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

RRP9

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs777793041	snp	G/T	1.65157e-05	0.0028736	missense	RRP9	GRCh38.p7	3:51937724	AATGCACGGGCCTCA[G/T]CCTTCTCCTCCTCTG	9136
rs777954663	snp	C/G			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940792	TGCTGGGATTAGAGG[C/G]ATGAGTTACCAGGCC	9136
rs777971460	snp	C/G	2.62671e-05	0.00362393	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943455	TTCCGCTCCACCGCT[C/G]AGGCCCTCAAGGCCA	9136
rs778116714	snp	C/T	1.66579e-05	0.00288595	missense	RRP9	GRCh38.p7	3:51934715	GCTCTCCCCGCAGCC[C/T]GTGAGCTTCACGCTG	9136
rs778130074	snp	C/T	1.6569e-05	0.00287824	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941528	CTTTGGTCAGGGGTC[C/T]AGACCACCCTGGCAT	9136
rs778215822	in-del	-/TC	1.64819e-05	0.00287066	frameshift-variant	RRP9	GRCh38.p7	3:51937223	TCTTTGGCAGCAGAG[-/TC]AAGATGGCTGAGTCA	9136
rs778278452	snp	C/T	1.64795e-05	0.00287045	missense	RRP9	GRCh38.p7	3:51933591	TTGATTCTCCACCAT[C/T]GGCCAAGCCTGCAGG	9136
rs778294303	snp	C/T	1.64779e-05	0.00287031	intron-variant	RRP9	GRCh38.p7	3:51936368	CAGGGATGAAGACAA[C/T]GATCACAGGCACCCA	9136
rs778494411	snp	C/G			intron-variant, upstream-variant-2KB	RRP9, PARP3	GRCh38.p7	3:51940304	AGCAAATTAAGGCAA[C/G]ACATACTCAATTTTA	9136
rs778543279	in-del	-/C	8.48421e-05	0.00651259	intron-variant	RRP9	GRCh38.p7	3:51933817	AAAGACATTAGAACG[-/C]CCCCCCGCCACCACC	9136
rs778581448	snp	C/T	1.65124e-05	0.00287331	missense	RRP9	GRCh38.p7	3:51937715	TCCTCCTCAAATGCA[C/T]GGGCCTCAGCCTTCT	9136
rs778629528	snp	A/C/T	8.26267e-05	0.00642708	intron-variant	RRP9	GRCh38.p7	3:51933823	CATTAGAACGCCCCC[A/C/T]GCCACCACCGTCCTC	9136
rs778682899	snp	C/T	1.64866e-05	0.00287106	missense	RRP9	GRCh38.p7	3:51933760	CAGAGCTGGAGAACT[C/T]GAGGCTGTTGATAAA	9136
rs778812042	snp	A/G	2.36275e-05	0.00343704	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943510	GCGTGGATCCAACAT[A/G]TCCACTCAGCAGCAA	9136
rs778813554	snp	C/T			intron-variant	RRP9	GRCh38.p7	3:51938895	CACAGCACCATCCTT[C/T]ACCCTGGGAACAAGG	9136
rs778869919	snp	A/T	4.09593e-05	0.00452526	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943399	AGACTGAGGGCCCTG[A/T]GAAGAAGAAGGGCCG	9136
rs778882732	snp	A/G	1.64727e-05	0.00286986	intron-variant	RRP9	GRCh38.p7	3:51937596	CTCAAGCTGCATGGA[A/G]AAGAGATGGATGAGA	9136
rs778914647	snp	C/G	1.67164e-05	0.00289101	intron-variant	RRP9	GRCh38.p7	3:51934604	CCCACCCGGCGACCC[C/G]TCCTCCCTGCCTCTC	9136
rs778951423	snp	C/G			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941265	AAGACTTTGCAGGAC[C/G]AGAAACTAAAGGAAA	9136
rs779002251	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	PARP3, RRP9	GRCh38.p7	3:51942932	CCCTCCCCCATAGCT[C/T]GGTGACTCGGCCCGG	9136
rs779007234	snp	A/C	0.000137052	0.00827691	synonymous-codon, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943451	CCCCTTCCGCTCCAC[A/C]GCTGAGGCCCTCAAG	9136
rs779112396	snp	C/T			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940984	AAAATACACACCTCA[C/T]TACAACACACTCTCT	9136
rs779284362	snp	C/G	1.64779e-05	0.00287031	missense	RRP9	GRCh38.p7	3:51936268	TCACCGACACTGCAT[C/G]CCGGTGTCCTGTGAA	9136
rs779377171	snp	A/C	3.29679e-05	0.00405991	missense	RRP9	GRCh38.p7	3:51933742	CAGCCACCAGGAAGT[A/C]CCCAGAGCTGGAGAA	9136
rs779438034	snp	A/G	4.94303e-05	0.00497119	upstream-variant-2KB, synonymous-codon	PARP3, RRP9	GRCh38.p7	3:51941426	CTCGCTCTCAGAGTC[A/G]CTGGAGATCTCCTCA	9136
rs779498896	snp	G/T	0.000118378	0.00769253	upstream-variant-2KB, synonymous-codon	PARP3, RRP9	GRCh38.p7	3:51941817	CCCCGCGCCAGCCCC[G/T]GCCCCAGAGGCCGGC	9136
rs779668485	snp	A/C			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940651	TCCTGAGTAGTTGGG[A/C]CTACAGGTGCACACC	9136
rs779715407	snp	C/T	2.90846e-05	0.00381332	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943443	GAGGAGGACCCCTTC[C/T]GCTCCACCGCTGAGG	9136
rs779834933	snp	C/T	1.65875e-05	0.00287984	synonymous-codon	RRP9	GRCh38.p7	3:51935416	ATCCCGGCCCCCAGC[C/T]GTCACACAGCACTCC	9136
rs779955723	snp	C/T	1.66319e-05	0.00288369	missense	RRP9	GRCh38.p7	3:51935345	AGGCCACCTTACTGG[C/T]GGCCATAGAAGACAA	9136
rs780010667	snp	C/T	6.59837e-05	0.00574348	intron-variant	RRP9	GRCh38.p7	3:51937328	CTGGATCTGGGCAGA[C/T]AGGGGCCAGGTCACT	9136
rs780025809	snp	A/G	4.59654e-05	0.00479381	synonymous-codon, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943391	CTGGGTACAGACTGA[A/G]GGCCCTGAGAAGAAG	9136
rs780045263	snp	C/T	1.66618e-05	0.00288628	missense	RRP9	GRCh38.p7	3:51934530	CCACACTGCCAAAGC[C/T]GCACACAGGAGCTGT	9136
rs780145600	snp	A/G			intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943198	GGGAATGCCGTCAGA[A/G]TGGACACAGGATGCA	9136
rs780423505	snp	C/T	2.06913e-05	0.0032164	synonymous-codon	RRP9	GRCh38.p7	3:51938135	GAGCTTGGCCAAGCG[C/T]AGCTTCTTTTCCTGT	9136
rs780503546	snp	A/G	1.64795e-05	0.00287045	synonymous-codon	RRP9	GRCh38.p7	3:51937235	AGAGAAGATGGCTGA[A/G]TCATCGGGGGTGACG	9136
rs780527382	snp	G/T			upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942177	CTGCTGGCCCACTTC[G/T]AAGTCGGAGCAAGAG	9136
rs780536046	snp	A/G	1.66158e-05	0.0028823	intron-variant	RRP9	GRCh38.p7	3:51937148	CTGACCAGCCCTCCC[A/G]GATCCGCCATGGGGG	9136
rs780800694	snp	C/T	0.000115345	0.00759337	missense	RRP9	GRCh38.p7	3:51937249	AGTCATCGGGGGTGA[C/T]GACCAAACATGTGAT	9136
rs781032974	snp	C/G	1.66994e-05	0.00288953	missense	RRP9	GRCh38.p7	3:51934503	AGAAGGTCAAGCTGC[C/G]GGAAGCCTTCCCCAC	9136
rs781058684	snp	A/G	3.31296e-05	0.00406985	intron-variant	RRP9	GRCh38.p7	3:51935507	GAGCAGGATAGTGGG[A/G]ATAGGGGTACTGCAT	9136
rs781073336	snp	A/G	0.000116598	0.00763448	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943495	AGAAGCGCATAATCC[A/G]CGTGGATCCAACATG	9136
rs781087944	snp	C/G	1.65053e-05	0.0028727	intron-variant	RRP9	GRCh38.p7	3:51936220	AACACTAGCATGTGC[C/G]CACTAAAGATCCACT	9136
rs781147960	snp	A/G	9.01429e-05	0.00671292	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942720	TTGGGTGAGTGTCCT[A/G]TGGTCCTGCCCACGG	9136
rs781151944	in-del	-/CTCCTCCTC	0.000102122	0.00714498	cds-indel	RRP9	GRCh38.p7	3:51938165	TGCAGTTTCCTCCAG[-/CTCCTCCTC]CTCCTCCTCCTCAGG	9136
rs781253966	snp	C/T	1.82068e-05	0.00301713	synonymous-codon	RRP9	GRCh38.p7	3:51938114	CTGACGGAGCTGCTC[C/T]AGGTAGAGCTTGGCC	9136
rs781267545	snp	A/C/G			intron-variant	RRP9	GRCh38.p7	3:51934328	GAGGGAAAGTGGGGA[A/C/G]GGTTCCTGCCAGGCC	9136
rs781379799	snp	C/T	1.6522e-05	0.00287414	missense	RRP9	GRCh38.p7	3:51937736	TCAGCCTTCTCCTCC[C/T]CTGTGCAGGACAGAC	9136
rs781469918	snp	C/G	8.32952e-05	0.00645296	upstream-variant-2KB, synonymous-codon	PARP3, RRP9	GRCh38.p7	3:51941799	TCGCCGCCGCTTGCC[C/G]GCCCCCGCGCCAGCC	9136
rs781518444	snp	A/C	0.000105302	0.00725534	synonymous-codon, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943535	CAGCAACCCCGGGAC[A/C]CAGGTGAGCTGCAGT	9136
rs781521220	snp	C/G	1.64936e-05	0.00287168	synonymous-codon	RRP9	GRCh38.p7	3:51936467	GATGGCCATGCAGAG[C/G]ACGTGGCTGCTGTGG	9136
rs781553335	snp	A/G	1.69364e-05	0.00290997	intron-variant	RRP9	GRCh38.p7	3:51934813	AGCAGTGAGGGGGCC[A/G]GAGGCAGAAAAGGCC	9136
rs781648041	snp	C/T	5.79895e-05	0.00538437	upstream-variant-2KB, utr-variant-5-prime	PARP3, RRP9	GRCh38.p7	3:51941872	GTTGCCGACATGCTG[C/T]CCACCAGGCGTGTAG	9136
rs781664738	snp	G/T	3.41921e-05	0.0041346	intron-variant	RRP9	GRCh38.p7	3:51936590	AGAAGCTACTGGGAT[G/T]GGGGGATAGGGCTGG	9136
rs796949617	multinucleotide-polymorphism	CTG/GTA			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941740	TGACGGTTGTCCCAG[CTG/GTA]CAGGGCTGACCGCGG	9136

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