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
rs884273	snp	A/G	0.0429648	0.14013	intron-variant	RNFT2	GRCh38.p7	12:116784335	CAGACCTTCTCCCAA[A/G]AGCTGAACTGGGGAA	84900
rs903771	snp	G/T	0.232943	0.249417	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853786	TCTCGTGGGAGCACT[G/T]CTGTAATAAATCACA	84900
rs903772	snp	A/G	0.29175	0.246489	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852796	CCTGGAGATGGCTAC[A/G]GGGAGGCTGAGTGAC	84900
rs903773	snp	A/G	0.105569	0.204058	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852350	GTGGCACACAGGGGC[A/G]AATGTCCTGAATCTA	84900
rs903774	snp	C/G	0.292008	0.246445	intron-variant	RNFT2	GRCh38.p7	12:116852291	AATACTGGCTGACAG[C/G]GAGGTGGCTACAAAG	84900
rs903775	snp	C/G	0.481148	0.0952395	intron-variant	RNFT2	GRCh38.p7	12:116851808	CTGGGCCAAAGCTGA[C/G]CTTTCTTTCTTTCCT	84900
rs924072	snp	C/G	0.335559	0.234904	intron-variant	RNFT2	GRCh38.p7	12:116808586	GATTTATTTATTTAT[C/G]TAGTCCCGCCTGGCT	84900
rs924073	snp	C/G	0.186421	0.24178	intron-variant	RNFT2	GRCh38.p7	12:116808831	AAATTCTTGCTCCCC[C/G]TCCTGTGCTCCCCCT	84900
rs924074	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116808872	CTCTCACCCCCAGCA[A/C]TGGGCCGTTGGAAAT	84900
rs924075	snp	C/T	0.373196	0.217538	intron-variant	RNFT2	GRCh38.p7	12:116812229	GAACACAGACTTATT[C/T]CCTGCTGCAGCCTTA	84900
rs924076	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116812366	AGGACGGGGATGGCA[A/G]AGGGAGGAAAGGAGG	84900
rs924077	snp	A/G	0	0	intron-variant	RNFT2	GRCh38.p7	12:116812375	ATGGCAAAGGGAGGA[A/G]AGGAGGGACAGCTCT	84900
rs924078	snp	A/T	0.348354	0.22984	intron-variant	RNFT2	GRCh38.p7	12:116816066	AAGACTATAGCTGAC[A/T]TGGGGACAGATAAGC	84900
rs924079	snp	C/G	0.470811	0.117228	intron-variant	RNFT2	GRCh38.p7	12:116816174	CTTAATCATCAACAT[C/G]TTATAATTAGGCCTC	84900
rs987560	snp	A/G	0.142609	0.225759	intron-variant	RNFT2	GRCh38.p7	12:116811074	TCACCTCCCTTCTCC[A/G]TGCCTCAGTTTCCTC	84900
rs1495933	snp	A/G	0.335559	0.234904	intron-variant	RNFT2	GRCh38.p7	12:116805938	catttacaaaatgcc[A/G]tcacagcaaaaccca	84900
rs1532395	snp	C/T	0.260227	0.249791	intron-variant	RNFT2	GRCh38.p7	12:116748511	TTCCTGAATAGAATT[C/T]CTGGGGGTGGGGGTG	84900
rs1565988	snp	C/T	0.111928	0.208413	intron-variant	RNFT2	GRCh38.p7	12:116767339	tcctcccacctcagc[C/T]tcccaagtagctggt	84900
rs1603327	snp	C/T	0.488666	0.0744214	intron-variant	RNFT2	GRCh38.p7	12:116800127	AGCTTCACCAGAGGC[C/T]GAGCATATGCAGGTG	84900
rs1603328	snp	A/G	0.209388	0.246679	intron-variant	RNFT2	GRCh38.p7	12:116800180	agaaccatgagccaa[A/G]ataaacctcttttct	84900
rs1845777	snp	A/G	0.486133	0.082104	intron-variant	RNFT2	GRCh38.p7	12:116800355	tacaaaaaattggcc[A/G]ggcacagtggcttac	84900
rs1969017	snp	A/G	0.229723	0.249176	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740059	AAAAATACAAAAATT[A/G]GGTGGGCGTGGTGTC	84900
rs1971306	snp	C/T	0.348794	0.229651	intron-variant	RNFT2	GRCh38.p7	12:116772468	AATACAAAAATCAGC[C/T]GGGCGTGGTGGCACA	84900
rs2016622	snp	A/G	0.195214	0.243923	intron-variant	RNFT2	GRCh38.p7	12:116806147	GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC	84900
rs2018152	snp	A/G	0.37138	0.218556	intron-variant	RNFT2	GRCh38.p7	12:116851609	GCCGGGCGCGGTGGC[A/G]GGTGCCTGTAATCCC	84900
rs2029852	snp	C/G	0.4973	0.0366419	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737461	AAGAAAGACGGAAGG[C/G]AAGGGAGAGGAAAAA	84900
rs2029853	snp	A/G	0.497933	0.032082	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737503	AAGAAAGGGAAGGGG[A/G]AGGAAGGAAAGGGGG	84900
rs2029854	snp	C/T	0.211819	0.247067	intron-variant	RNFT2	GRCh38.p7	12:116755245	ttgttgaaaagggtg[C/T]cctttccccacttta	84900
rs2029855	snp	A/T	0.0540123	0.155206	intron-variant	RNFT2	GRCh38.p7	12:116755370	GCCCAGAGGTCTTTT[A/T]TTTTTTTTTTTTTAA	84900
rs2029856	snp	C/T	0.213635	0.247341	intron-variant	RNFT2	GRCh38.p7	12:116755408	TATGCCATGAATTCA[C/T]AGGGAATAGGTTCCA	84900
rs2088230	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116851764	cctccctccctccct[G/T]ctttctttctttttt	84900
rs2088231	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116851762	tccctccctcccttc[G/T]ttctttctttttttt	84900
rs2088232	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116799945	acaggggtgaatctc[A/C]tgtgaatggcgtggt	84900
rs2088233	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116799951	gtgaatctcatgtga[A/C]tggcgtggtaccctc	84900
rs2088234	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116800012	tagttcatgcacgat[A/C]tgactgtttaaaaga	84900
rs2088235	snp	C/T	0.133435	0.221162	intron-variant	RNFT2	GRCh38.p7	12:116800738	agaattgcttgagcc[C/T]gggaggtggaggttg	84900
rs2088236	snp	C/T	0.47614	0.106587	intron-variant	RNFT2	GRCh38.p7	12:116787273	GATCATCTGCCAGAT[C/T]GGCCAGGTGCTAGAG	84900
rs2101868	snp	A/G	0.106278	0.204558	intron-variant	RNFT2	GRCh38.p7	12:116787118	tatccttgagtggcc[A/G]ttatttcctttacta	84900
rs2132389	snp	A/G	0.450985	0.148678	intron-variant	RNFT2	GRCh38.p7	12:116781553	TGCCATCACTGACTC[A/G]GAAGACGGaggaaga	84900
rs2172953	snp	C/T	0.0648419	0.167978	intron-variant	RNFT2	GRCh38.p7	12:116740307	GCAGATTCAAGGTAT[C/T]GCAGGGACTGTTCAT	84900
rs2220936	snp	A/C			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739262	GCCCTTATTACCTTG[A/C]TAGGGTGAAAGGTGG	84900
rs2393084	snp	A/C	0.1652	0.235179	intron-variant	RNFT2	GRCh38.p7	12:116791793	atgatccagaattct[A/C]tgcctatgtatttac	84900
rs2393085	snp	C/T	0.165853	0.235413	intron-variant	RNFT2	GRCh38.p7	12:116791734	gtctgcgaaagctca[C/T]agcagcactattcac	84900
rs2393086	snp	A/G	0.208779	0.246578	intron-variant	RNFT2	GRCh38.p7	12:116757392	tcttcttgtttctct[A/G]gttccttgaggggtg	84900
rs2393087	snp	C/T	0.208779	0.246578	intron-variant	RNFT2	GRCh38.p7	12:116757579	tgatgtcatttttga[C/T]ccaatgctcattcag	84900
rs2393089	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116845262	tctATATATATATAT[A/T]TAttttttttttttt	84900
rs2393090	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116845260	tATATATATATATAt[A/T]ttttttttttttttt	84900
rs2393107	snp	A/G	0.112631	0.208878	intron-variant	RNFT2	GRCh38.p7	12:116800870	aaataaaaACCATTT[A/G]ACAGATAAAACAGAG	84900
rs2893689	snp	A/T	0.295599	0.245806	intron-variant	RNFT2	GRCh38.p7	12:116847839	taaattaaaTTTTTT[A/T]AAAAAGAGAGAGggc	84900
rs2893690	snp	A/C	0.139903	0.224452	intron-variant	RNFT2	GRCh38.p7	12:116845280	tctctctctctctct[A/C]tctctATATATATAT	84900
rs2893691	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116845278	tctctctctctctct[A/C]tctATATATATATAT	84900
rs2893692	snp	A/G	0.202959	0.245534	intron-variant	RNFT2	GRCh38.p7	12:116842251	agtgaaggtgatggg[A/G]tgtcccttctgggat	84900
rs3069215	in-del	-/CTCT			intron-variant	RNFT2	GRCh38.p7	12:116845293	GAGCTCTCTCTCTCT[-/CTCT]CTCTCTATATATATA	84900
rs3069310	in-del	-/TAAAA			intron-variant	RNFT2	GRCh38.p7	12:116800813	AGCAAGACTCCATCT[-/TAAAA]TAAAATAAAATAAAA	84900
rs3088107	snp	A/G	0.400282	0.220572	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853334	CTCAAGTTCCACGAA[A/G]TCCTTAGAAATGGAC	84900
rs3203930	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116852298	GCCACCTCCCTGTCA[C/G]CCAGTATTAACATGT	84900
rs3809191	snp	A/G	0.0912534	0.193131	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738576	TCGGTGCAGTCCTGT[A/G]ACGGGCCCCAGGGGC	84900
rs3809192	snp	A/G	0.247621	0.249989	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738747	GTACGGCCTGCTTCC[A/G]ACAAAGAATCCGAAG	84900
rs3809193	snp	A/G	0.114036	0.209795	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738900	TGGAGGGAGGGGCGA[A/G]AGGAGGATTAAGTTG	84900
rs3840786	in-del	-/T	0.5	0	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738388	AAAAAGAGAACGCGA[-/T]TTTTTTTTTCTTTTC	84900
rs3863382	snp	A/C	0	0	intron-variant	RNFT2	GRCh38.p7	12:116845276	TCTCTCTCTCTCTCT[A/C]TATATATATATATAT	84900
rs3926590	snp	C/G	0.209084	0.246629	intron-variant	RNFT2	GRCh38.p7	12:116755518	GGTACCTTTCTCTTC[C/G]GCTTCTTTCTTTTTC	84900
rs3933908	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737554	gtgaggaaggtaagg[A/G]aggaagg	84900
rs3933909	snp	A/C			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737558	ggaaggtaaggaagg[A/C]agg	84900
rs3941210	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116851745	tctttcttttttttt[G/T]tagacagagtctcac	84900
rs4238048	snp	A/G	0.199564	0.24486	intron-variant	RNFT2	GRCh38.p7	12:116806671	gatcccttgagcctg[A/G]gagttcgaggctgca	84900
rs4275719	snp	A/G	0.379354	0.213933	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737570	AGGAAGGGAGGCAGG[A/G]AGAGGGGAAGGAAGG	84900
rs4301877	snp	C/T	0.303938	0.244112	intron-variant	RNFT2	GRCh38.p7	12:116750660	gtgtgatgctaggtg[C/T]attatttaacctctc	84900
rs4326894	snp	G/T	0.347253	0.230308	intron-variant	RNFT2	GRCh38.p7	12:116819871	acagaaatataagag[G/T]agtcacacagacgat	84900
rs4468446	snp	A/G	0.208779	0.246578	intron-variant	RNFT2	GRCh38.p7	12:116757413	ttgaggggtgacctt[A/G]gagtgtcagtttgtg	84900
rs4480639	snp	A/G	0.337386	0.23423	intron-variant	RNFT2	GRCh38.p7	12:116807341	CGTGATAGTAATAAA[A/G]TAAGAAATATTAGAT	84900
rs4486720	snp	C/G	0.180383	0.240111	intron-variant	RNFT2	GRCh38.p7	12:116750754	tgatgttaaatttga[C/G]ttaatatgtgtaaaa	84900
rs4608187	snp	C/T	0.0916144	0.193427	intron-variant	RNFT2	GRCh38.p7	12:116800813	AGCAAGACTCCATCT[C/T]AAAATAAAATAAAAT	84900
rs4612912	snp	A/G	0.113685	0.209567	intron-variant	RNFT2	GRCh38.p7	12:116753654	GGCTTAGAGAGGTGC[A/G]GTGACTTGCCCAAGC	84900
rs4766805	snp	C/T	0.280256	0.248162	intron-variant	RNFT2	GRCh38.p7	12:116825164	ACCGTTGGCTGGTTT[C/T]CATGTTTCTCCTCCA	84900
rs4766806	snp	C/T	0.28578	0.247426	intron-variant	RNFT2	GRCh38.p7	12:116841465	ctcaaaaaaataaaa[C/T]gactgggcatggtgg	84900
rs4767443	snp	C/T	0.291235	0.246576	intron-variant	RNFT2	GRCh38.p7	12:116745552	AGGCATGAGCCACCA[C/T]GCCTGGCCTCACTAG	84900
rs4767444	snp	A/G	0.00755907	0.0610114	intron-variant	RNFT2	GRCh38.p7	12:116753888	CTGTCAACTCTGAGG[A/G]GACCAGGGATGTGCC	84900
rs4767445	snp	C/T	0.211516	0.24702	intron-variant	RNFT2	GRCh38.p7	12:116754322	tttatggctgtgtag[C/T]attccaccatgtata	84900
rs4767446	snp	C/T	0.209084	0.246629	intron-variant	RNFT2	GRCh38.p7	12:116756722	gtaatttgttggatt[C/T]ggttagcaagtattt	84900
rs4767447	snp	A/T	0.119978	0.213528	intron-variant	RNFT2	GRCh38.p7	12:116756981	ttgttggtaattttt[A/T]aattaccatttcaat	84900
rs4767448	snp	A/G	0.138886	0.22395	intron-variant	RNFT2	GRCh38.p7	12:116759756	ccagtgcctgttgcc[A/G]tggaggtggtggagg	84900
rs4767449	snp	A/G	0.110519	0.207473	intron-variant	RNFT2	GRCh38.p7	12:116771860	GCCATGCACCTGGAA[A/G]TTCTTTTGAAACGAG	84900
rs4767450	snp	A/G	0.110519	0.207473	intron-variant	RNFT2	GRCh38.p7	12:116772009	CTCCGATGTTTTTTA[A/G]TGAGTTTGTTTCCCC	84900
rs4767451	snp	A/G	0.348574	0.229746	intron-variant	RNFT2	GRCh38.p7	12:116774099	TACCTAAAGTAGTCA[A/G]ATTTATAGACAGAAA	84900
rs4767452	snp	C/T	0.206005	0.246099	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779336	CAAGATCATCCTGGC[C/T]GTCAAGTCCAAGGTA	84900
rs4767453	snp	G/T	0.449599	0.150533	intron-variant	RNFT2	GRCh38.p7	12:116786754	CTCACAGTTCTGGAA[G/T]CCAGAAATCCAAAAT	84900
rs4767454	snp	G/T	0.11963	0.213316	intron-variant	RNFT2	GRCh38.p7	12:116797922	tggtaactcctgggt[G/T]ttgccatggcaatgg	84900
rs4767455	snp	C/G	0.103438	0.202533	intron-variant	RNFT2	GRCh38.p7	12:116798331	ATATACAGCTCCCAC[C/G]TTGCTTTTATTATCC	84900
rs4767456	snp	A/T	0.0558544	0.157504	intron-variant	RNFT2	GRCh38.p7	12:116798360	CCATCTATCTTAGAG[A/T]TTGTTCGGATAAATA	84900
rs4767457	snp	C/G	0.42803	0.175514	intron-variant	RNFT2	GRCh38.p7	12:116820288	gatttcattatgttt[C/G]ccagtctggtctcga	84900
rs4767458	snp	C/T	0.143284	0.226079	intron-variant	RNFT2	GRCh38.p7	12:116820373	AGGTGTGAGCCACCA[C/T]GCCCAGCTATCCCTG	84900
rs4767459	snp	A/G	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116825208	CTGCTCCCCTTCCAC[A/G]TGtcctcttcactgg	84900
rs4767460	snp	A/T	0.171057	0.237209	intron-variant	RNFT2	GRCh38.p7	12:116841063	AAGTCAGATGCTTTT[A/T]gtatcagttatcaat	84900
rs4767461	snp	C/T	0.492188	0.0620098	intron-variant	RNFT2	GRCh38.p7	12:116849176	AGTATTTTGGAGTCG[C/T]ATTGTCTCCCCAACG	84900
rs5801197	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116744226	GTGAGACTCCTCCTC[-/A]AAAAAAAAAAAAAAA	84900
rs5801198	in-del	-/A	0.486	0.0824865	intron-variant	RNFT2	GRCh38.p7	12:116775261	TGAAACTCCCGTCTC[-/A]AAAAAAAAAAAAAAA	84900
rs5801199	in-del	-/AAGTCACCAG	0	0	intron-variant	RNFT2	GRCh38.p7	12:116775332	TACTGAAGTCACCAG[-/AAGTCACCAG]TCTAGACGGTGCTTG	84900
rs6490086	snp	A/C	0.18325	0.240924	intron-variant	RNFT2	GRCh38.p7	12:116752595	TTAAAAGAGTAAGTG[A/C]GACCAGGTACGGTGG	84900
rs6490091	snp	A/G	0.110519	0.207473	intron-variant	RNFT2	GRCh38.p7	12:116776022	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT	84900

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