Sox15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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20 records found for search term Sox15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156257782	CV2369001	single nucleotide variant	NM_006942.2(SOX15):c.5C>A (p.Ala2Glu)	not specified [RCV004207943]	uncertain significance	17	7589672	7589672	Human		name
156225990	CV2203095	single nucleotide variant	NM_006942.2(SOX15):c.47C>T (p.Pro16Leu)	not specified [RCV004069340]	uncertain significance	17	7589630	7589630	Human		name
597756541	CV3603901	single nucleotide variant	NM_006942.2(SOX15):c.61G>T (p.Ala21Ser)	not specified [RCV004868416]	uncertain significance	17	7589616	7589616	Human		name
401752918	CV2682980	single nucleotide variant	NM_006942.2(SOX15):c.119C>T (p.Ala40Val)	not specified [RCV004283769]	likely benign	17	7589558	7589558	Human		name
401769468	CV2689778	single nucleotide variant	NM_006942.2(SOX15):c.274G>A (p.Glu92Lys)	not specified [RCV004297687]	uncertain significance	17	7589403	7589403	Human		name
407504759	CV3485147	single nucleotide variant	NM_006942.2(SOX15):c.280G>C (p.Glu94Gln)	not specified [RCV004670640]	uncertain significance	17	7589397	7589397	Human		name
407504767	CV3485149	single nucleotide variant	NM_006942.2(SOX15):c.208C>A (p.Gln70Lys)	not specified [RCV004670642]	uncertain significance	17	7589469	7589469	Human		name
156319750	CV2200585	single nucleotide variant	NM_006942.2(SOX15):c.677C>T (p.Ala226Val)	not specified [RCV004078925]	uncertain significance	17	7588403	7588403	Human		name
155918705	CV2206066	single nucleotide variant	NM_006942.2(SOX15):c.429C>A (p.Ser143Arg)	not specified [RCV004078477]	uncertain significance	17	7589248	7589248	Human		name
156364941	CV2272022	single nucleotide variant	NM_006942.2(SOX15):c.508A>G (p.Thr170Ala)	not specified [RCV004124827]	uncertain significance	17	7589169	7589169	Human		name
156390572	CV2383219	single nucleotide variant	NM_006942.2(SOX15):c.626A>T (p.His209Leu)	not specified [RCV004220228]	uncertain significance	17	7588454	7588454	Human		name
156040146	CV2390415	single nucleotide variant	NM_006942.2(SOX15):c.566C>T (p.Pro189Leu)	not specified [RCV004234113]	uncertain significance	17	7588514	7588514	Human		name
329367762	CV2427545	single nucleotide variant	NM_006942.2(SOX15):c.569G>C (p.Cys190Ser)	not specified [RCV004250183]	uncertain significance	17	7588511	7588511	Human		name
329399558	CV2470153	single nucleotide variant	NM_006942.2(SOX15):c.551T>C (p.Leu184Pro)	not specified [RCV004287400]	likely benign	17	7588529	7588529	Human		name
401753100	CV2720631	single nucleotide variant	NM_006942.2(SOX15):c.604G>C (p.Glu202Gln)	not specified [RCV004327994]	uncertain significance	17	7588476	7588476	Human		name
401859198	CV2771472	single nucleotide variant	NM_006942.2(SOX15):c.397C>A (p.Arg133Ser)	not specified [RCV004348517]	uncertain significance	17	7589280	7589280	Human		name
405774568	CV3333510	single nucleotide variant	NM_006942.2(SOX15):c.356G>A (p.Arg119Gln)	not specified [RCV004457579]	uncertain significance	17	7589321	7589321	Human		name
407504757	CV3485146	single nucleotide variant	NM_006942.2(SOX15):c.607C>A (p.Leu203Met)	not specified [RCV004670639]	uncertain significance	17	7588473	7588473	Human		name
597756536	CV3603900	single nucleotide variant	NM_006942.2(SOX15):c.437C>T (p.Pro146Leu)	not specified [RCV004868415]	uncertain significance	17	7589240	7589240	Human		name
598247273	CV3922405	single nucleotide variant	NM_006942.2(SOX15):c.574C>T (p.Leu192Phe)	not specified [RCV005277265]	uncertain significance	17	7588506	7588506	Human		name

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