Has3 Variant Search Result - Rat Genome Database

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44 records found for search term Has3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407514191	CV3443991	single nucleotide variant	NM_001199280.2(HAS3):c.5C>T (p.Pro2Leu)	not specified [RCV004627455]	uncertain significance	16	69109400	69109400	Human		name
11087684	CV227789	single nucleotide variant	NM_001199280.2(HAS3):c.279A>G (p.Ala93=)	anthracyclines and related substances response - Toxicity/ADR [RCV000211138]	drug response	16	69109674	69109674	Human		name
8689353	CV97441	single nucleotide variant	NM_001199280.2(HAS3):c.141G>T (p.Leu47=)	not provided [RCV000122520]	uncertain significance	16	69109536	69109536	Human		name
329351645	CV2459223	single nucleotide variant	NM_001199280.2(HAS3):c.92C>T (p.Thr31Met)	not specified [RCV004274662]	uncertain significance	16	69109487	69109487	Human		name
401734015	CV2688378	single nucleotide variant	NM_001199280.2(HAS3):c.29G>A (p.Arg10His)	not specified [RCV004299371]	uncertain significance	16	69109424	69109424	Human		name
597709459	CV3682132	single nucleotide variant	NM_001199280.2(HAS3):c.59C>T (p.Ala20Val)	not specified [RCV004917319]	uncertain significance	16	69109454	69109454	Human		name
8635872	CV91095	single nucleotide variant	NM_001199280.1(HAS3):c.636G>A (p.Gln212=)	Malignant melanoma [RCV000071193]	not provided	16	69110031	69110031	Human		name
150406841	CV1200053	single nucleotide variant	NM_001199280.2(HAS3):c.202C>T (p.Arg68Trp)	not provided [RCV001579529]	uncertain significance	16	69109597	69109597	Human		name
156040956	CV2261341	single nucleotide variant	NM_001199280.2(HAS3):c.136G>A (p.Gly46Ser)	not specified [RCV004129988]	uncertain significance	16	69109531	69109531	Human		name
401895024	CV2792691	single nucleotide variant	NM_001199280.2(HAS3):c.184T>C (p.Phe62Leu)	not specified [RCV004365469]	uncertain significance	16	69109579	69109579	Human		name
405789074	CV3269965	single nucleotide variant	NM_001199280.2(HAS3):c.113C>T (p.Thr38Met)	not specified [RCV004399141]	uncertain significance	16	69109508	69109508	Human		name
407514189	CV3443990	single nucleotide variant	NM_001199280.2(HAS3):c.247C>T (p.Arg83Trp)	not specified [RCV004627454]	uncertain significance	16	69109642	69109642	Human		name
407514199	CV3443995	single nucleotide variant	NM_001199280.2(HAS3):c.118A>C (p.Lys40Gln)	not specified [RCV004627459]	uncertain significance	16	69109513	69109513	Human		name
597709453	CV3682131	single nucleotide variant	NM_001199280.2(HAS3):c.220G>A (p.Gly74Ser)	not specified [RCV004917318]	uncertain significance	16	69109615	69109615	Human		name
597781194	CV3682133	single nucleotide variant	NM_001199280.2(HAS3):c.148G>A (p.Ala50Thr)	not specified [RCV004930833]	uncertain significance	16	69109543	69109543	Human		name
15118645	CV715029	single nucleotide variant	NM_001199280.2(HAS3):c.1590A>G (p.Leu530=)	not provided [RCV000962415]	benign	16	69115194	69115194	Human		name
15160574	CV726754	single nucleotide variant	NM_001199280.2(HAS3):c.214C>T (p.Arg72Cys)	not provided [RCV000881408]	benign	16	69109609	69109609	Human		name
156022003	CV2223073	single nucleotide variant	NM_001199280.2(HAS3):c.524G>A (p.Arg175Gln)	not specified [RCV004103928]	uncertain significance	16	69109919	69109919	Human		name
156068281	CV2317977	single nucleotide variant	NM_001199280.2(HAS3):c.430G>A (p.Glu144Lys)	not specified [RCV004177096]	uncertain significance	16	69109825	69109825	Human		name
329357281	CV2431317	single nucleotide variant	NM_001199280.2(HAS3):c.317G>A (p.Arg106His)	not specified [RCV004252439]	uncertain significance	16	69109712	69109712	Human		name
329390600	CV2437112	single nucleotide variant	NM_001199280.2(HAS3):c.785G>A (p.Arg262Gln)	not specified [RCV004262919]	uncertain significance	16	69114389	69114389	Human		name
329394625	CV2461454	single nucleotide variant	NM_001199280.2(HAS3):c.488C>T (p.Thr163Met)	not specified [RCV004267598]	uncertain significance	16	69109883	69109883	Human		name
401777950	CV2718397	single nucleotide variant	NM_001199280.2(HAS3):c.514G>A (p.Asp172Asn)	not specified [RCV004318223]	uncertain significance	16	69109909	69109909	Human		name
401863935	CV2770939	single nucleotide variant	NM_001199280.2(HAS3):c.455G>A (p.Arg152His)	not specified [RCV004343606]	uncertain significance	16	69109850	69109850	Human		name
401897246	CV2789967	single nucleotide variant	NM_001199280.2(HAS3):c.661G>C (p.Asp221His)	not specified [RCV004363932]	uncertain significance	16	69113465	69113465	Human		name
405789085	CV3269968	single nucleotide variant	NM_001199280.2(HAS3):c.517C>T (p.Arg173Cys)	not specified [RCV004399144]	uncertain significance	16	69109912	69109912	Human		name
405789089	CV3269969	single nucleotide variant	NM_001199280.2(HAS3):c.880C>T (p.Leu294Phe)	not specified [RCV004399145]	uncertain significance	16	69114484	69114484	Human		name
407514195	CV3443993	single nucleotide variant	NM_001199280.2(HAS3):c.535C>T (p.Arg179Trp)	not specified [RCV004627457]	uncertain significance	16	69109930	69109930	Human		name
597781189	CV3682129	single nucleotide variant	NM_001199280.2(HAS3):c.595A>G (p.Thr199Ala)	not specified [RCV004930831]	uncertain significance	16	69109990	69109990	Human		name
597781192	CV3682130	single nucleotide variant	NM_001199280.2(HAS3):c.492G>C (p.Glu164Asp)	not specified [RCV004930832]	uncertain significance	16	69109887	69109887	Human		name
597781199	CV3682134	single nucleotide variant	NM_001199280.2(HAS3):c.377G>A (p.Arg126His)	not specified [RCV004930834]	uncertain significance	16	69109772	69109772	Human		name
597709465	CV3682135	single nucleotide variant	NM_001199280.2(HAS3):c.480G>C (p.Glu160Asp)	not specified [RCV004917320]	uncertain significance	16	69109875	69109875	Human		name
597709474	CV3682136	single nucleotide variant	NM_001199280.2(HAS3):c.545C>A (p.Thr182Asn)	not specified [RCV004917321]	uncertain significance	16	69109940	69109940	Human		name
598265427	CV3971396	single nucleotide variant	NM_001199280.2(HAS3):c.498C>G (p.Ser166Arg)	not specified [RCV005349057]	uncertain significance	16	69109893	69109893	Human		name
598265432	CV3971397	single nucleotide variant	NM_001199280.2(HAS3):c.388G>A (p.Ala130Thr)	not specified [RCV005349058]	uncertain significance	16	69109783	69109783	Human		name
156381758	CV2215217	single nucleotide variant	NM_001199280.2(HAS3):c.1244C>T (p.Thr415Met)	not specified [RCV004086927]	uncertain significance	16	69114848	69114848	Human		name
156314892	CV2253327	single nucleotide variant	NM_001199280.2(HAS3):c.1346G>A (p.Ser449Asn)	not specified [RCV004123160]	uncertain significance	16	69114950	69114950	Human		name
156199169	CV2312973	single nucleotide variant	NM_001199280.2(HAS3):c.1398G>C (p.Trp466Cys)	not specified [RCV004159478]	uncertain significance	16	69115002	69115002	Human		name
156308298	CV2369906	single nucleotide variant	NM_001199280.2(HAS3):c.1657G>C (p.Val553Leu)	not specified [RCV004208375]	uncertain significance	16	69115261	69115261	Human		name
407514193	CV3443992	single nucleotide variant	NM_001199280.2(HAS3):c.1613G>A (p.Arg538Gln)	not specified [RCV004627456]	uncertain significance	16	69115217	69115217	Human		name
407514197	CV3443994	single nucleotide variant	NM_001199280.2(HAS3):c.1088G>A (p.Arg363Gln)	not specified [RCV004627458]	uncertain significance	16	69114692	69114692	Human		name
407514204	CV3443997	single nucleotide variant	NM_001199280.2(HAS3):c.1252C>A (p.Leu418Met)	not specified [RCV004627461]	uncertain significance	16	69114856	69114856	Human		name
597709479	CV3682137	single nucleotide variant	NM_001199280.2(HAS3):c.1157C>T (p.Thr386Met)	not specified [RCV004917322]	uncertain significance	16	69114761	69114761	Human		name
15174685	CV740315	single nucleotide variant	NM_001199280.2(HAS3):c.1577C>G (p.Ala526Gly)	not provided [RCV000906027]	benign	16	69115181	69115181	Human		name

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