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
rs717060	snp	A/G	0.00909072	0.0668036	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107897046	tacatgaagcaatta[A/G]aatagtgcctaacat	11043
rs742584	snp	A/T	0.257866	0.249876	utr-variant-3-prime, intron-variant	MID2, LOC101928335	GRCh38.p7	X:107930939	TAAAGTAAAACCTGT[A/T]TTGAGAGTATGAAAG	11043
rs1008503	snp	A/G/T	0.104127	0.20303	intron-variant	MID2	GRCh38.p7	X:107831270	CTCAGCTTCCTTCCC[A/G/T]TAGGTCAGACTCCGC	11043
rs1158303	snp	G/T	0	0	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107923922	AAACATGGAAACTCA[G/T]CCAAAGGGACACAta	11043
rs1159681	snp	A/C	0	0	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107918225	ACCGTAACATGTGAG[A/C]TAAACAACAGCTTTG	11043
rs2050192	snp	C/T	0.00397613	0.0444101	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107900030	GTCCTTAAGTGTTTT[C/T]TGAACAGGAAATACT	11043
rs2236083	snp	A/C	0.152361	0.230145	synonymous-codon	MID2	GRCh38.p7	X:107840845	TCGCATTTTGGTATC[A/C]AGCTGCAGCTCTGGT	11043
rs2267975	snp	A/C	0.0622094	0.165029	intron-variant	MID2	GRCh38.p7	X:107865573	AGGACTGAAAAGAAC[A/C]CTTTGGGGTGGGCGG	11043
rs2273377	snp	C/T	0.00105904	0.0229869	intron-variant	MID2	GRCh38.p7	X:107854835	AGTTTTAGAAAGTCT[C/T]ATTCCTTTAGGATGC	11043
rs2300099	snp	C/T	0.0026455	0.0362733	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107919571	CCATATGAAGAGCAA[C/T]TGAAAGAAAGGAAGA	11043
rs2300100	snp	C/T	0.000529661	0.016265	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107914946	gttatttccattttg[C/T]gaatgagaaagttgg	11043
rs2300101	snp	C/T	0.443854	0.157862	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107898327	CAGAAAAATAGAAAA[C/T]GTGCTTGGTTAAAGC	11043
rs2300102	snp	C/T	0.022522	0.1037	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107896408	AGTTACTGTCTCCCC[C/T]ATATTCTCTTTGTAA	11043
rs2300103	snp	A/T	0.253421	0.249977	intron-variant	MID2	GRCh38.p7	X:107867978	TTAATTATATTTATG[A/T]CTATCCTAAGTCTCT	11043
rs2300104	snp	C/T	0.00158814	0.0281345	intron-variant	MID2	GRCh38.p7	X:107867842	TACATCCTGTTCCAT[C/T]AAATCTGATTCTTCT	11043
rs2300105	snp	C/T	0.445441	0.155894	intron-variant	MID2	GRCh38.p7	X:107853951	AAAACCATAACAATC[C/T]CACAAAGTAGAAGAT	11043
rs2300106	snp	G/T	0.444914	0.156552	intron-variant	MID2	GRCh38.p7	X:107847004	AACCTCACTTCTTTG[G/T]GTTCAGTAATTCTTG	11043
rs2300107	snp	C/T	0.00370173	0.0428621	intron-variant	MID2	GRCh38.p7	X:107846965	ATCTTTCCTCACCTA[C/T]ATTATATTTCTGTAA	11043
rs2300108	snp	A/C	0.0660089	0.169255	intron-variant	MID2	GRCh38.p7	X:107844468	ATATATCATGAACTA[A/C]GATATATATTGGGAC	11043
rs2344566	snp	C/G	0.399909	0.200068	intron-variant	MID2	GRCh38.p7	X:107851780	GCGTCCCCCACTACT[C/G]TCTTTCTACCCTCTG	11043
rs2473631	snp	A/T	0	0	intron-variant	MID2	GRCh38.p7	X:107893361	GATATTAACAAAATA[A/T]AAACATTCTAGTAAT	11043
rs2473632	snp	A/C	0	0	intron-variant	MID2	GRCh38.p7	X:107893267	GACTGTGTTTTTTAC[A/C]CGAAGTGAGAAGATC	11043
rs2473635	snp	G/T	0.000529661	0.016265	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107922447	AATTAAATGAATACA[G/T]ATGGGAAAATTGGGG	11043
rs2500127	snp	C/G	0	0	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107915534	ctgcactgcaacctg[C/G]gtgacacagcaagac	11043
rs3060813	in-del	-/CAAAA			intron-variant	MID2	GRCh38.p7	X:107884708	caaaacaaaacaaaa[-/CAAAA]aCAGGGCAGATTAGA	11043
rs3813784	snp	C/T	0.0358881	0.129059	utr-variant-3-prime, intron-variant	MID2, LOC101928335	GRCh38.p7	X:107931519	TGGACCAATAGTGTC[C/T]CTCCTAGTGACAGAA	11043
rs4036984	snp	A/G	0.44579	0.155455	intron-variant	MID2	GRCh38.p7	X:107851767	TCCATTTCCAGCTGC[A/G]TCCCCCACTACTCTC	11043
rs4460524	snp	C/T	0	0	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107907047	tcagatactctcttt[C/T]caatattctcaatcc	11043
rs5903309	in-del	-/C			intron-variant	MID2	GRCh38.p7	X:107852656	GCTGGTCCTCATAAT[-/C]CCAGTTTGAGAAAAT	11043
rs5903310	in-del	-/AAAAC/AAAC	0.0645269	0.16763	intron-variant	MID2	GRCh38.p7	X:107884684	GCTACAAAGAGACCA[-/AAAAC/AAAC]AAAACAAAACAAAAC	11043
rs5916793	snp	A/C	0.0204249	0.0989712	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107904318	ttcattgagctgtac[A/C]cttaggatttgggtg	11043
rs5917074	snp	A/T	0.432112	0.171275	intron-variant	MID2	GRCh38.p7	X:107845525	CACACACACACACAC[A/T]CTCTCTCTCTCTCTC	11043
rs5917075	snp	C/T	0.0323082	0.122924	intron-variant	MID2	GRCh38.p7	X:107884747	TGGCAGAAGTCTTGG[C/T]CTtggagttaggatg	11043
rs5962410	snp	C/T	0.435581	0.16751	intron-variant	MID2	GRCh38.p7	X:107829818	TCGTCTGGCATGTTG[C/T]ACCCTGCAAGGCCAC	11043
rs5962411	snp	C/T	0.0470497	0.145984	intron-variant	MID2	GRCh38.p7	X:107845980	TGAGTGTGTATATTC[C/T]TGCATAAATATGTGG	11043
rs5962412	snp	A/T	0.0470497	0.145984	intron-variant	MID2	GRCh38.p7	X:107846003	ATATGTGGCTGAGAA[A/T]GACTCTGTGTCTGTG	11043
rs5962413	snp	A/G	0.151636	0.229836	intron-variant	MID2	GRCh38.p7	X:107854911	ACGGTGATGATGGAC[A/G]GTGGGGGGATAATAG	11043
rs5962414	snp	A/G	0.150308	0.229263	intron-variant	MID2	GRCh38.p7	X:107854966	TCCAAACAGCAGGCA[A/G]TATGAAAATCAGACA	11043
rs5962415	snp	A/G	0.443854	0.157862	intron-variant	MID2	GRCh38.p7	X:107882892	ttctactataaagac[A/G]catgcacacatatgt	11043
rs5962896	snp	C/G	0.05658	0.158394	intron-variant	MID2	GRCh38.p7	X:107829578	TAGCACCTAGTAGCA[C/G]AGTCAACAATATTAA	11043
rs5962897	snp	A/G	0.0525796	0.153379	intron-variant	MID2	GRCh38.p7	X:107840042	CTCAGTTTACTAGGA[A/G]TAGAATGGAACGGAA	11043
rs5962898	snp	A/T	0.05658	0.158394	intron-variant	MID2	GRCh38.p7	X:107843491	CAGATTTTGAATAGT[A/T]CCCCTTTCATATTTT	11043
rs5962899	snp	A/G	0	0	intron-variant	MID2	GRCh38.p7	X:107847313	AAGTGGGAAATTCCA[A/G]TTCAGTATGGTAAGT	11043
rs5962901	snp	A/G	0.151194	0.229646	intron-variant	MID2	GRCh38.p7	X:107859068	TCTCTTTAGAGTTCA[A/G]ACTTCAGATGGGCTG	11043
rs5962902	snp	C/T	0.085528	0.188279	intron-variant	MID2	GRCh38.p7	X:107861045	TGGTTCCTGGACCCA[C/T]TGTGAGGATGACTTG	11043
rs5962903	snp	C/T	0.445616	0.155675	intron-variant	MID2	GRCh38.p7	X:107865764	GGCACAAAACAATCA[C/T]TGGCTTTGGAATAAT	11043
rs5962904	snp	C/T	0.445441	0.155894	intron-variant	MID2	GRCh38.p7	X:107868178	AGCAAGGTACTGGCA[C/T]GTAGAGAGTAACTGA	11043
rs5962906	snp	A/G	0.444562	0.156989	intron-variant	MID2	GRCh38.p7	X:107871726	agtctagctgtcccc[A/G]gctggactcctcttc	11043
rs5962907	snp	G/T	0.0220041	0.102557	intron-variant	MID2	GRCh38.p7	X:107871783	tgaagtcaagctgct[G/T]ctttccaacttccaa	11043
rs5962909	snp	A/G	0.308702	0.24301	intron-variant	MID2	GRCh38.p7	X:107887856	gtttagtcttgggag[A/G]gtgtatgtgttgagg	11043
rs5962910	snp	A/G	0.445266	0.156113	intron-variant	MID2	GRCh38.p7	X:107893163	ACGGCTTTCTGAAAA[A/G]CAGTGCTATTATTGA	11043
rs5962911	snp	C/T	0.313263	0.241863	intron-variant	MID2	GRCh38.p7	X:107893858	TGTCCTTTTGCCATC[C/T]GTACTTTATATGCTG	11043
rs6523981	snp	A/G	0.443677	0.15808	intron-variant	MID2	GRCh38.p7	X:107881506	TTTCTTCTCTCTGGT[A/G]TGTCCTTCAAAACTT	11043
rs6523982	snp	A/C	0.241753	0.249864	intron-variant	MID2	GRCh38.p7	X:107888942	aggctaggattgcag[A/C]ccctgcctttttttg	11043
rs6523983	snp	A/C/G	0.445796	0.157699	intron-variant	MID2	GRCh38.p7	X:107891081	gtgaggcgatgcctc[A/C/G]ccctgcttcggctca	11043
rs6523985	snp	A/C	0.444386	0.157208	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107906557	cagtttttaactata[A/C]cctctacttaacaac	11043
rs6616669	snp	C/T	0	0	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107910939	gctcactgcaatctc[C/T]gcctcccagattcaa	11043
rs6622267	snp	C/G	0.0204488	0.0990265	intron-variant	MID2	GRCh38.p7	X:107835150	aggagccttttgtga[C/G]tggcttcttttactt	11043
rs6622268	snp	A/G	0.438029	0.164757	intron-variant	MID2	GRCh38.p7	X:107838787	TGATGACAAGATAAT[A/G]AACAAAAGCTACTCA	11043
rs6622271	snp	C/T	0	0	intron-variant	MID2	GRCh38.p7	X:107846849	AATATTTGAAAGGAG[C/T]TAACAATCGTTTGTT	11043
rs6622274	snp	C/T			intron-variant	MID2	GRCh38.p7	X:107893149	TCTTTCATGTTCTTA[C/T]GGCTTTCTGAAAAAC	11043
rs6622275	snp	A/G			intron-variant	MID2, LOC101928335	GRCh38.p7	X:107897917	CTTGATAATTCATCA[A/G]ATGTCCAATTTACCT	11043
rs6652967	snp	C/T	0.444562	0.156989	intron-variant	MID2	GRCh38.p7	X:107871317	CTTGCTTGGCCCCAC[C/T]GTGTTCCACGCCTTG	11043
rs6652968	snp	A/G	0.444562	0.156989	intron-variant	MID2	GRCh38.p7	X:107871499	ttagctttgctgtcc[A/G]tgaatggcttaagtg	11043
rs7051357	snp	A/C			intron-variant	MID2	GRCh38.p7	X:107857335	gcccaggctagagtg[A/C]agtggcacaatctcg	11043
rs7053430	snp	A/G	0.445441	0.155894	intron-variant	MID2	GRCh38.p7	X:107859919	ttgggcccaaataat[A/G]aagagccttgtaggc	11043
rs7053643	snp	C/T	0.103655	0.20269	intron-variant	MID2	GRCh38.p7	X:107836400	ctgggactacaggca[C/T]gcgccactacgcctg	11043
rs7053850	snp	A/G	0.104127	0.20303	intron-variant	MID2	GRCh38.p7	X:107854206	CTTCATCATAAGTTG[A/G]GGGACATGTGTAATA	11043
rs7054585	snp	A/C/G	0.151636	0.229836	intron-variant	MID2	GRCh38.p7	X:107854452	ATTATTAATTTGTAC[A/C/G]TAGATTAGTGCTTGG	11043
rs7055611	snp	A/G	0.103655	0.20269	intron-variant	MID2	GRCh38.p7	X:107872254	tctaggtgcaaagaa[A/G]caagttttacagggt	11043
rs7060291	snp	A/G	0.0440191	0.141675	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107903048	aattctctacgcctc[A/G]gtttccccgtatgtg	11043
rs7066710	snp	C/G	0.151636	0.229836	intron-variant	MID2	GRCh38.p7	X:107853141	CTCTTTTTCACATAA[C/G]GAATGGGAAACAGTA	11043
rs7067117	snp	A/G	0.0214859	0.101397	intron-variant	MID2	GRCh38.p7	X:107853188	ACATGCTAGAATTCC[A/G]GCTACTGTTGTAACA	11043
rs7878008	snp	A/G	0	0	intron-variant	MID2	GRCh38.p7	X:107841460	TCTCTAATAAAATAG[A/G]TGACTTTTCCTATAT	11043
rs7879230	snp	C/T	0.33977	0.233327	intron-variant	MID2	GRCh38.p7	X:107829243	TTGACTGGGTGTAAG[C/T]AGGAATCTTAGCTTA	11043
rs7879425	snp	A/G	0.339469	0.233442	intron-variant	MID2	GRCh38.p7	X:107829196	TACTTTTCAAAGAAA[A/G]CACTTCCTTTACCTT	11043
rs7879884	snp	C/G	0.00791544	0.0624105	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107924611	GGGAGCAGTGGTACT[C/G]GGTAGAGGAGCTATA	11043
rs7880389	snp	C/G	0.327548	0.237668	upstream-variant-2KB, utr-variant-5-prime	MID2	GRCh38.p7	X:107824101	ttttttgaggaacct[C/G]catactattttccat	11043
rs7880672	snp	C/T	0.327548	0.237668	upstream-variant-2KB, utr-variant-5-prime	MID2	GRCh38.p7	X:107824314	ctcttgcctcagcat[C/T]ccctcctgagtagct	11043
rs7882633	snp	A/T	0.154285	0.230951	intron-variant	MID2	GRCh38.p7	X:107833431	tatatatatatatat[A/T]tTTTTTAAAAACCTA	11043
rs7882634	snp	A/T			intron-variant	MID2	GRCh38.p7	X:107833433	tatatatatatattt[A/T]ttttaaaaaCCTACA	11043
rs7883542	snp	A/G	0.313263	0.241863	intron-variant	MID2	GRCh38.p7	X:107881863	ggaattattttattc[A/G]ctgtgattatgcaaa	11043
rs7885256	snp	A/C	0.403433	0.197379	intron-variant	MID2	GRCh38.p7	X:107839734	TCTTAAAATTTCTGG[A/C]ACTTTGCTAATTTCT	11043
rs7887181	snp	C/T	0.0869739	0.189532	intron-variant	MID2	GRCh38.p7	X:107834958	aagttgtgcaatcat[C/T]gtcactatctaattt	11043
rs7888271	snp	A/G	0.0965482	0.197364	downstream-variant-500B, intron-variant	MID2, LOC101928335	GRCh38.p7	X:107931823	ACTTTGATTTCAGGA[A/G]CATGATATGGTCAAG	11043
rs7888338	snp	A/G	0.016289	0.0887646	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107912871	CTGAAATTTTCCCCC[A/G]CCATTATGCATTGTA	11043
rs9699225	snp	G/T	0.104127	0.20303	intron-variant	MID2	GRCh38.p7	X:107842656	CAATGACTATGGTTT[G/T]TGCCTCTTTTGGTTA	11043
rs9919100	snp	C/T	0.0525796	0.153379	intron-variant	MID2	GRCh38.p7	X:107854308	gggcgaaatgagata[C/T]tgcctatgaaatact	11043
rs10481933	snp	C/G	0.445441	0.155894	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107909326	tagctggtaggaaca[C/G]acactattgctagac	11043
rs11092600	snp	A/G	0.0194105	0.0965841	intron-variant	MID2	GRCh38.p7	X:107849033	AGACTCAGGTTTGGG[A/G]TGAATTGGCCTTTCT	11043
rs11541084	snp	C/G			utr-variant-5-prime, intron-variant	MID2	GRCh38.p7	X:107826053	TCCGCCTCCCTTTTG[C/G]AAGGGATTGCCTTTT	11043
rs11797581	snp	G/T			intron-variant	MID2	GRCh38.p7	X:107871961	cactttgggacacgg[G/T]tccaggcttgagggc	11043
rs11797607	snp	A/G	0.00938946	0.0678717	intron-variant	MID2, LOC101928335	GRCh38.p7	X:107911229	gactggtgacctcta[A/G]ctctgggaaatgttc	11043
rs12011005	snp	C/G	0.0399626	0.135589	intron-variant	MID2	GRCh38.p7	X:107875258	aggtacttgagatag[C/G]agggtatacagattg	11043
rs12012633	snp	C/T	0.0399626	0.135589	intron-variant	MID2	GRCh38.p7	X:107836542	aggcgtgagccacca[C/T]gcccagccTACtttt	11043
rs12012669	snp	A/C	0.0540818	0.155294	intron-variant	MID2	GRCh38.p7	X:107887177	tgaataggagtggtg[A/C]gagagggcatccctg	11043
rs12013286	snp	A/C	0.0333324	0.12472	utr-variant-3-prime, intron-variant	MID2, LOC101928335	GRCh38.p7	X:107929811	ACTTGATGATGCATC[A/C]CTCTTTAGAGATCCA	11043
rs12013687	snp	A/G	0.0245906	0.108123	intron-variant	MID2	GRCh38.p7	X:107887671	attccctctttttct[A/G]ttgattggaatagtt	11043
rs12387575	snp	G/T	0.00317376	0.039709	intron-variant	MID2	GRCh38.p7	X:107884450	gtttctattttacca[G/T]tcagaaagatagctc	11043
rs12394544	snp	G/T	0.0470497	0.145984	intron-variant	MID2	GRCh38.p7	X:107857207	GGACCCTACAGGATG[G/T]CTTATGGAAGGCCAT	11043

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