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
rs13636	snp	G/T	0	0	utr-variant-5-prime, synonymous-codon	LYN	GRCh38.p7	8:55880028	GGGCGCGACGGGGCG[G/T]CCCAGCAGGACCTGC	4067
rs167999	snp	A/G	0.272188	0.249013	intron-variant	LYN	GRCh38.p7	8:55880126	CTCTGCGCGAGCCCA[A/G]GGGTGGGCGCGGGCA	4067
rs170783	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911223	atatatatatatata[C/T]acacacacacacgta	4067
rs179692	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911157	atatatgtatatgta[C/T]atatatatacacgtg	4067
rs182832	snp	G/T	0.247337	0.249986	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878302	TTAGGGAGTTGGGGA[G/T]CTGGTTGCAAGCTCA	4067
rs182833	snp	C/T	0.252421	0.249988	intron-variant	LYN	GRCh38.p7	8:55880265	GCACCGCCTCTGGGC[C/T]CCGGCGGCGAAGGCT	4067
rs333612	snp	C/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55912212	GGGGCACACAGAAAT[C/G]TGTTACACGGTGAAA	4067
rs333614	snp	G/T	0.250732	0.249999	intron-variant	LYN	GRCh38.p7	8:55884176	GCAATCTCAGCTCAC[G/T]GCAATCTCCGCCTCC	4067
rs333615	snp	A/G	0.261884	0.249717	intron-variant	LYN	GRCh38.p7	8:55886397	ggcatgcaccaatgc[A/G]ccaccatgcccggct	4067
rs333616	snp	C/T	0.356597	0.226135	intron-variant	LYN	GRCh38.p7	8:55888438	TAGTATGAAGCTAAT[C/T]TTTTTGTCCATCACA	4067
rs333617	snp	C/G	0.373799	0.217195	intron-variant	LYN	GRCh38.p7	8:55889048	tttgagatggggtct[C/G]actctgtcgcccagg	4067
rs333618	snp	G/T	0.199564	0.24486	intron-variant	LYN	GRCh38.p7	8:55889248	tttgagacCAGGCTG[G/T]AACcccaggcaggag	4067
rs333619	snp	A/T	0.498323	0.0289051	intron-variant	LYN	GRCh38.p7	8:55889510	accacacccagccCA[A/T]GTATATTTATCGAGT	4067
rs867586	snp	A/G	0.0119091	0.0762411	intron-variant	LYN	GRCh38.p7	8:55984760	ACTCTCAGCCCTCCA[A/G]TTCTTCTTGGCTTCA	4067
rs868541	snp	A/G	0.481396	0.0946345	intron-variant	LYN	GRCh38.p7	8:55964201	AAAAATGCAGTACAA[A/G]ATAAGTGTTAGAACA	4067
rs907422	snp	A/C	0.0707826	0.174302	intron-variant	LYN	GRCh38.p7	8:55971324	CCAACCCCACCTATT[A/C]CTCTTACTGCAGAGA	4067
rs907423	snp	C/G	0.460589	0.13473	intron-variant	LYN	GRCh38.p7	8:55971059	GAGGATGCCTGAGCA[C/G]TGTGACTCACCCATC	4067
rs907424	snp	A/G	0.482234	0.0925596	intron-variant	LYN	GRCh38.p7	8:55963660	TGCATTTCTCTGGTT[A/G]CTAATAAGATTGAGT	4067
rs907425	snp	C/T	0.491104	0.0660973	intron-variant	LYN	GRCh38.p7	8:55963732	AAATGCCCTTCCAAG[C/T]CTTTGCCTATTTCTT	4067
rs925448	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006776	AAGCAGATCACCAGC[C/T]AATGGGTGTTTACTT	4067
rs952784	snp	A/G	0.319616	0.240112	intron-variant	LYN	GRCh38.p7	8:55971530	GGGCTATGGAACATC[A/G]GGACACATGGCCTGG	4067
rs1027985	snp	C/G	0.461813	0.132798	intron-variant	LYN	GRCh38.p7	8:55970612	TGAGGGAAGAAGTGG[C/G]AGTGAAAAAGGAAGA	4067
rs1027986	snp	C/T	0.460589	0.13473	intron-variant	LYN	GRCh38.p7	8:55969912	TCTTTTTCTCATAAC[C/T]GCTGCTGGGAAACAT	4067
rs1027987	snp	C/T	0.460589	0.13473	intron-variant	LYN	GRCh38.p7	8:55969624	CTATTACAGGGGAAC[C/T]CCCCACAAAATGATT	4067
rs1027989	snp	C/G	0.164873	0.23506	intron-variant	LYN	GRCh38.p7	8:55901862	CTGAAAGTCATTTTT[C/G]ATTTAGGTTCTTCCC	4067
rs1027990	snp	C/T	0.445987	0.155207	intron-variant	LYN	GRCh38.p7	8:55901750	ACATCCAGCTCCGCG[C/T]TGGAAATATCTGAAG	4067
rs1050855	snp	A/G	0.497933	0.0320782	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55880027	CGCAGGTCCTGCTGG[A/G]CCGCCCCGTCGCGCC	4067
rs1050875	snp	A/C/T	1.64798e-05	0.00287047	synonymous-codon	LYN	GRCh38.p7	8:55998432	GGTCTCCGAGTCACT[A/C/T]ATGTGCAAAATTGCA	4067
rs1123750	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55926951	AGATTCAGATAAATT[A/G]GGCAGAAATTACAGA	4067
rs1124745	snp	A/G	0.0955749	0.196603	intron-variant	LYN	GRCh38.p7	8:55901611	TTGCTCTGTGGGGTC[A/G]GGTAGGGCCGGGGGA	4067
rs1126327	snp	C/T	0.147991	0.228242	intron-variant	LYN	GRCh38.p7	8:55938860	CTGTGTGAGTGAGTC[C/T]TAGCCTCACCCCTCC	4067
rs1397974	snp	C/T	0.493793	0.055364	intron-variant	LYN	GRCh38.p7	8:55886552	TGTGGTCAAATAAGT[C/T]TGACAggctgggcgc	4067
rs1397975	snp	G/T	0.165853	0.235413	intron-variant	LYN	GRCh38.p7	8:55912838	AGTCCATTAAAAGAA[G/T]ACATATTTTTAATCA	4067
rs1397976	snp	A/G	0.422158	0.181278	intron-variant	LYN	GRCh38.p7	8:55912826	GAATACATATTTTTA[A/G]TCAGGAAATATAATA	4067
rs1450738	snp	C/T	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55882538	ACATTGTTATAAGCT[C/T]ACTCCTACTGATGAT	4067
rs1450739	snp	C/T	0.297382	0.245469	intron-variant	LYN	GRCh38.p7	8:55882672	ACTGGCTCTTCCTAG[C/T]GATGATGGTGAAGGT	4067
rs1450740	snp	A/C	0.133093	0.220981	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877987	CCAGTAGTTGAGGAG[A/C]CAAGCCTAACATGGG	4067
rs1450741	snp	C/T	0.406986	0.194565	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879600	AAGCCCAGGCTCCTC[C/T]GGAGATCCTTCCGTC	4067
rs1466138	snp	A/C	0.182933	0.240836	intron-variant	LYN	GRCh38.p7	8:55895382	ATCCATACCTATATT[A/C]TTCACCAAGATTAGT	4067
rs1470707	snp	C/T	0.421842	0.181577	intron-variant	LYN	GRCh38.p7	8:55903935	TGAGATGGGAGGATC[C/T]GCTTGAGCCTCGGAG	4067
rs1470708	snp	A/G	0.499897	0.00718776	intron-variant	LYN	GRCh38.p7	8:55904151	AAAAAAAATAATAGC[A/G]GGACTTTAATAGATA	4067
rs1473075	snp	C/G/T	0.0498117	0.149749	intron-variant	LYN	GRCh38.p7	8:55941113	CCCTACCTATGTTTA[C/G/T]CTGGAGCCAGGTTCT	4067
rs1511723	snp	C/T	0.17461	0.238362	intron-variant	LYN	GRCh38.p7	8:55890620	acacaagtgtacaaa[C/T]atctctgagacccca	4067
rs1511724	snp	C/G	0.499824	0.00938333	intron-variant	LYN	GRCh38.p7	8:55884138	CACTCCAGGCTGGGC[C/G]ACAGAGTGAGCCTTC	4067
rs1546518	snp	C/G	0.422	0.181428	intron-variant	LYN	GRCh38.p7	8:55912335	CTAGGAGTATTCAAG[C/G]CTGATTTCTTTCCTT	4067
rs1546519	snp	C/T	0.283158	0.247791	intron-variant	LYN	GRCh38.p7	8:55911999	AAGGGCTAGAAGGGA[C/T]GTGGTAGAACACACC	4067
rs1562818	snp	C/T	0.163892	0.234703	intron-variant	LYN	GRCh38.p7	8:55891915	TCAGCCAGCAATCCA[C/T]GTGGCCATGTATTAA	4067
rs1828527	snp	C/T	0.16618	0.23553	intron-variant	LYN	GRCh38.p7	8:55912542	TACGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT	4067
rs1849195	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930828	CATCAGCTCATCCCA[A/G]GACCTTGGCAGGGCC	4067
rs1877301	snp	A/T	0.463881	0.12944	intron-variant	LYN	GRCh38.p7	8:55964031	ACAATAACTCTTAAG[A/T]TCTACAGAAAAGGCC	4067
rs1912818	snp	G/T	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55991762	TGGTGCACCCCCACA[G/T]GCTCCCTTGTCCCTG	4067
rs1963650	snp	A/G	0.474453	0.110094	intron-variant	LYN	GRCh38.p7	8:55902250	gaggcaaaaatgggc[A/G]gatcacctgaggttg	4067
rs1973610	snp	C/T	0.474272	0.110462	intron-variant	LYN	GRCh38.p7	8:55902236	cagatcacctgaggt[C/T]gggagttcgagacca	4067
rs1979128	snp	A/G	0.473174	0.112665	intron-variant	LYN	GRCh38.p7	8:55901451	TCAAGGCCAGGCTTT[A/G]GACTCCTTCTTGGGC	4067
rs1980041	snp	A/G	0.445064	0.156365	intron-variant	LYN	GRCh38.p7	8:55900446	GTTCAAGGCTGCAGA[A/G]AGCAATGATCACATC	4067
rs1980042	snp	C/T	0.474	0.111014	intron-variant	LYN	GRCh38.p7	8:55900083	TTGTCTTCCTGAAGT[C/T]CGAGTGGCAGCGCAT	4067
rs1995976	snp	A/G	0.343701	0.231776	intron-variant	LYN	GRCh38.p7	8:56009508	gtgctagccaggttg[A/G]tttctcctgaggcct	4067
rs2012149	snp	C/T	0.149999	0.229128	intron-variant	LYN	GRCh38.p7	8:55902516	GTGTACTTTGTACAA[C/T]TCAACTTctagaaaa	4067
rs2036897	snp	A/G	0.455383	0.142541	intron-variant	LYN	GRCh38.p7	8:55972576	AGGAGGAGGAGGAGC[A/G]CTGGGTAGCAGTGGT	4067
rs2036898	snp	C/G	0.205723	0.246048	intron-variant	LYN	GRCh38.p7	8:55972539	TGAGGGCATCCCAGG[C/G]GGACGAGGGAGCAGG	4067
rs2100245	snp	C/T	0.380724	0.213099	intron-variant	LYN	GRCh38.p7	8:55937541	CACTGCACAGGGGCA[C/T]AAGGATGTTCCCGCT	4067
rs2137126	snp	A/C	0.497881	0.0324789	intron-variant	LYN	GRCh38.p7	8:55898968	gcacagtggtgtaca[A/C]ctgtggtcccagcta	4067
rs2175487	snp	C/T	0.206947	0.246265	intron-variant	LYN	GRCh38.p7	8:55999302	GCGGAGTTTCACTCT[C/T]GTCACCCAGGCTGGA	4067
rs2227978	snp	C/T	0.018945	0.0954651	synonymous-codon	LYN	GRCh38.p7	8:55998369	GGGAATGGCATACAT[C/T]GAGCGGAAGAACTAC	4067
rs2227979	snp	C/T	0.00872672	0.0654768	synonymous-codon	LYN	GRCh38.p7	8:55953956	GGTGAAAAGGCTTGG[C/T]GCTGGGCAGTTTGGG	4067
rs2227980	snp	A/G	0.114597	0.210157	synonymous-codon	LYN	GRCh38.p7	8:55953893	TCCCAAGCCACAGAA[A/G]CCATGGGATAAAGAT	4067
rs2271400	snp	A/G	0.416218	0.186739	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878685	GAGAAGGGGTGGGTT[A/G]CCCATGGAAATACCC	4067
rs2292419	snp	C/T	0.301932	0.244547	intron-variant	LYN	GRCh38.p7	8:55954221	TAAGGAGGGGAGTAA[C/T]GGGTATTTATCTTGA	4067
rs2317199	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55973126	ATCTGTATCTGGCCT[C/T]TTCTTCCCGCTCCCC	4067
rs2317200	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55973129	TGTATCTGGCCTCTT[C/T]TTCCCGCTCCCCACT	4067
rs2443049	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55909012	tgtgtgtgtgtgtgt[A/G]tatatatatatatat	4067
rs2458083	snp	A/G	0.15698	0.23205	intron-variant	LYN	GRCh38.p7	8:55986226	TTATGTATATGCTAA[A/G]GGAGTAGTCATGGCA	4067
rs2466007	snp	A/G	0.488118	0.0761554	intron-variant	LYN	GRCh38.p7	8:55976628	TAGCATGCGGTGCCC[A/G]CTCTGACAGCCCTTG	4067
rs2667971	snp	A/G	0.394904	0.203722	intron-variant	LYN	GRCh38.p7	8:55994601	GCCACACAGGTGGGC[A/G]TGATGGCAGGGACCC	4067
rs2667972	snp	A/G	0.157311	0.232183	intron-variant	LYN	GRCh38.p7	8:55994102	TGGTCTATTTACTAC[A/G]GCTAAGTAAATCCAG	4067
rs2667973	snp	G/T	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55994031	GCTGATTGAATGTAG[G/T]GTCAACTTTTCATGG	4067
rs2667974	snp	G/T	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55992818	AGTTTGACCCTTTTT[G/T]TGCCCTTCCACCTTC	4067
rs2667975	snp	A/G	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55992571	TTGGGGAGGAAGTCC[A/G]GATGCAACTCAGCTT	4067
rs2667976	snp	G/T	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55992164	AATGTCAGGCCCAGG[G/T]GTGAACAAAGACAAG	4067
rs2667977	snp	C/T	0.336474	0.234568	intron-variant	LYN	GRCh38.p7	8:55991685	GCCTGTGCCTGAAGC[C/T]GATGACAAAGAAGAC	4067
rs2667978	snp	C/T	0.210909	0.246925	intron-variant	LYN	GRCh38.p7	8:55985392	TCAAAATACCATGTG[C/T]TTGCGAGGGAAGCCT	4067
rs2667979	snp	C/T	0.373598	0.21731	intron-variant	LYN	GRCh38.p7	8:55985242	GCTCACCAGGTAGGA[C/T]TTGTCCATGCCTAGT	4067
rs2667980	snp	A/T	0.15665	0.231917	intron-variant	LYN	GRCh38.p7	8:55983982	AGAGGTACGGAAGGA[A/T]TCTTCCCAAGAACCT	4067
rs2667981	snp	A/T	0.157311	0.232183	intron-variant	LYN	GRCh38.p7	8:55981744	CAGGAAAGTAAACCT[A/T]TAGTTAGAGGAAGGG	4067
rs2667982	snp	A/C	0.398534	0.201091	intron-variant	LYN	GRCh38.p7	8:55981608	AGCACTTTGGGAGGC[A/C]GAGGTGGGAGGACTG	4067
rs2667983	snp	A/C	0.156319	0.231784	intron-variant	LYN	GRCh38.p7	8:55981528	TCTCTATATTAAAAA[A/C]AATTTTTTTAAACAC	4067
rs2667984	snp	A/G	0.25045	0.25	intron-variant	LYN	GRCh38.p7	8:55973851	TCAAGCAATCCTCCC[A/G]TTTCAGCCTCCCAAG	4067
rs2667985	snp	C/G	0.140242	0.224618	intron-variant	LYN	GRCh38.p7	8:55967799	TTGATTCAAAGTCTT[C/G]TATATGAAGGTGATC	4067
rs2667986	snp	C/T	0.156319	0.231784	intron-variant	LYN	GRCh38.p7	8:55967462	ctgggcatggtggca[C/T]gtgcctgtagtccca	4067
rs2667987	snp	A/G	0.254105	0.249966	intron-variant	LYN	GRCh38.p7	8:55967406	aatcgcttgaacccg[A/G]gaggcaggggttgca	4067
rs2667988	snp	C/G	0.48155	0.0942576	intron-variant	LYN	GRCh38.p7	8:55966554	ACAGTGAAACCCCAT[C/G]TCTACTAAAAATACA	4067
rs2667989	snp	A/G	0.258288	0.249863	intron-variant	LYN	GRCh38.p7	8:55966384	TGCGACTCCGTCTCA[A/G]TTAAAAAAAAAAAAA	4067
rs2667990	snp	C/G	0.373196	0.217538	intron-variant	LYN	GRCh38.p7	8:56000661	ggctcactgcaacct[C/G]tgcttcccaggttga	4067
rs2668010	snp	C/T	0.373397	0.217424	intron-variant	LYN	GRCh38.p7	8:56007884	AGCACTTTGGGAGGC[C/T]GAGACAGGCAGACGA	4067
rs2668011	snp	C/T	0.256897	0.249905	utr-variant-3-prime	LYN	GRCh38.p7	8:56011499	TGCTTTAAACTTGCC[C/T]AAGTTCTACCTCCTT	4067
rs2668015	snp	A/G	0.417845	0.185278	intron-variant	LYN	GRCh38.p7	8:55956896	AGAAGACAGGAGGAA[A/G]GGAGAAAAGAGTGTA	4067
rs2668016	snp	C/T	0.306927	0.243432	intron-variant	LYN	GRCh38.p7	8:55957046	CAGATAAGCAACTTA[C/T]TCAAGGTCATTCAAG	4067
rs2668017	snp	C/T	0.307176	0.243374	intron-variant	LYN	GRCh38.p7	8:55957307	TCTAGTTATTGGAAG[C/T]TATATTTTGGTGTAT	4067
rs2668018	snp	C/T	0.424348	0.179172	intron-variant	LYN	GRCh38.p7	8:55959543	GCAAAGGCTATACAG[C/T]AGAGGAAAGAAATTG	4067
rs2668019	snp	C/G	0.418169	0.184985	intron-variant	LYN	GRCh38.p7	8:55959748	aaagtacaaacaact[C/G]aaatgtccatcagat	4067

Full records

It may take some time, please wait.