Slc16a13 Variant Search Result - Rat Genome Database

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34 records found for search term Slc16a13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597675436	CV3599637	single nucleotide variant	NM_201566.3(SLC16A13):c.5C>G (p.Ala2Gly)	not specified [RCV004856860]	uncertain significance	17	7036387	7036387	Human		name
598208943	CV3894815	deletion	NM_201566.3(SLC16A13):c.24del (p.Asp9fs)	Short stature with nonspecific skeletal abnormalities 1 [RCV005358291]	pathogenic	17	7036401	7036401	Human	1	name
405710909	CV3328855	single nucleotide variant	NM_201566.3(SLC16A13):c.11G>A (p.Arg4Lys)	not specified [RCV004448459]	uncertain significance	17	7036393	7036393	Human		name
8628069	CV83213	single nucleotide variant	NM_201566.2(SLC16A13):c.693C>T (p.Phe231=)	Malignant melanoma [RCV000063293]	not provided	17	7038501	7038501	Human		name
156096665	CV2310200	single nucleotide variant	NM_201566.3(SLC16A13):c.293C>G (p.Ser98Cys)	not specified [RCV004163305]	uncertain significance	17	7036820	7036820	Human		name
405710914	CV3328856	single nucleotide variant	NM_201566.3(SLC16A13):c.158C>A (p.Ser53Tyr)	not specified [RCV004448460]	uncertain significance	17	7036540	7036540	Human		name
407519489	CV3477198	single nucleotide variant	NM_201566.3(SLC16A13):c.103G>T (p.Gly35Trp)	not specified [RCV004676532]	uncertain significance	17	7036485	7036485	Human		name
407519494	CV3477202	single nucleotide variant	NM_201566.3(SLC16A13):c.232G>C (p.Gly78Arg)	not specified [RCV004676534]	uncertain significance	17	7036759	7036759	Human		name
407519496	CV3477203	single nucleotide variant	NM_201566.3(SLC16A13):c.154G>A (p.Val52Ile)	not specified [RCV004676535]	uncertain significance	17	7036536	7036536	Human		name
598268424	CV3921613	single nucleotide variant	NM_201566.3(SLC16A13):c.205G>A (p.Val69Ile)	not specified [RCV005281765]	uncertain significance	17	7036732	7036732	Human		name
156205230	CV2249859	single nucleotide variant	NM_201566.3(SLC16A13):c.847C>T (p.Leu283Phe)	not specified [RCV004122841]	uncertain significance	17	7038655	7038655	Human		name
156059349	CV2391740	single nucleotide variant	NM_201566.3(SLC16A13):c.568C>T (p.Arg190Cys)	not specified [RCV004242277]	uncertain significance	17	7038376	7038376	Human		name
329355697	CV2445580	single nucleotide variant	NM_201566.3(SLC16A13):c.760C>G (p.Leu254Val)	not specified [RCV004259668]	uncertain significance	17	7038568	7038568	Human		name
401739914	CV2683204	single nucleotide variant	NM_201566.3(SLC16A13):c.659C>T (p.Thr220Ile)	not specified [RCV004286200]	uncertain significance	17	7038467	7038467	Human		name
401774028	CV2702540	single nucleotide variant	NM_201566.3(SLC16A13):c.569G>A (p.Arg190His)	not specified [RCV004317032]	uncertain significance	17	7038377	7038377	Human		name
401877302	CV2769407	single nucleotide variant	NM_201566.3(SLC16A13):c.752C>T (p.Ala251Val)	not specified [RCV004357394]	uncertain significance	17	7038560	7038560	Human		name
405710922	CV3328857	single nucleotide variant	NM_201566.3(SLC16A13):c.538C>T (p.Leu180Phe)	not specified [RCV004448461]	uncertain significance	17	7038346	7038346	Human		name
405710929	CV3328858	single nucleotide variant	NM_201566.3(SLC16A13):c.875G>C (p.Gly292Ala)	not specified [RCV004448462]	uncertain significance	17	7038683	7038683	Human		name
405710935	CV3328859	single nucleotide variant	NM_201566.3(SLC16A13):c.877G>T (p.Val293Leu)	not specified [RCV004448463]	uncertain significance	17	7038685	7038685	Human		name
405710941	CV3328860	single nucleotide variant	NM_201566.3(SLC16A13):c.895C>A (p.Pro299Thr)	not specified [RCV004448464]	uncertain significance	17	7038703	7038703	Human		name
407503066	CV3477199	single nucleotide variant	NM_201566.3(SLC16A13):c.649C>G (p.Leu217Val)	not specified [RCV004670137]	uncertain significance	17	7038457	7038457	Human		name
407519492	CV3477200	single nucleotide variant	NM_201566.3(SLC16A13):c.613G>T (p.Ala205Ser)	not specified [RCV004676533]	uncertain significance	17	7038421	7038421	Human		name
407503070	CV3477201	single nucleotide variant	NM_201566.3(SLC16A13):c.731T>C (p.Leu244Pro)	not specified [RCV004670138]	uncertain significance	17	7038539	7038539	Human		name
597675446	CV3599638	single nucleotide variant	NM_201566.3(SLC16A13):c.813G>C (p.Trp271Cys)	not specified [RCV004856861]	uncertain significance	17	7038621	7038621	Human		name
598199921	CV3921615	single nucleotide variant	NM_201566.3(SLC16A13):c.442G>A (p.Val148Met)	not specified [RCV005268465]	uncertain significance	17	7038250	7038250	Human		name
598268436	CV3921616	single nucleotide variant	NM_201566.3(SLC16A13):c.460A>G (p.Thr154Ala)	not specified [RCV005281767]	likely benign	17	7038268	7038268	Human		name
598268442	CV3921617	single nucleotide variant	NM_201566.3(SLC16A13):c.349G>A (p.Gly117Ser)	not specified [RCV005281768]	uncertain significance	17	7038157	7038157	Human		name
155975134	CV2270044	single nucleotide variant	NM_201566.3(SLC16A13):c.1091G>A (p.Arg364Gln)	not specified [RCV004129022]	uncertain significance	17	7039772	7039772	Human		name
156036038	CV2303635	single nucleotide variant	NM_201566.3(SLC16A13):c.1160T>C (p.Ile387Thr)	not specified [RCV004161717]	uncertain significance	17	7039841	7039841	Human		name
156283155	CV2360549	single nucleotide variant	NM_201566.3(SLC16A13):c.1258A>G (p.Lys420Glu)	not specified [RCV004211309]	uncertain significance	17	7039939	7039939	Human		name
329378717	CV2459913	single nucleotide variant	NM_201566.3(SLC16A13):c.1226C>G (p.Thr409Arg)	not specified [RCV004279404]	uncertain significance	17	7039907	7039907	Human		name
405710899	CV3328854	single nucleotide variant	NM_201566.3(SLC16A13):c.1058G>A (p.Gly353Glu)	not specified [RCV004448458]	uncertain significance	17	7038866	7038866	Human		name
407503076	CV3477204	single nucleotide variant	NM_201566.3(SLC16A13):c.1106A>C (p.Asn369Thr)	not specified [RCV004670139]	uncertain significance	17	7039787	7039787	Human		name
598268419	CV3921612	single nucleotide variant	NM_201566.3(SLC16A13):c.1207G>A (p.Gly403Arg)	not specified [RCV005281764]	likely benign	17	7039888	7039888	Human		name

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