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
rs1127489	snp	A/G	0.35574	0.226537	intron-variant	PHF10	GRCh38.p7	6:169707606	TGTAAAGAATCTCCT[A/G]TGAGGAGTTCTGTTT	55274
rs3088034	snp	C/G	0.426507	0.177046	intron-variant	PHF10	GRCh38.p7	6:169708321	AACAGTATTGTTTAG[C/G]TTACATTAACCTGAA	55274
rs3211062	snp	A/G	0.415563	0.18732	intron-variant	PHF10	GRCh38.p7	6:169708703	ACAGGCTGGAAATCA[A/G]CTATTCAACACTATC	55274
rs3807063	snp	A/G	0.0267878	0.112589	intron-variant	PHF10	GRCh38.p7	6:169718998	GAGGATATTTTGAAA[A/G]CTATTTTAAGTATTT	55274
rs3807064	snp	A/G	0.387074	0.209071	intron-variant	PHF10	GRCh38.p7	6:169719195	GCATTTTTAGTTTAA[A/G]GGACCTATGAGGGCA	55274
rs3807065	snp	C/T	0.31503	0.241394	intron-variant	PHF10	GRCh38.p7	6:169719393	CATCATATCATAAAC[C/T]GTAACTGTTTGTTCT	55274
rs3924590	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706223	GGTATAGTGGTATTT[A/T]AAAAAAAATCAGTTT	55274
rs3924825	snp	A/G	0.491732	0.0637633	intron-variant	PHF10	GRCh38.p7	6:169717073	cctggccaacatggt[A/G]aaaccccgtctctaa	55274
rs4286788	snp	C/T	0.0024695	0.0350521	utr-variant-3-prime, synonymous-codon	C6orf120, PHF10	GRCh38.p7	6:169705629	ACCACTATTCTCACA[C/T]TGGGAGCAGTGTATA	55274
rs4626430	snp	C/G	0.494057	0.0541878	intron-variant	PHF10	GRCh38.p7	6:169711889	TATTCTCCTTCAGGT[C/G]CACAGAATACACCAA	55274
rs4716384	snp	A/T	0.350109	0.229081	intron-variant	PHF10	GRCh38.p7	6:169709088	AAAAAAAAAAAAGAA[A/T]TTTTAAGTTAATTAC	55274
rs5881838	in-del	-/T	0.314301	0.241589	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	C6orf120, WDR27, PHF10	GRCh38.p7	6:169703412	TAACCGAAGTTGGTG[-/T]TAAGTTTTCAAGAGT	55274
rs5881839	in-del	-/ACTT	0.0142736	0.0832652	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706086	ACCATTATGTGTAAG[-/ACTT]ACTCTAAAAAGACCA	55274
rs6459654	snp	C/T	0.387074	0.209071	intron-variant	PHF10	GRCh38.p7	6:169720831	actatcataaaaTTG[C/T]TTTTTAATTACACTC	55274
rs6459655	snp	A/G	0.391397	0.206172	intron-variant	PHF10	GRCh38.p7	6:169723100	CACACGGCACACCGC[A/G]CACCGCACGAAGGCT	55274
rs6911713	snp	A/G	0.0271762	0.113356	upstream-variant-2KB, downstream-variant-500B	PHF10, TCTE3	GRCh38.p7	6:169725478	GCCGATCCTAATCCA[A/G]CTTGGTTCTCTCAGC	55274
rs6931721	snp	A/G	0.0952156	0.196321	intron-variant	PHF10	GRCh38.p7	6:169722138	CTTAGAACAAGGACT[A/G]GCGAGTTATCTGATA	55274
rs7453621	snp	C/T			downstream-variant-500B, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706733	atacatacatacaca[C/T]acacacacacacaca	55274
rs7740499	snp	A/G	0.182296	0.240658	intron-variant	PHF10	GRCh38.p7	6:169711505	ATGGAACTTAAATTG[A/G]TAAGACTGTCAAAAT	55274
rs7752243	snp	A/G	0.19459	0.243782	intron-variant	PHF10	GRCh38.p7	6:169714067	cagaggttgcagtga[A/G]ccgaaatcacactac	55274
rs7753546	snp	C/G	0.4941	0.0539917	intron-variant	PHF10	GRCh38.p7	6:169723484	TATGCGCGGAATGAA[C/G]GCTGAGCGAACGCGC	55274
rs7759105	snp	A/T	0	0	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169705332	ATGGCCTAAATCAAA[A/T]CCAGTATTAGTGGTA	55274
rs7760142	snp	C/T	0	0	intron-variant	PHF10	GRCh38.p7	6:169717989	GCTTAAAAACCTTGA[C/T]TTTTTAAAGTATTCA	55274
rs7762018	snp	A/C	0.349233	0.229462	intron-variant	PHF10	GRCh38.p7	6:169713148	CTAGGTCAGACAGCA[A/C]TGCTTCGTGCCACCT	55274
rs7768116	snp	G/T	0.426507	0.177046	intron-variant	PHF10	GRCh38.p7	6:169709604	CTCCTTTACTCTGAG[G/T]ATAATCAGATCAACA	55274
rs7773552	snp	A/G	0.386313	0.209568	intron-variant	PHF10	GRCh38.p7	6:169713199	CCCCATTCAGGAGGC[A/G]ACCCTAGATGAAGAC	55274
rs9371126	snp	C/T	0.42666	0.176893	intron-variant	PHF10	GRCh38.p7	6:169708593	TTTAGGTACTAAAAA[C/T]GTTCACAGATTATGT	55274
rs9371169	snp	G/T	0	0	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169705902	TGCCTACTGAAGAAA[G/T]CATTAATTTCATCAT	55274
rs9396950	snp	C/T			downstream-variant-500B, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706779	acacacacacacaca[C/T]GTAGATGAACTGGGA	55274
rs9396952	snp	G/T	0.322721	0.23919	intron-variant	PHF10	GRCh38.p7	6:169708344	ATACTGTTCTATGAA[G/T]TAAGGGCAAGCACTA	55274
rs9396953	snp	A/G	0.335101	0.23507	intron-variant	PHF10	GRCh38.p7	6:169708971	ACATAAGCTATATAT[A/G]TAAAAACAAGTACAA	55274
rs9478004	snp	A/G	0.181022	0.240296	intron-variant	PHF10	GRCh38.p7	6:169713510	GAAGCTGAAGCAGGA[A/G]AATCACTTGAACCAG	55274
rs9478095	snp	A/G			intron-variant	PHF10	GRCh38.p7	6:169707789	TTGTTAAATCACTTA[A/G]TTTTTCTTACCCAAC	55274
rs9478098	snp	C/G	0.181022	0.240296	intron-variant	PHF10	GRCh38.p7	6:169722607	GCATTATTATATAAA[C/G]TGAGCATCTGGGCAG	55274
rs11372372	in-del	-/T	0.0279526	0.114869	intron-variant	PHF10	GRCh38.p7	6:169719394	TCATATCATAAACCG[-/T]TAACTGTTTGTTCTC	55274
rs11546265	snp	C/T	0.352721	0.227922	intron-variant	PHF10	GRCh38.p7	6:169708267	TCCGGCCTATAAATA[C/T]AATAATTAAAATCTA	55274
rs11546266	snp	C/T			intron-variant	PHF10	GRCh38.p7	6:169707848	ACAAAGCTGTCTCTC[C/T]TCCCCTTCTCTCATG	55274
rs11750951	snp	G/T	0	0	intron-variant	PHF10	GRCh38.p7	6:169716223	AAGCAAAATATCTTA[G/T]TACATTTGAAAATAA	55274
rs11963331	snp	C/T	0	0	downstream-variant-500B, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706731	acatacatacataca[C/T]acacacacacacaca	55274
rs12663375	snp	A/G	0.183568	0.241012	intron-variant	PHF10	GRCh38.p7	6:169710147	GAGGTACAGCAGGCA[A/G]AAGCTCCACAATCGT	55274
rs17860601	snp	C/T	0.0819801	0.18512	synonymous-codon, intron-variant	PHF10	GRCh38.p7	6:169710308	AGTGGCAGCTTTGTC[C/T]TTTGATTTCTGTCTT	55274
rs17860603	snp	G/T	0.0376037	0.131863	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	C6orf120, WDR27, PHF10	GRCh38.p7	6:169703900	TTTTTTGCAAATTAT[G/T]AGCTTAAAATCTGCA	55274
rs17860604	snp	A/C	0.000393895	0.0140283	intron-variant	PHF10	GRCh38.p7	6:169721131	ACATTTAAAAGATTC[A/C]AAAATAATAATTAGA	55274
rs17860605	snp	C/T	0.0103295	0.0711199	intron-variant	PHF10	GRCh38.p7	6:169721265	TTGGCATGAGCAAGA[C/T]CTGGAATAAAATTTA	55274
rs17860613	snp	A/G	0.0180464	0.0932604	intron-variant	PHF10	GRCh38.p7	6:169715683	TAAACTAAGTTCAGG[A/G]GGTACTAAATTTAAG	55274
rs17860614	in-del	-/TT	0.140242	0.224618	intron-variant	PHF10	GRCh38.p7	6:169709304	TTCACTTGGCAAAAC[-/TT]TCTCATCAGCTTACT	55274
rs17860618	snp	A/C	0.000798403	0.0199641	intron-variant	PHF10	GRCh38.p7	6:169708398	CAGATACATTACTTC[A/C]TTGAATCTCGTACTT	55274
rs17860886	snp	G/T	0.0437281	0.141251	upstream-variant-2KB, downstream-variant-500B	PHF10, TCTE3	GRCh38.p7	6:169725113	GCTGCATTTATTACT[G/T]ATCTCGGGCTGCACC	55274
rs33910456	in-del	-/TT			upstream-variant-2KB, intron-variant	PHF10, TCTE3	GRCh38.p7	6:169725634	AGCGGTTTTTTTTTT[-/TT]AAGAAAAAAAACAAA	55274
rs34033798	in-del	-/TT	0.350109	0.229081	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706324	TGTGTGATTATTCTC[-/TT]TGCATGTCTAATAAA	55274
rs34227712	snp	A/G	9.88386e-05	0.00702919	missense, intron-variant	PHF10	GRCh38.p7	6:169710265	GGTCCCAAACGTTCT[A/G]TACTGTCCAAGTCAG	55274
rs34283211	in-del	-/A			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	C6orf120, WDR27, PHF10	GRCh38.p7	6:169703815	AAGGTTACTATAAAA[-/A]TACTTTGGAAGATGA	55274
rs34406607	in-del	-/A			intron-variant	PHF10	GRCh38.p7	6:169707035	CAGAGGCATTCAAAA[-/A]GAATTTTTGGCTTAT	55274
rs34468626	in-del	-/G			intron-variant	PHF10	GRCh38.p7	6:169715396	ATGGTAAAACACCAT[-/G]CTCTACTAAAAATAC	55274
rs34564229	in-del	-/A	0.0441095	0.141807	intron-variant	PHF10	GRCh38.p7	6:169711954	AAAAAAAAGTCATAC[-/A]GGAAAACCCAACAAA	55274
rs35206456	in-del	-/C			intron-variant	PHF10	GRCh38.p7	6:169709454	ACAGCTAATTCTTCC[-/C]TTTTATGATATTCTT	55274
rs35381106	in-del	-/G			intron-variant	PHF10	GRCh38.p7	6:169707447	TCCATCAAAACTAAG[-/G]AAATCTCTTGGTTAT	55274
rs35531685	in-del	-/A/AA			intron-variant	PHF10	GRCh38.p7	6:169719981	CTACAACAAAAAAAA[-/A/AA]CCCCAAATAAAAAAT	55274
rs35601906	in-del	-/G			intron-variant	PHF10	GRCh38.p7	6:169707563	TCACTAAAGTCAGGG[-/G]AAGTAACCAAACAAT	55274
rs35676225	in-del	-/T			intron-variant	PHF10	GRCh38.p7	6:169716455	AAAATTCAACATATT[-/T]ATAGTTCCCAGTCTT	55274
rs35892429	in-del	-/TACT			utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706089	ATTATGTGTAAGACT[-/TACT]CTAAAAAGACCATTT	55274
rs36114980	in-del	-/A	0.0232847	0.105357	upstream-variant-2KB, intron-variant	PHF10, TCTE3	GRCh38.p7	6:169725852	GCCACAAAACTACAC[-/A]AAAAAAATGCTTCAA	55274
rs41265395	snp	A/G	0.0460142	0.144533	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169705014	ATCACAGCTTTGGTC[A/G]TATTTGCACATAAGA	55274
rs41265397	snp	A/C			intron-variant	PHF10	GRCh38.p7	6:169710474	ACTATGGAAAATATT[A/C]AAAGAAAGTTTTAAA	55274
rs41265399	snp	A/T	0.0859241	0.188624	intron-variant	PHF10	GRCh38.p7	6:169718935	TAAGTACAGAAATAC[A/T]TATTATGCATTAAAT	55274
rs55829134	in-del	-/AC			downstream-variant-500B, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706778	CACACACACACACAC[-/AC]GTAGATGAACTGGGA	55274
rs58285745	snp	A/C			upstream-variant-2KB, intron-variant	PHF10, TCTE3	GRCh38.p7	6:169725584	TCTGCCAAGAAGAAA[A/C]TGCATCTTTCAGCTA	55274
rs58588902	in-del	-/GGA			intron-variant	PHF10	GRCh38.p7	6:169721693	TTTTTTTAAAGAAGA[-/GGA]TTATATATTTTTAAT	55274
rs61747680	snp	A/C	1.6489e-05	0.00287128	synonymous-codon	PHF10	GRCh38.p7	6:169715810	TTTCTTAATATACTC[A/C]GGCACTTTACTGGCT	55274
rs61757711	snp	A/G	0.000462039	0.0151923	intron-variant	PHF10	GRCh38.p7	6:169714847	ACCTGGATAACCTAC[A/G]TTAACATAAAGAGAA	55274
rs71010613	in-del	-/ACACAC	0	0	downstream-variant-500B, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706774	CACACACACACACAC[-/ACACAC]GTAGATGAACTGGGA	55274
rs71574971	snp	A/C	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169717982	TTTAAAAGCTTAAAA[A/C]CCTTGATTTTTTAAA	55274
rs73039197	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169705424	CAGAGAATGGCTATA[A/G]TGTCAAATCGCCAAA	55274
rs73039200	snp	A/T	0.00279162	0.0372561	intron-variant	PHF10	GRCh38.p7	6:169710055	AACCATAGCCAAAAG[A/T]GACAGAAAAGCCACC	55274
rs73039202	snp	A/T	0.0023933	0.0345097	intron-variant	PHF10	GRCh38.p7	6:169713939	GCATCCTGGCCAACA[A/T]GGTAAAACCCACCTC	55274
rs73041103	snp	G/T	0.0023933	0.0345097	intron-variant	PHF10	GRCh38.p7	6:169713940	CATCCTGGCCAACAT[G/T]GTAAAACCCACCTCT	55274
rs73242910	snp	A/G	0.352504	0.228019	intron-variant	PHF10	GRCh38.p7	6:169714574	TTCTGACTACAGGGT[A/G]TTGTTTACCACAGAA	55274
rs73242916	snp	C/T	0.0763149	0.179815	intron-variant	PHF10	GRCh38.p7	6:169719154	ACACTGGGAAGAACG[C/T]AGAATCACAATTGCT	55274
rs74528745	snp	A/G	0.00557542	0.0525036	intron-variant	PHF10	GRCh38.p7	6:169719176	ACAATTGCTAAGAAC[A/G]AAGGCATTTTTAGTT	55274
rs74958830	snp	A/T	0.00953873	0.0683987	intron-variant	PHF10	GRCh38.p7	6:169717500	ATAAAGTGTTGAATA[A/T]GTCATGTGACTTGTT	55274
rs75365863	snp	C/T	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169714154	TTAGCCCTGTTTTTT[C/T]CAGTTACATTTAATT	55274
rs75404814	snp	A/G	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169710839	AAGCGCTGCAGTTAG[A/G]AAAAAAAAAAAAAAG	55274
rs75557160	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, intron-variant	C6orf120, PHF10	GRCh38.p7	6:169706177	AACTAGAGCTATAAA[A/G]TCTAAGTTAAAAAAT	55274
rs75598299	in-del	-/CAA			intron-variant	PHF10	GRCh38.p7	6:169715594	AAACAAACAAACAAA[-/CAA]AAAAACACACACACA	55274
rs75663289	snp	A/G	0	0	intron-variant	PHF10	GRCh38.p7	6:169710842	CGCTGCAGTTAGGAA[A/G]AAAAAAAAAAAGTCC	55274
rs75830361	snp	A/G	0.0479149	0.147179	intron-variant	PHF10	GRCh38.p7	6:169712023	GAAGCATAAGATTAA[A/G]CAAATGCACTCCCCT	55274
rs77090339	snp	A/G	0	0	intron-variant	PHF10	GRCh38.p7	6:169721691	TTTTTTTTTTAAAGA[A/G]GATTATATATTTTTA	55274
rs77273105	snp	A/G	0.102014	0.201495	intron-variant	PHF10	GRCh38.p7	6:169713397	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	55274
rs77535897	snp	A/G	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169710841	GCGCTGCAGTTAGGA[A/G]AAAAAAAAAAAAGTC	55274
rs77811390	snp	A/C			intron-variant	PHF10	GRCh38.p7	6:169717909	CGTCGCTCTAAATCT[A/C]CAAAAAAAAGATCAA	55274
rs77919800	snp	A/G	0.000379091	0.0137623	missense	PHF10	GRCh38.p7	6:169715755	CTTCCATGCGTTCCC[A/G]GTTTAAGTTGCTATT	55274
rs78116410	snp	A/C	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169714119	AGCAAGACTGTCTCA[A/C]AAAAAAAAAAAAGAA	55274
rs78315194	snp	C/T	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169711120	TGTATCTACTTTATC[C/T]TTTTTCTGGGTGTCC	55274
rs78641408	snp	A/G	0.000565131	0.0168002	intron-variant	PHF10	GRCh38.p7	6:169715862	TGTTGCATTTGCTGG[A/G]AAAAAAAAATACAGT	55274
rs78780499	snp	C/T	0.00318978	0.0398085	intron-variant	PHF10	GRCh38.p7	6:169718632	ATAATCGCACCAGTG[C/T]GCTCTAGCCTGGGTT	55274
rs78856832	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-3-prime	PHF10, TCTE3	GRCh38.p7	6:169725532	CCTCTGTCCCACCAC[A/G]TGCAGGTGTAAGCTT	55274
rs79175710	snp	A/G	0.0345262	0.126772	intron-variant	PHF10	GRCh38.p7	6:169720723	GAAATGGATGGTGGT[A/G]ATGGCTGCACAACAC	55274
rs79626796	snp	A/G	0.000399281	0.0141238	intron-variant	PHF10	GRCh38.p7	6:169717470	TGGGCAAAATCAGCT[A/G]ACACAAATTTTAATA	55274
rs79720232	snp	A/G	0.5	0	intron-variant	PHF10	GRCh38.p7	6:169714987	GGAGCTATAACCTAA[A/G]AGGACAGTTGGTGCT	55274
rs80102757	snp	A/C	0.00557542	0.0525036	intron-variant	PHF10	GRCh38.p7	6:169714400	GTTGGGCCTGAGATT[A/C]TGCATTTCCAACAAG	55274

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