Srrd 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 Srrd

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405701904	CV3330672	single nucleotide variant	NM_001013694.3(SRRD):c.10G>C (p.Ala4Pro)	not specified [RCV004460512]	uncertain significance	22	26483900	26483900	Human		name
405871626	CV3397984	single nucleotide variant	NM_001013694.3(SRRD):c.150C>T (p.Gly50=)	not provided [RCV004574984]	likely benign	22	26484040	26484040	Human		name
155978415	CV2222684	single nucleotide variant	NM_001013694.3(SRRD):c.64T>G (p.Ser22Ala)	not specified [RCV004101545]	uncertain significance	22	26483954	26483954	Human		name
156384445	CV2231085	single nucleotide variant	NM_001013694.3(SRRD):c.82C>G (p.Arg28Gly)	not specified [RCV004094309]	uncertain significance	22	26483972	26483972	Human		name
156291549	CV2296664	single nucleotide variant	NM_001013694.3(SRRD):c.56A>G (p.Lys19Arg)	not specified [RCV004154716]	likely benign	22	26483946	26483946	Human		name
156094350	CV2300294	single nucleotide variant	NM_001013694.3(SRRD):c.36G>C (p.Trp12Cys)	not specified [RCV004153248]	uncertain significance	22	26483926	26483926	Human		name
405701949	CV3330678	single nucleotide variant	NM_001013694.3(SRRD):c.74G>A (p.Arg25Gln)	not specified [RCV004460518]	uncertain significance	22	26483964	26483964	Human		name
407516711	CV3474813	single nucleotide variant	NM_001013694.3(SRRD):c.29A>G (p.Glu10Gly)	not specified [RCV004675386]	uncertain significance	22	26483919	26483919	Human		name
597779292	CV3611545	single nucleotide variant	NM_001013694.3(SRRD):c.32C>T (p.Ser11Phe)	not specified [RCV004873501]	uncertain significance	22	26483922	26483922	Human		name
597680946	CV3611546	single nucleotide variant	NM_001013694.3(SRRD):c.74G>C (p.Arg25Pro)	not specified [RCV004857474]	uncertain significance	22	26483964	26483964	Human		name
597680964	CV3611553	single nucleotide variant	NM_001013694.3(SRRD):c.52C>T (p.Arg18Trp)	not specified [RCV004857476]	uncertain significance	22	26483942	26483942	Human		name
598173295	CV3912330	single nucleotide variant	NM_001013694.3(SRRD):c.61C>T (p.Arg21Cys)	not specified [RCV005285155]	uncertain significance	22	26483951	26483951	Human		name
155996085	CV2375896	single nucleotide variant	NM_001013694.3(SRRD):c.116C>T (p.Ala39Val)	not specified [RCV004217738]	uncertain significance	22	26484006	26484006	Human		name
329357831	CV2427852	single nucleotide variant	NM_001013694.3(SRRD):c.119C>T (p.Ala40Val)	not specified [RCV004252625]	uncertain significance	22	26484009	26484009	Human		name
329377062	CV2435795	single nucleotide variant	NM_001013694.3(SRRD):c.140C>T (p.Ala47Val)	not specified [RCV004253419]	uncertain significance	22	26484030	26484030	Human		name
401742091	CV2697696	single nucleotide variant	NM_001013694.3(SRRD):c.173A>G (p.Asp58Gly)	not specified [RCV004300435]	uncertain significance	22	26484063	26484063	Human		name
405701912	CV3330673	single nucleotide variant	NM_001013694.3(SRRD):c.151C>A (p.Pro51Thr)	not specified [RCV004460513]	uncertain significance	22	26484041	26484041	Human		name
405701920	CV3330674	single nucleotide variant	NM_001013694.3(SRRD):c.296C>A (p.Ala99Asp)	not specified [RCV004460514]	uncertain significance	22	26488074	26488074	Human		name
597779300	CV3611549	single nucleotide variant	NM_001013694.3(SRRD):c.156G>C (p.Glu52Asp)	not specified [RCV004873503]	uncertain significance	22	26484046	26484046	Human		name
597779307	CV3611551	single nucleotide variant	NM_001013694.3(SRRD):c.154G>A (p.Glu52Lys)	not specified [RCV004873505]	uncertain significance	22	26484044	26484044	Human		name
156180375	CV2201732	single nucleotide variant	NM_001013694.3(SRRD):c.342C>G (p.Asp114Glu)	not specified [RCV004082177]	uncertain significance	22	26488120	26488120	Human		name
156381378	CV2214915	single nucleotide variant	NM_001013694.3(SRRD):c.726G>A (p.Met242Ile)	not specified [RCV004084704]	uncertain significance	22	26490160	26490160	Human		name
156284646	CV2231272	single nucleotide variant	NM_001013694.3(SRRD):c.397G>A (p.Val133Ile)	not specified [RCV004094463]	uncertain significance	22	26488175	26488175	Human		name
156245389	CV2283420	single nucleotide variant	NM_001013694.3(SRRD):c.733A>G (p.Ile245Val)	not specified [RCV004139645]	uncertain significance	22	26490167	26490167	Human		name
156070137	CV2341174	single nucleotide variant	NM_001013694.3(SRRD):c.694A>C (p.Ser232Arg)	not specified [RCV004181646]	uncertain significance	22	26490128	26490128	Human		name
155991610	CV2355492	single nucleotide variant	NM_001013694.3(SRRD):c.878C>T (p.Thr293Ile)	not specified [RCV004205342]	uncertain significance	22	26491530	26491530	Human		name
156094480	CV2398836	single nucleotide variant	NM_001013694.3(SRRD):c.747C>G (p.Phe249Leu)	not specified [RCV004245159]	uncertain significance	22	26490181	26490181	Human		name
401736526	CV2683043	single nucleotide variant	NM_001013694.3(SRRD):c.607G>A (p.Glu203Lys)	not specified [RCV004283820]	uncertain significance	22	26488486	26488486	Human		name
401723770	CV2684861	single nucleotide variant	NM_001013694.3(SRRD):c.803T>C (p.Ile268Thr)	not specified [RCV004296367]	uncertain significance	22	26491063	26491063	Human		name
401748709	CV2713319	single nucleotide variant	NM_001013694.3(SRRD):c.305G>A (p.Gly102Glu)	not specified [RCV004316832]	uncertain significance	22	26488083	26488083	Human		name
401778440	CV2714727	single nucleotide variant	NM_001013694.3(SRRD):c.298C>T (p.Pro100Ser)	not specified [RCV004320299]	uncertain significance	22	26488076	26488076	Human		name
401728652	CV2729716	single nucleotide variant	NM_001013694.3(SRRD):c.796C>A (p.Pro266Thr)	not specified [RCV004331971]	uncertain significance	22	26491056	26491056	Human		name
405701926	CV3330675	single nucleotide variant	NM_001013694.3(SRRD):c.365T>C (p.Val122Ala)	not specified [RCV004460515]	uncertain significance	22	26488143	26488143	Human		name
405701932	CV3330676	single nucleotide variant	NM_001013694.3(SRRD):c.500A>G (p.Glu167Gly)	not specified [RCV004460516]	uncertain significance	22	26488278	26488278	Human		name
407487448	CV3474812	single nucleotide variant	NM_001013694.3(SRRD):c.925G>A (p.Asp309Asn)	not specified [RCV004675385]	uncertain significance	22	26491577	26491577	Human		name
407516713	CV3474814	single nucleotide variant	NM_001013694.3(SRRD):c.454T>G (p.Cys152Gly)	not specified [RCV004675387]	uncertain significance	22	26488232	26488232	Human		name
597680954	CV3611547	single nucleotide variant	NM_001013694.3(SRRD):c.592G>A (p.Val198Ile)	not specified [RCV004857475]	uncertain significance	22	26488471	26488471	Human		name
597779297	CV3611548	single nucleotide variant	NM_001013694.3(SRRD):c.559G>A (p.Glu187Lys)	not specified [RCV004873502]	uncertain significance	22	26488438	26488438	Human		name
597779303	CV3611550	single nucleotide variant	NM_001013694.3(SRRD):c.454T>C (p.Cys152Arg)	not specified [RCV004873504]	uncertain significance	22	26488232	26488232	Human		name
597779311	CV3611552	single nucleotide variant	NM_001013694.3(SRRD):c.620G>A (p.Arg207Gln)	not specified [RCV004873506]	uncertain significance	22	26490054	26490054	Human		name
597779315	CV3611554	single nucleotide variant	NM_001013694.3(SRRD):c.859A>C (p.Met287Leu)	not specified [RCV004873507]	uncertain significance	22	26491511	26491511	Human		name
598173282	CV3912328	single nucleotide variant	NM_001013694.3(SRRD):c.631G>A (p.Gly211Arg)	not specified [RCV005285153]	uncertain significance	22	26490065	26490065	Human		name
598173289	CV3912329	single nucleotide variant	NM_001013694.3(SRRD):c.922A>G (p.Ile308Val)	not specified [RCV005285154]	uncertain significance	22	26491574	26491574	Human		name

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