Dgat2l6 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Dgat2l6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15187679	CV731483	single nucleotide variant	NM_198512.3(DGAT2L6):c.267+8C>T	DGAT2L6-related disorder [RCV003940578]\|not provided [RCV000887320]	benign	X	70199890	70199890	Human		name , trait , alternate_id
21075155	CV798375	single nucleotide variant	NM_198512.3(DGAT2L6):c.472+3G>A	not provided [RCV000995938]	uncertain significance	X	70200462	70200462	Human		name
401927261	CV2829196	single nucleotide variant	NM_198512.3(DGAT2L6):c.171C>T (p.Thr57=)	not provided [RCV003438476]	likely benign	X	70199356	70199356	Human		name
405266532	CV3213141	single nucleotide variant	NM_198512.3(DGAT2L6):c.174T>C (p.Tyr58=)	DGAT2L6-related disorder [RCV003969295]	likely benign	X	70199359	70199359	Human		name , trait , alternate_id
597658358	CV3655508	single nucleotide variant	NM_198512.3(DGAT2L6):c.26T>C (p.Leu9Pro)	not specified [RCV004911438]	uncertain significance	X	70177608	70177608	Human		name
401927262	CV2829197	single nucleotide variant	NM_198512.3(DGAT2L6):c.684C>T (p.Asn228=)	not provided [RCV003438477]	likely benign	X	70204341	70204341	Human		name
405258118	CV3208152	single nucleotide variant	NM_198512.3(DGAT2L6):c.801G>T (p.Arg267=)	DGAT2L6-related disorder [RCV003941593]	likely benign	X	70204458	70204458	Human		name , trait , alternate_id
405295222	CV3211127	single nucleotide variant	NM_198512.3(DGAT2L6):c.978T>C (p.Tyr326=)	DGAT2L6-related disorder [RCV003937119]	likely benign	X	70205070	70205070	Human		name , trait , alternate_id
407466620	CV3426985	single nucleotide variant	NM_198512.3(DGAT2L6):c.47T>C (p.Phe16Ser)	not specified [RCV004614006]	uncertain significance	X	70177629	70177629	Human		name
597658364	CV3655509	single nucleotide variant	NM_198512.3(DGAT2L6):c.80T>C (p.Phe27Ser)	not specified [RCV004911439]	uncertain significance	X	70177662	70177662	Human		name
329361576	CV2437655	single nucleotide variant	NM_198512.3(DGAT2L6):c.205C>T (p.Arg69Cys)	not specified [RCV004260973]	uncertain significance	X	70199820	70199820	Human		name
329398626	CV2471616	single nucleotide variant	NM_198512.3(DGAT2L6):c.107T>C (p.Ile36Thr)	not specified [RCV004286911]	uncertain significance	X	70199292	70199292	Human		name
401870592	CV2755919	single nucleotide variant	NM_198512.3(DGAT2L6):c.283G>A (p.Asp95Asn)	not specified [RCV004336008]	uncertain significance	X	70200270	70200270	Human		name
401891383	CV2770493	single nucleotide variant	NM_198512.3(DGAT2L6):c.282T>G (p.His94Gln)	not specified [RCV004358127]	uncertain significance	X	70200269	70200269	Human		name
405275038	CV3204559	single nucleotide variant	NM_198512.3(DGAT2L6):c.133T>A (p.Phe45Ile)	DGAT2L6-related disorder [RCV003951977]	likely benign	X	70199318	70199318	Human		name , trait , alternate_id
405681243	CV3237216	single nucleotide variant	NM_198512.3(DGAT2L6):c.191G>C (p.Ser64Thr)	not specified [RCV004371176]	uncertain significance	X	70199376	70199376	Human		name
597658345	CV3655506	single nucleotide variant	NM_198512.3(DGAT2L6):c.280C>A (p.His94Asn)	not specified [RCV004911436]	uncertain significance	X	70200267	70200267	Human		name
597658351	CV3655507	single nucleotide variant	NM_198512.3(DGAT2L6):c.248G>A (p.Arg83Gln)	not specified [RCV004911437]	likely benign	X	70199863	70199863	Human		name
9687170	CV171691	single nucleotide variant	NM_198512.3(DGAT2L6):c.769C>A (p.Leu257Met)	Prostate cancer [RCV000149389]	uncertain significance	X	70204426	70204426	Human	2	name
156165967	CV2243548	single nucleotide variant	NM_198512.3(DGAT2L6):c.719C>T (p.Thr240Met)	not specified [RCV004112500]	uncertain significance	X	70204376	70204376	Human		name
156267228	CV2243924	single nucleotide variant	NM_198512.3(DGAT2L6):c.842G>A (p.Arg281Gln)	not specified [RCV004108433]	uncertain significance	X	70204499	70204499	Human		name
156108484	CV2304251	single nucleotide variant	NM_198512.3(DGAT2L6):c.677G>A (p.Gly226Asp)	not specified [RCV004170267]	uncertain significance	X	70204334	70204334	Human		name
155976247	CV2324639	single nucleotide variant	NM_198512.3(DGAT2L6):c.841C>T (p.Arg281Trp)	not specified [RCV004172890]	uncertain significance	X	70204498	70204498	Human		name
156179807	CV2327693	single nucleotide variant	NM_198512.3(DGAT2L6):c.386G>A (p.Arg129Gln)	not specified [RCV004177265]	uncertain significance	X	70200373	70200373	Human		name
156285870	CV2360847	single nucleotide variant	NM_198512.3(DGAT2L6):c.906G>T (p.Lys302Asn)	not specified [RCV004213618]	uncertain significance	X	70204998	70204998	Human		name
155931767	CV2362640	single nucleotide variant	NM_198512.3(DGAT2L6):c.631A>G (p.Met211Val)	not specified [RCV004215291]	uncertain significance	X	70202048	70202048	Human		name
156222279	CV2394624	single nucleotide variant	NM_198512.3(DGAT2L6):c.731T>G (p.Leu244Trp)	not specified [RCV004240965]	uncertain significance	X	70204388	70204388	Human		name
401768132	CV2675055	single nucleotide variant	NM_198512.3(DGAT2L6):c.833C>A (p.Pro278His)	not specified [RCV004289839]	uncertain significance	X	70204490	70204490	Human		name
401891952	CV2777162	single nucleotide variant	NM_198512.3(DGAT2L6):c.814G>A (p.Gly272Arg)	not specified [RCV004354207]	uncertain significance	X	70204471	70204471	Human		name
405275598	CV3196410	single nucleotide variant	NM_198512.3(DGAT2L6):c.928C>T (p.Leu310Phe)	DGAT2L6-related disorder [RCV003974247]	uncertain significance	X	70205020	70205020	Human		name , trait , alternate_id
405289923	CV3213934	single nucleotide variant	NM_198512.3(DGAT2L6):c.385C>T (p.Arg129Trp)	DGAT2L6-related disorder [RCV003926787]	likely benign	X	70200372	70200372	Human		name , trait , alternate_id
405681249	CV3237217	single nucleotide variant	NM_198512.3(DGAT2L6):c.334C>G (p.Leu112Val)	not specified [RCV004371177]	likely benign	X	70200321	70200321	Human		name
405681255	CV3237218	single nucleotide variant	NM_198512.3(DGAT2L6):c.533A>G (p.Asn178Ser)	not specified [RCV004371178]	uncertain significance	X	70201950	70201950	Human		name
405681260	CV3237219	single nucleotide variant	NM_198512.3(DGAT2L6):c.581G>A (p.Arg194Gln)	not specified [RCV004371179]	likely benign	X	70201998	70201998	Human		name
405681266	CV3237220	single nucleotide variant	NM_198512.3(DGAT2L6):c.731T>C (p.Leu244Ser)	not specified [RCV004371180]	uncertain significance	X	70204388	70204388	Human		name
405681273	CV3237221	single nucleotide variant	NM_198512.3(DGAT2L6):c.782T>G (p.Phe261Cys)	not specified [RCV004371181]	uncertain significance	X	70204439	70204439	Human		name
405681277	CV3237222	single nucleotide variant	NM_198512.3(DGAT2L6):c.881C>T (p.Pro294Leu)	not specified [RCV004371182]	uncertain significance	X	70204973	70204973	Human		name
405681282	CV3237223	single nucleotide variant	NM_198512.3(DGAT2L6):c.900C>G (p.Asn300Lys)	not specified [RCV004371183]	uncertain significance	X	70204992	70204992	Human		name
407466604	CV3426981	single nucleotide variant	NM_198512.3(DGAT2L6):c.465G>A (p.Met155Ile)	not specified [RCV004614002]	uncertain significance	X	70200452	70200452	Human		name
407466608	CV3426982	single nucleotide variant	NM_198512.3(DGAT2L6):c.788C>T (p.Thr263Ile)	not specified [RCV004614003]	uncertain significance	X	70204445	70204445	Human		name
407466612	CV3426983	single nucleotide variant	NM_198512.3(DGAT2L6):c.587G>A (p.Gly196Glu)	not specified [RCV004614004]	uncertain significance	X	70202004	70202004	Human		name
597658371	CV3655510	single nucleotide variant	NM_198512.3(DGAT2L6):c.356A>G (p.Asn119Ser)	not specified [RCV004911440]	uncertain significance	X	70200343	70200343	Human		name
598161218	CV3952898	single nucleotide variant	NM_198512.3(DGAT2L6):c.419C>A (p.Thr140Asn)	not specified [RCV005328933]	uncertain significance	X	70200406	70200406	Human		name

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