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

KLHL41

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs772854250	in-del	-/T	0.00268976	0.0365739	intron-variant	KLHL41	GRCh38.p7	2:169525566	CTGCTTATTGATTAC[-/T]TTTTTTTTCCTCCAT	10324
rs772934126	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169523984	TCTCAGTATACAACA[C/T]TCTCAACATAGACCC	10324
rs772944683	snp	A/G			utr-variant-3-prime	KLHL41	GRCh38.p7	2:169525897	TAAAACCATTTTCTA[A/G]TAATAAATTAAATCT	10324
rs772975075	snp	A/G	3.31082e-05	0.00406854	intron-variant	KLHL41	GRCh38.p7	2:169514774	TAAGCATTCAAGTAT[A/G]TGCGTGCCTACAACA	10324
rs773033779	snp	A/G	1.65034e-05	0.00287253	splice-donor-variant	KLHL41	GRCh38.p7	2:169521008	CAATGACATATGGAA[A/G]TAAGTTCTCATCACT	10324
rs773331535	snp	C/T	3.79903e-05	0.00435818	intron-variant	KLHL41	GRCh38.p7	2:169515001	TTATGTCTAAATGAC[C/T]TTTTATTAGAAGGGT	10324
rs773594703	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169516827	GGGAATTTGAGACCA[A/G]CCTGTCCAACGTGGA	10324
rs773708864	snp	A/G	3.30863e-05	0.00406719	missense	KLHL41	GRCh38.p7	2:169510535	CTCCAGAAAAAAATC[A/G]AAGTTCTAAAAGATG	10324
rs773713203	in-del	-/AAC	1.65748e-05	0.00287874	cds-indel	KLHL41	GRCh38.p7	2:169525688	TCTTCAAACTGTCTA[-/AAC]AACTGTGAACAAGGT	10324
rs773715604	snp	C/G			intron-variant	KLHL41	GRCh38.p7	2:169512834	TGCATTAATTTAGGA[C/G]TAATTTGACCTTTGA	10324
rs773723368	snp	C/T	4.94482e-05	0.00497209	synonymous-codon	KLHL41	GRCh38.p7	2:169525639	GGAAATACGTTATGC[C/T]TCAGGAGCTAGTTGC	10324
rs773869984	snp	G/T	6.58935e-05	0.00573955	missense	KLHL41	GRCh38.p7	2:169510621	TGAGGTGAATGGTGA[G/T]GTTGGTGATGAAGAT	10324
rs774105660	snp	C/T	3.29511e-05	0.00405887	missense	KLHL41	GRCh38.p7	2:169509933	ACAGATTGATTTTGT[C/T]AGCTTGTAGTCCTTA	10324
rs774108134	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169521955	ATTTTGAACTGAGAT[C/T]GCGCCACTGCACTCC	10324
rs774274795	snp	C/T	5.00856e-05	0.00500403	intron-variant	KLHL41	GRCh38.p7	2:169514819	GAACCTGGAATTTAC[C/T]GAAGGTATATAAATT	10324
rs774398791	snp	C/T	1.70799e-05	0.00292227	intron-variant	KLHL41	GRCh38.p7	2:169518397	TGCCACATCTTAGTA[C/T]ATAGCATGTGAACAA	10324
rs774434260	snp	A/G	1.70592e-05	0.0029205	missense	KLHL41	GRCh38.p7	2:169514961	GAAAGACAGATGACA[A/G]GTAAGTACCCTGAAC	10324
rs774465298	snp	A/G	3.29984e-05	0.00406179	missense	KLHL41	GRCh38.p7	2:169518256	AGATCTGGCTCCAAT[A/G]AAAATTCCTCGTTCC	10324
rs774827735	snp	A/C/G	9.88361e-05	0.00702917	missense	KLHL41	GRCh38.p7	2:169510647	AAGATTTACTTCCTG[A/C/G]TTACCTGAATGACAT	10324
rs774846657	snp	A/G	6.58957e-05	0.00573964	missense	KLHL41	GRCh38.p7	2:169510661	GGTTACCTGAATGAC[A/G]TTCCCAGGCATGGAA	10324
rs774922275	snp	A/C/G			intron-variant	KLHL41	GRCh38.p7	2:169520063	GGAATGCAGCAATGC[A/C/G]ATCATAGCTCACCGC	10324
rs775002789	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169519889	ATGAGCCACCGTGCC[C/T]GGCCTTAGGGTTGCC	10324
rs775129813	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169514366	TTGAAGATTTTGATA[C/T]CTTTATCTGGTAGGC	10324
rs775196099	snp	G/T	1.78512e-05	0.00298752	intron-variant	KLHL41	GRCh38.p7	2:169514983	ACCCTGAACTCTCAT[G/T]ATTTATGTCTAAATG	10324
rs775340986	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169521646	GATCCACCCGCCTCA[A/G]TCTCCCAAAGTGCTA	10324
rs775513051	in-del	-/A	3.29905e-05	0.0040613	frameshift-variant	KLHL41	GRCh38.p7	2:169509985	GAAATTGATGAGGCG[-/A]AAAAAAAAGGAGGTA	10324
rs775529378	snp	C/G			intron-variant	KLHL41	GRCh38.p7	2:169523763	CCTGGGTACTTATCA[C/G]AAAGGCAGATTCTCA	10324
rs775891967	snp	A/G	0.000120301	0.00775473	intron-variant	KLHL41	GRCh38.p7	2:169518403	ATCTTAGTATATAGC[A/G]TGTGAACAACTATAC	10324
rs776119431	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169514550	CTAACAGGCTCCACA[A/G]TCTCTCATATATGTT	10324
rs776170658	snp	A/T	5.00329e-05	0.0050014	missense	KLHL41	GRCh38.p7	2:169510860	ATGAAGAAAATAAGG[A/T]TCAACCTCTACAGTC	10324
rs776266534	in-del	-/A	1.65401e-05	0.00287572	frameshift-variant	KLHL41	GRCh38.p7	2:169510337	GTCATTTCAAATGAC[-/A]GCCTAAATGTAGAAA	10324
rs776338095	snp	A/C/G	3.57918e-05	0.00423023	utr-variant-3-prime	KLHL41	GRCh38.p7	2:169525741	GGTGGTTTGTTTGGT[A/C/G]AATGGGGCTTTAATT	10324
rs776458387	snp	C/G	1.65542e-05	0.00287695	missense	KLHL41	GRCh38.p7	2:169510202	GCCATCCTAAGATTA[C/G]GACTTCTTCTTGACT	10324
rs776517407	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169511270	GCCCCGGCTGGTCTC[A/G]AACTCCTGGGCTCAA	10324
rs776571020	in-del	-/TTTA			intron-variant	KLHL41	GRCh38.p7	2:169517878	TAAAAGGTTTATGAT[-/TTTA]TTTTTTACTCAAATA	10324
rs776592055	in-del	-/TTG	3.58715e-05	0.00423491	intron-variant	KLHL41	GRCh38.p7	2:169518426	AACTATACATTTTAA[-/TTG]TTAACTTTGGATAAA	10324
rs776743734	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169523456	GAACCACTGGATTGG[A/G]TAAAGAGAAGAGGGG	10324
rs776837529	snp	A/G			missense	KLHL41	GRCh38.p7	2:169514661	GAGGTGGATGATAAA[A/G]TCTATGTAGTTGCAG	10324
rs776839011	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169521682	ACAGGCGTGAGCCAC[A/G]TACCCAGCCTAAAGA	10324
rs777120116	snp	A/G	8.23866e-05	0.00641767	synonymous-codon	KLHL41	GRCh38.p7	2:169520972	TCAACTGGAGTCTAA[A/G]GAATTTGCACCCACT	10324
rs777151398	snp	A/G	0.00018206	0.00953924	missense	KLHL41	GRCh38.p7	2:169510529	CCAGACCTCCAGAAA[A/G]AAATCAAAGTTCTAA	10324
rs777173274	snp	C/T	1.76561e-05	0.00297115	intron-variant	KLHL41	GRCh38.p7	2:169518418	ATGTGAACAACTATA[C/T]ATTTTAATTGTTAAC	10324
rs777250281	snp	A/G	1.64743e-05	0.00287	missense	KLHL41	GRCh38.p7	2:169510025	AATGTGGATCCTGCT[A/G]TACTTGATTTAATCA	10324
rs777285517	snp	A/G	1.64866e-05	0.00287106	synonymous-codon	KLHL41	GRCh38.p7	2:169525603	TGAAGATGATAAAAA[A/G]GAATGGGCTGGGATG	10324
rs777303663	snp	A/T	0.000252655	0.0112367	intron-variant	KLHL41	GRCh38.p7	2:169518164	AAAAAAGGTTCTAAA[A/T]GGAACATTTGTTTTT	10324
rs777331306	snp	A/G	1.6585e-05	0.00287962	missense	KLHL41	GRCh38.p7	2:169514927	ATTTCACATAAAGGG[A/G]TGATATATTGTCTAG	10324
rs777345943	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169516967	CAGTGAGCTGATATC[A/G]CGCCACTGCACTCCA	10324
rs777495507	snp	C/T			synonymous-codon	KLHL41	GRCh38.p7	2:169509901	CCTAAAAGCAGGTGA[C/T]AAAAGTCTTCCTTGC	10324
rs777511235	snp	A/G	1.65831e-05	0.00287945	missense	KLHL41	GRCh38.p7	2:169510482	AATATTTTAAGGATC[A/G]TGTTGAGAAAGATGA	10324
rs777586212	snp	A/T			intron-variant	KLHL41	GRCh38.p7	2:169521267	GAGTTGGACCTTTGA[A/T]ACTCTCAGTTTCATT	10324
rs777665141	snp	C/G			utr-variant-3-prime	KLHL41	GRCh38.p7	2:169526238	AAAAGTCTCTTGTAA[C/G]TAAAAGTAGTCAAAT	10324
rs777665811	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169513809	ATTTAAATTACCAAA[A/G]GTAAGTGATGAAACA	10324
rs777667473	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169515550	TTCACTGATTTATAA[C/T]TGTATTTTACTACAT	10324
rs777708003	snp	A/G			synonymous-codon	KLHL41	GRCh38.p7	2:169509997	GGCGAAAAAAAAGGA[A/G]GTAGTGCTAGACAAT	10324
rs777872730	snp	A/G			missense	KLHL41	GRCh38.p7	2:169510821	AGCAAAATCAGATAT[A/G]TGTGGTAGGAGGACT	10324
rs777968201	snp	C/T	7.09207e-05	0.00595444	intron-variant	KLHL41	GRCh38.p7	2:169510908	GAAGGACTTTTTGTA[C/T]ATGTAGTTGCTTAAA	10324
rs778003504	snp	A/G	1.675e-05	0.00289391	missense	KLHL41	GRCh38.p7	2:169518375	ACCTTACAACAAATA[A/G]GTGAGTTGCCACATC	10324
rs778040771	in-del	-/AA	1.64761e-05	0.00287015	frameshift-variant	KLHL41	GRCh38.p7	2:169509902	CTAAAAGCAGGTGAC[-/AA]AAGTCTTCCTTGCCA	10324
rs778064930	snp	A/C			intron-variant	KLHL41	GRCh38.p7	2:169525196	AAGGCATAATTAAGT[A/C]TACCGATAGTCCCTG	10324
rs778165438	in-del	-/TT	3.80409e-05	0.00436108	intron-variant	KLHL41	GRCh38.p7	2:169515001	TTATGTCTAAATGAC[-/TT]TTTATTAGAAGGGTT	10324
rs778451557	snp	A/C	1.64762e-05	0.00287016	missense	KLHL41	GRCh38.p7	2:169510056	TCAAATACCTGTACT[A/C]TGCCAGTATTGATCT	10324
rs778483560	snp	C/T	1.65373e-05	0.00287548	missense	KLHL41	GRCh38.p7	2:169510149	TTACTGTCTGCGTTT[C/T]TTATCTTCAGAAAAG	10324
rs778531652	snp	A/T	1.64866e-05	0.00287106	missense	KLHL41	GRCh38.p7	2:169518295	AGTAGCAGTCCATAA[A/T]GGCAAAATTGTGATT	10324
rs778568999	snp	G/T			intron-variant	KLHL41	GRCh38.p7	2:169520027	CCCTTAAAGACAGGG[G/T]TTTGCTCTATCACCC	10324
rs778816761	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169512138	ATACTATTATACCTT[C/T]AATCAACTTTTTCTA	10324
rs778843381	in-del	-/TA	1.70342e-05	0.00291836	intron-variant	KLHL41	GRCh38.p7	2:169518394	GTTGCCACATCTTAG[-/TA]TATATAGCATGTGAA	10324
rs778940575	snp	A/C	3.34526e-05	0.00408965	synonymous-codon	KLHL41	GRCh38.p7	2:169518203	AGAAAATGTACAAAC[A/C]GGGTGTTTATCTTCA	10324
rs779057487	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169525565	GCTGCTTATTGATTA[C/T]TTTTTTTTTCCTCCA	10324
rs779057492	snp	C/T	6.61332e-05	0.00574998	synonymous-codon	KLHL41	GRCh38.p7	2:169510313	CTGTCTCCACAGGAA[C/T]TGATCTCAGTCATTT	10324
rs779110067	snp	C/T	5.35681e-05	0.00517505	utr-variant-5-prime	KLHL41	GRCh38.p7	2:169509751	TAAGGCCTTCAGTGT[C/T]CCCTTCCTTACCCAG	10324
rs779134378	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169515713	TCATAAGAGGGACTT[C/T]AGATAGGTCAGTTTG	10324
rs779140230	snp	C/T	3.29527e-05	0.00405898	stop-gained	KLHL41	GRCh38.p7	2:169510805	TCCAGCATTGTTACC[C/T]AGCAAAATCAGATAT	10324
rs779210560	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169511037	TTTGCTGTATAGAGC[A/G]TTGACAGAAAAATAT	10324
rs779433733	snp	A/T			intron-variant	KLHL41	GRCh38.p7	2:169511066	ATTTGACTGCTTTGT[A/T]AATGTGTAATAAAAA	10324
rs779485358	snp	A/G	1.81764e-05	0.00301461	intron-variant	KLHL41	GRCh38.p7	2:169510925	TGTAGTTGCTTAAAG[A/G]GAAGGCTGTTACTCA	10324
rs779488836	snp	A/T			intron-variant	KLHL41	GRCh38.p7	2:169516274	ACTCTATTCTGGAGT[A/T]AATGATTATTGGGTA	10324
rs779505405	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169513125	AAGGTAGGCAGTACT[A/G]TACAGTATGAGAGTT	10324
rs779578696	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169517413	TTCGAGACCAGCCTG[A/G]CCAACATGGCGAAAC	10324
rs779598362	snp	A/C			downstream-variant-500B	KLHL41	GRCh38.p7	2:169526685	AAGTCATCAATTAAT[A/C]ATCACTTTTAGCCAC	10324
rs779629881	snp	C/T	6.80816e-05	0.00583405	intron-variant	KLHL41	GRCh38.p7	2:169514536	CTTCTAATTTTTTTC[C/T]AACAGGCTCCACAAT	10324
rs779691989	snp	A/G	1.6534e-05	0.00287519	missense	KLHL41	GRCh38.p7	2:169510280	GTACAGATTTGTAAG[A/G]AAGAGGACTTTATGC	10324
rs779872706	snp	A/G	1.64939e-05	0.0028717	missense	KLHL41	GRCh38.p7	2:169518326	GCAGGAGGTGTCACT[A/G]AAGATGGTCTTTCAG	10324
rs779897118	snp	C/G	1.65658e-05	0.00287795	missense	KLHL41	GRCh38.p7	2:169518222	TGTTTATCTTCAACC[C/G]CAAAAAAGGAGATTG	10324
rs780063055	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169521582	ATTTTTAGTAGAGAC[A/G]GCATTTCGCCATGTT	10324
rs780236874	snp	C/G			intron-variant	KLHL41	GRCh38.p7	2:169524316	TTGAGAACTAATTTG[C/G]AACATTGATGAAATT	10324
rs780253296	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169513612	GGCTTCCACAGACAC[C/T]CCTGTCTATACCACA	10324
rs780264253	snp	A/G	1.65781e-05	0.00287902	missense	KLHL41	GRCh38.p7	2:169510499	GTTGAGAAAGATGAT[A/G]TAATTAAAAGCAACC	10324
rs780328749	snp	A/G			upstream-variant-2KB	KLHL41	GRCh38.p7	2:169509629	AAATTCCCGTTGTTA[A/G]AGTTGGTATCTATAT	10324
rs780335197	snp	A/G	1.67781e-05	0.00289634	utr-variant-3-prime	KLHL41	GRCh38.p7	2:169525705	ACTGTGAACAAGGTG[A/G]CAAAACATAATAGAT	10324
rs780361528	snp	G/T	1.64991e-05	0.00287215	missense	KLHL41	GRCh38.p7	2:169509843	CCCTTCTTCAGGATG[G/T]TCTAAAAGATCTCCT	10324
rs780442771	snp	A/G			missense	KLHL41	GRCh38.p7	2:169514934	ATAAAGGGATGATAT[A/G]TTGTCTAGGAGGAAA	10324
rs780672614	snp	C/T	3.50643e-05	0.004187	utr-variant-5-prime	KLHL41	GRCh38.p7	2:169509769	CTTCCTTACCCAGGT[C/T]TCTCACAGAATGGAT	10324
rs780689781	in-del	-/CTCA			intron-variant	KLHL41	GRCh38.p7	2:169511244	TAGCAGAGATGGGCT[-/CTCA]CTATGTTGCCCCGGC	10324
rs780783546	snp	C/T	1.6531e-05	0.00287493	synonymous-codon	KLHL41	GRCh38.p7	2:169514896	ACTCCCTATCAAAGT[C/T]TATGGCCATAATGTG	10324
rs781142922	snp	A/G	1.65795e-05	0.00287914	missense	KLHL41	GRCh38.p7	2:169510446	TGTTTGATTGTATCC[A/G]TTTTCGCCTTATGAC	10324
rs781168942	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169512227	TCCAGTGAAGAATGT[C/T]ATAAGTATTTGAATG	10324
rs781196871	snp	C/T			intron-variant	KLHL41	GRCh38.p7	2:169523328	TGCTTCAAAAAATAT[C/T]AACACCTCTATCCCA	10324
rs781233657	snp	C/T			synonymous-codon	KLHL41	GRCh38.p7	2:169509913	TGACAAAAGTCTTCC[C/T]TGCCACAGATTGATT	10324
rs781404051	snp	A/G			upstream-variant-2KB	KLHL41	GRCh38.p7	2:169509622	CTCTCCTAAATTCCC[A/G]TTGTTAGAGTTGGTA	10324
rs781536513	snp	C/T	6.58913e-05	0.00573945	missense	KLHL41	GRCh38.p7	2:169510737	TGGCTTATGACCCCA[C/T]GGAAAATGAATGCTA	10324
rs781663837	in-del	-/ATTA			upstream-variant-2KB	KLHL41	GRCh38.p7	2:169509071	ATAATTTAATTCAAT[-/ATTA]ATTACAGTTTTTCCA	10324
rs781712235	snp	A/G			missense	KLHL41	GRCh38.p7	2:169509789	ACAGAATGGATTCCC[A/G]GCGGGAACTTGCAGA	10324
rs781747838	snp	C/G	1.72264e-05	0.00293477	utr-variant-3-prime	KLHL41	GRCh38.p7	2:169525730	ATAGATTGGGAGGTG[C/G]TTTGTTTGGTGAATG	10324
rs796881135	snp	A/G			intron-variant	KLHL41	GRCh38.p7	2:169512628	TCTGTATAACAGAAC[A/G]TTAACAATAACAGTT	10324
rs864309595	snp	A/G			missense	KLHL41	GRCh38.p7	2:169520937	GGATCTCTGTATGCA[A/G]TTGGTGGTTTTGCTA	10324

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