Cisd3 Variant Search Result - Rat Genome Database

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16 records found for search term Cisd3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156179127	CV2355988	single nucleotide variant	NM_001136498.2(CISD3):c.29C>T (p.Pro10Leu)	not specified [RCV004201367]	uncertain significance	17	38730387	38730387	Human		name
156198562	CV2362801	single nucleotide variant	NM_001136498.2(CISD3):c.86C>T (p.Ala29Val)	not specified [RCV004208918]	uncertain significance	17	38731321	38731321	Human		name
156165305	CV2376341	single nucleotide variant	NM_001136498.2(CISD3):c.47G>C (p.Arg16Pro)	not specified [RCV004222601]	uncertain significance	17	38730405	38730405	Human		name
329356953	CV2460627	single nucleotide variant	NM_001136498.2(CISD3):c.85G>A (p.Ala29Thr)	not specified [RCV004268893]	uncertain significance	17	38731320	38731320	Human		name
401781874	CV2689974	single nucleotide variant	NM_001136498.2(CISD3):c.34G>A (p.Ala12Thr)	not specified [RCV004297858]	uncertain significance	17	38730392	38730392	Human		name
598231571	CV3948195	single nucleotide variant	NM_001136498.2(CISD3):c.85G>C (p.Ala29Pro)	not specified [RCV005319575]	uncertain significance	17	38731320	38731320	Human		name
156149386	CV2234771	single nucleotide variant	NM_001136498.2(CISD3):c.250C>T (p.Pro84Ser)	not specified [RCV004111214]	uncertain significance	17	38733321	38733321	Human		name
401748165	CV2700019	single nucleotide variant	NM_001136498.2(CISD3):c.236G>A (p.Arg79His)	not specified [RCV004310446]	uncertain significance	17	38733307	38733307	Human		name
405683908	CV3293910	single nucleotide variant	NM_001136498.2(CISD3):c.174G>C (p.Arg58Ser)	not specified [RCV004443970]	uncertain significance	17	38731409	38731409	Human		name
405683919	CV3293912	single nucleotide variant	NM_001136498.2(CISD3):c.282G>A (p.Met94Ile)	not specified [RCV004443972]	uncertain significance	17	38733353	38733353	Human		name
407456522	CV3419197	single nucleotide variant	NM_001136498.2(CISD3):c.187G>A (p.Gly63Ser)	not specified [RCV004610757]	uncertain significance	17	38731422	38731422	Human		name
407456524	CV3419198	single nucleotide variant	NM_001136498.2(CISD3):c.275C>T (p.Thr92Ile)	not specified [RCV004610758]	uncertain significance	17	38733346	38733346	Human		name
407456527	CV3419199	single nucleotide variant	NM_001136498.2(CISD3):c.188G>A (p.Gly63Asp)	not specified [RCV004610759]	uncertain significance	17	38731423	38731423	Human		name
597781441	CV3650393	single nucleotide variant	NM_001136498.2(CISD3):c.118G>A (p.Val40Met)	not specified [RCV004899782]	uncertain significance	17	38731353	38731353	Human		name
597781445	CV3650394	single nucleotide variant	NM_001136498.2(CISD3):c.161G>A (p.Gly54Glu)	not specified [RCV004899783]	uncertain significance	17	38731396	38731396	Human		name
156238969	CV2217130	single nucleotide variant	NM_001136498.2(CISD3):c.350G>A (p.Arg117His)	not specified [RCV004085802]	uncertain significance	17	38733421	38733421	Human		name