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
rs2272308	snp	C/T	0.302686	0.244385	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163446	GGCATCGGCAGTGGC[C/T]TGTCTCAGCTCTGTC	102465519
rs2293432	snp	A/C	0.244205	0.249933	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164004	ACGAGGACCTAGGTC[A/C]GGTGACAGGTGGATT	102465519
rs12306627	snp	C/T	0.0379877	0.132479	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164382	GGTGGGGTCTACCCT[C/T]GGCCGTGTAGATGAG	102465519
rs35084322	in-del	-/G			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163530	GCCCAGCCTGGCCCT[-/G]GGGATGTCTACCTTG	102465519
rs57142641	snp	C/T	0.00672897	0.0576125	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162989	AGCCCCAGTTCCAAA[C/T]AGAGAAAGGCTAGTG	102465519
rs61748839	snp	C/T	0.00692832	0.0584479	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163713	GCTCCGGATGGCTGC[C/T]GCGTAGATGTCCTTG	102465519
rs77746486	snp	A/G	0.00139218	0.0263467	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163563	GAACTCGAGGTTGAT[A/G]TAGGGGAGGCCGCAG	102465519
rs78121431	snp	C/T	0	0	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164625	CTAATTATGCTTGCT[C/T]TTTTTTTTTTTTGAG	102465519
rs78614777	snp	G/T	0	0	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164637	GCTTTTTTTTTTTTT[G/T]GAGACGGAGTTTTGC	102465519
rs78987995	snp	A/G	0.0444908	0.142359	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163794	AGAGGCTGGGTCTGG[A/G]GGCCACACCCACTCA	102465519
rs111277819	snp	A/T	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163929	TCTTAGTAAACCCCT[A/T]CTGCTGAGGACCCTC	102465519
rs112704220	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164653	GAGACGGAGTTTTGC[C/T]CTTGTTGCCCAGGCT	102465519
rs114772167	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164031	TCGTGTCATTGCCCA[G/T]GAACAGATGCTGCTG	102465519
rs114947184	snp	C/G	0.0134861	0.0810011	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163437	TGTGGCAAGGACAGA[C/G]CTGAGACAGGCCACT	102465519
rs140424049	in-del	-/C			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164070	GGCTGGCTGGCCGGG[-/C]CCAGCCCCTGCCAGC	102465519
rs141828248	snp	A/G	0.000167434	0.00914817	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163629	CAGCAGCTGCAGGGG[A/G]ATGATGGAGCCCAGG	102465519
rs142106640	snp	C/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164917	GTGAGCCACTGCACC[C/T]AGACCGCTTTTTCTT	102465519
rs145874584	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163372	GGGGCAGGGTGCAAC[A/G]TGTGGGCTGTGAGCA	102465519
rs147125643	in-del	-/CCC			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163771	AGGTGAGGGAGAACA[-/CCC]CCGCCGAAGAGGCTG	102465519
rs147715633	snp	A/G	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163799	CTGGGTCTGGGGGCC[A/G]CACCCACTCAGCTGG	102465519
rs149761829	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HECTD4, MIR6861	GRCh38.p7	12:112163291	AGGTCCAGGTGTCAG[A/G]AGCCCTGGAGCCCCA	102465519
rs181634938	snp	C/T	0.000542446	0.0164599	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163651	GAGCCCAGGCCGGCC[C/T]GCACGGCCGTCACGC	102465519
rs182300912	snp	A/G			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164747	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	102465519
rs183122979	snp	A/T			intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162788	TTTTTTTTTTTAACC[A/T]TTTTTCTGCATTTAA	102465519
rs183882784	snp	C/T	0.0133539	0.0806141	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163079	GATCTTCATGGGGTA[C/T]GGGGGCACATGGGCA	102465519
rs185247666	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164766	AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC	102465519
rs186770263	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163802	GGTCTGGGGGCCACA[C/T]CCACTCAGCTGGAGG	102465519
rs188611917	snp	A/G	8.28837e-05	0.006437	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163208	CTCCAGGGCCCCCCA[A/G]AAGAACTCGATGTGC	102465519
rs189956579	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164822	AGACTGGGTTTCACT[A/G]TGTTGGCCAGGCTGG	102465519
rs190623100	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164692	ATGGCGCAATCTTGG[C/G]TCGCTGCAACCCCTC	102465519
rs192743323	snp	C/T			intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162768	CCCAGCAAATTGTTT[C/T]TTTTTTTTTTTTTTT	102465519
rs200268404	snp	A/G	0.000569285	0.0168617	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164214	CTGTCAGGGCTCTCC[A/G]TGGCCAGGTGCTGGG	102465519
rs201265123	snp	C/G	0.000844476	0.0205311	missense, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163160	GTTGCAGGCAAACTT[C/G]ATGAACTTGCACAGC	102465519
rs202119425	snp	C/T	0.000657266	0.0181163	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164124	GCCACAAGGATGTGC[C/T]GGCCCCGGCTGCACA	102465519
rs367606627	snp	C/T	4.27451e-05	0.00462285	intron-variant, nc-transcript-variant	HECTD4, MIR6861	GRCh38.p7	12:112163281	TGGGGAGGAGAGGTC[C/T]AGGTGTCAGGAGCCC	102465519
rs368281795	snp	A/G	0.000132514	0.00813876	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163151	GCGCTCCTGGTTGCA[A/G]GCAAACTTGATGAAC	102465519
rs369547696	snp	G/T	1.75145e-05	0.00295921	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164153	CAGCTCCACCTCCTC[G/T]CCCGTCATGGTCAGG	102465519
rs369564664	snp	C/T	0.00112945	0.0237371	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164096	CCAGCCCCTGACACG[C/T]GCACACACTCACGCC	102465519
rs370063916	snp	A/C/T	3.34965e-05	0.00409235	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164242	GGGAGGCGATCTCAG[A/C/T]GCACAGGGCCTCCAG	102465519
rs371033442	snp	A/G	0.000156924	0.0088565	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164321	ATGAGGCCATGGGAG[A/G]TGGAACCCTGATCCC	102465519
rs371115604	snp	C/T	8.36897e-05	0.00646822	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164233	CCAGGTGCTGGGAGG[C/T]GATCTCAGCGCACAG	102465519
rs371332898	snp	C/G	0.000163987	0.00905353	intron-variant, nc-transcript-variant	HECTD4, MIR6861	GRCh38.p7	12:112163294	TCCAGGTGTCAGGAG[C/G]CCTGGAGCCCCACCT	102465519
rs371389017	snp	C/G	3.31697e-05	0.00407231	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163106	GGCAGTGTCGGGACC[C/G]CCATCTTTGCAGGGG	102465519
rs371880099	snp	C/G	8.28246e-05	0.00643471	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163172	CTTGATGAACTTGCA[C/G]AGCTCCTCCTGGGTG	102465519
rs372003631	snp	C/T			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163925	GTTTTCTTAGTAAAC[C/T]CCTTCTGCTGAGGAC	102465519
rs372573928	snp	C/T	0.000190221	0.0097506	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164156	CTCCACCTCCTCGCC[C/T]GTCATGGTCAGGTAG	102465519
rs374029714	snp	C/T	3.31724e-05	0.00407248	missense, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163216	CCCCCCAGAAGAACT[C/T]GATGTGCTGGTCCGT	102465519
rs374497789	snp	C/T	0.000461969	0.0151911	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164295	AGGGTGGAGGCAGAG[C/T]GAGGCTCATTATGAG	102465519
rs375061280	snp	A/T	0.000161987	0.00899817	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164091	CCCTGCCAGCCCCTG[A/T]CACGCGCACACACTC	102465519
rs375330854	snp	C/T	0.000326371	0.0127702	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164130	AGGATGTGCCGGCCC[C/T]GGCTGCACAGCTCCA	102465519
rs375445453	snp	A/G	3.70501e-05	0.00430391	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163017	GTGTGTCCCTACTTG[A/G]GACATGGCCAGGGGA	102465519
rs375590063	snp	C/T			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163976	ATCCTGCCTCATCTC[C/T]CTCTCCTGGTGAAAT	102465519
rs375635285	snp	C/T	1.65839e-05	0.00287953	missense, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163107	GCAGTGTCGGGACCC[C/T]CATCTTTGCAGGGGC	102465519
rs375938583	snp	C/T	0.000187982	0.00969308	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163551	GTCTACCTTGAGGAA[C/T]TCGAGGTTGATGTAG	102465519
rs376711869	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164922	CCACTGCACCCAGAC[C/T]GCTTTTTCTTTTTTT	102465519
rs377053677	snp	A/G	0.000938702	0.0216442	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163656	CAGGCCGGCCCGCAC[A/G]GCCGTCACGCACTCC	102465519
rs377506093	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162895	TGGCTGGTTCCTGCC[A/G]GGCCCTAATCCTCAA	102465519
rs527298215	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164642	TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG	102465519
rs527424635	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165265	CAGAGGCCTGAGACC[A/G]ATACCAGATGATACT	102465519
rs527546674	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164015	CACCTGACCTAGGTC[C/T]TCGTGTCATTGCCCA	102465519
rs528812083	snp	C/G	0.000182208	0.00954311	synonymous-codon, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112163184	GCACAGCTCCTCCTG[C/G]GTGAACATCTCCAGG	102465519
rs528961462	snp	A/G			intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162929	TGTCTGAGTTTTGGC[A/G]CGTGGGGCTCCTGTT	102465519
rs529747953	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164886	CTCAGCCTTCCAAAG[C/T]GCTGGGATTACAGGT	102465519
rs532706721	in-del	-/GCCAGCCCCT	0.00183206	0.0302105	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164069	TGGCTGGCTGGCCGG[-/GCCAGCCCCT]GCCAGCCCCTGCCAG	102465519
rs533056922	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164446	CATCAGTTCAGGGCC[A/G]GGCGTGTGACCCAGG	102465519
rs533087892	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163855	GGCCTGGGGCCCAGC[C/T]GCCCTGGTCATCCCA	102465519
rs533769191	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162837	CATTCTGGATTTTCA[A/G]CTTCTTTTAAGATAT	102465519
rs534136597	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163512	TGGGGCTCACCACCT[C/G]CCCGCCCAGCCTGGC	102465519
rs535516940	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163612	AGTGGGCTGAGCATG[A/G]TCAGCAGCTGCAGGG	102465519
rs535743680	snp	A/C			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164351	CCAGGTGGCTGGGTA[A/C]ACCCCAAGCGCAGCT	102465519
rs537674422	snp	C/T	0.00782583	0.0620618	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164067	CCCTGGCTGGCTGGC[C/T]GGGCCAGCCCCTGCC	102465519
rs540965990	snp	C/G	0.000399281	0.0141238	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163719	GATGGCTGCCGCGTA[C/G]ATGTCCTTGTTCTCC	102465519
rs542012726	snp	G/T	0.000326554	0.0127738	intron-variant, nc-transcript-variant	HECTD4, MIR6861	GRCh38.p7	12:112163270	TGGTGTGGGCCTGGG[G/T]AGGAGAGGTCCAGGT	102465519
rs542595027	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165308	GGATTTGGCCCTGCC[G/T]GAAGTCAAACCCATC	102465519
rs544745123	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165154	TTGAACTCCTGACCT[C/T]GTGATCTACCCGCCT	102465519
rs544961944	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165069	GGGATTACAGGCACC[C/T]GCCACCATGCCTGGC	102465519
rs545092155	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164540	CTCACTGGCATGGAC[C/T]GACTATGATGGGAAA	102465519
rs545772641	snp	C/T	0.000767361	0.0195727	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163687	ACATTCTGCAGCTCC[C/T]GCAGCCGCAGGCTCC	102465519
rs545807973	snp	C/T			intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162930	GTCTGAGTTTTGGCA[C/T]GTGGGGCTCCTGTTC	102465519
rs547440179	snp	A/G			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163856	GCCTGGGGCCCAGCC[A/G]CCCTGGTCATCCCAG	102465519
rs548543216	in-del	-/TGAT	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164329	TGGGAGGTGGAACCC[-/TGAT]TGATCCCCAGGTGGC	102465519
rs549270232	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164029	CCTCGTGTCATTGCC[C/G]AGGAACAGATGCTGC	102465519
rs549747227	snp	A/G			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164018	CTGACCTAGGTCCTC[A/G]TGTCATTGCCCAGGA	102465519
rs550697417	snp	A/G	0.000394878	0.0140457	intron-variant, nc-transcript-variant	HECTD4, MIR6861	GRCh38.p7	12:112163298	GGTGTCAGGAGCCCT[A/G]GAGCCCCACCTACCC	102465519
rs553952531	snp	C/T			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165029	TGGGTTCAAGCAATT[C/T]TCTGCCTCAGGCTCC	102465519
rs555564729	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162894	ATGGCTGGTTCCTGC[C/T]GGGCCCTAATCCTCA	102465519
rs555824604	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164980	CAGCTGGAGTGCAGT[A/G]GCGCAATCTCAGCTC	102465519
rs555940034	snp	A/G			intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164541	TCACTGGCATGGACC[A/G]ACTATGATGGGAAAC	102465519
rs555971026	snp	C/T	0.000432121	0.0146926	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164094	TGCCAGCCCCTGACA[C/T]GCGCACACACTCACG	102465519
rs556039865	snp	A/G	0	0	synonymous-codon, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164240	CTGGGAGGCGATCTC[A/G]GCGCACAGGGCCTCC	102465519
rs556748614	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165070	GGATTACAGGCACCC[A/G]CCACCATGCCTGGCT	102465519
rs557862489	snp	A/G	2.20524e-05	0.0033205	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164131	GGATGTGCCGGCCCC[A/G]GCTGCACAGCTCCAC	102465519
rs558239335	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164897	AAAGCGCTGGGATTA[C/T]AGGTGTGAGCCACTG	102465519
rs559854710	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164600	GTGCGCTGGGAGAGA[A/C]TGCTTGAGGCTAATT	102465519
rs560216408	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112165165	ACCTCGTGATCTACC[C/T]GCCTCAGCCTCCCAA	102465519
rs560687679	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164383	GTGGGGTCTACCCTC[A/G]GCCGTGTAGATGAGC	102465519
rs562592155	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163853	GAGGCCTGGGGCCCA[A/G]CCGCCCTGGTCATCC	102465519
rs563109255	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112164384	TGGGGTCTACCCTCG[G/T]CCGTGTAGATGAGCA	102465519
rs563297363	snp	C/T	1.88525e-05	0.00307016	intron-variant, downstream-variant-500B	HECTD4, MIR6861	GRCh38.p7	12:112162999	CCAAACAGAGAAAGG[C/T]TAGTGTGTCCCTACT	102465519
rs564542020	snp	C/T	0.000399281	0.0141238	missense, upstream-variant-2KB	HECTD4, MIR6861	GRCh38.p7	12:112163702	CGCAGCCGCAGGCTC[C/T]GGATGGCTGCCGCGT	102465519

Full records

It may take some time, please wait.