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
rs7789166	snp	C/T	0.443598	0.158176	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701482	CATTTGGAGATATAC[C/T]TAATGTTAAATGACG	378925
rs7790381	snp	G/T	0.01005	0.0701712	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702088	ACTTCGCCTCCTGGT[G/T]AAAGAATTGGGCACT	378925
rs28541748	snp	A/T			intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701465	GAAGCGGGGAGGGAT[A/T]GCATTTGGAGATATA	378925
rs35322616	in-del	-/C			intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704056	TGTATAGGTTATCTT[-/C]CTATGTGCTCAGCAT	378925
rs35372605	snp	C/G	0.181978	0.240568	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704947	AAGAAATTATGTGGT[C/G]CAAAATATCAATAGT	378925
rs73220287	snp	C/T	0.0209421	0.100162	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702835	AAGATAGCTTGTTGG[C/T]GGCAGATTACTAAAG	378925
rs73220288	snp	G/T	0.221439	0.248363	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704353	TCCTTACAGGTAGAC[G/T]TTTTTTTTTTCATGT	378925
rs73437705	snp	A/G	0.0104602	0.071559	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702715	TCCAGATGAAACAGA[A/G]CTATGCGTCGAAGGG	378925
rs75461294	snp	A/G	0.0115144	0.0749975	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702836	AGATAGCTTGTTGGC[A/G]GCAGATTACTAAAGC	378925
rs76137038	snp	A/T			intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704537	CTTTTTATTTTGCAG[A/T]TTTTTTGTGGGTGAA	378925
rs76233656	in-del	-/T	0.172997	0.237846	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704537	TTTTTATTTTGCAGA[-/T]TTTTTTGTGGGTGAA	378925
rs77687318	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704364	AGACTTTTTTTTTTT[C/T]ATGTTCAAATGGAGT	378925
rs77929503	snp	C/G	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702807	ACAACATCAGTTGTA[C/G]AAGAACATAAAGAAG	378925
rs78593990	snp	A/C	0.0788843	0.182262	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703773	GAGCTTAGGCAAAAG[A/C]AGATAGTGGCTTGGA	378925
rs78832865	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704363	TAGACTTTTTTTTTT[C/T]CATGTTCAAATGGAG	378925
rs113197000	snp	C/T	0.00914312	0.0669923	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701296	TCCTTTGTAGGGACA[C/T]GGATGAAGCTGGAAA	378925
rs117448502	snp	C/T	0.0279526	0.114869	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704717	CCCTCTCTTCTGCCC[C/T]CGTCTTACAACAAAA	378925
rs117586487	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702945	TCATAATGAAACAAA[A/G]TAACAAGACTTGTGA	378925
rs117830557	snp	C/T	0.0256215	0.110247	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702831	AAAGAAGATAGCTTG[C/T]TGGCGGCAGATTACT	378925
rs118066697	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704048	TTTCTATCATGTATA[C/G]GTTATCTTCTATGTG	378925
rs138284424	snp	A/C/G	0.00268409	0.0365442	intron-variant, synonymous-codon, missense	CADPS2, RNF148	GRCh38.p7	7:122701931	AATGTTTGCAAGTTA[A/C/G]AATGCGTACTACATC	378925
rs138600624	snp	C/T	1.65674e-05	0.00287809	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702422	TTATGTGTAAAAGTA[C/T]AGCCTCCACGTTCGA	378925
rs139011944	snp	C/T	0.0103295	0.0711199	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701481	GCATTTGGAGATATA[C/T]CTAATGTTAAATGAC	378925
rs139576419	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704657	AGCTCATTCATTCTA[C/T]TTTTCTCATTATAAT	378925
rs139751883	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703108	AATGAGTCAAGATAC[A/G]TAACAATTTGAATAG	378925
rs142695415	snp	G/T	0.000399281	0.0141238	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702560	TCCAGAGGAGAATGA[G/T]TCCCGAACACTCCAC	378925
rs142716487	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703238	TTTCTAGCTGTAAGG[C/T]AAAGGCAAAGATAAA	378925
rs145027837	snp	C/T	0.0221141	0.102801	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701477	GATAGCATTTGGAGA[C/T]ATACCTAATGTTAAA	378925
rs147169344	snp	C/G/T	9.9373e-05	0.00704824	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702295	GTTGCTTATCATCAC[C/G/T]GCGACTATATTTTCC	378925
rs147362816	snp	C/T	0.00275622	0.0370204	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702724	AACAGAACTATGCGT[C/T]GAAGGGGTAATTCTA	378925
rs149475218	snp	C/T	0.00250196	0.0352806	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122701947	AATGCGTACTACATC[C/T]TGGGGTTTGTATGTG	378925
rs150450224	snp	A/C/T	4.97701e-05	0.00498828	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701909	TCAATGCATGCCTTA[A/C/T]GGAAAAAATGTTTGC	378925
rs150554227	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703502	CAGTGTAAACTCTTA[C/T]TGTTAGCCTAATACA	378925
rs180849511	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703186	TTTCTTCCTTAGTTC[G/T]GGAGAGACTGAAAAT	378925
rs181995389	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702871	AAATGGAAAAGGTCT[A/C]CCTGGATCAAAGCTA	378925
rs182748737	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704636	AAGGACCAATTTGAG[G/T]AACTTAGCTCATTCA	378925
rs182867883	snp	A/G	0.00318978	0.0398085	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701334	TCTCAGCGAACTATC[A/G]CAAGGACAAAAAACC	378925
rs182993272	snp	A/C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703389	GATGGTTCAACACTA[A/C/T]CCAGTATGGCATTCT	378925
rs183114321	snp	C/T	0.00358779	0.0422022	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701428	GGGAACGTCACACAC[C/T]GGGGCCTGTTGTGGG	378925
rs183241405	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704060	ATAGGTTATCTTCTA[C/T]GTGCTCAGCATGCCA	378925
rs184065081	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704831	TGCTTCTGCAGACAT[A/T]TTTTGATTGTCACAA	378925
rs184474405	snp	C/T	0.00358779	0.0422022	intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702829	ATAAAGAAGATAGCT[C/T]GTTGGCGGCAGATTA	378925
rs184801351	snp	C/G/T	0.000198733	0.00996641	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702270	AGTGCAAAATTTCCA[C/G/T]GCCTTTCAGGTTGCT	378925
rs185927409	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703683	AAGCCAGGGAGGTGA[C/T]AAATGTGTTTCAAAA	378925
rs186520802	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703351	TGGGATGGTTCAACA[C/T]TACCGAATATGGCAT	378925
rs187208331	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122702968	ACTTGTGATTGGTAC[A/C]ATGTGATTTCAAGAA	378925
rs187667058	snp	A/G	0.00142988	0.0267001	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702036	GAACTCGCAGTTGAA[A/G]CTGGTCAATAGCTTT	378925
rs187856840	snp	C/T	0.000798403	0.0199641	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701355	ACAAAAAACCAAACA[C/T]CGCATGTTCTCACTC	378925
rs188118563	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704763	CAATCATCTATCTCT[C/T]AAAAAGTGGTTTTCA	378925
rs188887592	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704403	GGCTGATTCTATTAA[C/T]AGTGACAAATTGAAG	378925
rs188936781	snp	A/T			intron-variant, utr-variant-5-prime	CADPS2, RNF148	GRCh38.p7	7:122702868	CATAAATGGAAAAGG[A/T]CTCCCTGGATCAAAG	378925
rs189215473	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703116	AAGATACATAACAAT[C/T]TGAATAGGCTGTAAA	378925
rs189837730	snp	C/T	0.000480287	0.0154891	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702399	CCTTCTCTGCTGCCA[C/T]GTTGATTTTATGTGT	378925
rs190386268	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703934	TTACAGAATCTTTAC[A/G]GCTTTAAAGATGCCT	378925
rs191326240	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703355	ATGGTTCAACACTAC[C/T]GAATATGGCATTCTG	378925
rs191835775	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704808	TTGCCTCTCAGGGGA[C/T]ATCTGGCTGCTTCTG	378925
rs192276120	snp	C/T	0.00599571	0.0544234	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702589	ACTCTCTCCTAATTC[C/T]GATGTGATCTCATTT	378925
rs192419960	snp	G/T	0.0107246	0.0724382	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701382	ACTCATAGGTGGGAA[G/T]TGAACAATGAGAACA	378925
rs192515188	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704455	ACATCATCATATTAG[A/G]GGTAATTTGTTAAAT	378925
rs192523053	snp	A/G	3.31241e-05	0.00406952	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702256	TCCTTTCTGAATCGA[A/G]TGCAAAATTTCCATG	378925
rs199691234	snp	A/G			intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122704045	TATTTTCTATCATGT[A/G]TAGGTTATCTTCTAT	378925
rs199764715	snp	C/T	3.31246e-05	0.00406955	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702253	GACTCCTTTCTGAAT[C/T]GAGTGCAAAATTTCC	378925
rs199897572	snp	A/G	0.000447231	0.0149471	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702400	CTTCTCTGCTGCCAC[A/G]TTGATTTTATGTGTA	378925
rs200113037	snp	A/C/G	0.000149779	0.00865273	intron-variant, missense, stop-gained	CADPS2, RNF148	GRCh38.p7	7:122702027	CTTCTTTGAGAACTC[A/C/G]CAGTTGAAGCTGGTC	378925
rs200171193	snp	C/T	0.000231873	0.0107649	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702356	CTGCCCGTACCTTGA[C/T]AGTTGTAGATGATCA	378925
rs200667006	snp	A/G	1.65723e-05	0.00287852	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702152	AAGTAGGCAATTGTG[A/G]CAGCCAGGAAGGTAA	378925
rs200865337	snp	C/T	8.28164e-05	0.00643439	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702297	TGCTTATCATCACCG[C/T]GACTATATTTTCCGT	378925
rs201098995	snp	A/G	0.000149282	0.00863822	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701937	TGCAAGTTAAAATGC[A/G]TACTACATCTTGGGG	378925
rs201141220	snp	C/G	0.00012055	0.00776277	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702720	ATGAAACAGAACTAT[C/G]CGTCGAAGGGGTAAT	378925
rs201215032	snp	A/G	4.98409e-05	0.00499179	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702590	CTCTCTCCTAATTCC[A/G]ATGTGATCTCATTTC	378925
rs201297535	in-del	-/A	0.0236746	0.106192	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701621	AAATAAAATTCACCT[-/A]AAAAAAACAATTAAA	378925
rs201395313	snp	A/G	6.62493e-05	0.00575502	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702296	TTGCTTATCATCACC[A/G]CGACTATATTTTCCG	378925
rs201540773	snp	A/C/T	0.000199659	0.00998958	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702026	CCTTCTTTGAGAACT[A/C/T]GCAGTTGAAGCTGGT	378925
rs201630707	snp	A/C	0.000166061	0.00911058	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701900	AGCCAGGGGTCAATG[A/C]ATGCCTTATGGAAAA	378925
rs201973741	snp	A/G	0.000132503	0.00813842	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702311	GCGACTATATTTTCC[A/G]TCCCCTGGTGAGACA	378925
rs202050897	snp	A/G	4.97146e-05	0.00498546	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702436	ACAGCCTCCACGTTC[A/G]ATGAGGGCCAGCCAT	378925
rs202141735	snp	C/T	0.00013287	0.0081497	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701981	AAGCAAACAACACAG[C/T]TGTCTTCATTTAGGT	378925
rs202200728	snp	C/T	0.000399062	0.0141199	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702077	GTCTTTATTTGACTT[C/T]GCCTCCTGGTGAAAG	378925
rs367569835	snp	A/G/T	0.000231851	0.0107645	intron-variant, stop-gained, missense	CADPS2, RNF148	GRCh38.p7	7:122702254	ACTCCTTTCTGAATC[A/G/T]AGTGCAAAATTTCCA	378925
rs368049014	snp	A/C	0.000161987	0.00899818	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702372	AGTTGTAGATGATCA[A/C]CCCATTTGCTCCCTT	378925
rs368078936	snp	C/T	3.56818e-05	0.0042237	intron-variant, utr-variant-3-prime	CADPS2, RNF148	GRCh38.p7	7:122701830	GAAAATTCTCCAGAT[C/T]TCTTAAGTTTTCAGG	378925
rs368118247	snp	A/C	0.000167986	0.00916323	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702740	GAAGGGGTAATTCTA[A/C]GGAAGCTCATGCCTC	378925
rs368198874	snp	A/G	7.38798e-05	0.00607737	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702722	GAAACAGAACTATGC[A/G]TCGAAGGGGTAATTC	378925
rs368588577	snp	A/G			intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701226	TACGATTAAGAAAAT[A/G]TGGCACATATACACC	378925
rs368632624	snp	A/G	4.98824e-05	0.00499387	intron-variant, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122701893	GGCTAAAAGCCAGGG[A/G]TCAATGCATGCCTTA	378925
rs368845403	snp	C/G/T	6.62706e-05	0.005756	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702431	AAAGTACAGCCTCCA[C/G/T]GTTCGATGAGGGCCA	378925
rs368944991	snp	A/G	4.97863e-05	0.00498906	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701960	TCTTGGGGTTTGTAT[A/G]TGTCAAAGCAAACAA	378925
rs369956136	snp	C/T	0.000159987	0.00894248	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702465	ATGAGTCTGCCTGTT[C/T]GGGCCTGCTGAAATT	378925
rs370147382	snp	C/G	1.72779e-05	0.00293916	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701852	GTTTTCAGGATGTCA[C/G]ACTTGCACATGGGAC	378925
rs370211791	snp	C/G/T	0.000328779	0.0128178	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702651	TCCAAATGGCTTTTC[C/G/T]GTTTGAGTCAGGAAA	378925
rs370238800	snp	A/G	0.000798403	0.0199641	intron-variant	CADPS2, RNF148	GRCh38.p7	7:122701214	GGCAAAAAGGGATAC[A/G]ATTAAGAAAATGTGG	378925
rs370904877	snp	C/T	1.65748e-05	0.00287874	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702140	CAATCTAAGTAAAAG[C/T]AGGCAATTGTGGCAG	378925
rs371390372	snp	A/T	1.65696e-05	0.00287828	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702434	GTACAGCCTCCACGT[A/T]CGATGAGGGCCAGCC	378925
rs371445644	snp	A/G			intron-variant, upstream-variant-2KB	CADPS2, RNF148	GRCh38.p7	7:122703325	TCAACACTACCCAAT[A/G]TGGCATTCTGTGGGA	378925
rs372584162	snp	C/G/T	1.65927e-05	0.00288029	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701952	GTACTACATCTTGGG[C/G/T]TTTGTATGTGTCAAA	378925
rs372978327	snp	C/T	3.32204e-05	0.00407542	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701898	AAAGCCAGGGGTCAA[C/T]GCATGCCTTATGGAA	378925
rs373122777	snp	A/C	1.65737e-05	0.00287864	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702473	GCCTGTTTGGGCCTG[A/C]TGAAATTGGTCAAAG	378925
rs373254243	snp	A/G/T	1.67913e-05	0.00289748	intron-variant, missense, synonymous-codon	CADPS2, RNF148	GRCh38.p7	7:122702628	AAATGTTATATTCAG[A/G/T]TGAGCTGTCCAAATG	378925
rs373309915	snp	C/T	0.000165986	0.00910855	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122701963	TGGGGTTTGTATGTG[C/T]CAAAGCAAACAACAC	378925
rs373686482	snp	A/T	1.65737e-05	0.00287864	intron-variant, missense	CADPS2, RNF148	GRCh38.p7	7:122702141	AATCTAAGTAAAAGT[A/T]GGCAATTGTGGCAGC	378925

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