Timm10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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16 records found for search term Timm10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155929152	CV2369672	single nucleotide variant	NM_012456.3(TIMM10):c.16G>T (p.Ala6Ser)	not specified [RCV004215073]	uncertain significance	11	57530174	57530174	Human		name
156156467	CV2238481	single nucleotide variant	NM_012456.3(TIMM10):c.97T>C (p.Cys33Arg)	not specified [RCV004113533]	uncertain significance	11	57528893	57528893	Human		name
407520449	CV3475691	single nucleotide variant	NM_012456.3(TIMM10):c.92G>A (p.Arg31Gln)	not specified [RCV004676961]	uncertain significance	11	57528898	57528898	Human		name
155959571	CV2390552	single nucleotide variant	NM_012456.3(TIMM10):c.242A>G (p.Lys81Arg)	not specified [RCV004239084]	uncertain significance	11	57528748	57528748	Human		name
405768353	CV3345885	single nucleotide variant	NM_012456.3(TIMM10):c.127C>T (p.Leu43Phe)	not specified [RCV004469847]	uncertain significance	11	57528863	57528863	Human		name
598176616	CV3924239	single nucleotide variant	NM_012456.3(TIMM10):c.139G>A (p.Glu47Lys)	not specified [RCV005285668]	uncertain significance	11	57528851	57528851	Human		name
598197706	CV3924240	single nucleotide variant	NM_012456.3(TIMM10):c.186T>G (p.His62Gln)	not specified [RCV005289615]	uncertain significance	11	57528804	57528804	Human		name
401726096	CV2699084	single nucleotide variant	NM_012192.4(TIMM10B):c.11A>C (p.Gln4Pro)	not specified [RCV004303596]	uncertain significance	11	6481527	6481527	Human		name
401890155	CV2763651	single nucleotide variant	NM_012192.4(TIMM10B):c.16C>G (p.Gln6Glu)	not specified [RCV004343157]	uncertain significance	11	6481532	6481532	Human		name
597764461	CV3613464	single nucleotide variant	NM_012192.4(TIMM10B):c.29A>C (p.Gln10Pro)	not specified [RCV004870143]	uncertain significance	11	6481545	6481545	Human		name
597764464	CV3613465	single nucleotide variant	NM_012192.4(TIMM10B):c.38A>G (p.Asn13Ser)	not specified [RCV004870144]	uncertain significance	11	6481554	6481554	Human		name
401751846	CV2702924	single nucleotide variant	NM_012192.4(TIMM10B):c.286C>G (p.Pro96Ala)	not specified [RCV004321254]	uncertain significance	11	6482195	6482195	Human		name
401871136	CV2766826	single nucleotide variant	NM_012192.4(TIMM10B):c.190A>C (p.Met64Leu)	not specified [RCV004349211]	uncertain significance	11	6482099	6482099	Human		name
407520452	CV3475692	single nucleotide variant	NM_012192.4(TIMM10B):c.207G>T (p.Gln69His)	not specified [RCV004676962]	uncertain significance	11	6482116	6482116	Human		name
598197715	CV3924241	single nucleotide variant	NM_012192.4(TIMM10B):c.158C>T (p.Ala53Val)	not specified [RCV005289616]	uncertain significance	11	6482067	6482067	Human		name
329353380	CV2469122	single nucleotide variant	NM_012192.4(TIMM10B):c.304G>C (p.Gly102Arg)	not specified [RCV004274352]	uncertain significance	11	6482213	6482213	Human		name