Kcnip4 Variant Search Result - Rat Genome Database

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37 records found for search term Kcnip4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8625765	CV80889	single nucleotide variant	KCNIP4:c.89-32038C>T	Malignant melanoma [RCV000060966]	not provided	4	20882705	20882705	Human		name
405284229	CV3196712	single nucleotide variant	NM_025221.6(KCNIP4):c.429+7T>C	KCNIP4-related disorder [RCV003979608]	benign	4	20749655	20749655	Human		name , trait , alternate_id
15137736	CV779201	single nucleotide variant	NM_025221.6(KCNIP4):c.289-7T>C	not provided [RCV000965671]	benign	4	20758897	20758897	Human		name
8579632	CV114034	single nucleotide variant	NM_025221.5(KCNIP4):c.61+191225G>T	Lung cancer [RCV000094557]	uncertain significance	4	21757346	21757346	Human		name
8579633	CV114035	single nucleotide variant	NM_025221.5(KCNIP4):c.61+152705C>G	Lung cancer [RCV000094558]	uncertain significance	4	21795866	21795866	Human		name
8579634	CV114036	single nucleotide variant	NM_025221.5(KCNIP4):c.61+120890T>A	Lung cancer [RCV000094559]	uncertain significance	4	21827681	21827681	Human		name
8579635	CV114037	single nucleotide variant	NM_025221.5(KCNIP4):c.61+101507A>G	Lung cancer [RCV000094560]	uncertain significance	4	21847064	21847064	Human		name
11087755	CV227749	single nucleotide variant	NM_025221.5(KCNIP4):c.62-506862C>T	Ace Inhibitors, Plain response - Toxicity/ADR [RCV000211329]	drug response	4	21389571	21389571	Human		name
21068799	CV795578	single nucleotide variant	NM_025221.6(KCNIP4):c.61+251149A>T	not provided [RCV000998231]	uncertain significance	4	21697422	21697422	Human		name
8579631	CV114033	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+2078G>T	Lung cancer [RCV000094556]	uncertain significance	4	21695272	21695272	Human		name
8579616	CV114018	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-82173A>G	Lung cancer [RCV000094541]	uncertain significance	4	20932840	20932840	Human		name
8579628	CV114030	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+95638G>A	Lung cancer [RCV000094553]	uncertain significance	4	21601712	21601712	Human		name
8579629	CV114031	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+65296T>A	Lung cancer [RCV000094554]	uncertain significance	4	21632054	21632054	Human		name
8579617	CV114019	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-152962G>T	Lung cancer [RCV000094542]	uncertain significance	4	21003629	21003629	Human		name
8579618	CV114020	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-236805C>G	Lung cancer [RCV000094543]	uncertain significance	4	21087472	21087472	Human		name
8579619	CV114021	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-291388C>A	Lung cancer [RCV000094544]	uncertain significance	4	21142055	21142055	Human		name
8579620	CV114022	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-326358C>G	Lung cancer [RCV000094545]	uncertain significance	4	21177025	21177025	Human		name
8579621	CV114023	single nucleotide variant	NM_001035003.1(KCNIP4):c.89-391883A>G	Lung cancer [RCV000094546]	uncertain significance	4	21242550	21242550	Human		name
8579622	CV114024	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+337612C>A	Lung cancer [RCV000094547]	uncertain significance	4	21359738	21359738	Human		name
8579623	CV114025	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+316795C>A	Lung cancer [RCV000094548]	uncertain significance	4	21380555	21380555	Human		name
8579624	CV114026	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+283936C>T	Lung cancer [RCV000094549]	uncertain significance	4	21413414	21413414	Human		name
8579625	CV114027	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+275840A>C	Lung cancer [RCV000094550]	uncertain significance	4	21421510	21421510	Human		name
8579626	CV114028	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+185538T>C	Lung cancer [RCV000094551]	uncertain significance	4	21511812	21511812	Human		name
8579627	CV114029	single nucleotide variant	NM_001035003.1(KCNIP4):c.88+173273G>A	Lung cancer [RCV000094552]	uncertain significance	4	21524077	21524077	Human		name
156273880	CV2254681	single nucleotide variant	NM_025221.6(KCNIP4):c.16G>A (p.Val6Met)	not specified [RCV004115167]	uncertain significance	4	21948616	21948616	Human		name
405287809	CV3217970	single nucleotide variant	NM_025221.6(KCNIP4):c.210T>C (p.Pro70=)	KCNIP4-related disorder [RCV003982094]	benign	4	20850621	20850621	Human		name , trait , alternate_id
405287886	CV3217972	single nucleotide variant	NM_025221.6(KCNIP4):c.288T>C (p.Asn96=)	KCNIP4-related disorder [RCV003982096]	benign	4	20850543	20850543	Human		name , trait , alternate_id
155927142	CV2345343	single nucleotide variant	NM_025221.6(KCNIP4):c.169G>A (p.Val57Met)	not specified [RCV004198123]	uncertain significance	4	20850662	20850662	Human		name
405806687	CV3268686	single nucleotide variant	NM_025221.6(KCNIP4):c.122T>C (p.Leu41Ser)	not specified [RCV004406200]	uncertain significance	4	20882649	20882649	Human		name
405806689	CV3268687	single nucleotide variant	NM_025221.6(KCNIP4):c.167G>A (p.Ser56Asn)	not specified [RCV004406201]	uncertain significance	4	20850664	20850664	Human		name
407511777	CV3445056	single nucleotide variant	NM_025221.6(KCNIP4):c.223C>T (p.Leu75Phe)	not specified [RCV004626573]	uncertain significance	4	20850608	20850608	Human		name
597766936	CV3687548	single nucleotide variant	NM_025221.6(KCNIP4):c.196G>A (p.Val66Ile)	not specified [RCV004927174]	uncertain significance	4	20850635	20850635	Human		name
597766945	CV3687550	single nucleotide variant	NM_025221.6(KCNIP4):c.202C>T (p.His68Tyr)	not specified [RCV004927176]	uncertain significance	4	20850629	20850629	Human		name
156072568	CV2325340	single nucleotide variant	NM_025221.6(KCNIP4):c.410A>G (p.Asn137Ser)	not specified [RCV004177721]	uncertain significance	4	20749681	20749681	Human		name
405806691	CV3268688	single nucleotide variant	NM_025221.6(KCNIP4):c.320C>A (p.Thr107Asn)	not specified [RCV004406202]	uncertain significance	4	20758859	20758859	Human		name
597766940	CV3687549	single nucleotide variant	NM_025221.6(KCNIP4):c.460C>T (p.Arg154Trp)	not specified [RCV004927175]	uncertain significance	4	20734705	20734705	Human		name
598259806	CV3976123	single nucleotide variant	NM_025221.6(KCNIP4):c.376C>T (p.His126Tyr)	not specified [RCV005347496]	uncertain significance	4	20749715	20749715	Human		name

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