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
rs9213	snp	C/T	0.399073	0.200692	utr-variant-3-prime, nc-transcript-variant	SH3YL1	GRCh38.p7	2:218386	AGTAATGTTTAGAGT[C/T]GTAGGTATTAACTAG	26751
rs300703	snp	C/T	0.141596	0.225274	intron-variant	SH3YL1	GRCh38.p7	2:239416	GCACTGGATACACCA[C/T]GTGGAAGGTACGGGA	26751
rs300704	snp	A/C	0.142609	0.225759	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:240255	aagccaagctactac[A/C]ccacccaaggctgca	26751
rs300705	snp	A/G	0.419296	0.183954	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:240785	acagtcagaacacct[A/G]tcatctcaggaaaac	26751
rs300754	snp	C/T	0.00119737	0.0244387	intron-variant	SH3YL1	GRCh38.p7	2:223892	ACCCTGGCCTCCCCT[C/T]CTGGGAGCCCACTCC	26751
rs300755	snp	C/T	0.142272	0.225598	intron-variant	SH3YL1	GRCh38.p7	2:228505	TAAATGAGAGGATTT[C/T]ATACATGCATATGCA	26751
rs300756	snp	A/G	0.357238	0.225832	intron-variant	SH3YL1	GRCh38.p7	2:233416	GAGGAAAAACAGGCC[A/G]GGGGAAGAACATACA	26751
rs370478	snp	C/G	0	0	intron-variant	SH3YL1	GRCh38.p7	2:226803	TATGTATTCTCCCCA[C/G]TATATGTACACTCCC	26751
rs394899	snp	C/T	0.000399281	0.0141238	intron-variant	SH3YL1	GRCh38.p7	2:235342	AAATGAGAGGCAGCA[C/T]GGGTCAGGGGAGGCA	26751
rs419692	snp	C/T	0	0	intron-variant	SH3YL1	GRCh38.p7	2:226812	TCCCCAGTATATGTA[C/T]TCTCCCCAGTATATG	26751
rs435371	snp	C/T	0.0217236	0.101931	intron-variant	SH3YL1	GRCh38.p7	2:226779	ATGGTGGGGAGTGTA[C/T]ATATGGTGGGGAGTG	26751
rs435378	snp	A/T			intron-variant	SH3YL1	GRCh38.p7	2:226793	ATATATGGTGGGGAG[A/T]GTACATATACTGGGG	26751
rs898671	snp	C/T	0.109461	0.206758	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:240926	TCCTAGGGGGAGAGG[C/T]TGAGCACCCAGAGTT	26751
rs1046207	snp	C/G	0.0368353	0.130617	utr-variant-3-prime, nc-transcript-variant	SH3YL1	GRCh38.p7	2:218476	AATCTTGAGGGTAGA[C/G]CCACAAATTTCAATT	26751
rs1128906	snp	A/G			missense, nc-transcript-variant	SH3YL1	GRCh38.p7	2:233218	GAAGGAACTTGGAAG[A/G]AAACGTGGCCCTGAG	26751
rs1461028	snp	A/G	0.429837	0.173662	intron-variant	SH3YL1	GRCh38.p7	2:238975	GATTGTCGAACATAA[A/G]TTAACCCCACGCCGG	26751
rs1474052	snp	G/T	0.445724	0.155538	intron-variant	SH3YL1	GRCh38.p7	2:224192	TGCAAATGTGAGTGG[G/T]ACACAAATTGAGGGC	26751
rs1474053	snp	A/T	0.47802	0.102502	intron-variant	SH3YL1	GRCh38.p7	2:224086	ATGCTGCTGGATATA[A/T]AACTGTCGGAGAATT	26751
rs2085852	snp	G/T	0.429837	0.173662	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:240630	gagcacaattttaac[G/T]ggatcaaactgtgga	26751
rs2290911	snp	A/G	0.429862	0.173636	intron-variant, synonymous-codon, nc-transcript-variant	SH3YL1	GRCh38.p7	2:224919	ATATTCATTTCTGTT[A/G]CCTGCCAAAAAAGAG	26751
rs2290912	snp	C/T	0.454803	0.143373	intron-variant	SH3YL1	GRCh38.p7	2:224970	CTGATTAGTATATAT[C/T]ATACAAAATACACAA	26751
rs2306060	snp	A/C	0.403334	0.197456	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:230912	AATGTGAAGTCAGTG[A/C]AACTACGAAGGAGGC	26751
rs2864044	snp	A/G	0.477768	0.103061	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:240054	agcatttctcttccc[A/G]cagctccttgtacag	26751
rs2902647	snp	G/T			intron-variant	SH3YL1	GRCh38.p7	2:227727	TGAAAGTTCATAATT[G/T]ATGTTGTGAACGTGG	26751
rs2952789	snp	G/T	0.391024	0.206427	intron-variant	SH3YL1	GRCh38.p7	2:242605	tctatatctcatgcc[G/T]tttttgtccctctgt	26751
rs3020766	snp	C/G/T	0.0205511	0.0992634	intron-variant, upstream-variant-2KB	ACP1, SH3YL1	GRCh38.p7	2:265241	TGCCATATATCCGGG[C/G/T]CTCTTGGCATCTGCA	26751
rs3020767	snp	C/G			intron-variant, upstream-variant-2KB	ACP1, SH3YL1	GRCh38.p7	2:266588	gtaccaaacccaatt[C/G]ctgtcaattggaaca	26751
rs3070147	in-del	-/GT/T/TG	0	0	intron-variant	SH3YL1	GRCh38.p7	2:227890	ATTTCCATAAAATTA[-/GT/T/TG]TGTGTGTGTGTGTGT	26751
rs3748872	snp	A/C	0.44288	0.159051	intron-variant	SH3YL1	GRCh38.p7	2:234130	TAGATGTTAGACAGT[A/C]AAGGTTTAACAACTG	26751
rs3791216	snp	G/T	0.142947	0.22592	intron-variant	SH3YL1	GRCh38.p7	2:237142	TGTATTTTCCGAGTG[G/T]GAAATGTGGGAAGCA	26751
rs3791217	snp	A/T	0.142609	0.225759	intron-variant	SH3YL1	GRCh38.p7	2:237140	TATTTTCCGAGTGGG[A/T]AATGTGGGAAGCATT	26751
rs3791219	snp	G/T	0.000399281	0.0141238	intron-variant	SH3YL1	GRCh38.p7	2:227978	TTTTAATGTTTTATG[G/T]TAAATCTGACCTTTT	26751
rs3791220	snp	C/T	0.396546	0.202545	intron-variant	SH3YL1	GRCh38.p7	2:227066	ACTATAGTTGCTTCC[C/T]GCCATAGGCATTTCC	26751
rs3791221	snp	C/T	0.396727	0.202413	intron-variant	SH3YL1	GRCh38.p7	2:226933	TCACCATGGTTACTA[C/T]CCACCATATGCATTC	26751
rs3791223	snp	A/G	0.383632	0.211288	intron-variant	SH3YL1	GRCh38.p7	2:222336	CCTCATGCAGGCTCC[A/G]TGAGAAAGTGGACTG	26751
rs3791224	snp	A/G	0.406468	0.194981	intron-variant	SH3YL1	GRCh38.p7	2:221981	ACTCACCTTTTATTG[A/G]TGAATTCTTTGTGGG	26751
rs3828165	snp	C/T	0.370974	0.218781	intron-variant	SH3YL1	GRCh38.p7	2:220889	CTGTGGCTCCCAGAA[C/T]ATTCCCTGATGTTCA	26751
rs3838489	in-del	-/TGGTAGTGTCAC	0.389152	0.207694	intron-variant	SH3YL1	GRCh38.p7	2:237347	GGTTCTCGGGCTAAT[-/TGGTAGTGTCAC]CAAAAAACACAATAT	26751
rs3838490	in-del	-/A	0.141258	0.225111	intron-variant	SH3YL1	GRCh38.p7	2:237138	TTTTCCGAGTGGGAA[-/A]TGTGGGAAGCATTAT	26751
rs3842545	in-del	-/T			intron-variant	SH3YL1	GRCh38.p7	2:238399	CCTAAGAATGGGATG[-/T]AAGGAAAAGATCTGT	26751
rs3842546	in-del	-/CA/CACACACACA/CACACACACACA			intron-variant	SH3YL1	GRCh38.p7	2:238260	ACACACACACACACA[-/CA/CACACACACA/CACACACACACA]AGGAGGGAGGAAAAG	26751
rs3842547	in-del	-/CA/CACA	0.382473	0.212016	intron-variant	SH3YL1	GRCh38.p7	2:227889	acacacacacacaca[-/CA/CACA]TAATTTTATGGAAAT	26751
rs3924770	snp	C/G	0.428786	0.174744	intron-variant	SH3YL1	GRCh38.p7	2:255580	aggcagggctttgcc[C/G]tgttgcccaggctgg	26751
rs3926131	snp	A/C/T			upstream-variant-2KB, intron-variant	ACP1, SH3YL1	GRCh38.p7	2:263581	TCGCCGGCGCCTAGC[A/C/T]AAGGCTTCCTCCCCG	26751
rs3926132	snp	C/T			upstream-variant-2KB, intron-variant	ACP1, SH3YL1	GRCh38.p7	2:263587	GCGCCTAGCAAAGGC[C/T]TCCTCCCCGGCGCCT	26751
rs3976788	in-del	-/AAT			intron-variant	SH3YL1	GRCh38.p7	2:220212	aataataataataat[-/AAT]aAAGTGAATTTGGTC	26751
rs4241316	snp	C/T	0.150333	0.229274	intron-variant	SH3YL1	GRCh38.p7	2:252197	GTTTAAGAACTGTGC[C/T]TTTATGGTCTAGGGG	26751
rs4255987	snp	C/G	0.428484	0.175052	intron-variant	SH3YL1	GRCh38.p7	2:259296	TGACCACATTTCACT[C/G]TCTCTATCAAAGGTT	26751
rs4447635	snp	C/G	0.429238	0.174281	intron-variant, upstream-variant-2KB	ACP1, SH3YL1	GRCh38.p7	2:265970	TTTATAAAGTCAAAC[C/G]TAAATATTTCCTCCT	26751
rs4455191	snp	C/T	0.401037	0.199218	intron-variant, utr-variant-5-prime	SH3YL1	GRCh38.p7	2:256278	CAACTGGTATTCTAA[C/T]GTGTGGACATAGCAC	26751
rs4497901	snp	C/T	0.412082	0.190341	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:239969	ggggaagggggtttg[C/T]aagaacacagacttc	26751
rs4854299	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:260594	GAGAGCAAAGCCTTC[A/G]TAGGGGAACCTGGCA	26751
rs4854300	snp	C/G	0.00199481	0.0315187	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ACP1, SH3YL1	GRCh38.p7	2:264895	GCGCGGGGCAAGAGG[C/G]TGGCAGTGCGCCTGC	26751
rs6548220	snp	A/G	0.477937	0.102688	intron-variant	SH3YL1	GRCh38.p7	2:225951	ACATGTAATGTTACC[A/G]TAATTAGCATTGAAA	26751
rs6710091	snp	C/G	0.383632	0.211288	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:239597	TTTACAGATTTGATT[C/G]AGGAAGATTAAGTAC	26751
rs6710233	snp	C/G	0.445987	0.155207	downstream-variant-500B	SH3YL1	GRCh38.p7	2:217826	TAATAGAGGGCATGA[C/G]ATAGAAGAACGAAAG	26751
rs6718259	snp	A/C	0.0883596	0.190715	intron-variant	SH3YL1	GRCh38.p7	2:245184	GTGACATCACTGCAC[A/C]CTCACAATTACACGC	26751
rs6718370	snp	A/G	0.0883596	0.190715	intron-variant	SH3YL1	GRCh38.p7	2:245257	GGTTAAGAAGTTTAA[A/G]ACTCATGTCTCCAAT	26751
rs6729224	snp	A/C	0.42263	0.180829	intron-variant	SH3YL1	GRCh38.p7	2:219461	TTCTTGCACCTTCCT[A/C]CTTGTGAGGACACAG	26751
rs6729496	snp	A/C	0.473266	0.112482	intron-variant	SH3YL1	GRCh38.p7	2:253411	ccaccaaaaccaaga[A/C]ggcaatgaacgtgac	26751
rs6742278	snp	A/G	0.110167	0.207236	intron-variant	SH3YL1	GRCh38.p7	2:226999	ATGCATATGGTGGGT[A/G]GCATACATGATGGAG	26751
rs6744062	snp	C/T	0.00874735	0.0655527	intron-variant	SH3YL1	GRCh38.p7	2:228450	TCATTTTTAAATCCG[C/T]ACTGATAAGGACCTG	26751
rs7556816	snp	C/T	0.426202	0.17735	intron-variant, utr-variant-5-prime, nc-transcript-variant	SH3YL1	GRCh38.p7	2:243504	aagacacaacatacc[C/T]acacttatggaaggc	26751
rs7568630	snp	G/T	0.144632	0.226711	intron-variant	SH3YL1	GRCh38.p7	2:244239	CGGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT	26751
rs7574889	snp	A/G	0.429837	0.173662	intron-variant	SH3YL1	GRCh38.p7	2:226231	ATTTAAAACTTTCAT[A/G]GAGTAAAATTATGAA	26751
rs7580141	snp	A/G	0.495596	0.0467178	intron-variant	SH3YL1	GRCh38.p7	2:248037	TCTAACGGTAACATA[A/G]TAATTGTTTCCATTG	26751
rs7584915	snp	A/G	0.405429	0.195811	upstream-variant-2KB, intron-variant, nc-transcript-variant	ACP1, SH3YL1	GRCh38.p7	2:264227	AGATCGAAAAGCCCA[A/G]AGCCCCGCGGCGGCT	26751
rs7588515	snp	A/G	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	ACP1, SH3YL1	GRCh38.p7	2:265104	GCCTAGGAACCATGA[A/G]GGGGAGGAGGCCAGG	26751
rs7595075	snp	A/C	0.443673	0.158085	upstream-variant-2KB, utr-variant-5-prime, intron-variant	ACP1, SH3YL1	GRCh38.p7	2:264019	CGCCCCGTCCCGAGG[A/C]TGCCCAGGAAGAGGA	26751
rs7596678	snp	C/T	0.474634	0.109726	intron-variant, nc-transcript-variant, upstream-variant-2KB	SH3YL1	GRCh38.p7	2:262553	AAAAATGGGATCTTC[C/T]CAGAGAAAATTTTTT	26751
rs7596838	snp	A/C	0.109461	0.206758	intron-variant	SH3YL1	GRCh38.p7	2:229536	agatcgagaccatcc[A/C]ggctaaaacggtgaa	26751
rs7597084	snp	C/T	0.0115144	0.0749975	intron-variant	SH3YL1	GRCh38.p7	2:229723	gacagagcgagactc[C/T]gtctcaaaaaaaaaa	26751
rs7601944	snp	A/G	0.411914	0.190483	intron-variant	SH3YL1	GRCh38.p7	2:229456	TCTTATGGGCCGGGC[A/G]CGGTGGCTCACGCCT	26751
rs7609512	snp	A/G	0.473081	0.112848	intron-variant	SH3YL1	GRCh38.p7	2:251673	AGACTGATTTGTGAC[A/G]TCTGAGCAGATTTCT	26751
rs9309729	snp	A/C	0.473174	0.112665	intron-variant	SH3YL1	GRCh38.p7	2:253566	CTAAAAAGGAGAGGA[A/C]CTCTCAGTTCCGGGA	26751
rs9808365	snp	C/G	0.40157	0.198813	intron-variant	SH3YL1	GRCh38.p7	2:232343	ACAACAAGGAATACT[C/G]ACTGACACATGAGTT	26751
rs10167992	snp	C/T	0.145978	0.227331	upstream-variant-2KB, intron-variant	ACP1, SH3YL1	GRCh38.p7	2:263270	GCCTCCACAGGAGCA[C/T]GGGCATATTGGTTCA	26751
rs10171229	snp	A/C	0.429688	0.173817	intron-variant	SH3YL1	GRCh38.p7	2:236950	CCACACAAGATGCTT[A/C]AGCTTGACGCTTGCC	26751
rs10174612	snp	A/T	0.429688	0.173817	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:241669	aatgactcatcacat[A/T]aaaggaaccccaatt	26751
rs10181015	snp	A/C	0.401037	0.199218	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:239736	GGTGGCATAAAGAGG[A/C]CACAGACCCTCTCCA	26751
rs10181051	snp	C/T	0.441617	0.16057	intron-variant, missense, nc-transcript-variant	SH3YL1	GRCh38.p7	2:242800	gattcaaagttacca[C/T]tagattgacagtaaa	26751
rs10188763	snp	A/G	0.428182	0.17536	intron-variant, nc-transcript-variant	SH3YL1	GRCh38.p7	2:260677	GCTCTGGACTTCTTC[A/G]TCAAATGGACCAGCA	26751
rs10193882	snp	A/T	0.145978	0.227331	intron-variant	SH3YL1	GRCh38.p7	2:246301	CTACATTTTACTTGC[A/T]CTTGTTTTTCAGGGC	26751
rs10205435	snp	C/T	0.498459	0.0277128	intron-variant	SH3YL1	GRCh38.p7	2:230442	AGGTGCTGTGGAACA[C/T]CATGAACAATGCACA	26751
rs10432714	snp	C/T	0.428635	0.174898	intron-variant, upstream-variant-2KB	SH3YL1	GRCh38.p7	2:256839	catttcaggcttcca[C/T]cagaaacttttataa	26751
rs10533035	in-del	-/GAGT	0.128976	0.218754	intron-variant	SH3YL1	GRCh38.p7	2:221800	ACATGAAAATCACAA[-/GAGT]GAGGCCAGCAGATCC	26751
rs10558174	in-del	-/GCA			intron-variant	SH3YL1	GRCh38.p7	2:236216	TCAGGGGAGGCAGCA[-/GCA]TGGGCCAGGGGAGGC	26751
rs10654359	in-del	-/AC			intron-variant	SH3YL1	GRCh38.p7	2:234670	ATCTCATCAGACTAA[-/AC]ACTTTGTAAAAGCCA	26751
rs10865544	snp	A/T	0.428484	0.175052	intron-variant	SH3YL1	GRCh38.p7	2:259774	AAATGATGTATTGCA[A/T]ACTAGATAATGTTCA	26751
rs11268733	in-del	-/GTGGCAGGCAC			intron-variant	SH3YL1	GRCh38.p7	2:221039	GAACTGCTCAGGCAC[-/GTGGCAGGCAC]ACACATGTGCTCCTC	26751
rs11273285	in-del	-/CAGGCACGTGG	0.483995	0.0880135	intron-variant	SH3YL1	GRCh38.p7	2:221032	CCACCGCGAACTGCT[-/CAGGCACGTGG]CAGGCACACACATGT	26751
rs11347402	in-del	-/A	0.0228947	0.104514	intron-variant	SH3YL1	GRCh38.p7	2:250196	TAGTACATAAAAGAT[-/A]AAAGCTACATTTTCA	26751
rs11370759	in-del	-/T	0.174288	0.23826	intron-variant	SH3YL1	GRCh38.p7	2:232445	GTTTCTTTTTTTTTT[-/T]AATATACTTTAAGTT	26751
rs11383620	in-del	-/A	0	0	intron-variant	SH3YL1	GRCh38.p7	2:243568	GTAAATGTGTCTATT[-/A]AAAAAAAAAACAGAC	26751
rs11544681	snp	C/G			synonymous-codon, nc-transcript-variant	SH3YL1	GRCh38.p7	2:233211	CTTGGAAGGAAACGT[C/G]GCCCTGAGAAGCTCC	26751
rs11682301	snp	A/G	0.0111196	0.0737302	intron-variant	SH3YL1	GRCh38.p7	2:223375	CTCAGCTCTTTTTCA[A/G]CCAGCTTCCCTCAGC	26751
rs11685739	snp	A/C	0.0111196	0.0737302	intron-variant	SH3YL1	GRCh38.p7	2:221384	GTTCTAAGCAGTTTC[A/C]GGAATATATTTTATG	26751
rs11689239	snp	C/G/T	0.00297832	0.0384755	intron-variant	SH3YL1	GRCh38.p7	2:230055	TTAGCCTGGGAGAAA[C/G/T]AAAAAGATAAATACA	26751
rs11691572	snp	C/G/T	0.00303115	0.0388127	missense, upstream-variant-2KB, nc-transcript-variant	ACP1, SH3YL1	GRCh38.p7	2:264985	GGAACAGGCTACCAA[C/G/T]TCCGTGCTGTTTGTG	26751
rs11696071	snp	C/T	0.00150353	0.0273771	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ACP1, SH3YL1	GRCh38.p7	2:264948	CGCGGTGTCTCGGCG[C/T]CTCTGCGCGCGGGAA	26751

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