Tbc1d14 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

66 records found for search term Tbc1d14

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155990887	CV2256383	single nucleotide variant	NM_020773.3(TBC1D14):c.14A>G (p.Lys5Arg)	not specified [RCV004116828]	uncertain significance	4	6923403	6923403	Human		name
15184090	CV709426	single nucleotide variant	NM_020773.3(TBC1D14):c.255C>T (p.His85=)	not provided [RCV000975029]	benign	4	6923644	6923644	Human		name
156335420	CV2211463	single nucleotide variant	NM_020773.3(TBC1D14):c.60T>G (p.Asp20Glu)	not specified [RCV004084376]	uncertain significance	4	6923449	6923449	Human		name
401880279	CV2770025	single nucleotide variant	NM_020773.3(TBC1D14):c.32A>G (p.Asn11Ser)	not specified [RCV004353849]	uncertain significance	4	6923421	6923421	Human		name
407512403	CV3475433	single nucleotide variant	NM_020773.3(TBC1D14):c.65G>A (p.Arg22Gln)	not specified [RCV004673371]	uncertain significance	4	6923454	6923454	Human		name
597760620	CV3609354	single nucleotide variant	NM_020773.3(TBC1D14):c.28A>G (p.Thr10Ala)	not specified [RCV004869266]	uncertain significance	4	6923417	6923417	Human		name
598195914	CV3916602	single nucleotide variant	NM_020773.3(TBC1D14):c.37G>C (p.Val13Leu)	not specified [RCV005289329]	uncertain significance	4	6923426	6923426	Human		name
15174427	CV709425	single nucleotide variant	NM_020773.3(TBC1D14):c.97G>A (p.Val33Ile)	not provided [RCV000972714]	benign	4	6923486	6923486	Human		name
156223859	CV2219222	single nucleotide variant	NM_020773.3(TBC1D14):c.128C>T (p.Ala43Val)	not specified [RCV004093483]	uncertain significance	4	6923517	6923517	Human		name
156210282	CV2259795	single nucleotide variant	NM_020773.3(TBC1D14):c.253C>T (p.His85Tyr)	not specified [RCV004117068]	uncertain significance	4	6923642	6923642	Human		name
156052538	CV2363470	single nucleotide variant	NM_020773.3(TBC1D14):c.260G>A (p.Arg87Lys)	not specified [RCV004216044]	likely benign	4	6923649	6923649	Human		name
329364773	CV2443849	single nucleotide variant	NM_020773.3(TBC1D14):c.248C>T (p.Ala83Val)	not specified [RCV004258189]	likely benign	4	6923637	6923637	Human		name
329371097	CV2461946	single nucleotide variant	NM_020773.3(TBC1D14):c.197C>T (p.Ser66Leu)	not specified [RCV004271846]	uncertain significance	4	6923586	6923586	Human		name
405780197	CV3324671	single nucleotide variant	NM_020773.3(TBC1D14):c.127G>C (p.Ala43Pro)	not specified [RCV004471819]	uncertain significance	4	6923516	6923516	Human		name
405780225	CV3324676	single nucleotide variant	NM_020773.3(TBC1D14):c.269A>G (p.Gln90Arg)	not specified [RCV004471824]	uncertain significance	4	6923658	6923658	Human		name
407512405	CV3475432	single nucleotide variant	NM_020773.3(TBC1D14):c.154C>T (p.Leu52Phe)	not specified [RCV004673370]	uncertain significance	4	6923543	6923543	Human		name
597760593	CV3609347	single nucleotide variant	NM_020773.3(TBC1D14):c.119T>A (p.Leu40His)	not specified [RCV004869260]	uncertain significance	4	6923508	6923508	Human		name
597760605	CV3609351	single nucleotide variant	NM_020773.3(TBC1D14):c.110C>T (p.Ala37Val)	not specified [RCV004869263]	uncertain significance	4	6923499	6923499	Human		name
597760610	CV3609352	single nucleotide variant	NM_020773.3(TBC1D14):c.295C>T (p.Arg99Trp)	not specified [RCV004869264]	uncertain significance	4	6923684	6923684	Human		name
597760624	CV3609355	single nucleotide variant	NM_020773.3(TBC1D14):c.142C>T (p.Pro48Ser)	not specified [RCV004869267]	uncertain significance	4	6923531	6923531	Human		name
598265402	CV3916600	single nucleotide variant	NM_020773.3(TBC1D14):c.101A>G (p.Asn34Ser)	not specified [RCV005280969]	uncertain significance	4	6923490	6923490	Human		name
156219469	CV2225936	single nucleotide variant	NM_020773.3(TBC1D14):c.412G>C (p.Val138Leu)	not specified [RCV004105108]	uncertain significance	4	6923801	6923801	Human		name
156205581	CV2297893	single nucleotide variant	NM_020773.3(TBC1D14):c.352A>C (p.Thr118Pro)	not specified [RCV004157829]	uncertain significance	4	6923741	6923741	Human		name
156068351	CV2320413	single nucleotide variant	NM_020773.3(TBC1D14):c.425G>A (p.Ser142Asn)	not specified [RCV004178565]	uncertain significance	4	6923814	6923814	Human		name
155920445	CV2350503	single nucleotide variant	NM_020773.3(TBC1D14):c.358C>T (p.Arg120Trp)	not specified [RCV004204866]	uncertain significance	4	6923747	6923747	Human		name
156339624	CV2367637	single nucleotide variant	NM_020773.3(TBC1D14):c.475G>A (p.Val159Met)	not specified [RCV004211560]	uncertain significance	4	6923864	6923864	Human		name
329381624	CV2441464	single nucleotide variant	NM_020773.3(TBC1D14):c.802C>T (p.Leu268Phe)	not specified [RCV004257259]	uncertain significance	4	6967383	6967383	Human		name
329367369	CV2456780	single nucleotide variant	NM_020773.3(TBC1D14):c.332C>T (p.Ala111Val)	not specified [RCV004270755]	uncertain significance	4	6923721	6923721	Human		name
401728381	CV2672905	single nucleotide variant	NM_020773.3(TBC1D14):c.316G>A (p.Ala106Thr)	not specified [RCV004283910]	uncertain significance	4	6923705	6923705	Human		name
401727863	CV2678528	single nucleotide variant	NM_020773.3(TBC1D14):c.305A>G (p.Gln102Arg)	not specified [RCV004292540]	uncertain significance	4	6923694	6923694	Human		name
401736933	CV2689524	single nucleotide variant	NM_020773.3(TBC1D14):c.779G>C (p.Trp260Ser)	not specified [RCV004308361]	uncertain significance	4	6967360	6967360	Human		name
405780238	CV3324678	single nucleotide variant	NM_020773.3(TBC1D14):c.410C>T (p.Ser137Leu)	not specified [RCV004471826]	uncertain significance	4	6923799	6923799	Human		name
405780245	CV3324679	single nucleotide variant	NM_020773.3(TBC1D14):c.464C>T (p.Ser155Phe)	not specified [RCV004471827]	uncertain significance	4	6923853	6923853	Human		name
405780247	CV3324680	single nucleotide variant	NM_020773.3(TBC1D14):c.535G>C (p.Asp179His)	not specified [RCV004471828]	uncertain significance	4	6923924	6923924	Human		name
405780252	CV3324681	single nucleotide variant	NM_020773.3(TBC1D14):c.767A>G (p.Asn256Ser)	not specified [RCV004471829]	likely benign	4	6967348	6967348	Human		name
405780258	CV3324682	single nucleotide variant	NM_020773.3(TBC1D14):c.782A>G (p.Lys261Arg)	not specified [RCV004471830]	uncertain significance	4	6967363	6967363	Human		name
407512409	CV3475431	single nucleotide variant	NM_020773.3(TBC1D14):c.592C>T (p.Pro198Ser)	not specified [RCV004673369]	uncertain significance	4	6923981	6923981	Human		name
407512395	CV3475436	single nucleotide variant	NM_020773.3(TBC1D14):c.419T>C (p.Leu140Pro)	not specified [RCV004673373]	uncertain significance	4	6923808	6923808	Human		name
597760846	CV3609348	single nucleotide variant	NM_020773.3(TBC1D14):c.588T>A (p.Asp196Glu)	not specified [RCV004869261]	uncertain significance	4	6923977	6923977	Human		name
597760600	CV3609349	single nucleotide variant	NM_020773.3(TBC1D14):c.607G>A (p.Val203Ile)	not specified [RCV004869262]	uncertain significance	4	6923996	6923996	Human		name
597760629	CV3609356	single nucleotide variant	NM_020773.3(TBC1D14):c.473G>C (p.Ser158Thr)	not specified [RCV004869268]	uncertain significance	4	6923862	6923862	Human		name
597760633	CV3609357	single nucleotide variant	NM_020773.3(TBC1D14):c.338C>T (p.Pro113Leu)	not specified [RCV004869269]	uncertain significance	4	6923727	6923727	Human		name
597760637	CV3609358	single nucleotide variant	NM_020773.3(TBC1D14):c.964A>T (p.Asn322Tyr)	not specified [RCV004869270]	uncertain significance	4	6996326	6996326	Human		name
597760642	CV3609359	single nucleotide variant	NM_020773.3(TBC1D14):c.835A>T (p.Ile279Leu)	not specified [RCV004869271]	uncertain significance	4	6967416	6967416	Human		name
597760652	CV3609362	single nucleotide variant	NM_020773.3(TBC1D14):c.606C>A (p.Asn202Lys)	not specified [RCV004869273]	uncertain significance	4	6923995	6923995	Human		name
598195909	CV3916601	single nucleotide variant	NM_020773.3(TBC1D14):c.449G>A (p.Arg150His)	not specified [RCV005289328]	uncertain significance	4	6923838	6923838	Human		name
598195920	CV3916603	single nucleotide variant	NM_020773.3(TBC1D14):c.762A>T (p.Lys254Asn)	not specified [RCV005289330]	uncertain significance	4	6967343	6967343	Human		name
156183630	CV2198526	single nucleotide variant	NM_020773.3(TBC1D14):c.1373A>G (p.Asp458Gly)	not specified [RCV004075553]	uncertain significance	4	7006653	7006653	Human		name
156010695	CV2291058	single nucleotide variant	NM_020773.3(TBC1D14):c.2029T>G (p.Leu677Val)	not specified [RCV004151590]	uncertain significance	4	7030339	7030339	Human		name
156260395	CV2322299	single nucleotide variant	NM_020773.3(TBC1D14):c.1096G>A (p.Val366Ile)	not specified [RCV004176063]	uncertain significance	4	6999135	6999135	Human		name
156088164	CV2359205	single nucleotide variant	NM_020773.3(TBC1D14):c.1474A>G (p.Ser492Gly)	not specified [RCV004212500]	uncertain significance	4	7009904	7009904	Human		name
401766440	CV2679690	single nucleotide variant	NM_020773.3(TBC1D14):c.1858C>G (p.Leu620Val)	not specified [RCV004282161]	uncertain significance	4	7025104	7025104	Human		name
401732724	CV2691090	single nucleotide variant	NM_020773.3(TBC1D14):c.1376G>A (p.Arg459Lys)	not specified [RCV004301088]	uncertain significance	4	7006656	7006656	Human		name
405780207	CV3324673	single nucleotide variant	NM_020773.3(TBC1D14):c.1354G>C (p.Ala452Pro)	not specified [RCV004471821]	uncertain significance	4	7006634	7006634	Human		name
405780213	CV3324674	single nucleotide variant	NM_020773.3(TBC1D14):c.1650G>C (p.Met550Ile)	not specified [RCV004471822]	uncertain significance	4	7014450	7014450	Human		name
407530600	CV3475434	single nucleotide variant	NM_020773.3(TBC1D14):c.1697C>T (p.Pro566Leu)	not specified [RCV004681996]	uncertain significance	4	7014497	7014497	Human		name
407512399	CV3475435	single nucleotide variant	NM_020773.3(TBC1D14):c.1891A>T (p.Thr631Ser)	not specified [RCV004673372]	uncertain significance	4	7025137	7025137	Human		name
597760614	CV3609353	single nucleotide variant	NM_020773.3(TBC1D14):c.1941G>C (p.Glu647Asp)	not specified [RCV004869265]	uncertain significance	4	7025187	7025187	Human		name
597794820	CV3609360	single nucleotide variant	NM_020773.3(TBC1D14):c.1319T>A (p.Leu440His)	not specified [RCV004877986]	uncertain significance	4	7004892	7004892	Human		name
597760646	CV3609361	single nucleotide variant	NM_020773.3(TBC1D14):c.1028T>C (p.Val343Ala)	not specified [RCV004869272]	uncertain significance	4	6996390	6996390	Human		name
597760656	CV3609363	single nucleotide variant	NM_020773.3(TBC1D14):c.1213A>C (p.Ser405Arg)	not specified [RCV004869274]	uncertain significance	4	7001194	7001194	Human		name
598195900	CV3916598	single nucleotide variant	NM_020773.3(TBC1D14):c.1622C>T (p.Ala541Val)	not specified [RCV005289326]	uncertain significance	4	7010756	7010756	Human		name
598195905	CV3916599	single nucleotide variant	NM_020773.3(TBC1D14):c.1393C>T (p.Leu465Phe)	not specified [RCV005289327]	uncertain significance	4	7006673	7006673	Human		name
598195927	CV3916604	single nucleotide variant	NM_020773.3(TBC1D14):c.1558A>T (p.Asn520Tyr)	not specified [RCV005289331]	uncertain significance	4	7010692	7010692	Human		name
598195931	CV3916605	single nucleotide variant	NM_020773.3(TBC1D14):c.1501C>T (p.Arg501Trp)	not specified [RCV005289332]	uncertain significance	4	7009931	7009931	Human		name
598265395	CV3916606	single nucleotide variant	NM_020773.3(TBC1D14):c.1640A>G (p.His547Arg)	not specified [RCV005280970]	uncertain significance	4	7010774	7010774	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