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
rs6157795	snp	C/G	0.5	0	intron-variant, missense, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94979181	ACTTCCGGGGAACTC[C/G]GGCGAGTAAGACCAG	320713
rs6158411	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94979296	TCTTTTTCCATTCAG[A/G]CGAGAGACCCTGCTT	320713
rs6159440	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB, nc-transcript-variant	Mysm1, LOC105244623	Mm_Celera	4:94979459	ATGGATAAGTAAATA[A/G]ACTCAGAAAACTGAC	320713
rs6405908	snp	A/C/G	0.5	0	intron-variant, missense, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94979121	ATGCGGCggggcggg[A/C/G]ccgggggcgggccca	320713
rs28150698	snp	C/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Mysm1, LOC105244623	GRCm38.p3	4:94981118	TGTGCAAGCCTTCCT[C/G]TGGTCCAAGTATGAG	320713
rs28150699	snp	C/T	0.48	0.0979796	upstream-variant-2KB, intron-variant	Mysm1, LOC105244623	GRCm38.p3	4:94981113	TACAGTGTGCAAGCC[C/T]TCCTGTGGTCCAAGT	320713
rs28150700	snp	C/T	0.486111	0.0821678	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94980952	GCCTGATTGGAATCC[C/T]AGGTGAGTGTGTATT	320713
rs28150701	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94980919	GAGGACTGAAGAAAC[C/T]TTGAGCGAATGTGTT	320713
rs28150702	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94980891	TGGTGCCTGTTTGCC[C/T]CAGACATTGTGTGAG	320713
rs28150703	snp	A/C	0.32	0.24	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94980843	CTACCAGAGGGAATA[A/C]TGCAGTACCCATTAC	320713
rs28150704	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB, nc-transcript-variant	Mysm1, LOC105244623	GRCm38.p3	4:94980665	CTTTTCAGGGCAACC[C/T]GGAACCATGGTGTTT	320713
rs28150705	snp	A/G	0.495868	0.0452663	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94980559	AAACGAGCTTACTTC[A/G]CACCTCAGCCTGAGA	320713
rs28150706	snp	C/T	0.473373	0.11227	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94980341	TGGCCGAAGCTACAG[C/T]CTACCCTGCTTGCCC	320713
rs28150707	snp	C/T	0.408163	0.193609	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94980107	AGACAGCTATTTGAG[C/T]CCAGCCATCTCAGAG	320713
rs28150708	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94980027	TGTCGTTTTCAGGCT[C/T]CATTTAATCATAGGG	320713
rs28150709	snp	A/G	0.415225	0.187619	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978831	TCCATCGCAGCCCAG[A/G]AAGTGGAGATAAACA	320713
rs28150710	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978763	CAGTGTTCAAGATGC[G/T]GTGAGGCGCCTGAGA	320713
rs28150711	snp	G/T	0.415225	0.187619	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978741	GGCGCAGGACTAAAT[G/T]AGACGCCAGTGTTCA	320713
rs28150712	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	GRCm38.p3	4:94978719	CGACTGGACCAGGTC[A/G]CTAGCGGGCGCAGGA	320713
rs28150713	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978356	AAAATCACACTGCCC[A/G]TCCTTGCAGGCACTG	320713
rs28150714	snp	A/C	0.231111	0.249285	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978141	TCTACAGTGGAGCAG[A/C]CCTCCTGTCAAATGA	320713
rs28150715	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94978118	GCCTTATAGAGGAGG[A/G]CTGGCAGTCTACAGT	320713
rs28150716	snp	C/T	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94977815	GAAAGTTAAAACGAA[C/T]CCTTGAGAGAGGCAC	320713
rs28150717	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94977801	CTAAACACAACCAGG[A/G]AAGTTAAAACGAACC	320713
rs28150718	snp	A/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94977774	AATGGTACAAGAAAA[A/T]GGGATGAAAAACTAA	320713
rs28150719	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94977725	TACGAGGTTAACATT[A/G]CAACATGCCACCAGT	320713
rs28150720	snp	A/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Mysm1, LOC105244623	Mm_Celera	4:94977711	TTTGAGACCTAACAT[A/T]CGAGGTTAACATTAC	320713
rs28150721	snp	A/G	0.391111	0.206368	intron-variant	Mysm1	Mm_Celera	4:94977042	TTCCACATAATGTCA[A/G]TGATGCTCCAGAAGC	320713
rs28150722	snp	A/G	0.207612	0.24638	intron-variant	Mysm1	Mm_Celera	4:94976716	GAAATTAAGTCAGGA[A/G]AGATGCCAGGCTTGG	320713
rs28150723	snp	C/T	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94976473	TGTTGCCATCATGCA[C/T]TGAACTAGGGACAGC	320713
rs28150724	snp	G/T	0.265928	0.249492	intron-variant	Mysm1	Mm_Celera	4:94976459	GGAGACTGTGTGGAT[G/T]TTGCCATCATGCACT	320713
rs28150725	snp	A/G	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94975866	TGGGTCAGTGCAGGA[A/G]AAAAAGCTAGCAAGC	320713
rs28150726	snp	C/G	0.260355	0.249785	intron-variant	Mysm1	Mm_Celera	4:94975775	ATCAATCTCCCTAGC[C/G]GTCCAAGACACTAGG	320713
rs28150727	snp	C/G	0.260355	0.249785	intron-variant	Mysm1	Mm_Celera	4:94975750	TGTATACTCTCTTAG[C/G]CCTTGTAACATCAAT	320713
rs28150728	snp	A/C	0.231111	0.249285	intron-variant	Mysm1	Mm_Celera	4:94975653	ATATGCATCAGAACA[A/C]CTACCTGAATCTCCT	320713
rs28150729	snp	A/C	0.124444	0.216185	intron-variant	Mysm1	GRCm38.p3	4:94975352	TTCAGCTACAGATCA[A/C]ATAAGACAGGGCCTG	320713
rs28150730	snp	A/G	0.132653	0.220748	intron-variant	Mysm1	Mm_Celera	4:94975072	CCTCTATTTTTAAAG[A/G]AAGTGTCTCCATATA	320713
rs28150731	snp	C/T	0.415225	0.187619	intron-variant	Mysm1	Mm_Celera	4:94974447	GACCTGTCCCTAAAT[C/T]AGCTGGATCTAAATT	320713
rs28150732	snp	A/C	0.359862	0.224567	intron-variant	Mysm1	Mm_Celera	4:94974373	TACATGAAGACATGA[A/C]CTCTAGGATTATCCC	320713
rs28150733	snp	C/T	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94973252	ATTCCCAAGTTCATG[C/T]GGTAATAACGGCCAC	320713
rs28150734	snp	C/T	0.48	0.0979796	intron-variant	Mysm1	Mm_Celera	4:94973246	TGTTGGATTCCCAAG[C/T]TCATGTGGTAATAAC	320713
rs28150735	snp	A/T	0.497778	0.0332592	intron-variant	Mysm1	Mm_Celera	4:94973190	TATCTGAAGCACTGG[A/T]GGCATGTTAAATGGA	320713
rs28150736	snp	C/T	0.444444	0.157135	intron-variant	Mysm1	Mm_Celera	4:94972790	ATAAGTGACATGAAA[C/T]TACACAATCAAAATC	320713
rs28150737	snp	A/G	0.387812	0.208586	intron-variant	Mysm1	Mm_Celera	4:94972757	CAGATTCACCAGTAA[A/G]CCATGCTTTTTGCAC	320713
rs28150738	snp	C/T	0.142012	0.225474	intron-variant	Mysm1	Mm_Celera	4:94972669	TTAAATATTCTACCG[C/T]TCCTAAGCATTTACG	320713
rs28150739	snp	C/T	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94972521	ATCAGTCTATTTTGT[C/T]TTTCATTAAAATTCT	320713
rs28150740	snp	A/G	0.391111	0.206368	intron-variant	Mysm1	Mm_Celera	4:94972445	CTCGAAGTTAAACTG[A/G]CGCAGAATACGCAGT	320713
rs28150741	snp	C/T	0.5	0	intron-variant	Mysm1	GRCm38.p3	4:94972340	GTTAGTAATCAATTT[C/T]TAAAGGCCAAAAAAA	320713
rs28150742	snp	C/G	0.391111	0.206368	intron-variant	Mysm1	Mm_Celera	4:94971320	TTGGAAGTGAACAAG[C/G]GACTCCTGTTCAATA	320713
rs28150743	snp	C/T	0.18	0.24	intron-variant	Mysm1	Mm_Celera	4:94971251	CACAAACACATATAT[C/T]CCTCTCTATTCTCAA	320713
rs28150744	snp	C/T	0.495868	0.0452663	intron-variant	Mysm1	Mm_Celera	4:94971193	TTCATTTAACAACTA[C/T]CAACCGCATGTCATA	320713
rs28150745	snp	A/G	0.152778	0.230321	intron-variant	Mysm1	Mm_Celera	4:94971099	ATTAATACAAGTAAC[A/G]TCAAATGTACCGAGA	320713
rs28150746	snp	G/T	0.497778	0.0332592	intron-variant	Mysm1	Mm_Celera	4:94971067	GTCACAGAAAAGAAC[G/T]CAGGATCCTTCTACA	320713
rs28150747	snp	A/C	0.495868	0.0452663	intron-variant	Mysm1	Mm_Celera	4:94970996	AATACAAGTAGTAAA[A/C]TGATGAATGTGTTGT	320713
rs28150748	snp	C/T	0.497778	0.0332592	intron-variant	Mysm1	Mm_Celera	4:94970887	AAACACACCACACAG[C/T]TCCTGCAGTCAGCAC	320713
rs28150749	snp	A/C	0.32	0.24	intron-variant	Mysm1	Mm_Celera	4:94970847	AAGCTGGTGCTTTCC[A/C]CAGCGTCAGTAGGAA	320713
rs28150750	snp	C/G	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94970738	TAAACAATATTAAAG[C/G]CATATAATTCTTATG	320713
rs28150751	snp	C/T	0.391111	0.206368	synonymous-codon, missense	Mysm1	GRCm38.p3	4:94970526	CATGGCTTTTGATGA[C/T]TTCTGCAGGCTGCAC	320713
rs28150752	snp	C/T	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94970099	ATCTTTAGGAAACTG[C/T]CTTTCTTTACTATGT	320713
rs28150753	snp	C/G	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94969987	AGTATTTACAAGTCA[C/G]AGATCCAAATAAAAC	320713
rs28150754	snp	A/C	0.46281	0.131194	intron-variant	Mysm1	Mm_Celera	4:94969588	CAGTAATATATTCCC[A/C]AAATCTAAGAGTTTA	320713
rs28150755	snp	C/T	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94969438	GTAAGGTTTACCCTG[C/T]TCTCTATCTCTATCA	320713
rs28150756	snp	C/T	0.497778	0.0332592	intron-variant	Mysm1	Mm_Celera	4:94969398	GAGGAGGGAAGGAGG[C/T]AGCTGAGGCAGCTGG	320713
rs28150757	snp	A/G	0.391111	0.206368	intron-variant	Mysm1	Mm_Celera	4:94969332	GAAAGGGGACTGGGA[A/G]CTGCTGTTAAACCAG	320713
rs28150758	snp	G/T	0.42	0.183303	intron-variant	Mysm1	Mm_Celera	4:94969120	AAATGAAATGGAACA[G/T]TCCATATTTATGCAG	320713
rs28150759	snp	A/C/G	0.336735	0.234472	missense, splice-acceptor-variant	Mysm1	GRCm38.p3	4:94969054	GTTTTGCAGGAGAAT[A/C/G]TACCCTGAAGGAAAA	320713
rs28150760	snp	A/G	0.152778	0.230321	missense	Mysm1	GRCm38.p3	4:94969030	TCCACTTTACTGAAT[A/G]ACTGGCTGGTTTTGC	320713
rs28150761	snp	C/T	0.497778	0.0332592	synonymous-codon	Mysm1	Mm_Celera	4:94969001	TTGTTCAAACAGCTC[C/T]TTCTCTTCTACTGTC	320713
rs28150762	snp	C/T	0.408163	0.193609	intron-variant	Mysm1	Mm_Celera	4:94968866	AAAGTATGGATTATG[C/T]ACAATGACAAACAGA	320713
rs28150763	snp	C/T	0.5	0	intron-variant	Mysm1	Mm_Celera	4:94968823	AGCATAACAAGAAAA[C/T]GTTTCTGGTCTTCAA	320713
rs28150764	snp	C/G	0.5	0	intron-variant	Mysm1	GRCm38.p3	4:94968444	ATCACATATTGAAAA[C/G]TTTGAAAAATCTCCA	320713
rs28150765	snp	A/G	0.336735	0.234472	intron-variant	Mysm1	Mm_Celera	4:94968380	CCTATTAAATGTCCT[A/G]TAGCAAACCTACTAC	320713
rs28150766	snp	A/G	0.497041	0.0383476	intron-variant	Mysm1	Mm_Celera	4:94968334	TCTGCACTAATTGCA[A/G]CTTTTAAACTCAGAG	320713
rs28150767	snp	C/T	0.152778	0.230321	intron-variant	Mysm1	Mm_Celera	4:94968329	CACCTTCTGCACTAA[C/T]TGCAACTTTTAAACT	320713
rs28150768	snp	A/G	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94968308	TTTTTTACAGAATCA[A/G]CTGGACACCTTCTGC	320713
rs28150769	snp	A/G	0.142012	0.225474	intron-variant	Mysm1	Mm_Celera	4:94967848	ATTTCGTCATTAATT[A/G]GGGTATCTGTACTCT	320713
rs28150770	snp	A/G	0.497778	0.0332592	intron-variant	Mysm1	Mm_Celera	4:94967807	TATAGTTTGCACTAA[A/G]TAATTATGCTCACTG	320713
rs28150771	snp	C/G/T	0.46875	0.121031	intron-variant	Mysm1	GRCm38.p3	4:94967446	AAACAAATAAAAAGC[C/G/T]AGTGGGCCAGTCAGA	320713
rs28150772	snp	C/T	0.32	0.24	intron-variant	Mysm1	Mm_Celera	4:94967291	GAATACACTGCTTTA[C/T]AGACTTTACAGCAGC	320713
rs28150773	snp	A/G	0.415225	0.187619	intron-variant	Mysm1	Mm_Celera	4:94966694	AAAAGGATCTCACCT[A/G]AGGCACTTCCAATTT	320713
rs28150774	snp	A/G	0.132653	0.220748	intron-variant	Mysm1	Mm_Celera	4:94966168	CTGAAGCTGTGGAGC[A/G]TCACACTGGATTTTA	320713
rs28150775	snp	C/T	0.387812	0.208586	missense	Mysm1	GRCm38.p3	4:94965496	TTTCAGCCCATGATG[C/T]AATTTCTGAGCTTGA	320713
rs28150776	snp	G/T	0.231111	0.249285	missense	Mysm1	Mm_Celera	4:94965337	GCATTTCATTTCCAC[G/T]TGAGTCCTGCCTCTC	320713
rs28150777	snp	C/T	0.132653	0.220748	intron-variant	Mysm1	Mm_Celera	4:94965071	ACAATTCTGCATGGG[C/T]CGAATCAATATACTT	320713
rs28150778	snp	A/C	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94965023	ACTACTGAAGGAAGA[A/C]ACGCAAAAGCTCTTT	320713
rs28150779	snp	G/T	0.244898	0.249948	intron-variant	Mysm1	Mm_Celera	4:94964803	TACATGTGAAAACTG[G/T]AAAGTCTCTCCTTTC	320713
rs28150780	snp	A/T	0.124444	0.216185	intron-variant	Mysm1	GRCm38.p3	4:94964488	ACTGAAACAGGACAG[A/T]GAAACCTTTGATAGA	320713
rs28150781	snp	C/T	0.124444	0.216185	intron-variant	Mysm1	GRCm38.p3	4:94964285	CGTCAGTTGTTTCTC[C/T]TGTGTATTCCTTACT	320713
rs28150782	snp	A/G	0.18	0.24	intron-variant	Mysm1	GRCm38.p3	4:94964110	ATGGGTCAGTGGCTC[A/G]TTGAAAGATCAAAGG	320713
rs28150783	snp	C/T	0.42	0.183303	intron-variant	Mysm1	Mm_Celera	4:94964032	AGATCTAGTTTAACC[C/T]ACATTTAAAAGCTAT	320713
rs28150784	snp	C/T	0.465374	0.126941	intron-variant	Mysm1	GRCm38.p3	4:94963967	TTTGAAGGCCTTCAA[C/T]TTTAGCTATCCATCT	320713
rs28150785	snp	A/T	0.188366	0.242283	intron-variant	Mysm1	GRCm38.p3	4:94963817	CGGACTTAGGAAACT[A/T]CTGCCATATAACTGA	320713
rs28150786	snp	A/T	0.132653	0.220748	intron-variant	Mysm1	Mm_Celera	4:94963606	AAAACCAATTGTACC[A/T]GTTCTCATGGAAAAG	320713
rs28150787	snp	A/G	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94963305	CATCGCCTTCCCTGA[A/G]TAGAACCAAAGAGCC	320713
rs28150788	snp	C/T	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94963281	AACAGGGAGGAGCAT[C/T]GCCACACACATCGCC	320713
rs28150789	snp	A/G	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94963215	ATTCACAAAATGGGA[A/G]CATTTTCAGTGGTGT	320713
rs28150790	snp	A/G	0.231111	0.249285	intron-variant	Mysm1	Mm_Celera	4:94962988	GGGGTCTGAGAACCG[A/G]CTTTGTCTACCTCTG	320713
rs28150791	snp	C/T	0.124444	0.216185	intron-variant	Mysm1	Mm_Celera	4:94962666	AGATGCAGACAGTGA[C/T]GCAGGCCTTAACTGA	320713
rs28150792	snp	G/T	0.188366	0.242283	intron-variant	Mysm1	GRCm38.p3	4:94962639	ACTTAACATGAAGAA[G/T]TGGAGAGATGCAGAT	320713
rs28150793	snp	A/C	0.18	0.24	intron-variant	Mysm1	Mm_Celera	4:94962523	GAAATCAATGCTGCA[A/C]TGTTAGGTAGACAGG	320713

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