Gap43 Variant Search Result - Rat Genome Database

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24 records found for search term Gap43

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156245887	CV2283459	single nucleotide variant	NM_002045.4(GAP43):c.31-12167G>A	not specified [RCV004139679]	uncertain significance	3	115663846	115663846	Human		name
401894012	CV2770223	single nucleotide variant	NM_002045.4(GAP43):c.31-12146T>A	not specified [RCV004356113]	likely benign	3	115663867	115663867	Human		name
405750672	CV3251153	single nucleotide variant	NM_002045.4(GAP43):c.31-12204C>T	not specified [RCV004392690]	uncertain significance	3	115663809	115663809	Human		name
15137592	CV708476	single nucleotide variant	NM_002045.4(GAP43):c.31-12223C>T	not provided [RCV000965647]	benign	3	115663790	115663790	Human		name
15151873	CV747905	single nucleotide variant	NM_002045.4(GAP43):c.48C>T (p.Asp16=)	not provided [RCV000923762]	likely benign	3	115676030	115676030	Human		name
405750680	CV3251154	single nucleotide variant	NM_002045.4(GAP43):c.222T>C (p.Val74=)	not specified [RCV004392691]	likely benign	3	115676204	115676204	Human		name
329359648	CV2462155	single nucleotide variant	NM_002045.4(GAP43):c.44A>T (p.Asp15Val)	not specified [RCV004266176]	uncertain significance	3	115676026	115676026	Human		name
405750666	CV3251152	single nucleotide variant	NM_002045.4(GAP43):c.68A>G (p.Asp23Gly)	not specified [RCV004392689]	uncertain significance	3	115676050	115676050	Human		name
598203766	CV3974015	single nucleotide variant	NM_002045.4(GAP43):c.70G>A (p.Gly24Ser)	not specified [RCV005337317]	uncertain significance	3	115676052	115676052	Human		name
156187224	CV2397857	single nucleotide variant	NM_002045.4(GAP43):c.184G>C (p.Ala62Pro)	not specified [RCV004239326]	uncertain significance	3	115676166	115676166	Human		name
407503631	CV3436370	single nucleotide variant	NM_002045.4(GAP43):c.251G>A (p.Gly84Asp)	not specified [RCV004623812]	uncertain significance	3	115676233	115676233	Human		name
597754306	CV3680837	single nucleotide variant	NM_002045.4(GAP43):c.259A>C (p.Thr87Pro)	not specified [RCV004924342]	uncertain significance	3	115676241	115676241	Human		name
598203772	CV3974016	single nucleotide variant	NM_002045.4(GAP43):c.254C>T (p.Thr85Ile)	not specified [RCV005337318]	uncertain significance	3	115676236	115676236	Human		name
156072619	CV2233383	single nucleotide variant	NM_002045.4(GAP43):c.605G>A (p.Ser202Asn)	not specified [RCV004105747]	uncertain significance	3	115676587	115676587	Human		name
156097335	CV2253178	single nucleotide variant	NM_002045.4(GAP43):c.478C>A (p.Pro160Thr)	not specified [RCV004120944]	uncertain significance	3	115676460	115676460	Human		name
156108924	CV2313853	single nucleotide variant	NM_002045.4(GAP43):c.392C>T (p.Ser131Leu)	not specified [RCV004164173]	uncertain significance	3	115676374	115676374	Human		name
156188743	CV2375414	single nucleotide variant	NM_002045.4(GAP43):c.406G>A (p.Gly136Ser)	not specified [RCV004232808]	uncertain significance	3	115676388	115676388	Human		name
405750696	CV3251156	single nucleotide variant	NM_002045.4(GAP43):c.446A>G (p.Asp149Gly)	not specified [RCV004392693]	uncertain significance	3	115676428	115676428	Human		name
407462138	CV3436369	single nucleotide variant	NM_002045.4(GAP43):c.532G>T (p.Ala178Ser)	not specified [RCV004634452]	uncertain significance	3	115676514	115676514	Human		name
597754310	CV3680838	single nucleotide variant	NM_002045.4(GAP43):c.403G>T (p.Ala135Ser)	not specified [RCV004924343]	uncertain significance	3	115676385	115676385	Human		name
598203753	CV3974013	single nucleotide variant	NM_002045.4(GAP43):c.403G>A (p.Ala135Thr)	not specified [RCV005337315]	uncertain significance	3	115676385	115676385	Human		name
598203760	CV3974014	single nucleotide variant	NM_002045.4(GAP43):c.339G>T (p.Lys113Asn)	not specified [RCV005337316]	uncertain significance	3	115676321	115676321	Human		name
8630546	CV85701	single nucleotide variant	NM_001130064.1(GAP43):c.441G>A (p.Glu147=)	Malignant melanoma [RCV000065784]	not provided	3	115676315	115676315	Human		name
8630545	CV85700	single nucleotide variant	NM_001130064.1(GAP43):c.439G>A (p.Glu147Lys)	Malignant melanoma [RCV000065783]	not provided	3	115676313	115676313	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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