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

RNF139

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs778858468	snp	A/G	1.76334e-05	0.00296924	missense, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475156	TGCGGATGGCCCATC[A/G]GCAGGTCTGGGCGGC	11236
rs778983313	snp	C/G			intron-variant	RNF139	GRCh38.p7	8:124481545	ACTCTTTCATGAGTT[C/G]AGTTCATATATAGTT	11236
rs778983581	snp	A/G			intron-variant	RNF139	GRCh38.p7	8:124483519	TCTCAGCTAACTGCA[A/G]TGCCTCCCGGGTTCA	11236
rs779030330	snp	C/T			intron-variant	RNF139	GRCh38.p7	8:124479896	AAATTATACTAGATG[C/T]CTACCTTATGTCAAT	11236
rs779193713	snp	C/T	1.64751e-05	0.00287007	synonymous-codon	RNF139	GRCh38.p7	8:124486708	ACTTATTCGCTTAAG[C/T]AGAAACATGTGCCTT	11236
rs779215538	snp	C/T	5.05574e-05	0.00502754	synonymous-codon, utr-variant-5-prime	RNF139	GRCh38.p7	8:124485844	AGGTGTATTTGCATC[C/T]AGTATTGTTCTGATC	11236
rs779232456	snp	C/G	0.000489836	0.0156422	utr-variant-5-prime, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475087	CCTGCCCGGCCCACC[C/G]AGCCCTGGTGTGGCA	11236
rs779310914	snp	G/T	1.6476e-05	0.00287014	missense, utr-variant-5-prime	RNF139	GRCh38.p7	8:124485993	ACACGTCAGCTTTTG[G/T]AATTGAGCTGCTTCC	11236
rs779361941	snp	C/G			upstream-variant-2KB, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474340	AGGATCCCGGGCGGC[C/G]TTCGCGGGATTTCTC	11236
rs779592058	snp	C/G	1.64789e-05	0.0028704	missense	RNF139	GRCh38.p7	8:124486106	CATTCCATCTATTCA[C/G]AATTAATTATTTTGG	11236
rs779594594	in-del	-/ATCTT	4.99571e-05	0.00499761	frameshift-variant, utr-variant-5-prime	RNF139	GRCh38.p7	8:124485857	TCCAGTATTGTTCTG[-/ATCTT]GTCACAACGATCACT	11236
rs779666925	snp	A/G			intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475935	GATGAGACATTTGCC[A/G]AAGAGACTTCTGAAA	11236
rs779682173	snp	A/T	3.35616e-05	0.0040963	synonymous-codon	RNF139	GRCh38.p7	8:124487614	GCACACAGGCGCAGC[A/T]GCTGAAGAATTTAAT	11236
rs779692844	snp	C/T	0.0013541	0.0259849	utr-variant-5-prime, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475066	CCGGGCCCTGCCCCG[C/T]GCGGCCCTGCCCGGC	11236
rs779733580	in-del	-/ATG	1.69612e-05	0.0029121	cds-indel	RNF139	GRCh38.p7	8:124487628	CAGCTGAAGAATTTA[-/ATG]ATGATACTGACTGAT	11236
rs779746111	snp	A/G			intron-variant	RNF139	GRCh38.p7	8:124481780	TGTCTCTGGACTTTT[A/G]TATTTTCTTAGACCT	11236
rs779868632	snp	C/G			intron-variant	RNF139	GRCh38.p7	8:124483930	GAATCCATAGATGGA[C/G]AGGGTAGGATCTTTG	11236
rs780250354	snp	C/T	1.65004e-05	0.00287227	synonymous-codon	RNF139	GRCh38.p7	8:124486486	GGACCTCATTTGCAA[C/T]CTTATAATTAGTGGG	11236
rs780340306	snp	C/T	1.73171e-05	0.00294249	intron-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488738	TTAAATCTCCAAGTA[C/T]ACATTTAGTTCTAAA	11236
rs780366891	snp	C/T	3.29489e-05	0.00405874	missense	RNF139	GRCh38.p7	8:124486698	CAGAAGAGAGACTTA[C/T]TCGCTTAAGTAGAAA	11236
rs780371413	snp	A/G			intron-variant	RNF139	GRCh38.p7	8:124484733	TCAGAGTACAAAGAA[A/G]GATGGTGTCTATGGA	11236
rs780401301	snp	C/T			intron-variant	RNF139	GRCh38.p7	8:124477474	TCAACCTCACTTTTT[C/T]CTTTAAAATTAATGT	11236
rs780437521	snp	C/G	1.64963e-05	0.00287192	missense	RNF139	GRCh38.p7	8:124487357	CATTATTTCCATGCA[C/G]TTTGCCTTCGGAAAT	11236
rs780776839	snp	A/G			intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124476277	GCAATAAATAGCCAT[A/G]TTTTACATTTATCTG	11236
rs780814940	snp	C/G	1.654e-05	0.00287571	missense, utr-variant-5-prime	RNF139	GRCh38.p7	8:124485870	TGATCTTGTCACAAC[C/G]ATCACTTTTCAAGTT	11236
rs780816498	snp	G/T	1.65573e-05	0.00287721	stop-gained	RNF139	GRCh38.p7	8:124487531	GCTGAATCTGACAGG[G/T]AATTGAACGAAGATG	11236
rs781107757	snp	A/C	1.65217e-05	0.00287412	synonymous-codon	RNF139	GRCh38.p7	8:124486444	AAATGAAACTGATTC[A/C]TTCTTTATTTCTTGG	11236
rs781135935	snp	C/G	1.65362e-05	0.00287538	missense, upstream-variant-2KB, utr-variant-5-prime	RNF139, RNF139-AS1	GRCh38.p7	8:124475271	CTGCATCGTGCTCCA[C/G]ATCTTCCTCCGGCTC	11236
rs781298403	snp	C/G	1.70175e-05	0.00291693	missense, utr-variant-3-prime, nc-transcript-variant	TATDN1, RNF139	GRCh38.p7	8:124488605	CCAATTATATTCCAG[C/G]AAAAAATACTTTAAT	11236
rs781420142	snp	A/T	6.68818e-05	0.00578242	splice-acceptor-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488698	TCTCCAATATTTGAC[A/T]AAAACAAAACAAAAA	11236
rs781504288	snp	A/C	3.31033e-05	0.00406823	missense	RNF139	GRCh38.p7	8:124487084	ATATTTGGAGTTGTA[A/C]TGTTTGGAAATGGGG	11236
rs781628113	snp	A/C	1.65029e-05	0.00287248	missense	RNF139	GRCh38.p7	8:124487270	AAAGGGAGCCGCTTA[A/C]AAGAAATAAATGATG	11236
rs781774668	snp	A/G			missense	RNF139	GRCh38.p7	8:124486473	GGGATGATTTTTGGG[A/G]CCTCATTTGCAATCT	11236
rs796151328	snp	A/T			intron-variant	RNF139	GRCh38.p7	8:124484708	ATCCTACTTAAAATA[A/T]GCATTTCTGTCAGAG	11236
rs796337797	in-del	-/A			intron-variant	RNF139	GRCh38.p7	8:124478290	TTGATTTTATGGGGG[-/A]AAAAAAAAAAGTACC	11236
rs796760114	snp	A/G			intron-variant, utr-variant-5-prime	RNF139	GRCh38.p7	8:124483362	TGGATTGTGAAATGC[A/G]TCTACTGTAATAATA	11236

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