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
rs6267385	snp	A/C	0.5	0	intron-variant	Ppwd1	GRCm38.p3	13:104221393	CAAAACATATGCCAA[A/C]GTTTNGATCTGATTT	238831
rs6267387	snp	A/T	0.345679	0.230967	intron-variant	Ppwd1	Mm_Celera	13:104221398	CATATGCCAANGTTT[A/T]GATCTGATTTATAGA	238831
rs6268013	snp	G/T	0.359862	0.224567	intron-variant	Ppwd1	GRCm38.p3	13:104221514	AGCTCATAAGGATGG[G/T]TGCCTAATCTAATGA	238831
rs6268458	snp	A/T	0.487293	0.0786907	intron-variant	Ppwd1	Mm_Celera	13:104221574	TTCTTTAACCAAATG[A/T]GGAAATGCCAAGAAG	238831
rs6268549	snp	C/T	0.207612	0.24638	intron-variant	Ppwd1	Mm_Celera	13:104221628	ATGAAATTGCTAGCA[C/T]TGAACCTTGGATTTG	238831
rs29229211	snp	A/T	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104221736	ACATTCTGATAATAG[A/T]ATGACTTTTAAGTTG	238831
rs29229228	snp	C/T	0.375	0.216506	intron-variant	Ppwd1	Mm_Celera	13:104213941	ACATCAACCTCTGAC[C/T]CCCTGCATACATGTG	238831
rs29233169	snp	C/T	0.444444	0.157135	synonymous-codon, intron-variant	Ppwd1	GRCm38.p3	13:104213667	TCCCTGAAACAAAGC[C/T]AGCTGCATCACTCTA	238831
rs29236088	snp	A/G	0.49827	0.0293608	intron-variant	Ppwd1	Mm_Celera	13:104214076	ACTATCCTAGATGAG[A/G]TATTTGATTCCGTGT	238831
rs29236179	snp	C/T	0.495	0.0497494	downstream-variant-500B	Ppwd1	Mm_Celera	13:104204829	GTTAGCAGTCAGTTA[C/T]GGAAAAGGGACGTGA	238831
rs29238783	snp	A/G	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104206417	ATTTAGTTGACACTC[A/G]TACTTTTTCTGCTTT	238831
rs29250833	snp	A/G	0.375	0.216506	intron-variant	Ppwd1	Mm_Celera	13:104220561	TAGACTATCTTTCAA[A/G]TCAAAATGCTCTGGC	238831
rs29493327	snp	C/T	0.444444	0.157135	downstream-variant-500B, utr-variant-3-prime	Ppwd1	Mm_Celera	13:104205064	TAAGCTGTAACTTGA[C/T]AGAAGAAAGATTAGT	238831
rs29495337	snp	C/T	0.48	0.0979796	intron-variant	Ppwd1	GRCm38.p3	13:104217332	ACATATATAATCACA[C/T]GTACATATATAAATT	238831
rs29496730	snp	G/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Cenpk, Ppwd1	Mm_Celera	13:104230245	TGGATCACCTTAGGT[G/T]CCATTTCACTTAGTT	238831
rs29508686	snp	A/G	0.48	0.0979796	intron-variant, downstream-variant-500B	Ppwd1	Mm_Celera	13:104206769	TGATTTTGTCTTAAT[A/G]AAAGTAAAAAGCACT	238831
rs29527815	snp	A/T	0.375	0.216506	intron-variant, downstream-variant-500B	Ppwd1	Mm_Celera	13:104216814	TTTTTTTTTTTTTTT[A/T]AAAGAAAAAAAAGAA	238831
rs29528893	snp	C/T	0.432133	0.171253	intron-variant	Ppwd1	GRCm38.p3	13:104221537	TCTAATGAGCCCTTG[C/T]CCTCATCTGCCAACT	238831
rs29550552	snp	A/G	0.401235	0.199068	downstream-variant-500B	Ppwd1	GRCm38.p3	13:104204602	GGTAAATGTAACAAA[A/G]GTACTAATGGAGTAA	238831
rs29552353	snp	C/T	0.484429	0.0868505	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104228053	ACCCTAAGACATTTA[C/T]GAAAAAGTTCCTAGA	238831
rs29574592	snp	C/T	0.375	0.216506	intron-variant	Ppwd1	Mm_Celera	13:104221887	AAATCAATATAAATA[C/T]ACAAGTTTGTATCTT	238831
rs29584942	snp	C/T	0.444444	0.157135	intron-variant	Ppwd1	GRCm38.p3	13:104214223	GCATGGGCTCCCCTA[C/T]CCCAAAATAAAGAAA	238831
rs29587587	snp	A/C	0.444444	0.157135	intron-variant	Ppwd1	GRCm38.p3	13:104213106	AAGTCAAGGAAATCC[A/C]TAAGTGTATTCCATA	238831
rs29723694	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104227904	GTCCTGCTTGGGGAA[A/G]TAAAGAGAGACAAAC	238831
rs29724923	snp	G/T	0.432133	0.171253	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104228011	TTGAGATTAACGCGT[G/T]AGCGAACGAACACAC	238831
rs29761753	snp	A/T	0.5	0	intron-variant	Ppwd1	Mm_Celera	13:104218465	GCTACACATAGCCTG[A/T]AAAATCTTGTATAAG	238831
rs29770866	snp	C/T	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104222237	CTGCTCAAAAATAGC[C/T]TATAATATGGTAAAG	238831
rs29817097	snp	A/T	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104221719	GCAAAGCAAGTTCCC[A/T]AACATTCTGATAATA	238831
rs29830206	snp	G/T	0.444444	0.157135	intron-variant	Ppwd1	GRCm38.p3	13:104211712	CATAGTTCATTAGTC[G/T]TCTAGTCATAGCCAG	238831
rs29832819	snp	A/G	0.484429	0.0868505	synonymous-codon	Ppwd1	GRCm38.p3	13:104205540	GATGCTGACGTCCTC[A/G]TAAGGCTTATCGGTT	238831
rs29852725	snp	A/G	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104218551	AAGTTATGTCTGTAT[A/G]TGTGTCATGTATATT	238831
rs29866988	snp	A/G	0.497778	0.0332592	intron-variant	Ppwd1	Mm_Celera	13:104209610	CAACAAAGGTTTTAC[A/G]TACTCAACAGGAAAA	238831
rs29874084	snp	C/T	0.456747	0.140554	downstream-variant-500B, utr-variant-3-prime	Ppwd1	Mm_Celera	13:104204908	TTATCTGGCATTATG[C/T]AGTCCAGGCTGACCT	238831
rs29881500	snp	A/G	0.432133	0.171253	intron-variant	Ppwd1	Mm_Celera	13:104221610	AGAGAGCCCTCATAA[A/G]AAATGAAATTGCTAG	238831
rs29912802	snp	C/T	0.5	0	intron-variant	Ppwd1	GRCm38.p3	13:104212329	CTGGGAAACTGCTAA[C/T]AAGTTTATCAATTAT	238831
rs29928474	snp	C/T	0.5	0	intron-variant	Ppwd1	GRCm38.p3	13:104212394	AGAGACATCAGAGTG[C/T]ACACTCCAACAGGTC	238831
rs29955900	snp	C/T	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104217687	CCTGGGTTTGATCCC[C/T]ATCAACCCCTACCCT	238831
rs29956532	snp	A/T	0.375	0.216506	intron-variant	Ppwd1	GRCm38.p3	13:104212994	AGTAAATGATCACTG[A/T]GCAGCACTCCCCACA	238831
rs29958955	snp	A/G	0.375	0.216506	intron-variant	Ppwd1	Mm_Celera	13:104210023	GGGCATATAAAGTTT[A/G]TGTGTCCAATGGGTC	238831
rs29991612	snp	C/G	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104206692	AACCCCAGAATGTGA[C/G]AGGCTGATTCTGAGG	238831
rs29997339	snp	A/G	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104217335	TATATAATCACACGT[A/G]CATATATAAATTTCA	238831
rs30057531	snp	A/T	0.493827	0.0552116	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104227920	TAAAGAGAGACAAAC[A/T]GCCTCATAATCCATG	238831
rs30057558	snp	A/G	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104218002	ACTGACTGCTCTTCC[A/G]AAGGCCCTGAGTTGA	238831
rs30062320	snp	C/T	0.5	0	intron-variant	Ppwd1	GRCm38.p3	13:104212467	GTCTCTATTTATTAA[C/T]TTTAAATCATCTGGA	238831
rs30064999	snp	A/G	0.489796	0.070696	intron-variant	Ppwd1	Mm_Celera	13:104214345	TTTATGTTGGTAGGT[A/G]TTACTAGGTTAAAAA	238831
rs30067781	snp	A/G	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104209589	GACATTGGTATTTGT[A/G]TAAGACAACAAAGGT	238831
rs30068290	snp	C/T	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104213124	AGTGTATTCCATATG[C/T]GCATAGATATGCATA	238831
rs30070971	snp	C/T	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104211090	CAGAGAGCAACTGAT[C/T]AAATAGTGTCCAGCT	238831
rs30076152	snp	C/T	0.5	0	intron-variant	Ppwd1	GRCm38.p3	13:104218675	ACTGAATTTGGGTCC[C/T]ACGCAAGAACAGTAA	238831
rs45672025	snp	C/T			intron-variant	Ppwd1	Mm_Celera	13:104218387	AACCCCTTTCCTCAC[C/T]TCCCACAAACAAGCA	238831
rs45675868	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104228333	ACACAGCAGCTATGA[A/G]GTCAAAAAAAGCATC	238831
rs45808431	snp	C/T	0.132653	0.220748	intron-variant	Ppwd1	Mm_Celera	13:104206224	TTTAAGAAGACTGTA[C/T]TTTGGCATAATTCAG	238831
rs45895919	snp	A/G			intron-variant, upstream-variant-2KB	Ppwd1	Mm_Celera	13:104225729	AATGAGGCCAGCAGA[A/G]GATGGTGAATGAATC	238831
rs45944104	snp	C/T			intron-variant	Ppwd1	GRCm38.p3	13:104213434	GTTTAGGAAGTTTGC[C/T]ATCATTGCCTACATT	238831
rs45951486	snp	G/T	0.489796	0.070696	intron-variant	Ppwd1	Mm_Celera	13:104220863	AATCATATCTGGGTC[G/T]TAAGGTATTCTGAGG	238831
rs45956616	snp	C/G			intron-variant	Ppwd1	GRCm38.p3	13:104213897	CACAGGGCAAACTGG[C/G]TAGCTAGACTTGGCA	238831
rs45959540	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Ppwd1	GRCm38.p3	13:104220238	TTTAGGGAACTTATA[C/T]TCGTGCGGCGGTCCA	238831
rs46000676	snp	C/T	0.497778	0.0332592	intron-variant	Ppwd1	Mm_Celera	13:104219665	CACCCCTCCGTGGAG[C/T]GTGGAATTACTCATC	238831
rs46083308	snp	C/G	0.391111	0.206368	intron-variant, nc-transcript-variant	Ppwd1	GRCm38.p3	13:104219832	GTCCTATCACCTCAA[C/G]AAATGCTGAGAGAGG	238831
rs46093578	snp	G/T			intron-variant	Ppwd1	GRCm38.p3	13:104210542	TTGTTGGTCACTGGA[G/T]CCTAGGAAGCACCCA	238831
rs46245555	snp	A/G	0.497778	0.0332592	synonymous-codon, nc-transcript-variant	Ppwd1	GRCm38.p3	13:104220265	TCCAGTCCAGTACTC[A/G]ATCATCCCGGATTTG	238831
rs46281166	snp	A/G	0.391111	0.206368	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	GRCm38.p3	13:104228322	ATTCCAACTTCACAC[A/G]GCAGCTATGAGGTCA	238831
rs46299568	snp	A/T	0.5	0	intron-variant	Ppwd1	Mm_Celera	13:104212392	TCAGAGACATCAGAG[A/T]GCACACTCCAACAGG	238831
rs46364765	snp	C/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Ppwd1	Mm_Celera	13:104219819	TGCTTGTCACTCAGT[C/G]CTATCACCTCAACAA	238831
rs46386526	snp	C/T	0.391111	0.206368	intron-variant	Ppwd1	GRCm38.p3	13:104217726	CTATACTAATAGTCA[C/T]TGATTTTTCTAACTG	238831
rs46554840	snp	A/G	0.124444	0.216185	synonymous-codon, intron-variant, nc-transcript-variant	Ppwd1	Mm_Celera	13:104222906	CGCTTTATCATCACC[A/G]ACAGAGCAGAACAAC	238831
rs46559366	snp	A/G	0.132653	0.220748	intron-variant	Ppwd1	Mm_Celera	13:104207668	GTATCTGATTTTTCC[A/G]TTTGCCATTTCTAAC	238831
rs46571367	snp	A/T			intron-variant	Ppwd1	GRCm38.p3	13:104223445	CTATTTTGACTTTGT[A/T]TTTAAATTTTCCTTT	238831
rs46634130	snp	G/T	0.48	0.0979796	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104227602	TTCTTACATGATTAG[G/T]CTAGTAGTGTTCAGG	238831
rs46774360	snp	G/T	0.244898	0.249948	synonymous-codon, downstream-variant-500B	Ppwd1	GRCm38.p3	13:104207183	GTACGGTCTGTCATG[G/T]CGTAATGTTGAGTGG	238831
rs46781842	snp	A/G			intron-variant	Ppwd1	Mm_Celera	13:104210104	AGAGTCAAGAGCTCT[A/G]GGGTACTGGTTAGTT	238831
rs46838311	snp	C/T	0.32	0.24	synonymous-codon, nc-transcript-variant	Ppwd1	GRCm38.p3	13:104220337	TTGAGTAAGAGGGGA[C/T]ACATGGAGTTTGTCA	238831
rs46984874	snp	A/G	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104223538	GAAAAAGGATTTACC[A/G]TTAAACAAACAAATC	238831
rs47088014	snp	C/T			intron-variant	Ppwd1	Mm_Celera	13:104225131	GCAGCTCAGTAGTTA[C/T]GAGCACCGGCTGCTG	238831
rs47128643	snp	C/T			intron-variant	Ppwd1	Mm_Celera	13:104219589	ACTAGACTAGTTAAA[C/T]AGTCTTAAATCACTG	238831
rs47162874	snp	C/G	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Ppwd1	Mm_Celera	13:104226112	ATCCTAGCAAATCTA[C/G]TTGAGTGCCTTTCAG	238831
rs47193923	snp	A/G	0.260355	0.249785	utr-variant-3-prime	Ppwd1	GRCm38.p3	13:104205216	TTTTAAAAAGAATCC[A/G]TTATTTAATACCAAA	238831
rs47238395	snp	A/G	0.497778	0.0332592	intron-variant	Ppwd1	Mm_Celera	13:104225047	AAATTACTTCTGTAA[A/G]TCCACTCATAATTAA	238831
rs47249694	snp	A/T	0.124444	0.216185	intron-variant	Ppwd1	Mm_Celera	13:104220938	AGCATGTAATAGTAT[A/T]CTTTGTAAATCCATG	238831
rs47263489	snp	A/C			intron-variant	Ppwd1	GRCm38.p3	13:104213437	TAGGAAGTTTGCTAT[A/C]ATTGCCTACATTCTC	238831
rs47372973	snp	A/C	0.32	0.24	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	GRCm38.p3	13:104227660	AAAAAGTAGTAAGTG[A/C]CTCGAAGGCAAAAGC	238831
rs47394152	snp	C/G	0.444444	0.157135	intron-variant	Ppwd1	Mm_Celera	13:104222990	AATTAAAACATTCTG[C/G]TAAATACAAATAACA	238831
rs47395459	snp	A/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppwd1	Mm_Celera	13:104226164	CCTAGAAAAATGGAA[A/T]ATCGATGATCATCAA	238831
rs47404115	snp	A/G	0.48	0.0979796	intron-variant	Ppwd1	Mm_Celera	13:104225328	AATGTAAAATGTAAA[A/G]GACAAAGTATGACAC	238831
rs47406513	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104229367	AAGGGCCTGCGTGTT[A/G]CGTTCCCGCGTCTCC	238831
rs47442866	snp	A/C	0.489796	0.070696	intron-variant	Ppwd1	Mm_Celera	13:104220648	CTCAGAATAGATACT[A/C]AATTTCTCTTTACTC	238831
rs47457478	snp	A/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	Mm_Celera	13:104228230	TGAAAATTCATTACT[A/T]GACGAGTCAGGGTTG	238831
rs47542701	snp	C/T	0.244898	0.249948	intron-variant	Ppwd1	GRCm38.p3	13:104206331	CCAACACTGAAGTAC[C/T]GTGAATCTTACATTA	238831
rs47562846	snp	G/T	0.32	0.24	upstream-variant-2KB, intron-variant	Cenpk, Ppwd1	GRCm38.p3	13:104229175	TCTAGAACCTACCTG[G/T]TTTTTCCCGAAAAAG	238831
rs47730361	snp	G/T	0.142012	0.225474	intron-variant	Ppwd1	GRCm38.p3	13:104213407	TTAGTGCTGTAGGCT[G/T]GTGTTTCAGGTGTTT	238831
rs47745191	snp	A/T	0.165289	0.235211	intron-variant	Ppwd1	Mm_Celera	13:104218817	ATTAATATTAGATGG[A/T]TGTGTTTAGAAAACA	238831
rs47763032	snp	C/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Ppwd1	GRCm38.p3	13:104219749	ACACACGGTTTTCTT[C/T]TGCCACATTCTCATT	238831
rs47792751	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Ppwd1, Cenpk	GRCm38.p3	13:104226745	TAATGCTGTTGTTTA[C/T]TGGAATTTTCTGTAG	238831
rs47794735	snp	C/T	0.46281	0.131194	intron-variant	Ppwd1	Mm_Celera	13:104208587	GCTTAGTTATAGAAA[C/T]GGCTTCTAAGTTTAA	238831
rs47804811	snp	C/T	0.5	0	intron-variant	Ppwd1	Mm_Celera	13:104220767	TCCCTCTTTCTACTA[C/T]CATCAGTGTAACAAT	238831
rs47812367	snp	C/T	0.345679	0.230967	intron-variant	Ppwd1	GRCm38.p3	13:104212875	CAGACTCTGTCCTTA[C/T]GCTGTCTGCCTAACG	238831
rs47813989	snp	A/T			intron-variant	Ppwd1	Mm_Celera	13:104211394	TGAAAGCAAGAGAAA[A/T]AGTCTCCCCCAGAGA	238831
rs47858442	snp	C/T			intron-variant	Ppwd1	Mm_Celera	13:104220555	CCTCCATAGACTATC[C/T]TTCAAATCAAAATGC	238831
rs47863804	snp	G/T	0.132653	0.220748	intron-variant	Ppwd1	Mm_Celera	13:104209276	AATCCCCACAAACCC[G/T]ATCTGGACCTTCAGT	238831
rs47864649	snp	A/C	0.231111	0.249285	intron-variant	Ppwd1	GRCm38.p3	13:104207606	TCTATTCCTCAAATA[A/C]TCTGGCTTTCCTAGT	238831

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