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
rs346447030	snp	A/G			intron-variant	RIN2	TAIR10	4:12926330	CTGAATTCCAGTTAG[A/G]AAACTCGTTTGATCT	828626
rs346484690	snp	G/T			intron-variant	RIN2	TAIR10	4:12924714	ACTATTGGGATGCAA[G/T]ATAAGCAATGTTTTT	828626
rs346503000	snp	C/T			intron-variant	RIN2	TAIR10	4:12927265	GCTATATGTCGGGTA[C/T]GCTTCTGCTATAGTC	828626
rs346529527	snp	A/C			intron-variant	RIN2	TAIR10	4:12926588	TCTTTCTTTCGTAGC[A/C]ATAGTCAACAAAATA	828626
rs346533682	snp	A/G			utr-variant-3-prime	RIN2	TAIR10	4:12928985	GAGTAACCACTCTTT[A/G]CAGCTGCTCTTTTGG	828626
rs346540021	snp	A/G			missense	RIN2	TAIR10	4:12928259	ACAAATGAAAGCTTA[A/G]CAAATATACTAGCTA	828626
rs346540691	snp	C/G			intron-variant	RIN2	TAIR10	4:12925048	ACTTTGGTTACGATC[C/G]AAAACATTATTATTA	828626
rs346541485	snp	A/G			intron-variant	RIN2	TAIR10	4:12924823	TACTTTAAGCGATTA[A/G]TACCTTTATGAAATT	828626
rs346546296	snp	A/T			utr-variant-3-prime	RIN2	TAIR10	4:12928882	GCTCTCTTGCGAAAA[A/T]AAGTTCGGATATTTA	828626
rs346560025	snp	A/T			intron-variant	RIN2	TAIR10	4:12925234	ATTGTCTGTGGTTCT[A/T]ATGTCTTCTCAACAT	828626
rs346599132	snp	A/T			intron-variant	RIN2	TAIR10	4:12928343	CAGGTAAATTTTAAG[A/T]GCATATTGGATTATC	828626
rs346663616	snp	A/T			intron-variant	RIN2	TAIR10	4:12928523	TGAACTGGTCTCTAT[A/T]TTCACTAGACTGGTC	828626
rs346680851	snp	C/T			synonymous-codon	RIN2	TAIR10	4:12927976	GAATTTAGGATTGGA[C/T]CCAAGTTGGCTGCAG	828626
rs346686001	snp	A/G			synonymous-codon	RIN2	TAIR10	4:12927698	CGAAAATGATACTTC[A/G]AGGTTCAGTTCATTC	828626
rs346687330	snp	C/T			intron-variant	RIN2	TAIR10	4:12926851	ACTCTTATCTTTGGA[C/T]AGGCTCACTGTTGGA	828626
rs346688189	snp	A/C			intron-variant, utr-variant-5-prime	RIN2	TAIR10	4:12924199	CAAATCTGATTTCAC[A/C]TGTATGCATACGACT	828626
rs346748222	snp	A/C			intron-variant	RIN2	TAIR10	4:12926601	GCCATAGTCAACAAA[A/C]TATAGAGCTCATCGG	828626
rs346751151	snp	C/T			intron-variant	RIN2	TAIR10	4:12924946	TGTTTCACTTGTTCT[C/T]GGGACATCTTTTTTA	828626
rs346764784	snp	A/G			intron-variant	RIN2	TAIR10	4:12926197	ACTGTGAGAGTTGTT[A/G]TCCTGAAATTCATCT	828626
rs346772520	snp	A/G			missense	RIN2	TAIR10	4:12927556	TTGGTAGAACTGAAA[A/G]TGAGGTGAACCCTCG	828626
rs346821942	snp	G/T			intron-variant	RIN2	TAIR10	4:12927466	GGTGATCCTGATGAT[G/T]TTTTGATTCCTGCAG	828626
rs346825521	snp	G/T			intron-variant	RIN2	TAIR10	4:12926536	GACCTTGCAGGTACT[G/T]AATTGATAACAGTTT	828626
rs346830866	snp	C/T			intron-variant	RIN2	TAIR10	4:12925842	ACACCCTAAACTGTA[C/T]CTTGTAATGTTATGT	828626
rs346875191	snp	G/T			intron-variant	RIN2	TAIR10	4:12925538	TTTACTTAGACAGTT[G/T]ATTCTGCCACATTTT	828626
rs346887896	snp	C/T			utr-variant-3-prime	RIN2	TAIR10	4:12929008	TCTTTTGGCTGCTGC[C/T]ACCTCTCCTGTATAA	828626
rs346918393	snp	C/G/T			intron-variant	RIN2	TAIR10	4:12926776	TGTTTTTCTATTAGA[C/G/T]CCCGAAAATGCATTC	828626
rs346965364	snp	A/C			utr-variant-3-prime	RIN2	TAIR10	4:12928808	TGTAGATATAAGGCA[A/C]TGTGTATCACTTTTT	828626
rs346983845	snp	A/T			intron-variant	RIN2	TAIR10	4:12924699	TAAGAGTAACCTTTT[A/T]CTATTGGGATGCAAT	828626
rs346990877	snp	A/G			intron-variant	RIN2	TAIR10	4:12927931	TTTACTGGATTGTAT[A/G]AGTTCTCATCCCTTT	828626
rs347086713	snp	A/G			missense	RIN2	TAIR10	4:12928034	GCTGGTCCTTCTACC[A/G]CTTCCAGGACAGTTG	828626
rs347131424	snp	A/T			intron-variant	RIN2	TAIR10	4:12927328	AAAATACAATTATAA[A/T]TGGCAGGAACCTATG	828626
rs347143468	snp	A/C			intron-variant	RIN2	TAIR10	4:12926611	ACAAAATATAGAGCT[A/C]ATCGGAACTTTTTGC	828626
rs347151709	snp	C/T			synonymous-codon	RIN2	TAIR10	4:12926724	TAAGTTTATTGATTC[C/T]ATGACAGCAGGTCGT	828626
rs347159590	snp	C/T			synonymous-codon	RIN2	TAIR10	4:12927665	TGGATTATTTCCTGC[C/T]GAGGTGCCAGATTCT	828626
rs347166800	snp	A/C			intron-variant	RIN2	TAIR10	4:12926379	TAGTAACCAGTTTCA[A/C]GCATGTCTAGATGAT	828626
rs347203255	snp	C/T			synonymous-codon	RIN2	TAIR10	4:12924665	AATGTGTATATTCTT[C/T]TGGTACTTTCTCTCA	828626
rs347287727	snp	C/T			intron-variant	RIN2	TAIR10	4:12925128	TTTATAAGAGTCAAA[C/T]TCTCGTTTCCGGTAG	828626
rs347301889	snp	A/G			synonymous-codon	RIN2	TAIR10	4:12927578	GAACCCTCGCACAGT[A/G]GAAGTCTCAAGTGAT	828626
rs347302530	snp	C/G			utr-variant-3-prime	RIN2	TAIR10	4:12929000	GCAGCTGCTCTTTTG[C/G]CTGCTGCCACCTCTC	828626
rs347322973	snp	C/G			intron-variant, utr-variant-5-prime	RIN2	TAIR10	4:12924255	ATTTTCCTCTGCTTT[C/G]GAGCTCAATTTTCTT	828626
rs347330279	snp	G/T			intron-variant	RIN2	TAIR10	4:12927798	GCGACTCCCTTGATC[G/T]TGGTACTGAGATACT	828626
rs347337443	snp	A/T			intron-variant	RIN2	TAIR10	4:12928376	TAAGCTTTGATGGGA[A/T]GTGCATACATGGTTG	828626
rs347338104	snp	A/T			intron-variant	RIN2	TAIR10	4:12926817	TTTTGGTCTATTGGA[A/T]CTCCAAATCTCAAGT	828626
rs347353712	snp	C/T			synonymous-codon	RIN2	TAIR10	4:12928015	AAGTCAGGGTTCTGA[C/T]GTCGCTGGTCCTTCT	828626
rs347364392	snp	A/G			utr-variant-3-prime	RIN2	TAIR10	4:12928904	GGATATTTACATAAG[A/G]TGATGATGCCCTGGT	828626
rs347372306	snp	C/G			intron-variant	RIN2	TAIR10	4:12926151	AACAACATAGAGAGA[C/G]TGCATAGCTTGCTTT	828626
rs347425535	snp	A/T			intron-variant	RIN2	TAIR10	4:12928527	CTGGTCTCTATATTC[A/T]CTAGACTGGTCCTTA	828626
rs347431800	snp	A/G			synonymous-codon	RIN2	TAIR10	4:12925952	TGTGTATTCAGTGCT[A/G]TTCTTGGTCCTCTCT	828626
rs347440791	snp	C/G			intron-variant	RIN2	TAIR10	4:12924871	GAGCTTGTTTGCCTC[C/G]TAATCTACATTAGTC	828626
rs347457027	snp	C/T			intron-variant	RIN2	TAIR10	4:12926809	GTGGACATTTTTGGT[C/T]TATTGGAACTCCAAA	828626
rs347485735	snp	A/G			utr-variant-3-prime	RIN2	TAIR10	4:12929077	AAAGAGTCTACTGTT[A/G]TTGATCCAATAGCCT	828626

Full records

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