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
rs762564	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239954	TTCCTTCTCTACCCA[A/G]AAGCCAGTCCTTGAG	84628
rs762565	snp	C/T			synonymous-codon	NTNG2	GRCh38.p7	9:132239246	GTTCTCATCATCCAG[C/T]TGTGCCGAGCCGTTG	84628
rs762566	snp	C/G/T	1.66421e-05	0.00288458	missense	NTNG2	GRCh38.p7	9:132239244	TCTCATCATCCAGTT[C/G/T]TGCCGAGCCGTTGCG	84628
rs762567	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132235562	CATCACAGCCCCGCA[A/C]CCCACAGGCCCCTTA	84628
rs762568	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132235248	TGCGAAGTGGGACAT[C/G]TCTTCCGGCCAAGAT	84628
rs762569	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132235246	CGAAGTGGGACATCT[C/G]TTCCGGCCAAGATCT	84628
rs869497	snp	C/G	0.134119	0.221521	intron-variant	NTNG2	GRCh38.p7	9:132163667	CAGCGCCCTCCCTCC[C/G]GTGCCCCCAggggcc	84628
rs870591	snp	A/G	0.20111	0.245173	intron-variant	NTNG2	GRCh38.p7	9:132187384	TTTACGCTGATTCAC[A/G]AGCGGGGAGGGTGAC	84628
rs870592	snp	A/G	0.142609	0.225759	intron-variant	NTNG2	GRCh38.p7	9:132187388	CGCTGATTCACAAGC[A/G]GGGAGGGTGACCTTG	84628
rs871461	snp	G/T	0.311369	0.242351	intron-variant	NTNG2	GRCh38.p7	9:132201974	GCTGTCTGCCATGTA[G/T]TGGCGCTGTGCAATC	84628
rs871462	snp	C/T	0.491936	0.0629843	intron-variant	NTNG2	GRCh38.p7	9:132201909	CTTCATCTGAAAACA[C/T]GAGGCTGGGGGAGCG	84628
rs871463	snp	G/T	0.447938	0.152711	intron-variant	NTNG2	GRCh38.p7	9:132201866	GGAGCGCTCCAGGGG[G/T]TGGGGATCAGGTCTG	84628
rs874653	snp	A/G	0.45946	0.136478	intron-variant	NTNG2	GRCh38.p7	9:132211751	GGCTGTGGAATTGTC[A/G]CAAGCCGCCAAGGCT	84628
rs876952	snp	C/G	0.499965	0.00419314	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244085	GAGATGTAAGCAGGA[C/G]TGATGGGTGGGCTTC	84628
rs876953	snp	A/G	0.397813	0.201621	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244197	CTCATCCCTCCCTCT[A/G]CTCTTCAGTCAGCAG	84628
rs883318	snp	A/G	0.49975	0.0111793	intron-variant	NTNG2	GRCh38.p7	9:132167498	CCAGCAGACGGTACC[A/G]TGAAGCTAGAGCATG	84628
rs914418	snp	A/G	0.498945	0.022939	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244768	GGGTGAGTTCTGCTC[A/G]GCTGCCCTGTGCTCA	84628
rs914419	snp	C/T	0.308414	0.24308	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229672	ACCCACTCCTTCCTC[C/T]ACCTCCATGTCTGGG	84628
rs914420	snp	A/G	0.342134	0.232404	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229399	GGAGAGACTTGGAGC[A/G]GATGGAGGGAAGTTC	84628
rs914422	snp	A/C	0.0759472	0.179459	intron-variant	NTNG2	GRCh38.p7	9:132167798	CAGCAGAGATGGTTG[A/C]GTGCGAGCTGTCTGA	84628
rs914423	snp	A/G	0.498754	0.0249289	intron-variant	NTNG2	GRCh38.p7	9:132168589	GGAGAAGGCGGCACG[A/G]AGCCAGGAGCTGGGG	84628
rs914424	snp	A/G	0.499997	0.00119808	intron-variant	NTNG2	GRCh38.p7	9:132168648	GGGGACCGCAGGGCC[A/G]AGCAAGGGGGCTGGG	84628
rs928912	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132233741	ATATGATGATACAAT[C/G]ATACGAGCACAGCCC	84628
rs933173	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132236548	GGGCGCTCAAAGCCC[G/T]GCTCGCTGCTCAGAG	84628
rs933174	snp	A/G	0.481242	0.0950111	intron-variant	NTNG2	GRCh38.p7	9:132236183	CTTCTCCCTTCACCC[A/G]CCACAGTCCACCCTC	84628
rs943754	snp	G/T	0.286042	0.247388	intron-variant	NTNG2	GRCh38.p7	9:132233475	GGAAATGCAGGGGAG[G/T]TGAGGGTCCCCAGGA	84628
rs1041501	snp	C/G	0.490287	0.0690083	intron-variant	NTNG2	GRCh38.p7	9:132197600	CCACACCTGGTGACA[C/G]TGTGCCTGGGCCTCC	84628
rs1041502	snp	C/T	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132197492	CCCTTCCACTCTGTC[C/T]GCCTCAAAAATTCCC	84628
rs1041504	snp	C/T	0.490343	0.0688145	intron-variant	NTNG2	GRCh38.p7	9:132196622	TGAAAATGTCACTAA[C/T]GTAGTGGTCCCCAGG	84628
rs1105684	snp	A/T	0.27278	0.24896	intron-variant	NTNG2	GRCh38.p7	9:132164221	AAAATAAATAAATTT[A/T]AAAAACCCTAACAAC	84628
rs1105685	snp	A/G	0.301177	0.244706	intron-variant	NTNG2	GRCh38.p7	9:132164169	AATGTGTTTACAACT[A/G]GTCAATCAATTGGGC	84628
rs1111393	snp	A/C/T	0.000164694	0.00907302	intron-variant	NTNG2	GRCh38.p7	9:132239006	CAGGTCATGCAGGGA[A/C/T]GGAGGAAGGCATCTT	84628
rs1331625	snp	C/G	0.208474	0.246527	intron-variant	NTNG2	GRCh38.p7	9:132184100	CCCACCCCCAACGAC[C/G]AGCCAGGGTTCATCC	84628
rs1331626	snp	C/T	0.454061	0.144427	intron-variant	NTNG2	GRCh38.p7	9:132216512	CCCACTGCAGAATCC[C/T]ACGGCTTTAGCTCTT	84628
rs1331627	snp	C/T	0.499563	0.0147699	intron-variant	NTNG2	GRCh38.p7	9:132216492	CTTTAGCTCTTCAGA[C/T]GGCAGCAAGAACGCT	84628
rs1810887	snp	A/G	0.493925	0.054776	intron-variant	NTNG2	GRCh38.p7	9:132235069	CCCCAGCATGAACCA[A/G]TGACACAACGCTCAG	84628
rs1887625	snp	C/T	0.305934	0.243663	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230068	ACGGCACGATTTACG[C/T]AGGGGATGCTGACAC	84628
rs1887626	snp	G/T	0.312348	0.242101	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230210	CTGTCCTGCACTGGA[G/T]GGCCCAAAAATCTGA	84628
rs1977549	snp	C/G	0.493386	0.0571263	intron-variant	NTNG2	GRCh38.p7	9:132216416	acatacacacacaca[C/G]agagagagagagaga	84628
rs1999033	snp	A/G	0.49941	0.0171624	intron-variant	NTNG2	GRCh38.p7	9:132232031	AGTTCAGCTTCCAAA[A/G]TCGTCTTCCTCCTGC	84628
rs1999389	snp	A/G	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132175146	CTCTCTGTCACCCAC[A/G]CACTTTCCCCTCGAA	84628
rs1999391	snp	A/G	0.497749	0.0334707	intron-variant	NTNG2	GRCh38.p7	9:132234482	GTCTTGGGGAGGGAG[A/G]GAGTCCTGGCTTGGC	84628
rs2011023	snp	C/T	0.490398	0.0686206	intron-variant	NTNG2	GRCh38.p7	9:132197112	gtgagccactgcgcc[C/T]ggccCCTGAGCCTTT	84628
rs2023364	snp	C/G	0.403158	0.197592	intron-variant	NTNG2	GRCh38.p7	9:132216418	acacatacacacaca[C/G]acagagagagagaga	84628
rs2026367	snp	C/T	0.18325	0.240924	intron-variant	NTNG2	GRCh38.p7	9:132173447	GTGAAAGGGCCCAGA[C/T]GGGACATCTTTCCAA	84628
rs2104852	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132211949	tgttcatgaatgaat[A/C]aatgaatgactgact	84628
rs2149171	snp	C/T	0.471983	0.114993	synonymous-codon	NTNG2	GRCh38.p7	9:132226867	CAAGTGCAACCTGCA[C/T]GCCAACCTGTGCTCC	84628
rs2183763	snp	C/T	0.0482946	0.147699	intron-variant	NTNG2	GRCh38.p7	9:132196612	ACTAACGTAGTGGTC[C/T]CCAGGGTCAGAGGGA	84628
rs2274852	snp	A/C	0.499424	0.0169631	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243197	CGGAGGTGGCCACCG[A/C]GACACAGTATAAATC	84628
rs2274853	snp	C/T	0.449428	0.150759	intron-variant	NTNG2	GRCh38.p7	9:132238978	CTTTGGAAAAGGTAC[C/T]GGAAGGTGCCCTAGG	84628
rs2274854	snp	A/T	0.227369	0.248974	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230667	CCCTTTTTTCTCTCC[A/T]GCTTTTTCCAGGACA	84628
rs2274855	snp	C/T	0.375637	0.216137	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230557	CCTGTGGGAGAGAGA[C/T]GGGCGTGAGCTGGCT	84628
rs2361547	snp	A/G	0.498611	0.0263212	intron-variant	NTNG2	GRCh38.p7	9:132216572	GCCTGGGAGGGGTCC[A/G]CTGGCCTCATGGGCT	84628
rs2361548	snp	G/T	0.413914	0.188765	intron-variant	NTNG2	GRCh38.p7	9:132225155	CTCCTGACCTCAAGT[G/T]ATCTGCCTGCCTTGG	84628
rs2361549	snp	C/T	0.386884	0.209196	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239701	AGCCTATCCCTCCTC[C/T]TGCAGGGGCCCAGTT	84628
rs2479527	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230197	CCATACGATGTCCCT[C/G]TCCTGCACTGGAGGG	84628
rs2482300	snp	C/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242682	GGAGGAGGAGAGAAG[C/G]AAGGGGTGGGGGGCC	84628
rs2482301	snp	C/G			intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242863	TCTTTCTGTGTTGGG[C/G]ACGGTGGGCAGGTGT	84628
rs2482302	snp	C/G			missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240990	CGCGAGGGCGCGGCG[C/G]GCCCCAAGTGCGACG	84628
rs2482303	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241314	gcctggtgagatggg[A/G]ccgacccgggggcgg	84628
rs2769644	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230079	tacgcaggggatgct[C/G]acaccgtgcctggca	84628
rs2769645	snp	A/C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230096	caccgtgcctggcac[A/C/G]tgggacgcactcCAC	84628
rs2769646	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230640	GGCCCCCACTGCACG[A/C]GCCTCTTTGCATGTC	84628
rs2769647	snp	A/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230740	CTCTAATTACACCCC[A/T]TCTGCTTCTCCACCT	84628
rs2769648	snp	A/G	0.00835141	0.0640778	intron-variant, splice-donor-variant	NTNG2	GRCh38.p7	9:132231569	GTCTGCACAGCCGTC[A/G]TAAGTTGCTTCTCTG	84628
rs2769649	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132231603	TGTCCCCACCCCGGC[A/C]ACCCCCCAACCCTCT	84628
rs2769650	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132231996	CCTGTTCCTGAGCCC[A/T]GCCAGGGGATTCAGG	84628
rs2769651	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132235279	GCCATTAGCCAGAGA[C/G]ATCAGCTCAGAGAGG	84628
rs2769652	snp	C/T	0	0	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132237223	TCCTTCAGGAAGGGG[C/T]CCCACCTCCCTGGGC	84628
rs2769653	snp	C/T	0	0	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237671	TAAACTGAGTCTCTC[C/T]TCCCTACAGGCCTCC	84628
rs2769654	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237792	TAGCCCATCCCGGCT[C/T]CCCTGGGAGGTGTGG	84628
rs2769655	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132238275	AATCCCTGAGAGCCT[G/T]GCCCCAGGCAGTCAC	84628
rs2769656	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132238844	GCTGCCCATGGCCCT[C/G]CCTGGTTCCCTGGGG	84628
rs2769658	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239769	AAGTCCCTTCCCGTT[C/G]CTGGGCCTCAGCTTC	84628
rs2769659	snp	C/G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243051	CCCCACCTGTTAGGA[C/G/T]CCTCCCCACACTGAA	84628
rs2769660	snp	C/G			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243165	AGAATCCTAGCAGAG[C/G]TTGAATCCAATGCTC	84628
rs2777465	snp	C/G	0.281841	0.247964	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230424	CCTGCAGGTCATCAT[C/G]ATTGCTAGCAGTTGT	84628
rs2777466	snp	C/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231294	CGGTCTCTCCTTTCA[C/G]CCTTGCAAACCCCTC	84628
rs2777467	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132232069	GCCATTGCTTGGAAG[G/T]GCTCCCAGACCATTG	84628
rs2777468	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132232349	GAGCCTCTGGAGCTG[A/C]GTTTGGACACCGTGG	84628
rs2777469	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132235563	AAGGGGCCTGTGGGG[A/T]GCGGGGCTGTGATGC	84628
rs2777470	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132238733	CAGGTGGCATGACCC[G/T]GCCCTCCTTGCATGA	84628
rs2777471	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132238734	AGGTGGCATGACCCT[G/T]CCCTCCTTGCATGAA	84628
rs2854925	snp	G/T	0.477853	0.102875	intron-variant	NTNG2	GRCh38.p7	9:132233164	CCCACCACAGGCTCA[G/T]CAGCAAAGCACAGGT	84628
rs2854926	snp	C/T	0.140581	0.224783	intron-variant	NTNG2	GRCh38.p7	9:132233123	TGGGCCAACCTATGT[C/T]TGAAGTCCAGAATTC	84628
rs2854927	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132232438	GCCTGTCTGTGGCAG[A/C]CCCCTGAGGGGCAGG	84628
rs2854930	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132231605	AGAGAGGGTTGGGGG[G/T]TGGCCGGGGTGGGGA	84628
rs2854934	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230380	GGTGGATTATCCCAT[C/T]TCATCCTCACTTCAG	84628
rs2854936	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132241790	ACAGGGTGTGCGAGA[C/T]CCCGGGGGCGCCGTC	84628
rs2854937	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132238531	ATTAGCCTGAGCTtt[C/G]tgcaagtttgattga	84628
rs2854938	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132238516	gtgcaagtttgattg[A/T]tttgcaggatgctaa	84628
rs2854939	snp	C/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242469	GTGTGTGTAAGTGTG[C/G]TGGGAGGCAGGACGG	84628
rs3065875	in-del	-/CA/CACA			intron-variant	NTNG2	GRCh38.p7	9:132233349	ACACACACACACACA[-/CA/CACA]GAGGAATCCATTTGC	84628
rs3739928	snp	C/T	0.4941	0.0539917	intron-variant	NTNG2	GRCh38.p7	9:132198716	AACATCCCAAGAACC[C/T]GGTCATGTTCCACAT	84628
rs3739929	snp	A/G	0.184203	0.241186	intron-variant	NTNG2	GRCh38.p7	9:132198676	CATCCCAGGTATCCA[A/G]TAACGTCCCAGGTAA	84628
rs3739930	snp	A/G	0.173589	0.238037	synonymous-codon	NTNG2	GRCh38.p7	9:132198580	GATGTTGGAGATGGC[A/G]TAGAAGTACTTGTAG	84628
rs3813389	snp	A/G	0.0970103	0.197722	intron-variant	NTNG2	GRCh38.p7	9:132167193	ACCAGACCTGGACCA[A/G]GTCTTTGTCCCACCT	84628
rs3813391	snp	A/G	0.0944967	0.195752	intron-variant	NTNG2	GRCh38.p7	9:132232034	TCAGCTTCCAAAGTC[A/G]TCTTCCTCCTGCCCT	84628
rs3824574	snp	A/G	0.433635	0.169641	synonymous-codon	NTNG2	GRCh38.p7	9:132198490	GTCGGTGAGGGTGAA[A/G]AACTCCTTGAGGCCC	84628
rs3829759	snp	A/G	0.0785177	0.181917	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166779	GTCCCGCCTGACCCC[A/G]TCGCTGCCTCTCCAG	84628

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