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
rs7856	snp	G/T	0.0444908	0.142359	utr-variant-3-prime, nc-transcript-variant	RNF13	GRCh38.p7	3:149961227	TATTCTACAGTTTAA[G/T]CAAATTACTGAAACA	11342
rs481885	snp	A/G			intron-variant	RNF13	GRCh38.p7	3:149915896	tcagcttaataagat[A/G]aaggctgtgaatgga	11342
rs481890	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149915900	cttaataagatgaag[G/T]ctgtgaatggatggt	11342
rs481984	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149915930	tagtgatggtagcac[A/C]acagtatgaatgtac	11342
rs484572	snp	A/T			intron-variant	RNF13	GRCh38.p7	3:149935133	gttatcattatatag[A/T]gattttttgggtctc	11342
rs484647	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149941722	ATTTTTTTCTTTTGT[C/T]GCCTGTGCTTATGGT	11342
rs485289	snp	A/T			intron-variant	RNF13	GRCh38.p7	3:149935157	gggtctctttttaag[A/T]gtttgttgtttattt	11342
rs485532	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149848687	ATTTGTAATGCCAGA[C/T]GCCTTTGATTTTTTG	11342
rs489315	snp	C/G	0	0	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF13	GRCh38.p7	3:149812740	TGAGTGTAGTGTGCA[C/G]GGAAGAGACGCGTCA	11342
rs501600	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149849069	CTTTTAGATTACTGT[G/T]TTTATCTCTTATCAT	11342
rs519335	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149920530	TTAAGCAGAGAAGTT[C/T]TTAACTTTGACATAG	11342
rs531758	snp	A/C			intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955461	CAAGAAATCTCAACA[A/C]AATACAACAGGATAA	11342
rs532668	snp	G/T			intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955358	ATTTATTATTAAGGT[G/T]AGATTAAAAGCTGTT	11342
rs541365	snp	A/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149897860	GTGAAGTGTCAACAG[A/G]AAGGGGCTTTTACAA	11342
rs542333	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149897739	CCTCTTCTGATAAAT[A/C]TATGCTTTTCTTACC	11342
rs544716	snp	G/T	0.0185938	0.0946107	upstream-variant-2KB	RNF13	GRCh38.p7	3:149811400	CTGTTGCCTATGCCC[G/T]AGTGCAGTGGTGGGA	11342
rs565608	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149853802	TTAGAATAAACTGAA[A/C]ACATTCTATGGTACA	11342
rs565615	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149853796	TAAACTGAAAACATT[A/C]TATGGTACATATCCA	11342
rs576857	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149863462	AACCCAGGAGGCATA[G/T]CTTGCAGTGAGCTGA	11342
rs589313	snp	G/T	0.0171766	0.0910674	utr-variant-5-prime, upstream-variant-2KB	RNF13	GRCh38.p7	3:149812700	GGCGGATGAGGCCTC[G/T]CCCTCTCCTCTTTAG	11342
rs589330	snp	G/T	0	0	utr-variant-5-prime, upstream-variant-2KB	RNF13	GRCh38.p7	3:149812706	TGAGGCCTCTCCCTC[G/T]CCTCTTTAGTAGGTC	11342
rs592231	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149897706	TTACCATTTTCATGT[G/T]TGCTATTACTCGGGA	11342
rs592244	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149897717	ATGTGTGCTATTACT[C/T]GGGAGAGGTAAGAAA	11342
rs592793	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149897873	TTCCTGTTGACACTT[C/T]ACGTAAGGAATATAC	11342
rs601859	snp	A/G			intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955335	AAGCTGTTAAAATGT[A/G]GTTATAAAAAAAGAA	11342
rs602881	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149861698	AAACATTAGAACTTA[C/T]ACCTTCTATCTAACT	11342
rs612849	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149919892	ccagtccctccactt[C/T]cgtgccaacgcttgg	11342
rs615729	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149906434	TCCCAAAGTGCCTTC[A/C]CCAACTTATATTCAC	11342
rs615754	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149906450	ccaatttatattcac[A/C]ccagcaatgtatgag	11342
rs622482	snp	A/T			intron-variant	RNF13	GRCh38.p7	3:149935255	tataaagacacatag[A/T]ctgaaagtaaagggg	11342
rs622877	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149935160	ataaaataaacaaca[A/C]actcttaaaaagaga	11342
rs636139	snp	A/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149816513	AAAAAAAAAAGGCTA[A/G]GGCATATAATTTACT	11342
rs641324	snp	G/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149916456	cagacccttgaacgg[G/T]gcctagttcaccata	11342
rs643851	snp	C/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149938738	CCACCATTTCCATGT[C/G]TGACCACCACTACTA	11342
rs651870	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149845042	TATACTTTAGCATGT[G/T]TTCATTTTTATTTCA	11342
rs670138	snp	G/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149923551	gcagacagatcacta[G/T]gtcaggagatcgaga	11342
rs674184	snp	A/C	0	0	intron-variant	RNF13	GRCh38.p7	3:149864194	attacagcagaagtc[A/C]ccaagccattcatga	11342
rs688199	snp	A/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149863396	cgagtctccatctta[A/T]aaaataaaaaaaaga	11342
rs716352	snp	C/T	0.45574	0.142025	intron-variant	RNF13	GRCh38.p7	3:149908643	TCCCCACTATTTCAT[C/T]TGACTACTTCCTTGA	11342
rs833036	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149950602	cagtagtcccagcta[C/T]tcaggaggctgaggc	11342
rs833037	snp	A/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149921359	cacaacgtgcaggtt[A/T]gttacataggtatac	11342
rs833038	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149921368	caggtttgttacata[G/T]gtatacatgtgccat	11342
rs833679	snp	A/C	0	0	intron-variant	RNF13	GRCh38.p7	3:149848737	acaaaacacaaaaca[A/C]aaaaaacacaaaaca	11342
rs844297	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149848744	CAaaaacacaaaaca[A/C]aaaacaaaaaaaaca	11342
rs855199	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149950569	gaggatggcttgaac[C/T]caggaggcagaggtt	11342
rs864414	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149950561	cttgaactcaggagg[C/T]agaggttgcggtgag	11342
rs864431	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149848751	CAACTGCCAaaaaca[A/C]aaaacaaaaaacaaa	11342
rs866234	snp	A/T	0	0	intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955276	aagtaaaaaattata[A/T]aatttaaaaaaatta	11342
rs866235	snp	A/C	0	0	intron-variant	RNF13	GRCh38.p7	3:149924265	ggaagattggtattg[A/C]acatatggaatttca	11342
rs866729	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955167	TCTTTCCCCTCCTGT[A/G]CATATAATCTTCAAA	11342
rs866741	snp	A/C	0	0	intron-variant	RNF13	GRCh38.p7	3:149848726	AACACAAAAAACACA[A/C]AACAAAACAACCAAC	11342
rs983456	snp	C/T	0.404384	0.196635	intron-variant	RNF13	GRCh38.p7	3:149904788	ATTAAAAAAAGACTT[C/T]AATTTATTCTTTAGT	11342
rs1038705	snp	C/T	0.030665	0.119967	intron-variant	RNF13	GRCh38.p7	3:149855833	aagagttagaaagac[C/T]gataatatccagtgt	11342
rs1043642	snp	C/T	0.183886	0.241099	utr-variant-3-prime, nc-transcript-variant	RNF13	GRCh38.p7	3:149961458	TCAGTGCTACAGCCA[C/T]CTAGCATGAACTAAC	11342
rs1239714	snp	C/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149893620	TGATTATTTGTTACA[C/T]ACATTAACTTATTAT	11342
rs1239715	snp	A/C	0	0	intron-variant	RNF13	GRCh38.p7	3:149878603	TGATTTACATTCACA[A/C]TCTGAATCCTCAGAT	11342
rs1262693	snp	A/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149933091	gcttgtgctctcaga[A/G]cagtgccccaaactg	11342
rs1268317	snp	C/T	0.00988443	0.0696026	intron-variant	RNF13	GRCh38.p7	3:149876748	ACCTTCCCTGATTTT[C/T]TTCAAGGTAGAAGTC	11342
rs1350349	snp	A/G	0.192088	0.2432	intron-variant	RNF13	GRCh38.p7	3:149908752	ACCAATCAAACTACT[A/G]AGCCTCAGTGGATTT	11342
rs1403026	snp	A/G	0.191461	0.24305	intron-variant	RNF13	GRCh38.p7	3:149826153	CCTTTGGGCCTGAGC[A/G]CAGTGCTGAGCTCCT	11342
rs1522238	snp	A/G	0.404559	0.196498	intron-variant	RNF13	GRCh38.p7	3:149859362	GAAATTAAGAGGAAA[A/G]GGTTTATTTTAGAAG	11342
rs1522239	snp	A/C	0.211819	0.247067	intron-variant	RNF13	GRCh38.p7	3:149859174	TCTGACCTTTGTTTT[A/C]GTTTATAAACTGAGG	11342
rs1522240	snp	A/G	0.156319	0.231784	intron-variant	RNF13	GRCh38.p7	3:149862738	TAAATATGTCTCCTT[A/G]TATATATTATAACTA	11342
rs1568568	snp	A/G	0.395453	0.203331	intron-variant	RNF13	GRCh38.p7	3:149836428	tattttagtatggct[A/G]tatgtatatatatat	11342
rs1585859	snp	C/T	0.0111196	0.0737302	intron-variant	RNF13	GRCh38.p7	3:149950599	cctgcctcagcctcc[C/T]gaatagctgggacta	11342
rs1673691	snp	C/G			intron-variant	RNF13	GRCh38.p7	3:149915829	gaatggtggttgcca[C/G]ggactgaggggactg	11342
rs1684819	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149915814	tagagacagaaacta[G/T]aatggtggttgccac	11342
rs1684820	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149889436	caacctcccaagtaa[A/C]taggactacaggcgt	11342
rs1686641	snp	A/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149827631	ATGTTTATTGTTTAG[A/T]GTTCAGCTTTGCCAC	11342
rs1686642	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF13	GRCh38.p7	3:149812850	GACCGACCGGGCCTG[C/T]CCGCTCGGTCCCGCG	11342
rs1718227	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149827635	CAAAGCTGAACACTA[A/C]ACAATAAACATAACA	11342
rs1802142	snp	A/C/G	4.94344e-05	0.00497139	synonymous-codon, missense, nc-transcript-variant	RNF13	GRCh38.p7	3:149960115	GATGGAGACAAACTC[A/C/G]GAATCCTTCCCTGTT	11342
rs1802144	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF13	GRCh38.p7	3:149961200	TTTCTGTAGAAATAA[A/C]TTATTTTTTAGTATT	11342
rs1840951	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149877495	TTTTTTTTTTTTTGG[G/T]GATTTTTTTGTTATC	11342
rs1840952	snp	A/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149877514	TTTTTTGTTATCTCA[A/G]AAAGTAGCCCTCTAG	11342
rs1980276	snp	A/T	0.465052	0.127485	intron-variant	RNF13	GRCh38.p7	3:149819990	TTAATAATTATTAAA[A/T]ATTAATAATTATGAA	11342
rs2035741	snp	A/G	0.212425	0.24716	intron-variant	RNF13	GRCh38.p7	3:149882039	CAGAGAAGGATATAC[A/G]GATGGAGGAAGTCCA	11342
rs2100633	snp	A/G	0.415891	0.18703	intron-variant	RNF13	GRCh38.p7	3:149950229	cctcagaatattaac[A/G]gtggttgttttaaat	11342
rs2125100	snp	G/T	0.19334	0.243495	intron-variant	RNF13	GRCh38.p7	3:149927667	CTATCCTAATGGGTA[G/T]GAAGTGGTACCTTAA	11342
rs2130320	snp	A/G	0.422315	0.181128	intron-variant	RNF13	GRCh38.p7	3:149831007	gtgttgagctgcaag[A/G]tgcacagaagtccag	11342
rs2130321	snp	A/T	0.404907	0.196224	intron-variant	RNF13	GRCh38.p7	3:149838049	ccccatgcaagtcca[A/T]aatccagcggggcag	11342
rs2130322	snp	C/T	0.211212	0.246973	intron-variant	RNF13	GRCh38.p7	3:149849612	gtctggccacagagc[C/T]ccagcccttaaccca	11342
rs2219386	snp	A/G	0.0232847	0.105357	intron-variant	RNF13	GRCh38.p7	3:149932390	TCCCAGTAGTATCCA[A/G]AGTCTTAACTCATTC	11342
rs2607906	snp	C/T	0.00337267	0.0409263			GRCh38.p7	3:149917490	GAGAAACACTTCCTC[C/T]TTCTGGCCAGTTCAT	11342
rs2607907	snp	C/G					GRCh38.p7	3:149931836	gccagcctcccttca[C/G]tgctcccttccaccc	11342
rs2607908	snp	C/G					GRCh38.p7	3:149937132	ctgagatgaagagca[C/G]ccccaagtttccttt	11342
rs2607909	snp	G/T					GRCh38.p7	3:149893628	ATAAACTTTGATTAT[G/T]TGTTACATACATTAA	11342
rs2607910	snp	C/G	0	0			GRCh38.p7	3:149876681	CTTCTACTTGTCTGT[C/G]TGGCCAATCTGACTT	11342
rs2631544	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149906643	TCATTTGTTCAATTC[C/T]GCttttttttttttt	11342
rs2631545	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149906646	TTTGTTCAATTCTGC[C/T]ttttttttttttttt	11342
rs2631546	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149897588	TGCTCAGAATTTTGG[G/T]TCTTGACTCTGTTGC	11342
rs2631547	snp	C/T			intron-variant	RNF13	GRCh38.p7	3:149897597	TTTTGGGTCTTGACT[C/T]TGTTGCTTAGATTAT	11342
rs2631548	snp	A/C/G	0.00517822	0.0506191	intron-variant	RNF13	GRCh38.p7	3:149897675	ATATGTACACAGACA[A/C/G]ATGTTGTAAAGATCT	11342
rs2631549	snp	A/T			intron-variant	RNF13	GRCh38.p7	3:149898989	acacctagttctaca[A/T]ttcaaagataaacct	11342
rs2631550	snp	C/G	0	0	intron-variant	RNF13	GRCh38.p7	3:149937049	AGGAGTTTGTGCGCA[C/G]AGGACCCGTGGAATG	11342
rs2631551	snp	G/T			intron-variant	RNF13	GRCh38.p7	3:149883953	GAGAACACGTGGTGT[G/T]TGGTTTTCTGTTTCT	11342
rs2631552	snp	G/T	0	0	intron-variant	RNF13	GRCh38.p7	3:149884205	TGTCATATGTCTTGG[G/T]CTTTAAAGACCTTTT	11342
rs2631554	snp	A/T			intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955290	GAGtaaaattttata[A/T]gtgaaaaattatata	11342
rs2631555	snp	A/G			intron-variant, upstream-variant-2KB	RNF13, LOC105374152	GRCh38.p7	3:149955287	taaaattttatatgt[A/G]aaaaattatataatt	11342
rs2635624	snp	A/C			intron-variant	RNF13	GRCh38.p7	3:149898210	CTTCTGACTCCTCAT[A/C]TAGGCTCCTCTCACT	11342

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