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
rs3656411	snp	A/G	0.42344	0.180051	intron-variant	Fchsd2	GRCm38.p3	7:101222804	TTCCATTTTTGTCTA[A/G]ATTCCTCTGTTCTGT	207278
rs3657035	snp	A/C	0.362812	0.2231	intron-variant	Fchsd2	GRCm38.p3	7:101222906	GAAAATAAACATAGA[A/C]ACCTAATCTCAAACC	207278
rs3674231	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101179628	CTTCCTTTTCCCTCT[C/T]CAAATCTTCCCGTAC	207278
rs3674798	snp	C/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101179704	TATTGCTACATATGT[C/G]TATGTGTGTATGCAT	207278
rs3679370	snp	C/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101217715	AGCCATCTCTCTAGC[C/T]CCAGTATTAATATTT	207278
rs6155955	snp	A/G	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101275245	GTATTTTTGTGTATG[A/G]TATTGTGTTCCTATT	207278
rs6156378	snp	A/T	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101275260	GTATTGTGTTCCTAT[A/T]GAAAGGATGGCCCTT	207278
rs6245271	snp	A/T	0.415225	0.187619	intron-variant	Fchsd2	Mm_Celera	7:101133405	GCACTGAATGACAGG[A/T]TTTTGAGGTGAACAA	207278
rs6250697	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214400	caaagagtacacacc[A/G]gggacccatggctcc	207278
rs6251625	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214561	aggagctccctcata[A/G]aggcagggggatggg	207278
rs6251648	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214581	agggggatgggggag[A/G]ggataggggtttgtg	207278
rs6252140	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101214684	TAAAAGGGCTTTTTA[C/T]AGCATACCAGCCTAT	207278
rs6284925	snp	C/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101222781	TTCCTCTGCAGAAAA[C/T]ATTAAATTTCCATTT	207278
rs13474820	snp	A/T			utr-variant-3-prime	Fchsd2	Mm_Celera	7:101284229	AAAATATGCCTCCtt[A/T]ttaaaaataaataaa	207278
rs13479429	snp	C/T	0.464806	0.127899	intron-variant	Fchsd2	Mm_Celera	7:101171025	TTTTTCCCCTGATGC[C/T]AGAACAGAACCTAGG	207278
rs31046427	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101274748	AGAAAGAGCATTGTG[C/T]GCTCAGAGAACAGGA	207278
rs31046740	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101255665	AGTATCTGTAAAATT[C/G]TCTTCAAATGAGCTC	207278
rs31049794	snp	C/T	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101228338	AACGACATGTTTTTT[C/T]CTCCTAATTCCTAGC	207278
rs31052011	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101282066	GATCACAAGTGTGTG[C/T]CACCCTGCCTGACTA	207278
rs31053090	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101275283	TGGCCCTTTGTAGTC[A/C]AGGCTAGCCTAGAAT	207278
rs31055185	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101238411	TTTCCCGGGCGGCGA[C/G]CGGGAATCCCTGTGA	207278
rs31056013	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101218378	TATGCAGCTGGAGCC[A/T]TGAGTCCCACCATGT	207278
rs31058533	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101136905	GTGTATGTGGAGGTC[A/G]AAGGACAACTTATGA	207278
rs31078157	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101230348	CAATAACCAAAAGAA[A/G]GACAGGCAAGCGTCA	207278
rs31080605	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101166911	AACAGCCAGGATGGT[A/C]CAGCCCACTATAAAA	207278
rs31085924	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101248528	GGTGAGTCTCTGTAA[A/C]TGGAACGCCTAGTCA	207278
rs31089870	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	Mm_Celera	7:101134634	TGATCATATCTTCTC[A/G]TGTGCTAAGTAGAGC	207278
rs31089872	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101219600	GGTGTTGCTGCCACA[C/T]CCAGCCATGATCTTA	207278
rs31089966	snp	C/T	0.444444	0.157135	synonymous-codon	Fchsd2	GRCm38.p3	7:101198522	TACCAAAGCTACCCA[C/T]GCAAGGAATGATTAC	207278
rs31090529	snp	G/T	0.304688	0.243945	intron-variant	Fchsd2	GRCm38.p3	7:101128545	CTAGTTCATGCGTTT[G/T]AAATTAATGATTTGT	207278
rs31092837	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101111675	CAAAAAAATCAAAAA[C/T]CCAAAGGTACTGTAA	207278
rs31099485	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101264114	GGGATTAAAAGCATG[C/T]TCCACCACCGCCTAG	207278
rs31103422	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101157650	TGGTATATTAAAAAA[A/T]TATTTTTTCTTTTTT	207278
rs31114260	snp	C/T	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101271849	TGAAATATTGAGTCT[C/T]TGCTGTCTGACTTTT	207278
rs31147670	snp	C/T	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101260007	TGGGCTATTGGTGTC[C/T]GTCCCCCAAACTTAT	207278
rs31148162	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101119228	ATTGGCCCAGGGACT[C/T]CCTGTGTGGCTGAAG	207278
rs31148715	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101248716	TAGTAATATGCCTAG[A/G]GTTAGTGGGTCATAC	207278
rs31149587	snp	C/T	0.415225	0.187619	intron-variant	Fchsd2	GRCm38.p3	7:101121845	TCTAGTCTTCACATG[C/T]GTGTGTGTTCATGTA	207278
rs31151822	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101224621	TAGAGCTTTCAGATG[C/T]AATTTTAAATTGTTG	207278
rs31151957	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101229335	AATAATTAAAAATAA[A/T]TTTTAAGAATAGTTT	207278
rs31152316	snp	A/G	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101222043	CAAAGATGTAGACAA[A/G]AAGAGCCTGCGGTAG	207278
rs31157140	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101266258	AATTGGCTCTTTTAT[A/G]ATTTTTTTTTTTCTT	207278
rs31160494	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101157652	GTATATTAAAAAAAT[A/T]TTTTTTCTTTTTTTT	207278
rs31182268	snp	C/T	0.359862	0.224567	intron-variant	Fchsd2	GRCm38.p3	7:101228162	CTATTTTAGAAATGT[C/T]CAGTGGTCTCAGAAA	207278
rs31183078	snp	G/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101269415	GGTTCATGTAGCCCA[G/T]ACTGGCCTGAACTCA	207278
rs31185067	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101139033	TCATAAAGAGGAATA[C/T]ACCCCCCTCCATATA	207278
rs31185770	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101242572	GTATATTGACGCCTA[C/T]TTGATTATGATGGAT	207278
rs31186959	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101275950	TGAGTTTCCTCCAGG[C/T]TCTGAGTCTCAGAAG	207278
rs31194822	snp	A/G	0.231111	0.249285	intron-variant	Fchsd2	Mm_Celera	7:101224475	TGTTGACTTTCTCAA[A/G]GAACCAGCTCTTGGT	207278
rs31196188	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101171411	TAGAATTAAAGTTAT[C/T]CACTACCATGCCATG	207278
rs31196675	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101238910	GCCGCTGACCAGTCC[A/G]CTACCTCTCCAGCTG	207278
rs31198525	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101110126	GAAATCCCAGGGTCC[G/T]GCCTGGCGAGGATGG	207278
rs31200488	snp	C/G	0.375	0.216506	upstream-variant-2KB	Fchsd2	Mm_Celera	7:101107253	TCACACTGTGGCTGC[C/G]TGTGGAGCTGTGGCT	207278
rs31200746	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101266948	CACACTGTCCTCAGC[C/T]TGGAAACTTCTTCTG	207278
rs31201734	snp	C/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101155369	TTCATACGTGTACTC[C/G]CAGCCCTCAGTAGGC	207278
rs31202802	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101210440	TTCAATATCTTTCCT[A/G]TGTTCCCTTGAATCC	207278
rs31211060	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101239513	GCCATGTCTTTTTAA[A/C]AACAAAAACCCCTGG	207278
rs31212386	snp	A/C	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101220378	AGCCTTGTCTATATA[A/C]ATTTAAAAATATTAC	207278
rs31229229	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101206890	CTTGGTGGCTATAGG[C/T]TGGGGTAATTCTCAT	207278
rs31236875	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101261072	CCTATCTGTAAGCAC[A/T]CCATAGCATCAGTAA	207278
rs31240750	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101208215	GCCACTGGTCAGTAA[C/T]TTCTAACTCCTCTTT	207278
rs31244614	snp	A/G	0.456747	0.140554	intron-variant	Fchsd2	GRCm38.p3	7:101276322	TTTGGAGTACATGGA[A/G]GTATTATGCTGAATA	207278
rs31245262	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266173	TGCTTTTTTGTTGTT[A/G]TTGTTTTCCTGTTTT	207278
rs31246396	snp	A/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101228149	CTTTTGCCCAGCACT[A/G]TTTTAGAAATGTCCA	207278
rs31251887	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101223653	AGTTCTCTGGCAGAG[G/T]TTTTGGGGCTACTTA	207278
rs31255913	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101162060	ATATATCCCTTGTCT[C/T]ACATGTACAGCTTTT	207278
rs31259501	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101129477	CAGGGGTAGTAATGT[C/T]CTTTTTATTGGGCAC	207278
rs31263421	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101167560	TTTGTATCTCCTCCC[A/G]TGGGTATTTTGTTCC	207278
rs31268927	snp	A/G	0.21875	0.248039	intron-variant	Fchsd2	GRCm38.p3	7:101117486	TTCCACAAGAAGAGC[A/G]AAGATGTGATTGTTT	207278
rs31269014	snp	A/G	0.493827	0.0552116	intron-variant	Fchsd2	GRCm38.p3	7:101116396	ACTATTACCTGCTAA[A/G]ACATGCTTTTAGGCC	207278
rs31280093	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101238412	TTCCCGGGCGGCGAG[C/T]GGGAATCCCTGTGAG	207278
rs31281962	snp	G/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101129251	GGAGAAGGATTTGCT[G/T]AGCTTGGGGAACAGT	207278
rs31283923	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101272338	AACAACTAGAGCTCC[C/T]TTTGCCCTTACAGAG	207278
rs31287431	snp	A/G	0.277778	0.248452	intron-variant	Fchsd2	GRCm38.p3	7:101123825	CTGCTGGGCTGGATG[A/G]GTGACAGGGATCCAC	207278
rs31287968	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101196647	GCCAGCAAACATGAA[A/T]AACTTATTGCAGGGG	207278
rs31297478	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101201824	TACAATGAGCAGATA[C/T]GTGACAGGGAGGTAG	207278
rs31299401	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261415	CACACACCTCCCGAG[A/G]TTACCTGTGCCTGTT	207278
rs31301721	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101131768	CTGTCTCAGACGCCT[A/G]AGAGCTGGGGTTAGT	207278
rs31313002	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153409	CATAAAACATATTTA[A/T]AAAAAAAACTAATTT	207278
rs31322659	snp	G/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101169409	AGGTTTTTGTTTTTT[G/T]GGGTTTTTTTTCTGA	207278
rs31323274	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153410	ATAAAACATATTTAA[A/T]AAAAAAACTAATTTG	207278
rs31328813	snp	G/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101132485	ATAGTTCAATCTACT[G/T]TGGGAAAGTCTGAGC	207278
rs31338986	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101219506	TGTGTAGCCTTAGCT[C/G]TCCTGGAATTCACTC	207278
rs31341364	snp	C/T	0.401235	0.199068	intron-variant	Fchsd2	Mm_Celera	7:101138968	TTGTTACTGCAACTG[C/T]TGTGAAAAACGGCAG	207278
rs31342117	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101263665	AGTTGCACTAAGGCA[A/G]TCTGACAGTCTGCTT	207278
rs31343984	snp	A/C	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101190709	GTGATAAAGTATATG[A/C]ACAGTTACAAGGCCC	207278
rs31359195	snp	A/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101209136	ACAATGGCATGTTAA[A/T]TAGTTGTACCAAGAG	207278
rs31373111	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101224410	AATTTTGTTAGTTTG[A/G]ATACTGTCTCTCTGC	207278
rs31373592	snp	C/T	0.42	0.183303	intron-variant	Fchsd2	GRCm38.p3	7:101187991	TACCAAAGCCTCTCA[C/T]ATTTTCTCATTCTGG	207278
rs31376575	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101267707	CCGCTACAGAAACTC[A/C]CACAGGGTTCTTCTT	207278
rs31381535	snp	C/T	0.401235	0.199068	synonymous-codon	Fchsd2	GRCm38.p3	7:101276925	CAGTCTTTGGCTGCT[C/T]TGGACAGTCGGTCAC	207278
rs31383500	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101209300	TGGCTGGAAGCCCAC[A/T]AGTGATTGTCCAGTG	207278
rs31389068	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101228809	ACTTCTTGATCTTAC[A/G]GAGGACCCTGGCATG	207278
rs31396415	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101209560	AAATTTGGTTTTTTT[G/T]GGGACAGTTTTTCTT	207278
rs31399591	snp	A/G	0.432133	0.171253	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284732	AACCTTTTACTCACT[A/G]AGCCATGGATGTGGA	207278
rs31405110	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101173930	AATTAATTAGTGTAG[A/G]TAATTTTCTTTGTAA	207278
rs31410606	snp	A/G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101247326	TCTTGTATTGAAGCA[A/G/T]ATGTCATTTCAGCAA	207278
rs31411954	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101208253	TCTTGCCTGTTATTT[A/T]TTTGTCTGTATAAAT	207278
rs31423807	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101144857	TGTGTGTTTTATCAC[C/T]AGTGGATTTGCTGGC	207278
rs31424196	snp	A/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101258466	CATTCAAAGACTCCT[A/G]AACACAGTTAGGAGA	207278

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