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
rs15700	snp	A/G	0	0	missense, nc-transcript-variant, utr-variant-3-prime	RHOBTB1	GRCh38.p7	10:60871570	ACCAGCGTGTGAAAA[A/G]GGAACGAGAGAAGGA	9886
rs750593	snp	C/T	0.44333	0.158505	intron-variant	RHOBTB1	GRCh38.p7	10:60902556	TTTGGTAATGCCTTT[C/T]GTGAATGAGTATTCT	9886
rs873602	snp	A/G	0.0189856	0.0955633	upstream-variant-2KB	RHOBTB1	GRCh38.p7	10:61002079	ACACGACAGGACCAT[A/G]TGTAACGACTAAGTA	9886
rs884403	snp	C/T	0.475613	0.107697	intron-variant	RHOBTB1	GRCh38.p7	10:60898101	GTCAATGATGACATA[C/T]AAAGAGGTGGGATCC	9886
rs884404	snp	C/T	0.496034	0.0443518	intron-variant	RHOBTB1	GRCh38.p7	10:60898080	GGTGGGATCCTACCA[C/T]GGAACAAAAGAATTT	9886
rs957854	snp	C/T	0.454544	0.143743	intron-variant	RHOBTB1	GRCh38.p7	10:60937884	GAGAGCTAACCCTTA[C/T]TGAGCACCTACTATG	9886
rs1013704	snp	C/G	0.0948562	0.196037	intron-variant	RHOBTB1	GRCh38.p7	10:60937660	ACTTTGGCAACCTTA[C/G]AGTGTGAAGAAAACA	9886
rs1013705	snp	A/C	0.11963	0.213316	intron-variant	RHOBTB1	GRCh38.p7	10:60937764	TATAACCATTCCTTA[A/C]AATATCAGAATTCAA	9886
rs1864756	snp	A/T			intron-variant	RHOBTB1	GRCh38.p7	10:60949804	ACTAACAATGAAAAG[A/T]ACACAGTATCTAATG	9886
rs1864757	snp	A/T	0.482979	0.0906686	intron-variant	RHOBTB1	GRCh38.p7	10:60949689	CCAAAGTTATGCTTT[A/T]AAAAAAAAAAAAAAA	9886
rs1864763	snp	A/T	0.478188	0.10213	intron-variant	RHOBTB1	GRCh38.p7	10:60916923	GAGAGAAATATGAAG[A/T]TGCTATACTGCTGGC	9886
rs1864764	snp	A/G	0.498009	0.0314867	intron-variant	RHOBTB1	GRCh38.p7	10:60917222	TTCTAAATGTTGTTT[A/G]TTACCTTTATATACA	9886
rs1897358	snp	C/G	0.480302	0.0972668			GRCh38.p7	10:60970907	TTTTTCTGATACTGA[C/G]TTTGACTCTCCATGA	9886
rs1897359	snp	A/G	0.480302	0.0972668			GRCh38.p7	10:60970687	TCTGACCACGGAACT[A/G]TTAAAAAGTATTTGA	9886
rs1897360	snp	A/C	0.0356815	0.128715			GRCh38.p7	10:60957431	cagcacatacgacag[A/C]ggtcccataacatta	9886
rs1897363	snp	A/G	0.480382	0.097079			GRCh38.p7	10:60975711	AGCAGGAACAAAATG[A/G]TTTTTCAGTTTTTCC	9886
rs1897364	snp	C/T	0.00835141	0.0640778			GRCh38.p7	10:60976759	ATAATAAAAATATTT[C/T]CTTTAAATTCACATC	9886
rs1897366	snp	A/G	0	0			GRCh38.p7	10:60901394	TGCCAATTATTATCA[A/G]ACAAATATAATTATG	9886
rs1897367	snp	A/G	0.404907	0.196224			GRCh38.p7	10:60906635	CTATTTTGCAGGCTC[A/G]CCACAAGAGTGAAGC	9886
rs1897368	snp	C/T	0.115788	0.21092			GRCh38.p7	10:60930657	TTATGAATAGAGAGG[C/T]ATGGCTTACCTCACC	9886
rs1897369	snp	A/G	0.450231	0.149691			GRCh38.p7	10:60938206	ACCCACCATATCTTT[A/G]CACGACTGGAATTCT	9886
rs1897370	snp	C/T	0.489376	0.0721049			GRCh38.p7	10:60972930	CACTGCACTTGTTTC[C/T]ATTTAAAAGGGGAGT	9886
rs1946591	snp	C/T	0.490175	0.0693959	intron-variant	RHOBTB1	GRCh38.p7	10:60967182	TGCTATTCCCTTGCC[C/T]GGACTACTACTCTTT	9886
rs1946592	snp	C/T	0.497586	0.0346604	intron-variant	RHOBTB1	GRCh38.p7	10:60925972	gtggtgtctcacacc[C/T]gtaatcctagcactt	9886
rs2001940	snp	C/T	0.422473	0.180978	intron-variant	RHOBTB1	GRCh38.p7	10:60897775	GAAGTGGCTCAATCT[C/T]GGCTCACTGCAACCT	9886
rs2082307	snp	A/G	0.492037	0.0625946	intron-variant	RHOBTB1	GRCh38.p7	10:60990908	CTCCCGTGATGTCTC[A/G]AGACATCTCAAACTC	9886
rs2116452	snp	G/T	0.490618	0.0678448	intron-variant	RHOBTB1	GRCh38.p7	10:60955371	AATTGAATTGTGGCA[G/T]TTTAAAACCATAAAG	9886
rs2116453	snp	A/G	0.0228947	0.104514	intron-variant	RHOBTB1	GRCh38.p7	10:61000374	CACCAGATCTGGGAA[A/G]AAACCCAAAATATAT	9886
rs2163602	snp	A/G	0.498158	0.0302955	intron-variant	RHOBTB1	GRCh38.p7	10:60985524	ACATGTCAATTTCCT[A/G]TACAAAATGCTACGC	9886
rs2271126	snp	A/G	0.325785	0.238236	utr-variant-5-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60911547	TCAGCGTCCATTTAT[A/G]AAACTCTGTAAGAAG	9886
rs2271127	snp	A/G	0.153665	0.230694	intron-variant, upstream-variant-2KB	RHOBTB1	GRCh38.p7	10:60911616	AGCAATCAAAGACGT[A/G]AGAGGTTCAGGGAGT	9886
rs2271128	snp	A/G	0.088636	0.190949	synonymous-codon, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60886115	GAAGGCACGTACCTC[A/G]CTGTTGGCACTTTCC	9886
rs2279942	snp	A/G	0.470618	0.117591	intron-variant, downstream-variant-500B	RHOBTB1	GRCh38.p7	10:60874863	TGCATCTGTCTAAAT[A/G]AAGATGTCACCACTG	9886
rs2393707	snp	C/T			intron-variant	RHOBTB1	GRCh38.p7	10:60903025	TTTCCCGCAATACAG[C/T]TATTGCTACGATAGG	9886
rs2393708	snp	C/T	0.479824	0.098392	intron-variant	RHOBTB1	GRCh38.p7	10:60984032	CTGAAAACTATACCA[C/T]TTAAAATCTCTCTAA	9886
rs2393709	snp	C/G	0.497855	0.0326773	intron-variant	RHOBTB1	GRCh38.p7	10:60996634	AAAAGCTCTGGACGT[C/G]CTCCTGAGAAAAATG	9886
rs2393712	snp	C/T			intron-variant	RHOBTB1	GRCh38.p7	10:60955043	TTCTTttctttcctt[C/T]ttttttttttttttt	9886
rs2893866	snp	C/T	0.0314385	0.121371	intron-variant	RHOBTB1	GRCh38.p7	10:60894322	GAGATTAAAATATTT[C/T]CAAATTATAAGAGAG	9886
rs2893868	snp	A/G	0.444267	0.157354	intron-variant	RHOBTB1	GRCh38.p7	10:60901367	CAGTGAAAGTGTTCT[A/G]TAACCGTTAAGTGCC	9886
rs2893869	snp	C/T	0.44306	0.158832	intron-variant	RHOBTB1	GRCh38.p7	10:60902203	GAATGGTACATGTAT[C/T]TTCTGTGCGCCAGAT	9886
rs2893870	snp	A/G	0.330482	0.236691	intron-variant	RHOBTB1	GRCh38.p7	10:60902893	AACTAACATCGATCA[A/G]GCTCCTACAAGACAC	9886
rs2893871	snp	A/G	0.338523	0.233803	intron-variant	RHOBTB1	GRCh38.p7	10:60903023	ATTTTCCCGCAATAC[A/G]GTTATTGCTACGATA	9886
rs2893872	snp	G/T	0.444533	0.157025	intron-variant	RHOBTB1	GRCh38.p7	10:60989359	ATGAATTTATTTCAT[G/T]GCATAAGTATATTTT	9886
rs2893873	snp	C/G	0.480775	0.0961398	intron-variant	RHOBTB1	GRCh38.p7	10:60993688	AAAATATACACCGTA[C/G]AGCAATATAAAATGT	9886
rs2893874	snp	C/T	0.480382	0.097079	intron-variant	RHOBTB1	GRCh38.p7	10:60963327	GCTCCCAATTTCAGA[C/T]GATGAAAGTGAATTT	9886
rs3049417	in-del	-/CAC			intron-variant	RHOBTB1	GRCh38.p7	10:60881017	agctcccataattcc[-/CAC]gtgttgtgggagaga	9886
rs3049452	in-del	-/TG	0	0	intron-variant	RHOBTB1	GRCh38.p7	10:60997104	gtgtgtgtgtgtgtg[-/TG]TACATAACCATGCTG	9886
rs3049595	in-del	-/TTT/TTTT/TTTTT/TTTTTT			intron-variant	RHOBTB1	GRCh38.p7	10:60932513	ttttttttttttttt[-/TTT/TTTT/TTTTT/TTTTTT]actttAAGAAAGtat	9886
rs3049597	in-del	-/GACTTCAA	0.0948562	0.196037	intron-variant	RHOBTB1	GRCh38.p7	10:60930998	GAGGGAAGACTTCAA[-/GACTTCAA]TATTGCTTCCTGTTA	9886
rs3763742	snp	C/T	0.220843	0.248294	utr-variant-3-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60870857	TACCAGCACTTAACA[C/T]GGCAAATATTGTAAA	9886
rs3999424	in-del	-/TTTT	0	0	intron-variant	RHOBTB1	GRCh38.p7	10:60955062	ttttnntttttttnt[-/TTTT]nnnaagatgtagtct	9886
rs4072139	snp	C/G	0.475348	0.108251	intron-variant	RHOBTB1	GRCh38.p7	10:60897598	AAGTTCTCCAGAAAG[C/G]TATGAGTGGGACAGC	9886
rs4309112	snp	A/G	0.0228947	0.104514	intron-variant	RHOBTB1	GRCh38.p7	10:60955500	CTTCCTTCTGATTGA[A/G]CAGGGTAATTATTCA	9886
rs4339988	snp	C/T	0	0	intron-variant	RHOBTB1	GRCh38.p7	10:60947110	ACAGACCGTATTTTG[C/T]TAATAGGAAAAGAGA	9886
rs4376852	snp	G/T	0.479744	0.0985793	intron-variant	RHOBTB1	GRCh38.p7	10:60927502	aaaagcatgggacag[G/T]cataaaaacagacac	9886
rs4408258	snp	A/G	0.0655868	0.168795	intron-variant	RHOBTB1	GRCh38.p7	10:60929978	GGCCCCAAATCCCCC[A/G]AAGTGTAAATTGTTG	9886
rs4437981	snp	C/T	0.44252	0.159487	intron-variant	RHOBTB1	GRCh38.p7	10:60902745	CAGGTTGATCCATCA[C/T]TTGTTATTCTTATTA	9886
rs4472883	snp	C/T	0.000399281	0.0141238	intron-variant	RHOBTB1	GRCh38.p7	10:60955524	TTATTCAAGGAGTAT[C/T]TGTCCTGAGCTATCC	9886
rs4485055	snp	A/G	0.4231	0.180378	intron-variant, upstream-variant-2KB	RHOBTB1	GRCh38.p7	10:60913297	ATTCAAGGAACAGAT[A/G]TGTGCTTAGGTTAGG	9886
rs4542350	snp	C/G	0.0952156	0.196321	intron-variant	RHOBTB1	GRCh38.p7	10:60937947	tcataaccctctgag[C/G]ggggaggggatgctg	9886
rs4545506	snp	C/T	0.422	0.181428	intron-variant	RHOBTB1	GRCh38.p7	10:60902761	TTGTTATTCTTATTA[C/T]AAAAGGGCATATATA	9886
rs4545508	snp	C/T	0.0941369	0.195465	intron-variant	RHOBTB1	GRCh38.p7	10:60938125	TAGAAGGGTGTTATG[C/T]TTTGAATAAGAGAAA	9886
rs4575214	snp	C/T	0.345037	0.231231	intron-variant	RHOBTB1	GRCh38.p7	10:60902710	GGCTAAGCACCAGTA[C/T]TTTCCATCTTCATCA	9886
rs4582920	snp	C/G	0.497586	0.0346604	intron-variant, upstream-variant-2KB	RHOBTB1, LOC107984236	GRCh38.p7	10:60942981	CTGGAGTTCAACAAG[C/G]CTCAGTGAACAGCAC	9886
rs4641412	snp	C/T	0.434687	0.168495	intron-variant	RHOBTB1	GRCh38.p7	10:60902887	TCGTTCAACTAACAT[C/T]GATCAAGCTCCTACA	9886
rs4643024	snp	A/G	0.4973	0.0366419	intron-variant	RHOBTB1	GRCh38.p7	10:60933780	GTCCAAACACAGGAG[A/G]TGGATTAAAAAAAAA	9886
rs4948437	snp	C/T	0.380333	0.213338	intron-variant	RHOBTB1	GRCh38.p7	10:60973559	GGAGGGCAAAGCTTG[C/T]TGAGTTTCATATTCA	9886
rs5785469	in-del	-/AAAA			intron-variant	RHOBTB1	GRCh38.p7	10:60932529	AAAAAAAAAAAAAAA[-/AAAA]AAAGACAGAAACAAG	9886
rs5785470	in-del	-/C	0.490727	0.0674567	intron-variant	RHOBTB1	GRCh38.p7	10:60951345	ATAATGGTTCCTAAT[-/C]TAAAAGCAAAGATGA	9886
rs5785471	in-del	-/AC			intron-variant	RHOBTB1	GRCh38.p7	10:60997065	ACAGCATGGTTATGT[-/AC]ACACACACACACACA	9886
rs6479741	snp	G/T	0.101763	0.201681	intron-variant, utr-variant-3-prime	RHOBTB1	GRCh38.p7	10:60885169	aaatagctaaaagac[G/T]attttaaatgttctc	9886
rs6479743	snp	C/T	0.489318	0.0722982	intron-variant	RHOBTB1	GRCh38.p7	10:60971083	TCATCATTATCATTA[C/T]TGATGTAATTAATAA	9886
rs6479744	snp	C/T	0.497329	0.0364438	intron-variant	RHOBTB1	GRCh38.p7	10:60989635	TGCCTTAGCACCTTG[C/T]TTCCTGTGCTGAGAC	9886
rs7067621	snp	A/T	0.405255	0.195948	intron-variant	RHOBTB1	GRCh38.p7	10:60907223	TACCAGTGTAAGAAC[A/T]GACTAATACAGGGAC	9886
rs7068842	snp	C/T	0	0	intron-variant	RHOBTB1	GRCh38.p7	10:60930841	GGGCTAGCCATCATT[C/T]TCTGCTTGTCTTATT	9886
rs7069036	snp	A/T	0.4944	0.0526182	intron-variant	RHOBTB1	GRCh38.p7	10:60891713	CAAAAAGTTCAACAT[A/T]AAAAAAACATAAAAA	9886
rs7073034	snp	C/T	0.139903	0.224452	intron-variant	RHOBTB1	GRCh38.p7	10:60873693	CTGTTTCAAAAGACC[C/T]CAAATTCCAAGTGTG	9886
rs7073240	snp	C/T	0.497613	0.0344622	intron-variant	RHOBTB1	GRCh38.p7	10:60931542	TGGCTGAAAAATATT[C/T]TTAGACATATTACTT	9886
rs7073817	snp	A/G	0.00159617	0.0282053	intron-variant	RHOBTB1	GRCh38.p7	10:60874019	CTCTGGCCACAGTAG[A/G]AAGGGCCTGAGCAGC	9886
rs7074600	snp	A/G	0.495708	0.0461266	intron-variant	RHOBTB1	GRCh38.p7	10:60896540	GAACCTGAATACTGA[A/G]AAGGGGTAGGAAGGA	9886
rs7074883	snp	C/T	0.0402882	0.136092	intron-variant	RHOBTB1	GRCh38.p7	10:60896686	GCTTGCCCTTGCCCA[C/T]GGAATGTTTATATCT	9886
rs7077303	snp	C/T	0.489376	0.0721049	intron-variant	RHOBTB1	GRCh38.p7	10:60993885	TAGTAATTAATTTTT[C/T]GGTGACATTTAGCTC	9886
rs7078521	snp	A/T	0.0988009	0.199095	intron-variant	RHOBTB1	GRCh38.p7	10:60893627	GTAATATTTAACATA[A/T]AACTAGGCGAGAATT	9886
rs7078938	snp	A/T	0.437965	0.164831	intron-variant, utr-variant-3-prime	RHOBTB1	GRCh38.p7	10:60883180	CAGGTCTTCAGTGGC[A/T]TGGTTCCGTGGTCTT	9886
rs7079085	snp	A/G	0.494609	0.0516363	intron-variant	RHOBTB1	GRCh38.p7	10:60897247	TGGTGGGAAAAGATC[A/G]GAGAAGCAACCAGAA	9886
rs7079357	snp	A/T	0.428333	0.175206	intron-variant, utr-variant-3-prime	RHOBTB1	GRCh38.p7	10:60883410	TGGAGACGATTACAG[A/T]CCATTCTTGGAAGGG	9886
rs7081336	snp	C/T	0.443732	0.158012	intron-variant	RHOBTB1	GRCh38.p7	10:60880730	ACACAGATGTTGGAA[C/T]ATTATTCTTCCCTTC	9886
rs7082246	snp	A/T	0	0	intron-variant, utr-variant-3-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60875471	tgaaatgtttccatc[A/T]ctgcagaaagttcta	9886
rs7083122	snp	A/C	0.416055	0.186885	intron-variant, utr-variant-3-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60875947	TCATCTGTAGCATTG[A/C]ATTTGTTCTTCTAAT	9886
rs7083267	snp	G/T	0.491525	0.0645418	intron-variant	RHOBTB1	GRCh38.p7	10:60894573	AAGCCAAGAATGCTT[G/T]GAATTTTACATTTTT	9886
rs7083452	snp	A/G	0	0	intron-variant	RHOBTB1	GRCh38.p7	10:60903681	CTGGGTCAGACTATG[A/G]GCCCCTGGGTCAGAC	9886
rs7084092	snp	G/T	0.480144	0.097642	intron-variant	RHOBTB1	GRCh38.p7	10:60972202	gagtttatacccaaa[G/T]gattataaaccattc	9886
rs7084565	snp	A/G	0.00358779	0.0422022	intron-variant	RHOBTB1	GRCh38.p7	10:60989034	TTCAATGCTCTAAAA[A/G]TTATAGGAGATTAAA	9886
rs7085867	snp	C/T	0.488545	0.074807	intron-variant	RHOBTB1	GRCh38.p7	10:60960257	AAGTGAAAAATCTAA[C/T]TAAATGATGCTTCCA	9886
rs7087218	snp	A/G	0.472335	0.114312	intron-variant, utr-variant-3-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60876352	TAATAACTAAACTAA[A/G]TGTTCATAGAAGTCT	9886
rs7087304	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	RHOBTB1	GRCh38.p7	10:60876639	GTAATTGCCCATGGA[A/C]gcctcccagagtgag	9886
rs7087599	snp	G/T	0.210301	0.246828	intron-variant	RHOBTB1	GRCh38.p7	10:60904255	CCTGGCCTATTTCTC[G/T]TCTTAAAGAATTTTT	9886
rs7089016	snp	C/T	0.489434	0.0719116	intron-variant, utr-variant-3-prime	RHOBTB1	GRCh38.p7	10:60885424	GGCTGACAAGTGATG[C/T]AGCTGCTTCCGCTAG	9886
rs7089671	snp	A/C	0.467337	0.123551	intron-variant	RHOBTB1	GRCh38.p7	10:60892581	TTAGAGAATTTACTT[A/C]AAGTGCTGTCCAATC	9886
rs7090226	snp	C/T	0.0232847	0.105357	intron-variant	RHOBTB1	GRCh38.p7	10:60913908	AGGTTGTTGTGAGGA[C/T]TACGTGAACTGATGA	9886

Full records

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