Slc25a35 Variant Search Result - Rat Genome Database

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27 records found for search term Slc25a35

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405853018	CV3393449	single nucleotide variant	NM_001320870.2(SLC25A35):c.183C>A (p.Ala61=)	not provided [RCV004546179]	likely benign	17	8294625	8294625	Human		name
401740156	CV2684281	single nucleotide variant	NM_001320870.2(SLC25A35):c.61G>C (p.Glu21Gln)	not specified [RCV004288938]	uncertain significance	17	8294747	8294747	Human		name
405768298	CV3321708	single nucleotide variant	NM_001320870.2(SLC25A35):c.53A>G (p.Asn18Ser)	not specified [RCV004456527]	uncertain significance	17	8294755	8294755	Human		name
156035761	CV2208246	single nucleotide variant	NM_001320870.2(SLC25A35):c.143A>T (p.His48Leu)	not specified [RCV004088697]	uncertain significance	17	8294665	8294665	Human		name
156040147	CV2310772	single nucleotide variant	NM_001320870.2(SLC25A35):c.160G>T (p.Gly54Cys)	not specified [RCV004157699]	uncertain significance	17	8294648	8294648	Human		name
156201073	CV2313121	single nucleotide variant	NM_001320870.2(SLC25A35):c.137T>C (p.Val46Ala)	not specified [RCV004161388]	uncertain significance	17	8294671	8294671	Human		name
401782181	CV2719215	single nucleotide variant	NM_001320870.2(SLC25A35):c.146C>A (p.Ala49Asp)	not specified [RCV004324869]	uncertain significance	17	8294662	8294662	Human		name
405768273	CV3321704	single nucleotide variant	NM_001320870.2(SLC25A35):c.292G>A (p.Gly98Ser)	not specified [RCV004456523]	uncertain significance	17	8294516	8294516	Human		name
597754941	CV3606358	single nucleotide variant	NM_001320870.2(SLC25A35):c.232G>T (p.Gly78Cys)	not specified [RCV004867988]	uncertain significance	17	8294576	8294576	Human		name
155990482	CV2276466	single nucleotide variant	NM_001320870.2(SLC25A35):c.409G>A (p.Glu137Lys)	not specified [RCV004144187]	uncertain significance	17	8292555	8292555	Human		name
156294337	CV2293179	single nucleotide variant	NM_001320870.2(SLC25A35):c.362G>A (p.Ser121Asn)	not specified [RCV004150693]	uncertain significance	17	8294446	8294446	Human		name
156274317	CV2344223	single nucleotide variant	NM_001320870.2(SLC25A35):c.386A>G (p.His129Arg)	not specified [RCV004197860]	uncertain significance	17	8292578	8292578	Human		name
156233494	CV2346206	single nucleotide variant	NM_001320870.2(SLC25A35):c.463G>A (p.Glu155Lys)	not specified [RCV004201659]	uncertain significance	17	8291464	8291464	Human		name
156154436	CV2374934	single nucleotide variant	NM_001320870.2(SLC25A35):c.506C>T (p.Ala169Val)	not specified [RCV004227955]	uncertain significance	17	8291421	8291421	Human		name
329397814	CV2456373	single nucleotide variant	NM_001320870.2(SLC25A35):c.392A>G (p.Gln131Arg)	not specified [RCV004275535]	uncertain significance	17	8292572	8292572	Human		name
329396841	CV2459060	single nucleotide variant	NM_001320870.2(SLC25A35):c.651T>G (p.Ile217Met)	not specified [RCV004272529]	uncertain significance	17	8290920	8290920	Human		name
405768279	CV3321705	single nucleotide variant	NM_001320870.2(SLC25A35):c.316G>A (p.Ala106Thr)	not specified [RCV004456524]	uncertain significance	17	8294492	8294492	Human		name
405768285	CV3321706	single nucleotide variant	NM_001320870.2(SLC25A35):c.413T>C (p.Ile138Thr)	not specified [RCV004456525]	uncertain significance	17	8292551	8292551	Human		name
405768290	CV3321707	single nucleotide variant	NM_001320870.2(SLC25A35):c.464A>G (p.Glu155Gly)	not specified [RCV004456526]	uncertain significance	17	8291463	8291463	Human		name
405768304	CV3321709	single nucleotide variant	NM_001320870.2(SLC25A35):c.644G>A (p.Ser215Asn)	not specified [RCV004456528]	uncertain significance	17	8290927	8290927	Human		name
597700527	CV3606360	single nucleotide variant	NM_001320870.2(SLC25A35):c.683T>C (p.Val228Ala)	not specified [RCV004859875]	uncertain significance	17	8290888	8290888	Human		name
597700537	CV3606361	single nucleotide variant	NM_001320870.2(SLC25A35):c.542C>A (p.Ser181Tyr)	not specified [RCV004859876]	uncertain significance	17	8291385	8291385	Human		name
597754731	CV3606362	single nucleotide variant	NM_001320870.2(SLC25A35):c.653C>A (p.Ala218Glu)	not specified [RCV004867989]	uncertain significance	17	8290918	8290918	Human		name
598168937	CV3918237	single nucleotide variant	NM_001320870.2(SLC25A35):c.644G>C (p.Ser215Thr)	not specified [RCV005284180]	uncertain significance	17	8290927	8290927	Human		name
598168943	CV3918238	single nucleotide variant	NM_001320870.2(SLC25A35):c.520C>T (p.Pro174Ser)	not specified [RCV005284181]	uncertain significance	17	8291407	8291407	Human		name
598200383	CV3918239	single nucleotide variant	NM_001320870.2(SLC25A35):c.524G>A (p.Arg175Gln)	not specified [RCV005268534]	uncertain significance	17	8291403	8291403	Human		name
598168955	CV3918241	single nucleotide variant	NM_001320870.2(SLC25A35):c.535G>A (p.Gly179Ser)	not specified [RCV005284183]	uncertain significance	17	8291392	8291392	Human		name

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