variant	NM_001387889.1(SFMBT2):c.2098G>C (p.Val700Leu)	not specified [RCV004191502]	uncertain significance	10	7172548	7172548	Human		name
156278335	CV2352162	single nucleotide variant	NM_001387889.1(SFMBT2):c.2146G>A (p.Gly716Arg)	not specified [RCV004191250]	uncertain significance	10	7172500	7172500	Human		name
156223672	CV2355596	single nucleotide variant	NM_001387889.1(SFMBT2):c.2347G>A (p.Gly783Arg)	not specified [RCV004205440]	likely benign	10	7171963	7171963	Human		name
155986760	CV2363706	single nucleotide variant	NM_001387889.1(SFMBT2):c.2434G>A (p.Glu812Lys)	not specified [RCV004216651]	uncertain significance	10	7171038	7171038	Human		name
156180597	CV2374769	single nucleotide variant	NM_001387889.1(SFMBT2):c.2213C>G (p.Ser738Cys)	not specified [RCV004225374]	uncertain significance	10	7172097	7172097	Human		name
156186241	CV2377939	single nucleotide variant	NM_001387889.1(SFMBT2):c.1810T>C (p.Tyr604His)	not specified [RCV004230505]	uncertain significance	10	7176164	7176164	Human		name
156045896	CV2381750	single nucleotide variant	NM_001387889.1(SFMBT2):c.1564G>A (p.Val522Ile)	not specified [RCV004232204]	uncertain significance	10	7197682	7197682	Human		name
329354151	CV2437012	single nucleotide variant	NM_001387889.1(SFMBT2):c.2083C>T (p.Arg695Trp)	not specified [RCV004260378]	uncertain significance	10	7172563	7172563	Human		name
329360830	CV2463024	single nucleotide variant	NM_001387889.1(SFMBT2):c.1130G>A (p.Gly377Asp)	not specified [RCV004272843]	uncertain significance	10	7227928	7227928	Human		name
401731202	CV2707774	single nucleotide variant	NM_001387889.1(SFMBT2):c.1358T>C (p.Ile453Thr)	not specified [RCV004307022]	uncertain significance	10	7205901	7205901	Human		name
401764721	CV2728046	single nucleotide variant	NM_001387889.1(SFMBT2):c.1213A>G (p.Ser405Gly)	not specified [RCV004324162]	uncertain significance	10	7220528	7220528	Human		name
401871740	CV2760034	single nucleotide variant	NM_001387889.1(SFMBT2):c.2098G>A (p.Val700Met)	not specified [RCV004345446]	uncertain significance	10	7172548	7172548	Human		name
401871318	CV2763497	single nucleotide variant	NM_001387889.1(SFMBT2):c.1681G>A (p.Val561Met)	not specified [RCV004343025]	uncertain significance	10	7197565	7197565	Human		name
405763680	CV3321463	single nucleotide variant	NM_001387889.1(SFMBT2):c.1288G>A (p.Val430Ile)	not specified [RCV004455755]	uncertain significance	10	7220453	7220453	Human		name
405763686	CV3321464	single nucleotide variant	NM_001387889.1(SFMBT2):c.1363G>A (p.Asp455Asn)	not specified [RCV004455756]	uncertain significance	10	7205896	7205896	Human		name
405763692	CV3321465	single nucleotide variant	NM_001387889.1(SFMBT2):c.1846G>A (p.Val616Ile)	not specified [RCV004455757]	uncertain significance	10	7176128	7176128	Human		name
405763697	CV3321466	single nucleotide variant	NM_001387889.1(SFMBT2):c.1850G>A (p.Arg617Gln)	not specified [RCV004455758]	uncertain significance	10	7176124	7176124	Human		name
405763704	CV3321467	single nucleotide variant	NM_001387889.1(SFMBT2):c.1925C>T (p.Pro642Leu)	not specified [RCV004455759]	uncertain significance	10	7176049	7176049	Human		name
405763710	CV3321468	single nucleotide variant	NM_001387889.1(SFMBT2):c.2044G>A (p.Asp682Asn)	not specified [RCV004455760]	uncertain significance	10	7172602	7172602	Human		name
405763716	CV3321469	single nucleotide variant	NM_001387889.1(SFMBT2):c.2065G>T (p.Ala689Ser)	not specified [RCV004455761]	uncertain significance	10	7172581	7172581	Human		name
405763722	CV3321470	single nucleotide variant	NM_001387889.1(SFMBT2):c.2081G>A (p.Arg694Gln)	not specified [RCV004455762]	uncertain significance	10	7172565	7172565	Human		name
405763729	CV3321471	single nucleotide variant	NM_001387889.1(SFMBT2):c.2125G>A (p.Val709Met)	not specified [RCV004455763]	uncertain significance	10	7172521	7172521	Human		name
405763735	CV3321472	single nucleotide variant	NM_001387889.1(SFMBT2):c.2243C>T (p.Ser748Leu)	not specified [RCV004455764]	uncertain significance	10	7172067	7172067	Human		name
405763741	CV3321473	single nucleotide variant	NM_001387889.1(SFMBT2):c.2272C>T (p.Arg758Trp)	not specified [RCV004455765]	uncertain significance	10	7172038	7172038	Human		name
405763747	CV3321474	single nucleotide variant	NM_001387889.1(SFMBT2):c.2311C>T (p.Arg771Cys)	not specified [RCV004455766]	uncertain significance	10	7171999	7171999	Human		name
405763753	CV3321475	single nucleotide variant	NM_001387889.1(SFMBT2):c.2324C>T (p.Pro775Leu)	not specified [RCV004455767]	uncertain significance	10	7171986	7171986	Human		name
407492609	CV3484004	single nucleotide variant	NM_001387889.1(SFMBT2):c.1661C>T (p.Ser554Leu)	not specified [RCV004667202]	uncertain significance	10	7197585	7197585	Human		name
407489838	CV3484005	single nucleotide variant	NM_001387889.1(SFMBT2):c.1415A>G (p.Tyr472Cys)	not specified [RCV004666171]	uncertain significance	10	7205844	7205844	Human		name
407489843	CV3484006	single nucleotide variant	NM_001387889.1(SFMBT2):c.2644G>A (p.Glu882Lys)	not specified [RCV004666172]	uncertain significance	10	7163811	7163811	Human		name
407489847	CV3484007	single nucleotide variant	NM_001387889.1(SFMBT2):c.2363C>T (p.Ser788Phe)	not specified [RCV004666173]	uncertain significance	10	7171947	7171947	Human		name
597672444	CV3595572	single nucleotide variant	NM_001387889.1(SFMBT2):c.2138C>T (p.Ala713Val)	not specified [RCV004856537]	uncertain significance	10	7172508	7172508	Human		name
597673410	CV3595574	single nucleotide variant	NM_001387889.1(SFMBT2):c.1345G>A (p.Val449Ile)	not specified [RCV004856539]	likely benign	10	7205914	7205914	Human		name
597673391	CV3595577	single nucleotide variant	NM_001387889.1(SFMBT2):c.2234C>T (p.Thr745Met)	not specified [RCV004856541]	uncertain significance	10	7172076	7172076	Human		name
597673362	CV3595580	single nucleotide variant	NM_001387889.1(SFMBT2):c.1889G>A (p.Cys630Tyr)	not specified [RCV004856544]	uncertain significance	10	7176085	7176085	Human		name
598198338	CV3921107	single nucleotide variant	NM_001387889.1(SFMBT2):c.1214G>A (p.Ser405Asn)	not specified [RCV005268236]	uncertain significance	10	7220527	7220527	Human		name
598198346	CV3921108	single nucleotide variant	NM_001387889.1(SFMBT2):c.2144C>T (p.Ser715Leu)	not specified [RCV005268237]	uncertain significance	10	7172502	7172502	Human		name
598198360	CV3921110	single nucleotide variant	NM_001387889.1(SFMBT2):c.1579T>A (p.Cys527Ser)	not specified [RCV005268239]	uncertain significance	10	7197667	7197667	Human		name
598198369	CV3921111	single nucleotide variant	NM_001387889.1(SFMBT2):c.2249C>T (p.Ala750Val)	not specified [RCV005268240]	uncertain significance	10	7172061	7172061	Human		name
598198381	CV3921113	single nucleotide variant	NM_001387889.1(SFMBT2):c.2393C>T (p.Pro798Leu)	not specified [RCV005268242]	uncertain significance	10	7171917	7171917	Human		name
598198390	CV3921114	single nucleotide variant	NM_001387889.1(SFMBT2):c.2040C>A (p.Asn680Lys)	not specified [RCV005268243]	uncertain significance	10	7172606	7172606	Human		name
598198398	CV3921115	single nucleotide variant	NM_001387889.1(SFMBT2):c.1343C>G (p.Pro448Arg)	not specified [RCV005268244]	uncertain significance	10	7205916	7205916	Human		name
598198407	CV3921116	single nucleotide variant	NM_001387889.1(SFMBT2):c.2180T>C (p.Met727Thr)	not specified [RCV005268245]	uncertain significance	10	7172130	7172130	Human		name
8633714	CV88930	single nucleotide variant	NM_001018039.1(SFMBT2):c.1066A>C (p.Ile356Leu)	Malignant melanoma [RCV000069026]	not provided	10	7243612	7243612	Human		name

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