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
rs959022	snp	A/T	0.431177	0.172264	intron-variant	RNF19A	GRCh38.p7	8:100283764	AGAAAAAATTCATAA[A/T]TTCACATCTAGCATT	25897
rs962451	snp	C/T	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100318782	CGGATTTACATAGCC[C/T]AATTTGATAGCATGC	25897
rs962452	snp	A/G	0.499587	0.0143711	intron-variant	RNF19A	GRCh38.p7	8:100319141	CCAAGACTCAAAGAT[A/G]GACATTCTATGGATG	25897
rs1020171	snp	C/T	0.431325	0.172108	intron-variant	RNF19A	GRCh38.p7	8:100276382	ttttgaaatgtcaaa[C/T]agattagtggttgcc	25897
rs1047901	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258056	AATTTCATTTTTTTT[C/T]TTCATATGCAATGTG	25897
rs1125706	snp	A/T	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100314511	TTCACTTAGGCTGTG[A/T]CACCAGGGAAGGGGC	25897
rs1348062	snp	C/G/T	0	0	intron-variant	RNF19A	GRCh38.p7	8:100327130	TTTTCTGTTTTTAAT[C/G/T]TTAGCCTCGCTAACA	25897
rs1371867	snp	A/C	0.495855	0.045338	intron-variant	RNF19A	GRCh38.p7	8:100317981	TGGATAGGGCCTAGA[A/C]CACCCCCTCCCCACC	25897
rs1371868	snp	C/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100318039	GCTCCTTCCTCCCCT[C/T]AGATTTCCTTAAAGA	25897
rs1440572	snp	G/T	0.181978	0.240568	intron-variant	RNF19A	GRCh38.p7	8:100287125	AAAAAAATAAAGAAG[G/T]TCATTTGAATTTATG	25897
rs1548046	snp	A/G	0.0659589	0.169201	intron-variant	RNF19A	GRCh38.p7	8:100326539	gcagtctagtgaggg[A/G]aactgaGGTAACCCC	25897
rs1548047	snp	A/C	0.476574	0.105661	intron-variant	RNF19A	GRCh38.p7	8:100327964	GTAAATAAATCCTAG[A/C]AAACAGGTAGGCTCT	25897
rs1612305	snp	C/T	0.0174175	0.0916809	intron-variant	RNF19A	GRCh38.p7	8:100260775	AATTTTTCCTACTTA[C/T]CTATATGGCTATTGA	25897
rs1612773	snp	C/G	0.496842	0.0396107	intron-variant	RNF19A	GRCh38.p7	8:100325590	ACACCTCTAGCCTAC[C/G]CCCTGGGTCCTCAAG	25897
rs1616833	snp	C/T	0.499642	0.0133738	intron-variant	RNF19A	GRCh38.p7	8:100259593	ATCACCACTACCTAA[C/T]TTCAGAACATTTTCA	25897
rs1619759	snp	C/T	0.429837	0.173662	intron-variant	RNF19A	GRCh38.p7	8:100325332	TCTTCCAAAAAGTAG[C/T]TACAATGTAACTGTG	25897
rs1629834	snp	A/G	0.4231	0.180378	intron-variant	RNF19A	GRCh38.p7	8:100305487	TCATGATAATCTTTC[A/G]GATCTATTGGCTTAA	25897
rs1660310	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100315698	actctgttgtccagg[G/T]gggagtgcagtggtg	25897
rs1660311	snp	C/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100318351	TATACTTAACTCACT[C/T]TTGGCTTAAATTCTC	25897
rs1660312	snp	C/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100318406	AGATTGAATTTTTCT[C/G]GTGCTATATTTTATG	25897
rs1660313	snp	A/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100320484	TAAAAGTTGAAAAAT[A/G]CTATAACCAACCTCT	25897
rs1660314	snp	C/T	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100320725	TTAGATAAAATAATA[C/T]ACGTAAAGCATTTAG	25897
rs1660315	snp	A/G	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100320728	gataaaataatatac[A/G]taaagcatttagcac	25897
rs1660316	snp	C/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100320821	accaccaaaataaaa[C/T]aaatattgcaataaa	25897
rs1660317	snp	G/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100321024	ataatctttttgctg[G/T]tggagagtcttgcct	25897
rs1660318	snp	C/T	0.495596	0.0467178	intron-variant	RNF19A	GRCh38.p7	8:100325051	AGCTGGAATTACAGG[C/T]GCCTACCACCACAAC	25897
rs1660319	snp	A/G	0.496681	0.0405994	intron-variant	RNF19A	GRCh38.p7	8:100325302	AGGGTTTTTGCAGAG[A/G]GTTTGGTTTCTGAGT	25897
rs1660320	snp	A/C	0.496714	0.0404017	intron-variant	RNF19A	GRCh38.p7	8:100325351	AATGTAACTGTGTAA[A/C]TTTATAAATTATAAA	25897
rs1660322	snp	C/T	0.379158	0.214052	intron-variant	RNF19A	GRCh38.p7	8:100265412	TACCAGAAGACAGGA[C/T]TGAATTCACTCAGCA	25897
rs1660323	snp	A/T	0.431769	0.17164	intron-variant	RNF19A	GRCh38.p7	8:100266496	CGATCAGCTAATATA[A/T]TTTGAAATTTTTTAT	25897
rs1660324	snp	C/T	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100269043	TATTTTTAAAAACTT[C/T]TCATAGTTAGGAGCT	25897
rs1660326	snp	A/G	0.431916	0.171483	intron-variant	RNF19A	GRCh38.p7	8:100278219	GCCAAATAAGCACAT[A/G]GCTGCTTTGATAACA	25897
rs1660327	snp	A/C	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100279978	TTTCTGATTTCTTTT[A/C]ATTTTTCATAACTTC	25897
rs1660328	snp	A/G	0.499598	0.0141716	intron-variant	RNF19A	GRCh38.p7	8:100291222	TGTTCTAAGAATAAT[A/G]TGAAATTGACATGTG	25897
rs1660329	snp	G/T	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100291820	GTCAAAATACTAAAT[G/T]TAAGAGCAGTGTACC	25897
rs1660330	snp	A/T	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100292787	TTTTTTAATTTCTTA[A/T]TTTTGAGACATTTAT	25897
rs1660331	snp	C/T	0.429837	0.173662	intron-variant	RNF19A	GRCh38.p7	8:100297228	TGAAAGAAAGCAATG[C/T]TACTAGATGTACAAT	25897
rs1660332	snp	C/T	0.499539	0.0151687	intron-variant	RNF19A	GRCh38.p7	8:100297262	AATACCTTTCAATTA[C/T]TTCAATGTGTCCTTA	25897
rs1660333	snp	C/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100297761	TCCACCATGAGATTT[C/T]GGGTTTTCTGTTACA	25897
rs1660334	snp	C/T	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100298052	GAATTACAGTACCTA[C/T]AGTCCATAGATTATA	25897
rs1660339	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100315098	ttgtcatgttgccta[G/T]gcccaaatcatctgc	25897
rs1660340	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100314932	GTCTCGCAGCACCTA[G/T]GGAAGGCATGTCATG	25897
rs1660341	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100314811	CTACAAATAATGACA[A/C]TGAAGTACTTTATAC	25897
rs1660342	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100314783	TACACAAAAATTATA[G/T]AGGTAAGCATGGTTG	25897
rs1660343	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100314694	GAAATGAGCCACGCA[C/G]AGGAGAGGGGAGGGG	25897
rs1660344	snp	C/T	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100312431	CCAGGCTAATTTTTG[C/T]ATTTTCGCCATCTTG	25897
rs1660345	snp	G/T	0.429837	0.173662	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310534	GCAGGTGAACCCTGA[G/T]AACACAAAGGAATGA	25897
rs1660346	snp	A/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100300269	GAGTATTTTCTAAAG[A/G]CAGAAAAATCTAGGT	25897
rs1660347	snp	A/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100302752	AGGGGGATCATGGAG[A/G]AATTACACTTTAAAG	25897
rs1660348	snp	A/G	0.499587	0.0143711	intron-variant	RNF19A	GRCh38.p7	8:100303020	GTTTAGTCTCTGATC[A/G]TCATAGCACATGATA	25897
rs1660349	snp	A/G	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100307098	TGGGCTTTTGCCCAA[A/G]GTGGCCTAATTTTTA	25897
rs1660351	snp	C/T	0.431769	0.17164	intron-variant	RNF19A	GRCh38.p7	8:100262806	CTAAGGGAAGGACAA[C/T]GAAGAGAGTAAGAAG	25897
rs1788164	snp	C/T	0.0452528	0.143452	intron-variant	RNF19A	GRCh38.p7	8:100334264	GTGCTAATTTTGACT[C/T]TTCAACTATTTTGAA	25897
rs1788166	snp	A/G	0.4231	0.180378	intron-variant	RNF19A	GRCh38.p7	8:100305724	TAAGTGCTAAGACTT[A/G]AAGAGTGAACAAAGA	25897
rs1788167	snp	C/T	0.499575	0.0145705	intron-variant	RNF19A	GRCh38.p7	8:100307768	TTACGACTTCACTTA[C/T]ATTCAAATTTGGGAA	25897
rs1788168	snp	G/T	0.499551	0.0149693	intron-variant	RNF19A	GRCh38.p7	8:100312732	agtttgataccagcc[G/T]ggacaacatgatgaa	25897
rs1788169	snp	C/T	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100314086	gaggttttgccatgt[C/T]gctcaggtgggtctt	25897
rs1788170	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100314794	ACCTCTATAATTTTT[C/G]TGTATAAAGTACTTC	25897
rs1788173	snp	C/T	0.49962	0.0137727	intron-variant	RNF19A	GRCh38.p7	8:100318711	TCAAGCTGGAACACT[C/T]TTAGATATGACCCAG	25897
rs1788174	snp	C/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100318729	AGATATGACCCAGAA[C/G]CTTGATACCAAATAA	25897
rs1788175	snp	A/G	0.499642	0.0133738	intron-variant	RNF19A	GRCh38.p7	8:100319861	ttttttcgagatgga[A/G]ttttgctcttgttgc	25897
rs1788176	snp	A/G	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100319884	cttgttgcccaggac[A/G]gagtgcaatggtagg	25897
rs1788177	snp	A/G	0.431029	0.17242	intron-variant	RNF19A	GRCh38.p7	8:100320083	TCAGGTGACCCAACT[A/G]CCTCAGCCTCCCAAA	25897
rs1788178	snp	A/C	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100320290	CCTTTATTTTTTAAA[A/C]AACAACAACAACAAC	25897
rs1788179	snp	A/G	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100321117	gtttcttaaaataag[A/G]taacaatgaagtttg	25897
rs1788180	snp	A/G	0.49962	0.0137727	intron-variant	RNF19A	GRCh38.p7	8:100321140	gaagtttgccacatc[A/G]attgactcttccttc	25897
rs1788181	snp	C/T	0.49962	0.0137727	intron-variant	RNF19A	GRCh38.p7	8:100321840	gaattgtcagtgaga[C/T]ataatattttgaaag	25897
rs1788182	snp	C/T	0.499693	0.0123764	intron-variant	RNF19A	GRCh38.p7	8:100322392	tagcttcaaactttt[C/T]ttctgaagcttcctt	25897
rs1788183	snp	A/C	0.499693	0.0123764	intron-variant	RNF19A	GRCh38.p7	8:100322690	cttgttttttggttt[A/C]aagtgagaggcatgc	25897
rs1788184	snp	A/G	0.499693	0.0123764	intron-variant	RNF19A	GRCh38.p7	8:100322878	aagttcactgtcttc[A/G]gtgggagtggttcat	25897
rs1788185	snp	C/T	0.432357	0.171014	intron-variant	RNF19A	GRCh38.p7	8:100323301	TCTCTGTAATATCAT[C/T]TTTGGAAGTTTTATC	25897
rs1788186	snp	C/T	0.499693	0.0123764	intron-variant	RNF19A	GRCh38.p7	8:100323458	CCTGTTTTTGCAGGA[C/T]GACCACGTTTCACCC	25897
rs1788187	snp	A/G	0.499693	0.0123764	intron-variant	RNF19A	GRCh38.p7	8:100323871	AAATGACTGTGCCAA[A/G]CCAACATTCCTGTCA	25897
rs1788193	snp	C/T	0.428333	0.175206	intron-variant	RNF19A	GRCh38.p7	8:100264449	GAAGTGCCAGGCCTC[C/T]GAACTGTACTTGGGG	25897
rs1788194	snp	C/T	0.432504	0.170857	intron-variant	RNF19A	GRCh38.p7	8:100265688	TATTACATGGTATAA[C/T]AACACCTTTGGCCTT	25897
rs1788196	snp	C/T	0.499587	0.0143711	intron-variant	RNF19A	GRCh38.p7	8:100277860	GTTTTAAAACAATAA[C/T]GTCAGTGAAAAGGAT	25897
rs1788197	snp	C/T	0.499673	0.0127754	intron-variant	RNF19A	GRCh38.p7	8:100278700	CTTTGTAGAAGGCTG[C/T]TCAATATACTAGTAT	25897
rs1788198	snp	A/G	0.418814	0.184396	intron-variant	RNF19A	GRCh38.p7	8:100280132	TCATTAAGGGGCAGG[A/G]CTGGATTTGAACAAA	25897
rs1788199	snp	A/G	0.432797	0.170544	intron-variant	RNF19A	GRCh38.p7	8:100280626	TGTTTTCATAAATGT[A/G]TAATCTGACAACAAA	25897
rs1788201	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290159	tgtgtctgttgccca[C/G]gctggagtgcagtga	25897
rs1788202	snp	C/T	0.430732	0.172731	intron-variant	RNF19A	GRCh38.p7	8:100290328	gctggcctcgaactc[C/T]tgacctcaagtgatc	25897
rs1788203	snp	C/T	0.430285	0.173197	intron-variant	RNF19A	GRCh38.p7	8:100291493	ACATGTTAAGTATCC[C/T]GACACTACAACTTCA	25897
rs1788204	snp	C/T	0.43088	0.172575	intron-variant	RNF19A	GRCh38.p7	8:100291708	TACATGGTCAAATAA[C/T]AGTTTTTGCTTCTGT	25897
rs1788205	snp	C/G	0.430285	0.173197	intron-variant	RNF19A	GRCh38.p7	8:100294318	GTAGATCTGTGGAAA[C/G]CACCCATGTTTACCA	25897
rs1788206	snp	A/G	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100294738	ttcatctaggctttg[A/G]gatacagtattcttg	25897
rs1788207	snp	A/G	0	0	intron-variant	RNF19A	GRCh38.p7	8:100298495	CCAACAAGTTCTTTA[A/G]AAAGTAAATGCTTAC	25897
rs1788208	snp	C/T	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100300287	GAAAAATCTAGGTAA[C/T]AATTACACAGCAGGT	25897
rs1788209	snp	C/T	0.495213	0.048687	intron-variant	RNF19A	GRCh38.p7	8:100324828	CTTCCTTCCTTCCTT[C/T]CTCCTTCTTCCTCCC	25897
rs1788210	snp	A/T	0.430136	0.173352	intron-variant	RNF19A	GRCh38.p7	8:100325084	GCTAATTTTTTGTAT[A/T]TTTAGTAGAGATGGG	25897
rs1866787	snp	C/G	0	0	intron-variant	RNF19A	GRCh38.p7	8:100300199	GTCTCCCGAAAATGA[C/G]ATTAAAAACTCACGT	25897
rs1962901	snp	C/T	0.49962	0.0137727	intron-variant	RNF19A	GRCh38.p7	8:100314200	TATATATAGTATGTA[C/T]GCAATAAAGAGTAGT	25897
rs2033920	snp	C/T	0.499396	0.0173617	intron-variant	RNF19A	GRCh38.p7	8:100335778	TTACCTTAGAAAGCA[C/T]CTAGGGACAGGCGGC	25897
rs2033921	snp	A/G	0.499653	0.0131743	intron-variant	RNF19A	GRCh38.p7	8:100319586	ccaggctggagtgta[A/G]tggcacaatctcggc	25897
rs2033922	snp	C/G	0.431325	0.172108	intron-variant	RNF19A	GRCh38.p7	8:100319637	caggttcaagtgatt[C/G]tcctgcctcagcctc	25897
rs2439452	snp	C/T	0.221439	0.248363	intron-variant	RNF19A	GRCh38.p7	8:100316993	ctgggggacccagta[C/T]actctccgcagccgc	25897
rs2439453	snp	C/T	0.49962	0.0137727	intron-variant	RNF19A	GRCh38.p7	8:100316996	ggggacccagtacac[C/T]ctccgcagccgctgg	25897
rs2439456	snp	C/T	0.502127	0.0552246	intron-variant	RNF19A	GRCh38.p7	8:100324646	TTGATTTTTCACAAA[C/T]GAAGAATTTCCAACC	25897
rs2439458	snp	C/T	0.499587	0.0143711	intron-variant	RNF19A	GRCh38.p7	8:100285756	TCCCGTCTTGGCCTC[C/T]CAAAGTGCTGGGATT	25897
rs2439460	snp	C/T	0.499563	0.0147699	intron-variant	RNF19A	GRCh38.p7	8:100300437	GGCAGGCAGATTACT[C/T]GAAATTAGGAGTTCA	25897
rs2510206	snp	A/G	0.090703	0.192677	intron-variant	RNF19A	GRCh38.p7	8:100276738	caaaaaaaaaaaaaa[A/G]aaaaagaaaaaaagg	25897

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