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
rs12910	snp	A/C	0.421209	0.182174	utr-variant-5-prime	FYN	GRCh38.p7	6:111780572	GTGATCGTTGGCGGA[A/C]ATTTTGGTAAGTGTT	2534
rs697640	snp	A/G	0.0588605	0.161139	intron-variant	FYN	GRCh38.p7	6:111718519	CCATATCCAGCACTC[A/G]TGAATGAATGAACAA	2534
rs697641	snp	A/G	0.166506	0.235645	intron-variant	FYN	GRCh38.p7	6:111723315	ACTGCTGCATCTTGC[A/G]TGGCCAGAACAGTGC	2534
rs697642	snp	A/G	0.44651	0.154543	intron-variant	FYN	GRCh38.p7	6:111731902	GTAAAGTTTTCACTA[A/G]AGGTCTGCATTTATG	2534
rs706861	snp	A/G	0.029116	0.117091	intron-variant	FYN	GRCh38.p7	6:111681758	TGACTCTTAGCAAGC[A/G]CTCAGTGTATGTTTA	2534
rs706862	snp	A/G	0.350327	0.228986	intron-variant	FYN	GRCh38.p7	6:111682545	AGCAAAAGTATCTGC[A/G]GTCTTCATTGGAGCA	2534
rs706863	snp	A/G	0.356169	0.226336	intron-variant	FYN	GRCh38.p7	6:111685624	TCCTTTTGCCAGCAA[A/G]GCAAGACAAGGAAGC	2534
rs706864	snp	A/G	0.0444908	0.142359	intron-variant	FYN, LOC105377945	GRCh38.p7	6:111691160	CCATGTCAGGGAGGT[A/G]GTCAAGGCCAGGCCC	2534
rs706865	snp	G/T	0.0569829	0.158885	intron-variant	FYN	GRCh38.p7	6:111704612	tacaaaaattagctt[G/T]gtgtggtggtgggca	2534
rs706866	snp	A/T	0.171704	0.237423	intron-variant	FYN	GRCh38.p7	6:111705063	cgagactctgtctca[A/T]aacaaaaaataaaca	2534
rs706867	snp	C/T	0.16911	0.236552	intron-variant	FYN	GRCh38.p7	6:111705797	GAGGTTGCAGTGAGC[C/T]GAGACAGGGCCACTG	2534
rs706868	snp	A/G	0.0588605	0.161139	intron-variant	FYN	GRCh38.p7	6:111706257	AACCCAAGGGAGAAT[A/G]CTGGAGCATTCAATT	2534
rs706869	snp	A/G	0.0596104	0.162024	intron-variant	FYN	GRCh38.p7	6:111706482	GTGCAACAATTCTTA[A/G]TCTAGCATTAGGTGG	2534
rs706870	snp	A/G	0.00835141	0.0640778	intron-variant	FYN	GRCh38.p7	6:111707758	ATTAAGTTAATAATA[A/G]TGCAAGTATTACACA	2534
rs706871	snp	A/G	0.192715	0.243348	intron-variant	FYN	GRCh38.p7	6:111708331	CTGGATTCCTTTTCC[A/G]TCCATCCAAGTTAAG	2534
rs706872	snp	C/T	0.267091	0.249415	intron-variant	FYN	GRCh38.p7	6:111708953	CAGGGCTACCTGTGA[C/T]GAAGAGCAGGAATGG	2534
rs706873	snp	A/G	0.193055	0.244361	intron-variant	FYN	GRCh38.p7	6:111709043	GGTGGAAGGTTCTGC[A/G]GATACTCAGTGGATG	2534
rs706874	snp	C/G	0.192715	0.243348	intron-variant	FYN	GRCh38.p7	6:111709132	TCTCCTGGGGCTCAG[C/G]ACCTTCTTTTCCTCC	2534
rs706875	snp	A/G	0.267091	0.249415	intron-variant	FYN	GRCh38.p7	6:111709260	AAAAAAAAATGTGTT[A/G]GCTTCTGGCCATGGT	2534
rs706876	snp	A/G	0.266819	0.249434	intron-variant	FYN	GRCh38.p7	6:111709497	TTTGTGGGCTATTCT[A/G]TTACTTATGCCACCA	2534
rs706877	snp	A/G	0.0437281	0.141251	intron-variant	FYN	GRCh38.p7	6:111709693	TCCTAACAAAGATCT[A/G]GACATGAACTAAATT	2534
rs706878	snp	A/C	0.0592355	0.161582	intron-variant	FYN	GRCh38.p7	6:111709891	GGCATAGAAATGAGA[A/C]CAGTACAAACTGTTA	2534
rs706879	snp	A/G	0.266819	0.249434	intron-variant	FYN	GRCh38.p7	6:111710108	GAGGGTGGAGGGGGA[A/G]GAGCTGGGTATTGTT	2534
rs706880	snp	A/T	0.0437281	0.141251	intron-variant	FYN	GRCh38.p7	6:111710238	TTTTTTCTTAATTTA[A/T]TTCAATTAGAACTAA	2534
rs706881	snp	A/G	0.0596104	0.162024	intron-variant	FYN	GRCh38.p7	6:111711210	GATAAAATTGTTACC[A/G]ACATAAAATGCTACA	2534
rs706882	snp	C/T	0.265453	0.249522	intron-variant	FYN	GRCh38.p7	6:111712167	GGACTGACTTTCCAA[C/T]GCCCTCCAGCGTAAT	2534
rs706883	snp	C/T	0.0592355	0.161582	intron-variant	FYN	GRCh38.p7	6:111712303	TCTAATCAACCTTGG[C/T]ATGTAGGGGAGGCTA	2534
rs706884	snp	C/T	0.0463947	0.145069	intron-variant	FYN	GRCh38.p7	6:111712797	aggtaacactcttct[C/T]gacctggctggtggc	2534
rs706885	snp	A/C	0.265453	0.249522	intron-variant	FYN	GRCh38.p7	6:111714654	CCTTACTGTATCTGA[A/C]AGAAACCTAGACCTG	2534
rs706886	snp	C/T	0.282632	0.247861	intron-variant	FYN	GRCh38.p7	6:111715370	ataggtgtgacctac[C/T]gtgcccaaccCAACA	2534
rs706887	snp	A/G	0.0592355	0.161582	intron-variant	FYN	GRCh38.p7	6:111715459	AGcccctccccttga[A/G]tgtgggctggatcta	2534
rs706888	snp	C/T	0.0387552	0.1337	intron-variant	FYN	GRCh38.p7	6:111716003	ACACAGTTATTTCTA[C/T]TTTAGTACATATAAG	2534
rs706889	snp	C/T	0.26518	0.249539	intron-variant	FYN	GRCh38.p7	6:111716410	ATTTTTTAAAAGTCA[C/T]GGTATCACTGGTTCT	2534
rs706890	snp	C/T	0.245631	0.249962	intron-variant	FYN	GRCh38.p7	6:111716800	ttttttttttttttt[C/T]tgagatggagtttca	2534
rs706891	snp	C/T	0.26518	0.249539	intron-variant	FYN	GRCh38.p7	6:111716853	GCAGTGGCATAATCT[C/T]AGCTCACTGCAACCT	2534
rs706892	snp	C/G	0.0588605	0.161139	intron-variant	FYN	GRCh38.p7	6:111717437	GAGTGCCTGCTATGA[C/G]CTACAGAAATGACAG	2534
rs706893	snp	C/T	0.0588605	0.161139	intron-variant	FYN	GRCh38.p7	6:111717549	tcactgcagcctccg[C/T]ctcccgggtttaagc	2534
rs706894	snp	C/T	0.0588605	0.161139	intron-variant	FYN	GRCh38.p7	6:111718869	TAATGTCCAAAGGCT[C/T]AGGGTCAGGCTCCTT	2534
rs706895	snp	C/T	0.499816	0.0095829	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111720156	ATTGACAAGGCTCAC[C/T]GTTGGCTATTTCAGG	2534
rs706896	snp	A/G	0.0592355	0.161582	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111720662	TGGATGAAAAATAAA[A/G]TCGGCAGAACCTAAG	2534
rs706897	snp	G/T	0.0329836	0.124112	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111720949	tcctgagaagcatcc[G/T]catttcctcctcctt	2534
rs706898	snp	C/T	0.195214	0.243923	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111721472	tctcactctgttgcc[C/T]aggctggagtgcagt	2534
rs706899	snp	A/T	0.26818	0.249338	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111721614	ttcaccatgttggtc[A/T]ggctggtcttgaact	2534
rs706900	snp	C/G	0.170408	0.236992	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111721675	ctcccaaagtactgg[C/G]attacaggcgtgaac	2534
rs706901	snp	A/C	0.268452	0.249318	intron-variant	FYN	GRCh38.p7	6:111722396	AAGGCATGATGTACT[A/C]AAGGAATTTCATCAT	2534
rs706902	snp	A/G	0.5	0.000399361	intron-variant	FYN	GRCh38.p7	6:111722655	CTTTACCACTCCCCT[A/G]CAAGAGACATATTGG	2534
rs706903	snp	A/G	0.499999	0.000599041	intron-variant	FYN	GRCh38.p7	6:111722853	AATCCTGATTTACAC[A/G]AAGGAAAGAATTTAT	2534
rs706904	snp	A/C	0.499999	0.000599041	intron-variant	FYN	GRCh38.p7	6:111722859	GATTTACACGAAGGA[A/C]AGAATTTATATCTAC	2534
rs706905	snp	A/G	0.5	0.000399361	intron-variant	FYN	GRCh38.p7	6:111723919	CCATGAGTTCATGGC[A/G]TGTGGTATTTTCCTG	2534
rs706906	snp	A/C	0.5	0.000399361	intron-variant	FYN	GRCh38.p7	6:111724275	GCCATGCTATGGGAG[A/C]TATGCTTCTCCACAT	2534
rs706907	snp	C/G	0.266546	0.249452	intron-variant	FYN	GRCh38.p7	6:111725206	TACATTCTCAGTGGA[C/G]AGAGTTAATCCATTG	2534
rs706908	snp	A/G	0.283684	0.24772	intron-variant	FYN	GRCh38.p7	6:111726253	TGTTTTAAGCTACTA[A/G]GTTTGTAGTACTTTG	2534
rs706909	snp	A/G	0.17138	0.237316	intron-variant	FYN	GRCh38.p7	6:111727086	CTCCGTTAGTAATGT[A/G]TACTAGTCCATTCTC	2534
rs706910	snp	C/T	0.267364	0.249396	intron-variant	FYN	GRCh38.p7	6:111727208	CTAGGTGCAGTGAGT[C/T]ACCATCTTCCTTCGT	2534
rs706911	snp	C/T	0.44768	0.153045	intron-variant	FYN	GRCh38.p7	6:111728849	attgaaatattaatc[C/T]aagagagttgaaaac	2534
rs706912	snp	C/G	0.0329836	0.124112	intron-variant	FYN	GRCh38.p7	6:111731327	AAAGGCAAAAGAAGT[C/G]AAATCTCCTTCTTCA	2534
rs706913	snp	A/G	0.409891	0.192184	intron-variant	FYN	GRCh38.p7	6:111732770	ACCAGCACCACACCC[A/G]CTTCCCAGCCCACAG	2534
rs706914	snp	C/T	0.0441095	0.141807	intron-variant	FYN	GRCh38.p7	6:111734448	TTTAAAGTACTCTTT[C/T]TTACTACAGTTTTCA	2534
rs706915	snp	A/G	0.0429648	0.14013	intron-variant	FYN	GRCh38.p7	6:111754269	TTTCTTGATGGTTGG[A/G]AAGAATCATTTGGGT	2534
rs752168	snp	A/G	0.27278	0.24896	intron-variant	FYN	GRCh38.p7	6:111835260	AATCTAGGTAATTTG[A/G]TTTTTCTTAAAAAAT	2534
rs784590	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	FYN	GRCh38.p7	6:111761679	AAGGGCAGAGCCTTC[C/T]GGGGCGACAACCACT	2534
rs784591	snp	A/G	0.00199481	0.0315187	intron-variant	FYN	GRCh38.p7	6:111742882	AACCAATGAGTTACA[A/G]TTTGTCCTACGTTTT	2534
rs784592	snp	A/G			intron-variant	FYN	GRCh38.p7	6:111743219	ccagcactttgggag[A/G]ccaaggtgggcagat	2534
rs804180	snp	A/T	0.0678174	0.1712	intron-variant	FYN	GRCh38.p7	6:111676908	GCCGTTGGTTTTTTT[A/T]AATCTGAAATTATGA	2534
rs804181	snp	C/T	0.105924	0.204309	intron-variant	FYN	GRCh38.p7	6:111673153	ACATCCTCGCCCTCC[C/T]GAGACCCGCACATTT	2534
rs804182	snp	C/G	0.0444908	0.142359	intron-variant	FYN	GRCh38.p7	6:111670909	TGTGAGAAATAAAAA[C/G]ACTTAAGTAAAAGCA	2534
rs804183	snp	C/T	0.499999	0.000798721	intron-variant	FYN	GRCh38.p7	6:111713847	TCACTCCCAAATTTT[C/T]GTTATAGGGAAACGC	2534
rs804184	snp	C/T	0.499999	0.000798721	intron-variant	FYN	GRCh38.p7	6:111713905	TAGCAGTTTATAAAA[C/T]AAAGAACTTGTTGCA	2534
rs804185	snp	A/G	0.046775	0.145601	intron-variant	FYN	GRCh38.p7	6:111700671	AAGGATATTTTCAGC[A/G]TTCCCAAAAACATGT	2534
rs804186	snp	A/C/T	0.0152632	0.0860206	intron-variant, nc-transcript-variant	FYN, LOC105377945	GRCh38.p7	6:111694620	CAGCACAGGTAGGCC[A/C/T]TGCAGGGTAACTTGA	2534
rs804187	snp	C/T	0.0159676	0.0879137	intron-variant, nc-transcript-variant	FYN, LOC105377945	GRCh38.p7	6:111694538	AGCCACCTGTGGAAA[C/T]CCAGGGAACAGGACA	2534
rs804188	snp	A/T	0.499946	0.00519141	intron-variant	FYN, LOC105377945	GRCh38.p7	6:111693708	AGGGAGAGTGGAGAG[A/T]GGACTTACACTACAG	2534
rs804189	snp	A/G	0.0444908	0.142359	intron-variant, nc-transcript-variant	FYN, LOC105377945	GRCh38.p7	6:111689929	CTTTTTGttctttat[A/G]agctataacacacat	2534
rs804190	snp	C/G	0.0444908	0.142359	intron-variant, nc-transcript-variant	FYN, LOC105377945	GRCh38.p7	6:111689903	cacatacagtaaaac[C/G]aacaaatctgaagtg	2534
rs804191	snp	A/G	0.138207	0.223612	intron-variant, upstream-variant-2KB	FYN, LOC105377945	GRCh38.p7	6:111689222	aagtaactggcctgc[A/G]gacaccaagcttgta	2534
rs804192	snp	A/G	0.404907	0.196224	intron-variant, upstream-variant-2KB	FYN, LOC105377945	GRCh38.p7	6:111688816	CCTCATCTCCGGCCA[A/G]CTTGCCTATTTTCTC	2534
rs804193	snp	A/G	0.107694	0.205546	intron-variant	FYN	GRCh38.p7	6:111686822	ATCAGCCGCTTCTGA[A/G]GCCCCTGTAATCCGG	2534
rs804194	snp	A/G	0.356383	0.226236	intron-variant	FYN	GRCh38.p7	6:111686782	AAGGCTGATCTCGCC[A/G]TGAGATGCCCTCCCT	2534
rs809192	snp	A/G	0.170084	0.236883	intron-variant	FYN	GRCh38.p7	6:111713799	CATTCAAGAGTGGGT[A/G]AAATCACTTCTTCTA	2534
rs809193	snp	A/G	0.5	0.00019968	intron-variant	FYN	GRCh38.p7	6:111699211	TAAGAAAGACCATGG[A/G]CGTTTTGCTCAATGG	2534
rs810747	snp	C/T	0.0111196	0.0737302	intron-variant	FYN	GRCh38.p7	6:111751046	ACTGGAAAAAAACAC[C/T]AAGAGAAGCAAAGCA	2534
rs811470	snp	A/C	0.499551	0.0149693	intron-variant	FYN	GRCh38.p7	6:111686077	TTTTCTTTTAATTTT[A/C]ATCTTTGGCTTTCAA	2534
rs811972	snp	C/G	0.109461	0.206758	intron-variant	FYN	GRCh38.p7	6:111683630	TTTATAATTAAAAAG[C/G]GCTCTGGGTGGCTCT	2534
rs811973	snp	G/T			intron-variant	FYN	GRCh38.p7	6:111743204	accaaggtgggcaga[G/T]cacgaggtcaggagt	2534
rs812500	snp	C/G	0.0152947	0.0861012	intron-variant, nc-transcript-variant	FYN, LOC105377945	GRCh38.p7	6:111696245	CCTGTCTCCAGCTCA[C/G]AGTGCCTTAAGGGGT	2534
rs910682	snp	A/G	0.407158	0.194426	intron-variant	FYN	GRCh38.p7	6:111854532	agaagggttaatgga[A/G]aacacagaaagttat	2534
rs910683	snp	C/T	0.107341	0.205301	intron-variant	FYN	GRCh38.p7	6:111862084	CATAATACTTTCAGG[C/T]CCAACAATACTGGCA	2534
rs910684	snp	C/G	0.21845	0.248001	intron-variant	FYN	GRCh38.p7	6:111862255	AACCTGATGGCAGAG[C/G]GCAAAGGAGTAACTA	2534
rs927010	snp	C/G	0.177503	0.239258	intron-variant	FYN	GRCh38.p7	6:111826120	AGGGAGGAGTGAAGA[C/G]GCCAGAGGACTGTCA	2534
rs994268	snp	A/G	0.424814	0.178718	intron-variant	FYN	GRCh38.p7	6:111750224	GGCCTGGTGGGAGGT[A/G]ATTGGGTCATGGGGG	2534
rs994269	snp	G/T	0.247337	0.249986	intron-variant	FYN	GRCh38.p7	6:111750644	TCCTCTCTCCTCCTT[G/T]CCTCATTTTCTTCCC	2534
rs1022646	snp	A/G	0.252421	0.249988	intron-variant	FYN	GRCh38.p7	6:111708128	ATCATCCTGCCACCC[A/G]ATTTCTCCAACCTAT	2534
rs1022647	snp	C/T	0.272511	0.248984	intron-variant	FYN	GRCh38.p7	6:111708199	CAGAAGGTTCCAGTT[C/T]GAGTCAGCCATGAGA	2534
rs1022648	snp	C/T	0.271432	0.24908	intron-variant	FYN	GRCh38.p7	6:111708401	TCTGGGAAGGGAAGC[C/T]TTTTAGGAGGTCTGA	2534
rs1022649	snp	A/G	0.462253	0.132093	intron-variant	FYN	GRCh38.p7	6:111798778	TGGTGAAGAATAAAC[A/G]AAAAGCGTTCTGGGC	2534
rs1022650	snp	G/T	0.222928	0.24853	intron-variant	FYN	GRCh38.p7	6:111805552	ACAAGGGTCCATGTG[G/T]TTCAGGTTCCTTCTG	2534
rs1022651	snp	C/T	0.135143	0.222054	intron-variant	FYN	GRCh38.p7	6:111805840	TGACTGAATTACAGG[C/T]CGTGTAAAAGTTGAA	2534
rs1057979	snp	C/G	0.494013	0.0543839	utr-variant-5-prime, upstream-variant-2KB	FYN, LOC102724646	GRCh38.p7	6:111873293	GAGACCCGCCCGCCG[C/G]CCGGCGGCGAGAGTA	2534
rs1058134	snp	A/C	0	0	missense, intron-variant	FYN	GRCh38.p7	6:111700152	CCTCGAGAATCCCTG[A/C]AGTTGATCAAGAGAC	2534
rs1067141	snp	A/G	0.499997	0.00119808	intron-variant	FYN	GRCh38.p7	6:111734073	TTGAGACAGGGTCTC[A/G]CTCTGTCACCCAGGC	2534

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