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
rs1267818	snp	A/G	0.230896	0.249269	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642037	GATAACTACTGGCCC[A/G]TCTCAAGGCAAGATG	154881
rs1610759	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66636760	cctgggtgacagaac[A/G]agatcctatctctta	154881
rs1618893	snp	C/T	0.230017	0.2492	intron-variant	KCTD7	GRCh38.p7	7:66631132	AGACCCAAAATTCAC[C/T]GAATGAATGAAAGAA	154881
rs1638732	snp	C/T	0.331874	0.236213	intron-variant	KCTD7	GRCh38.p7	7:66637231	aggtatggtggtggg[C/T]gtctgtaatcccagc	154881
rs1638733	snp	A/C	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66635916	TCTAGATCTTCAGCA[A/C]ACCTTGGTGAGCTCT	154881
rs1638734	snp	G/T	0.231189	0.249291	intron-variant	KCTD7	GRCh38.p7	7:66632552	TTATAGGTTGTTCAC[G/T]GCATAAAAGCACCTG	154881
rs1638735	snp	C/T	0.367297	0.220775	intron-variant	KCTD7	GRCh38.p7	7:66630751	CTTTCCCTCAAACCA[C/T]ATCATTTTCCCAATG	154881
rs1638736	snp	A/T	0.187053	0.241946	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66627321	accttgtttaaacac[A/T]gatgaaaaggaatga	154881
rs1796214	snp	A/G/T	0.49706	0.0382258	intron-variant	KCTD7	GRCh38.p7	7:66635701	AGGAGCCCCTGGTCA[A/G/T]ATAACTTGCTTGGAA	154881
rs1796223	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66636881	ATGCCTAACTCTAAT[A/G]TCTGAACAAACTGGT	154881
rs1796224	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66636873	CTCTAATGTCTGAAC[A/G]AACTGGTTTCAGGGC	154881
rs1860468	snp	A/G	0.495745	0.0459295	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642265	TGGTGAACAAGGCAG[A/G]GGTAAAATAAGGAAG	154881
rs1860469	snp	C/T	0.469544	0.119585	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66641888	CCAACCCTTCTTCTG[C/T]TCTGGGCCTGGCCAT	154881
rs1860470	snp	C/G	0.496279	0.0429702	intron-variant	KCTD7	GRCh38.p7	7:66638707	GGGGCCAATGAAGGG[C/G]ACAAACTTAAACAAG	154881
rs2159468	snp	C/T	0.000399281	0.0141238	intron-variant	KCTD7	GRCh38.p7	7:66636887	GGTAAAATGCCTAAC[C/T]CTAATGTCTGAACAA	154881
rs2420820	snp	C/T	0.486332	0.08153	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66626920	tatatatatatttta[C/T]tttttgtagaggcag	154881
rs2420821	snp	G/T	0.466204	0.125522	intron-variant	KCTD7	GRCh38.p7	7:66632346	CAAAAAATTAGCCAG[G/T]CGTGGTGGCAGGCAC	154881
rs2420822	snp	G/T			intron-variant	KCTD7	GRCh38.p7	7:66636886	TTTGTTCAGACATTA[G/T]AGTTAGGCATTTTAC	154881
rs2901263	snp	C/G			intron-variant	KCTD7	GRCh38.p7	7:66636868	ATTCAGCCCTGAAAC[C/G]AGTTTGTTCAGACAT	154881
rs3069693	in-del	-/ATAT/ATATATATATAT/ATATATATATATATAT/ATGT/TG	0	0	intron-variant	KCTD7	GRCh38.p7	7:66634137	TATATATATATATAT[lengthTooLong]GTATATATATGAGCT	154881
rs3069694	in-del	-/CTAT			intron-variant	KCTD7	GRCh38.p7	7:66634229	TATCTATCTATCTAT[-/CTAT]AAAAATAAAGATAGG	154881
rs3764902	snp	A/T	0.0587695	0.161031	intron-variant	KCTD7	GRCh38.p7	7:66633595	AAAAAAAAAAAAAAA[A/T]ATTGATCTCTTTCAA	154881
rs3764903	snp	C/T	0.494597	0.0516922	intron-variant	KCTD7	GRCh38.p7	7:66633495	CCATACTCAAGCCTA[C/T]GCTAATCACCTGCTA	154881
rs3764904	snp	C/T	0.183631	0.241029	KCTD7	7	allele_origin=T(germline)/C(germline)	7:66633397	CCGGCCCTCGGAGTC[C/T]GTGGGGATGTAGTGC	154881
rs3764905	snp	C/T	0.00177692	0.029754	intron-variant	KCTD7	GRCh38.p7	7:66633239	CTCTCAGGCAGGCAA[C/T]GGGGAATGAGAGCTG	154881
rs3981081	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66636688	tgaggcaagaggact[A/G]cttgagcccaggagt	154881
rs4717307	snp	C/G/T	0.00755907	0.0610114	intron-variant	KCTD7	GRCh38.p7	7:66636244	GTTCCCCATTGTCAT[C/G/T]AGCTTGCTGCACTCT	154881
rs4718381	snp	A/G	0.0821764	0.185298	intron-variant	KCTD7	GRCh38.p7	7:66636191	TTATGTATCCCTAGC[A/G]TCCACCGTGAAGGCT	154881
rs4718382	snp	C/G	0.078151	0.181571	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66639922	CCCTGTCTTAGGGCC[C/G]CGGCTTCTCTTATCT	154881
rs4718383	snp	C/T	0.469544	0.119585	downstream-variant-500B	KCTD7	GRCh38.p7	7:66643422	TTCCTCCTGTCATAT[C/T]ACCACTTCCTTTTCA	154881
rs6963242	snp	A/T	0.0919752	0.193722	intron-variant	KCTD7	GRCh38.p7	7:66632887	TCTCTACTAAAAAAA[A/T]ATATATATATATACA	154881
rs7793469	snp	A/T	0	0	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66627688	aaaaaaaaaaaaaaa[A/T]tttttttttcttttt	154881
rs9791712	snp	C/G	0.469346	0.119947	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640176	TCTTTAAACCCTGTT[C/G]CTCTGTCCTGGTAAC	154881
rs9791713	snp	A/C	0.469445	0.119766	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640211	TCCTTCTAGGAGAGC[A/C]TCTCTTCTGAGAAGG	154881
rs9791890	snp	A/G	0.49621	0.0433651	intron-variant	KCTD7	GRCh38.p7	7:66636343	GAGCCTCTGGCAGCG[A/G]TGGCTACTTGAGCAA	154881
rs9791892	snp	A/G	0.474634	0.109726	intron-variant	KCTD7	GRCh38.p7	7:66636497	GGAGTAATACTTAGC[A/G]AGTGTTAGCTGGTGT	154881
rs10263935	snp	A/G	0.496279	0.0429702	intron-variant	KCTD7	GRCh38.p7	7:66631041	ACCTACAGAATAAGC[A/G]CAAGGCATTTTCATG	154881
rs10266041	snp	C/G	0.166832	0.235761	intron-variant	KCTD7	GRCh38.p7	7:66636323	AATCAGCCATGGCTG[C/G]ATCTGAGCCTCTGGC	154881
rs10281544	snp	C/T	0.169435	0.236663	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66627721	agacggagtttcgct[C/T]ttgttgcccaggttg	154881
rs10601698	in-del	-/ACA	0.49645	0.0419827	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66643166	TTGGGGATGCCCCAC[-/ACA]ACAAGACAGGCTTTT	154881
rs12531758	snp	C/T	0.0718919	0.175435	intron-variant	KCTD7	GRCh38.p7	7:66629477	GTGATTTACTCCCAT[C/T]GCCATGTCCCACTTT	154881
rs12536586	snp	A/G	0.0788843	0.182262	intron-variant	KCTD7	GRCh38.p7	7:66634662	ATTTTGGGGCTCAGC[A/G]TTGCCATGGGAAGGA	154881
rs13307386	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66634092	cacatatatatatat[A/G]tatatatgggtgtGT	154881
rs13307923	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66634094	catatatatatatgt[A/G]tatatgggtgtgtgt	154881
rs13309185	snp	G/T	0	0	intron-variant	KCTD7	GRCh38.p7	7:66634189	TGGTCTTGATGTGTG[G/T]GATtctatctatcta	154881
rs17229513	snp	C/G	0.0715223	0.175059	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640959	GGAAGAGAAGACCAA[C/G]CCCTGGGACTTTGGC	154881
rs28480509	snp	A/G	0.469642	0.119404	intron-variant	KCTD7	GRCh38.p7	7:66634237	CTATCTATAAAAATA[A/G]AGATAGGATCTTGCT	154881
rs28671466	snp	A/C/T	0.0873957	0.190361	intron-variant	KCTD7	GRCh38.p7	7:66637600	ATACATTTCAAAAAC[A/C/T]TTATGTTAAAGGAAA	154881
rs34184629	in-del	-/T	0.375	0.216506	intron-variant	KCTD7	GRCh38.p7	7:66631718	CTTAAAATGCAAGGC[-/T]TTTTTTTTTTTCCTG	154881
rs34420265	in-del	-/AT/TA/TT			intron-variant	KCTD7	GRCh38.p7	7:66632886	GTATATATATATATA[-/AT/TA/TT]TTTTTTTAGTAGAGA	154881
rs34883818	snp	A/T	0.359364	0.22481	intron-variant	KCTD7	GRCh38.p7	7:66630959	TAATAATACTTAACA[A/T]TTCTGGAGCTCTTTA	154881
rs34917150	in-del	-/C			downstream-variant-500B	KCTD7	GRCh38.p7	7:66643280	TGGGGTGGGCACATG[-/C]CCTACATGAAACAGG	154881
rs35317589	in-del	-/C			intron-variant	KCTD7	GRCh38.p7	7:66632142	TGGCATCTACTCATT[-/C]CTAGAAATTTCTATT	154881
rs35512905	in-del	-/A			intron-variant	KCTD7	GRCh38.p7	7:66632017	GTGTCATATTCTCCT[-/A]CTATAATAGCACCTA	154881
rs35526611	snp	A/G	0.488284	0.0756358	utr-variant-5-prime	KCTD7	GRCh38.p7	7:66629021	TTCGGGCGGGCGGAG[A/G]CGGCGGCCCCGGGCA	154881
rs35633983	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642844	TGTTTGTTCCCACCT[C/T]CCTCAACCCCTGCCA	154881
rs35686816	in-del	-/C			splice-donor-variant	KCTD7	GRCh38.p7	7:66633445	AGAGGGAGAGACATA[-/C]CCCAAAGTGTGTGCC	154881
rs35694149	in-del	-/GAG/GGA			intron-variant	KCTD7	GRCh38.p7	7:66634762	CTTGGCAAAATTAAA[-/GAG/GGA]GAACAACACTGTATC	154881
rs35961913	in-del	-/TTG			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66643170	AGGGAAAAGCCTGTC[-/TTG]TTGTGTGGGGCATCC	154881
rs55764000	snp	C/T			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640982	ACTTTGGCTGAATTC[C/T]TCCGTGGGGCTGGAC	154881
rs56904178	snp	G/T			intron-variant	KCTD7	GRCh38.p7	7:66637564	CAAACTACTGGTTTG[G/T]TTTTATTATTTATTT	154881
rs57116165	snp	C/G	0.00597247	0.0543191	intron-variant	KCTD7	GRCh38.p7	7:66630793	ACAGATTGCAGACCA[C/G]GGCCCCACCACCAGT	154881
rs57580125	in-del	-/AGGA	0.224423	0.248688	intron-variant	KCTD7	GRCh38.p7	7:66638448	GTCAGCTGCCCAGGA[-/AGGA]TGGTGGGTATGTGGG	154881
rs57784651	in-del	-/CCT	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66634763	ATACAGTGTTGTTCT[-/CCT]TTAATTTTGCCAAGG	154881
rs58026597	snp	A/T	0.0310518	0.120672	intron-variant	KCTD7	GRCh38.p7	7:66634590	GTGGAGAGGAATAAG[A/T]GTAATCCCACATAGG	154881
rs62469066	snp	A/G	0.0785177	0.181917	intron-variant	KCTD7	GRCh38.p7	7:66631196	TCAGCTTTATTTAAT[A/G]TATTTGTACCCTATT	154881
rs62469067	snp	C/T	0.0788843	0.182262	intron-variant	KCTD7	GRCh38.p7	7:66634803	AAAAAAAAAAAAACC[C/T]TCTGTTGTTCTTGTC	154881
rs62469069	snp	A/G	0.0722614	0.17581	intron-variant	KCTD7	GRCh38.p7	7:66636805	AAATCTGAAAAGTGA[A/G]TTAGAAGGACTGAAT	154881
rs62469070	snp	A/T	0.0785177	0.181917	intron-variant	KCTD7	GRCh38.p7	7:66637308	CCAGGCTGGTCTTAA[A/T]CTCCTGAGCTCAGAT	154881
rs62469071	snp	A/G	0.00318978	0.0398085	intron-variant	KCTD7	GRCh38.p7	7:66637638	GGTATGAAAGAGAAC[A/G]TACTATATAATTCTG	154881
rs62469072	snp	C/T	0.0766824	0.180169	intron-variant	KCTD7	GRCh38.p7	7:66637726	TAGAGTGGTTGCTTC[C/T]GTAGGGATTAACTGG	154881
rs62469073	snp	A/G	0.5	0	downstream-variant-500B	KCTD7	GRCh38.p7	7:66643284	GTTTCATGTAGGCAT[A/G]TGCCCACCCCAGCCT	154881
rs68184930	in-del	-/T	0.378765	0.214288	intron-variant	KCTD7	GRCh38.p7	7:66635031	TTTTTTTTTTTTTTT[-/T]GAGTCAGCGTCTTGC	154881
rs71261622	snp	A/G	0.00199481	0.0315187	intron-variant	KCTD7	GRCh38.p7	7:66636219	GCTGCTTGGGCCTCA[A/G]TCTGGGGTCGTTCCC	154881
rs71261623	snp	C/T	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66636270	ACTCTGGTCTAAATG[C/T]TTCTGCTGAAGCTGG	154881
rs71276648	multinucleotide-polymorphism	CGTG/GGTA	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66636294	CTGAAGCTGGACCAT[CGTG/GGTA]GATGTGGGTGTAGAA	154881
rs71276649	multinucleotide-polymorphism	ATCAGC/GTCAGT	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66636309	AGATGTGGGTGTAGA[ATCAGC/GTCAGT]CATGGCTGGATCTGA	154881
rs72073419	in-del	-/A	0.369958	0.21934	intron-variant	KCTD7	GRCh38.p7	7:66631707	GCAGTGCAAAACAGG[-/A]AAAAAAAAAAAGCCT	154881
rs73133851	snp	C/G	0.200182	0.244986	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642984	AGTTCATGTACCTGT[C/G]TGTGAGTGCTTTGGT	154881
rs73375381	snp	A/T	0.00636936	0.0560724	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640630	ATGTGTAAAGAATTG[A/T]TGCGAGCCAGGAACA	154881
rs73375385	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	KCTD7	GRCh38.p7	7:66643604	ACATCATGGATTAAC[A/G]CAGAAAGGTGAGTTC	154881
rs73702137	snp	C/G	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66634759	GACTGATACAGTGTT[C/G]TTCTTTAATTTTGCC	154881
rs73702138	snp	C/T	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66634761	CTGATACAGTGTTGT[C/T]CTTTAATTTTGCCAA	154881
rs73702140	snp	A/G	0.0850919	0.187897	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66641312	TGTTCATTTTTTGAC[A/G]GAGAGGCAGACTATT	154881
rs74360055	snp	G/T	0.00597247	0.0543191	intron-variant	KCTD7	GRCh38.p7	7:66629692	ACTGGAAAAACAAAG[G/T]CATTTTGGGTTGGAT	154881
rs74362924	snp	C/G	0.0298908	0.118541	intron-variant	KCTD7	GRCh38.p7	7:66638488	GTCTGCAAGGCATCT[C/G]TGAGTGTTTAGGTCT	154881
rs75054368	snp	C/T	0.00597247	0.0543191	intron-variant	KCTD7	GRCh38.p7	7:66633154	GTGTTCAGATGGACC[C/T]GTGGGCTTGAGTGAC	154881
rs75672175	snp	C/T	0.0396425	0.135091	intron-variant	KCTD7	GRCh38.p7	7:66638229	TAAGCTCCTTGTCAC[C/T]GACCCTCTTTCCTTC	154881
rs75774733	snp	A/G	0.00318978	0.0398085	intron-variant	KCTD7	GRCh38.p7	7:66633155	TGTTCAGATGGACCC[A/G]TGGGCTTGAGTGACT	154881
rs76376025	in-del	-/CTC	0.469839	0.119042	intron-variant	KCTD7	GRCh38.p7	7:66634761	TGATACAGTGTTGTT[-/CTC]CTTTAATTTTGCCAA	154881
rs76436939	snp	A/G	0.00159617	0.0282053	intron-variant	KCTD7	GRCh38.p7	7:66630302	AAAAGCAAGAGAAGG[A/G]AAACGATGCCAGGTG	154881
rs76519909	in-del	-/CTATCTATCTATCT			intron-variant	KCTD7	GRCh38.p7	7:66634198	TGTGTGTGATTCTAT[-/CTATCTATCTATCT]ATCTATCTATCTATC	154881
rs77241642	snp	A/G	0.00517822	0.0506191	intron-variant	KCTD7	GRCh38.p7	7:66631860	AGGAGAGGAGTAGAT[A/G]CCTGGAAGTATTCAA	154881
rs77341088	snp	A/G	0.0659589	0.169201	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66639448	GCCTGCAGGCACTCC[A/G]GCCAGCGCTCACCTG	154881
rs77480434	snp	C/T	0.0596104	0.162024	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66627259	GTGCCTGGCTTATTT[C/T]ACTTAACATAATGAC	154881
rs79736939	snp	C/T	0.031825	0.122064	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66639940	GCTTCTCTTATCTTC[C/T]ACCACCTTCCTTGCT	154881
rs79812221	snp	C/T	0.5	0	intron-variant	KCTD7	GRCh38.p7	7:66635013	AGAGTGAGACTGTCT[C/T]TTTTTTTTTTTTTTT	154881
rs79868578	in-del	-/AA			intron-variant	KCTD7	GRCh38.p7	7:66632504	AAAAAAAAAAAAAAA[-/AA]GAAAAAGGGCACATA	154881
rs80028027	snp	G/T	0.5	0	upstream-variant-2KB	KCTD7	GRCh38.p7	7:66628330	CACTGTCATTATTCA[G/T]TGAACTCAAGCGCTC	154881
rs80101541	snp	C/T	0.0422008	0.138995	intron-variant	KCTD7	GRCh38.p7	7:66630261	GTGATAGAGTAAGAC[C/T]GTACCTACAAACAAA	154881

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