iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1064197	snp	C/G	0.000181203	0.00951675	missense	FKBP6	GRCh38.p7	7:73330252	ATGGAACGCTGGGCT[C/G]CCCTCCCTTGATCCC	135892
rs2178022	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73328201	GGATCATACCTCGCA[A/C]CTCACCGCGTGGCCT	135892
rs2353062	snp	C/T	0.210301	0.246828	intron-variant, upstream-variant-2KB	TRIM50	GRCh38.p7	7:73326044	AGGTGCATGCCACCA[C/T]GCCAAGCTAATATTT	135892
rs2463283	snp	A/G			intron-variant	TRIM50	GRCh38.p7	7:73319744	TGTGCCTCTCACTTC[A/G]GGAGATCAGCCAGGG	135892
rs2463284	snp	C/T	0.0111196	0.0737302	intron-variant	TRIM50	GRCh38.p7	7:73319867	GGGGCGGAGGAGTCA[C/T]GCCCATGCTTTGAGC	135892
rs2463285	snp	C/T	0.0107246	0.0724382	intron-variant	TRIM50	GRCh38.p7	7:73320088	CCAATGAGAACTGAG[C/T]TCTACAGGAAAGTGA	135892
rs2463287	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327551	AACACAATGGAAGAG[A/G]GAAAGTGAAAGAAGG	135892
rs2530528	snp	C/G	0.012068	0.0767355	intron-variant, utr-variant-5-prime	TRIM50	GRCh38.p7	7:73319071	GGACAGGGAGGGCTG[C/G]TCACTGCAGAGTCAC	135892
rs2695365	snp	A/G			intron-variant	TRIM50	GRCh38.p7	7:73319250	GCCGTGGGGAGGGTG[A/G]CCCCAGCTCCCGTTT	135892
rs2695366	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327538	CTAAATTCTCTAGAA[C/T]ACAATGGAAGAGAGA	135892
rs2695368	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327891	TTCCCGCTCGCTCTC[A/G]TTACGTACCCAGCCT	135892
rs2695369	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	FKBP6, TRIM50	GRCh38.p7	7:73328005	CCACCTAACCCCCCA[C/T]GTCCGTGCCTCATCA	135892
rs2695370	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73328372	AGAGTCACAGCCAGG[A/G]AGGGCAGCGGGGCGC	135892
rs2950497	snp	A/C/T	0.000332069	0.0128813	intron-variant	TRIM50	GRCh38.p7	7:73324839	ACCTCAGTCCTGTCC[A/C/T]CTCCCCTCCCCCTGT	135892
rs2950498	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73324865	CCTGTCCAGCACTCA[C/T]CCACCACCCTCAACC	135892
rs2950499	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73324955	ACATGACCTTGGGCC[C/T]CAGTTTCCGCAGCTG	135892
rs2950500	snp	A/G	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73324964	TGGGCCCCAGTTTCC[A/G]CAGCTGTAAAACAAA	135892
rs3108461	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, utr-variant-5-prime	TRIM50	GRCh38.p7	7:73320198	GAAGCAGGAGCAGAA[A/G]AAGGTGGATGAGCTC	135892
rs3108462	snp	A/G	0.209693	0.246729	intron-variant	TRIM50	GRCh38.p7	7:73325451	AGGTATTCCAATGTC[A/G]GGCTCCCCCGGGGGC	135892
rs3750075	snp	A/C/T	0.00467241	0.0481079	missense, synonymous-codon, intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329400	CATGGACAGACCCTT[A/C/T]GATTCTAATTACTTT	135892
rs3888061	snp	A/G	0.0217236	0.101931	intron-variant	TRIM50	GRCh38.p7	7:73317770	GAAGGCTTGGGAACT[A/G]CACGTGTTCGTTTGT	135892
rs3950375	snp	A/C/G/T	0.0214532	0.101332	intron-variant	FKBP6	GRCh38.p7	7:73330140	CCACCTTCTTTGTCC[A/C/G/T]TTCTTACAGATATTA	135892
rs3950376	snp	A/G	0.000247233	0.0111155	missense	FKBP6	GRCh38.p7	7:73330192	GCCTTCTGAGCATGC[A/G]GAGAGGAGAGCTGGC	135892
rs4030977	snp	C/T	0.0345262	0.126772	intron-variant	TRIM50	GRCh38.p7	7:73323464	aagtgatccacccac[C/T]tcggcctcccaaagt	135892
rs4030979	snp	C/G			intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329986	ataaaatttctatca[C/G]tagaagctgggcaca	135892
rs4030981	snp	A/G	3.41618e-05	0.00413276	intron-variant	FKBP6	GRCh38.p7	7:73330100	GAAACTGATAGCACT[A/G]AGCAGGATACTGAGC	135892
rs4717748	snp	A/T	0.345925	0.230864	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73326559	ACAAGATGTAGAGTG[A/T]TTccagaaagctccc	135892
rs4717749	snp	C/T	0.00953873	0.0683987	utr-variant-5-prime, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73328178	CATGTTTCGTGCGCT[C/T]CCATTACGGATCATA	135892
rs5884900	in-del	-/C	0.0345262	0.126772	intron-variant	TRIM50	GRCh38.p7	7:73323316	CTATCTCACCCCCAC[-/C]GATGTTCCCTCCAGC	135892
rs6943491	snp	C/T	0.0345262	0.126772	intron-variant, upstream-variant-2KB	TRIM50	GRCh38.p7	7:73325638	CTTTCCCAGCAACAC[C/T]CCTGTGTCCCCAAGG	135892
rs6949855	snp	A/G	0.210301	0.246828	intron-variant	TRIM50	GRCh38.p7	7:73314130	AGGAAAGAAGGCCAA[A/G]GGGAAGAAGGTGGCT	135892
rs6950193	snp	A/C	0	0	intron-variant	TRIM50	GRCh38.p7	7:73314271	TCGCCCACTTTGTGC[A/C]ATGGTCCTGCTCGGT	135892
rs6980124	snp	A/G	0.00133074	0.0257604	missense, intron-variant	TRIM50	GRCh38.p7	7:73324765	CAGTCCTCCAGCTCC[A/G]GCAGGCTCACCTGCC	135892
rs6980258	snp	C/T	0.00136312	0.0260711	synonymous-codon, intron-variant	TRIM50	GRCh38.p7	7:73324764	CCAGTCCTCCAGCTC[C/T]AGCAGGCTCACCTGC	135892
rs7776916	snp	C/T	0.02016	0.0983543	intron-variant	TRIM50	GRCh38.p7	7:73316108	ctggacttgaactcc[C/T]gacctcagaagatcc	135892
rs7784181	snp	C/T	0.34659	0.230587	intron-variant	TRIM50	GRCh38.p7	7:73314485	TGCCAGCAAAGGGGA[C/T]GTCCCCACTAAGAGG	135892
rs7793813	snp	C/T	0.021333	0.101051	intron-variant	TRIM50	GRCh38.p7	7:73316069	tattattagtagaga[C/T]ggggtttcaccatgt	135892
rs7797242	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329298	TGATCATGAGAGACT[C/T]GATATTATGGTGGCG	135892
rs7801936	snp	A/C	0.34659	0.230587	intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329980	GTTTGAATAAAATTT[A/C]TATCAGTAGAAGCTG	135892
rs9791481	snp	A/G			upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327429	ggagtggcggctgca[A/G]tgagctgagatccat	135892
rs9791841	snp	A/G			upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327394	cgggaggctgaggca[A/G]gaggatctcttgagc	135892
rs9918672	snp	A/G	0.319136	0.24025	intron-variant	TRIM50	GRCh38.p7	7:73316042	cacactaccacgccc[A/G]gctaattcttgtatt	135892
rs11984428	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73324881	CCACCACCCTCAACC[C/T]TAAGGAGCACCAGAA	135892
rs13227775	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323095	TTGTCCCAGTTCCCA[C/T]CGACTTAGGTCCTGG	135892
rs13227882	snp	G/T	0.00119737	0.0244387	intron-variant	TRIM50	GRCh38.p7	7:73323179	GAGAGATCTGAGCAT[G/T]TCATCACTGGCTTAA	135892
rs13227889	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323207	TAAAACCCTCCAGCC[C/T]CCGCCTTGCTCCCTC	135892
rs13228013	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323322	TCACCCCCACCGATG[C/T]TCCCTCCAGCCTTAT	135892
rs13228104	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323363	caggagtggccactg[C/T]gcctggccaacaagg	135892
rs13228429	snp	G/T			intron-variant	TRIM50	GRCh38.p7	7:73323720	caccctcatgCACCA[G/T]AGAGTGCAAACAGGG	135892
rs13240587	snp	A/C			intron-variant	TRIM50	GRCh38.p7	7:73323198	TCACTGGCTTAAAAC[A/C]CTCCAGCCTCCGCCT	135892
rs13240602	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM50	GRCh38.p7	7:73323247	ATAAACTCCAAATCC[A/C]TTCCCGGGTCACACT	135892
rs13240614	snp	A/G			intron-variant	TRIM50	GRCh38.p7	7:73323309	CGCTGGCCCTATCTC[A/G]CCCCCACCGATGTTC	135892
rs13240664	snp	A/G	0.0119091	0.0762411	intron-variant	TRIM50	GRCh38.p7	7:73323097	GTCCCAGTTCCCATC[A/G]ACTTAGGTCCTGGCA	135892
rs13240714	snp	A/C			intron-variant	TRIM50	GRCh38.p7	7:73323375	ctgtgcctggccaac[A/C]aggctaattttgaaa	135892
rs13240715	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323333	GATGTTCCCTCCAGC[C/T]TTATgctgggattac	135892
rs13240783	snp	G/T			intron-variant	TRIM50	GRCh38.p7	7:73323215	TCCAGCCTCCGCCTT[G/T]CTCCCTCATCCTGTG	135892
rs13240897	snp	C/G			intron-variant	TRIM50	GRCh38.p7	7:73323318	TATCTCACCCCCACC[C/G]ATGTTCCCTCCAGCC	135892
rs13240936	snp	C/T			intron-variant	TRIM50	GRCh38.p7	7:73323550	ATATATAACAGCCAG[C/T]CAGGTATTATTATTA	135892
rs13241149	snp	C/G			intron-variant	TRIM50	GRCh38.p7	7:73323545	TTTATATATATAACA[C/G]CCAGCCAGGTATTAT	135892
rs13241244	snp	A/G			intron-variant	TRIM50	GRCh38.p7	7:73323569	GTATTATTATTACTC[A/G]TCTTAAAGAATGATC	135892
rs28626137	snp	A/G	0.000676294	0.0183768	missense, intron-variant	TRIM50	GRCh38.p7	7:73324751	TGGGACACTGAAGCC[A/G]GTCCTCCAGCTCCAG	135892
rs35621939	in-del	-/A	0	0	downstream-variant-500B	TRIM50	GRCh38.p7	7:73312488	AAAAAAAAAAAAAAA[-/A]GACTCGAGCATAAAG	135892
rs36063137	in-del	-/T	0	0	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73326404	TTTTTTTTTTTTTTT[-/T]AAGATATTCAAAGGT	135892
rs55761041	in-del	-/GTGTGT			intron-variant	TRIM50	GRCh38.p7	7:73325048	TGTGTGTGTGTGTGT[-/GTGTGT]CTACATTTTTTACTC	135892
rs55963844	in-del	-/G	5.00249e-05	0.00500104	intron-variant	TRIM50	GRCh38.p7	7:73324351	GGATCTGGTCCCCGC[-/G]GGCCTCTCCAGCCGC	135892
rs57292425	in-del	-/GTGTGTGT	0	0	intron-variant	TRIM50	GRCh38.p7	7:73325046	TGTGTGTGTGTGTGT[-/GTGTGTGT]CTACATTTTTTACTC	135892
rs57889282	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM50	GRCh38.p7	7:73321414	TCACAAAAAGGCCGG[C/T]GCCAGGTGAGGCTAA	135892
rs58165529	snp	C/T	0.0955749	0.196603	intron-variant	TRIM50	GRCh38.p7	7:73314257	GGCCAAAACGGACCT[C/T]GCCCACTTTGTGCAA	135892
rs60799075	snp	C/T	0.0733688	0.176922	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327080	ACAGGTGTGAGCCAC[C/T]GCGCCTGTCCTGTTA	135892
rs61735966	snp	A/G	0.00949353	0.0682396	synonymous-codon	FKBP6	GRCh38.p7	7:73330244	CTACGCCTATGGAAC[A/G]CTGGGCTGCCCTCCC	135892
rs61741334	snp	G/T	0.0400535	0.135735	synonymous-codon, intron-variant	TRIM50	GRCh38.p7	7:73324563	GAGCCTCAGGGCTTC[G/T]ATCACCCTGGCCAGG	135892
rs61743386	snp	A/G	0.277778	0.248452	synonymous-codon, intron-variant	TRIM50	GRCh38.p7	7:73324592	GGGAGACGTTGGGCA[A/G]GGAGCTGCTGCCGTC	135892
rs61743391	snp	A/C/T	0.000545441	0.0165052	missense, intron-variant	TRIM50	GRCh38.p7	7:73324625	CCGCCTGCCGGCACA[A/C/T]GGGGCAGCGCAGCTC	135892
rs62465083	snp	A/G	0.0191752	0.0960203	intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73328543	GCCGGGTGGGTCTGC[A/G]GCTCTGAGGCCTGGC	135892
rs71071927	in-del	-/A/T	0.277334	0.248501	intron-variant	TRIM50	GRCh38.p7	7:73315346	AAAAAGAAAAGAATG[-/A/T]AAAAAAAAAAAAAGG	135892
rs71517385	in-del	-/A	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73323862	CCTGGGCAACATAAC[-/A]AGACCCCATTTCTAC	135892
rs73131580	snp	A/G	0.0475873	0.146728	intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329313	CGATATTATGGTGGC[A/G]TGGGTGTTTTTGGTC	135892
rs75299722	snp	A/C	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73321024	AGTGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAG	135892
rs75868672	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM50	GRCh38.p7	7:73314241	CTGGACAGGACTTCC[A/G]GGCCAAAACGGACCT	135892
rs76450125	snp	C/T			upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73326177	TTACAGGCGTGAGCC[C/T]TACTGCACCCAGCCT	135892
rs77500933	snp	C/G			intron-variant	TRIM50	GRCh38.p7	7:73322372	CAACAACAAAATTAA[C/G]CCCAAATCTAAAACA	135892
rs77664691	snp	C/T	0.00338016	0.0409714	synonymous-codon, intron-variant	TRIM50	GRCh38.p7	7:73324425	GGAGACGGGCGTGAC[C/T]GGGTGGTGTTGGTGG	135892
rs78297984	snp	G/T			intron-variant	TRIM50	GRCh38.p7	7:73314449	GAAGCAGAGACTGTT[G/T]GCCCTGACTGAGAAG	135892
rs79749432	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73327387	AGCTACTTGGGAGGC[C/T]GAGGCAGGAGGATCT	135892
rs79866895	snp	C/T	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73323467	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	135892
rs80101953	snp	C/T	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73315360	TCCTTTTTTTTTTTT[C/T]CATTCTTTTCTTTTT	135892
rs80274720	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	FKBP6, TRIM50	GRCh38.p7	7:73328045	CGCTATGGTTACATG[C/G]CCCGCCTCGCGCTAC	135892
rs111279110	snp	C/T	0.00569429	0.0530539	missense, downstream-variant-500B	TRIM50	GRCh38.p7	7:73313160	TGCGGTGGGGGTGGC[C/T]GGCCACGGGCAGGGG	135892
rs111398281	snp	A/C	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73324262	GCTAAGGAATGAATG[A/C]GCCAGGGCACAGCTG	135892
rs111399096	snp	C/T	0.5	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73328368	CACCAGAGTCACAGC[C/T]AGGGAGGGCAGCGGG	135892
rs111638818	snp	A/G/T	3.30914e-05	0.00406753	missense, intron-variant	TRIM50	GRCh38.p7	7:73324531	TGCACGCAGACCTTG[A/G/T]GCTCCGGGTCCCCAG	135892
rs111773860	snp	C/G	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73319312	AATTTTTTTTTTTAA[C/G]AGACAGGGTCTCACT	135892
rs111844626	snp	C/T	0.00478085	0.0486577	intron-variant	TRIM50	GRCh38.p7	7:73322168	TCCTGGCTAACACGG[C/T]GAAACCCCGCCTCTA	135892
rs112003602	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM50	GRCh38.p7	7:73325802	ACCGTCCACACCTCA[C/T]GACCCCAACAGGAGC	135892
rs112290231	snp	A/C	0.0372196	0.131242	intron-variant	TRIM50	GRCh38.p7	7:73316179	AGCCACTGTGCCCAG[A/C]CAAAAAGTACATTAC	135892
rs112475552	snp	A/G	0.5	0	intron-variant	TRIM50	GRCh38.p7	7:73322328	CGCTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT	135892
rs112809122	in-del	-/T	0.5	0	upstream-variant-2KB, intron-variant	FKBP6, TRIM50	GRCh38.p7	7:73326731	ATATTGAATTGTGAG[-/T]TTTTTTTTTTAATGT	135892
rs112910219	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM50	GRCh38.p7	7:73320558	CAAAAATTAGCCAGG[C/T]GTGGTGGCATACACC	135892
rs113241101	snp	A/C/T	1.65138e-05	0.00287343	missense, intron-variant	TRIM50	GRCh38.p7	7:73324568	TCAGGGCTTCGATCA[A/C/T]CCTGGCCAGGGAGAC	135892
rs113247135	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FKBP6, TRIM50	GRCh38.p7	7:73329538	AAGACTGCTCAGAGC[A/G]CAGGTTCTTTGAGTT	135892

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