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
rs3141633	snp	A/G	0.124444	0.216185	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Arhgap4, Avpr2	Mm_Celera	X:73894622	GCATAAGAGGAGCTC[A/G]TCTCCAGCTTCCTTC	171207
rs3157222	snp	A/G			frameshift-variant, intron-variant, nc-transcript-variant	Arhgap4	GRCm38.p3	X:73904431	GTGTAGCTCCGGAGC[A/G]CCTGCTCCAGGGCCA	171207
rs3161197	snp	C/G			synonymous-codon, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73904431	TGTGTAGCTCCGGAG[C/G]ACCTGCTCCAGGGCC	171207
rs29038708	snp	A/G/T	0.35503	0.226867	upstream-variant-2KB	Arhgap4	GRCm38.p3	X:73913257	AACTAGCCTTCAAAT[A/G/T]TTCTTAGTCCTTAAT	171207
rs29038709	snp	A/G	0.142012	0.225474	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73913202	CCCATCCAAGCAGCA[A/G]AGCCAGACCAGGATT	171207
rs29038710	snp	A/C	0.142012	0.225474	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73911848	CCCTTCTACTCAGCC[A/C]CAAAGGAAAGAACTA	171207
rs29038711	snp	A/C	0.142012	0.225474	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73911709	GACATCAGATGCCAC[A/C]CTCCTTCCAGAGTCA	171207
rs29038712	snp	A/G	0.152778	0.230321	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73911520	AAAGCAGCAATGCAA[A/G]ACAACCTCAACATGT	171207
rs29038713	snp	A/T	0.142012	0.225474	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73911423	GTGGGCCTCTGAAAG[A/T]CTAGGCACCCCTTTT	171207
rs29039104	snp	C/T	0.277778	0.248452	utr-variant-5-prime, nc-transcript-variant	Arhgap4	Mm_Celera	X:73911296	GGCGAGACCGCCAAG[C/T]GCAGGGACTAGGGGC	171207
rs29039105	snp	C/T	0.142012	0.225474	utr-variant-5-prime, nc-transcript-variant	Arhgap4	Mm_Celera	X:73911264	CTTCGAGTCCCAATG[C/T]TCCCACGCGGAAGCG	171207
rs29039106	snp	C/G	0.426035	0.177515	utr-variant-5-prime, nc-transcript-variant	Arhgap4	Mm_Celera	X:73911234	TGCGCCGCCATGGCC[C/G]AAGGCCGTTCGCGAC	171207
rs29039107	snp	A/C	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73911100	CCTGCTCCAGGCACC[A/C]CTGAGATCAGCAGCG	171207
rs29039108	snp	A/G	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73910839	GAGGTGAAGGTGCTA[A/G]GAATTCATAGATTCT	171207
rs29039109	snp	C/T	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73910812	ACCTGCAAGCTAATA[C/T]AGTGCCAAAGGGAGG	171207
rs29039110	snp	A/T	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73910392	TTGCTTGCACCAAAT[A/T]AGTACATTGGAATTT	171207
rs29039111	snp	C/T	0.375	0.216506	intron-variant	Arhgap4	Mm_Celera	X:73910355	AACAGCAACACATCA[C/T]GAAGATACACTTTGT	171207
rs29039112	snp	A/T	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73909127	TAAAGAATGGCAATT[A/T]AAGTTCAAGTAGGGT	171207
rs29039113	snp	A/G	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73909081	CTGACTTCTATCGGG[A/G]AAATCTCCACTAAAT	171207
rs29039544	snp	A/G	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73908937	GTTAGGCAGATGGGA[A/G]CTGGTGTGTATGTAT	171207
rs29039545	snp	C/T	0.35503	0.226867	intron-variant	Arhgap4	Mm_Celera	X:73908910	ATTGCTAATTTTCCA[C/T]TAAGGGTACAAGTTA	171207
rs29039546	snp	C/T	0.277778	0.248452	intron-variant	Arhgap4	Mm_Celera	X:73908790	ACTCTATGGTAATAC[C/T]GACTTCTCCAGCTGC	171207
rs29039547	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908698	TGAAAAGCCTTGTTA[A/G]GTATTTCCTATCCAG	171207
rs29039548	snp	A/C	0.165289	0.235211	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908620	TATTCAAAGAAACCC[A/C]CTGTAAAGAAATCAG	171207
rs29039549	snp	C/T	0.277778	0.248452	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908588	AGCAAGTCTGAAAGG[C/T]AAGACCCAGGAGTAT	171207
rs29039550	snp	A/C	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908576	TGGGACTCAGAGAGC[A/C]AGTCTGAAAGGTAAG	171207
rs29039551	snp	G/T	0.35503	0.226867	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908428	CTTGTGGTCTAGAAT[G/T]CTCATCTGGATGCCC	171207
rs29039552	snp	A/G	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908383	GAAAAGCAAGTGGGA[A/G]GAATCTGGGAGGGAG	171207
rs29039553	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73907226	AGCCATGGCCAAGTG[C/T]TGATAAGTGAAGGGA	171207
rs29039974	snp	C/T	0.165289	0.235211	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73907072	AGAAGCCCCTGTGCA[C/T]TTGGGAAGGGCCCTA	171207
rs29039975	snp	C/T	0.142012	0.225474	synonymous-codon, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73905792	CCGCTTCTCCTCTTG[C/T]CGCTCCGCTTCCCGA	171207
rs29039976	snp	C/T	0.260355	0.249785	intron-variant	Arhgap4	Mm_Celera	X:73905613	CAGAGCTATCAGAGA[C/T]GGACAGAGACAGGAG	171207
rs29039977	snp	A/G	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73905444	TTTAGGTCTGTTGAA[A/G]CATCTGTAACCTAAT	171207
rs29039978	snp	C/T	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73904798	CTACAGACAAGCATG[C/T]CCAATGTGCCGCAGG	171207
rs29039979	snp	C/T	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73904727	CTCAAGACACCAAGG[C/T]ACACCAGGGTCACTC	171207
rs29039980	snp	C/G	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73904237	AGTGGGTGTAATAAA[C/G]TAACCCTCACCTCAT	171207
rs29039981	snp	A/G	0.142012	0.225474	intron-variant	Arhgap4	Mm_Celera	X:73904077	TGGGCCAGAGGCTAT[A/G]GAATGGAGGACTGAG	171207
rs29039982	snp	C/G	0.426035	0.177515	intron-variant	Arhgap4	Mm_Celera	X:73904053	AGCTGCCACAGAAAA[C/G]TGTTCTAATGGGCCA	171207
rs29039983	snp	C/T	0.21875	0.248039	intron-variant	Arhgap4	Mm_Celera	X:73900987	GGAACACATAAAATA[C/T]GTGTCATGTTAAAAA	171207
rs29040394	snp	A/C	0.32	0.24	intron-variant	Arhgap4	Mm_Celera	X:73900765	TACCAGGGATGAGGA[A/C]TAGGTCAGAGCAGAG	171207
rs29040395	snp	C/G	0.32	0.24	intron-variant	Arhgap4	Mm_Celera	X:73900503	GGCAGTAAGTCAGGA[C/G]AGTATGGGAGGAACA	171207
rs29040396	snp	A/G	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Arhgap4	Mm_Celera	X:73900404	CAAAGAGTCCAGTAT[A/G]TCCCCATCCTCTGAT	171207
rs29040397	snp	A/C	0.391111	0.206368	missense, nc-transcript-variant	Arhgap4	Mm_Celera	X:73900147	TGGCCTGCAGCTTGG[A/C]AAGGATGCTCCGGCC	171207
rs29040398	snp	C/T	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Arhgap4	Mm_Celera	X:73900112	ACCTTGTTGTATGGC[C/T]TCCTGAAGTTTTTCA	171207
rs29040399	snp	C/T	0.391111	0.206368	intron-variant	Arhgap4	Mm_Celera	X:73899894	AGGAGAAAATATTTT[C/T]TTGTCTCTCAGGCTG	171207
rs29040400	snp	C/T	0.124444	0.216185	intron-variant	Arhgap4	Mm_Celera	X:73899828	GTGAATAGGCCAGCA[C/T]CCCATGAAGGACTCA	171207
rs29040401	snp	A/G	0.32	0.24	intron-variant, missense	Arhgap4	Mm_Celera	X:73899397	CAATAGCTTGCGCAG[A/G]AAGGAACACCTGAGA	171207
rs29040402	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Arhgap4	Mm_Celera	X:73898881	TGACAAAATTTGGGC[C/T]GGAAGTATGGCCTAT	171207
rs29040403	snp	A/T	0.32	0.24	intron-variant	Arhgap4	Mm_Celera	X:73898323	GATTTGCTGGTGACA[A/T]TGACATGGCATTTTA	171207
rs29040854	snp	A/G	0.124444	0.216185	intron-variant	Arhgap4	Mm_Celera	X:73897475	AGGCTGGGGAAACAC[A/G]AAGATCACAGGCAGG	171207
rs29040855	snp	A/G	0.32	0.24	synonymous-codon, nc-transcript-variant	Arhgap4	Mm_Celera	X:73897399	CACAGGCAACAGTGT[A/G]GGCCCAAAACATACA	171207
rs29040856	snp	C/T	0.32	0.24	missense, nc-transcript-variant	Arhgap4	Mm_Celera	X:73897305	CTGGAGGTGGGAAAA[C/T]CCGTGCTGGTTGCAG	171207
rs29040857	snp	A/G	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Arhgap4	Mm_Celera	X:73897240	ATACCCCAGGCAGCT[A/G]GCAGAAGGTGGTGCC	171207
rs29040858	snp	C/T	0.32	0.24	intron-variant	Arhgap4	Mm_Celera	X:73896185	AGAACCTCTCCAAGT[C/T]ACAAAAAGGCTGACT	171207
rs29040859	snp	A/G	0.32	0.24	synonymous-codon, nc-transcript-variant	Arhgap4	Mm_Celera	X:73896046	GGGTGCCTAGTTCCA[A/G]CCTACAAAGCAGAGA	171207
rs29040860	snp	A/C	0.32	0.24	intron-variant	Arhgap4	Mm_Celera	X:73895410	GGGACCATTCTTCCT[A/C]AGACTTAGTAACAGT	171207
rs31234007	snp	C/G	0.5	0	intron-variant	Arhgap4	Mm_Celera	X:73903296	ACACACACACACACA[C/G]ACAGAGAGAGAGAGA	171207
rs31663888	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Arhgap4	Mm_Celera	X:73913114	AATCAGGCACCAATG[C/T]CTTTATTAGTTAAAG	171207
rs31663889	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908443	GCTCATCTGGATGCC[C/T]AAGGAGATATAAGCC	171207
rs31663890	snp	C/T	0.142012	0.225474	synonymous-codon, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73905798	CTCCTCTTGCCGCTC[C/T]GCTTCCCGAAGTTTA	171207
rs31663891	snp	A/C	0.35503	0.226867	intron-variant	Arhgap4	Mm_Celera	X:73905201	CCTACTTAGCATGGG[A/C]GCCTCCCCACTCTTT	171207
rs31663892	snp	A/G	0.260355	0.249785	intron-variant	Arhgap4	Mm_Celera	X:73904785	TTTCTCATTCCCTCT[A/G]CAGACAAGCATGCCC	171207
rs31663893	snp	A/C	0.165289	0.235211	intron-variant	Arhgap4	Mm_Celera	X:73904528	GTCAAGGACTCCAAG[A/C]TTTTAAGCTCCAGTT	171207
rs31664644	snp	C/T	0.152778	0.230321	intron-variant	Arhgap4	Mm_Celera	X:73904011	GTTGTGATGGTTGCA[C/T]TGTGTTTGAGGGCAG	171207
rs31664645	snp	A/G	0.231111	0.249285	intron-variant	Arhgap4	Mm_Celera	X:73899968	GTTCAGGATAATCCA[A/G]TGACCTACACTGGGT	171207
rs31664646	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Arhgap4	Mm_Celera	X:73898990	CTGAGTTCCTTAAGT[A/G]TTTCCTTTAAAACTG	171207
rs31664647	snp	A/G	0.124444	0.216185	intron-variant	Arhgap4	Mm_Celera	X:73897052	ACACAGGAAAAAGAT[A/G]GGGTAGCGTCTCCCT	171207
rs33877140	snp	A/C	0.444444	0.157135	intron-variant	Arhgap4	Mm_Celera	X:73902482	AATTGTGCAGGAATT[A/C]TTTTTTTTTTTTTGA	171207
rs45856635	snp	A/C			intron-variant	Arhgap4	Mm_Celera	X:73910411	ACATTGGAATTTCAT[A/C]TACAGGTTGGAAAAC	171207
rs211796553	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73903223	AAGATATCCAATGGC[C/T]TCTTCTGACTTCTGT	171207
rs211955875	snp	C/G			missense, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73904359	CAAAGCCTCCAGAGC[C/G]TCTTCCAGGCTGCCT	171207
rs212256945	snp	A/G			intron-variant	Arhgap4	Mm_Celera	X:73905415	CATGGCCCTGTGGTT[A/G]TCTTTCCCCATCTTT	171207
rs212298677	snp	A/G			intron-variant	Arhgap4	Mm_Celera	X:73901395	GGAGAGGGGAACCTG[A/G]TCTGGTATTGGGTTA	171207
rs213128060	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73910005	ATTAGAGTGCCAAAA[C/T]AGTGCCCCTGTTCCA	171207
rs213284729	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73895617	AGCTCTAGGTGTCAG[C/T]CTTGAAGTTTGTCCT	171207
rs213330985	snp	A/G			intron-variant	Arhgap4	Mm_Celera	X:73905913	AGGTCATGACTAAGA[A/G]GAGTCCCTCAGCCCC	171207
rs213477692	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73908133	CCCCCCCAAAAAAAA[A/C]AAAAACAAAAACAAA	171207
rs214329924	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73904251	ACTAACCCTCACCTC[A/G]TCATCTTCATGGGGC	171207
rs214413837	snp	A/T			intron-variant	Arhgap4	Mm_Celera	X:73903116	TGAAGAGACGCCCAG[A/T]GGTTAGAAGTGATTA	171207
rs214456420	snp	G/T			upstream-variant-2KB	Arhgap4	Mm_Celera	X:73912128	CACTTTGTAGCCCTG[G/T]TTGGCTTTACACAAT	171207
rs214469135	in-del	-/TATTT			intron-variant	Arhgap4	Mm_Celera	X:73903742	TAATTAGAAATGATG[-/TATTT]CTACATGCTGTATTT	171207
rs214617395	snp	C/T			upstream-variant-2KB	Arhgap4	Mm_Celera	X:73913226	CAGGATTCAGGCACA[C/T]AAGAAATGGCTACTG	171207
rs215006550	snp	A/G			intron-variant	Arhgap4	Mm_Celera	X:73898673	TTGCAAATGACACTG[A/G]GGTTTTTTCCCTTCC	171207
rs215302036	snp	A/G			missense, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73899618	GGGGATGGCTCTTGT[A/G]GAATTTTCTCTCTGT	171207
rs215498043	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73909893	GGGACCCAGGCCCCC[C/T]AGCACTTCCTGTGAG	171207
rs215563609	snp	A/G/T			intron-variant	Arhgap4	GRCm38.p3	X:73909053	CTGTGCCAGCCACTC[A/G/T]CTAGGATGAGTGCTG	171207
rs215793677	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73895228	GGTTCCCCCTCTTTC[C/T]ACTCCTACTTTTTCT	171207
rs216109201	in-del	-/GTA			intron-variant	Arhgap4	Mm_Celera	X:73896294	AGCTTAGCAGTGTAG[-/GTA]GTAGCCTCTGGCCCA	171207
rs216810677	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73903077	TAAAATAATGATCTA[C/T]TTCAAAGCAGACATA	171207
rs216951787	snp	G/T			intron-variant	Arhgap4	Mm_Celera	X:73904561	CATAGCCCCACCTGC[G/T]TGCCCACACAAAACT	171207
rs217769237	in-del	-/AGTC			intron-variant	Arhgap4	Mm_Celera	X:73905914	GTCATGACTAAGAAG[-/AGTC]AGTCCCTCAGCCCCA	171207
rs217963253	in-del	-/AG			upstream-variant-2KB	Arhgap4	Mm_Celera	X:73912791	TTTGGCCTCGAACTC[-/AG]AAATCCACCTGCCTC	171207
rs217992703	snp	C/G			intron-variant	Arhgap4	Mm_Celera	X:73902144	GCCCCAGGGAGTTTC[C/G]AGGTCAGGTGGGTGG	171207
rs218035119	snp	A/G			intron-variant	Arhgap4	Mm_Celera	X:73901475	AACCTCAGGAAATAA[A/G]AGGTTGGGGGACCCT	171207
rs218340600	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73910052	TTCTTTTGAGGGAGG[C/T]TGGTGAGAAATAATA	171207
rs218473497	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73897942	TGCCTACTGAAGCCA[C/T]TGCCACATTTGTCCA	171207
rs218641218	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	Arhgap4	Mm_Celera	X:73899580	TCCAAAAAGTCTCTG[A/G]TTATACTGGAATCTA	171207
rs218684542	snp	C/T			intron-variant	Arhgap4	Mm_Celera	X:73896799	GGACCCTCCCTAGGG[C/T]TATAGCTCACTCACC	171207
rs218722345	snp	A/T			intron-variant	Arhgap4	Mm_Celera	X:73908982	CCGAAGCCAATGCAA[A/T]GCAGAGCCCACAATA	171207
rs218920509	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap4	Mm_Celera	X:73907538	TAAGGCACACTGTCT[C/T]GGCTTCTGGTAAACA	171207

Full records

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