Tssk4 Variant Search Result - Rat Genome Database

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24 records found for search term Tssk4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155960827	CV2285445	single nucleotide variant	NM_001184739.2(TSSK4):c.56T>G (p.Leu19Arg)	not specified [RCV004139299]	uncertain significance	14	24205979	24205979	Human		name
405799343	CV3341056	single nucleotide variant	NM_001184739.2(TSSK4):c.98A>G (p.His33Arg)	not specified [RCV004476801]	uncertain significance	14	24206021	24206021	Human		name
597788767	CV3618197	single nucleotide variant	NM_001184739.2(TSSK4):c.79G>T (p.Val27Leu)	not specified [RCV004875937]	uncertain significance	14	24206002	24206002	Human		name
156131331	CV2235229	single nucleotide variant	NM_001184739.2(TSSK4):c.250T>A (p.Tyr84Asn)	not specified [RCV004107277]	uncertain significance	14	24206533	24206533	Human		name
329359091	CV2435284	single nucleotide variant	NM_001184739.2(TSSK4):c.113C>T (p.Ser38Leu)	not specified [RCV004252949]	uncertain significance	14	24206036	24206036	Human		name
597788757	CV3618195	single nucleotide variant	NM_001184739.2(TSSK4):c.269G>A (p.Arg90Gln)	not specified [RCV004875935]	likely benign	14	24206552	24206552	Human		name
598252704	CV3925031	single nucleotide variant	NM_001184739.2(TSSK4):c.242G>A (p.Arg81Gln)	not specified [RCV005298942]	uncertain significance	14	24206525	24206525	Human		name
156246466	CV2219093	single nucleotide variant	NM_001184739.2(TSSK4):c.902C>T (p.Ser301Phe)	not specified [RCV004087254]	uncertain significance	14	24208031	24208031	Human		name
156088044	CV2290650	single nucleotide variant	NM_001184739.2(TSSK4):c.688T>G (p.Ser230Ala)	not specified [RCV004149182]	uncertain significance	14	24207363	24207363	Human		name
156056553	CV2326674	single nucleotide variant	NM_001184739.2(TSSK4):c.308A>G (p.Glu103Gly)	not specified [RCV004185253]	uncertain significance	14	24206591	24206591	Human		name
156116745	CV2349410	single nucleotide variant	NM_001184739.2(TSSK4):c.439C>T (p.Arg147Cys)	not specified [RCV004199340]	uncertain significance	14	24206722	24206722	Human		name
329399899	CV2444349	single nucleotide variant	NM_001184739.2(TSSK4):c.487A>C (p.Asn163His)	not specified [RCV004263101]	uncertain significance	14	24207162	24207162	Human		name
405799336	CV3341054	single nucleotide variant	NM_001184739.2(TSSK4):c.586C>G (p.Arg196Gly)	not specified [RCV004476799]	uncertain significance	14	24207261	24207261	Human		name
405799340	CV3341055	single nucleotide variant	NM_001184739.2(TSSK4):c.914A>G (p.Lys305Arg)	not specified [RCV004476800]	uncertain significance	14	24208043	24208043	Human		name
407528693	CV3487113	single nucleotide variant	NM_001184739.2(TSSK4):c.719A>G (p.Tyr240Cys)	not specified [RCV004680520]	uncertain significance	14	24207394	24207394	Human		name
407528696	CV3487114	single nucleotide variant	NM_001184739.2(TSSK4):c.689C>G (p.Ser230Cys)	not specified [RCV004680521]	uncertain significance	14	24207364	24207364	Human		name
407528697	CV3487115	single nucleotide variant	NM_001184739.2(TSSK4):c.856C>T (p.Arg286Cys)	not specified [RCV004680522]	uncertain significance	14	24207985	24207985	Human		name
597788762	CV3618196	single nucleotide variant	NM_001184739.2(TSSK4):c.500A>C (p.Asp167Ala)	not specified [RCV004875936]	uncertain significance	14	24207175	24207175	Human		name
597788771	CV3618198	single nucleotide variant	NM_001184739.2(TSSK4):c.695C>T (p.Thr232Ile)	not specified [RCV004875938]	uncertain significance	14	24207370	24207370	Human		name
597788775	CV3618199	single nucleotide variant	NM_001184739.2(TSSK4):c.928C>G (p.Gln310Glu)	not specified [RCV004875939]	uncertain significance	14	24208057	24208057	Human		name
597788780	CV3618201	single nucleotide variant	NM_001184739.2(TSSK4):c.654G>C (p.Glu218Asp)	not specified [RCV004875940]	uncertain significance	14	24207329	24207329	Human		name
597788784	CV3618202	single nucleotide variant	NM_001184739.2(TSSK4):c.518A>G (p.Lys173Arg)	not specified [RCV004875941]	uncertain significance	14	24207193	24207193	Human		name
598217038	CV3925030	single nucleotide variant	NM_001184739.2(TSSK4):c.857G>A (p.Arg286His)	not specified [RCV005292965]	likely benign	14	24207986	24207986	Human		name
156033259	CV2376574	single nucleotide variant	NM_001184739.2(TSSK4):c.1010C>T (p.Thr337Met)	not specified [RCV004220737]	uncertain significance	14	24208139	24208139	Human		name

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