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
rs3090410	snp	C/T	0.21875	0.248039	intron-variant	Fbxo10	GRCm38.p3	4:45077664	AAGGTTCTCTGCTTC[C/T]GCCTGTGGGTTCCAA	269529
rs3090411	snp	A/T	0.21875	0.248039	intron-variant	Fbxo10	Mm_Celera	4:45077625	TTCAAGTTGTAAGAT[A/T]TAATGGCCATTTTGC	269529
rs6211837	snp	G/T	0.415225	0.187619	intron-variant	Fbxo10	Mm_Celera	4:45040277	GGAAGAACACTGTAC[G/T]AATCACACACGTGTG	269529
rs6212390	snp	C/T	0.290657	0.246672	intron-variant	Fbxo10	Mm_Celera	4:45040394	CCAACTACAACTGCA[C/T]GTGCCTAAATGAAAG	269529
rs6212883	snp	A/C	0.5	0	intron-variant	Fbxo10	Mm_Celera	4:45040488	tgtgctcacacagga[A/C]gtgcattacccaggg	269529
rs27826398	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Fbxo10	Mm_Celera	4:45086405	ACGAGGGCACATACA[A/G]TCTCCACGGCCATGT	269529
rs27826399	snp	C/T	0.35503	0.226867	upstream-variant-2KB	Fbxo10	Mm_Celera	4:45086365	CTTAGCAGCCTGGCA[C/T]GTCATTCGTATTTAT	269529
rs27826400	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Fbxo10	Mm_Celera	4:45086333	CTACTTCATTTGACT[A/G]GAGTGGGCTTGCTCA	269529
rs27826401	snp	A/G	0.142012	0.225474	upstream-variant-2KB	Fbxo10	Mm_Celera	4:45086029	ATTCAAAGGACAACA[A/G]TGGGGCCCGTCTAAC	269529
rs27826402	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Fbxo10	Mm_Celera	4:45085860	GCTTACGTTTGGCAA[A/G]CCGATCGCACGTCTA	269529
rs27826403	snp	A/T	0.124444	0.216185	intron-variant	Fbxo10	Mm_Celera	4:45073623	CTAATTTGGACTGAC[A/T]GCATTCAGCTAGGAG	269529
rs27826404	snp	G/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45073337	AGGTTTCACAGCTGG[G/T]GATGGTACAGGACCC	269529
rs27826405	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45073160	TATTTTGAGGACTTA[C/T]TGTGTCACCTCAGTG	269529
rs27826406	snp	A/C	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45072679	GTTTCTTCGAGCCTT[A/C]GTCCTCTTCAGCCTG	269529
rs27826407	snp	C/G/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45071866	GCGTAAGGCGGGTGT[C/G/T]AGGACAAGCTCTGAG	269529
rs27826408	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45071853	CAGATGAGCACAGGC[A/G]TAAGGCGGGTGTGAG	269529
rs27826409	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45071852	TCAGATGAGCACAGG[C/T]GTAAGGCGGGTGTGA	269529
rs27826410	snp	A/C/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45071086	ATGGCACATGGTTTC[A/C/G]GTGGTCTTCTGACCT	269529
rs27826411	snp	A/T	0.124444	0.216185	intron-variant	Fbxo10	Mm_Celera	4:45070997	TGCATGCAAGCAACA[A/T]CCTGGCTCAAAAAAA	269529
rs27826412	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45070263	AAAGGACAAAGTGCA[C/T]ATAACATCCTTCAAG	269529
rs27826413	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45070110	CAGGCCATCAGGGAC[A/G]GTCTCTAGGGAAGTG	269529
rs27826414	snp	A/G	0.142012	0.225474	intron-variant	Fbxo10	Mm_Celera	4:45069761	CGAGTCTATTTCCCC[A/G]ATCTCTCACCAAATG	269529
rs27826415	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45069452	CCCCTGGGCCTGTGC[A/G]CTTGTAGTGTGACGT	269529
rs27826416	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45068320	GCCTATGATGTAGCC[A/G]TTGGTGGCAGTTCAC	269529
rs27826417	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45067882	GGTGTCTGGCTCTTA[A/G]TTACTTCCTCAGTCG	269529
rs27826418	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45067862	GCTCCTCTCAAAGCT[A/G]AGCAGGTGTCTGGCT	269529
rs27826419	snp	A/T	0.142012	0.225474	intron-variant	Fbxo10	Mm_Celera	4:45067784	GCTGTTCTGAAGACA[A/T]GAGGCGATACCTCTG	269529
rs27826420	snp	A/G	0.244898	0.249948	intron-variant	Fbxo10	Mm_Celera	4:45067498	AGAAGCTAAGAGCTC[A/G]GGGCTAGTCTGTTAC	269529
rs27826421	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45067099	AATTGTTTCCTCAAC[C/T]GGATGTAAATTTACC	269529
rs27826422	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45066953	AAAGGATGCCCTAGG[C/T]CACAATTCAACGACT	269529
rs27826423	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45066593	TCTTTCAGGGAGCAC[C/T]ACATGGCAGGAGTGC	269529
rs27826424	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45066560	TCACACTGGTCCTCC[A/G]GAGTGAATGTGCACT	269529
rs27826425	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45066507	GGCTCTGACCTACTT[C/T]TACACCCATGCTTTC	269529
rs27826426	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45066366	GACTTCAATTTAAAA[C/T]CACCAGAGCTACCAC	269529
rs27826427	snp	A/C	0.124444	0.216185	intron-variant	Fbxo10	Mm_Celera	4:45066288	AGTTCCAGTTGATCT[A/C]TCCAGTGCTCATTTA	269529
rs27826428	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065747	GGGCATCCCAGTTTC[C/T]GGCCAGTCTCTAAGC	269529
rs27826429	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065616	GCTCTAGATGTACAC[A/G]ATATTCTGGTTGCTG	269529
rs27826430	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065565	ACAGCCGGCCCTCCA[C/T]AGGCTGCATCTGATA	269529
rs27826431	snp	A/C	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065403	CTGGCTTGGCGACTC[A/C]CTGGTGTAATCCTAG	269529
rs27826432	snp	G/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065398	TGGTCCTGGCTTGGC[G/T]ACTCCCTGGTGTAAT	269529
rs27826433	snp	C/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065281	CGGTCCTAGAGTCTG[C/G]ATGTCCTAGATACAA	269529
rs27826434	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45065171	AAAAAAAAGGTGAGG[A/G]CAGGTGCATGTATCC	269529
rs27826435	snp	G/T	0.132653	0.220748	intron-variant	Fbxo10	Mm_Celera	4:45063852	GACTTCTCAGGGATT[G/T]TCACCCAATAGTCTC	269529
rs27826436	snp	A/T	0.277778	0.248452	intron-variant	Fbxo10	Mm_Celera	4:45062590	TTATTGTTCCCTTTT[A/T]AAAAATAACACCTCC	269529
rs27826437	snp	C/T	0.132653	0.220748	synonymous-codon, downstream-variant-500B	Fbxo10, Gm30939	GRCm38.p3	4:45062090	CTTCAGGATGATTTC[C/T]CCTTGCTCCTCGTAC	269529
rs27826438	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061691	GCTCTTGCTGATCTT[A/G]TTAGGAATAGAAGAG	269529
rs27826439	snp	G/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061659	TGCATGACTGCCACC[G/T]CACCACTCTACCTGG	269529
rs27826440	snp	G/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061633	GCTCAGCTAATGTCC[G/T]GTCACCACACTGCAT	269529
rs27826441	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061575	CTGCACAGGATGAGG[A/G]TTCAGATCCTGAGGG	269529
rs27826442	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061523	TGGACTGGTATTTCC[C/T]GACTTCCCTCCAGGT	269529
rs27826443	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061483	TGTTCAGAAGGTGAC[C/T]GCTCTGTGCTAATGA	269529
rs27826444	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061454	CAGGGCCACCAGCTC[C/T]TCTACACACGCTTTG	269529
rs27826445	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061437	ATAGGCTCTGTGTTT[C/T]ACAGGGCCACCAGCT	269529
rs27826446	snp	G/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061409	CTGTAACAGGGCCAC[G/T]TCCAGCCAATGCATA	269529
rs27826447	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061344	ACTGAGTGTCTGGAA[C/T]GGCCAGTGAGGTACT	269529
rs27826448	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061259	CTATAAAACCAGGTG[A/G]CACAACATCCTCTGA	269529
rs27826449	snp	A/G	0.142012	0.225474	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45061106	CTCATCTGCCCAAGG[A/G]CACCACAGCTACTGA	269529
rs27826450	snp	C/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060683	AAAACTTCTGGGACA[C/T]TGTCAGATCTCTGTG	269529
rs27826451	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060601	CAGTGAAGCCCATCT[A/G]CCCTCTTGGCCCTTT	269529
rs27826452	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060353	GTAGGATGGGAACGT[A/G]CCGAACCTGCTAAGT	269529
rs27826453	snp	C/T	0.142012	0.225474	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060326	AAGACACAAGGACCT[C/T]GGGAGTCTGGGGTAG	269529
rs27826454	snp	A/C	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060297	ACTCAGACAGCTATT[A/C]TTATCTGAGGTCAAA	269529
rs27826455	snp	C/G	0.142012	0.225474	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060292	GTCAGACTCAGACAG[C/G]TATTATTATCTGAGG	269529
rs27826456	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45060069	GTTTGCAATGCAAAC[A/G]ACAGGTCTCATCTTC	269529
rs27826457	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45059976	CAAGAAGAGATTTAA[C/T]ACTTCTGTGACCAGG	269529
rs27826458	snp	G/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45059691	TGGATTTCACAAACA[G/T]AGGAGCTAGTGCAAT	269529
rs27826459	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Fbxo10, Gm30939	Mm_Celera	4:45059566	GTACAGTGCTTGCCT[A/G]GCACGCAGGCAGGAA	269529
rs27826460	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45059399	CCCACACTCTACAGC[A/G]GGACCCAGTATGTAT	269529
rs27826461	snp	G/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45059216	GGTTATCACCAAGCT[G/T]CTCTTCAAGGAGGGC	269529
rs27826462	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45059180	GAGAAGACTCAGTCA[A/G]AAGCCTACACTTGTT	269529
rs27826463	snp	A/G	0.132653	0.220748	synonymous-codon, intron-variant	Fbxo10, Gm30939	GRCm38.p3	4:45059088	GCAGGTACCTGGACC[A/G]TGGACCTGGATGTGT	269529
rs27826464	snp	A/G	0.124444	0.216185	synonymous-codon, intron-variant	Fbxo10, Gm30939	GRCm38.p3	4:45058839	CCAGGCCTGGTCCCG[A/G]CTCTCTAAGTCCAAG	269529
rs27826465	snp	A/G	0.244898	0.249948	synonymous-codon, intron-variant	Fbxo10, Gm30939	GRCm38.p3	4:45058650	TGTGAGCTGTTCGTC[A/G]TCCTCATCCTCCCCG	269529
rs27826466	snp	A/C	0.132653	0.220748	synonymous-codon, intron-variant	Fbxo10, Gm30939	GRCm38.p3	4:45058518	CTGCAGCTCCTGATG[A/C]AGTGAATTCAGCACT	269529
rs27826467	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45057822	CGTGGGTGACTCAGC[C/T]TCGCAAACAGCTCAG	269529
rs27826468	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45057807	AATGTGTTCCAGCTG[C/T]GTGGGTGACTCAGCC	269529
rs27826469	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45057338	TGAGACCCAAGGCCA[C/T]GGTAGTGCTATGCTC	269529
rs27826470	snp	A/G	0.244898	0.249948	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45056628	TGTGTGAAGAGAAAA[A/G]TCCTCTGCAGGGACC	269529
rs27826471	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45056159	CTCACCTCTTGTACT[A/G]GGAGTCTTCACCTGC	269529
rs27826472	snp	A/G	0.124444	0.216185	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45056013	GTGCTTCTTAGTCAC[A/G]TTCCAGAATCTCACC	269529
rs27826473	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45055916	CCTGGCCCTTCTCTC[C/T]CAGGTTGCCCTGTGC	269529
rs27826474	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45055764	AGAAGACGGCAGCTC[C/T]GCTGAGTGTCAATGT	269529
rs27826475	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45055720	GTGCACCCAGCGTGT[A/G]AGCACACACCTTTCC	269529
rs27826476	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45055541	TTATTGTCAGAATCC[C/T]TGAAAATCAGTTGCC	269529
rs27826477	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45055536	TTCCCTTATTGTCAG[A/G]ATCCCTGAAAATCAG	269529
rs27826478	snp	C/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45054770	ATGTGTCTCTGGTCC[C/T]ATTCTTTGTTGTGCA	269529
rs27826479	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45054730	AGTCATATGGCCATG[A/G]AGTATACACATTTTA	269529
rs27826480	snp	A/C	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45054525	GGTAAAGGCAACACA[A/C]CCCAGGACCCTTAGG	269529
rs27826481	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45053685	TTCCAGCATATTTGA[A/G]TATGGAGGAATGTGG	269529
rs27826482	snp	A/C	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45053556	GCACAAGACAACTCA[A/C]ACATATTAAAGGAAT	269529
rs27826483	snp	C/T	0.142012	0.225474	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45053262	TGAAAAAAAGGAACC[C/T]GAGAGAGCTCAGTCT	269529
rs27826484	snp	A/G	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45053258	TGCATGAAAAAAAGG[A/G]ACCCGAGAGAGCTCA	269529
rs27826485	snp	A/T	0.132653	0.220748	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45052375	CAGTCTCCTGTATCC[A/T]GCGTGACCCTGCCCT	269529
rs27826486	snp	C/T	0.142012	0.225474	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45052368	GAGGACACAGTCTCC[C/T]GTATCCAGCGTGACC	269529
rs27826487	snp	C/T	0.132653	0.220748	missense, intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45051699	CATTCCTGAGCATGA[C/T]GATCTAAACAGAACA	269529
rs27826488	snp	C/T	0.32	0.24	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45050223	TAAGAACATCAAGCA[C/T]GGGCCACACTGCCCT	269529
rs27826489	snp	C/T	0.124444	0.216185	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45050122	TAGGGACATGGGTAG[C/T]CATGACACATTTCAC	269529
rs27826490	snp	A/G	0.124444	0.216185	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45049892	TGTGCACAGTCCCAA[A/G]TAAAGCCCTAAGCTC	269529
rs27826491	snp	C/T	0.124444	0.216185	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45049871	TGCTTTCTCCATGAC[C/T]GAGCATGTGCACAGT	269529
rs27826492	snp	A/G	0.124444	0.216185	intron-variant	Fbxo10, Gm30939	Mm_Celera	4:45049673	CTACCCTTTCTCTCC[A/G]GCTGCAGCTATGGCA	269529

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