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
rs2883	snp	A/T	0.489024	0.0732638	intron-variant	SMARCAD1	GRCh38.p7	4:94237459	GAGTCAGCATTTATT[A/T]AAAAACTGGACACGC	56916
rs8026	snp	A/G	0.499546	0.0150616	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	SMARCAD1	GRCh38.p7	4:94291034	CTAAAAGGAGTCTTC[A/G]TGTGTTAATACTACC	56916
rs8336	snp	A/G	0.476647	0.105504	utr-variant-3-prime, nc-transcript-variant	SMARCAD1	GRCh38.p7	4:94290459	TCAGTCTGCTTTGAA[A/G]TGAAATAGCTTTAAG	56916
rs14696	snp	A/C	0.000721891	0.0189848	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	SMARCAD1	GRCh38.p7	4:94291178	CAACAACAATAACAA[A/C]AAAAAAAGAAACAGC	56916
rs169488	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94219618	TGGAATTACTCCCTA[G/T]GGCCATGGAGTCTTC	56916
rs183993	snp	C/T	0.497356	0.0912703	intron-variant, upstream-variant-2KB	SMARCAD1, LOC101929210	GRCh38.p7	4:94208874	CTGAATCACTGACAT[C/T]GCTCTTCCAATAGCA	56916
rs192527	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94210735	tgttggccaggctgg[G/T]cttgtgatctcaggt	56916
rs204755	snp	C/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94210788	ctccaccatgcctgg[C/G]taatttttgtagttt	56916
rs282447	snp	A/G	0.488965	0.0734569	intron-variant	SMARCAD1	GRCh38.p7	4:94220274	tgtttttgagatgga[A/G]ttttgctttgttgcc	56916
rs282448	snp	G/T	0.497121	0.0378299	intron-variant	SMARCAD1	GRCh38.p7	4:94220260	atttattattattat[G/T]tttttgagatggagt	56916
rs282449	snp	A/G	0.497091	0.0380279	intron-variant	SMARCAD1	GRCh38.p7	4:94220077	TTTGAATTAAAAAGC[A/G]TCATTGCAGCAGGAA	56916
rs282450	snp	C/G	0.489083	0.0730708	intron-variant	SMARCAD1	GRCh38.p7	4:94218447	ACAGGCATGCATCAC[C/G]ACGCCCAGCTAATAT	56916
rs728989	snp	C/G	0.43655	0.16643	intron-variant	SMARCAD1	GRCh38.p7	4:94243330	TGCATGTGCAGATGT[C/G]TCAGACTCTCATGGT	56916
rs1352265	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94262095	TGCTGATGAGATTAC[A/C]TAAGGAAAAGCACAT	56916
rs1352266	snp	A/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94278025	AAATGGCCCCAAAAG[A/G]AAGCTAGTGCAGACT	56916
rs1352267	snp	G/T	0	0	intron-variant, utr-variant-5-prime, nc-transcript-variant	SMARCAD1	GRCh38.p7	4:94266066	CTACACCATCCCATA[G/T]CACCCTATAAGGGCA	56916
rs1386532	snp	A/C			intron-variant	SMARCAD1	GRCh38.p7	4:94278123	TCATGTATCGATTAC[A/C]TAGATAACTCTCATT	56916
rs1386533	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94278021	GGCCCCAAAAGGAAG[A/C]TAGTGCAGACTGATG	56916
rs1386534	snp	A/C			intron-variant	SMARCAD1	GRCh38.p7	4:94277925	AAGTAGAATTTTATT[A/C]TAGGATGTGAAGGAG	56916
rs1487368	snp	C/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94248132	gctggaaaccatttc[C/T]taagcaagctaatgt	56916
rs1565062	snp	C/T	0.4582	0.138394	intron-variant	SMARCAD1	GRCh38.p7	4:94261849	gccaaggcaagagca[C/T]tgtttgagcctagga	56916
rs1906237	snp	A/G	0	0			GRCh38.p7	4:94251757	cctgtgaatgaaggt[A/G]acaccattattttat	56916
rs1955242	snp	A/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94228794	aactaaatccactgt[A/G]aaaAAAAAATTACCA	56916
rs1955243	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94228615	GCAAGATATTCTTGG[G/T]GAAGGAATCAGTACC	56916
rs1955244	snp	A/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94228583	TGATTTGCATTCTAA[A/G]ACATATTCCTTATTT	56916
rs2016428	snp	C/T			intron-variant	SMARCAD1	GRCh38.p7	4:94210675	tgggattacaggctt[C/T]agccaccgcgcATAA	56916
rs2046595	snp	G/T	0.0581437	0.160285	intron-variant	SMARCAD1	GRCh38.p7	4:94218624	TAAATTTGAAATGGG[G/T]TTTTTTCCCTCATTT	56916
rs2087170	snp	A/C	0.499104	0.0211472	intron-variant	SMARCAD1	GRCh38.p7	4:94241809	GCATGCAAGTCAACA[A/C]GGTAAGACTTTCTAC	56916
rs2129596	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94229497	aacacaaCAGCCTGT[G/T]TGAAGAGGCCCTCAG	56916
rs2129597	snp	A/G			intron-variant	SMARCAD1	GRCh38.p7	4:94229377	TTTGATATTTATTGT[A/G]CCACATAAATAAAAG	56916
rs2129598	snp	A/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94229340	TGGGGAGAAAAAGGA[A/G]CATTACAGACTACCA	56916
rs2129601	snp	C/G	0	0	upstream-variant-2KB, intron-variant	SMARCAD1, LOC101929210	GRCh38.p7	4:94205842	agatggagttgccca[C/G]gctggagtgcaatgg	56916
rs2171383	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94229295	GTTCTAGAACACTGG[G/T]TAGTATACCACATTT	56916
rs2220338	snp	A/G	0.0134861	0.0810011	intron-variant	SMARCAD1	GRCh38.p7	4:94262414	GTCTGTGTTGGACAC[A/G]GAGAAACTGATAAGA	56916
rs2276910	snp	C/T	0.462285	0.132043	intron-variant, nc-transcript-variant, upstream-variant-2KB	SMARCAD1, LOC101929210	GRCh38.p7	4:94208087	TAAGAGGAGGTTGCA[C/T]GAGGGTCAGCTCGTG	56916
rs2306802	snp	C/T	0.476321	0.106202	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	SMARCAD1	GRCh38.p7	4:94264904	CAACAAAGATTACCT[C/T]TGGTTTAGAATGGAA	56916
rs2306803	snp	A/G	0.445724	0.155538	intron-variant	SMARCAD1	GRCh38.p7	4:94240845	AAAAATCAATTTAAT[A/G]TAAAACAAAGGCAAA	56916
rs2632387	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94235733	TTTAATACTCCATGT[G/T]TATTCTATTAGAAGC	56916
rs2632395	snp	C/T	0.0923359	0.194016	intron-variant	SMARCAD1	GRCh38.p7	4:94235342	ATCCTGCAACAGCGA[C/T]GAATCTTTTCCACTA	56916
rs2632396	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94235330	cgacgaatcttttcc[A/C]ctaggtgaaagcagc	56916
rs2632397	snp	C/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94234146	TTTATCATCATTACA[C/G]CTACACTAACCAATG	56916
rs2632398	snp	A/G	0.0154232	0.0864508	missense, nc-transcript-variant, utr-variant-5-prime	SMARCAD1	GRCh38.p7	4:94234003	TATCATCATTTCTAC[A/G]TGCCATGGTAGGAAG	56916
rs2632399	snp	A/C	0.497091	0.0380279	intron-variant	SMARCAD1	GRCh38.p7	4:94232590	GTAACGAGGCAAATA[A/C]ACCTCTTCCTTTATC	56916
rs2632400	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94232573	CCTCTTCCTTTATCA[A/C]TATGCCTGTCCTTCA	56916
rs2632401	snp	C/G	0.499137	0.0207489	intron-variant	SMARCAD1	GRCh38.p7	4:94225904	GTTATTTTGCAGTTT[C/G]CACTAAAGTCTTGTT	56916
rs2632405	snp	A/C	0.489142	0.0728777	intron-variant	SMARCAD1	GRCh38.p7	4:94231064	CATCTTTCGCACAAC[A/C]ACTCAGTGAAACTGT	56916
rs2632406	snp	A/G			intron-variant	SMARCAD1	GRCh38.p7	4:94230029	attaattaataatCC[A/G]AGTGCATTGAGTGTA	56916
rs2632407	snp	C/G	0	0	intron-variant, upstream-variant-2KB	SMARCAD1, LOC101929210	GRCh38.p7	4:94209060	TTCTGAGGACATCCA[C/G]GAAGTCAGGTGGATG	56916
rs2632410	snp	A/T	0.489024	0.0732638	intron-variant	SMARCAD1	GRCh38.p7	4:94228356	aaagtgttcagtagt[A/T]attgtaattgctgtt	56916
rs2632411	snp	C/T	0.485324	0.0843964	intron-variant	SMARCAD1	GRCh38.p7	4:94228283	gtaattctgaaaaga[C/T]tgtgagagttgataa	56916
rs2632412	snp	A/C	0.372995	0.217652	intron-variant	SMARCAD1	GRCh38.p7	4:94228168	TTTTATCTTGGAGTA[A/C]ATTTCAGAATTAGGC	56916
rs2632413	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94227632	cctttatctcagtac[A/C]tagtaactccatcct	56916
rs2632416	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94216430	TTAACAGACATACTA[G/T]AGGAAAATATGAATG	56916
rs2632417	snp	C/G	0.488965	0.0734569	intron-variant	SMARCAD1	GRCh38.p7	4:94216391	TATAGTGTGGTAATG[C/G]GGAATGCAGAAGACT	56916
rs2632418	snp	C/G			intron-variant	SMARCAD1	GRCh38.p7	4:94216382	GTAATGCGGAATGCA[C/G]AAGACTTATAGGAAA	56916
rs2632419	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94216373	AATGCACAAGACTTA[G/T]AGGAAAGGATGAACA	56916
rs2632420	snp	A/G			intron-variant	SMARCAD1	GRCh38.p7	4:94216207	tgctggagggaggaa[A/G]gggtattaggtgatg	56916
rs2632421	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94216093	aaagattgtggtcta[G/T]gaatatggccctgag	56916
rs2632422	snp	C/G/T	0.000399281	0.0141238	intron-variant	SMARCAD1	GRCh38.p7	4:94216087	tgtggtctatgaata[C/G/T]ggccctgagatacct	56916
rs2632423	snp	C/T	0.439224	0.163383	intron-variant	SMARCAD1	GRCh38.p7	4:94214327	TGCAGTGAGTTGAGA[C/T]TGCGCCACTGCACTC	56916
rs2664871	snp	C/T	0.49706	0.0382258	intron-variant	SMARCAD1	GRCh38.p7	4:94225130	TAATACTTTATTGAC[C/T]TGTTTTTGAACAGAC	56916
rs2664872	snp	A/G	0.488965	0.0734569	intron-variant	SMARCAD1	GRCh38.p7	4:94225801	GGAATCTTTTGGGCT[A/G]TGGTGTTCATGCTGT	56916
rs2664873	snp	C/T			intron-variant	SMARCAD1	GRCh38.p7	4:94226738	accatccccagcttt[C/T]tttctgccctcacac	56916
rs2664874	snp	C/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94226742	tccccagctttcttt[C/T]tgccctcacacagct	56916
rs2664875	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94228446	aacagtaatatttca[A/C]acccagaaataccaa	56916
rs2664880	snp	A/T	0.488965	0.0734569	intron-variant	SMARCAD1	GRCh38.p7	4:94223026	TGTTTTTCTCCCTTA[A/T]ACAGACTGTAGTACA	56916
rs2664881	snp	C/T	0.489024	0.0732638	intron-variant	SMARCAD1	GRCh38.p7	4:94222333	TTGTATCTCTGATAC[C/T]TACCATACTTGAAAA	56916
rs2664882	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94220763	atacattgactacta[G/T]aaccgtctagagcct	56916
rs2664883	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94220753	tactagaaccgtcta[G/T]agccttggccttgat	56916
rs2664884	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94235755	TTTGGCCCTTTATGT[G/T]GAATATTTTAATACT	56916
rs2664885	snp	C/G			intron-variant	SMARCAD1	GRCh38.p7	4:94235676	CTTTAGCCCTCATGT[C/G]TACATTTGTTTCCAC	56916
rs2664886	snp	A/C	0.375	0.216506	intron-variant	SMARCAD1	GRCh38.p7	4:94235659	ACATTTGTTTCCACA[A/C]AAAAAAAAAAAAAAA	56916
rs2664887	snp	C/T			intron-variant	SMARCAD1	GRCh38.p7	4:94235337	GCAACAGCGATGAAT[C/T]TTTTCCACTAGGTGA	56916
rs2664888	snp	C/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94235293	CAAAATATCACATAT[C/T]TGAATCCATTTATAT	56916
rs2664889	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94234209	CGTAAGATATCTTTA[G/T]AAAAATGACTATCCA	56916
rs2664890	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94234181	CCACTACTAACTATA[G/T]CACTGAATGCAGGAG	56916
rs2664891	snp	A/G	0	0	missense, nc-transcript-variant, utr-variant-5-prime	SMARCAD1	GRCh38.p7	4:94233988	GTGCCATGGTAGGAA[A/G]GCCTTGGGACTCTTC	56916
rs2664892	snp	A/G	0.498392	0.028309	intron-variant	SMARCAD1	GRCh38.p7	4:94233035	AACATGTGATGCCTA[A/G]GAACATCTAAAAGCA	56916
rs2664893	snp	C/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94233004	AATTTCCAAAGAACA[C/G]AATATGTGTGttttt	56916
rs2664894	snp	A/G	0.489024	0.0732638	intron-variant	SMARCAD1	GRCh38.p7	4:94232680	CAGGTGTGAGCCACC[A/G]TGCCTAGCCAGTGTA	56916
rs2664895	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94229946	catacttgatgactg[A/C]acagattagtaaaat	56916
rs2865345	snp	A/G	0.478188	0.10213	intron-variant	SMARCAD1	GRCh38.p7	4:94235414	AAAAATAAACATGCT[A/G]TTCAAGCCAAACAAC	56916
rs2865350	snp	A/T	0.373196	0.217538	downstream-variant-500B	SMARCAD1	GRCh38.p7	4:94291662	TTGAAACATTACTGT[A/T]GTTCCTAACAGTTGG	56916
rs2902979	snp	C/G	0.49703	0.0384237	intron-variant	SMARCAD1	GRCh38.p7	4:94256723	ATTGGCCACTTAAAG[C/G]ATGGTAATACATATT	56916
rs2902980	snp	A/C	0.165853	0.235413	intron-variant	SMARCAD1	GRCh38.p7	4:94256724	TTGGCCACTTAAAGC[A/C]TGGTAATACATATTT	56916
rs2941218	snp	A/C			intron-variant	SMARCAD1	GRCh38.p7	4:94230343	CTAAGTAAATAAAAG[A/C]ACAAATGAATATACA	56916
rs2941219	snp	C/T			intron-variant	SMARCAD1	GRCh38.p7	4:94230331	AAGAACAAATGAATA[C/T]ACACACATGTAGTAT	56916
rs2941220	snp	A/C			intron-variant	SMARCAD1	GRCh38.p7	4:94230297	ATCTTTTGTGTAAGA[A/C]ACAAAAAAAAAAATA	56916
rs2941221	snp	C/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94230270	AATACACGAAAGTAT[C/G]ACAATGAACTAAACA	56916
rs2941222	snp	A/C	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94230242	ACAAACTGGTTAGTT[A/C]TAAGGTTTGAATGGA	56916
rs3066293	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94239442	TTGTTTTGAAAGTTT[G/T]TTTTTGAATATGAAA	56916
rs3103115	snp	C/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94250221	GGCCTTTTAGCAACA[C/G]GATGCGTGGCATGAG	56916
rs3103116	snp	A/G	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94249932	TATAGTAAACAAGGT[A/G]AATAAACAACATAAA	56916
rs3103117	snp	G/T	0.017122	0.0909277	missense, nc-transcript-variant, utr-variant-5-prime	SMARCAD1	GRCh38.p7	4:94249682	TCCCAATTACTGCTA[G/T]ATTCTGCAGACTCAT	56916
rs3103118	snp	A/C/G	0.000399281	0.0141238	intron-variant	SMARCAD1	GRCh38.p7	4:94249591	CACTGGGCTTAAAGC[A/C/G]ATTATCATTGTGTTT	56916
rs3103119	snp	A/G			intron-variant	SMARCAD1	GRCh38.p7	4:94249579	AGCGATTATCATTGT[A/G]TTTTGACTCGATCTG	56916
rs3103120	snp	G/T			intron-variant	SMARCAD1	GRCh38.p7	4:94246244	taatcccagctactc[G/T]ggaggctgaggtggg	56916
rs3103121	snp	C/G/T	0.000798403	0.0199641	intron-variant	SMARCAD1	GRCh38.p7	4:94245556	GTGGTAGCTCACTGT[C/G/T]CTTGTGTTATGTGTG	56916
rs3103122	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94245162	CCGAGTCCAAACTGT[G/T]TTTCTTAGATCAATA	56916
rs3103125	snp	G/T	0	0	intron-variant	SMARCAD1	GRCh38.p7	4:94253954	TTGCTCCCTAACTTA[G/T]GGAATAAAACTTTCT	56916

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