Slc4a1ap Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

68 records found for search term Slc4a1ap

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405727308	CV3325578	single nucleotide variant	NM_018158.3(SLC4A1AP):c.4G>C (p.Ala2Pro)	not specified [RCV004463891]	uncertain significance	2	27663918	27663918	Human		name
598245326	CV3911353	single nucleotide variant	NM_018158.3(SLC4A1AP):c.8A>G (p.Asp3Gly)	not specified [RCV005276979]	uncertain significance	2	27663922	27663922	Human		name
155959829	CV2252617	single nucleotide variant	NM_018158.3(SLC4A1AP):c.17C>G (p.Ser6Cys)	not specified [RCV004118493]	uncertain significance	2	27663931	27663931	Human		name
405867082	CV2842602	single nucleotide variant	NM_018158.3(SLC4A1AP):c.150G>A (p.Gly50=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557959]	likely benign	2	27664064	27664064	Human		name
156155528	CV2266149	single nucleotide variant	NM_018158.3(SLC4A1AP):c.88G>A (p.Ala30Thr)	not specified [RCV004128733]	uncertain significance	2	27664002	27664002	Human		name
155946441	CV2266150	single nucleotide variant	NM_018158.3(SLC4A1AP):c.89C>A (p.Ala30Glu)	not specified [RCV004128734]	uncertain significance	2	27664003	27664003	Human		name
156091389	CV2300044	single nucleotide variant	NM_018158.3(SLC4A1AP):c.98G>A (p.Ser33Asn)	not specified [RCV004151249]	uncertain significance	2	27664012	27664012	Human		name
156388845	CV2376141	single nucleotide variant	NM_018158.2(SLC4A1AP):c.86A>C (p.Glu29Ala)	not specified [RCV004220371]	uncertain significance	2	27663838	27663838	Human		name
401857932	CV2765526	single nucleotide variant	NM_018158.2(SLC4A1AP):c.82G>A (p.Gly28Arg)	not specified [RCV004341836]	uncertain significance	2	27663834	27663834	Human		name
405727338	CV3325581	single nucleotide variant	NM_018158.3(SLC4A1AP):c.49A>T (p.Ser17Cys)	not specified [RCV004463894]	uncertain significance	2	27663963	27663963	Human		name
405727362	CV3325584	single nucleotide variant	NM_018158.3(SLC4A1AP):c.83C>T (p.Ser28Phe)	not specified [RCV004463897]	uncertain significance	2	27663997	27663997	Human		name
405727894	CV3325585	single nucleotide variant	NM_018158.3(SLC4A1AP):c.89C>T (p.Ala30Val)	not specified [RCV004463898]	uncertain significance	2	27664003	27664003	Human		name
597689339	CV3596826	single nucleotide variant	NM_018158.2(SLC4A1AP):c.97G>C (p.Asp33His)	not specified [RCV004870678]	uncertain significance	2	27663849	27663849	Human		name
598245309	CV3911351	single nucleotide variant	NM_018158.2(SLC4A1AP):c.61A>G (p.Thr21Ala)	not specified [RCV005276977]	likely benign	2	27663813	27663813	Human		name
156148660	CV2321762	single nucleotide variant	NM_018158.3(SLC4A1AP):c.295C>G (p.Pro99Ala)	not specified [RCV004179755]	uncertain significance	2	27664209	27664209	Human		name
155980586	CV2343566	single nucleotide variant	NM_018158.2(SLC4A1AP):c.106G>C (p.Val36Leu)	not specified [RCV004190598]	uncertain significance	2	27663858	27663858	Human		name
156199098	CV2362839	single nucleotide variant	NM_018158.3(SLC4A1AP):c.173A>G (p.Asn58Ser)	not specified [RCV004208951]	likely benign	2	27664087	27664087	Human		name
156129290	CV2364608	single nucleotide variant	NM_018158.3(SLC4A1AP):c.196C>T (p.Pro66Ser)	not specified [RCV004219502]	uncertain significance	2	27664110	27664110	Human		name
155927712	CV2391494	single nucleotide variant	NM_018158.3(SLC4A1AP):c.158C>A (p.Ala53Glu)	not specified [RCV004239880]	uncertain significance	2	27664072	27664072	Human		name
329365371	CV2444831	single nucleotide variant	NM_018158.3(SLC4A1AP):c.262G>T (p.Val88Phe)	not specified [RCV004259072]	uncertain significance	2	27664176	27664176	Human		name
401865674	CV2755592	single nucleotide variant	NM_018158.3(SLC4A1AP):c.233A>G (p.Gln78Arg)	not specified [RCV004340164]	uncertain significance	2	27664147	27664147	Human		name
597766719	CV3596820	single nucleotide variant	NM_018158.3(SLC4A1AP):c.293C>T (p.Pro98Leu)	not specified [RCV004870673]	uncertain significance	2	27664207	27664207	Human		name
598237440	CV3911350	single nucleotide variant	NM_018158.3(SLC4A1AP):c.173A>C (p.Asn58Thr)	not specified [RCV005275655]	uncertain significance	2	27664087	27664087	Human		name
155998098	CV2288701	single nucleotide variant	NM_018158.3(SLC4A1AP):c.463T>C (p.Tyr155His)	not specified [RCV004153992]	uncertain significance	2	27664377	27664377	Human		name
156189999	CV2325433	single nucleotide variant	NM_018158.3(SLC4A1AP):c.754A>G (p.Lys252Glu)	not specified [RCV004179888]	uncertain significance	2	27665190	27665190	Human		name
156189302	CV2328782	single nucleotide variant	NM_018158.3(SLC4A1AP):c.632T>C (p.Phe211Ser)	not specified [RCV004178007]	uncertain significance	2	27664546	27664546	Human		name
156275207	CV2330657	single nucleotide variant	NM_018158.3(SLC4A1AP):c.908A>C (p.Glu303Ala)	not specified [RCV004183686]	uncertain significance	2	27667316	27667316	Human		name
401747503	CV2688932	single nucleotide variant	NM_018158.3(SLC4A1AP):c.709C>G (p.Gln237Glu)	not specified [RCV004303937]	uncertain significance	2	27665145	27665145	Human		name
401776802	CV2721476	single nucleotide variant	NM_018158.3(SLC4A1AP):c.950A>G (p.Lys317Arg)	not specified [RCV004322206]	uncertain significance	2	27667358	27667358	Human		name
405727882	CV3325586	single nucleotide variant	NM_018158.3(SLC4A1AP):c.379C>G (p.Arg127Gly)	not specified [RCV004463899]	uncertain significance	2	27664293	27664293	Human		name
405727877	CV3325587	single nucleotide variant	NM_018158.3(SLC4A1AP):c.505G>A (p.Glu169Lys)	not specified [RCV004463900]	uncertain significance	2	27664419	27664419	Human		name
405727869	CV3325588	single nucleotide variant	NM_018158.3(SLC4A1AP):c.629G>A (p.Arg210His)	not specified [RCV004463901]	uncertain significance	2	27664543	27664543	Human		name
407515153	CV3480840	single nucleotide variant	NM_018158.3(SLC4A1AP):c.976C>G (p.Arg326Gly)	not specified [RCV004674827]	uncertain significance	2	27667384	27667384	Human		name
407515169	CV3480845	single nucleotide variant	NM_018158.3(SLC4A1AP):c.497C>T (p.Pro166Leu)	not specified [RCV004674832]	uncertain significance	2	27664411	27664411	Human		name
407515172	CV3480846	single nucleotide variant	NM_018158.3(SLC4A1AP):c.901G>A (p.Val301Ile)	not specified [RCV004674833]	uncertain significance	2	27667309	27667309	Human		name
597766713	CV3596819	single nucleotide variant	NM_018158.3(SLC4A1AP):c.524C>T (p.Pro175Leu)	not specified [RCV004870672]	uncertain significance	2	27664438	27664438	Human		name
597766729	CV3596822	single nucleotide variant	NM_018158.3(SLC4A1AP):c.304G>C (p.Glu102Gln)	not specified [RCV004870675]	uncertain significance	2	27664218	27664218	Human		name
597723924	CV3596823	single nucleotide variant	NM_018158.3(SLC4A1AP):c.725G>A (p.Arg242His)	not specified [RCV004862279]	uncertain significance	2	27665161	27665161	Human		name
597766734	CV3596824	single nucleotide variant	NM_018158.3(SLC4A1AP):c.939A>G (p.Ile313Met)	not specified [RCV004870676]	uncertain significance	2	27667347	27667347	Human		name
597766745	CV3596827	single nucleotide variant	NM_018158.3(SLC4A1AP):c.646C>T (p.Arg216Trp)	not specified [RCV004870679]	uncertain significance	2	27664560	27664560	Human		name
598245301	CV3911349	single nucleotide variant	NM_018158.3(SLC4A1AP):c.794A>T (p.Asp265Val)	not specified [RCV005276976]	uncertain significance	2	27665230	27665230	Human		name
156306313	CV2252719	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1172G>A (p.Arg391Gln)	not specified [RCV004118574]	uncertain significance	2	27669376	27669376	Human		name
156310416	CV2260038	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2088G>T (p.Lys696Asn)	not specified [RCV004119051]	uncertain significance	2	27688746	27688746	Human		name
156053499	CV2269507	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1199A>T (p.Lys400Ile)	not specified [RCV004124617]	uncertain significance	2	27675547	27675547	Human		name
156116058	CV2273479	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1498C>T (p.Arg500Trp)	not specified [RCV004132228]	uncertain significance	2	27677821	27677821	Human		name
155902786	CV2386338	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1937A>G (p.Lys646Arg)	not specified [RCV004228677]	uncertain significance	2	27685260	27685260	Human		name
329372894	CV2428699	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1898T>A (p.Val633Glu)	not specified [RCV004255491]	uncertain significance	2	27685221	27685221	Human		name
401738488	CV2676302	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2015C>T (p.Thr672Ile)	not specified [RCV004286338]	uncertain significance	2	27687994	27687994	Human		name
401760640	CV2706029	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1985A>G (p.Gln662Arg)	not specified [RCV004314730]	uncertain significance	2	27687964	27687964	Human		name
401738367	CV2714430	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1613A>C (p.Gln538Pro)	not specified [RCV004317960]	uncertain significance	2	27682259	27682259	Human		name
401874502	CV2759239	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1737A>T (p.Glu579Asp)	not specified [RCV004335837]	uncertain significance	2	27685060	27685060	Human		name
405711903	CV3325577	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1303G>C (p.Ala435Pro)	not specified [RCV004461909]	uncertain significance	2	27675651	27675651	Human		name
405727319	CV3325579	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1724C>G (p.Pro575Arg)	not specified [RCV004463892]	uncertain significance	2	27685047	27685047	Human		name
405727346	CV3325582	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2171C>T (p.Pro724Leu)	not specified [RCV004463895]	uncertain significance	2	27693746	27693746	Human		name
405727353	CV3325583	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2204A>G (p.His735Arg)	not specified [RCV004463896]	uncertain significance	2	27694658	27694658	Human		name
407515155	CV3480841	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1283G>A (p.Arg428His)	not specified [RCV004674828]	uncertain significance	2	27675631	27675631	Human		name
407515159	CV3480842	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2072G>A (p.Gly691Asp)	not specified [RCV004674829]	likely benign	2	27688730	27688730	Human		name
407515162	CV3480843	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1358A>G (p.Asn453Ser)	not specified [RCV004674830]	uncertain significance	2	27677308	27677308	Human		name
407515166	CV3480844	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1039G>A (p.Val347Met)	not specified [RCV004674831]	uncertain significance	2	27668899	27668899	Human		name
407515174	CV3480847	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2192A>G (p.Asp731Gly)	not specified [RCV004674834]	uncertain significance	2	27694646	27694646	Human		name
407515178	CV3480849	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1477A>G (p.Ser493Gly)	not specified [RCV004674835]	uncertain significance	2	27677800	27677800	Human		name
597766724	CV3596821	single nucleotide variant	NM_018158.3(SLC4A1AP):c.2071G>C (p.Gly691Arg)	not specified [RCV004870674]	uncertain significance	2	27688729	27688729	Human		name
597766740	CV3596825	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1709T>C (p.Val570Ala)	not specified [RCV004870677]	uncertain significance	2	27682355	27682355	Human		name
597766750	CV3596828	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1345G>T (p.Val449Phe)	not specified [RCV004870680]	uncertain significance	2	27677295	27677295	Human		name
598245295	CV3911347	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1234A>G (p.Ser412Gly)	not specified [RCV005276975]	uncertain significance	2	27675582	27675582	Human		name
598237433	CV3911348	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1189C>T (p.Arg397Trp)	not specified [RCV005275654]	uncertain significance	2	27675537	27675537	Human		name
598245318	CV3911352	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1827G>T (p.Glu609Asp)	not specified [RCV005276978]	uncertain significance	2	27685150	27685150	Human		name
598245332	CV3911354	single nucleotide variant	NM_018158.3(SLC4A1AP):c.1359T>A (p.Asn453Lys)	not specified [RCV005276980]	uncertain significance	2	27677309	27677309	Human		name

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

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message