Akt1s1 Variant Search Result - Rat Genome Database

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39 records found for search term Akt1s1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155935460	CV2371805	single nucleotide variant	NM_001098633.4(AKT1S1):c.8C>T (p.Ser3Leu)	not specified [RCV004219462]	uncertain significance	19	49873288	49873288	Human		name
401910703	CV2818616	single nucleotide variant	NM_001098633.4(AKT1S1):c.99G>A (p.Ala33=)	not provided [RCV003425348]	likely benign	19	49873197	49873197	Human		name
401910704	CV2818617	single nucleotide variant	NM_001098633.4(AKT1S1):c.48C>T (p.Ala16=)	not provided [RCV003425349]	likely benign	19	49873248	49873248	Human		name
156275251	CV2202724	single nucleotide variant	NM_001098633.4(AKT1S1):c.19G>A (p.Glu7Lys)	not specified [RCV004082968]	uncertain significance	19	49873277	49873277	Human		name
15180491	CV728348	single nucleotide variant	NM_001098633.4(AKT1S1):c.165G>A (p.Ala55=)	not provided [RCV000885541]	benign	19	49873131	49873131	Human		name
156062664	CV2321014	single nucleotide variant	NM_001098633.4(AKT1S1):c.46G>C (p.Ala16Pro)	not specified [RCV004172806]	uncertain significance	19	49873250	49873250	Human		name
156062678	CV2321015	single nucleotide variant	NM_001098633.4(AKT1S1):c.83T>C (p.Leu28Pro)	not specified [RCV004172807]	uncertain significance	19	49873213	49873213	Human		name
155989003	CV2371885	single nucleotide variant	NM_001098633.4(AKT1S1):c.67C>T (p.Arg23Trp)	not specified [RCV004221574]	uncertain significance	19	49873229	49873229	Human		name
401767749	CV2729881	single nucleotide variant	NM_001098633.4(AKT1S1):c.55C>T (p.Arg19Cys)	not specified [RCV004332885]	uncertain significance	19	49873241	49873241	Human		name
405792229	CV3263654	single nucleotide variant	NM_001098633.4(AKT1S1):c.37G>A (p.Val13Met)	not specified [RCV004400124]	uncertain significance	19	49873259	49873259	Human		name
405792384	CV3263705	single nucleotide variant	NM_001098633.4(AKT1S1):c.95C>T (p.Thr32Ile)	not specified [RCV004400175]	uncertain significance	19	49873201	49873201	Human		name
598202099	CV3977124	single nucleotide variant	NM_001098633.4(AKT1S1):c.77C>T (p.Thr26Met)	not specified [RCV005337029]	uncertain significance	19	49873219	49873219	Human		name
15194235	CV728347	single nucleotide variant	NM_001098633.4(AKT1S1):c.348C>T (p.Ser116=)	not provided [RCV000889167]	benign	19	49872948	49872948	Human		name
156382209	CV2212644	single nucleotide variant	NM_001098633.4(AKT1S1):c.226C>T (p.Arg76Trp)	not specified [RCV004085169]	uncertain significance	19	49873070	49873070	Human		name
156054871	CV2326542	single nucleotide variant	NM_001098633.4(AKT1S1):c.190G>A (p.Asp64Asn)	not specified [RCV004183092]	uncertain significance	19	49873106	49873106	Human		name
155908848	CV2387456	single nucleotide variant	NM_001098633.4(AKT1S1):c.146A>G (p.His49Arg)	not specified [RCV004240321]	uncertain significance	19	49873150	49873150	Human		name
401885400	CV2762914	single nucleotide variant	NM_001098633.4(AKT1S1):c.164C>T (p.Ala55Val)	not specified [RCV004342665]	uncertain significance	19	49873132	49873132	Human		name
405792211	CV3267482	single nucleotide variant	NM_001098633.4(AKT1S1):c.236C>T (p.Ala79Val)	not specified [RCV004400118]	uncertain significance	19	49873060	49873060	Human		name
597757863	CV3677831	single nucleotide variant	NM_001098633.4(AKT1S1):c.178C>T (p.Arg60Cys)	not specified [RCV004925163]	uncertain significance	19	49873118	49873118	Human		name
597755145	CV3677841	single nucleotide variant	NM_001098633.4(AKT1S1):c.226C>G (p.Arg76Gly)	not specified [RCV004924544]	uncertain significance	19	49873070	49873070	Human		name
598158232	CV3977133	single nucleotide variant	NM_001098633.4(AKT1S1):c.152G>A (p.Arg51Gln)	not specified [RCV005327949]	uncertain significance	19	49873144	49873144	Human		name
156229197	CV2234953	single nucleotide variant	NM_001098633.4(AKT1S1):c.590G>C (p.Arg197Thr)	not specified [RCV004113153]	uncertain significance	19	49871584	49871584	Human		name
155975267	CV2235842	single nucleotide variant	NM_001098633.4(AKT1S1):c.758A>G (p.Lys253Arg)	not specified [RCV004111958]	uncertain significance	19	49869930	49869930	Human		name
156065464	CV2272509	single nucleotide variant	NM_001098633.4(AKT1S1):c.344C>A (p.Thr115Asn)	not specified [RCV004133415]	uncertain significance	19	49872952	49872952	Human		name
156147525	CV2377255	single nucleotide variant	NM_001098633.4(AKT1S1):c.385T>A (p.Phe129Ile)	not specified [RCV004225445]	uncertain significance	19	49871884	49871884	Human		name
401730059	CV2683928	single nucleotide variant	NM_001098633.4(AKT1S1):c.702G>T (p.Gln234His)	not specified [RCV004284647]	uncertain significance	19	49869986	49869986	Human		name
401783191	CV2716172	single nucleotide variant	NM_001098633.4(AKT1S1):c.509C>A (p.Pro170His)	not specified [RCV004323406]	uncertain significance	19	49871665	49871665	Human		name
401892178	CV2775983	single nucleotide variant	NM_001098633.4(AKT1S1):c.735C>G (p.Asn245Lys)	not specified [RCV004344998]	uncertain significance	19	49869953	49869953	Human		name
405792223	CV3263652	single nucleotide variant	NM_001098633.4(AKT1S1):c.319G>A (p.Glu107Lys)	not specified [RCV004400122]	uncertain significance	19	49872977	49872977	Human		name
405792255	CV3263663	single nucleotide variant	NM_001098633.4(AKT1S1):c.403G>A (p.Ala135Thr)	not specified [RCV004400133]	likely benign	19	49871866	49871866	Human		name
405792314	CV3263683	single nucleotide variant	NM_001098633.4(AKT1S1):c.712G>C (p.Asp238His)	not specified [RCV004400153]	uncertain significance	19	49869976	49869976	Human		name
405792341	CV3263691	single nucleotide variant	NM_001098633.4(AKT1S1):c.755T>A (p.Leu252Gln)	not specified [RCV004400161]	uncertain significance	19	49869933	49869933	Human		name
407464527	CV3433572	single nucleotide variant	NM_001098633.4(AKT1S1):c.341A>G (p.Glu114Gly)	not specified [RCV004635101]	uncertain significance	19	49872955	49872955	Human		name
407464568	CV3443608	single nucleotide variant	NM_001098633.4(AKT1S1):c.425C>G (p.Pro142Arg)	not specified [RCV004635111]	uncertain significance	19	49871844	49871844	Human		name
407464596	CV3443617	single nucleotide variant	NM_001098633.4(AKT1S1):c.365T>C (p.Ile122Thr)	not specified [RCV004635120]	uncertain significance	19	49872931	49872931	Human		name
407464628	CV3443625	single nucleotide variant	NM_001098633.4(AKT1S1):c.724C>T (p.Pro242Ser)	not specified [RCV004635128]	uncertain significance	19	49869964	49869964	Human		name
597757848	CV3677822	single nucleotide variant	NM_001098633.4(AKT1S1):c.479C>A (p.Thr160Asn)	not specified [RCV004925160]	uncertain significance	19	49871695	49871695	Human		name
598202174	CV3977144	single nucleotide variant	NM_001098633.4(AKT1S1):c.425C>A (p.Pro142His)	not specified [RCV005337045]	uncertain significance	19	49871844	49871844	Human		name
598202225	CV3977155	single nucleotide variant	NM_001098633.4(AKT1S1):c.577T>C (p.Phe193Leu)	not specified [RCV005337054]	uncertain significance	19	49871597	49871597	Human		name

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