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
rs200517	snp	C/G			intron-variant	ARMC4	GRCh38.p7	10:27872320	tcaattaggaaaaga[C/G]gaagtcaaattgtcc	55130
rs200518	snp	C/T			intron-variant	ARMC4	GRCh38.p7	10:27872033	ctacaaaccactgct[C/T]aaggaaataaaagag	55130
rs394249	snp	A/T			intron-variant	ARMC4	GRCh38.p7	10:27872822	gcagagacacaacca[A/T]aaaagagaattttag	55130
rs880706	snp	G/T	0.462363	0.131916	intron-variant	ARMC4	GRCh38.p7	10:27904958	CACAAACAATATTTA[G/T]GTTAAAGGACTTAAG	55130
rs880707	snp	G/T	0.463126	0.13068	intron-variant	ARMC4	GRCh38.p7	10:27904011	AAATAAGGACTACCT[G/T]TTGCCAAAAAGGGTA	55130
rs880708	snp	C/T	0.463126	0.13068	intron-variant	ARMC4	GRCh38.p7	10:27904103	ACTCCCCAAACTGTT[C/T]CCTCATACAGAATGA	55130
rs915174	snp	C/T	0.437542	0.165312	intron-variant	ARMC4	GRCh38.p7	10:27844600	GGGCAAGTTATTTAA[C/T]CTTTATGAAACTCAA	55130
rs915175	snp	C/T	0.444	0.157683	intron-variant	ARMC4	GRCh38.p7	10:27844758	AAAACGATATGACTT[C/T]CATTATTATCTAGCT	55130
rs933065	snp	A/C	0.452842	0.146134	intron-variant	ARMC4	GRCh38.p7	10:27949394	GAGCTGTGGAAGCAC[A/C]TCACAGGGAACTTTG	55130
rs952403	snp	A/G	0.113685	0.209567	intron-variant	ARMC4	GRCh38.p7	10:27825215	agtgatggtaatggg[A/G]agatgtcaggacaga	55130
rs952404	snp	C/T	0.154661	0.231107	intron-variant	ARMC4	GRCh38.p7	10:27825192	aggacagattctggg[C/T]ttattttgaaggtaa	55130
rs983258	snp	C/T	0.166832	0.235761	intron-variant	ARMC4	GRCh38.p7	10:27939088	ATCTACACTAACTTT[C/T]TGTGTATGATACATT	55130
rs1041661	snp	A/G	0.0310518	0.120672	intron-variant	ARMC4	GRCh38.p7	10:27877435	ATAAGCTTCCTAATG[A/G]CTCCTAATCTGTGGG	55130
rs1061577	snp	A/G	0.106278	0.204558	utr-variant-3-prime, intron-variant	ARMC4	GRCh38.p7	10:27812382	AATGAAAACACACAA[A/G]TTGAAAATGCACAGA	55130
rs1090967	snp	A/C			intron-variant	ARMC4	GRCh38.p7	10:27872779	gatgaacatcaatgc[A/C]aaaatcctcaataaa	55130
rs1090968	snp	A/G			intron-variant	ARMC4	GRCh38.p7	10:27872750	aaatactggcaaacc[A/G]aatccagcagcacat	55130
rs1095911	snp	C/T	0	0	intron-variant	ARMC4	GRCh38.p7	10:27872504	ccaaaataataagag[C/T]tatgtatgacaaacc	55130
rs1319351	snp	C/T	0.0271762	0.113356	intron-variant	ARMC4	GRCh38.p7	10:27884194	actcaaacaagggaa[C/T]ctcattaagctcaac	55130
rs1334719	snp	A/C	0.462144	0.132269	intron-variant	ARMC4	GRCh38.p7	10:27894494	TGATAAAACAAATAT[A/C]TGGGGAGCTATGCTA	55130
rs1334720	snp	C/T	0.0111196	0.0737302	intron-variant	ARMC4	GRCh38.p7	10:27894637	GCTTGAGTGCAGTGG[C/T]GCAATCACGCCTCAC	55130
rs1334721	snp	G/T	0.0490535	0.14873	intron-variant	ARMC4	GRCh38.p7	10:27866708	ggaagcaagagaggg[G/T]agggaggtgccagac	55130
rs1413772	snp	C/T	0.462582	0.131564	intron-variant	ARMC4	GRCh38.p7	10:27897177	CACCCGCCTGCCTTC[C/T]TTCTTTACTTCActc	55130
rs1419366	snp	A/G	0.485731	0.0832509	intron-variant	ARMC4	GRCh38.p7	10:27931024	TGAGGCATCAGAAGT[A/G]GAGCCTTGGGAAAAG	55130
rs1547327	snp	C/G	0.437542	0.165312	intron-variant	ARMC4	GRCh38.p7	10:27856511	TAGATATTTCCCAGG[C/G]CTCTCTAAACTCTCT	55130
rs1556641	snp	A/G	0.49706	0.0382258	intron-variant	ARMC4	GRCh38.p7	10:27877047	ACTCAGTGAACATTC[A/G]AAAATATTTGTTGAA	55130
rs1556642	snp	A/G	0.499853	0.008585	intron-variant	ARMC4	GRCh38.p7	10:27877568	TTTTAAACATATGAC[A/G]TCTTGCCTCGCATAG	55130
rs1812592	snp	C/T	0.437542	0.165312	intron-variant	ARMC4	GRCh38.p7	10:27845260	gaagagagtgggggc[C/T]gatattcaacattct	55130
rs1832003	snp	C/T			intron-variant	ARMC4	GRCh38.p7	10:27949089	AGCAAATGTTTATTT[C/T]TTCCTTATCAATGGT	55130
rs1832004	snp	A/C	0.462472	0.13174	intron-variant	ARMC4	GRCh38.p7	10:27900223	cttctaacagtcagg[A/C]ctctctgctgcaggt	55130
rs1832005	snp	C/T	0.462472	0.13174	intron-variant	ARMC4	GRCh38.p7	10:27900438	ttccagttttgttcc[C/T]ttgctggtgaggagt	55130
rs1832006	snp	G/T	0.217851	0.247924	intron-variant	ARMC4	GRCh38.p7	10:27900525	TGGGTTAGAACATGC[G/T]CCTTTAGCTCAGACG	55130
rs1833058	snp	C/G	0.454784	0.1434	intron-variant	ARMC4	GRCh38.p7	10:27966397	CAAGCTCCTGGAGTT[C/G]AGGGCAGAGTGAATT	55130
rs1857616	snp	C/T	0.00279162	0.0372561	intron-variant	ARMC4	GRCh38.p7	10:27920271	CATTATTCACTTTCC[C/T]TTATGTATAGTTTAC	55130
rs1857617	snp	A/C	0.497121	0.0378299	intron-variant	ARMC4	GRCh38.p7	10:27883064	TCCTGGGAATCTAAA[A/C]GGCTACATACATGTG	55130
rs1889522	snp	C/T	0.437542	0.165312			GRCh38.p7	10:27853909	agcagaagtttttaa[C/T]gctggtgaagtccaa	55130
rs1889523	snp	C/G	0.49703	0.0384237			GRCh38.p7	10:27844532	TGGTGGTTCAGAGAG[C/G]AGCCTCTAAACCCAC	55130
rs1892115	snp	A/G	0	0			GRCh38.p7	10:27965022	GCTTGATGGACAGGA[A/G]GCAACAGTCAGTAAG	55130
rs1931888	snp	C/T	0.392511	0.205404	intron-variant	ARMC4	GRCh38.p7	10:27818128	CAGCCTGGATGCCAA[C/T]GGATCCTGATATTCA	55130
rs1931889	snp	C/T	0.451856	0.147493	intron-variant	ARMC4	GRCh38.p7	10:27946744	ATAAGAAGGAGGAGG[C/T]GTGTGGGAAGCTTGT	55130
rs1931890	snp	A/C/G	0.00676848	0.0578101	intron-variant	ARMC4	GRCh38.p7	10:27921046	TGTTTACTTTACAAC[A/C/G]TGTGGAAGGAAAATA	55130
rs1931891	snp	C/G	0.00597247	0.0543191	intron-variant	ARMC4	GRCh38.p7	10:27921252	gtgacccctcatcat[C/G]ccactgtactttagc	55130
rs1962094	snp	A/T	0.451732	0.147663	intron-variant	ARMC4	GRCh38.p7	10:27963710	ctacagaaatgctca[A/T]gtttttgattacagg	55130
rs1963750	snp	C/G	0.111224	0.207945	intron-variant	ARMC4	GRCh38.p7	10:27841445	ctgtcacctaggctg[C/G]agtgcagtggtgcga	55130
rs1963751	snp	A/C	0.498774	0.02473	intron-variant	ARMC4	GRCh38.p7	10:27841474	gatctcagctcactg[A/C]aacctccacctccca	55130
rs1964950	snp	C/T	0.499653	0.0131743	intron-variant	ARMC4	GRCh38.p7	10:27841437	gtcttgctctgtcac[C/T]taggctggagtgcag	55130
rs1970631	snp	C/T	0.494358	0.0528145	intron-variant	ARMC4	GRCh38.p7	10:27942806	AAATATGTAATAAAA[C/T]GAATGTGGCAGAATG	55130
rs1974220	snp	G/T	0.498794	0.0245311	intron-variant	ARMC4	GRCh38.p7	10:27845194	GGGTTACACACAAAG[G/T]GAAGCCCATCAGACT	55130
rs1974221	snp	G/T	0.498794	0.0245311	intron-variant	ARMC4	GRCh38.p7	10:27845217	ATCAGACTAACAGAG[G/T]ATCTCTTGGCAGAAA	55130
rs2003191	snp	C/G	0.311369	0.242351	intron-variant	ARMC4	GRCh38.p7	10:27904730	ATGGAAAATAAACAT[C/G]TCGGAATAGCCAGGG	55130
rs2003192	snp	C/T	0.49999	0.00219646	intron-variant	ARMC4	GRCh38.p7	10:27903943	ATCTCCTCTTCCTCC[C/T]CTCTGGGGTTCCCTT	55130
rs2065687	snp	C/T	0.497121	0.0378299	intron-variant	ARMC4	GRCh38.p7	10:27864586	GGTGAGAATGGGGAG[C/T]GAGGTGAGAGTGGGG	55130
rs2065688	snp	C/T	0.497151	0.037632	intron-variant	ARMC4	GRCh38.p7	10:27864782	TACTTGGCTCTATCA[C/T]TTTCTCAAATAATAA	55130
rs2065689	snp	G/T	0.309648	0.24278	intron-variant	ARMC4	GRCh38.p7	10:27821715	TGTACCAAATTTGTA[G/T]TTCACTTTCCTGAGA	55130
rs2065690	snp	A/G	0.463989	0.129263	intron-variant	ARMC4	GRCh38.p7	10:27898823	gtgtgaTTCCAGTAA[A/G]GATTTGAGATCTTTT	55130
rs2152016	snp	C/T	0.218151	0.247963	intron-variant	ARMC4	GRCh38.p7	10:27899714	AGCTGTGGTGGGCTC[C/T]GCCCAGTTCGAACTT	55130
rs2152018	snp	C/G	0.449091	0.151204	intron-variant	ARMC4	GRCh38.p7	10:27867445	GGATGATGCTATTCC[C/G]TGTAGTTTCTCTTCT	55130
rs2152019	snp	A/G	0.448836	0.15154	intron-variant	ARMC4	GRCh38.p7	10:27867356	CAGGCCTAACAGAAC[A/G]CCCCAGCACCATCAG	55130
rs2184418	snp	A/C	0.463343	0.130326	intron-variant	ARMC4	GRCh38.p7	10:27899420	GGGGTATGAAAAAAA[A/C]ACTCCTGCAGCTAGC	55130
rs2184419	snp	A/C	0.141934	0.225437	intron-variant	ARMC4	GRCh38.p7	10:27924951	caaagcccaggtagt[A/C]ccattgctcaataaa	55130
rs2225713	snp	A/G	0.0973687	0.197999	intron-variant	ARMC4	GRCh38.p7	10:27844258	GCAAGAGCAGCAAAG[A/G]AGGTTGGAAAATTGC	55130
rs2297646	snp	A/C	0.447291	0.153545	intron-variant	ARMC4	GRCh38.p7	10:27936968	CTAGAAAGAAGTTTC[A/C]TAGCTACTAGAATGG	55130
rs2368265	snp	C/T	0.0260105	0.111035	intron-variant	ARMC4	GRCh38.p7	10:27845345	atctgtaaaggattt[C/T]atttctccttcactt	55130
rs2368266	snp	A/G	0.484561	0.0864924	intron-variant	ARMC4	GRCh38.p7	10:27855401	TAGTATATATTCATC[A/G]ATACCAATTGGTTCT	55130
rs2368267	snp	C/T	0.0271762	0.113356	intron-variant	ARMC4	GRCh38.p7	10:27860217	aacactttgggaggc[C/T]gaagcaggaggatca	55130
rs2368268	snp	A/C	0.489142	0.0728777	intron-variant	ARMC4	GRCh38.p7	10:27951296	gatctagaatgaaaa[A/C]tccaaaaaataagtt	55130
rs2368269	snp	G/T	0.442926	0.158996	intron-variant	ARMC4	GRCh38.p7	10:27889490	AGTAAGAAAGCTGGG[G/T]GGCCAGGCTGGAAAA	55130
rs2368270	snp	C/T	0.0189856	0.0955633	intron-variant	ARMC4	GRCh38.p7	10:27901543	aaagatcaagaccca[C/T]cggtgtgctgtattc	55130
rs2368271	snp	C/G	0.462691	0.131387	intron-variant	ARMC4	GRCh38.p7	10:27901570	attcaggagacccat[C/G]ttacgtgcaaagaca	55130
rs2368272	snp	A/G	0.493748	0.0555599	intron-variant	ARMC4	GRCh38.p7	10:27901649	gaaagcaaaaaaagc[A/G]ggggttgcaatccta	55130
rs2368273	snp	A/T	0.493748	0.0555599	intron-variant	ARMC4	GRCh38.p7	10:27901816	GATTCATAAAACAAT[A/T]CTTGGAGACCTACAA	55130
rs2368274	snp	G/T	0.312348	0.242101	intron-variant	ARMC4	GRCh38.p7	10:27904347	GGCAGGAAGCAGAGC[G/T]GGAATCTTGGGCTGA	55130
rs2368286	snp	G/T	0.411242	0.191052	intron-variant	ARMC4	GRCh38.p7	10:27970647	GAAAAATATTGAATA[G/T]ATATTTACATGTCCC	55130
rs2368288	snp	A/T	0.00358779	0.0422022	intron-variant	ARMC4	GRCh38.p7	10:27963108	AGGCAGGAGAATCAC[A/T]TGAACCCGGCAGGCG	55130
rs2554077	snp	A/C					GRCh38.p7	10:27872581	agaaaaggcctttga[A/C]aacattcaacagctc	55130
rs2815507	snp	G/T	0.404035	0.196909	downstream-variant-500B, intron-variant	ARMC4	GRCh38.p7	10:27811674	GATAAAATGCTATTT[G/T]TTTTGTAGCCACTTT	55130
rs2887205	snp	C/G	0.49706	0.0382258	intron-variant	ARMC4	GRCh38.p7	10:27845526	TGATGTTAGCTGGTT[C/G]TTTTGCTTGTTAGTT	55130
rs2887206	snp	A/G	0.0275645	0.114116	intron-variant	ARMC4	GRCh38.p7	10:27864490	tgcaaattagagagt[A/G]aggagtgaagtgaga	55130
rs2887210	snp	A/T			intron-variant	ARMC4	GRCh38.p7	10:27972811	gagagttttgaagtc[A/T]accaattatggattt	55130
rs2991935	snp	A/G	0.499683	0.0125759	intron-variant	ARMC4	GRCh38.p7	10:27828993	TATTAGAAGAAATTC[A/G]AAACCAAAGACAAGC	55130
rs2991936	snp	A/G	0.10237	0.201756	intron-variant	ARMC4	GRCh38.p7	10:27867817	ggattacaggttcac[A/G]ccaccatgcccagct	55130
rs2991937	snp	A/G	0	0	intron-variant	ARMC4	GRCh38.p7	10:27849440	TCATTTACATTAGGT[A/G]TATCTCCTAATGCTA	55130
rs2991938	snp	A/G	0.00318978	0.0398085	intron-variant	ARMC4	GRCh38.p7	10:27875632	agtgatgcagaagac[A/G]ggtgatttctgcatt	55130
rs2991939	snp	A/G	0.0123036	0.0774623	intron-variant	ARMC4	GRCh38.p7	10:27875733	caccgagcatgagcc[A/G]aagcagggcaaggca	55130
rs3004196	snp	A/T	0.0283406	0.115616	intron-variant	ARMC4	GRCh38.p7	10:27849616	CTTTTTAAGTTTTCC[A/T]TGGGGAGCTCTAGGC	55130
rs3004197	snp	A/C	0.00755907	0.0610114	intron-variant	ARMC4	GRCh38.p7	10:27829029	ATGAATTCTATATCC[A/C]ATCATGTATTTTAAA	55130
rs3060459	in-del	-/CCTTC/TC	0	0	intron-variant	ARMC4	GRCh38.p7	10:27873252	GATTCTTCTCTCTTC[-/CCTTC/TC]TTTATTAGTCTGGCT	55130
rs3221658	microsatellite	(CA)19/21/22/23	0.480984	0.203874	intron-variant	ARMC4	GRCh38.p7	10:27979431	naaaacctaaGAATA[(CA)19/21/22/23]AGAGNTAAATGAAAT	55130
rs3737184	snp	A/C	0.090938	0.192871	missense, intron-variant	ARMC4	GRCh38.p7	10:27812526	TTCAAGTGTATCTTG[A/C]CTTCTCTGTAGCAAG	55130
rs3802517	snp	A/T	0.475259	0.108435	intron-variant	ARMC4	GRCh38.p7	10:27944540	TTTTTTAAGAAATCA[A/T]TTCCATTCCCAGAGG	55130
rs3808909	snp	A/G	0.341506	0.232651	intron-variant	ARMC4	GRCh38.p7	10:27987344	TTTCCCAGCAAGATT[A/G]TTTCTAAAAGTTCAA	55130
rs3824590	snp	A/C	0.482645	0.0917714	intron-variant	ARMC4	GRCh38.p7	10:27944191	GTGGCGGCTGGCACT[A/C]GATGACGATGACAAC	55130
rs3831254	in-del	-/A	0.143622	0.226238	intron-variant	ARMC4	GRCh38.p7	10:27856272	TAAATGTGTTAATCA[-/A]TCCCCTCCAATACAG	55130
rs3839908	in-del	-/T			intron-variant	ARMC4	GRCh38.p7	10:27907889	ATATTTTGCTTAGAA[-/T]TTTTTTTTTTTTTGC	55130
rs3897931	snp	A/G	0.490727	0.0674567	intron-variant	ARMC4	GRCh38.p7	10:27885297	tgggcagatcacgag[A/G]tcaagagatcgaaac	55130
rs3901839	snp	C/T	0.497121	0.0378299	intron-variant	ARMC4	GRCh38.p7	10:27869182	GATTATCCATTATCT[C/T]TATTTGTTCTTGTGC	55130
rs3902895	snp	A/G	0.45762	0.139261	intron-variant	ARMC4	GRCh38.p7	10:27964783	ACACTACAAGAAAAC[A/G]CAGAAATAAAAATTT	55130
rs3952837	snp	C/T	0.461259	0.133677	intron-variant	ARMC4	GRCh38.p7	10:27962768	TCCGGCGGTGGGAGG[C/T]GGAGACAAGCTGGTG	55130
rs4237386	snp	G/T	0.492435	0.0610346	intron-variant	ARMC4	GRCh38.p7	10:27926811	TATCAGAAAATTATG[G/T]TCCCCAAAACATAAA	55130
rs4237388	snp	A/G	0.454302	0.144085	intron-variant	ARMC4	GRCh38.p7	10:27965422	GGGTGAGGATATAAG[A/G]AAATTCATTTCCTTG	55130
rs4262624	snp	C/T			intron-variant	ARMC4	GRCh38.p7	10:27971525	AAACTCACACCTCTG[C/T]TGCAGCACAACAGAT	55130

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