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
rs3657238	snp	C/T	0.498866	0.0237825	intron-variant	Lnx1	GRCm38.p3	5:74605619	TGAAGCCATGATGTT[C/T]TGCTGCGCTGCTGTG	16924
rs3659100	snp	C/G	0.290657	0.246672	intron-variant	Lnx1	GRCm38.p3	5:74605910	TTTGCCAACAGAAGA[C/G]AGTTATTCCCAACAG	16924
rs6299799	snp	C/T	0.21875	0.248039	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74652373	AGGAGAGAGAGAAAA[C/T]CATGAATGAAATTGA	16924
rs6313089	snp	A/G	0.207612	0.24638	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74652505	AGGACATCCTTCCAT[A/G]TATGAAGTCAGCAAT	16924
rs6313107	snp	A/G	0.21875	0.248039	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74652522	ATGAAGTCAGCAATG[A/G]TCATATCCATGAATG	16924
rs6330646	snp	A/G	0.456747	0.140554	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74653487	taatcctagctcttg[A/G]cagaaagcattacaa	16924
rs6331099	snp	C/T	0.5	0	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74653533	ggtcaccctcagcca[C/T]acagcaagttcaagt	16924
rs13473461	snp	C/T			missense, utr-variant-3-prime	Lnx1, Fip1l1	Mm_Celera	5:74597929	TCTATTTCAGGTACT[C/T]ATGTAACTGTAAAGA	16924
rs13473462	snp	C/T	0.231111	0.249285	synonymous-codon, intron-variant	Fip1l1, Lnx1	Mm_Celera	5:74595128	AGGCTATGAGCGCCA[C/T]AGAGCTAGTCGGGAG	16924
rs13473463	snp	A/G			utr-variant-3-prime, intron-variant	Fip1l1, Lnx1	Mm_Celera	5:74596065	TAATGTTTAAGAAAT[A/G]TACCTTTAATCTTGT	16924
rs13478327	snp	C/T	0.498998	0.0223656	synonymous-codon	Lnx1	GRCm38.p3	5:74607852	GGTCATGCCGAGAGA[C/T]TCGCTGGGGTCTTTC	16924
rs29502174	snp	A/G	0.375	0.216506	intron-variant	Lnx1	Mm_Celera	5:74609507	GTGCATGGATATTTT[A/G]CCTACTACAGGTATA	16924
rs29503228	snp	C/T	0.375	0.216506	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74648806	TTAAGAAAGAAACAA[C/T]TTTCTGAGTAACGCC	16924
rs29506577	snp	G/T	0.375	0.216506	intron-variant	Lnx1	Mm_Celera	5:74659903	GGCTAAATACTAATG[G/T]CTTATTTCAAAAAGA	16924
rs29506611	snp	A/T	0.432133	0.171253	intron-variant	Lnx1	GRCm38.p3	5:74689345	TCTTGCTTTTAGACA[A/T]ACATGAGCCTAGCTA	16924
rs29508193	snp	C/T	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Lnx1	Mm_Celera	5:74697376	TGAACCCTACAGAGA[C/T]GAGGTAAATCTGCCC	16924
rs29508656	snp	C/T	0.401235	0.199068	intron-variant	Lnx1	GRCm38.p3	5:74638648	GAGGCATAGCAGCTG[C/T]AGCCAAGGTGTAGAC	16924
rs29509012	snp	A/G	0.48	0.0979796	intron-variant	Lnx1	Mm_Celera	5:74644857	GACCCAGGAGGAAAC[A/G]GAGTCCCTAGATTTG	16924
rs29511368	snp	G/T	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74621203	TTCCATGTGTGTGTG[G/T]GGGGGGAGAGAGAGA	16924
rs29526454	snp	A/G	0.375	0.216506	intron-variant	Lnx1	Mm_Celera	5:74639432	AAACAGCTCCGGGGG[A/G]TGGGGTGGGGGGGCT	16924
rs29527436	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	GRCm38.p3	5:74682116	GGTAGCCCATATCTG[C/T]GTTGAACTCCCTATA	16924
rs29527439	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74642560	TTTTCTGTAAACTGT[C/T]TAGGGATTGGGAATA	16924
rs29527869	snp	A/G	0.401235	0.199068	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74647883	AGGTTTGTCTTGGAC[A/G]GAATCATGGCAGGCC	16924
rs29532337	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74643075	ATGTTTTTTACTTCA[A/G]GGTTGATGGGAAACG	16924
rs29542881	snp	C/T	0.493827	0.0552116	intron-variant	Lnx1	Mm_Celera	5:74696895	TGTGTATGTGGACAT[C/T]GGCTACAGAATGAGT	16924
rs29544225	snp	A/G	0.48	0.0979796	intron-variant	Lnx1	GRCm38.p3	5:74677326	CACAAAGCACTAAGC[A/G]TGCTGCTTCAACTGC	16924
rs29545653	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74667111	TGAGTGCAGCATGTC[C/T]TCCCTTCTGAGCAGG	16924
rs29546535	snp	A/G	0.188366	0.242283	intron-variant, utr-variant-3-prime	Fip1l1, Lnx1	Mm_Celera	5:74592729	ATGACAGTATGGCAT[A/G]TACATGTAAGTGGGA	16924
rs29548239	snp	C/T	0.387812	0.208586	intron-variant	Lnx1	Mm_Celera	5:74611673	GCCATGGATCGATTT[C/T]CTGTATCTCTGATTG	16924
rs29549902	snp	G/T	0.489796	0.070696	intron-variant	Lnx1	Mm_Celera	5:74696883	GACAGGGATGGCTGT[G/T]TATGTGGACATCGGC	16924
rs29560463	snp	A/C	0.444444	0.157135	intron-variant, nc-transcript-variant	Lnx1, Gm32304	Mm_Celera	5:74655088	CAGAGGGCCTGGGCT[A/C]TGGAAGGAAGAACTG	16924
rs29563201	snp	C/G	0.5	0	intron-variant, nc-transcript-variant	Lnx1, Gm32304	Mm_Celera	5:74648328	CAGACGCTCAGTGTG[C/G]TGTTATCCTGTTTCC	16924
rs29564836	snp	A/G	0.401235	0.199068	intron-variant	Lnx1	Mm_Celera	5:74667636	TAAAGTTAAGGATCT[A/G]CCTTGATATTTTTCC	16924
rs29565269	snp	A/C	0.465374	0.126941	intron-variant	Lnx1	GRCm38.p3	5:74677132	GTCTGCTTGCAAGCT[A/C]TGGTCTTAATTGCTC	16924
rs29566096	snp	A/G	0.33241	0.236027	intron-variant	Lnx1	Mm_Celera	5:74642066	AGCTAGGGATGTGGT[A/G]GAGGAGTTCCTGGTT	16924
rs29568252	snp	A/G	0.290657	0.246672	intron-variant	Lnx1	Mm_Celera	5:74633788	AACTTTGGATACGCT[A/G]TCTGCTGAAACAAGT	16924
rs29568542	snp	C/T	0.493827	0.0552116	intron-variant	Lnx1	GRCm38.p3	5:74609711	GTTTTTAGTAACAAG[C/T]GCCACAATGGCCTGT	16924
rs29568613	snp	A/G	0.231111	0.249285	intron-variant	Lnx1	Mm_Celera	5:74661576	AGTTACCCTGGCCTC[A/G]TAGTTAGAAGCAGAC	16924
rs29579422	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	GRCm38.p3	5:74682477	TACAGTATAGAAGTC[A/G]AGGTCAATTTCCTCT	16924
rs29580542	snp	A/C	0.456747	0.140554	intron-variant, nc-transcript-variant	Lnx1, Gm32304	Mm_Celera	5:74655500	GATATCGTCTGCAAT[A/C]TGTGGGCTTCTGTTT	16924
rs29581122	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	Lnx1, Fip1l1	GRCm38.p3	5:74598555	CAACTAGGAGAGTCG[C/T]GGCTGTCAGACCTAA	16924
rs29581360	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74642565	TGTAAACTGTTTAGG[A/G]ATTGGGAATATGTAC	16924
rs29582494	snp	C/G	0.32	0.24	upstream-variant-2KB, intron-variant	Lnx1, Gm15984	Mm_Celera	5:74704394	AAAAGCAAAAGGTTC[C/G]AAAAGGAGGGAGGGG	16924
rs29586174	snp	A/G	0.432133	0.171253	intron-variant	Lnx1	Mm_Celera	5:74660063	TTGGCAAGTCTGAGG[A/G]CCAGGTTTGCACAAA	16924
rs29626910	snp	C/T	0.484429	0.0868505	intron-variant	Lnx1	GRCm38.p3	5:74632609	ATGCTTCTAACAGTC[C/T]GTAGCATCCTCAATG	16924
rs29626964	snp	A/G	0.456747	0.140554	intron-variant	Lnx1	Mm_Celera	5:74660664	AGCCAAACAGCTGAT[A/G]AACATTCAAGTCCAG	16924
rs29628632	snp	A/G	0.387812	0.208586	intron-variant, nc-transcript-variant	Lnx1, Gm32304	Mm_Celera	5:74657499	AGCTCACTCCCATAG[A/G]GCTGGAACTGCCTGT	16924
rs29629187	snp	C/T	0.32	0.24	intron-variant	Lnx1	Mm_Celera	5:74644474	AGCCTGCACAGGTTC[C/T]AAGCACTCTATCTCA	16924
rs29629762	snp	C/T	0.493827	0.0552116	intron-variant	Lnx1	GRCm38.p3	5:74667922	GGAGTAACTTGAAGA[C/T]GTGCTAGTAATCCTA	16924
rs29629859	snp	A/C	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74642518	GGGGAGGGGAGCTGG[A/C]GAGTCCCAAGCTACA	16924
rs29629987	snp	G/T	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74696803	ACAACATGAGATGTA[G/T]TAAAGGGTTGATGTA	16924
rs29630350	snp	C/T	0.188366	0.242283	intron-variant	Lnx1	Mm_Celera	5:74690545	TACCCTCCATTAGAC[C/T]TTTACATCTAGGGAA	16924
rs29631617	snp	C/T	0.33241	0.236027	intron-variant	Lnx1	Mm_Celera	5:74642165	TTCCAATGGCTGCTT[C/T]AATATGTTCTTTTAC	16924
rs29633942	snp	A/C	0.429688	0.173817	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74648010	ATCCTTTGTGAGCTC[A/C]CATCCACTTTCTGGA	16924
rs29636644	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	Lnx1, Fip1l1	Mm_Celera	5:74598908	ACTCAAGTGGCTGGG[C/T]TCACCTATGAGGGAT	16924
rs29637979	snp	C/T	0.32	0.24	intron-variant	Lnx1	Mm_Celera	5:74626682	AGCCACCTCCACCCA[C/T]ACACTATAAATAAAT	16924
rs29668312	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	GRCm38.p3	5:74642747	GCTGAGGCAGGAGGA[C/T]AATAGGTTCTGCGTT	16924
rs29669864	snp	C/G	0.487535	0.077957	intron-variant, upstream-variant-2KB	Lnx1	GRCm38.p3	5:74679246	CAATCTCTTCTTACA[C/G]ATGCTCACCCTAGAG	16924
rs29675747	snp	A/C	0.375	0.216506	intron-variant	Lnx1	Mm_Celera	5:74619009	CAAACACCCCCCCCC[A/C]AAAAAAAAAACCTCC	16924
rs29676660	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74675850	GTGGGTGTGGTCTTA[C/T]ATCCTGATTTCAAGT	16924
rs29678941	snp	C/G	0.32	0.24	intron-variant	Lnx1	Mm_Celera	5:74603303	GACTGAAGAAGGCAC[C/G]GTTCCCTTTGTATAT	16924
rs29680820	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74610307	GCAGGTTGGGAAACC[A/G]AAAAAAAAAACAAAT	16924
rs29682304	snp	A/C	0.475309	0.108333	intron-variant, upstream-variant-2KB	Lnx1	Mm_Celera	5:74698667	TGTTATATATGTGGA[A/C]TAATGCTCACTTTCA	16924
rs29684846	snp	C/T	0.5	0	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74650706	AGAGCATGGAACTCC[C/T]CAATGCTCAGGGCAT	16924
rs29728436	snp	A/C	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74682202	GGTAACAGATGTGCG[A/C]CCCTGCCCTTGGTTG	16924
rs29728920	snp	A/G	0.375	0.216506	intron-variant	Lnx1	GRCm38.p3	5:74669085	AAGCTAAACATCGAG[A/G]CAAGTGTGGCCCTAG	16924
rs29730500	snp	C/T	0.432133	0.171253	intron-variant, upstream-variant-2KB	Lnx1	GRCm38.p3	5:74678836	AATCTCACCGAGGCC[C/T]GAATTGAACTTGACT	16924
rs29730868	snp	A/T	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74665160	AGCGGTGTGAGGGAG[A/T]CTGTTCCCACAAGCC	16924
rs29731028	snp	C/T	0.415225	0.187619	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74648771	TCTAGCCCATGTGTA[C/T]GTCATGCTCTGAAGT	16924
rs29731125	snp	C/G	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74674100	TGTGTTCTCTTTGGG[C/G]TCTAAGAAGGTCAGA	16924
rs29731556	snp	A/C	0.444444	0.157135	synonymous-codon	Lnx1	GRCm38.p3	5:74620271	CAGCACCGTTAGCCG[A/C]AGCACCTGGCAGGGC	16924
rs29733557	snp	A/G	0.493827	0.0552116	intron-variant, downstream-variant-500B	Fip1l1, Lnx1	Mm_Celera	5:74592233	ACAGGTTTCCTTCTT[A/G]TCACCTAAACATGAT	16924
rs29773890	snp	C/T	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74612143	TGAATGTATGTGTCC[C/T]CCATGGGTGGAAATT	16924
rs29776410	snp	C/T	0.49827	0.0293608	intron-variant	Lnx1	Mm_Celera	5:74694944	GAATAAGATGTCCTC[C/T]CACATCCGAGCTATA	16924
rs29778987	snp	C/T	0.498615	0.0262793	intron-variant	Fip1l1, Lnx1	Mm_Celera	5:74594692	TTCTACTGTAGAAGC[C/T]ACTGTGAGCTATATA	16924
rs29780431	snp	A/T	0.188366	0.242283	intron-variant	Lnx1	Mm_Celera	5:74675568	ATCCAACTGGGTCCA[A/T]GCATGGTGGCAATAT	16924
rs29810466	snp	C/T	0.375	0.216506	intron-variant	Lnx1	GRCm38.p3	5:74608559	CACTCATAGAAAAGC[C/T]AACCATATAAAATGG	16924
rs29812219	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Lnx1	GRCm38.p3	5:74679033	AGAGCATCAGCAACA[A/G]CAAACAGTATTCTAA	16924
rs29817977	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	GRCm38.p3	5:74642855	TAAATGGCAAAGAGG[A/G]TTGGAGATGTGGCTC	16924
rs29821863	snp	A/G	0.475309	0.108333	intron-variant	Lnx1	Mm_Celera	5:74699593	CCAGAATAATCGAGC[A/G]CCTAGAACCGAACAC	16924
rs33032651	snp	A/C	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74691895	CGGCCCCCCCCCCCC[A/C]CACACACACACACTT	16924
rs33039339	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	GRCm38.p3	5:74675641	CTAGGTGTGGTACCC[A/G]GTACTGCAGGTAAAC	16924
rs33054473	snp	A/G	0.5	0	intron-variant	Lnx1	GRCm38.p3	5:74676790	AATTTACCCAAGACT[A/G]TTTTAAAGATATACA	16924
rs33060279	snp	A/G	0.5	0	intron-variant	Lnx1	GRCm38.p3	5:74688677	AACTAAGCAGGCCGA[A/G]CTACCAGACTGTCTT	16924
rs33071651	snp	C/T	0.277778	0.248452	intron-variant	Lnx1	Mm_Celera	5:74659233	AGACTGCCTTGGGTC[C/T]AACAGTTTTTAACCG	16924
rs33071888	snp	A/C	0.359862	0.224567	intron-variant	Lnx1	Mm_Celera	5:74630689	TCTGAGGTCAGTGCA[A/C]TGGGGACACTGAGCA	16924
rs33073763	snp	A/G	0.277778	0.248452	intron-variant	Lnx1	GRCm38.p3	5:74638755	CATGCTGGATGCAGG[A/G]AATGGTAGGTTCCAT	16924
rs33076299	snp	A/G	0.444444	0.157135	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74647925	TGGGATGGTGCTGGG[A/G]GAGGGGCGGGGTGTG	16924
rs33082958	snp	A/G	0.484429	0.0868505	intron-variant	Lnx1	GRCm38.p3	5:74632622	TCCGTAGCATCCTCA[A/G]TGTGATGAAATGTGG	16924
rs33094159	snp	C/T	0.375	0.216506	intron-variant, utr-variant-3-prime	Lnx1, Fip1l1	Mm_Celera	5:74598296	CATTCTCAGAATTAG[C/T]GATTAATTGCAAGGA	16924
rs33095986	snp	A/T	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74627797	ACATATCTCACTATT[A/T]AAAAAAAAAAAAATC	16924
rs33099056	snp	A/G	0.484429	0.0868505	intron-variant	Lnx1	GRCm38.p3	5:74676233	AATGACTTGCCTCAA[A/G]TGTCTTTTTCTATTT	16924
rs33103488	snp	C/G	0.5	0	intron-variant	Lnx1	Mm_Celera	5:74622398	GTGCCACATCCCAGC[C/G]ACCAGTGGGAATGTC	16924
rs33107628	snp	C/T	0.5	0	intron-variant	Lnx1	GRCm38.p3	5:74682205	AACAGATGTGCGACC[C/T]TGCCCTTGGTTGATA	16924
rs33109364	snp	C/T	0.5	0	intron-variant	Lnx1	GRCm38.p3	5:74682208	AGATGTGCGACCCTG[C/T]CCTTGGTTGATATGG	16924
rs33110068	snp	A/G	0.375	0.216506	intron-variant	Lnx1	GRCm38.p3	5:74638568	GGGAGCTCAGAGCAG[A/G]AGAGCACACACCCTG	16924
rs33117899	snp	A/C	0.429688	0.173817	intron-variant	Lnx1	Mm_Celera	5:74610470	TGGAGTTAAACACTG[A/C]CCAGCGCCTTCCTCC	16924
rs33117903	snp	A/G	0.465374	0.126941	intron-variant	Lnx1	Mm_Celera	5:74700322	GATTCAAGGTCATTG[A/G]TGGGTACAACATATT	16924
rs33118660	snp	A/G	0.444444	0.157135	intron-variant	Lnx1	Mm_Celera	5:74619675	TGTGTGTGTGTGTGT[A/G]TATATATATATATAT	16924
rs33141836	snp	A/G	0.5	0	intron-variant	Lnx1, Gm32304	Mm_Celera	5:74653672	AACTACTTAATTTAA[A/G]TTTGCTCTAGACAGT	16924

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