Csnk2a2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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34 records found for search term Csnk2a2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150493647	CV1267189	single nucleotide variant	NM_001896.4(CSNK2A2):c.-37C>T	not provided [RCV001688217]	benign	16	58197773	58197773	Human		name
150511700	CV1229527	single nucleotide variant	NM_001896.4(CSNK2A2):c.104+50C>T	not provided [RCV001637456]	benign	16	58197583	58197583	Human		name
150457891	CV1237138	single nucleotide variant	NM_001896.4(CSNK2A2):c.727-29T>G	not provided [RCV001648817]	benign	16	58166713	58166713	Human		name
150481116	CV1239718	single nucleotide variant	NM_001896.4(CSNK2A2):c.514-60T>C	not provided [RCV001652881]	benign	16	58167855	58167855	Human		name
150489408	CV1265418	single nucleotide variant	NM_001896.4(CSNK2A2):c.977-88C>G	not provided [RCV001687454]	benign	16	58164235	58164235	Human		name
150470732	CV1269910	single nucleotide variant	NM_001896.4(CSNK2A2):c.828-58G>A	not provided [RCV001695197]	benign	16	58165766	58165766	Human		name
150332102	CV1163622	single nucleotide variant	NM_001896.4(CSNK2A2):c.319-275C>T	not provided [RCV001528079]	benign	16	58184585	58184585	Human		name
150333177	CV1172872	single nucleotide variant	NM_001896.4(CSNK2A2):c.828-140C>A	not provided [RCV001539354]	benign	16	58165848	58165848	Human		name
150515494	CV1217511	single nucleotide variant	NM_001896.4(CSNK2A2):c.514-150G>A	not provided [RCV001608417]	benign	16	58167945	58167945	Human		name
150435048	CV1221546	single nucleotide variant	NM_001896.4(CSNK2A2):c.216+313T>C	not provided [RCV001609234]	benign	16	58196420	58196420	Human		name
150504520	CV1223966	single nucleotide variant	NM_001896.4(CSNK2A2):c.370-122A>G	not provided [RCV001621615]	benign	16	58174632	58174632	Human		name
150512150	CV1228436	single nucleotide variant	NM_001896.4(CSNK2A2):c.976+261C>A	not provided [RCV001637568]	benign	16	58165299	58165299	Human		name
150483106	CV1245055	single nucleotide variant	NM_001896.4(CSNK2A2):c.828-242G>A	not provided [RCV001653232]	benign	16	58165950	58165950	Human		name
150458435	CV1248934	single nucleotide variant	NM_001896.4(CSNK2A2):c.369+188A>G	not provided [RCV001669110]	benign	16	58184072	58184072	Human		name
150444935	CV1249491	single nucleotide variant	NM_001896.4(CSNK2A2):c.104+271G>A	not provided [RCV001666924]	benign	16	58197362	58197362	Human		name
150449641	CV1254003	single nucleotide variant	NM_001896.4(CSNK2A2):c.726+138G>A	not provided [RCV001667640]	benign	16	58167069	58167069	Human		name
150466018	CV1277334	single nucleotide variant	NM_001896.4(CSNK2A2):c.514-232A>G	not provided [RCV001710629]	benign	16	58168027	58168027	Human		name
156301011	CV2248914	single nucleotide variant	NM_001896.4(CSNK2A2):c.13G>A (p.Ala5Thr)	not specified [RCV004115920]	uncertain significance	16	58197724	58197724	Human		name
150442263	CV1266200	single nucleotide variant	NM_001896.4(CSNK2A2):c.585A>G (p.Ser195=)	not provided [RCV001690635]	benign	16	58167724	58167724	Human		name
405277727	CV3196096	single nucleotide variant	NM_001896.4(CSNK2A2):c.81C>G (p.Tyr27Ter)	CSNK2A2-related disorder [RCV003904614]	uncertain significance	16	58197656	58197656	Human		name , trait , alternate_id
407465438	CV3430017	single nucleotide variant	NM_001896.4(CSNK2A2):c.76G>A (p.Asp26Asn)	not specified [RCV004613704]	uncertain significance	16	58197661	58197661	Human		name
405687335	CV3236283	single nucleotide variant	NM_001896.4(CSNK2A2):c.220G>C (p.Val74Leu)	not specified [RCV004372607]	uncertain significance	16	58186853	58186853	Human		name
156029730	CV2238339	single nucleotide variant	NM_001896.4(CSNK2A2):c.656T>G (p.Leu219Trp)	not specified [RCV004113413]	uncertain significance	16	58167277	58167277	Human		name
156326899	CV2332021	single nucleotide variant	NM_001896.4(CSNK2A2):c.979C>T (p.Pro327Ser)	not specified [RCV004189076]	uncertain significance	16	58164145	58164145	Human		name
156000462	CV2391752	single nucleotide variant	NM_001896.4(CSNK2A2):c.884G>C (p.Ser295Thr)	not specified [RCV004242288]	uncertain significance	16	58165652	58165652	Human		name
401759718	CV2698603	single nucleotide variant	NM_001896.4(CSNK2A2):c.920G>A (p.Arg307Gln)	not specified [RCV004299083]	uncertain significance	16	58165616	58165616	Human		name
405687338	CV3236284	single nucleotide variant	NM_001896.4(CSNK2A2):c.394T>G (p.Phe132Val)	not specified [RCV004372608]	uncertain significance	16	58174486	58174486	Human		name
407465442	CV3430018	single nucleotide variant	NM_001896.4(CSNK2A2):c.812A>G (p.Asn271Ser)	not specified [RCV004613705]	uncertain significance	16	58166599	58166599	Human		name
596948294	CV3549376	single nucleotide variant	NM_001896.4(CSNK2A2):c.871A>G (p.Arg291Gly)	not provided [RCV004812196]	uncertain significance	16	58165665	58165665	Human		name
597805086	CV3654712	single nucleotide variant	NM_001896.4(CSNK2A2):c.316G>A (p.Val106Met)	not specified [RCV004908283]	uncertain significance	16	58186757	58186757	Human		name
597805088	CV3654713	single nucleotide variant	NM_001896.4(CSNK2A2):c.733C>A (p.Arg245Ser)	not specified [RCV004908284]	uncertain significance	16	58166678	58166678	Human		name
598219015	CV3959417	single nucleotide variant	NM_001896.4(CSNK2A2):c.613G>A (p.Val205Met)	not specified [RCV005317328]	uncertain significance	16	58167696	58167696	Human		name
401922310	CV2827577	single nucleotide variant	NM_001368165.1(CSNK2A2IP):c.87A>G (p.Gln29=)	not provided [RCV003433674]	likely benign	3	88465444	88465444	Human		name
401926487	CV2827578	single nucleotide variant	NM_001368165.1(CSNK2A2IP):c.591C>T (p.Ile197=)	not provided [RCV003437920]	likely benign	3	88465948	88465948	Human		name

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