Slc25a18 Variant Search Result - Rat Genome Database

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36 records found for search term Slc25a18

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156077939	CV2198266	single nucleotide variant	NM_031481.3(SLC25A18):c.272G>A (p.Arg91Gln)	not specified [RCV004081822]	likely benign	22	17582635	17582635	Human		name
156322970	CV2205306	single nucleotide variant	NM_031481.3(SLC25A18):c.187G>T (p.Gly63Cys)	not specified [RCV004079923]	uncertain significance	22	17581401	17581401	Human		name
156396191	CV2326142	single nucleotide variant	NM_031481.3(SLC25A18):c.122G>A (p.Gly41Glu)	not specified [RCV004180415]	uncertain significance	22	17581138	17581138	Human		name
156343091	CV2364061	single nucleotide variant	NM_031481.3(SLC25A18):c.268C>T (p.Arg90Trp)	not specified [RCV004221445]	uncertain significance	22	17582631	17582631	Human		name
407509250	CV3473961	single nucleotide variant	NM_031481.3(SLC25A18):c.237G>T (p.Lys79Asn)	not specified [RCV004672303]	uncertain significance	22	17582600	17582600	Human		name
156329813	CV2213908	single nucleotide variant	NM_031481.3(SLC25A18):c.412G>A (p.Val138Ile)	not specified [RCV004083639]	uncertain significance	22	17587138	17587138	Human		name
156233221	CV2227744	single nucleotide variant	NM_031481.3(SLC25A18):c.860G>A (p.Arg287Gln)	not specified [RCV004094130]	uncertain significance	22	17590148	17590148	Human		name
156184985	CV2239302	single nucleotide variant	NM_031481.3(SLC25A18):c.479C>T (p.Thr160Ile)	not specified [RCV004114050]	uncertain significance	22	17587205	17587205	Human		name
156340662	CV2268153	single nucleotide variant	NM_031481.3(SLC25A18):c.656C>T (p.Ala219Val)	not specified [RCV004138471]	uncertain significance	22	17588005	17588005	Human		name
156175612	CV2278218	single nucleotide variant	NM_031481.3(SLC25A18):c.312G>A (p.Met104Ile)	not specified [RCV004141404]	uncertain significance	22	17583437	17583437	Human		name
156237169	CV2285780	single nucleotide variant	NM_031481.3(SLC25A18):c.470C>T (p.Ser157Leu)	not specified [RCV004141915]	uncertain significance	22	17587196	17587196	Human		name
156354151	CV2324215	single nucleotide variant	NM_031481.3(SLC25A18):c.428C>T (p.Ser143Leu)	not specified [RCV004176955]	uncertain significance	22	17587154	17587154	Human		name
156039433	CV2332720	single nucleotide variant	NM_031481.3(SLC25A18):c.646G>A (p.Ala216Thr)	not specified [RCV004189394]	likely benign	22	17587995	17587995	Human		name
156331701	CV2339676	single nucleotide variant	NM_031481.3(SLC25A18):c.523C>T (p.Arg175Cys)	not specified [RCV004196380]	uncertain significance	22	17587249	17587249	Human		name
156388127	CV2380121	single nucleotide variant	NM_031481.3(SLC25A18):c.583C>T (p.Pro195Ser)	not specified [RCV004224498]	uncertain significance	22	17587932	17587932	Human		name
156387905	CV2383437	single nucleotide variant	NM_031481.3(SLC25A18):c.762A>C (p.Lys254Asn)	not specified [RCV004222457]	uncertain significance	22	17589621	17589621	Human		name
156082025	CV2384816	single nucleotide variant	NM_031481.3(SLC25A18):c.796G>A (p.Asp266Asn)	not specified [RCV004225706]	uncertain significance	22	17589655	17589655	Human		name
155928016	CV2391627	single nucleotide variant	NM_031481.3(SLC25A18):c.418C>T (p.His140Tyr)	not specified [RCV004241791]	uncertain significance	22	17587144	17587144	Human		name
401749227	CV2710025	single nucleotide variant	NM_031481.3(SLC25A18):c.662T>G (p.Phe221Cys)	not specified [RCV004315087]	uncertain significance	22	17588011	17588011	Human		name
401885541	CV2778131	single nucleotide variant	NM_031481.3(SLC25A18):c.655G>C (p.Ala219Pro)	not specified [RCV004348071]	uncertain significance	22	17588004	17588004	Human		name
405767652	CV3325436	single nucleotide variant	NM_031481.3(SLC25A18):c.299G>A (p.Arg100Gln)	not specified [RCV004456418]	uncertain significance	22	17583424	17583424	Human		name
405767658	CV3325437	single nucleotide variant	NM_031481.3(SLC25A18):c.325G>A (p.Gly109Arg)	not specified [RCV004456419]	uncertain significance	22	17583450	17583450	Human		name
405767662	CV3325438	single nucleotide variant	NM_031481.3(SLC25A18):c.376C>T (p.Leu126Phe)	not specified [RCV004456420]	uncertain significance	22	17583501	17583501	Human		name
405767667	CV3325439	single nucleotide variant	NM_031481.3(SLC25A18):c.403C>T (p.Arg135Cys)	not specified [RCV004456421]	uncertain significance	22	17583528	17583528	Human		name
405767681	CV3325441	single nucleotide variant	NM_031481.3(SLC25A18):c.658T>C (p.Ser220Pro)	not specified [RCV004456423]	uncertain significance	22	17588007	17588007	Human		name
405767687	CV3325442	single nucleotide variant	NM_031481.3(SLC25A18):c.665C>T (p.Ala222Val)	not specified [RCV004456424]	uncertain significance	22	17588014	17588014	Human		name
405767693	CV3325443	single nucleotide variant	NM_031481.3(SLC25A18):c.695G>T (p.Gly232Val)	not specified [RCV004456425]	uncertain significance	22	17588044	17588044	Human		name
405767699	CV3325444	single nucleotide variant	NM_031481.3(SLC25A18):c.712G>A (p.Ala238Thr)	not specified [RCV004456426]	uncertain significance	22	17588061	17588061	Human		name
405767705	CV3325445	single nucleotide variant	NM_031481.3(SLC25A18):c.872T>C (p.Ile291Thr)	not specified [RCV004456427]	uncertain significance	22	17590160	17590160	Human		name
597700213	CV3606274	single nucleotide variant	NM_031481.3(SLC25A18):c.526A>C (p.Thr176Pro)	not specified [RCV004859839]	uncertain significance	22	17587252	17587252	Human		name
597700223	CV3606275	single nucleotide variant	NM_031481.3(SLC25A18):c.707C>T (p.Ala236Val)	not specified [RCV004859840]	uncertain significance	22	17588056	17588056	Human		name
597700231	CV3606276	single nucleotide variant	NM_031481.3(SLC25A18):c.367A>T (p.Met123Leu)	not specified [RCV004859841]	uncertain significance	22	17583492	17583492	Human		name
598168522	CV3918155	single nucleotide variant	NM_031481.3(SLC25A18):c.524G>A (p.Arg175His)	not specified [RCV005284109]	uncertain significance	22	17587250	17587250	Human		name
598168528	CV3918156	single nucleotide variant	NM_031481.3(SLC25A18):c.866T>C (p.Leu289Pro)	not specified [RCV005284110]	uncertain significance	22	17590154	17590154	Human		name
598168534	CV3918157	single nucleotide variant	NM_031481.3(SLC25A18):c.835G>C (p.Ala279Pro)	not specified [RCV005284111]	uncertain significance	22	17590123	17590123	Human		name
598177751	CV4008339	duplication	NC_000007.14:g.18033369_18033372dup	SLC25A18-related disorder [RCV005393858]	uncertain significance	7	18033368	18033369	Human		trait

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