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
rs8154	snp	C/T	0.402893	0.197797	synonymous-codon, intron-variant, nc-transcript-variant	ATG7	GRCh38.p7	3:11554828	CTGGGACATGAGCGA[C/T]GATGAGACCATCTGA	10533
rs14016	snp	C/T	0.330058	0.236835	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG7	GRCh38.p7	3:11554874	GGGCTGACTTCTCCC[C/T]GGCCGCCTGCTGAGG	10533
rs16340	in-del	-/TGTC	0.232359	0.249377	utr-variant-3-prime, intron-variant	VGLL4, ATG7	GRCh38.p7	3:11557335	CACCATATCACAGAT[-/TGTC]TGTCAGTAATCTGCT	10533
rs346077	snp	A/C	0.206642	0.246211	intron-variant	ATG7	GRCh38.p7	3:11284416	TTTCTCATTTAGGCT[A/C]CTTATTTAGAGTAAT	10533
rs346078	snp	C/G	0.350327	0.228986	intron-variant	ATG7	GRCh38.p7	3:11286154	tagcacacagtgtct[C/G]tttgtcacgttgctg	10533
rs346079	snp	A/G	0.499703	0.0121769	intron-variant	ATG7	GRCh38.p7	3:11286453	GTAATTGGCTTCTGG[A/G]GTTTGTTCTCATAGT	10533
rs346080	snp	C/T	0.277778	0.248452	intron-variant	ATG7	GRCh38.p7	3:11286587	tttctttctttcttt[C/T]ttttttttttttttt	10533
rs346081	snp	A/G	0.157972	0.232445	intron-variant, upstream-variant-2KB	ATG7	GRCh38.p7	3:11287399	GGGAGAACAGGGAAC[A/G]CTTTTCAGACAGAGG	10533
rs346082	snp	C/G	0.148996	0.228688	intron-variant, upstream-variant-2KB	ATG7	GRCh38.p7	3:11287530	GGAAGGCAGCAGCGG[C/G]GGTCTGGGAGAAAGC	10533
rs384989	snp	C/T	0.499609	0.0139722	intron-variant	ATG7	GRCh38.p7	3:11278434	gtttctctgctgcag[C/T]tccagccggtccctc	10533
rs388407	snp	C/T	0.148996	0.228688	intron-variant	ATG7	GRCh38.p7	3:11279023	GGGGTGTTTCTGCAG[C/T]TGATGATGTGGAGCT	10533
rs439738	snp	C/G	0.139564	0.224285	intron-variant	ATG7	GRCh38.p7	3:11280891	GACTAAGCCAAAGAC[C/G]TACTGCTATTAGCTC	10533
rs719519	snp	A/G	0.0611083	0.163768	intron-variant	ATG7	GRCh38.p7	3:11329562	CAAAAAACATTCACC[A/G]AGTGTCTGCTCTGTA	10533
rs719520	snp	A/T	0	0	intron-variant	ATG7	GRCh38.p7	3:11329577	GAGTGTCTGCTCTGT[A/T]TTTATGAAGGAGAGA	10533
rs752759	snp	A/G	0.0577344	0.159793	intron-variant	ATG7	GRCh38.p7	3:11543592	CCAAAGGGAGGCACC[A/G]GGGTGGTGTGTTAGG	10533
rs754015	snp	C/T	0.499998	0.000998401	intron-variant	ATG7	GRCh38.p7	3:11452471	ACATATTAAAAGCCA[C/T]TGAACTGTTAAATTG	10533
rs768096	snp	G/T	0	0	intron-variant	ATG7	GRCh38.p7	3:11306489	CTGAGAGGTGGCGTA[G/T]GCACagcacagtacc	10533
rs892938	snp	C/T	0	0	utr-variant-3-prime, downstream-variant-500B, intron-variant	ATG7	GRCh38.p7	3:11555423	AGCTCACTCAGTCCT[C/T]GGTGGAAATCTGGCG	10533
rs904474	snp	C/G	0.499913	0.00658888	intron-variant	ATG7	GRCh38.p7	3:11483174	GGGGACGGGGAGAAT[C/G]CTTATTAAAATGTGA	10533
rs904475	snp	C/T	0.499913	0.00658888	intron-variant	ATG7	GRCh38.p7	3:11493943	ATGCTTCTTATAACA[C/T]AGTTTCCAGTCATGG	10533
rs921226	snp	C/T	0.393434	0.20476	intron-variant	ATG7	GRCh38.p7	3:11283108	TGGGCTCAGAGAAAT[C/T]GGACACTGAGTGCTC	10533
rs954171	snp	A/C	0.00338409	0.040995	intron-variant	ATG7	GRCh38.p7	3:11391164	CTTTTTTGTCAACTT[A/C]TAAAGATGGAAAGTT	10533
rs955057	snp	A/G	0.000399281	0.0141238	intron-variant	ATG7	GRCh38.p7	3:11413085	tatgattttacatgt[A/G]caaaaccctacagtc	10533
rs955058	snp	G/T			intron-variant	ATG7	GRCh38.p7	3:11413192	ttcaacacagtacta[G/T]aagttctagccagag	10533
rs956493	snp	A/G	0.058509	0.160828	intron-variant	ATG7	GRCh38.p7	3:11391343	ATCAGTGCATGCTCC[A/G]GGGAACATTAAACCT	10533
rs1046593	snp	C/T	0.254385	0.249962	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG7	GRCh38.p7	3:11554928	CTGCTGACCCCAGGC[C/T]TGGTGATTCTGGGCC	10533
rs1046595	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG7	GRCh38.p7	3:11554937	CCAGGCCTGGTGATT[C/T]TGGGCCCCTCCTCCA	10533
rs1056994	snp	C/T	0	0	utr-variant-3-prime, downstream-variant-500B, intron-variant	VGLL4, ATG7	GRCh38.p7	3:11557862	TCTCTCTCTAGATTT[C/T]AGGTGCTTGCAACTG	10533
rs1375204	snp	C/G	0.0912534	0.193131	intron-variant	ATG7	GRCh38.p7	3:11346242	TAATGCTGAACATTA[C/G]GAGAAGGGTTCAGTA	10533
rs1375205	snp	C/T	0.0648419	0.167978	intron-variant	ATG7	GRCh38.p7	3:11345887	CTTTTATATTTTCTA[C/T]AATGGCTTTATGTTG	10533
rs1375206	snp	C/G	0.49975	0.0111793	intron-variant, upstream-variant-2KB	ATG7	GRCh38.p7	3:11297643	GAAATTTTGTATTTT[C/G]TGCCATGATATATAT	10533
rs1391903	snp	C/G	0.219049	0.248077	intron-variant	ATG7	GRCh38.p7	3:11381797	TTAAATTTCTTTTGT[C/G]CTGGAAAGGTTGCTT	10533
rs1470612	snp	A/G	0.397452	0.201886	intron-variant	ATG7	GRCh38.p7	3:11295492	TAACTGACTGTGTCC[A/G]TAGCAAGTTCCAGTG	10533
rs1470613	snp	A/G	0.390838	0.206555	intron-variant	ATG7	GRCh38.p7	3:11306051	GAAGAGACCAGATTT[A/G]TCCACATCTGAATTC	10533
rs1499082	snp	A/G	0.371177	0.218669	intron-variant	ATG7	GRCh38.p7	3:11386481	CTATCAAATCTGAGA[A/G]GCAGGGAGTATCCTC	10533
rs1499119	snp	A/C	0.339429	0.233457	intron-variant	ATG7	GRCh38.p7	3:11291605	TCATTCTGTACCAAG[A/C]ACTACACTAAACAGT	10533
rs1546230	snp	C/T	0.397452	0.201886	intron-variant	ATG7	GRCh38.p7	3:11430296	TATTTTGCTTATATG[C/T]GCATACACACATTTT	10533
rs1546231	snp	G/T	0.187685	0.242109	intron-variant	ATG7	GRCh38.p7	3:11472204	ccactagatccaagt[G/T]tttaaaaatgtcaat	10533
rs1562615	snp	A/C	0.393803	0.204501	intron-variant	ATG7	GRCh38.p7	3:11331883	taaaaccataatgag[A/C]tgctactacatatcc	10533
rs1562616	snp	C/T	0.394171	0.204242	intron-variant	ATG7	GRCh38.p7	3:11332677	TGTGAGCATTTTTTC[C/T]GCATTTAAAAGATTT	10533
rs1802496	snp	A/C			missense, intron-variant, nc-transcript-variant	ATG7	GRCh38.p7	3:11426903	GGTCTTACATTGCTG[A/C]ATCAAGAAACCCAAG	10533
rs1803490	snp	G/T			utr-variant-3-prime, intron-variant	VGLL4, ATG7	GRCh38.p7	3:11557501	TGGGTCAGCTGCGGT[G/T]TGGGATGCTGGAGTT	10533
rs1803491	snp	G/T			utr-variant-3-prime, downstream-variant-500B, intron-variant	VGLL4, ATG7	GRCh38.p7	3:11557768	GAGCTGAGGTTGGAG[G/T]ATTCCATAGTGCTTT	10533
rs1803492	snp	G/T			utr-variant-3-prime, downstream-variant-500B, intron-variant	VGLL4, ATG7	GRCh38.p7	3:11558101	GTGCGTGTGTATACT[G/T]GAAGAGAACTGTCGT	10533
rs1809876	snp	C/T	0	0	intron-variant	ATG7	GRCh38.p7	3:11481458	GAAATTCTAGGTCTT[C/T]GTGGTAAGTCACATA	10533
rs1846118	snp	G/T			intron-variant	ATG7	GRCh38.p7	3:11348726	gtggccagcttttat[G/T]cccttatttgtcccc	10533
rs1874957	snp	A/C	0.0916144	0.193427	intron-variant	ATG7	GRCh38.p7	3:11372164	ATCACCCCCAGGCCC[A/C]AAAGGGCCAAGCACT	10533
rs2036231	snp	A/G	0.0146672	0.084371	intron-variant	ATG7	GRCh38.p7	3:11449192	CACCATCTGCTAACT[A/G]ATAAGCTAGGTGGGC	10533
rs2036232	snp	A/C	0.480539	0.0967035	intron-variant	ATG7	GRCh38.p7	3:11449382	CTCTTAAACCAACAA[A/C]AACAAAAAACCCTGA	10533
rs2084465	snp	A/C	0.499631	0.0135733	intron-variant	ATG7	GRCh38.p7	3:11348938	attgtaaacgcacca[A/C]tcagcactctgtaaa	10533
rs2084466	snp	C/T	0.499722	0.0117779	intron-variant	ATG7	GRCh38.p7	3:11348901	ccaatcagcgctcta[C/T]gtctagctaaaggat	10533
rs2088602	snp	C/T	0.186105	0.241697	intron-variant	ATG7	GRCh38.p7	3:11492150	accaggagattgtat[C/T]ccacacctggctcgg	10533
rs2088603	snp	A/G	0.185788	0.241613	intron-variant	ATG7	GRCh38.p7	3:11492110	tgaccacggagtctc[A/G]ctgattgctagcaca	10533
rs2122031	snp	C/T	0.499933	0.00579035	intron-variant, utr-variant-5-prime	ATG7	GRCh38.p7	3:11272457	AGCAAGACCCCACTA[C/T]ACCCTCGCCCGCCGC	10533
rs2133412	snp	A/G			intron-variant	ATG7	GRCh38.p7	3:11413783	atctttaattcttta[A/G]aaaagtttgaaaagc	10533
rs2244617	snp	C/T	0.145978	0.227331	intron-variant	ATG7	GRCh38.p7	3:11461623	TAGAATGAGAATTCT[C/T]AGTGGTTTTAAGAAA	10533
rs2245381	snp	C/T	0.24019	0.249807	intron-variant	ATG7	GRCh38.p7	3:11370349	ACTCTAGCTTAATAG[C/T]GAGAGTTGGGTCAGT	10533
rs2248971	snp	C/T	0.499203	0.0199521	intron-variant	ATG7	GRCh38.p7	3:11361967	AACTCATATCTCTTT[C/T]GGATGACTGGCTTTT	10533
rs2249051	snp	A/G	0.499325	0.0183582	intron-variant	ATG7	GRCh38.p7	3:11361760	AAGTGGGTCAAGTGC[A/G]ACAGTGCTTTGAACA	10533
rs2252601	snp	A/G	0.164219	0.234823	intron-variant	ATG7	GRCh38.p7	3:11439760	GTGCAGGAGAGAAAA[A/G]GCTTTCCAGAAGGGC	10533
rs2256773	snp	C/G	0.499515	0.0155675	intron-variant	ATG7	GRCh38.p7	3:11344855	gcctgcgtgataaag[C/G]aagacactgtctcaa	10533
rs2305686	snp	A/G	0.363764	0.222615	intron-variant	ATG7	GRCh38.p7	3:11309079	AACCTCGGTGCAACC[A/G]AGAGCCCATTTACTT	10533
rs2344131	snp	A/C	0.0707826	0.174302	intron-variant	ATG7	GRCh38.p7	3:11294378	GGTGCACTCCACTAC[A/C]CCCGGCTAATTTTTT	10533
rs2344132	snp	C/T	0.00953873	0.0683987	intron-variant	ATG7	GRCh38.p7	3:11354501	taaaaatacaaaaat[C/T]agctgggtgtggtgg	10533
rs2344133	snp	C/T			intron-variant	ATG7	GRCh38.p7	3:11354509	caaaaatcagctggg[C/T]gtggtggcgcacacc	10533
rs2344134	snp	A/C			intron-variant	ATG7	GRCh38.p7	3:11354672	aaaaaaaaaaaaaaa[A/C]aaaGATGTTGGATTA	10533
rs2344826	snp	A/G	0.134802	0.221877	intron-variant	ATG7	GRCh38.p7	3:11521153	ATCATGAGATAATAC[A/G]TGTGCAGCATTTCAG	10533
rs2437681	snp	C/T	0.484279	0.0872533	intron-variant	ATG7	GRCh38.p7	3:11552601	GGGCTCTCCACTGGC[C/T]TCGTCCCATTGGCTG	10533
rs2437682	snp	C/G			intron-variant	ATG7	GRCh38.p7	3:11552525	ACCAGAACAGGGACT[C/G]CTGGGGATAGGGACA	10533
rs2437683	snp	A/G	0.0836354	0.186609	intron-variant	ATG7	GRCh38.p7	3:11551811	TAGTGAGCTGAGATC[A/G]CACCACTATACTCCA	10533
rs2437684	snp	A/G	0.243061	0.249904	intron-variant	ATG7	GRCh38.p7	3:11551787	TACTCCAGCCTGGGC[A/G]ACAGGGTGAGACCCT	10533
rs2437685	snp	A/G	0.284733	0.247575	intron-variant	ATG7	GRCh38.p7	3:11551539	AATAAACCTAACATC[A/G]GATGTACAGAATCCA	10533
rs2437686	snp	C/T	0.281313	0.248031	intron-variant	ATG7	GRCh38.p7	3:11547515	actgcccaagagaaa[C/T]gacaacgtgtccaca	10533
rs2442768	snp	A/G			intron-variant	ATG7	GRCh38.p7	3:11540157	gtcgtttttgctgtt[A/G]ccaccagcagagttt	10533
rs2442769	snp	A/G	0.116488	0.211364	intron-variant	ATG7	GRCh38.p7	3:11449612	CTTGGGTTATGGCTC[A/G]CTAAATCAAGCATCA	10533
rs2442770	snp	A/G	0	0	intron-variant	ATG7	GRCh38.p7	3:11552427	GTGCCCTGTGTCCAC[A/G]CCAGTTGCACTGCCA	10533
rs2442771	snp	A/G	0.409212	0.192748	intron-variant	ATG7	GRCh38.p7	3:11452251	CTAGCTGGGCATGGT[A/G]GCACATGCCTGTAAT	10533
rs2442772	snp	A/G	0.479824	0.098392	intron-variant	ATG7	GRCh38.p7	3:11452452	ATGGTTTACACAGCT[A/G]TGAACATATTAAAAG	10533
rs2442779	snp	C/T	0.367503	0.220665	intron-variant	ATG7	GRCh38.p7	3:11441531	ACAGGCGTGAGTCAC[C/T]GCAACCAGCCTGCAT	10533
rs2442780	snp	A/G	0.180064	0.240019	intron-variant	ATG7	GRCh38.p7	3:11469094	TGTCAACAGAAGATG[A/G]GATGGTTGAAGAGGG	10533
rs2442781	snp	A/G	0.321769	0.239477	intron-variant	ATG7	GRCh38.p7	3:11442295	ACTCCTGGCCCCATC[A/G]CTAGTTGCATCACTT	10533
rs2442782	snp	C/T	0.406296	0.19512	intron-variant	ATG7	GRCh38.p7	3:11442319	ATCACTTCATCTTGC[C/T]TGGATTTCATCTGTA	10533
rs2442783	snp	C/G	0	0	intron-variant	ATG7	GRCh38.p7	3:11475864	TCCATCTCTCTGTCT[C/G]TGAGacacacacaca	10533
rs2442785	snp	C/T	0.182933	0.240836	intron-variant	ATG7	GRCh38.p7	3:11480354	accagctgggcaaca[C/T]agcaagaccctgtct	10533
rs2442786	snp	A/G	0.499937	0.0055907	intron-variant	ATG7	GRCh38.p7	3:11491448	cagagtagtttgatc[A/G]tcagaagccttcttc	10533
rs2442788	snp	C/T	0.0345262	0.126772	intron-variant	ATG7	GRCh38.p7	3:11444167	TCATTTTCGTTGCTA[C/T]GTAGTGTTTCATAAT	10533
rs2442789	snp	C/T	0.205723	0.246048	intron-variant	ATG7	GRCh38.p7	3:11498714	CTCTTTTTCCTCTTT[C/T]CCCTTCTAATTGCTC	10533
rs2442790	snp	C/T	0.0174175	0.0916809	intron-variant	ATG7	GRCh38.p7	3:11498822	TGGGCTCCAGGCCAA[C/T]TGTGCTCCTTCTCTC	10533
rs2442791	snp	C/G			intron-variant	ATG7	GRCh38.p7	3:11499954	ATATTTTATGAGCAT[C/G]TTAATCCTTATTTCG	10533
rs2442793	snp	C/T	0.0441095	0.141807	intron-variant	ATG7	GRCh38.p7	3:11506221	CAGAATATCACAGTT[C/T]AAACATGGTAGAAAT	10533
rs2442794	snp	A/G	0.352287	0.228117	intron-variant	ATG7	GRCh38.p7	3:11509527	TGACAAATTGTTTGT[A/G]TTTTATGAGCGTTTA	10533
rs2442795	snp	G/T	0.177182	0.23916	intron-variant	ATG7	GRCh38.p7	3:11509726	ATTGAATTCATTTTA[G/T]AGCCAACTTTTCAGG	10533
rs2442796	snp	A/C	0.143622	0.226238	intron-variant	ATG7	GRCh38.p7	3:11511742	ctgagccctgccccg[A/C]gggaaggcagctaag	10533
rs2442797	snp	C/T	0.147991	0.228242	intron-variant	ATG7	GRCh38.p7	3:11514461	TGGTGATTTTCCCAC[C/T]GGGAGAGGGAGACAT	10533
rs2442798	snp	A/G	0.401037	0.199218	intron-variant	ATG7	GRCh38.p7	3:11446417	TACTTTTGTAAATGC[A/G]TTATATAAAGGAGGA	10533
rs2442799	snp	A/G	0.17332	0.23795	intron-variant, downstream-variant-500B	ATG7	GRCh38.p7	3:11447166	TGAACTCTTTTTAGC[A/G]TAAAAGAGTAATTTA	10533
rs2443700	snp	C/T	0.238171	0.24972	intron-variant	ATG7	GRCh38.p7	3:11551844	GGAGAATGGCTTGAA[C/T]TCAGGAGGTAGAAGT	10533
rs2443701	snp	A/G	0.203575	0.245652	intron-variant	ATG7	GRCh38.p7	3:11547299	CCTGAGGACAATGGT[A/G]TCACATGTTTGCCCC	10533
rs2443702	snp	A/G	0.202343	0.245416	intron-variant	ATG7	GRCh38.p7	3:11544961	CTTGGTTCCTCCTGC[A/G]ACCCCACCATAATTT	10533
rs2443703	snp	C/T	0.148326	0.228391	intron-variant	ATG7	GRCh38.p7	3:11522717	TGAATTTACTGTTCA[C/T]AGTCATATGAAATTA	10533

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