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
rs919743	snp	C/T	0.0894459	0.191631	upstream-variant-2KB	RNF145	GRCh38.p7	5:159211860	GAAGTGGGGGTGGGG[C/T]GGGTGAATCGAGAGC	153830
rs975023	snp	A/G	0.093777	0.195178	intron-variant	RNF145	GRCh38.p7	5:159172929	CATCCCTACTTTTTA[A/G]AGTGACAATGAGCAA	153830
rs975024	snp	C/T	0.0998734	0.199905	intron-variant	RNF145	GRCh38.p7	5:159173292	TGCTAGTGTATTTTA[C/T]GTATAGCCCAAGACA	153830
rs1137598	snp	A/C			intron-variant	RNF145	GRCh38.p7	5:159196329	aatcttttggcttcc[A/C]tggaccacattagga	153830
rs1368373	snp	C/T	0.0279526	0.114869	upstream-variant-2KB, nc-transcript-variant	RNF145, LOC107986468	GRCh38.p7	5:159210123	CAAAGAATTTTATTG[C/T]AGTATGAAATTAAAT	153830
rs1432870	snp	A/G	0.0279526	0.114869	upstream-variant-2KB	RNF145	GRCh38.p7	5:159211028	CTAGCCTGGTAAGTA[A/G]AAAAATTACAGAGGT	153830
rs1432871	snp	A/T	0.0952156	0.196321	intron-variant	RNF145	GRCh38.p7	5:159182360	TTGAGAGCTGATCTC[A/T]CTCAACTCTACTACA	153830
rs1469681	snp	C/G	0.0898077	0.191933	intron-variant	RNF145	GRCh38.p7	5:159205978	GCTAGGGAAGAAAAA[C/G]TCCCTAATCCGTACA	153830
rs1473247	snp	C/T	0.499722	0.0117779	intron-variant	RNF145	GRCh38.p7	5:159176563	GAAATAAAAATGAAC[C/T]ATAACTTTAATGTAC	153830
rs1897565	snp	C/T	0.497387	0.0360476			GRCh38.p7	5:159191257	AGGTAAGGAAACAAT[C/T]TGTATCAAGTCTGAT	153830
rs2043268	snp	A/G	0.359575	0.224707	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF145, LOC107986468	GRCh38.p7	5:159208416	GAACTCATTCCAGAA[A/G]GGGGGTTCACGGGTC	153830
rs2043269	snp	A/G	0.0998734	0.199905	intron-variant	RNF145	GRCh38.p7	5:159170928	AGCTTTAATTTTCAA[A/G]GAAGAATTTCACTGA	153830
rs2043270	snp	A/G	0.0998734	0.199905	intron-variant	RNF145	GRCh38.p7	5:159170973	TCATTCAGGCAATCA[A/G]TGCTTGTCCCTTACT	153830
rs2060211	snp	C/G/T	0.0998734	0.199905	intron-variant	RNF145	GRCh38.p7	5:159173913	AAGTAATCTGCAAAA[C/G/T]TTACTATTCCTAGAT	153830
rs2060212	snp	A/G	0.0435799	0.141035	synonymous-codon	RNF145	GRCh38.p7	5:159174087	GAGCCAGAAAACCAT[A/G]AAAAGAACAGGGACT	153830
rs2116785	snp	C/T	0.0898077	0.191933	intron-variant	RNF145	GRCh38.p7	5:159191925	AAACTACTTAGGTCC[C/T]CTTTTTCCTTATATA	153830
rs2163775	snp	A/C	0.488786	0.0740357	intron-variant	RNF145	GRCh38.p7	5:159199339	GAAGTCTAAAGAAAA[A/C]AAATCAAAAGAATCA	153830
rs2195933	snp	G/T	0.18134	0.240387	upstream-variant-2KB	RNF145	GRCh38.p7	5:159210988	CCTGTCACATCCCAG[G/T]GATGCAGTTCATGAG	153830
rs2304056	snp	C/G	0.499995	0.00165172	intron-variant	RNF145	GRCh38.p7	5:159162890	TGGGAGGAAAAATAA[C/G]AAAATTGGTTATTAT	153830
rs2901183	snp	C/T	0.0901694	0.192235	intron-variant	RNF145	GRCh38.p7	5:159201179	AACATGCAAAACCCA[C/T]GTATACAGAGGGCCA	153830
rs3172947	snp	A/T			intron-variant	RNF145	GRCh38.p7	5:159173830	ACTGGATACCTAGGT[A/T]TGGCAATGCAGGGAG	153830
rs3213859	snp	C/T	0.354235	0.227234	intron-variant	RNF145	GRCh38.p7	5:159181817	AAAAAAAAAAACCAC[C/T]AAACAATGGGTATAT	153830
rs4318763	snp	C/G	0	0	intron-variant	RNF145	GRCh38.p7	5:159173130	AAAAACCGAGTCTTA[C/G]AATTATTTTGGGTTA	153830
rs4602609	snp	A/C/G	0	0	intron-variant	RNF145	GRCh38.p7	5:159175297	TCCATTCAAGAAACA[A/C/G]ACCACTAAAAAAACC	153830
rs5009411	snp	C/G/T	1.66994e-05	0.00288953	missense	RNF145	GRCh38.p7	5:159176676	CAAGGTTATAAGGTA[C/G/T]CAAAAGATTAGACCC	153830
rs5016135	snp	C/T	0.000742769	0.019257	synonymous-codon	RNF145	GRCh38.p7	5:159169813	AGTGCTGCAGCATTC[C/T]GCAATACTGGAAAAA	153830
rs6420104	snp	C/T	0.182933	0.240836	intron-variant	RNF145	GRCh38.p7	5:159198196	GCAGTGAGCTAAGAT[C/T]GTACCACTGCACTCC	153830
rs6556402	snp	A/G	0.352938	0.227824	intron-variant	RNF145	GRCh38.p7	5:159173338	TGGCCCAGGAAAGCC[A/G]AAAGATTGAACACCC	153830
rs6556403	snp	A/G	0	0	intron-variant	RNF145	GRCh38.p7	5:159184931	TCCAGAAGAATAAAT[A/G]ATCAACCTTTAGGCC	153830
rs6556404	snp	A/T	0.39527	0.203462	intron-variant	RNF145	GRCh38.p7	5:159188929	TAAGCTAGTTTTTAA[A/T]TTTTTTTTTCTTGTT	153830
rs6556405	snp	C/T	0.49753	0.0350569	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF145, LOC107986468	GRCh38.p7	5:159208094	TTGATGCCTGCTCAC[C/T]GCACAGGCCCCTTCC	153830
rs6863147	snp	A/G	0.00159617	0.0282053	intron-variant	RNF145	GRCh38.p7	5:159188509	AGGAATAGTAGTATC[A/G]GTGTATGGTTTTTCT	153830
rs6871659	snp	A/C	0.162909	0.23434	intron-variant	RNF145	GRCh38.p7	5:159186781	TGTTCAAAAGCAGAA[A/C]ACATGTCAAACAGTG	153830
rs6879008	snp	C/G	0.354881	0.226936	intron-variant	RNF145	GRCh38.p7	5:159183401	TGCTGCTAAATATTC[C/G]TCAATGCAAAGGCTA	153830
rs6880417	snp	A/G	0.00398564	0.0444627	intron-variant	RNF145	GRCh38.p7	5:159163742	TAAATTTTTGAGCCT[A/G]GCATTTGAGGTCCTC	153830
rs6884239	snp	A/G	0.360632	0.224189	intron-variant	RNF145	GRCh38.p7	5:159197561	AAAACTTTGAGAGAC[A/G]ATGAATACTAACTAT	153830
rs6885498	snp	G/T			intron-variant	RNF145	GRCh38.p7	5:159194575	ATTAATCCTGTGTAA[G/T]ATTTGGAAAATGAGT	153830
rs6888950	snp	G/T	0.497749	0.0334707	intron-variant	RNF145	GRCh38.p7	5:159197743	GGCAAAGCTGTTAGT[G/T]TTTAAATTATACACA	153830
rs6891575	snp	A/G	0.488666	0.0744214	intron-variant	RNF145	GRCh38.p7	5:159203033	TCAGCTGATGTTAAT[A/G]TTTTCGTTTATCTCA	153830
rs6893046	snp	C/T	0.49703	0.0384237	intron-variant	RNF145	GRCh38.p7	5:159203038	TGATGTTAATGTTTT[C/T]GTTTATCTCAGGGAA	153830
rs6894840	snp	G/T	0.404733	0.196361	intron-variant	RNF145	GRCh38.p7	5:159198780	TAATCCTAGCACTCT[G/T]GGAGGCTGAGGCAGG	153830
rs7443845	snp	C/G	0.352504	0.228019	intron-variant	RNF145	GRCh38.p7	5:159173449	CAAAGGCAAAGTATA[C/G]AGAGTAAGTCACAGG	153830
rs7448744	snp	C/T	0.161924	0.233971	intron-variant	RNF145	GRCh38.p7	5:159183847	GGGAGATGAGAGTAA[C/T]GGCTTAATGAGTACT	153830
rs7705300	snp	C/G	0.00398564	0.0444627	intron-variant	RNF145	GRCh38.p7	5:159167952	GAGATTAGCTGTTCC[C/G]TTACTATAAAAGGCT	153830
rs7707106	snp	C/G	0.352287	0.228117	intron-variant	RNF145	GRCh38.p7	5:159185948	GAAAAGGGCCTCCGG[C/G]CATGGTAGCTCAAGC	153830
rs7718670	snp	C/T	0.499451	0.0165644	intron-variant	RNF145	GRCh38.p7	5:159166365	CATTAATTCTAATAT[C/T]AATCATTAAATGTAT	153830
rs7726254	snp	C/G	0.391884	0.205837	intron-variant	RNF145	GRCh38.p7	5:159165200	AGGTGAAGGCCTGGA[C/G]AATAAACCACATCTA	153830
rs7728067	snp	C/T	0.360421	0.224293	intron-variant	RNF145	GRCh38.p7	5:159162070	TATGTTTTCCTTTAC[C/T]TAGGTAGCAAAGATC	153830
rs7728606	snp	C/T	0.00398564	0.0444627	intron-variant	RNF145	GRCh38.p7	5:159167878	GAATCTGATGTACTA[C/T]AATTAAAATGTTAAT	153830
rs7732603	snp	A/C	0.499017	0.0221427	intron-variant	RNF145	GRCh38.p7	5:159187349	AAAAATTTTTTTTTG[A/C]GATAGTCTCACACTG	153830
rs7732652	snp	A/C	0.486398	0.0813386	intron-variant	RNF145	GRCh38.p7	5:159162559	CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA	153830
rs9687130	snp	C/G	0	0	intron-variant	RNF145	GRCh38.p7	5:159167347	ATTCAAAGTACCCCG[C/G]CCCACATACAACACT	153830
rs10035989	snp	C/T	0.161924	0.233971	utr-variant-3-prime	RNF145	GRCh38.p7	5:159157983	ATATACATCAAAATA[C/T]TGAAGACTCCGTCAT	153830
rs10041650	snp	C/T	0.354881	0.226936	intron-variant	RNF145	GRCh38.p7	5:159186130	CTTGGGAGGCTGAGG[C/T]GGGAGAATTGTGTGG	153830
rs10057691	snp	A/T	0.396694	0.202437	intron-variant	RNF145	GRCh38.p7	5:159190517	ACAGCAAGAAACCCA[A/T]CTCTACAAAAAAATA	153830
rs10065135	snp	A/G	0.0193772	0.0965046	intron-variant	RNF145	GRCh38.p7	5:159191601	ttcaagaccagcctg[A/G]ccaacatggtaaaac	153830
rs10070253	snp	A/G	0.02016	0.0983543	intron-variant	RNF145	GRCh38.p7	5:159204528	AGGGCAAACAAggcc[A/G]ggcgcagtggcacac	153830
rs10072037	snp	C/T	0.264084	0.249603	intron-variant	RNF145	GRCh38.p7	5:159187599	CCCAAAGTGCTGGGA[C/T]TACAGGCGTGTGCCA	153830
rs10075570	snp	A/G	0.499722	0.0117779	intron-variant	RNF145	GRCh38.p7	5:159172350	GCCAGGTGTGGTGGC[A/G]CATGCCTGTAATCCC	153830
rs10076782	snp	A/G	0.499713	0.0119774	intron-variant	RNF145	GRCh38.p7	5:159177955	TTTCTGCTAGAATAC[A/G]TATCCTACTGCCTGA	153830
rs10077526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF145	GRCh38.p7	5:159186393	ATTATAACAGTCTCT[C/T]CAGCGACCTGACTCA	153830
rs10077858	snp	A/C	0.499954	0.00479211	intron-variant	RNF145	GRCh38.p7	5:159187079	TGAGGTCAGGAGTTC[A/C]AGAACAGCCTGGCCA	153830
rs10079720	snp	A/G	0.41325	0.18934	intron-variant	RNF145	GRCh38.p7	5:159187617	CAGGCGTGTGCCACC[A/G]CTCCCGGCCTATCTA	153830
rs10475670	snp	A/G	0.18	0.24	intron-variant	RNF145	GRCh38.p7	5:159204827	AAAAAAAAAAAAAAA[A/G]GCAAACAAAAGTGGG	153830
rs10476286	snp	A/G	0.0023933	0.0345097	intron-variant	RNF145	GRCh38.p7	5:159196167	ccatgggctacatgt[A/G]gcccaggatggcttt	153830
rs10515774	snp	C/T	0.110872	0.20771	intron-variant	RNF145	GRCh38.p7	5:159162850	ACTTATAATCATTCA[C/T]CTTGAAAAAATTTAA	153830
rs10515775	snp	C/T	0.239902	0.249796	intron-variant	RNF145	GRCh38.p7	5:159163446	ATTTGTGGTCTTTTT[C/T]AAATCTTATGACACC	153830
rs10515776	snp	C/T	0.239902	0.249796	intron-variant	RNF145	GRCh38.p7	5:159169365	TATTAACATCAAATA[C/T]TGTATAGAAATCAGA	153830
rs10515777	snp	A/G	0.177182	0.23916	intron-variant	RNF145	GRCh38.p7	5:159205559	GACTTACTTTGGTGA[A/G]CAAACTGATAACCCA	153830
rs10565309	in-del	-/TAAATAAA	0.34101	0.232846	intron-variant	RNF145	GRCh38.p7	5:159198240	GTGAGACTCTATCTC[-/TAAATAAA]TAAATAAATAAATAA	153830
rs11135052	snp	C/T	0.177503	0.239258	intron-variant	RNF145	GRCh38.p7	5:159171373	ATTTCTCTATTTTTA[C/T]GGACCTTTCTCCATA	153830
rs11360125	in-del	-/T	0.429388	0.174127	intron-variant	RNF145	GRCh38.p7	5:159196230	TTAAAATATTATGAG[-/T]TTTTTTTTTTTTTTT	153830
rs11555238	snp	A/T			utr-variant-3-prime	RNF145	GRCh38.p7	5:159157487	CTACTAAAAATAAAA[A/T]AAAGTCACATCCCAC	153830
rs11555239	snp	A/T			utr-variant-3-prime	RNF145	GRCh38.p7	5:159157482	ATTTGCTACTAAAAA[A/T]AAAATAAAGTCACAT	153830
rs11738949	snp	C/T	0	0	utr-variant-3-prime	RNF145	GRCh38.p7	5:159157606	ATAAAAAATTACATT[C/T]CCCCCTCCCCAGTTC	153830
rs11750842	snp	C/T	0.0715223	0.175059	intron-variant	RNF145	GRCh38.p7	5:159196881	TTTTCCTTTCCAGAA[C/T]GGTCTTGTCTTTTCT	153830
rs11957203	snp	C/T	0.00398564	0.0444627	intron-variant	RNF145	GRCh38.p7	5:159177987	CGAAATAGTAATCCT[C/T]AGTCACATGATTGCA	153830
rs12055000	snp	A/G	0.239902	0.249796	intron-variant	RNF145	GRCh38.p7	5:159166662	TGTGGGTCAGTCTGT[A/G]GTCTCTATTCCACTG	153830
rs12109660	snp	C/T	0.0287284	0.116357	intron-variant	RNF145	GRCh38.p7	5:159180983	GCACATTGGGTACAG[C/T]ATACACTCCTCAGGC	153830
rs12110198	snp	C/T	0.354665	0.227036	intron-variant	RNF145	GRCh38.p7	5:159181078	TGTTCCCCCAGAAAC[C/T]TATCTAAAAAATGTT	153830
rs12188266	snp	A/G	0.177824	0.239355	intron-variant	RNF145	GRCh38.p7	5:159171955	AATTATGTTAGCAAG[A/G]TATCTAAACTTCACA	153830
rs12522797	snp	A/T	0.479663	0.0987666	upstream-variant-2KB	RNF145	GRCh38.p7	5:159210750	TGGTAAACCCCCAAT[A/T]CTGAACACTCTTGTA	153830
rs12655958	snp	A/G	0.0984431	0.198823	intron-variant	RNF145	GRCh38.p7	5:159175686	CTGGGAAAACTGCCC[A/G]AGTTAATCACTGTGT	153830
rs12656023	snp	A/C	0.0948562	0.196037	intron-variant	RNF145	GRCh38.p7	5:159175999	AGTAATTTATCTTAG[A/C]GCAAAGGCTGAAAAA	153830
rs12657093	snp	C/G/T	0.0298908	0.118541	intron-variant, upstream-variant-2KB	RNF145, LOC107986468	GRCh38.p7	5:159207362	CACCTCCTAAACTTT[C/G/T]TTTTAAAAAGACAAA	153830
rs13158488	snp	C/T	0.187369	0.242028	intron-variant	RNF145	GRCh38.p7	5:159176263	AACACATATGGAACA[C/T]TGTCTGCCTGGTACT	153830
rs13165660	snp	C/T	0.185788	0.241613	intron-variant	RNF145	GRCh38.p7	5:159165143	TCTAATTAACTATTG[C/T]CAATAATGTAACAAG	153830
rs13178603	snp	C/G	0.187685	0.242109	intron-variant	RNF145	GRCh38.p7	5:159165007	CTAACTTGAGAATTA[C/G]GACGCTTTTCCTTTC	153830
rs13184675	snp	C/G	0	0	intron-variant	RNF145	GRCh38.p7	5:159203089	TAAAAAGCTTACTTT[C/G]TGAATTACTACCAAA	153830
rs13187955	snp	A/C	0	0	intron-variant	RNF145	GRCh38.p7	5:159200004	GAAAAACTCCCACTT[A/C]CGATAGCAATAAAAA	153830
rs13188097	snp	A/C	0	0	intron-variant	RNF145	GRCh38.p7	5:159200037	ATAAAATACCTAGAA[A/C]CAATAAATGtcagga	153830
rs17052525	snp	A/G	0.209388	0.246679	intron-variant	RNF145	GRCh38.p7	5:159164158	AATCAGTAATTCAGA[A/G]AAGAAAGTTAATTAT	153830
rs17056583	snp	C/G	0.239902	0.249796	intron-variant	RNF145	GRCh38.p7	5:159161741	TATTTCAAATATACA[C/G]AAGAGTATCCAGGGG	153830
rs17056588	snp	C/G	0.239902	0.249796	intron-variant	RNF145	GRCh38.p7	5:159164683	AAACCTCGTGCAATA[C/G]GTTAAGTACTATAAA	153830
rs17663669	snp	A/G	0.0729998	0.176553	intron-variant	RNF145	GRCh38.p7	5:159177503	TCCCACAACCCAAAG[A/G]TAGTCCTAAGAACAC	153830
rs17663721	snp	C/T	0.194278	0.243711	intron-variant	RNF145	GRCh38.p7	5:159177632	TATGACATCCTTGTA[C/T]AAACTACTTGGAACA	153830
rs17663989	snp	C/T	0.182614	0.240747	intron-variant	RNF145	GRCh38.p7	5:159199103	TAACAGTTGGGAAAA[C/T]AGATAAGCATATGGA	153830
rs17719770	snp	C/T	0.177182	0.23916	intron-variant	RNF145	GRCh38.p7	5:159169981	ACTCCATTAATAATT[C/T]AACCATCTTATTCAC	153830
rs17720062	snp	A/G	0.177182	0.23916	intron-variant	RNF145	GRCh38.p7	5:159177376	CCAAATAACTAAATC[A/G]TAAGTTAAAACTAAA	153830
rs17720456	snp	C/T	0.0189856	0.0955633	intron-variant	RNF145	GRCh38.p7	5:159204266	TATGGTCTAAAATTC[C/T]CATAATCTGCCTTCA	153830

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