iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

VHL

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs766377552	snp	A/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10150811	GGACAAATAAGTTTT[A/T]GCTAAATGTGAGTAT	7428
rs766389960	snp	A/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10140152	TTACCTGAGGTGAGG[A/G]GTTCAAGACCAGCCT	7428
rs766474372	in-del	-/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10141252	CGCGTCTGACATGAA[-/G]AAAAAAAAAATTCAG	7428
rs766571541	snp	G/T	1.64746e-05	0.00287002	intron-variant	VHL	GRCh38.p7	3:10146677	GATAAGGTTGTTGTG[G/T]TAAGTACAGGATAGA	7428
rs766576246	snp	C/T	9.23489e-05	0.00679455	missense	VHL	GRCh38.p7	3:10141996	CGGAGGAACTGGGCG[C/T]CGAGGAGGAGATGGA	7428
rs766583052	snp	A/G			synonymous-codon	VHL	GRCh38.p7	3:10142150	GCCCTACCCAACGCT[A/G]CCGCCTGGCACGGGC	7428
rs766830181	snp	C/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10153652	TAATACATTAAATGG[C/T]GCTGAGTAAAGGAAA	7428
rs767062290	snp	C/G	2.20383e-05	0.00331944	missense	VHL	GRCh38.p7	3:10142185	GCATCCACAGCTACC[C/G]AGGTACGGGCCCGGC	7428
rs767136348	snp	A/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant	VHL	GRCh38.p7	3:10146515	GCTTGTCCCGATAGG[A/T]CACCTTTGGCTCTTC	7428
rs767439665	snp	A/T			upstream-variant-2KB	VHL	GRCh38.p7	3:10140324	AGACTGAGCCACTGC[A/T]CTCCAGCCTGGGTGA	7428
rs767780451	snp	A/G	1.65149e-05	0.00287353	missense	VHL	GRCh38.p7	3:10149858	AATTACAGGAGACTG[A/G]ACATCGTCAGGTCGC	7428
rs767933516	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10144141	GAATTTTGTATTTTA[C/T]TCCAAAATTTTTCTG	7428
rs767939209	in-del	-/A			intron-variant	VHL	GRCh38.p7	3:10146326	CTACAGGCGCTCGCC[-/A]CCACACCTGGCTAAT	7428
rs768104793	snp	C/T	2.30742e-05	0.00339655	synonymous-codon	VHL	GRCh38.p7	3:10142072	GCCCTCCCAGGTCAT[C/T]TTCTGCAATCGCAGT	7428
rs768390987	snp	A/T	3.30535e-05	0.00406518	missense	VHL	GRCh38.p7	3:10149876	ATCGTCAGGTCGCTC[A/T]ACGAAGATCTGGAAG	7428
rs768452685	snp	C/G			missense	VHL	GRCh38.p7	3:10141913	GGCAGGCGTCGAAGA[C/G]TACGGCCCTGAAGAA	7428
rs768453720	snp	A/G/T	0.000753012	0.0193891	utr-variant-5-prime	VHL	GRCh38.p7	3:10141827	CGGCGTCCGGCCCGG[A/G/T]TGGTCTGGATCGCGG	7428
rs768483736	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10143386	CACCCGCCTTGGCCT[C/T]CCAAAGTGCTGAGAT	7428
rs768547253	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10146363	GTATTTTTAGTAGAG[A/G]CGAGGTTTCACCACG	7428
rs768637170	snp	C/G	1.64727e-05	0.00286986	missense, intron-variant	VHL	GRCh38.p7	3:10146591	TTATTTGTGCCATCT[C/G]TCAATGTTGACGGAC	7428
rs768650092	snp	C/G	0.000145613	0.00853144	missense	VHL	GRCh38.p7	3:10141962	GGCGCCGAGGAGTCC[C/G]GCCCGGAAGAGTCCG	7428
rs768802298	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10145121	ATTGCTTGAACCTGG[A/G]AGGCGGAGGTGGCAG	7428
rs768931039	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10149593	AGGTGAAATTACTAC[A/G]GAGGCATGAACACCA	7428
rs769102979	snp	C/G	4.08806e-05	0.00452091	synonymous-codon	VHL	GRCh38.p7	3:10142162	GCTGCCGCCTGGCAC[C/G]GGCCGCCGCATCCAC	7428
rs769290824	snp	A/C			upstream-variant-2KB	VHL	GRCh38.p7	3:10139999	GAGATAATGACATAG[A/C]CTTAATTCACGTGGG	7428
rs769658318	snp	C/G	3.47929e-05	0.00417076	missense	VHL	GRCh38.p7	3:10142048	GCTGCGCTCGGTGAA[C/G]TCGCGCGAGCCCTCC	7428
rs769903189	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10146071	TGAGATAATGTTACT[A/G]GAAGGGCTTTGTATA	7428
rs770268755	in-del	-/A/ACACTGTTTCATA	2.1539e-05	0.00328162	utr-variant-3-prime	VHL	GRCh38.p7	3:10149983	TTTCTGTTGAAACTT[-/A/ACACTGTTTCATA]ACACTGTTTCATCTC	7428
rs770543651	snp	C/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10139769	CTCCTGCTTCAGCCT[C/G]CTGAGTAGCTGGGAC	7428
rs770746627	snp	A/T	3.60698e-05	0.0042466	missense	VHL	GRCh38.p7	3:10149949	AGCGCATTGCACATC[A/T]ACGGATGGGAGATTG	7428
rs770795777	snp	G/T			intron-variant	VHL	GRCh38.p7	3:10143628	AATTTTTTGTATTCT[G/T]AGTAGAGACAGGGTT	7428
rs770804230	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10147440	TGCGATTTCAGCTCA[C/T]TGCAACCTCTGCATC	7428
rs771141091	snp	A/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10150892	TTGTTGTTGTTGTTT[A/T]GTTTTGTTTTGTTTT	7428
rs771222897	snp	A/C	1.67961e-05	0.00289789	intron-variant	VHL	GRCh38.p7	3:10149759	AGACCCTAGTCTGCC[A/C]CTGAGGATTTGGTTT	7428
rs771626617	snp	C/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10150113	TTAAAAGAAAGTTAA[C/G]TGACTTCACTAGGCA	7428
rs771727849	snp	A/C/G	1.6473e-05	0.00286988	VHL	3	allele_origin=G(germline)/C(germline)	3:10146608	CAATGTTGACGGACA[A/C/G]CCTATTTTTGCCAAT	7428
rs771759826	snp	A/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10151336	ATTAACTCAAATTCA[A/G]TGCTTCTATCAGACT	7428
rs771880989	snp	A/G	0.00019104	0.00977157	utr-variant-5-prime	VHL	GRCh38.p7	3:10141821	ATCCCGCGGCGTCCG[A/G]CCCGGGTGGTCTGGA	7428
rs771904956	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10143478	TTTTGAGTTGGAGTC[C/T]GGATCTGTCGCCAGA	7428
rs772300829	snp	C/T	1.98002e-05	0.00314638	synonymous-codon	VHL	GRCh38.p7	3:10142148	CAGCCCTACCCAACG[C/T]TGCCGCCTGGCACGG	7428
rs772327484	snp	A/C			utr-variant-3-prime	VHL	GRCh38.p7	3:10150152	TTTAGGGGCAAACAT[A/C]ACAAAATGTAATTTA	7428
rs772489344	snp	C/T	0.000510679	0.0159712	intron-variant	VHL	GRCh38.p7	3:10146463	ACAGGTGTGGGCCAC[C/T]GTGCCCAGCCACCGG	7428
rs772766527	snp	G/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10150750	TGTAACTTGCCATCC[G/T]CACAGAAAATACGAG	7428
rs772944298	snp	C/T			utr-variant-5-prime	VHL	GRCh38.p7	3:10141784	AGCGCGCACGCAGCT[C/T]CGCCCCGCGTCCGAC	7428
rs773040874	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10143508	ACTGGAGTGCTGTTG[C/T]ACAATCTTGGCTCAC	7428
rs773246608	snp	C/G	3.28316e-05	0.00405151	synonymous-codon	VHL	GRCh38.p7	3:10142051	GCGCTCGGTGAACTC[C/G]CGCGAGCCCTCCCAG	7428
rs773519476	snp	A/G	1.71687e-05	0.00292986	synonymous-codon	VHL	GRCh38.p7	3:10141982	GGAAGAGTCCGGCCC[A/G]GAGGAACTGGGCGCC	7428
rs773556807	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	VHL	GRCh38.p7	3:10146602	ATCTCTCAATGTTGA[C/T]GGACAGCCTATTTTT	7428
rs773684010	snp	C/T			missense, intron-variant	VHL	GRCh38.p7	3:10146525	ATAGGTCACCTTTGG[C/T]TCTTCAGAGATGCAG	7428
rs773903601	snp	G/T			intron-variant	VHL	GRCh38.p7	3:10149288	TGGCTAATTTTTTGT[G/T]TATTTTGTAGAGACG	7428
rs774164881	in-del	-/C			intron-variant	VHL	GRCh38.p7	3:10148315	GTTGTACTAGATTTT[-/C]TTTTTTTTTTTTTTT	7428
rs774380450	snp	C/T	0.00010897	0.00738059	missense	VHL	GRCh38.p7	3:10149951	CGCATTGCACATCAA[C/T]GGATGGGAGATTGAA	7428
rs774557051	snp	C/T	2.58997e-05	0.0035985	synonymous-codon	VHL	GRCh38.p7	3:10142063	CTCGCGCGAGCCCTC[C/T]CAGGTCATCTTCTGC	7428
rs774645008	snp	C/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10153515	AATTAAAAACCTGTA[C/G]CATGAATAATGTTTG	7428
rs774753107	snp	A/G	1.96581e-05	0.00313507	synonymous-codon	VHL	GRCh38.p7	3:10142144	GCCGCAGCCCTACCC[A/G]ACGCTGCCGCCTGGC	7428
rs774821221	in-del	-/CTC			utr-variant-3-prime	VHL	GRCh38.p7	3:10150429	CAGGGACAAGTCTTT[-/CTC]CTCTTTGAGACCCCA	7428
rs774869200	snp	C/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10140082	TTTATTTTTGAGCTG[C/G]GCACGGTGGCTCACA	7428
rs775038762	snp	G/T	1.6473e-05	0.00286988	missense, intron-variant	VHL	GRCh38.p7	3:10146617	CGGACAGCCTATTTT[G/T]GCCAATATCACACTG	7428
rs775446934	snp	C/G	0.000955749	0.0218394	utr-variant-5-prime	VHL	GRCh38.p7	3:10141822	TCCCGCGGCGTCCGG[C/G]CCGGGTGGTCTGGAT	7428
rs775470306	snp	A/G			utr-variant-5-prime	VHL	GRCh38.p7	3:10141661	TTACAACGGCCTACG[A/G]TGCTGGAGGATCCTT	7428
rs775614995	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10143760	CAACGTCCGACCGAA[A/G]GTTTTTAAGCAGGGA	7428
rs775624944	snp	C/T	7.72544e-05	0.0062146	synonymous-codon	VHL	GRCh38.p7	3:10149962	TCAACGGATGGGAGA[C/T]TGAAGATTTCTGTTG	7428
rs775645886	in-del	-/AAAG			downstream-variant-500B	VHL	GRCh38.p7	3:10153865	TTTATTTTTCTTATA[-/AAAG]AAATGTATCACTATA	7428
rs776071666	snp	C/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10153134	ATAGAAAAAATTAGG[C/T]GGGCGTGGTGGTGAG	7428
rs776399733	snp	A/C	0.000144498	0.00849872	missense	VHL	GRCh38.p7	3:10141965	GCCGAGGAGTCCGGC[A/C]CGGAAGAGTCCGGCC	7428
rs776744176	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10142720	CCCCACGTGTATTTT[C/T]CCCTCAAAGAAAAGC	7428
rs776768994	snp	C/T	0.000184723	0.00960872	utr-variant-5-prime	VHL	GRCh38.p7	3:10141833	CCGGCCCGGGTGGTC[C/T]GGATCGCGGAGGGAA	7428
rs776793408	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10143558	GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCA	7428
rs776841447	snp	A/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10150186	CCTGCCCATTAGAGA[A/G]GTATTTATCAGGAGA	7428
rs776865943	in-del	-/CT			upstream-variant-2KB	VHL	GRCh38.p7	3:10140513	GCCTTCTATAGTACC[-/CT]GTCTCTTTTTGTCGT	7428
rs776975601	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10142390	TCGCTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG	7428
rs777033554	snp	A/G	1.6476e-05	0.00287014	intron-variant	VHL	GRCh38.p7	3:10146480	TGCCCAGCCACCGGT[A/G]TGGCTCTTTAACAAC	7428
rs777130107	snp	A/G	3.40837e-05	0.00412804	missense	VHL	GRCh38.p7	3:10149937	GGCTGACACAGGAGC[A/G]CATTGCACATCAACG	7428
rs777355462	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10145574	AGCCGGGCGTGGTGG[C/T]GGGCACCTGTGGTCC	7428
rs777358147	snp	A/G/T			utr-variant-3-prime	VHL	GRCh38.p7	3:10152858	CTCTTGTTAAAACCT[A/G/T]CAGGCCGAGCACAGT	7428
rs777536042	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10144728	GGTCTTGCTATGTTG[C/T]CCAGGCTGAGACCTC	7428
rs777618560	in-del	-/AA			utr-variant-3-prime	VHL	GRCh38.p7	3:10152062	CAAGACCCTGCCTCA[-/AA]AAAAAAAAAAAAAAA	7428
rs777622214	snp	C/G/T	4.83188e-05	0.00491503	intron-variant	VHL	GRCh38.p7	3:10142197	ACCGAGGTACGGGCC[C/G/T]GGCGCTTAGGCCCGA	7428
rs777662240	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10149028	CTCAGCTAGGCAGTT[A/G]CTCTGCTGGTGGTAG	7428
rs777754174	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10147257	CCTCATGATCTGCCC[A/G]CCTACGCCTCCCAAA	7428
rs777923008	snp	A/C			downstream-variant-500B	VHL	GRCh38.p7	3:10153931	GAAAAACATTCACAT[A/C]GGAAACAAAGTTTTT	7428
rs778005138	snp	A/C	2.05126e-05	0.00320248	utr-variant-3-prime	VHL	GRCh38.p7	3:10149972	GGAGATTGAAGATTT[A/C]TGTTGAAACTTACAC	7428
rs778132298	snp	A/C			intron-variant	VHL	GRCh38.p7	3:10142887	TGGCGCCGGAAGAGC[A/C]GACCGTGTGTGGCGT	7428
rs778205243	snp	A/G	4.95561e-05	0.00497751	missense	VHL	GRCh38.p7	3:10149867	AGACTGGACATCGTC[A/G]GGTCGCTCTACGAAG	7428
rs778294945	snp	C/T	3.36723e-05	0.00410305	intron-variant	VHL	GRCh38.p7	3:10149755	ACTGAGACCCTAGTC[C/T]GCCACTGAGGATTTG	7428
rs778550164	snp	G/T			intron-variant	VHL	GRCh38.p7	3:10144418	GAGTTGGAGGCTACA[G/T]TGAACTATGATGGTG	7428
rs778674343	snp	C/G	6.4348e-05	0.00567185	synonymous-codon	VHL	GRCh38.p7	3:10141880	GAACTGGGACGAGGC[C/G]GAGGTAGGCGCGGAG	7428
rs778846471	snp	G/T	4.94173e-05	0.00497053	synonymous-codon, intron-variant	VHL	GRCh38.p7	3:10146560	ACACGATGGGCTTCT[G/T]GTTAACCAAACTGAA	7428
rs779042401	in-del	-/AATC			utr-variant-3-prime	VHL	GRCh38.p7	3:10152279	AGGCTGAGGCAGGAG[-/AATC]AATCACTTGAACCCA	7428
rs779124495	in-del	-/ACGGCCT			utr-variant-5-prime	VHL	GRCh38.p7	3:10141650	CTCGCCTCCGTTACA[-/ACGGCCT]ACGGCCTACGGTGCT	7428
rs779157605	snp	C/G/T	1.65277e-05	0.00287464	synonymous-codon	VHL	GRCh38.p7	3:10149875	CATCGTCAGGTCGCT[C/G/T]TACGAAGATCTGGAA	7428
rs779228671	snp	C/G	2.7755e-05	0.00372515	intron-variant	VHL	GRCh38.p7	3:10142214	GCGCTTAGGCCCGAC[C/G]CAGCAGGGACGATAG	7428
rs779237956	snp	A/T			upstream-variant-2KB	VHL	GRCh38.p7	3:10139751	TCCCAGGCTCAAGTG[A/T]TCCTCCTGCTTCAGC	7428
rs779380656	snp	C/T			upstream-variant-2KB	VHL	GRCh38.p7	3:10140420	TCTGAGCTGCTTCTC[C/T]ACTTGAGTCCATCCC	7428
rs779457437	snp	C/G			intron-variant	VHL	GRCh38.p7	3:10143314	TTTTTTTTTAGTAGA[C/G]ACGGGGGTTTCGTCA	7428
rs779514074	snp	C/T	3.367e-05	0.00410291	missense	VHL	GRCh38.p7	3:10149928	ACCTGGAGCGGCTGA[C/T]ACAGGAGCGCATTGC	7428
rs779592055	snp	A/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10141158	GTTAGTTGACTTTTT[A/G]TACTTTATAAGCGTG	7428
rs779747717	in-del	-/AAC	3.29495e-05	0.00405877	intron-variant	VHL	GRCh38.p7	3:10146490	CCGGTGTGGCTCTTT[-/AAC]AACCTTTGCTTGTCC	7428
rs779824452	snp	C/T			intron-variant	VHL	GRCh38.p7	3:10147211	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	7428
rs779910104	snp	G/T	0.000149981	0.00865841	missense	VHL	GRCh38.p7	3:10141959	TCGGGCGCCGAGGAG[G/T]CCGGCCCGGAAGAGT	7428
rs780167833	snp	A/T	3.29538e-05	0.00405904	intron-variant	VHL	GRCh38.p7	3:10146474	CCACCGTGCCCAGCC[A/T]CCGGTGTGGCTCTTT	7428
rs780178275	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	VHL	GRCh38.p7	3:10146586	CTGAATTATTTGTGC[C/T]ATCTCTCAATGTTGA	7428
rs780199564	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10146292	CATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG	7428
rs780557277	snp	C/T	2.48827e-05	0.00352714	utr-variant-3-prime	VHL	GRCh38.p7	3:10150002	CTGTTTCATCTCAGC[C/T]TTTGATGGTACTGAT	7428
rs780783479	snp	C/G			upstream-variant-2KB	VHL	GRCh38.p7	3:10139835	CATTTTTTATAGAGA[C/G]AGGACCTCGCTATGT	7428
rs780967763	snp	C/G			intron-variant	VHL	GRCh38.p7	3:10143238	TGGGGTCAAGTGGTT[C/G]TCTTGCCTCAGCCTC	7428
rs781038836	in-del	-/TTTT			utr-variant-3-prime	VHL	GRCh38.p7	3:10153607	CTATTTCAAGTTTTT[-/TTTT]TTTTTTTTTTTTTTA	7428
rs781063331	snp	C/G/T	9.80029e-05	0.00699954	synonymous-codon	VHL	GRCh38.p7	3:10142105	GCGCGTCGTGCTGCC[C/G/T]GTATGGCTCAACTTC	7428
rs781065296	snp	C/G			intron-variant	VHL	GRCh38.p7	3:10149524	CCTAGAATTGCCAGT[C/G]TCGCTTCATCCACAT	7428
rs781141216	in-del	-/T	1.6513e-05	0.00287336	utr-variant-3-prime	VHL	GRCh38.p7	3:10150013	AGCTTTTGATGGTAC[-/T]TGATGAGTCTTGATC	7428
rs781248221	snp	A/G	1.64795e-05	0.00287045	intron-variant	VHL	GRCh38.p7	3:10146688	TGTGGTAAGTACAGG[A/G]TAGACCACTTGAAAA	7428
rs781618785	snp	G/T	1.64727e-05	0.00286986	missense, intron-variant	VHL	GRCh38.p7	3:10146596	TGTGCCATCTCTCAA[G/T]GTTGACGGACAGCCT	7428
rs786201557	snp	C/T			synonymous-codon	VHL	GRCh38.p7	3:10149924	AAAGACCTGGAGCGG[C/T]TGACACAGGAGCGCA	7428
rs786202787	snp	A/G			missense	VHL	GRCh38.p7	3:10142085	ATCTTCTGCAATCGC[A/G]GTCCGCGCGTCGTGC	7428
rs786202857	snp	A/G			missense	VHL	GRCh38.p7	3:10142056	CGGTGAACTCGCGCG[A/G]GCCCTCCCAGGTCAT	7428
rs786203104	snp	A/G			missense	VHL	GRCh38.p7	3:10141942	AAGACGGCGGGGAGG[A/G]GTCGGGCGCCGAGGA	7428
rs786204065	snp	A/T			missense	VHL	GRCh38.p7	3:10141876	CGGAGAACTGGGACG[A/T]GGCCGAGGTAGGCGC	7428
rs794726890	snp	C/G			missense	VHL	GRCh38.p7	3:10142092	GCAATCGCAGTCCGC[C/G]CGTCGTGCTGCCCGT	7428
rs794727253	in-del	-/A			frameshift-variant, intron-variant	VHL	GRCh38.p7	3:10146622	AGCCTATTTTTGCCA[-/A]TATCACACTGCCAGG	7428
rs794729660	in-del	-/ATC			cds-indel	VHL	GRCh38.p7	3:10142070	GAGCCCTCCCAGGTC[-/ATC]TTCTGCAATCGCAGT	7428
rs796222009	snp	A/G			intron-variant	VHL	GRCh38.p7	3:10143179	GCAGTGGCCCACGCT[A/G]GAATGCAGTGGCGCG	7428
rs796247536	in-del	-/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10153614	AGTTTTTTTTTTTTT[-/G]TTTTTTTTTTAAAGC	7428
rs796478545	snp	A/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10150187	CTGCCCATTAGAGAA[A/G]TATTTATCAGGAGAA	7428
rs796510465	in-del	-/A			utr-variant-3-prime	VHL	GRCh38.p7	3:10152082	AAAAAAAAAAAAAAA[-/A]TCAGGCCGGGCATGG	7428
rs796876776	in-del	-/TCTC			intron-variant	VHL	GRCh38.p7	3:10144482	CACAGCAAGACCCTG[-/TCTC]TCTATCTTGTCTTTT	7428
rs796939406	in-del	-/G			utr-variant-3-prime	VHL	GRCh38.p7	3:10153615	GTTTTTTTTTTTTTT[-/G]TTTTTTTTTAAAGCT	7428
rs863224371	snp	C/T			synonymous-codon	VHL	GRCh38.p7	3:10142174	CACGGGCCGCCGCAT[C/T]CACAGCTACCGAGGT	7428
rs863224372	snp	C/T			synonymous-codon, intron-variant	VHL	GRCh38.p7	3:10146548	AGATGCAGGGACACA[C/T]GATGGGCTTCTGGTT	7428
rs863224688	snp	C/T			missense	VHL	GRCh38.p7	3:10142136	GACGGCGAGCCGCAG[C/T]CCTACCCAACGCTGC	7428
rs863224839	in-del	-/AGAGTCCGGCCCGGA			cds-indel	VHL	GRCh38.p7	3:10141970	GGAGTCCGGCCCGGA[-/AGAGTCCGGCCCGGA]GGAACTGGGCGCCGA	7428
rs864321640	in-del	-/A			frameshift-variant	VHL	GRCh38.p7	3:10149911	CCAAATGTGCAGAAA[-/A]GACCTGGAGCGGCTG	7428
rs864321641	snp	A/T			missense	VHL	GRCh38.p7	3:10149802	TGTATACTCTGAAAG[A/T]GCGATGCCTCCAGGT	7428
rs864321642	snp	C/T			missense	VHL	GRCh38.p7	3:10149832	TTGTCCGGAGCCTAG[C/T]CAAGCCTGAGAATTA	7428
rs864321643	snp	A/C			missense	VHL	GRCh38.p7	3:10142140	GCGAGCCGCAGCCCT[A/C]CCCAACGCTGCCGCC	7428
rs864622109	snp	C/T			synonymous-codon	VHL	GRCh38.p7	3:10149878	CGTCAGGTCGCTCTA[C/T]GAAGATCTGGAAGAC	7428
rs864622267	snp	C/G			missense	VHL	GRCh38.p7	3:10142154	TACCCAACGCTGCCG[C/G]CTGGCACGGGCCGCC	7428
rs864622313	snp	A/T			missense, intron-variant	VHL	GRCh38.p7	3:10146607	TCAATGTTGACGGAC[A/T]GCCTATTTTTGCCAA	7428
rs864622334	snp	C/T			synonymous-codon	VHL	GRCh38.p7	3:10142168	GCCTGGCACGGGCCG[C/T]CGCATCCACAGCTAC	7428
rs864622379	snp	A/C			missense	VHL	GRCh38.p7	3:10141894	CCGAGGTAGGCGCGG[A/C]GGAGGCAGGCGTCGA	7428
rs864622545	in-del	-/C			frameshift-variant	VHL	GRCh38.p7	3:10142105	GCGCGTCGTGCTGCC[-/C]GTATGGCTCAACTTC	7428
rs864622645	snp	C/T			synonymous-codon	VHL	GRCh38.p7	3:10141976	CGGCCCGGAAGAGTC[C/T]GGCCCGGAGGAACTG	7428
rs864622646	snp	C/T			synonymous-codon, intron-variant	VHL	GRCh38.p7	3:10146518	TGTCCCGATAGGTCA[C/T]CTTTGGCTCTTCAGA	7428
rs864622714	snp	C/G			synonymous-codon	VHL	GRCh38.p7	3:10142015	GGAGGAGATGGAGGC[C/G]GGGCGGCCGCGGCCC	7428

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