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

SUMO2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs774741055	snp	C/T			intron-variant	SUMO2	GRCh38.p7	17:75179041	AAAGTGCTGGATTAC[C/T]ACGCCCAGCCTATGA	6613
rs774853171	snp	A/G	1.7336e-05	0.00294409	intron-variant, synonymous-codon	SUMO2	GRCh38.p7	17:75174788	ATTGATTGGTTGCCC[A/G]TCAAATCGGAATCTG	6613
rs774860064	in-del	-/AAAAAAAAAAAAAAAAAA			intron-variant	SUMO2	GRCh38.p7	17:75180393	TGAGACTCCCAGCTT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAACGAC	6613
rs774908703	snp	A/G	3.32309e-05	0.00407607	intron-variant	SUMO2	GRCh38.p7	17:75181007	TCCCATGAAAATAAG[A/G]TTTTTAAAAATAGTT	6613
rs774916978	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75176685	GAACTTCCTGGAATA[A/G]CTTTAAAAAAGCACC	6613
rs774923798	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75170280	CAAATCTCAATAAAA[A/G]CCCAAATTAGGCTGG	6613
rs775099333	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75181301	TTTCTCATACTGTAT[A/G]CTAAAACGGCATACT	6613
rs775247760	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75179397	GCTGGGCGTGGTGGC[A/G]TGCGCCCGTAGTCCC	6613
rs775447862	snp	A/T			intron-variant	SUMO2	GRCh38.p7	17:75171037	CTCGGTGCACTGACT[A/T]TATAAGTTAGCCATG	6613
rs775524639	in-del	-/A	2.06797e-05	0.0032155	intron-variant	SUMO2	GRCh38.p7	17:75174847	GAATTTAAAAGCAAT[-/A]AACAGCATTAAGAGA	6613
rs775607606	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75175280	GAGCCATGGTGCCCA[A/G]CCTCTCATTTTCAGT	6613
rs775614950	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75175398	CGATCTCGGCTCACT[A/G]CAACCTCCACCTTTT	6613
rs775785193	in-del	-/AC			intron-variant	SUMO2	GRCh38.p7	17:75179919	CAAAGTGCTGGGATT[-/AC]AGATATGAGCCACTG	6613
rs775915972	snp	A/C/G	3.54178e-05	0.00420807	intron-variant	SUMO2	GRCh38.p7	17:75181213	GAAAAATAAAAGTAT[A/C/G]ATTTGGGAAATGTGA	6613
rs776065301	snp	G/T			intron-variant	SUMO2	GRCh38.p7	17:75182487	GCGCCCTAACGCCCC[G/T]CCTCACGCGCGCCGG	6613
rs776147766	snp	C/T	1.65792e-05	0.00287912	intron-variant	SUMO2	GRCh38.p7	17:75181028	AAAAATAGTTTTATT[C/T]AGTGGAAGTACACAT	6613
rs776163680	in-del	-/AG			intron-variant	SUMO2	GRCh38.p7	17:75174514	TTCAACCCGGGCAAC[-/AG]AGAGGCCCTGTCCCT	6613
rs776311393	in-del	-/A	3.44643e-05	0.00415102	intron-variant	SUMO2	GRCh38.p7	17:75181193	TGACTCCTTCCTGTT[-/A]AAAAGAAAAATAAAA	6613
rs776314209	in-del	-/C			intron-variant	SUMO2	GRCh38.p7	17:75179396	AGCTGGGCGTGGTGG[-/C]GTGCGCCCGTAGTCC	6613
rs776683482	snp	A/G/T	0.000101687	0.00712987	utr-variant-3-prime	SUMO2	GRCh38.p7	17:75168330	GGAGTAAAGAAGCAG[A/G/T]TTCCCTTTTCAGTAG	6613
rs776685588	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75173916	AAAATGAAGTGGTAC[A/G]TAAAGAGTTAAAGGA	6613
rs776740490	snp	G/T	4.09333e-05	0.00452382	intron-variant	SUMO2	GRCh38.p7	17:75174737	AATTTTTCTAATTAG[G/T]AGAGATTTTTTTACC	6613
rs776954062	snp	C/T	3.55638e-05	0.00421671	intron-variant	SUMO2	GRCh38.p7	17:75181217	AATAAAAGTATAATT[C/T]GGGAAATGTGATCAA	6613
rs777112418	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75172771	TGAGCCACTGCGCCC[A/G]GCGATGCCTGGCTAA	6613
rs777127173	in-del	-/CTT			upstream-variant-2KB	SUMO2	GRCh38.p7	17:75184729	CAGCAACATTCCTGA[-/CTT]CTTCTCCTTCACACA	6613
rs777145576	snp	G/T			intron-variant	SUMO2	GRCh38.p7	17:75180932	CACGACAAAACTGAC[G/T]TGCCAAGTGCATATT	6613
rs777200160	snp	A/G	1.72961e-05	0.00294071	utr-variant-5-prime	SUMO2	GRCh38.p7	17:75182842	TCGGCCATGGCGAGC[A/G]CCGGAGTCTCCTCAG	6613
rs777316008	snp	A/C	2.92325e-05	0.00382301	intron-variant	SUMO2	GRCh38.p7	17:75168420	GCATAAAAGAAAAAA[A/C]AAATGTAAAAGCACT	6613
rs777321825	in-del	-/GTT			intron-variant	SUMO2	GRCh38.p7	17:75181906	TCGACCCAACCTAAA[-/GTT]GTTGTCCAAAATCGA	6613
rs777470882	snp	C/T			intron-variant	SUMO2	GRCh38.p7	17:75179803	AGGTGGGATTATGCG[C/T]GTGTAACACCACGCC	6613
rs777667501	snp	A/C	8.19169e-05	0.00639935	utr-variant-3-prime	SUMO2	GRCh38.p7	17:75168296	GAATGTAATCTTGGT[A/C]TTTAAAGAACAGAGT	6613
rs777718501	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75178343	ATATTGTGAAACCCC[A/G]TCTCTACAAAAAATA	6613
rs777861977	in-del	-/G			intron-variant	SUMO2	GRCh38.p7	17:75178174	TCTCAAAAAAAAAAA[-/G]GGCAAAATTTTGCAA	6613
rs778071064	snp	A/C			intron-variant	SUMO2	GRCh38.p7	17:75181835	TATTCTCCCCTCCCC[A/C]CCTTTGTTGTCATGG	6613
rs778439397	snp	A/T			intron-variant	SUMO2	GRCh38.p7	17:75173019	TTTTCAAAGATTATC[A/T]ACAAAACTACAATCT	6613
rs778550296	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75177786	TCACCTGAGCTCAGG[A/G]GTTCAAGACCAGCCT	6613
rs778662924	snp	C/T	3.66831e-05	0.00428255	intron-variant	SUMO2	GRCh38.p7	17:75168443	AAAGCACTGATTAAG[C/T]TCTGAAAATTAATGA	6613
rs778870586	in-del	-/G			intron-variant	SUMO2	GRCh38.p7	17:75173165	TATGTTTCAGAAACT[-/G]TAAGTCTTCTATTTT	6613
rs779036721	in-del	-/A	5.95776e-05	0.00545759	intron-variant	SUMO2	GRCh38.p7	17:75174743	CTAATTAGGAGAGAT[-/A]TTTTTTACCTGTGCA	6613
rs779081178	snp	C/T	0.000221166	0.0105135	intron-variant	SUMO2	GRCh38.p7	17:75182811	GGCCGGCGGCGAGCT[C/T]ACCTTGGGCTTTTCG	6613
rs779238179	snp	A/T			intron-variant	SUMO2	GRCh38.p7	17:75171616	TTGGGAGAATAATTC[A/T]AAAACGAATCAATTC	6613
rs779266858	in-del	-/C			intron-variant	SUMO2	GRCh38.p7	17:75180412	AAAAAAAAAAAAAAA[-/C]AAAAAAAAACGACTT	6613
rs779280020	in-del	-/A			intron-variant	SUMO2	GRCh38.p7	17:75179529	CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA	6613
rs779312549	snp	A/G	1.66496e-05	0.00288522	synonymous-codon	SUMO2	GRCh38.p7	17:75181168	ATTAATATGATCGTT[A/G]TTCTCAGTCTTGACT	6613
rs779374279	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75172738	CCTCGGCCTCCCAAA[A/G]TGCTGGGATCACAGG	6613
rs779704830	snp	C/T			intron-variant	SUMO2	GRCh38.p7	17:75175812	TAATTTTTGTGTTTT[C/T]AGTAGAGACAGGGTT	6613
rs779765054	snp	C/T	1.65899e-05	0.00288005	synonymous-codon	SUMO2	GRCh38.p7	17:75181141	AGAACCATCCTGCCC[C/T]GCCACCTTCAAATTA	6613
rs780067186	snp	C/T			intron-variant	SUMO2	GRCh38.p7	17:75178650	CATGGCTCACTGCAG[C/T]CTAGACCTGCCAAGC	6613
rs780264298	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75171501	TCTGGGAGACAGGGC[A/G]AAACTCCGTCTCGAA	6613
rs780326909	snp	C/T	7.73784e-05	0.00621958	utr-variant-5-prime	SUMO2	GRCh38.p7	17:75182837	TTTCGTCGGCCATGG[C/T]GAGCGCCGGAGTCTC	6613
rs780621338	snp	A/G			upstream-variant-2KB	SUMO2	GRCh38.p7	17:75184234	CTGGTGCTGTCCCCA[A/G]AGTTCCACTAAAACT	6613
rs781167490	snp	A/G			intron-variant	SUMO2	GRCh38.p7	17:75181465	TCAGTGTATTGCAAC[A/G]TTCTCTTGAAGTTAA	6613
rs781216652	snp	C/G/T	0.000157493	0.00887252	intron-variant	SUMO2	GRCh38.p7	17:75182800	CGAGGCGAAGGGGCC[C/G/T]GCGGCGAGCTCACCT	6613
rs781295203	snp	C/T			intron-variant	SUMO2	GRCh38.p7	17:75179998	AACTCAAACTCAATT[C/T]CCCAACTTACATAGG	6613
rs781592545	snp	G/T			upstream-variant-2KB	SUMO2	GRCh38.p7	17:75184138	TATCTCTCTCCATTC[G/T]TGGCCAAACAGCTCG	6613
rs796178767	in-del	-/A			intron-variant	SUMO2	GRCh38.p7	17:75169068	ACAAAAAAAAAAAGG[-/A]AAAAAAAAAAAAAAT	6613
rs796254179	snp	A/C			intron-variant	SUMO2	GRCh38.p7	17:75176570	GCAGTGAGCCAAGAT[A/C]GTGCCCTAGCACTCC	6613

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