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
rs4225162	snp	A/G	0.21875	0.248039	utr-variant-3-prime	Whsc1	Mm_Celera	5:33895453	AAATAGAAATGGGAG[A/G]GCACCTTGACGCTGG	107823
rs4225163	snp	A/C	0.21875	0.248039	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33895383	GCTTGTTTATCCTGG[A/C]CCACCAAGCCTGCCT	107823
rs4225164	snp	A/G	0.21875	0.248039	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33895337	CAGTGCAGACGCAGC[A/G]CAGCTGCTGAGGATG	107823
rs4225165	snp	C/T	0.375	0.216506	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33895272	CAGGCCTATACACAG[C/T]GCTAGGAGCTGGGTC	107823
rs4225166	snp	A/G	0.21875	0.248039	synonymous-codon	Whsc1	GRCm38.p3	5:33895150	TGTGACCCTTCGCCA[A/G]CACCGCCTTTTCTTC	107823
rs4225167	snp	C/T	0.362812	0.2231	synonymous-codon	Whsc1	GRCm38.p3	5:33895123	CTTCCTCTTTCCTTT[C/T]GACTTCAGTGATTCT	107823
rs4225168	snp	A/G	0.4608	0.1344	missense	Whsc1	GRCm38.p3	5:33895113	CCTTTTGACTTCAGT[A/G]ATTCTGGAAAGGGTT	107823
rs6341465	snp	A/G	0.5	0	intron-variant	Whsc1	Mm_Celera	5:33864938	GGCCACTGAAGAAAG[A/G]ACATGTTCATTGGAG	107823
rs6342476	snp	C/T	0.5	0	intron-variant	Whsc1	Mm_Celera	5:33865113	gtggttgtgagccac[C/T]atgtggttgctggga	107823
rs6343025	snp	A/G	0.5	0	intron-variant	Whsc1	Mm_Celera	5:33865210	TTGAGTAGTATTTTA[A/G]GTAATGATTTTTTTT	107823
rs6343121	snp	C/T	0.290657	0.246672	intron-variant	Whsc1	Mm_Celera	5:33865279	TCAAGTAGCGTGAGC[C/T]TGACCTTCAGTTTGA	107823
rs13478176	snp	A/G	0.0798611	0.183174	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33895413	TCAAGTGTAGAGGTG[A/G]CGCTGTGTAGTAAGG	107823
rs29499601	snp	A/T	0.444444	0.157135	intron-variant	Whsc1	Mm_Celera	5:33856207	TGCCTGTGTCTCATT[A/T]CCTTTGTAAGGAACC	107823
rs29509643	snp	A/C	0.444444	0.157135	missense	Whsc1	Mm_Celera	5:33882145	CCATGTCAATGTGAG[A/C]TGGTGCTTTGTGTGC	107823
rs29530942	snp	A/G	0.32	0.24	intron-variant	Whsc1	Mm_Celera	5:33833517	GGAAGCAATCTCAGT[A/G]GTGACTCTGAAGTTT	107823
rs29548214	snp	G/T	0.375	0.216506	intron-variant, utr-variant-3-prime	Whsc1	GRCm38.p3	5:33875798	CCACTCTCTGACTAA[G/T]TGGCCACTGCTCTCA	107823
rs29567650	snp	C/T	0.484429	0.0868505	intron-variant	Whsc1	Mm_Celera	5:33827751	CATTACAGTTTTGTA[C/T]TTACGACTCTCATTT	107823
rs29583299	snp	A/G	0.444444	0.157135	intron-variant	Whsc1	GRCm38.p3	5:33831047	TGCTGGCCTCCATGG[A/G]CATTGCATGAATGTG	107823
rs29626965	snp	A/G	0.459184	0.136902	intron-variant, downstream-variant-500B	Whsc1	Mm_Celera	5:33877386	AGTGGGTTGGTGGAC[A/G]GAACATGGGCTCTCT	107823
rs29627816	snp	A/G	0.32	0.24	intron-variant, utr-variant-3-prime	Whsc1	GRCm38.p3	5:33871985	TGAAAGGCAGGAAGA[A/G]TTTTGATTCTGTCCT	107823
rs29628307	snp	C/T	0.444444	0.157135	intron-variant	Whsc1	GRCm38.p3	5:33836628	AGCCAAAGGAGCCTC[C/T]GAGACTTATCTGGAG	107823
rs29632368	snp	A/G	0.188366	0.242283	intron-variant	Whsc1, LOC105244765	Mm_Celera	5:33822540	TTTTTGTGCAACCAC[A/G]CTATACAGGGCTGTT	107823
rs29635623	snp	C/T	0.32	0.24	intron-variant	Whsc1	GRCm38.p3	5:33838726	TGGTTTCTCACACCA[C/T]CATTTGGGTCCCTAT	107823
rs29680834	snp	C/T	0.465374	0.126941	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33895579	CTGATGGTGCAGGCT[C/T]CTATTCACATACTGC	107823
rs29731148	snp	A/T	0.32	0.24	intron-variant, utr-variant-3-prime	Whsc1	Mm_Celera	5:33872789	GGTAAATAAAAAAAA[A/T]TTTAAATATAGATCA	107823
rs29731305	snp	A/G	0.375	0.216506	upstream-variant-2KB, utr-variant-3-prime	Whsc1, LOC105244765	GRCm38.p3	5:33819530	CCGAGGAATAGGGGT[A/G]GAGGTCTGTGGGCTG	107823
rs29776940	snp	A/G	0.444444	0.157135	intron-variant	Whsc1	GRCm38.p3	5:33863171	TTTCTAAATAGTGAG[A/G]CCTGGTGGTAAACAC	107823
rs29777320	snp	G/T	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33893749	GGTAAATGTCTCCAG[G/T]CCAGGGGACCTGCTG	107823
rs29780292	snp	C/G	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33852953	TATGTGCATTGTATG[C/G]GTATTGTGTGTGTAT	107823
rs33118842	snp	A/G	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33837109	ACATGTGATGCTTGT[A/G]CATAGTACACAAGAG	107823
rs33143888	snp	A/G	0.475309	0.108333	intron-variant	Whsc1	GRCm38.p3	5:33887158	GAGATCACTTAACGC[A/G]TTACCCTAGACTGAT	107823
rs33202951	snp	C/T	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33866866	CCGTACCTTTTGAAC[C/T]AGATTTTCCTTTCAT	107823
rs33250155	snp	A/C	0.197531	0.244432	intron-variant, downstream-variant-500B	Whsc1	Mm_Celera	5:33877643	ACTCAGAGCATTTCG[A/C]GTTGCCTCTTTCTGG	107823
rs33301297	snp	A/G	0.5	0	upstream-variant-2KB, utr-variant-3-prime	Whsc1, LOC105244765	GRCm38.p3	5:33818810	AGTGACCTATAGACT[A/G]AAAATCTTGACTTGG	107823
rs33314363	snp	C/T	0.475309	0.108333	intron-variant	Whsc1	GRCm38.p3	5:33884188	GAAAAGCTTAGAGTG[C/T]GCCCATGAGTCATGC	107823
rs33386042	snp	A/C	0.5	0	intron-variant	Whsc1	GRCm38.p3	5:33893676	GCTGTTCTTACTAGG[A/C]CTTTCTTTACTGACT	107823
rs33397572	snp	A/G	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33837654	CCATTAACTTAGAGT[A/G]GTCCCTTAGGAGAGG	107823
rs33398193	snp	A/G	0.375	0.216506	intron-variant	Whsc1	Mm_Celera	5:33827823	AAATAGTCTTGCTGT[A/G]TAACCCTGGGTGGTT	107823
rs33430301	snp	C/T	0.444444	0.157135	intron-variant	Whsc1	Mm_Celera	5:33885743	GCATGTGCTGTGGCG[C/T]GTGTGTGTGTGTGTG	107823
rs33458511	snp	C/T	0.444444	0.157135	intron-variant	Whsc1	GRCm38.p3	5:33838215	AGAATTTCCTTTAAC[C/T]CTGCACTTGGCAGGA	107823
rs33458702	snp	A/G	0.375	0.216506	intron-variant	Whsc1	GRCm38.p3	5:33836250	GCAGCAAGGTGGCTT[A/G]CAAGCTTCTGGAGAT	107823
rs33487419	snp	A/T	0.465374	0.126941	intron-variant	Whsc1	GRCm38.p3	5:33880915	CTGCTCCAAAGTAGC[A/T]GCCTTGTGCTAGTTG	107823
rs33562718	snp	A/C/T	0.203704	0.261891	utr-variant-3-prime	Whsc1	GRCm38.p3	5:33896337	ATGGCTTTGGAAAAA[A/C/T]CACAAAGTTAAACTA	107823
rs33566797	snp	A/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-3-prime	Whsc1, LOC105244765	GRCm38.p3	5:33819107	ATCTGGCATTAAGTA[A/T]GCTACATGGTATCTC	107823
rs33646831	snp	C/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Whsc1	GRCm38.p3	5:33842690	AGTGTTAGACTCTTA[C/T]AACTTGAGTTGCAGG	107823
rs33755429	snp	C/T	0.444444	0.157135	intron-variant	Whsc1	Mm_Celera	5:33856173	TACTTTTATTTTTTA[C/T]TATAAAATATATCAC	107823
rs45651877	snp	A/C	0.132653	0.220748	intron-variant	Whsc1	Mm_Celera	5:33865259	TCTTAAATGTTCTTG[A/C]TTGCTCAAGTAGCGT	107823
rs45694950	snp	A/G	0.18	0.24	intron-variant, utr-variant-3-prime	Whsc1	Mm_Celera	5:33875054	TTCCTAACATGCTTT[A/G]GAGCTTTTATTGCTT	107823
rs45729556	snp	A/G	0.197531	0.244432	intron-variant	Whsc1	Mm_Celera	5:33868321	TATGCTGCACAACAT[A/G]ATCAAGTTTTTAAAA	107823
rs45732888	snp	G/T	0.132653	0.220748	intron-variant	Whsc1	Mm_Celera	5:33892121	GCTTTCTAGTAAGCA[G/T]CACCTCTTCCCAGTA	107823
rs45795609	snp	A/C	0.495868	0.0452663	intron-variant, utr-variant-3-prime	Whsc1	GRCm38.p3	5:33875548	TCCTAGTTTTGGTAC[A/C]GGGGCATTGCCAGTC	107823
rs45893836	snp	C/G	0.48	0.0979796	intron-variant	Whsc1	GRCm38.p3	5:33862714	GCTCTGGGTATTTAT[C/G]GAAAAGAGTGACAGT	107823
rs45977241	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33862256	TCTCATTTAAACACT[A/G]GAGTTCCATATCAGC	107823
rs45982795	snp	A/G	0.489796	0.070696	intron-variant	Whsc1	Mm_Celera	5:33863402	GTGCAAATGAAAATA[A/G]AGAATTTGTATTCAA	107823
rs46057882	snp	C/T	0.124444	0.216185	synonymous-codon	Whsc1	Mm_Celera	5:33854650	TCATGTACAGTTCTT[C/T]GGTGATGCCCCAGAA	107823
rs46084153	snp	A/T			intron-variant	Whsc1	Mm_Celera	5:33857716	AAATATTGGAGTAGT[A/T]TTTTAAAAAAAAAAA	107823
rs46114084	snp	A/C	0.32	0.24	intron-variant	Whsc1	Mm_Celera	5:33860508	TCTCACTCCATGCTC[A/C]TAGGAACATTTTTGT	107823
rs46121779	snp	A/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33852615	TGGGTATGGGACCTC[A/T]TAGAGTGATGCTACA	107823
rs46145942	snp	G/T	0.124444	0.216185	downstream-variant-500B	Whsc1, Nelfa	Mm_Celera	5:33898140	TTGGTCTCAGAGCAG[G/T]GAGTCAAGCTCGCCT	107823
rs46308602	snp	G/T	0.231111	0.249285	intron-variant	Whsc1	Mm_Celera	5:33862867	GAGTGAGTTAGTTCC[G/T]GGTGTCCTCAGCTTT	107823
rs46324640	snp	A/C	0.231111	0.249285	missense	Whsc1	Mm_Celera	5:33881169	GCCTCCAACCCTTCA[A/C]ATCCACGGCCATCAA	107823
rs46327767	snp	G/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33879757	CATCTGTGGAAGGTG[G/T]CGTTTATGATGAAAA	107823
rs46423881	snp	A/G	0.132653	0.220748	intron-variant	Whsc1, LOC105244765	Mm_Celera	5:33823523	ACTCTGTTAGTTTTG[A/G]GCACCCTGGTTTCTG	107823
rs46435310	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33880316	TTCACTGTACTGTAT[C/T]AACTTGAATGACAGT	107823
rs46504755	snp	C/G	0.142012	0.225474	intron-variant	Whsc1, LOC105244765	Mm_Celera	5:33823777	CTGTTTTGGAAGGCT[C/G]TTGTAGGCATGATTT	107823
rs46507850	snp	A/G			intron-variant	Whsc1	Mm_Celera	5:33858172	CCTCTGCCTGGTCTA[A/G]AACTCACAAAGATCT	107823
rs46548215	snp	C/T			intron-variant	Whsc1	Mm_Celera	5:33857690	GGGTAGTTTAGAAGT[C/T]TTCCCAGAGAAAATA	107823
rs46554282	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33886723	TTTGCAATATATCCC[C/T]ATCATAGAGACACAA	107823
rs46604501	snp	A/C/G	0.165289	0.235211	intron-variant, utr-variant-3-prime	Whsc1	Mm_Celera	5:33874827	TCTCACATGTATTCA[A/C/G]ACATACAGGATGCTA	107823
rs46617532	snp	A/C	0.32	0.24	intron-variant	Whsc1	Mm_Celera	5:33855961	TGGGAACTGAGTTTC[A/C]CTGGGCCTCCCTTTG	107823
rs46625224	snp	A/C			intron-variant	Whsc1	Mm_Celera	5:33857672	GTTATTTTTGTCCCT[A/C]CAGGGTAGTTTAGAA	107823
rs46641607	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33879223	CTGATGTATTGGTGA[A/G]GGTGTCTCATGAAGT	107823
rs46667252	snp	G/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33893072	GTTCCTAACAGGTCA[G/T]TACTCTGACGTCTTT	107823
rs46718143	snp	G/T			intron-variant, upstream-variant-2KB	Whsc1, LOC105244765	GRCm38.p3	5:33825973	GCTGTGTGGGCTGTT[G/T]GAATCAGACTCAGGT	107823
rs46795769	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33890598	TCTCCTGGAGTGAAT[C/T]CTGAGTTCTGGGCTG	107823
rs46810425	snp	C/T			intron-variant	Whsc1	Mm_Celera	5:33834213	TAGATCTGGGGGGTC[C/T]GACTCTCTTGGCTCC	107823
rs46838274	snp	C/T			intron-variant	Whsc1	Mm_Celera	5:33857718	ATATTGGAGTAGTTT[C/T]TTAAAAAAAAAAATT	107823
rs46842374	snp	C/T			intron-variant	Whsc1	Mm_Celera	5:33857790	ACCAATATTTGGAGA[C/T]TGATCCAGGATGATT	107823
rs46881499	snp	A/C			intron-variant	Whsc1	Mm_Celera	5:33857739	AAAAAAAATTTGTAA[A/C]CCATGTTAAGTGTGG	107823
rs46924451	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33888881	TTCTTAAACAGTCCC[C/T]AAGTTTAGCTCTTAA	107823
rs46930998	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33878552	TGGGTGGGATGTTAG[A/G]TTTTGAGAAGAGAGA	107823
rs47000799	snp	A/C	0.32	0.24	intron-variant, utr-variant-3-prime	Whsc1	Mm_Celera	5:33872309	CTATGCACGGGGTGT[A/C]TGAGCGGTGCCCAGG	107823
rs47101762	snp	C/T	0.132653	0.220748	intron-variant	Whsc1	Mm_Celera	5:33863612	GATAAAACTTTGCTA[C/T]TTAAAAATTTGTTAT	107823
rs47127493	snp	G/T	0.244898	0.249948	synonymous-codon	Whsc1	Mm_Celera	5:33843392	GAAAGATCTTACTTC[G/T]TGTGTTTTTAATGGA	107823
rs47132345	snp	A/G	0.48	0.0979796	intron-variant	Whsc1	GRCm38.p3	5:33859977	TTCTTTTATGTTTCT[A/G]GGACCCAGATTCATT	107823
rs47155046	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Whsc1	Mm_Celera	5:33895639	GCCCTGGGCTCCTTC[C/T]GATCAGGATTGGTAA	107823
rs47196642	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33891131	GTGCCTCTCCCTCTC[A/G]TGTCAGCACAGCATC	107823
rs47200368	snp	A/G			intron-variant	Whsc1	Mm_Celera	5:33834141	GTACTTATGCCCTTG[A/G]TAAGAACCTGGTTTT	107823
rs47295271	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33894620	CAAATAAAAAAGTGA[C/T]TTTAAGTTAGGTATG	107823
rs47304912	snp	A/G	0.231111	0.249285	intron-variant	Whsc1	Mm_Celera	5:33864810	CTTTGGCCTGTGAGC[A/G]TGTATTCTATATAAT	107823
rs47356957	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33890687	TTCTCTTTCTATTCT[C/T]GTATCAACTGATGGG	107823
rs47367577	snp	C/G			intron-variant	Whsc1	Mm_Celera	5:33857776	ATAGCTGTACTATCA[C/G]CAATATTTGGAGATT	107823
rs47420830	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33886765	GTTTACCTTGTCACA[A/G]ACTGGCCCTGAAGTG	107823
rs47505634	snp	A/C	0.32	0.24	missense	Whsc1	Mm_Celera	5:33855583	TGATCCTGGCACAGA[A/C]AAGAGTACACCTCCA	107823
rs47527512	snp	A/G	0.345679	0.230967	missense	Whsc1	Mm_Celera	5:33867634	AAGGCTATAGAGGCA[A/G]CCTCCTCACTCAAGA	107823
rs47555616	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33894529	TGCCTGGCCTTTGAG[C/T]ACCAATTACAAGCTT	107823
rs47566172	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33880740	GATTCTAGTCTTCCT[C/T]CAGCCACAGCAAGTC	107823
rs47566759	snp	C/T	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33852310	TAGTTTCATTTGCTG[C/T]TGTTTTACTTACTAC	107823
rs47590178	snp	C/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33853956	TAAAGGTCTCTTTTC[C/G]TCTTGTTATTGAAAT	107823
rs47590966	snp	A/G	0.124444	0.216185	intron-variant	Whsc1	Mm_Celera	5:33845915	AGGGAAACATTCTCT[A/G]AAGATCAGGCCCTTA	107823

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