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

RNF146

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs763056478	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127271491	ATTAACATTGAATTC[A/G]TTGTCTCTATTAAAC	81847
rs763075186	snp	A/G	0.000115501	0.0075985	missense	RNF146	GRCh38.p7	6:127287331	CCATCCCCTGATGCA[A/G]GCACTTCTCTGGAAG	81847
rs763084258	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127279457	TTATTTCTGGACTCT[A/C]AATTCTATATCATTG	81847
rs763133290	snp	A/G	1.65064e-05	0.00287279	synonymous-codon	RNF146	GRCh38.p7	6:127287480	CATTGAAGAAACTGA[A/G]TCAGATGCCAGTAGT	81847
rs763188969	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127267552	CATTTTTGCCTTTTC[C/T]CGGAGTGTCTCTGGC	81847
rs763356793	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127268824	TTTCAGTCTCCACCA[A/G]CCTAACTTGTCAGAG	81847
rs763368413	snp	C/T	3.31592e-05	0.00407167	synonymous-codon	RNF146	GRCh38.p7	6:127286862	TCCCGAGGATTTCCT[C/T]GACAAGCCAACCTTG	81847
rs763702459	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127271025	TTCACCATGTTGGCC[A/C]GGATGGTATTGATCT	81847
rs763783725	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127281766	ATCTTAATTGATTTT[G/T]ATACTTAGGGACAGA	81847
rs763812686	snp	C/G/T	0.000265251	0.0115137	synonymous-codon	RNF146	GRCh38.p7	6:127286850	TCGACAAGAAATTCC[C/G/T]GAGGATTTCCTTGAC	81847
rs763855105	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127285953	GGTGTTTAGTAAATG[C/T]TTATCTGAATCAATA	81847
rs763902493	snp	A/G	1.65743e-05	0.00287869	missense	RNF146	GRCh38.p7	6:127286655	TCATTCAATAAACAT[A/G]CTTCCTACAAACAGG	81847
rs764129860	snp	A/G	1.6531e-05	0.00287493	missense	RNF146	GRCh38.p7	6:127287565	CTTTTGGTTTCTAAT[A/G]CAAACCAGACAGTAC	81847
rs764161627	in-del	-/AG			intron-variant, utr-variant-3-prime, downstream-variant-500B	ECHDC1, RNF146	GRCh38.p7	6:127288516	AGAGATTATTTAAAC[-/AG]AATCTATAGGCAGTG	81847
rs764177858	snp	G/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127266304	TCAGGCACTATTCTG[G/T]TTTTTTTAAAAAAAG	81847
rs764339585	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127267735	GGAACAATTAAGAGA[A/T]CTCAGAATATCCCTT	81847
rs764500638	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127276526	TATGAGATAAAGATA[G/T]GAGGGGGCCAAGGGT	81847
rs764648313	snp	C/T	1.6522e-05	0.00287414	missense	RNF146	GRCh38.p7	6:127287215	GCTCTGCTGACGGAG[C/T]GGACAGTGTATCAGC	81847
rs764739440	snp	A/T	1.6838e-05	0.0029015	missense	RNF146	GRCh38.p7	6:127287647	CAGTGAGTGTCAGTG[A/T]CAGATCTAGAAGGCC	81847
rs764859732	snp	C/G			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283444	AAAGGGAGGGGAAAA[C/G]CTTTCTTATTTACAT	81847
rs764896810	snp	G/T			utr-variant-3-prime	RNF146	GRCh38.p7	6:127288190	TTATAGTAAAGTTAT[G/T]GAAATGGAAATGAAA	81847
rs765236104	snp	C/T	4.95086e-05	0.00497512	missense	RNF146	GRCh38.p7	6:127287320	GCCCTGCAACACCAT[C/T]CCCTGATGCAAGCAC	81847
rs765334083	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127278100	TGTGTTTACTGTGAG[A/T]TCTATCATTTCTTTA	81847
rs765371140	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127266178	AAAAAGGAAATGTAC[A/G]TGCTAAAATGGTGAA	81847
rs765449163	snp	A/G	3.30442e-05	0.0040646	missense	RNF146	GRCh38.p7	6:127287223	GACGGAGCGGACAGT[A/G]TATCAGCACAGAGTG	81847
rs765489600	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127279245	TATTAAGAGTTTTAT[G/T]GTTTTATTTCTTATA	81847
rs765505242	in-del	-/CGATCGATCAGATCGATCGGGAACTGAT	1.65378e-05	0.00287552	frameshift-variant	RNF146	GRCh38.p7	6:127287582	AAACCAGACAGTACC[-/CGATCGATCAGATCGATCGGGAACTGAT]CGATCAGTAGCAGGG	81847
rs765545736	snp	C/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265112	AACAGTCTGTGGGGT[C/T]AAAGAGGTAATGAGG	81847
rs765605292	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127278310	ATTATAGATTTTCCA[C/G]AACTTTTTTTTAGCA	81847
rs765669763	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127273516	TTTGATGTTTCAAGA[C/G]TACATGATTCATCTG	81847
rs765731863	in-del	-/CT			intron-variant, downstream-variant-500B, utr-variant-3-prime	ECHDC1, RNF146	GRCh38.p7	6:127288651	ATTAGTAGTCTAACA[-/CT]CTGGATTAAATGGCA	81847
rs766073428	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127282028	AATAGGGAAAGAAAG[A/C]TGTCTTGGCCGAGTA	81847
rs766080708	in-del	-/TACC			intron-variant	RNF146	GRCh38.p7	6:127280028	GTTTTACTTCCTCCT[-/TACC]TACCCGTCTGTATGC	81847
rs766220292	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ECHDC1, RNF146	GRCh38.p7	6:127288605	CAAATAGCATATACC[A/G]TTAATATTTTATATT	81847
rs766236672	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127285854	TAATTATCTGCATGT[A/G]TGTTTCCTTATTTAA	81847
rs766280382	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127269124	ACATCTTTGTGGATA[C/T]AGAAACTAATTTATG	81847
rs766445819	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127277915	TTTAAAACAAATTGT[A/T]TGTTCTGTTAAACAT	81847
rs766683949	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127276856	TGTTTCTCAGATTGT[A/G]TTTGAAGGACTAAAG	81847
rs766813850	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127286527	TGCATATAATGCACA[C/T]CATAGGTGGTTAGTG	81847
rs766857368	snp	C/T	1.6582e-05	0.00287936	missense	RNF146	GRCh38.p7	6:127286870	ATTTCCTTGACAAGC[C/T]AACCTTGTTGTCACC	81847
rs766895672	in-del	-/AGAAGA			cds-indel	RNF146	GRCh38.p7	6:127287410	TCATAGGGGAGAAGG[-/AGAAGA]AGAAGAAGATCATGA	81847
rs766901437	in-del	-/TTAT			intron-variant	RNF146	GRCh38.p7	6:127281197	AAAAGTATGACCATA[-/TTAT]TTTTATTCAGTATTG	81847
rs767056539	snp	A/G	0.0023438	0.0341527	utr-variant-5-prime	RNF146	GRCh38.p7	6:127280326	GCAGGCATCTGTGGG[A/G]TCTGTAATAGAAATG	81847
rs767057832	snp	C/T	1.66186e-05	0.00288254	missense	RNF146	GRCh38.p7	6:127286645	GTGAAATTGATCATT[C/T]AATAAACATGCTTCC	81847
rs767237415	in-del	-/GATCGATCAGATCGATCGGGAACT	0.000314218	0.0125304	cds-indel	RNF146	GRCh38.p7	6:127287582	AACCAGACAGTACCC[-/GATCGATCAGATCGATCGGGAACT]GATCGATCAGATCGA	81847
rs767421986	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283078	TCTTGGAGATTTCCA[C/T]TAACTCTGCCCATAC	81847
rs767427529	snp	A/G	1.65266e-05	0.00287455	synonymous-codon	RNF146	GRCh38.p7	6:127287543	GCACTCCTTGACCCA[A/G]CAGAGACTTTTGGTT	81847
rs767517501	snp	A/G	1.65004e-05	0.00287227	missense	RNF146	GRCh38.p7	6:127287370	GCTCATTTACAACTC[A/G]GTGGAGACAACACAG	81847
rs767588075	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127274871	GAGGCCAGGAGTTTG[A/T]GGTTTAAGTTACCTG	81847
rs767781185	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127275857	ACAACTAGATTATTA[A/G]TCTATGGGTGGTTGT	81847
rs767980724	snp	A/C	1.65787e-05	0.00287907	synonymous-codon	RNF146	GRCh38.p7	6:127286886	AACCTTGTTGTCACC[A/C]GAAGAACTCAAGGCA	81847
rs768137076	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127264810	CCTCCTGTGTCTTGC[A/G]TCCTAATGTGATGAG	81847
rs768225194	snp	C/T	1.65351e-05	0.00287528	synonymous-codon	RNF146	GRCh38.p7	6:127287174	GCTAGACTGTGATGC[C/T]AATACCGTAAACCTA	81847
rs768259967	snp	G/T			utr-variant-3-prime	RNF146	GRCh38.p7	6:127288047	TCTTATTTTTCTGCA[G/T]GGATTGGCATAAGAC	81847
rs768293915	snp	C/T			synonymous-codon	RNF146	GRCh38.p7	6:127287570	GGTTTCTAATGCAAA[C/T]CAGACAGTACCCGAT	81847
rs768301618	in-del	-/TATG	0.000240833	0.0109708	intron-variant	RNF146	GRCh38.p7	6:127286599	ATGACTTTAATATTA[-/TATG]TATTTTTTCTTAGGA	81847
rs768311096	snp	C/G/T	3.31588e-05	0.00407167	missense	RNF146	GRCh38.p7	6:127287015	TTCCAAAGGTAAAAA[C/G/T]AACACTGAAATGTTA	81847
rs768348624	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127272733	TAAGAGGGCAGTACA[A/G]TTGACCCTTGAGCAA	81847
rs768485384	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127271103	ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTCCTT	81847
rs768679707	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127274628	TAATTGAATCTTCAC[A/T]CTAGAGGTTTTACCA	81847
rs768850858	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127268833	CCACCAACCTAACTT[C/G]TCAGAGGAAAGGAAC	81847
rs768908607	snp	G/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283878	TTCACTTCATTCTGA[G/T]GATGGAACCAAAATA	81847
rs768951941	snp	A/G			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284290	CTGTCCTTTGTTCAT[A/G]AGGTACTTAGATGGT	81847
rs769038880	snp	A/G	1.64958e-05	0.00287187	synonymous-codon	RNF146	GRCh38.p7	6:127287438	TGAATCACCATCTTC[A/G]GGCAGGGTACCAGCA	81847
rs769061636	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127271748	ATTGAAACATACTGA[A/G]GCAGTAATGTAGAAA	81847
rs769124693	snp	A/T	3.30224e-05	0.00406326	missense	RNF146	GRCh38.p7	6:127287298	TCAGTAGATGGTCAG[A/T]TAACAAGCCCTGCAA	81847
rs769146036	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127278468	CATACTTTTCTGTAT[G/T]TGGCTTATTAGTATG	81847
rs769213516	snp	A/G	1.65119e-05	0.00287327	missense	RNF146	GRCh38.p7	6:127287259	TCTGTTCAGCCCCTA[A/G]TGTCTTCTGTAAGGC	81847
rs769305632	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265637	AATAAAGCACTTAGA[A/G]CAACACCTGGCACAT	81847
rs769359963	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127277427	AGTAAAACAAAAAGG[C/T]TACTTAGAAACCTTG	81847
rs769421846	snp	A/G	1.73294e-05	0.00294353	splice-acceptor-variant	RNF146	GRCh38.p7	6:127286614	TATGTATTTTTTCTT[A/G]GGATGGCTGGCTGTG	81847
rs769455993	in-del	-/TC			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265545	TCTCAGCTGTGTGTG[-/TC]TCTCTCTCTCTGTAA	81847
rs769808714	snp	G/T			synonymous-codon	RNF146	GRCh38.p7	6:127287246	ACAGAGTGGAGCTTC[G/T]GTTCAGCCCCTAGTG	81847
rs769840887	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127272653	TGGTTGTGTTGTTCT[A/G]CGCAAATGTATTTTT	81847
rs769998378	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127274335	ATTTTTTTGTACTTA[C/T]TTTGAAGCTGCTTTG	81847
rs770155008	snp	A/G			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127282471	AGCTGTCATCTACCT[A/G]TCTCCACCTGGAGAC	81847
rs770171920	snp	A/T	0.000115816	0.00760886	synonymous-codon	RNF146	GRCh38.p7	6:127287591	AGTACCCGATCGATC[A/T]GATCGATCGGGAACT	81847
rs770654841	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127276388	GGTGGGGGAGCAGGG[A/G]GCTGTGTGGTGAGAG	81847
rs770671561	snp	A/G	9.90622e-05	0.00703714	synonymous-codon	RNF146	GRCh38.p7	6:127287285	AAGGCCCCTAACATC[A/G]GTAGATGGTCAGTTA	81847
rs770825666	snp	C/G	1.66754e-05	0.00288746	missense	RNF146	GRCh38.p7	6:127286638	GGCTGTGGTGAAATT[C/G]ATCATTCAATAAACA	81847
rs771043881	snp	A/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284654	CTATTTTAAAAACAT[A/T]TGCCTTCTTTTGTAA	81847
rs771078767	snp	G/T	1.85424e-05	0.00304481	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287718	TCTTCAGCTCCATGC[G/T]CAAGGTTGAAAGGGT	81847
rs771092790	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127272495	TCACCAAAGCATGCA[A/G]GATTTACTAAAATTA	81847
rs771170597	snp	C/T	6.62186e-05	0.00575369	missense	RNF146	GRCh38.p7	6:127287599	ATCGATCAGATCGAT[C/T]GGGAACTGATCGATC	81847
rs771351988	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127279130	AAAATTTTAAACTTA[C/T]ATAAAGCCCAATTTA	81847
rs771423509	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284763	ACATACTAAGACGTC[C/T]TATTAGGGTTTACTT	81847
rs771554791	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127267340	TCTTCCGCCTGAGCC[C/T]GCTTCGCTGCCTCGG	81847
rs771708764	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127275362	AGAACTTAGATATTT[C/T]TATGTATCTTACAGA	81847
rs771872003	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127276363	CAGAATTTATGGTGT[C/G]GTTGGTTGGGGTGGG	81847
rs771910185	snp	C/T			missense	RNF146	GRCh38.p7	6:127287539	CACAGCACTCCTTGA[C/T]CCAACAGAGACTTTT	81847
rs771960571	snp	A/G	3.30764e-05	0.00406659	synonymous-codon	RNF146	GRCh38.p7	6:127286790	CGTTTTCTGCTATCT[A/G]TGTGTAAAAGGAGCT	81847
rs772068992	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284389	ATTTTTCTATTTAGT[C/T]TCATGAATAGAATCA	81847
rs772224271	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127270088	TGAAAAAAACTCTTG[A/G]CTTTGATCTTGTGAC	81847
rs772226037	in-del	-/TTG	1.65825e-05	0.00287941	cds-indel	RNF146	GRCh38.p7	6:127286875	CTTGACAAGCCAACC[-/TTG]TTGTCACCAGAAGAA	81847
rs772329120	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127271303	TTTTGACTGCGCAGG[G/T]TGTAGACATTCTTAA	81847
rs772357043	snp	A/G	1.65263e-05	0.00287452	synonymous-codon	RNF146	GRCh38.p7	6:127287192	TACCGTAAACCTAGC[A/G]AGAGAGAGCTCTGCT	81847
rs772380757	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127285252	TTGAGGAACCAAGAA[C/T]ACAGAAAAGGCAGTA	81847
rs772398151	snp	A/G	1.86719e-05	0.00305542	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287731	GCTCAAGGTTGAAAG[A/G]GTTACCTGTAAATTT	81847
rs772702089	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127278768	TTACCTTCCTACCAG[A/C]AGTTTTCAAAGGTCC	81847
rs772751907	snp	C/G			utr-variant-3-prime	RNF146	GRCh38.p7	6:127288068	GGCATAAGACCATTA[C/G]TAAAATTTGGCACCT	81847
rs772793384	snp	G/T	4.9579e-05	0.00497866	missense	RNF146	GRCh38.p7	6:127287188	CTAATACCGTAAACC[G/T]AGCAAGAGAGAGCTC	81847
rs772805333	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127276364	AGAATTTATGGTGTG[A/G]TTGGTTGGGGTGGGG	81847
rs772860214	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127275415	GAACTCAAGTGTTGT[A/G]TTATTTGAATAAATC	81847
rs772899281	in-del	-/AGAGG			intron-variant	RNF146	GRCh38.p7	6:127275662	AAACATACAAAACAT[-/AGAGG]AGAGAACAGTTAACT	81847
rs772904903	in-del	-/G			utr-variant-3-prime	RNF146	GRCh38.p7	6:127287837	ACTCATAATTAAAAT[-/G]GTCTAACATGTCTCT	81847
rs772983266	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127268986	ACTACCAGGAAACAT[C/T]TAACAGCACTGACAG	81847
rs773162790	snp	C/T	1.65061e-05	0.00287277	missense	RNF146	GRCh38.p7	6:127287467	CACCAGACACCTCCA[C/T]TGAAGAAACTGAATC	81847
rs773163307	snp	G/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284440	TTATTACTTGTAAAT[G/T]GATCACTTTCTTGTT	81847
rs773286847	in-del	-/ACATAGATAG	1.65732e-05	0.00287859	frameshift-variant	RNF146	GRCh38.p7	6:127287002	GGAAGATGCTTTTTC[-/ACATAGATAG]CAAAGGTAAAAAGAA	81847
rs773323532	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127270395	AAAATTTACAGGTCA[C/T]TCATTCCAGTAGGAA	81847
rs773377870	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127271309	CTGCGCAGGGTGTAG[A/G]CATTCTTAACTCCTC	81847
rs773700569	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127277641	GCATCCAGTACAGGA[C/G]AAAGATGTAGGCTGG	81847
rs773806915	snp	C/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265905	AGATTGGGTTACATA[C/T]TGATATATATGAATG	81847
rs773819934	snp	G/T	1.65493e-05	0.00287652	missense	RNF146	GRCh38.p7	6:127287596	CCGATCGATCAGATC[G/T]ATCGGGAACTGATCG	81847
rs773836989	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127286405	ACTGATGGAATTTTT[A/T]TACATTCCCAAGGTA	81847
rs773862030	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127278858	CTTATAGATGTATCA[C/T]TGTGATTTTGATTTA	81847
rs773863875	snp	G/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127264835	GATGAGAAATATGAT[G/T]AAGATTAGTAAGTAA	81847
rs773984148	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127264605	TGATCTACTGACCTC[A/G]TGATCCGCCCACTTC	81847
rs774017170	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127272870	GTTGTTTGTTATATG[C/T]ATTACATACTATATT	81847
rs774206251	snp	A/T	1.6513e-05	0.00287336	synonymous-codon	RNF146	GRCh38.p7	6:127286748	TCTGCAAACATGTGT[A/T]CATCCAGTCAGTCTG	81847
rs774323082	snp	A/T	1.66621e-05	0.00288631	missense	RNF146	GRCh38.p7	6:127286640	CTGTGGTGAAATTGA[A/T]CATTCAATAAACATG	81847
rs774338701	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127274704	AGACTTGTAAGATAG[C/T]GAAGGATAGGCAGTG	81847
rs774466537	snp	G/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127282967	TTGCAAGCTAAAAAT[G/T]TCTTGAATACTACAC	81847
rs774510344	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127270061	GATAATCGCTTGCTT[C/G]AATCTATTACCTGAA	81847
rs774595976	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127267908	CTAAAGAATGTAAAA[-/T]TTGTTTTAAGAGTGG	81847
rs774652896	snp	C/T	1.65869e-05	0.00287979	stop-gained	RNF146	GRCh38.p7	6:127287610	CGATCGGGAACTGAT[C/T]GATCAGTAGCAGGGG	81847
rs774705162	in-del	-/CTT	3.30256e-05	0.00406346	cds-indel	RNF146	GRCh38.p7	6:127286702	GTTCTAATACTGCAC[-/CTT]CTTTAACCGTCCCTG	81847
rs774774509	snp	C/T	1.65811e-05	0.00287929	synonymous-codon	RNF146	GRCh38.p7	6:127287057	TCTGTATGTCGCTGA[C/T]CTTGAAAACATGGTT	81847
rs775060855	snp	G/T	1.65666e-05	0.00287802	missense	RNF146	GRCh38.p7	6:127286822	CATGGCTTGGAAAGC[G/T]GTGTGCTCTTTGTCG	81847
rs775124641	snp	C/T			missense	RNF146	GRCh38.p7	6:127287454	GGCAGGGTACCAGCA[C/T]CAGACACCTCCATTG	81847
rs775148358	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127267674	TTGTCCTAGTGAAGC[C/G]CAGCGCTGCATATTC	81847
rs775268035	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265646	CTTAGAGCAACACCT[A/G]GCACATTGTTAGTTA	81847
rs775335553	snp	G/T	3.31296e-05	0.00406985	missense	RNF146	GRCh38.p7	6:127286985	GCGCACTAGTAGAGA[G/T]CTGGAAGATGCTTTT	81847
rs775356278	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127272698	AATGAGAGGTGAAAT[A/G]AAAGAATGCTCAAAG	81847
rs775391334	snp	C/T	1.66266e-05	0.00288323	missense	RNF146	GRCh38.p7	6:127287620	CTGATCGATCAGTAG[C/T]AGGGGGTGGAACAGT	81847
rs775709941	snp	C/T	1.65105e-05	0.00287315	synonymous-codon	RNF146	GRCh38.p7	6:127287291	CCTAACATCAGTAGA[C/T]GGTCAGTTAACAAGC	81847
rs775745668	in-del	-/TG			utr-variant-3-prime	RNF146	GRCh38.p7	6:127288028	ATCTGACTCCTGCAT[-/TG]TGTCTTATTTTTCTG	81847
rs775799333	snp	A/G	1.86761e-05	0.00305576	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287732	CTCAAGGTTGAAAGG[A/G]TTACCTGTAAATTTC	81847
rs775893066	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127268749	GCTGGTCTTTTAGAC[A/G]AGAGAAGAAAAAAGA	81847
rs776005576	snp	A/C	1.65225e-05	0.00287419	missense	RNF146	GRCh38.p7	6:127287195	CGTAAACCTAGCAAG[A/C]GAGAGCTCTGCTGAC	81847
rs776022080	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127275618	CAAATGAATTGAAAT[A/T]AGTGCATGTGATAAA	81847
rs776208447	snp	G/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127264475	CCAGGTTCAAGCGAT[G/T]CTCCTGCCTCAGCCT	81847
rs776321830	snp	A/G			utr-variant-3-prime	RNF146	GRCh38.p7	6:127288124	GAAACATAATTTAAT[A/G]TATGAATAGATGTGA	81847
rs776373818	snp	A/G	1.87376e-05	0.0030608	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287742	AAAGGGTTACCTGTA[A/G]ATTTCTGCCCACATA	81847
rs776558245	snp	A/G			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284691	GTTGTTTCAAGTTAC[A/G]AGATCTTTGAAGGCA	81847
rs776658424	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127271458	TTTTTAATGTGTCTT[C/T]GGCAAAAGTCTAGGT	81847
rs776679679	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127279175	CATGCTTTTGATGTC[A/G]TATCTAGGAATCCAT	81847
rs776710876	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127285489	AGTCTTTTTTACTTA[C/T]CAGTGGTTTACTCCA	81847
rs776760149	in-del	-/A			intron-variant	RNF146	GRCh38.p7	6:127281493	GAAGGGTTCAGAATG[-/A]ACAGAATAAGTTTCA	81847
rs776841514	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127266024	AATCAAACAGTTAAT[A/G]AAATCCCAAAATGCA	81847
rs776982531	in-del	-/GCACTCCTT	1.65214e-05	0.0028741	cds-indel	RNF146	GRCh38.p7	6:127287527	TGCAGTTGTTGCACA[-/GCACTCCTT]GCACTCCTTGACCCA	81847
rs777035038	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127280884	TTTAAAGTGTTACAC[A/G]CTACCTTGGATTTGT	81847
rs777131925	snp	A/G	1.64977e-05	0.00287203	missense	RNF146	GRCh38.p7	6:127287388	GGAGACAACACAGCT[A/G]AAAGGAGTCATAGGG	81847
rs777145473	snp	A/G	1.65097e-05	0.00287308	missense	RNF146	GRCh38.p7	6:127287301	GTAGATGGTCAGTTA[A/G]CAAGCCCTGCAACAC	81847
rs777263871	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127267366	CTCGGGTGGCAGGCG[A/G]GTCCCTCTCCTCCCC	81847
rs777444811	snp	C/G	1.65116e-05	0.00287324	synonymous-codon	RNF146	GRCh38.p7	6:127287276	GTCTTCTGTAAGGCC[C/G]CTAACATCAGTAGAT	81847
rs777602712	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127278883	GATTTACATTTCCCT[A/G]ATTACTAATAATGTT	81847
rs777619442	snp	A/G			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265373	GAAGGAAGAGCCAAC[A/G]GGTTATATGCCAAAT	81847
rs777743885	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127278191	GAGGTGGAGATGGAA[A/G]TACTAAATGAGAAGA	81847
rs777815520	in-del	-/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284711	CTTTGAAGGCAAGTG[-/T]TTATCTCAAAATATT	81847
rs777877427	snp	C/T			missense	RNF146	GRCh38.p7	6:127286971	TGGCAGTACGATGAG[C/T]GCACTAGTAGAGAGC	81847
rs777980589	snp	A/G			intron-variant, splice-donor-variant	RNF146	GRCh38.p7	6:127285349	CAATTTTTGATGAGC[A/G]TAAGCATTCTTGTTG	81847
rs778027482	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127273912	ATAACTGGACTAGAG[A/G]AGTGTAATGAGGGCA	81847
rs778210775	snp	C/T	4.97253e-05	0.004986	synonymous-codon	RNF146	GRCh38.p7	6:127287111	ACGTCGCAGGAAGAT[C/T]AAGCGAGATATAATA	81847
rs778292666	in-del	-/TCT			intron-variant	RNF146	GRCh38.p7	6:127278935	TTGGCCATTTGTGTA[-/TCT]TCTTTAAGTTCTTTA	81847
rs778497238	snp	A/C			missense	RNF146	GRCh38.p7	6:127287581	CAAACCAGACAGTAC[A/C]CGATCGATCAGATCG	81847
rs778539602	snp	G/T			utr-variant-5-prime, intron-variant	RNF146	GRCh38.p7	6:127266902	AGAAAAGACTGCGAG[G/T]TGGCCGCAGCTGTGG	81847
rs778581193	snp	C/G	1.64974e-05	0.00287201	missense	RNF146	GRCh38.p7	6:127287431	AAGATCATGAATCAC[C/G]ATCTTCAGGCAGGGT	81847
rs778664929	snp	A/G	3.31214e-05	0.00406935	missense	RNF146	GRCh38.p7	6:127286972	GGCAGTACGATGAGC[A/G]CACTAGTAGAGAGCT	81847
rs778827268	snp	G/T			utr-variant-5-prime, intron-variant	RNF146	GRCh38.p7	6:127282324	TGTGGTTGGCCCTTT[G/T]GACTGCTCTCTCTAC	81847
rs779008835	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284242	TTTCATTTTACCAGA[C/T]TCTGTTTTTATTTAT	81847
rs779149321	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127285169	TTACTAGATATGTGC[C/T]ATCTTTTTAAAAACT	81847
rs779154662	in-del	-/TTT/TTTT			intron-variant	RNF146	GRCh38.p7	6:127285525	TCTCCCCTTTTAAAA[-/TTT/TTTT]TGTCTTTTTTTTTTT	81847
rs779329201	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127279978	TAGCTTTCTTGGGGA[-/T]TCTATGAGATCTTCT	81847
rs779347710	snp	C/T	4.55747e-05	0.00477339	intron-variant	RNF146	GRCh38.p7	6:127286578	AGATATTGCAAGAAT[C/T]AAAACATGACTTTAA	81847
rs779455713	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127272030	ATTAGATAATACGTG[A/C]CCTTTTCTGTGAGAG	81847
rs779617371	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127270925	GATTCAAGAGATTCT[C/T]CTGCCTCAGCCTCCC	81847
rs779724130	snp	G/T	1.79422e-05	0.00299513	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287695	TAACTGAAGTTTAAA[G/T]AAAAATGTCTTCAGC	81847
rs779729618	snp	A/G	1.65192e-05	0.00287391	missense	RNF146	GRCh38.p7	6:127287238	GTATCAGCACAGAGT[A/G]GAGCTTCTGTTCAGC	81847
rs779731781	snp	A/C	0.00011583	0.0076093	synonymous-codon	RNF146	GRCh38.p7	6:127287586	CAGACAGTACCCGAT[A/C]GATCAGATCGATCGG	81847
rs779919135	snp	C/G			utr-variant-5-prime	RNF146	GRCh38.p7	6:127280233	TTTTCTTTTGCAGCA[C/G]AAAGAATGAACCAGC	81847
rs779967177	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127276004	CACATATGGAAGAAA[A/C]CTGGTCCATTTTGCC	81847
rs779999370	snp	C/G	1.65386e-05	0.00287559	missense	RNF146	GRCh38.p7	6:127287167	GACTTAGGCTAGACT[C/G]TGATGCTAATACCGT	81847
rs779999931	snp	A/C			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127282844	CAGCTTCATAGAAAT[A/C]CTTAAGCCCCTTGAA	81847
rs780230337	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127280034	ACTTCCTCCTTACCC[A/G]TCTGTATGCCTTTAT	81847
rs780364388	snp	G/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283795	ATTGATAGTTAAGAG[G/T]GCTTCAGATGAAATA	81847
rs780452985	in-del	-/TGG			upstream-variant-2KB	RNF146	GRCh38.p7	6:127266187	ATGTACATGCTAAAA[-/TGG]TGAATTACTGCTAGA	81847
rs780655462	snp	A/G	1.65323e-05	0.00287505	synonymous-codon	RNF146	GRCh38.p7	6:127286676	TACAAACAGGAAAGC[A/G]AACGAGTCCTGTTCT	81847
rs780960899	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127277363	TTGAAGTTGGTGAAA[A/G]GGTTGAGAGGAAAGT	81847
rs781071785	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	ECHDC1, RNF146	GRCh38.p7	6:127288523	ATTTAAACAGAATCT[A/G]TAGGCAGTGTGTATA	81847
rs781234549	snp	A/G	1.95181e-05	0.00312389	intron-variant	RNF146	GRCh38.p7	6:127286600	TGACTTTAATATTAT[A/G]TGTATTTTTTCTTAG	81847
rs781237519	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	RNF146	GRCh38.p7	6:127266432	CTCCCCTCCGTCCCC[C/G]CCCTCCCCATTTTTT	81847
rs781385183	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127272557	GATTCCTGTTTACAT[C/G]TGTTAAGTTTTTTGT	81847
rs781464224	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127269792	CTACTCCTTTTATGT[A/G]TATATAATTTTTTTT	81847
rs781490874	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127268429	TGATTAGCAAATATT[A/G]TTTGTATAGAGTGTC	81847
rs781575953	in-del	-/AACA			intron-variant, downstream-variant-500B, utr-variant-3-prime	ECHDC1, RNF146	GRCh38.p7	6:127288646	ATTCATTAGTAGTCT[-/AACA]AACACTCTGGATTAA	81847
rs781611513	snp	G/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127282415	GTCACCAGACTTTTT[G/T]CAGCTCAGATTTATT	81847
rs781673535	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127266721	ACAGGCAAGAGAGTA[C/T]CGGCAGACAGCGGCG	81847
rs781680024	snp	C/T			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283604	ACTAGCAGTTTGGGG[C/T]TACTTTGTGTCTATC	81847
rs796081295	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127275351	AAGCAAGGATTAGAA[C/G]TTAGATATTTTTATG	81847
rs796162785	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127267633	GTCTCGGTCTTGCCT[A/G]AAACGAAGAGAGCAA	81847
rs796206372	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127270687	CCACTTATACAATAC[-/T]TTTTTTTTTCTGCCC	81847
rs796224729	snp	A/C			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283546	TGTGTAGGGTAGATT[A/C]AAATGGTTTTTTAAA	81847
rs796229021	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127270391	GTGTAAAATTTACAG[G/T]TCATTCATTCCAGTA	81847
rs796298835	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127268852	AGGAAAGGAACAGAC[-/T]TTTTTTTTTTAAAGG	81847
rs796310834	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127278798	CTATTTTTCTACATC[C/G]TCACCAACACTTATT	81847
rs796333670	snp	A/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265087	CTTTCTGGGAATACA[A/T]AGCTGGGTAAACAGT	81847
rs796390932	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127278283	CATTTACAATGTTAT[G/T]CAACTATCACCATTA	81847
rs796404929	snp	G/T			upstream-variant-2KB	RNF146	GRCh38.p7	6:127265388	AGGTTATATGCCAAA[G/T]GCATATAAGACATAA	81847
rs796464979	multinucleotide-polymorphism	AC/CT			intron-variant	RNF146	GRCh38.p7	6:127277597	CCCAAAACTGAAGAA[AC/CT]TGGAGTCTGATGTTC	81847
rs796503528	in-del	-/TTTG			intron-variant	RNF146	GRCh38.p7	6:127268086	TCAAGTTTTGAACAT[-/TTTG]TTTAATATTTTTGTA	81847
rs796530091	in-del	-/CT			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127282517	ATGTCTGAGACAGAA[-/CT]CTCCTCAAATTCTGA	81847
rs796534986	multinucleotide-polymorphism	CACT/TGCC			upstream-variant-2KB	RNF146	GRCh38.p7	6:127264615	CCTCGTGATCCGCCC[CACT/TGCC]CGGCCTCCTAAAGTC	81847
rs796662016	in-del	-/CTTTT			intron-variant	RNF146	GRCh38.p7	6:127286314	ATGATTCAAGGTATC[-/CTTTT]CCCCTCACTGGATGC	81847
rs796677833	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	RNF146	GRCh38.p7	6:127266523	GCGCCCCAGAGCTTC[C/T]TCAGGATAGCAAAGC	81847
rs796707195	snp	A/C			intron-variant	RNF146	GRCh38.p7	6:127275916	ATTTACAGTTTAGAT[A/C]TTTAAAACCTTTTAA	81847
rs796826917	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127268406	GTGATTTTGGCTTTG[C/G]TGTTTTATGATTAGC	81847
rs796841729	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127276008	TATGGAAGAAACCTG[A/G]TCCATTTTGCCTTTT	81847
rs796849076	in-del	CTTAGAGAGAAATA/TTTT			intron-variant	RNF146	GRCh38.p7	6:127268051	TTCTCTAAGTGCCAT[CTTAGAGAGAAATA/TTTT]GTGAGCACTTATTTC	81847
rs796873027	multinucleotide-polymorphism	AG/CA			utr-variant-3-prime	RNF146	GRCh38.p7	6:127287778	TACTCATCCCTAGTA[AG/CA]GCATTTTGGGAGTTG	81847
rs796930777	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127271620	AGTTATTGAGCACTT[A/G]ACATGTATCCAGTCT	81847
rs796936580	in-del	-/TTTTTT			intron-variant	RNF146	GRCh38.p7	6:127285530	CCCTTTTAAAATGTC[-/TTTTTT]TTTTTTTTTTTACCA	81847

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