Slc1a6 Variant Search Result - Rat Genome Database

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30 records found for search term Slc1a6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8585941	CV120535	single nucleotide variant	NM_001272087.1(SLC1A6):c.*821C>A	Lung cancer [RCV000101055]	uncertain significance	19	14961177	14961177	Human		name
156358873	CV2260837	single nucleotide variant	NM_005071.3(SLC1A6):c.86G>T (p.Ser29Ile)	not specified [RCV004125747]	uncertain significance	19	14972825	14972825	Human		name
405712348	CV3314745	single nucleotide variant	NM_005071.3(SLC1A6):c.435C>T (p.Ile145=)	not specified [RCV004448665]	likely benign	19	14968416	14968416	Human		name
156174886	CV2326976	single nucleotide variant	NM_005071.3(SLC1A6):c.141G>T (p.Glu47Asp)	not specified [RCV004176783]	uncertain significance	19	14972770	14972770	Human		name
156042081	CV2381422	single nucleotide variant	NM_005071.3(SLC1A6):c.107G>A (p.Arg36His)	not specified [RCV004229910]	uncertain significance	19	14972804	14972804	Human		name
401877858	CV2757646	single nucleotide variant	NM_005071.3(SLC1A6):c.230G>A (p.Arg77His)	not specified [RCV004334762]	uncertain significance	19	14971850	14971850	Human		name
405712327	CV3314742	single nucleotide variant	NM_005071.3(SLC1A6):c.152G>A (p.Arg51His)	not specified [RCV004448662]	uncertain significance	19	14972759	14972759	Human		name
155941601	CV2229216	single nucleotide variant	NM_005071.3(SLC1A6):c.346A>G (p.Met116Val)	not specified [RCV004101033]	uncertain significance	19	14968505	14968505	Human		name
156081328	CV2249053	single nucleotide variant	NM_005071.3(SLC1A6):c.967G>T (p.Ala323Ser)	not specified [RCV004116331]	uncertain significance	19	14956678	14956678	Human		name
329378319	CV2446965	single nucleotide variant	NM_005071.3(SLC1A6):c.649G>A (p.Gly217Arg)	not specified [RCV004257808]	uncertain significance	19	14962288	14962288	Human		name
401743659	CV2688001	single nucleotide variant	NM_005071.3(SLC1A6):c.851G>T (p.Gly284Val)	not specified [RCV004305076]	uncertain significance	19	14962086	14962086	Human		name
405712339	CV3314744	single nucleotide variant	NM_005071.3(SLC1A6):c.433A>G (p.Ile145Val)	not specified [RCV004448664]	uncertain significance	19	14968418	14968418	Human		name
405712356	CV3314746	single nucleotide variant	NM_005071.3(SLC1A6):c.627G>C (p.Arg209Ser)	not specified [RCV004448666]	uncertain significance	19	14962310	14962310	Human		name
597677154	CV3596404	single nucleotide variant	NM_005071.3(SLC1A6):c.388C>T (p.Arg130Trp)	not specified [RCV004857040]	uncertain significance	19	14968463	14968463	Human		name
598269141	CV3921785	single nucleotide variant	NM_005071.3(SLC1A6):c.389G>A (p.Arg130Gln)	not specified [RCV005281908]	uncertain significance	19	14968462	14968462	Human		name
598269146	CV3921786	single nucleotide variant	NM_005071.3(SLC1A6):c.377G>A (p.Arg126Gln)	not specified [RCV005281909]	uncertain significance	19	14968474	14968474	Human		name
598200114	CV3921789	single nucleotide variant	NM_005071.3(SLC1A6):c.472G>A (p.Gly158Ser)	not specified [RCV005268494]	uncertain significance	19	14968379	14968379	Human		name
8628216	CV83360	single nucleotide variant	NM_005071.2(SLC1A6):c.712G>A (p.Glu238Lys)	Malignant melanoma [RCV000063440]	not provided	19	14962225	14962225	Human		name
156075046	CV2198064	single nucleotide variant	NM_005071.3(SLC1A6):c.1063G>A (p.Gly355Ser)	not specified [RCV004079667]	uncertain significance	19	14956582	14956582	Human		name
156262682	CV2201110	single nucleotide variant	NM_005071.3(SLC1A6):c.1540A>G (p.Ile514Val)	not specified [RCV004075230]	uncertain significance	19	14950350	14950350	Human		name
155975004	CV2221274	single nucleotide variant	NM_005071.3(SLC1A6):c.1670G>A (p.Arg557Gln)	not specified [RCV004094706]	uncertain significance	19	14950220	14950220	Human		name
156204268	CV2252471	single nucleotide variant	NM_005071.3(SLC1A6):c.1150G>A (p.Ala384Thr)	not specified [RCV004116591]	uncertain significance	19	14956495	14956495	Human		name
156368113	CV2266944	single nucleotide variant	NM_005071.3(SLC1A6):c.1412C>T (p.Ala471Val)	not specified [RCV004131600]	uncertain significance	19	14953015	14953015	Human		name
329394506	CV2469907	single nucleotide variant	NM_005071.3(SLC1A6):c.1486G>A (p.Val496Met)	not specified [RCV004285374]	uncertain significance	19	14952941	14952941	Human		name
401756229	CV2687042	single nucleotide variant	NM_005071.3(SLC1A6):c.1157G>C (p.Gly386Ala)	not specified [RCV004304364]	uncertain significance	19	14956488	14956488	Human		name
401750156	CV2701034	single nucleotide variant	NM_005071.3(SLC1A6):c.1036G>A (p.Val346Ile)	not specified [RCV004309639]	uncertain significance	19	14956609	14956609	Human		name
405712319	CV3314741	single nucleotide variant	NM_005071.3(SLC1A6):c.1525G>A (p.Val509Ile)	not specified [RCV004448661]	uncertain significance	19	14950365	14950365	Human		name
405712334	CV3314743	single nucleotide variant	NM_005071.3(SLC1A6):c.1681G>A (p.Glu561Lys)	not specified [RCV004448663]	uncertain significance	19	14950209	14950209	Human		name
597677146	CV3596403	single nucleotide variant	NM_005071.3(SLC1A6):c.1664G>A (p.Arg555Gln)	not specified [RCV004857039]	uncertain significance	19	14950226	14950226	Human		name
598269156	CV3921788	single nucleotide variant	NM_005071.3(SLC1A6):c.1480A>G (p.Ile494Val)	not specified [RCV005281911]	uncertain significance	19	14952947	14952947	Human		name

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