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

FBXW10

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs960608	snp	C/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18756650	CACATATTTCTGTAA[C/T]CCAGCCCAGCAAAGT	10517
rs1024657	snp	C/T	0.0104662	0.071579	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779192	TTGATCCAGGAAAAG[C/T]CAGCAAAGCTGCATG	10517
rs1026259	snp	A/G	0.159882	0.233193	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778600	CTCCTGACTGTTAGC[A/G]CCCTGCAGCACGCCC	10517
rs1318979	snp	A/G	0.029198	0.117245	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779086	CCTTTTAGAGTGAAC[A/G]CTGAGTTCGTGCTGT	10517
rs2014354	snp	A/G	0.0121512	0.0769931	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779319	CCTTGGGAAATTACA[A/G]TGTTTTACAATAAAC	10517
rs2014360	snp	A/G	0.4488	0.151587	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779419	ATGTGGGAACTCCCA[A/G]TTATCTTCCCCTGAG	10517
rs2123375	snp	A/G	0.424659	0.17887			GRCh38.p7	17:18741366	AGCCAGCAGGGACTC[A/G]GGAAAGCACACAGGT	10517
rs2323786	snp	G/T	0.0252325	0.109451			GRCh38.p7	17:18741087	ATGTGGTATTACACT[G/T]GTTGGAAGTTGAATT	10517
rs2323787	snp	C/T	0.0252325	0.109451			GRCh38.p7	17:18741057	TTTAAAAAGCTTggc[C/T]gggcgcggtggttca	10517
rs3032059	snp	A/T	0.41275	0.189769	intron-variant	FBXW10	GRCh38.p7	17:18761962	aaaaaaaagaaaaag[A/T]aaaagaaaaaccaat	10517
rs3826384	snp	A/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18756277	TCATGTGCAAGTTTA[A/G]GGCTGGAGCTTGAGG	10517
rs4244595	snp	A/G	0.487113	0.0792303	intron-variant	FBXW10	GRCh38.p7	17:18774016	ATGTAAGACTAGATC[A/G]GCTACTATTGATTAC	10517
rs4315390	snp	A/G	0.492966	0.0588865	intron-variant	FBXW10	GRCh38.p7	17:18745734	TTCTGTATTTCTAAC[A/G]AGTTTCCAGCTAGTG	10517
rs4349204	snp	C/T	0.499551	0.0149693	intron-variant	FBXW10	GRCh38.p7	17:18745604	attttttagtagaga[C/T]ggggtttcaccatgc	10517
rs4520890	snp	A/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18759652	gagtctcactgtgtc[A/G]cccaggctggagagc	10517
rs4611519	snp	A/G	0.482534	0.0918038	intron-variant	FBXW10	GRCh38.p7	17:18766965	GAGCAACTGAGTATG[A/G]CCTTCAAGAAGGACA	10517
rs4630608	snp	C/T	0.495615	0.0466161	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775235	AGGGAACAAGTGGCA[C/T]GGATGGTGGGCAGGA	10517
rs4924769	snp	C/T	0.499987	0.00259581	intron-variant	FBXW10	GRCh38.p7	17:18749295	TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG	10517
rs4924770	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18757189	ATCACCATACTATCT[A/G]TATTTCTTTTTTCAG	10517
rs4924914	snp	C/T	0.490453	0.0684267			GRCh38.p7	17:18740329	CTCAGATTTCAGCAC[C/T]GACTCCCTCCCTCTG	10517
rs4924915	snp	A/G	0.5	0.000399361	intron-variant	FBXW10	GRCh38.p7	17:18753346	tgcagaaagatgtat[A/G]gggacagacacacaa	10517
rs4924917	snp	C/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18757188	TATCACCATACTATC[C/T]GTATTTCTTTTTTCA	10517
rs4924918	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18757296	TCAAGCGATTCTCCT[C/G]CCTCAGTCTCCTAAG	10517
rs4924920	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757340	AGGCACATGCCACCA[C/T]GCCTGGCTAATTTCT	10517
rs4924921	snp	C/T	0.375	0.216506	intron-variant	FBXW10	GRCh38.p7	17:18757440	GACTATACATCCCTG[C/T]TTATTGGAACAATCC	10517
rs4924923	snp	C/T	0.132653	0.220748	intron-variant	FBXW10	GRCh38.p7	17:18766028	CACTGGGCCCGGCAT[C/T]AACTTCTTCATTTTA	10517
rs4924924	snp	C/G	0.478354	0.101757	intron-variant	FBXW10	GRCh38.p7	17:18774461	AGATGGAAGGGATAA[C/G]TTCCAGCGTTTGGTT	10517
rs4924925	snp	G/T	0.475702	0.107512	intron-variant	FBXW10	GRCh38.p7	17:18777256	tttagtacagacggg[G/T]tttctccatgttggt	10517
rs5819658	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18767444	AGATCATGCGTCTCA[-/A]AAAAAAAAAAAAAAA	10517
rs6502669	snp	A/G	0.459687	0.136129	intron-variant	FBXW10	GRCh38.p7	17:18759758	gctgagactacaggg[A/G]cccgccaccacacca	10517
rs7209610	snp	A/G	0.00107037	0.0231093	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751045	CCGAAGTGGAAGCTG[A/G]GAACGAAGGTGGGTT	10517
rs7212014	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18747724	ATAAACAACTCGAGA[A/C]ATTTTACAATGGGGG	10517
rs7215492	snp	C/T	0.45762	0.139261	intron-variant	FBXW10	GRCh38.p7	17:18752174	acacaaaggaggaga[C/T]gggtcgtgtgggcag	10517
rs7216988	snp	A/G	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18766446	AGCACTTGGGCCTCA[A/G]GGCTAAGTTCCAGGG	10517
rs7217866	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18747486	acttgaacccaggag[A/G]cggaggttgcagtga	10517
rs7217902	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18747542	ccctgggcaataaga[C/G]caaaactcagtctca	10517
rs7223011	snp	C/T	0.0091458	0.0670019	intron-variant	FBXW10	GRCh38.p7	17:18766880	AAGTGGGCAGTGGGC[C/T]ACCTTGGCGGAAAGG	10517
rs7223948	snp	A/G	0.473909	0.111197	intron-variant	FBXW10	GRCh38.p7	17:18757485	GTCCTAGTGTCATTA[A/G]TAATAGTGTCCCCAG	10517
rs7225387	snp	A/G	0.131723	0.220251	intron-variant	FBXW10	GRCh38.p7	17:18764402	agacagggtttcacc[A/G]tgttggccagtatgg	10517
rs8069260	snp	A/G	0.100588	0.200439	intron-variant	FBXW10	GRCh38.p7	17:18774049	tctaatggttgctta[A/G]cattctgctgtaaag	10517
rs8070267	snp	C/T	0.118933	0.212888	intron-variant	FBXW10	GRCh38.p7	17:18774075	taaagaggtgacaat[C/T]acaaggggAGTTGCT	10517
rs8073523	snp	C/T	0.310632	0.242536	intron-variant	FBXW10	GRCh38.p7	17:18771432	AGGGAGGCAGTGCTG[C/T]GGGGGCACAGGAAGG	10517
rs8076246	snp	A/G	0.317692	0.240661	intron-variant, synonymous-codon	FBXW10	GRCh38.p7	17:18771630	GGTCTATGAAGGAGA[A/G]GAGGCCTCCCCATTA	10517
rs8076572	snp	C/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18763281	cctgcctcagcctcc[C/G]gagtagctgggacta	10517
rs8077093	snp	A/G	0.133777	0.221342	intron-variant	FBXW10	GRCh38.p7	17:18752662	agcttgcagtgagcc[A/G]agattgcgccactgc	10517
rs9674521	snp	C/T	0.00557542	0.0525036	intron-variant	FBXW10	GRCh38.p7	17:18777381	AAGACAGGTTTTATT[C/T]TGGGCAACATTCAAG	10517
rs9674947	snp	C/T	0.482384	0.0921818	intron-variant	FBXW10	GRCh38.p7	17:18769834	AGTTATGGCCAGTGC[C/T]GCTCAATCACACACA	10517
rs9783820	snp	A/C	0.475789	0.107327	intron-variant	FBXW10	GRCh38.p7	17:18757008	AATTCTAGGTATGAC[A/C]AACGGAATAAGGGCA	10517
rs9891495	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18752903	TTCAAGTCTGTTGCT[C/G]TTTTAAGTATAACAC	10517
rs9892842	snp	G/T	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18753318	aaagcagactcgggg[G/T]tatgcctgcagctgc	10517
rs9892969	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18752880	TTGAACGTGGACCTG[C/T]TTTTGTTTTCAAGTC	10517
rs9893944	snp	C/T	0.379746	0.213696			GRCh38.p7	17:18740728	GTATATATGTGCATG[C/T]GCTGGTTTCTCATGA	10517
rs9894485	snp	A/G	0.0376037	0.131863			GRCh38.p7	17:18741026	tcggcctcccaaagt[A/G]ctgggattacaagcg	10517
rs9895749	snp	A/G	0.460046	0.135575	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749757	CTCCGGTGTATATCC[A/G]AAATGAATAGGCTGT	10517
rs9895898	snp	C/T	0.387263	0.208947			GRCh38.p7	17:18740829	GCAGTGGTGCTATCT[C/T]GGCTCACTGCAAGCT	10517
rs9897266	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18778050	ggtcaggagatcgag[A/G]ccatcctggctaaca	10517
rs9898589	snp	C/T	0.316726	0.240931	intron-variant	FBXW10	GRCh38.p7	17:18769637	AAAAAATTAGCCAGG[C/T]GTGGTGGCGCATCAC	10517
rs9898823	snp	A/T	0.499816	0.0095829	intron-variant	FBXW10	GRCh38.p7	17:18750519	ATAAGGCTGCAAAGT[A/T]TTTTTTTAAGTTAAA	10517
rs9899562	snp	A/G	0.0263992	0.111815	intron-variant	FBXW10	GRCh38.p7	17:18757596	aggttacagggagtt[A/G]ttattgcgcccctgt	10517
rs9903004	snp	A/G	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18750784	CCAGAGGAACTGGCC[A/G]GAAGTGGGCCTGCCT	10517
rs9906011	snp	C/G	0.380529	0.213219	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779680	TTTCTGGTATTTTTG[C/G]ACAGAAGCCTGATAA	10517
rs9906823	snp	A/C	0.153997	0.230832	intron-variant	FBXW10	GRCh38.p7	17:18773984	ATTCAGTTTTCCATA[A/C]AAAGGCTAACATACA	10517
rs9907023	snp	A/G	0.43102	0.172429	intron-variant	FBXW10	GRCh38.p7	17:18754740	AGAGGAAGCAAAGGA[A/G]GGAGGGAAGGAGGGA	10517
rs9907681	snp	A/T	0.356811	0.226034	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779662	AGGGTCATGCATTGG[A/T]GTTTTCTGGTATTTT	10517
rs9908564	snp	C/T	0.489024	0.0732638			GRCh38.p7	17:18739168	CGAGAGCAGCCTGAC[C/T]AACATGGTGAAACTC	10517
rs9908821	snp	A/G	0.481396	0.0946345	intron-variant	FBXW10	GRCh38.p7	17:18776091	taggaggtggagatg[A/G]gcggattgcctgagg	10517
rs9909417	snp	A/G	0.467439	0.123371	intron-variant	FBXW10	GRCh38.p7	17:18776129	gtcgagaccagtctg[A/G]ccaacatggtgaaac	10517
rs9910784	snp	A/G	0.222928	0.24853	intron-variant	FBXW10	GRCh38.p7	17:18762558	caatctcctgacctc[A/G]tgatctgcccacctc	10517
rs9910881	snp	A/G	0.292008	0.246445	intron-variant	FBXW10	GRCh38.p7	17:18762350	ttgagatggagtctc[A/G]ctctgttgccaggct	10517
rs9911451	snp	A/T	0.473081	0.112848	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779697	CAGAAGCCTGATAAA[A/T]CCCATTAAGAATTTA	10517
rs9911990	snp	C/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18752187	gacgggtcgtgtggg[C/G]agtagcggacggtgt	10517
rs9912804	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18752645	gtgaacccgggaggc[A/G]gagcttgcagtgagc	10517
rs9914084	snp	A/G	0.0267878	0.112589	intron-variant	FBXW10	GRCh38.p7	17:18758896	TACGTggccaggcgc[A/G]gtggctcacgcctgt	10517
rs9914942	snp	A/G	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18767692	GGATCACAGTGAAAA[A/G]TGGCTGGCTTGGCCT	10517
rs10153280	snp	C/T	0.436976	0.165952	intron-variant	FBXW10	GRCh38.p7	17:18766504	GCTCCCTCAACCACC[C/T]GTATTCAGGGCGCTC	10517
rs10580273	in-del	-/AA	0.412416	0.190055	intron-variant	FBXW10	GRCh38.p7	17:18749375	AACCCCGCCTCTACT[-/AA]AAAAAAAAAAAATAC	10517
rs10659921	in-del	-/TTA/TTATT			intron-variant	FBXW10	GRCh38.p7	17:18758640	TAGAATACCTTCAGC[-/TTA/TTATT]TTTTTTTTGGCAAGG	10517
rs10775382	snp	A/C	0.314057	0.241654	intron-variant	FBXW10	GRCh38.p7	17:18768420	GTACCTACCGAGTGA[A/C]TGGCAGTCACAGATT	10517
rs11078420	snp	C/G	0.49655	0.04139	intron-variant	FBXW10	GRCh38.p7	17:18761065	AACCTGCCACTTCCT[C/G]CATTGATTTGAGGTG	10517
rs11331150	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18751240	TTTTTTTTTTTTTTT[-/T]AATGAGATGGAGTCT	10517
rs11336827	in-del	-/A	0.499853	0.008585	intron-variant	FBXW10	GRCh38.p7	17:18749547	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAGATTC	10517
rs11372212	in-del	-/T	0.444931	0.15653	intron-variant	FBXW10	GRCh38.p7	17:18758827	GGGAACGTGGTTTTT[-/T]ATGGGTTTGAGACAG	10517
rs11489009	snp	A/G	0.48178	0.0936921	intron-variant	FBXW10	GRCh38.p7	17:18771339	AAGAAACCTGTGCAG[A/G]GTATTTTCATTTCTT	10517
rs11510298	snp	C/G	0.469642	0.119404	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743783	TCATTGGGATAGCCA[C/G]TTTGTAACTGAACAG	10517
rs11544711	snp	A/T	0.4889	0.0736681	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744312	AGGGAACCGATTCCA[A/T]CCCTCTATGCCGGAA	10517
rs11651007	snp	C/T	0.484491	0.0866827	intron-variant	FBXW10	GRCh38.p7	17:18768874	ACTGTTAACCTCTTC[C/T]ACTCTCCCTTGTTTT	10517
rs11654164	snp	A/C	0.133777	0.221342			GRCh38.p7	17:18740500	ATGTGCCTAGTTTTT[A/C]ATCTCTATTTCTGGC	10517
rs11655952	snp	A/G	0.132066	0.220435	intron-variant	FBXW10	GRCh38.p7	17:18756959	ATGCTTAGTGTGGTG[A/G]TAACTGCTCTTTAGA	10517
rs11657036	snp	A/G	0.444444	0.157135	intron-variant	FBXW10	GRCh38.p7	17:18770343	TAGTTTCACTCTGTC[A/G]CACAGGCTGGAGTGC	10517
rs11657414	snp	C/G	0.416382	0.186593	intron-variant	FBXW10	GRCh38.p7	17:18765228	TGAACAACAATGGCT[C/G]CCATTTACTGAGTAC	10517
rs11657709	snp	C/T	0.131038	0.219882	intron-variant	FBXW10	GRCh38.p7	17:18755388	ggtgaaaccctgtct[C/T]tactaaaaatacaaa	10517
rs11657859	snp	G/T	0.497613	0.0344622	intron-variant	FBXW10	GRCh38.p7	17:18776035	AGAAAAAAAAAAAAA[G/T]TGGCCGGGCGCGGTG	10517
rs11867536	snp	C/T	0.109814	0.206997	intron-variant	FBXW10	GRCh38.p7	17:18759761	gagactacaggggcc[C/T]gccaccacaccaggc	10517
rs11870736	snp	C/T	0.130008	0.219321	intron-variant	FBXW10	GRCh38.p7	17:18766148	CAGTAAACCCACCCC[C/T]AGCTGTGACCATTTC	10517
rs12150401	snp	A/G	0.130351	0.219509	intron-variant	FBXW10	GRCh38.p7	17:18746651	GACTGGAGATCAACC[A/G]ACTTAATATCCTTAA	10517
rs12150592	snp	A/G	0.16618	0.23553	intron-variant	FBXW10	GRCh38.p7	17:18776520	GAGGGCTGCGCTAAC[A/G]ATGGGCATccttgta	10517
rs12452278	snp	C/T	0.38821	0.208322	intron-variant	FBXW10	GRCh38.p7	17:18769645	AGCCAGGTGTGGTGG[C/T]GCATCACTGTAATCC	10517
rs12452607	snp	A/T	0.00914312	0.0669923	intron-variant	FBXW10	GRCh38.p7	17:18765908	atttttttttttttt[A/T]agtagagacggggtt	10517
rs12602546	snp	A/G	0.464947	0.127663			GRCh38.p7	17:18741051	CAAGCGTGAACCACC[A/G]CGCCCAGCCAAGCTT	10517
rs12603304	snp	C/T	0.486	0.0824865	intron-variant	FBXW10	GRCh38.p7	17:18757963	ACTGTGTTCCTCTGA[C/T]GTTTTCCAAGAAAAA	10517
rs12603319	snp	C/T	0.212728	0.247206	intron-variant	FBXW10	GRCh38.p7	17:18758014	ATCCGGGCAATGCCA[C/T]ATACTCCATTCTCTC	10517
rs12603903	snp	C/T	0.00676609	0.0577691	intron-variant	FBXW10	GRCh38.p7	17:18752440	catttCTGggccagg[C/T]gcagcagctcacgcc	10517
rs12935972	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18761531	cggcctcccaaagtg[C/G]tgggattacaggcat	10517
rs12940441	snp	C/G	0.000116429	0.00762895	intron-variant	FBXW10	GRCh38.p7	17:18766697	CCCATGTCTTCCTCT[C/G]TCTCCCTCCTGTTCA	10517
rs12940935	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18766708	CTCTCTCTCCCTCCT[G/T]TTCAGTATGGGATGT	10517
rs12943180	snp	A/G	0.192715	0.243348	intron-variant	FBXW10	GRCh38.p7	17:18760490	GTTCATAGTATCTAC[A/G]TGAATTTTGTTGAAC	10517
rs12945049	snp	A/G	0.0146672	0.084371	intron-variant	FBXW10	GRCh38.p7	17:18770796	ATTATAGGAGAGTGG[A/G]GGGTGGCAGCAGCAG	10517
rs12946756	snp	A/G/T	0.604469	0.110764	intron-variant	FBXW10	GRCh38.p7	17:18777790	cctcgtgatccaccc[A/G/T]cctgggtctcccaaa	10517
rs12949129	snp	A/G	0.484279	0.0872533	intron-variant	FBXW10	GRCh38.p7	17:18758960	GTCACGAGGTCAGGA[A/G]ATCAAGACCATCCTG	10517
rs17852530	snp	C/T	0	0	synonymous-codon, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769948	GCTCGACGTGTCCCT[C/T]CTCTTCCTCCGGGTC	10517
rs28387012	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742015	CCGAGTAGCTGGAAC[C/T]ACAGGCGCCTGCCAC	10517
rs28407398	snp	G/T	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18765145	TAACTTTTTATTTCT[G/T]CAAAGGGCTCATTGT	10517
rs28490167	snp	A/G	0.0322114	0.122752			GRCh38.p7	17:18741238	GAGCTAGGTAGGACC[A/G]TGGTCTCTACTTCAT	10517
rs28496816	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742013	TCCCGAGTAGCTGGA[A/G]CTACAGGCGCCTGCC	10517
rs28529731	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18752446	TGggccaggtgcagc[A/G]gctcacgcctgtaat	10517
rs28602749	snp	C/T	0.316243	0.241064	intron-variant	FBXW10	GRCh38.p7	17:18770559	CACCCGTCACGGCCT[C/T]CCAAAGCGCTGGGAT	10517
rs28626269	snp	A/G	0.422	0.181428	intron-variant	FBXW10	GRCh38.p7	17:18759563	TTGGATGATTGTATC[A/G]TAACTCATTTATTTG	10517
rs28635232	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757103	ACATATACACATATG[C/T]ACATGTATATATATA	10517
rs28705187	snp	A/T			intron-variant	FBXW10	GRCh38.p7	17:18752673	agccgagattgcgcc[A/T]ctgcactccagcctg	10517
rs28707484	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18752497	aggcgggcggatcac[G/T]aggtcaggagtttga	10517
rs28711770	snp	A/G	0.172674	0.237741	intron-variant	FBXW10	GRCh38.p7	17:18762049	CTCACTGCCAGCTCC[A/G]CCTCCTGGGTTCATG	10517
rs28751991	snp	C/T					GRCh38.p7	17:18740769	TTTAAATTTTTTTTT[C/T]TTTTTTTTTGAGACG	10517
rs28757628	snp	C/T	0.481627	0.0940692	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779677	TGTTTTCTGGTATTT[C/T]TGCACAGAAGCCTGA	10517
rs34169181	in-del	-/G			intron-variant	FBXW10	GRCh38.p7	17:18774012	TCAATAGTAGCCGAT[-/G]CTAGTCTTACATCTG	10517
rs35123331	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18772947	GAGCGAAACTCCATC[-/T]CAAAAAAAAAAAAAA	10517
rs55791632	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18749389	TAAAAAAAAAAAAAA[C/T]ACAAAAAATTAGCCG	10517
rs55815282	in-del	-/T	0.499693	0.0123764	intron-variant	FBXW10	GRCh38.p7	17:18750630	ACTTGGATTTTTTTT[-/T]CCCCCAGCAGAGAGG	10517
rs55828488	snp	A/G	0.388398	0.208197	intron-variant	FBXW10	GRCh38.p7	17:18768362	TGAGCCACCGCACCC[A/G]GCCTCCATCGGCCTT	10517
rs55897765	snp	A/G	0.492871	0.0592773	intron-variant	FBXW10	GRCh38.p7	17:18778110	TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGAC	10517
rs55965678	in-del	-/CAG	0.483563	0.0891524	intron-variant	FBXW10	GRCh38.p7	17:18768119	CACCAGGCTGGAGCA[-/CAG]GCAGTGGTGAGATCT	10517
rs56009532	snp	A/G/T	0.164428	0.234899	intron-variant	FBXW10	GRCh38.p7	17:18771105	TTTCAGTCATGCTGC[A/G/T]AAAAAAAAAAAACAA	10517
rs56098216	in-del	-/AA					GRCh38.p7	17:18738286	AAAAAAAAAAAAAAA[-/AA]GATATGCTATGTCTG	10517
rs56195816	snp	A/G	0.270892	0.249126	intron-variant	FBXW10	GRCh38.p7	17:18751522	GGCGTGAGCCACCGC[A/G]CTCAGCCCGACACTT	10517
rs56296620	snp	A/T	0.100231	0.200173	intron-variant	FBXW10	GRCh38.p7	17:18760080	TGTATTAATTTACAT[A/T]CCCATTAGCAGCATA	10517
rs56355161	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18748341	GCGTGAAGCCGGGAG[G/T]CAGAGCTTGCAGTGA	10517
rs57336039	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18748432	AAAAAAAAAAAAAAA[-/A]GAAAGCCAATATGCA	10517
rs58696259	in-del	-/AAAA			intron-variant	FBXW10	GRCh38.p7	17:18748429	AAAAAAAAAAAAAAA[-/AAAA]GAAAGCCAATATGCA	10517
rs59007149	in-del	-/T/TT	0	0	intron-variant	FBXW10	GRCh38.p7	17:18768954	TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTCGC	10517
rs59130773	snp	C/G	0.401215	0.199083	intron-variant	FBXW10	GRCh38.p7	17:18766051	TCATTTTAGAAAACC[C/G]TGTTCTGCCACCCAC	10517
rs60883080	snp	C/T	0.330016	0.236849	intron-variant	FBXW10	GRCh38.p7	17:18776277	GCAGTGAGCTGAGAT[C/T]GTGCCACTGCAACTC	10517
rs60946049	in-del	-/T	0.499464	0.016365	intron-variant	FBXW10	GRCh38.p7	17:18770306	TTTTTTTTTTTTTTT[-/T]GAGACATAGTTTCAC	10517
rs61273748	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18769794	AAAAAAAAAAAAAAA[-/A]GACAGCAAACACCAT	10517
rs62073743	snp	C/T	0.473909	0.111197	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743514	GAGAGGACAGGTTGC[C/T]TGCTCGAGACCATAT	10517
rs62073745	snp	A/G	0.433473	0.169817	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744226	CGCAGGGCTAAAATG[A/G]ACTGGTTATCTTAGG	10517
rs62073747	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18758101	GTTTTTAAATTTAAC[A/G]GAAATGGATTTTTGT	10517
rs62073748	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18759817	AGAAGGGGTTTCCCC[A/G]TGTTAGCCAGGATGG	10517
rs62073749	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18759824	GTTTCCCCATGTTAG[C/T]CAGGATGGTCTCGAT	10517
rs62073750	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18759837	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	10517
rs62073751	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18759851	CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC	10517
rs62075096	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18774129	ACAATCACAAGGGGA[G/T]TTGCTTAACATTCTG	10517
rs62075097	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18774650	AATACAAAAAAATTA[A/G]CCGGTGTGGTGGCGC	10517
rs67053020	snp	C/G	0.474903	0.109173	intron-variant	FBXW10	GRCh38.p7	17:18776748	AGCTGGCATTTTGTA[C/G]TTGCTTGTATAAGTA	10517
rs67338964	snp	C/T	0.418653	0.184544	intron-variant	FBXW10	GRCh38.p7	17:18770497	TTAGTAGAGACGGGG[C/T]TTCACCATCTTGGCC	10517
rs71155351	in-del	-/A	0.48178	0.0936921	intron-variant	FBXW10	GRCh38.p7	17:18759619	GTGAGACTCCATCTC[-/A]AAAAAAAAAAACAAA	10517
rs71155352	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18760780	TTTTTTTTTTTTTTT[-/T]GAGACCGAGTTTCGC	10517
rs71185818	snp	A/G	0.0178098	0.0926698	intron-variant	FBXW10	GRCh38.p7	17:18754798	TTCATTTGCTTCCCA[A/G]TCTTTCTTTATTTCC	10517
rs71284781	in-del	-/A	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18761283	GCGAGACTCCGTCTT[-/A]AAAAAAAAAAAAAAG	10517
rs71284782	multinucleotide-polymorphism	GTGACAA/TTGACAG	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18754821	CAATTTTATCAAGTC[GTGACAA/TTGACAG]GGGCGCTTTCATTTG	10517
rs71367476	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18745596	TTTTTTGTATTTTTT[A/G]GTAGAGATGGGGTTT	10517
rs71367477	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18745710	TGAGCCACTGCACTC[A/G]ACCAGGGATTCTGTA	10517
rs71367478	snp	A/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18745763	TGCTGATGTTGCTGG[A/T]CTGGGGATCTGTCTT	10517
rs71367479	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18745876	TGGTGTCTGTTTTGC[C/T]TTGCTATAAAGGAAT	10517
rs71367480	snp	C/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18745880	GTCTGTTTTGCTTTG[C/G]TATAAAGGAATACCT	10517
rs71367481	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746010	TGGTGAGGGCTTCAG[A/G]AAGCTTCCACTTATG	10517
rs71367482	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746047	TGCAAGGGAAATCAA[C/T]GTATCATGAGGCAAG	10517
rs71367483	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746053	GGAAATCAATGTATC[A/G]TGAGGCAAGAGAAGT	10517
rs71367484	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746175	GGAAGGGCACCAAGC[C/T]ATTCATGAGGAATCT	10517
rs71367485	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746220	AAAACCTCCCATCAA[A/G]CCTTACTTCCAGCAC	10517
rs71367486	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746224	CCTCCCATCAAGCCT[C/T]ACTTCCAGCACTGGG	10517
rs71367487	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746235	GCCTTACTTCCAGCA[C/T]TGGGGGTCACATTTC	10517
rs71367488	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18746310	GCAAGAGAATTGAGC[C/T]TTGGAGGGGTCCAGG	10517
rs71372286	snp	C/T	0.307919	0.243198	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742311	GGGAGTGAGGCGCTG[C/T]CCTCTCGCACTCACT	10517
rs71372287	snp	A/G	0.475613	0.107697	intron-variant	FBXW10	GRCh38.p7	17:18757697	AAAACTCTCAGTTTG[A/G]ACAATACATTATTTG	10517
rs71372288	snp	A/C	0.417196	0.185864	intron-variant	FBXW10	GRCh38.p7	17:18763384	GATGGTCTCGATCTC[A/C]TGACCTCGTGATCTG	10517
rs71954242	in-del	-/AA/AAA			intron-variant	FBXW10	GRCh38.p7	17:18776021	AAGAAAAAAAAAAAA[-/AA/AAA]AGTGGCCGGGCGCGG	10517
rs72275127	in-del	-/CTTC			intron-variant	FBXW10	GRCh38.p7	17:18768027	TTCCTTCCTTCCTTT[-/CTTC]CTTCCTTCCTTCCTT	10517
rs72490632	in-del	-/AAAAA			intron-variant	FBXW10	GRCh38.p7	17:18762337	AGCGAGACTCCATCT[-/AAAAA]CAAAAAAAAAAAAAA	10517
rs73291490	snp	C/T	0.0267878	0.112589	intron-variant	FBXW10	GRCh38.p7	17:18758120	ATGGATTTTTGTCAT[C/T]GTGTGAGAGTGGGGA	10517
rs73293113	snp	C/G	0.474544	0.10991	intron-variant	FBXW10	GRCh38.p7	17:18776918	ACTAACTTGGAAAGA[C/G]ATCCACAATACATTA	10517
rs73981358	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18750639	ACTTGGATTTTTTTT[C/T]CCCCAGCAGAGAGGA	10517
rs74422951	snp	A/C	0.5	0	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742864	AGCGAGACTCTGCCT[A/C]CAAAAAAAAAAAATG	10517
rs74621204	snp	A/C	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18759169	AGCGAGACTCCATCT[A/C]AAAAAAAACCACATA	10517
rs74869072	snp	A/C	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760780	GCGAAACTCGGTCTC[A/C]AAAAAAAAAAAAAAA	10517
rs75131337	snp	G/T	0.109814	0.206997	intron-variant	FBXW10	GRCh38.p7	17:18748300	TGGCAGGCACCTGTA[G/T]TCCCAGCTACTGAGG	10517
rs75223724	snp	G/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18745433	CTTTTCTTTTTTTTT[G/T]GAGATGGAGTCTCGC	10517
rs75308505	snp	A/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18761283	CTTTTTTTTTTTTTT[A/T]AAGACGGAGTCTCGC	10517
rs75366322	snp	A/C	0.0955749	0.196603	intron-variant	FBXW10	GRCh38.p7	17:18775693	TATATATGTGAGATA[A/C]AGAGATAAGGGAGAA	10517
rs75549328	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18763685	GGGCAAGTGTTCTTG[C/T]TAAAAAACAGATAAT	10517
rs75742232	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18765916	TTTTTTTTAGTAGAG[A/C]CGGGGTTTCACCATG	10517
rs75892641	snp	C/T	0.0132779	0.0803907	intron-variant	FBXW10	GRCh38.p7	17:18772733	ACCCACAGAGCAGGT[C/T]GGGGTTTGGTGGGGG	10517
rs76349899	snp	C/T	0.0543475	0.155628			GRCh38.p7	17:18741655	GATAGGGGACTGGCA[C/T]GAAGCCTCCAGGCTG	10517
rs76656770	snp	A/G	0.114036	0.209795	intron-variant	FBXW10	GRCh38.p7	17:18748236	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	10517
rs76683595	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760371	GTCCAAAATCTGCAG[C/T]GTGGGGCCAGCAGGC	10517
rs76866171	snp	C/T	0.111224	0.207945	intron-variant	FBXW10	GRCh38.p7	17:18747678	TTCCCTGTTGCAATT[C/T]CTGACCTCGACTCTC	10517
rs76877955	snp	C/G	0.329084	0.237162	intron-variant	FBXW10	GRCh38.p7	17:18778156	TACTTGGGAGGCTGA[C/G]GCAGGAGAACGGCGT	10517
rs77010258	snp	C/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18766089	CTCTCATCCCCACTA[C/G]AAGATGCCAGGCAGT	10517
rs77420787	snp	A/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760794	CAAAAAAAAAAAAAA[A/T]ATCTCAATATGAATG	10517
rs77454435	snp	A/C	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760779	AGCGAAACTCGGTCT[A/C]AAAAAAAAAAAAAAA	10517
rs77764459	snp	A/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18749386	TACTAAAAAAAAAAA[A/T]AATACAAAAAATTAG	10517
rs77817142	snp	C/T	0.0104478	0.0715175	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779096	TGAACACTGAGTTCG[C/T]GCTGTTGACCGTGAA	10517
rs78522068	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18761285	TTTTTTTTTTTTTTA[A/G]GACGGAGTCTCGCTC	10517
rs78640521	snp	A/G/T	0.000115309	0.00759218	missense, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772479	AAGTGGCAGTATGCC[A/G/T]TGGAAAAAACGAAAC	10517
rs78709540	snp	A/G	0.109814	0.206997	intron-variant	FBXW10	GRCh38.p7	17:18750703	GGCGACAGTCTGACC[A/G]TCTTTACTGGTCCCC	10517
rs78926552	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18755550	ACAGAGCGAGACTCC[G/T]TCTGAAAAAAAAAAA	10517
rs78991050	snp	A/C	0	0	intron-variant	FBXW10	GRCh38.p7	17:18752714	TGAGATTCCATCTCA[A/C]AAAAAAAAAAAAAGA	10517
rs79326915	snp	A/C/G	0.0263992	0.111815	intron-variant	FBXW10	GRCh38.p7	17:18759907	GGTGTGAGCCACCGC[A/C/G]CCGGGCCCTTGTTTC	10517
rs79377474	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18762081	CATTCTCCTTCCTCA[G/T]CCTCCCGAGTAGCTG	10517
rs79431518	snp	C/T	0.0588605	0.161139	intron-variant	FBXW10	GRCh38.p7	17:18745709	GTGAGCCACTGCACT[C/T]GACCAGGGATTCTGT	10517
rs79883718	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18774531	GGGCGCAGTGACTCA[G/T]GCCTGTAATCCCAGC	10517
rs80167378	snp	A/C	0.492037	0.0625946			GRCh38.p7	17:18738265	CCGGGGCAACAGAGC[A/C]AGAAAAAAAAAAAAA	10517
rs80173819	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760772	CAACAAGAGCGAAAC[G/T]CGGTCTCAAAAAAAA	10517
rs80244261	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18777562	TCTTTTTTTTTTTTT[G/T]AGACTGAGTCTTGCT	10517
rs111636289	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18761152	TGATCTAGTCCACTG[C/T]CTTTCTGTTTTTAAT	10517
rs111726697	snp	A/C	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18755221	TGAGCCAAGATCATG[A/C]CATTGCACTCCAGCC	10517
rs111771692	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18765253	GAGTACCAGTTTTGT[G/T]ACAGATGCTTAACAT	10517
rs112015776	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760767	CAGGGCAACAAGAGC[A/G]AAACTCGGTCTCAAA	10517
rs112031344	snp	A/T			intron-variant	FBXW10	GRCh38.p7	17:18748622	GAGGAGCAAGGATTA[A/T]ATTGATCAATATGGC	10517
rs112087876	snp	C/T	0.27008	0.249192	intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18745075	CCTTAATGCTGGTGT[C/T]GTTCCTGCTTTAGGG	10517
rs112251084	snp	A/C	0.0185938	0.0946107	intron-variant	FBXW10	GRCh38.p7	17:18765826	CTGCCTCCCGGGTTC[A/C]AGTGATTCTCCTGCC	10517
rs112345740	snp	G/T	0.0622301	0.165053	intron-variant	FBXW10	GRCh38.p7	17:18770884	CTGCATTGTATACAG[G/T]ACTGTGCTTTATATA	10517
rs112397760	snp	G/T	0.130008	0.219321	intron-variant	FBXW10	GRCh38.p7	17:18762718	CCATGGCAGGCAGTA[G/T]CAGTGAGAGTGGGCA	10517
rs112401670	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18768055	TTCCTTCCTTCCTTC[C/T]TTCTTTCTTTCTTTC	10517
rs112512764	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18761132	GAGAATGTCCCTGAG[C/T]TCTCTGATCTAGTCC	10517
rs112514629	snp	A/T	0.132066	0.220435	intron-variant	FBXW10	GRCh38.p7	17:18771208	AGTCTAAAAGGGATT[A/T]CTTATTGGAATGACA	10517
rs112612709	in-del	-/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18757688	CACAATAAAAAACTC[-/T]TCAGTTTGGACAATA	10517
rs112635679	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18755803	AAAGTTCATGGAATC[A/G]GGGCACATGGAAAAT	10517
rs112698715	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743156	TTCTCCAGATTCCTC[C/T]TCAGACAGAAGAGGT	10517
rs112705082	snp	C/G	0.5	0	intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771714	CTTAAAACAAACAAA[C/G]AAACAAAAACACTGA	10517
rs112767708	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18761096	CTATCTTTATCACAT[G/T]GAAATTTCCCATATG	10517
rs112851417	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760878	CCCTCTTCTAGGTCA[C/T]AGAGATATTTTCTAA	10517
rs112945350	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760983	TGTGGCATTAGGTAG[A/G]GTTTCCATTTCATTT	10517
rs113012809	in-del	-/A	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18752713	GTGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAG	10517
rs113034979	snp	C/T	0.475081	0.108804	intron-variant	FBXW10	GRCh38.p7	17:18777809	GGGTCTCCCAAAGTG[C/T]GGGGATTACAGGCGT	10517
rs113103355	snp	A/G	0.270892	0.249126	intron-variant	FBXW10	GRCh38.p7	17:18760101	TAGCAGCATATGAGA[A/G]TATCTCTTCTTATAT	10517
rs113240009	in-del	-/A/AA	0.644684	0.0773268	intron-variant	FBXW10	GRCh38.p7	17:18755554	GCGAGACTCCGTCTG[-/A/AA]AAAAAAAAAAATGCA	10517
rs113241523	snp	C/T	0.00438332	0.0466095	intron-variant	FBXW10	GRCh38.p7	17:18776587	AAGGGTAAAGTCCTA[C/T]GAGTGAAATTGCTAA	10517
rs113244333	snp	A/G	0.5	0	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742852	CCTGGGGGATAGAGC[A/G]AGACTCTGCCTCCAA	10517
rs113270520	snp	A/G	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760974	AACCTTGTATGTGGC[A/G]TTAGGTAGGGTTTCC	10517
rs113295874	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18757211	TTTTTTCAGAGTGAA[C/T]CTCATTCTGTCGTCC	10517
rs113309595	snp	A/C					GRCh38.p7	17:18738272	AACAGAGCCAGAAAA[A/C]AAAAAAAAAAAAAAA	10517
rs113432878	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18768026	CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT	10517
rs113487778	snp	A/G	0.00835141	0.0640778	intron-variant	FBXW10	GRCh38.p7	17:18753906	AAGAGAGAGAAAAGG[A/G]AGAGAAGCAGAGAAG	10517
rs113490240	snp	C/T	0.5	0			GRCh38.p7	17:18740783	TCTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT	10517
rs113518293	snp	C/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760325	AGATTTACTATAAAG[C/T]ATTGACTTGTGTGAT	10517
rs113535784	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771702	TTGGAAGCTGTGCTT[A/C]AAACAAACAAAGAAA	10517
rs113552455	snp	A/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18751893	ACTAGTTCTTGGGCA[A/T]TAATGAAGAGTGACC	10517
rs113598378	snp	G/T	0.5	0	intron-variant	FBXW10	GRCh38.p7	17:18760473	GACTATCTATTAACT[G/T]TGTTCATAGTATCTA	10517
rs113607588	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18777072	ACTCAGTTTTTTTTT[C/T]TTTTTTTGAGATGGA	10517
rs113755907	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18756625	TTTTAGTAGAAGTGG[G/T]GTTATATTACACATA	10517
rs113783531	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18766031	TGGGCCCGGCATTAA[A/C]TTCTTCATTTTAGAA	10517
rs114067349	snp	C/T	0.0119091	0.0762411	intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18745377	CCTCCCCCAGAACTT[C/T]GGACTCAGCAGGTCT	10517
rs114381083	snp	A/T	0.211373	0.246998	intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744865	CAGAGATTGCACAGA[A/T]CTCAGCATAGGTTTT	10517
rs114608528	snp	G/T	0.140919	0.224948	intron-variant	FBXW10	GRCh38.p7	17:18748688	CCCACAAGACACATC[G/T]GAAGATAGAGATCAG	10517
rs115378294	snp	C/T	0.131723	0.220251	intron-variant	FBXW10	GRCh38.p7	17:18756737	GACATCATTTCAATA[C/T]GCTGAGAGACGAAGT	10517
rs115894780	snp	C/T	0.0123036	0.0774623	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18772182	GGAACATATGTGCCC[C/T]GATCATGTTTATTTT	10517
rs117084603	snp	A/G	0.0103295	0.0711199	intron-variant	FBXW10	GRCh38.p7	17:18776788	TCCGCATTTTCTTCT[A/G]GGTTGACCATTAACA	10517
rs117585894	snp	A/G	0.00284574	0.0376135	synonymous-codon, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18770032	CTGTATGAAGGTGTT[A/G]AAAGCCAATGGCAGA	10517
rs117869831	snp	C/T	0.00953873	0.0683987	intron-variant	FBXW10	GRCh38.p7	17:18775855	CCACTTAGCAAGACC[C/T]TTGTCTCTACCAAAA	10517
rs117902994	snp	C/T	0.0138799	0.0821421	intron-variant	FBXW10	GRCh38.p7	17:18752877	CATTTGAACGTGGAC[C/T]TGTTTTTGTTTTCAA	10517
rs137911010	snp	A/C	0.00398564	0.0444627	intron-variant	FBXW10	GRCh38.p7	17:18761091	AGGTGCTATCTTTAT[A/C]ACATTGAAATTTCCC	10517
rs137965030	snp	A/C	0.000115322	0.00759261	missense, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772498	AAAAAACGAAACAAA[A/C]GAAGAATAAGGAGAA	10517
rs138093156	snp	C/T	6.63438e-05	0.00575912	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758491	CCTAAGCGGGAGCTA[C/T]GACCTAAGTATCAGG	10517
rs138178982	snp	A/G	0.00517822	0.0506191	intron-variant	FBXW10	GRCh38.p7	17:18767654	GCGGGTGGTGTTGAT[A/G]TATGATTTGCAGCAG	10517
rs138269216	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18774919	AAGATGATGGATATC[C/T]TAATTATCTTGATCT	10517
rs138370993	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760996	AGGGTTTCCATTTCA[C/T]TTATTCATATTTAGA	10517
rs138485280	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18755275	TCTTAAAAAAATTGC[A/G]GCCGGGCCTGGTGGC	10517
rs138524337	snp	C/T	0.104859	0.203554	intron-variant	FBXW10	GRCh38.p7	17:18753313	AAGCTAAAGCAGACT[C/T]GGGGGTATGCCTGCA	10517
rs138532528	snp	A/C	0.137527	0.223271	intron-variant	FBXW10	GRCh38.p7	17:18749421	GCGTGGTGGCGGGCT[A/C]CTGTAGTCCCAGCTA	10517
rs138571078	snp	C/T	0.0166325	0.0896639	intron-variant	FBXW10	GRCh38.p7	17:18747127	GAGACGGGGTTTCAC[C/T]GTGTTAGCCCGGATG	10517
rs138625739	snp	C/T	0.00234426	0.034156	stop-gained, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766815	GTGAGCAGCTGTGAG[C/T]GAGGGCTGGTGAAAG	10517
rs138647311	snp	C/T	0.00174474	0.0294843	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744350	ACGTGTGTCTTAGCC[C/T]GGAAGATCTTCTCTA	10517
rs138657360	snp	A/G	1.64749e-05	0.00287005	missense, nc-transcript-variant, synonymous-codon	FBXW10	GRCh38.p7	17:18772463	CCAGTTTGAGCACAT[A/G]AAGTGGCAGTATGCC	10517
rs138784093	in-del	-/T	0.114387	0.210022	intron-variant	FBXW10	GRCh38.p7	17:18760834	ATCAGTTTATCAGGG[-/T]TTTTTTTTTCTTCAT	10517
rs139071521	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18776819	AACTAAATGTCCATC[A/G]ATGGGCAATGGCTAA	10517
rs139177136	snp	C/T	0.000807362	0.0200756	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772625	TGTGATCCAAGAGCT[C/T]CTACCAGGCAAACCT	10517
rs139181456	snp	A/G	0.130351	0.219509	intron-variant	FBXW10	GRCh38.p7	17:18747427	ATAGCCAGGTGTCAT[A/G]CACTTGTAATCCCAG	10517
rs139214917	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18760466	TTGCCAGGACTATCT[A/G]TTAACTGTGTTCATA	10517
rs139219182	snp	C/G	0.0111196	0.0737302	intron-variant	FBXW10	GRCh38.p7	17:18753172	ATAAGACATCTAGGG[C/G]ACAGAGGGAAGTGGG	10517
rs139437992	snp	A/G					GRCh38.p7	17:18739283	GAATTGCATGAACCC[A/G]GAGGCAGAGGTTGCA	10517
rs139505028	snp	A/G	0.02016	0.0983543	intron-variant	FBXW10	GRCh38.p7	17:18757223	GAACCTCATTCTGTC[A/G]TCCAGGCTGGGCTGC	10517
rs139583755	snp	A/T	0.00318978	0.0398085	intron-variant	FBXW10	GRCh38.p7	17:18773578	CATTATGTGTGGGTT[A/T]GAGTAGCAAGACTCC	10517
rs139592358	snp	A/G	0.0123036	0.0774623			GRCh38.p7	17:18739056	ATTTGGGCCGGGTGC[A/G]GTGGCTCATGCCTGT	10517
rs139724959	snp	C/T	0.000153988	0.00877328	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778882	CAGCCCATGATTATC[C/T]GCTCCAGGTTCTCTG	10517
rs139736412	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18741045	GGATTACAAGCGTGA[A/G]CCACCGCGCCCAGCC	10517
rs139842854	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749822	CGATCCCTGCAATCT[A/G]TTGGTTGACCTGGAT	10517
rs139854520	snp	A/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18751909	TAATGAAGAGTGACC[A/G]GAAGACTCTTCGAGC	10517
rs139952195	snp	C/T	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18768308	CCTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC	10517
rs140032131	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18764201	ATGATGTAAATACTC[-/T]TTTTTTTTTTTTTTT	10517
rs140063499	snp	C/G	6.77381e-05	0.00581932	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778793	AACGAACCAGTATTC[C/G]CCTTGAAATCCAGAA	10517
rs140154912	snp	A/C	0.147656	0.228091	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743461	ACCCACCTTTATCTT[A/C]TCCATCCTCATAACT	10517
rs140161487	snp	A/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18760497	GTATCTACATGAATT[A/T]TGTTGAACAAAAATT	10517
rs140249969	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18751520	CAGGCGTGAGCCACC[A/G]CGCTCAGCCCGACAC	10517
rs140324566	snp	A/G	0.0256215	0.110247	intron-variant	FBXW10	GRCh38.p7	17:18772959	TTGAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG	10517
rs140412541	snp	A/G	0.00120068	0.0244724	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758483	AACTTTCTCCTAAGC[A/G]GGAGCTATGACCTAA	10517
rs140472895	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18774302	AGCTGCGCTATGTGA[C/T]TCAGTTTCCAGGGTT	10517
rs140493980	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759993	TGGTGCCCATGTGCA[C/T]GAGTTTTTTAAAGGT	10517
rs140625978	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18776046	AAAAGTGGCCGGGCG[C/T]GGTGGCTCACACCTG	10517
rs140734253	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18754987	GCAAATGCAGGCTGG[G/T]CGTGGTGGCTCACAC	10517
rs140740094	snp	A/C/G	0.0283518	0.115709	intron-variant	FBXW10	GRCh38.p7	17:18764683	CTACATGGGTTCTAC[A/C/G]CAGTATGATCCTCTG	10517
rs140944543	snp	A/G	0.00378164	0.0433188	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751006	AAAATGGTAGATGAC[A/G]GGAAGAGCATGCGTG	10517
rs140982768	snp	A/G	3.2962e-05	0.00405954	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768630	GTCATGGCCTGGAGC[A/G]TGGTGGGGAAGTACG	10517
rs141000193	snp	A/T	0.000620529	0.0176034	intron-variant	FBXW10	GRCh38.p7	17:18750911	TTTATTTTTATTTTT[A/T]ATTTTTTGTCTTTTT	10517
rs141060553	snp	A/G	0.0138799	0.0821421	intron-variant	FBXW10	GRCh38.p7	17:18756624	ATTTTAGTAGAAGTG[A/G]TGTTATATTACACAT	10517
rs141093964	snp	C/T	0.021333	0.101051	intron-variant	FBXW10	GRCh38.p7	17:18774119	TAAAGAGGTGACAAT[C/T]ACAAGGGGAGTTGCT	10517
rs141190398	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18760393	CCAGCAGGCTGGAGA[C/T]CCAGGAGAGCCAACG	10517
rs141241128	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18772166	GAGAAGTGAAACAAT[C/T]GGAACATATGTGCCC	10517
rs141626132	snp	A/G	0.00838913	0.0642198	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766816	TGAGCAGCTGTGAGC[A/G]AGGGCTGGTGAAAGT	10517
rs141641344	snp	C/T	0.0170251	0.090679	intron-variant	FBXW10	GRCh38.p7	17:18747220	CATGAACCATCACGC[C/T]GGGCCAACAACCTTC	10517
rs141775838	snp	A/G	0.00636936	0.0560724	intron-variant	FBXW10	GRCh38.p7	17:18775935	GAAGCTGAGGCGGGA[A/G]GATCCTTTGAGTCCA	10517
rs142015040	snp	A/T	0.00318978	0.0398085	intron-variant	FBXW10	GRCh38.p7	17:18764534	TCCATTTTATCAATG[A/T]GGAAAGGAAACGTAA	10517
rs142047019	snp	C/G/T	0.00212922	0.0325597	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756154	GCATTCTCTCTGACA[C/G/T]GTAGGTACTGGGGTC	10517
rs142357409	snp	C/T	0.0345262	0.126772	intron-variant	FBXW10	GRCh38.p7	17:18752273	TCTGGCTAATTATTG[C/T]CTTGAGAGATTGTCT	10517
rs142382185	in-del	-/TTAAAGTCTATT	0.456095	0.141508	intron-variant	FBXW10	GRCh38.p7	17:18751993	TGCCCCCCACTCTGC[-/TTAAAGTCTATT]TTAAAGTCTATTTAA	10517
rs142465313	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18761095	GCTATCTTTATCACA[C/T]TGAAATTTCCCATAT	10517
rs142498785	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18767415	AACCAGGGAGGCAGA[C/T]GTTGCAGTGAGCCGA	10517
rs142528410	snp	A/G	3.29636e-05	0.00405964	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744587	TTGGATAAAACAGTA[A/G]AACAGAAGATGAAAG	10517
rs142568223	snp	C/T	0.000307953	0.0124049	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766747	GGAAGTGCCTGAAGA[C/T]GTTTAGACACAAAGA	10517
rs142829135	snp	C/T	0.00398564	0.0444627	intron-variant	FBXW10	GRCh38.p7	17:18760120	CTCTTCTTATATATT[C/T]TCACCAACACTTACT	10517
rs142899455	snp	A/C	0.00517822	0.0506191	intron-variant	FBXW10	GRCh38.p7	17:18773603	GACTCCTTCCTTTTA[A/C]CAGCCCTATATTTGG	10517
rs142904621	snp	C/T	0.0033463	0.0407671	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778862	GAGTCCAGTCCACCA[C/T]ACCCCAGCCCATGAT	10517
rs142907451	snp	C/T					GRCh38.p7	17:18741400	CAGGCCAGGTGGCAG[C/T]AGGGGAAGGCAAAGG	10517
rs143215236	snp	A/G	0.000724542	0.0190196	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769992	CAGATGGCAAGATCC[A/G]AATTTACAATTTCCT	10517
rs143308813	snp	C/T	0.00040765	0.0142709	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778753	GTTGATCGGTTGAGA[C/T]TGAGCAATCCTCCTA	10517
rs143325815	snp	A/C/G	0.0186378	0.0950629	intron-variant	FBXW10	GRCh38.p7	17:18767549	TTTTTTTTTCTCCAT[A/C/G]CTCTCTAATGAAGAG	10517
rs143459755	snp	A/G	0.000263791	0.0114815	missense, upstream-variant-2KB, intron-variant, downstream-variant-500B	FBXW10, TVP23B	GRCh38.p7	17:18779051	AGAAAGAACGGCCTC[A/G]CATCTATACAGCCCT	10517
rs143545979	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775579	ATGTCATCAATCTGA[A/G]AAATGGGCACAATAA	10517
rs143573197	snp	C/T	0.000153988	0.00877328	stop-gained, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744476	TTCCAAAATATCCTT[C/T]AGACCACACAGGGAA	10517
rs143595427	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18748940	TACATGAAATATCAT[C/T]GGAAACACAATATCA	10517
rs143662391	snp	C/G/T	0.0139261	0.0824398	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744338	CGGAAGTGTGAGACG[C/G/T]GTGTCTTAGCCTGGA	10517
rs143834097	snp	C/T	0.030665	0.119967	intron-variant	FBXW10	GRCh38.p7	17:18769498	AAAATGACAGCAGGC[C/T]GGGCATGGTGGCGCA	10517
rs144179290	snp	A/G	0.0115593	0.0751402	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756082	CATACCAGAACGAGG[A/G]AACGCAGCAGGTCCT	10517
rs144291569	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18773168	AAACTCCCGACCTCA[A/G]GTGATCCTCCCGGCT	10517
rs144304817	snp	G/T	0.0551013	0.156571	intron-variant	FBXW10	GRCh38.p7	17:18767866	TCTGGCCCTCTCTAG[G/T]GCTCCAAGAAGGTAG	10517
rs144354447	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18770814	GTGGCAGCAGCAGGG[A/G]GTACAGTGGGGGAAA	10517
rs144428015	snp	A/G	0.132167	0.220489	intron-variant	FBXW10	GRCh38.p7	17:18750160	CTGCAAGTCTGAAAG[A/G]GGAATGTCTGAGACC	10517
rs144460161	snp	A/G	0.00143346	0.0267334	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766830	CGAGGGCTGGTGAAA[A/G]TGTGGCACATTGCCA	10517
rs144567782	snp	A/G	0.000182305	0.00954564	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766715	TCCCTCCTGTTCAGT[A/G]TGGGATGTAGACACA	10517
rs144641799	snp	C/T	0.0894459	0.191631			GRCh38.p7	17:18739228	CTGGGCATGGTGGTG[C/T]GTGCCTGTAATCCCA	10517
rs144724584	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766766	TAGACACAAAGACCC[C/T]ATCTTGGCCACCAGG	10517
rs144799584	snp	C/T	0.00795532	0.062565	intron-variant	FBXW10	GRCh38.p7	17:18763779	GTGATTGGTAAAGGA[C/T]TCTGTTGCTCTTGTT	10517
rs144820718	snp	C/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18770048	AAAGCCAATGGCAGA[C/G]GTGATCCTGTGCTGT	10517
rs144924038	snp	A/G	0.0166325	0.0896639	intron-variant	FBXW10	GRCh38.p7	17:18751289	GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC	10517
rs144992749	snp	A/G	0.0333695	0.124785			GRCh38.p7	17:18739306	AGGTTGCAGTGAGCC[A/G]ATATTGCACCACTGC	10517
rs145174674	snp	C/T	0.00517822	0.0506191	intron-variant	FBXW10	GRCh38.p7	17:18756388	TATGCTGACCAACAA[C/T]CTTTTGCACAAGTCA	10517
rs145231603	snp	A/G	0.0001318	0.00811681	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769940	AGGGAGGTGCTCGAC[A/G]TGTCCCTTCTCTTCC	10517
rs145299110	snp	A/G	0.00199481	0.0315187			GRCh38.p7	17:18741063	ACCGCGCCCAGCCAA[A/G]CTTTTTAAAATTCAA	10517
rs145368701	snp	A/G	0.000177579	0.00942114	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750105	GACTTGTCAGCGCAC[A/G]GCTTCATTCAGAACC	10517
rs145424802	snp	A/G	0.030665	0.119967	intron-variant	FBXW10	GRCh38.p7	17:18750811	GCCTGCTGCAGCCAG[A/G]GCTTACCCATCCTTC	10517
rs145569250	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18765223	GTCCATGAACAACAA[C/T]GGCTGCCATTTACTG	10517
rs145674248	snp	C/T	0.128632	0.218563	intron-variant	FBXW10	GRCh38.p7	17:18745537	TCTCCTGCCTCAGCC[C/T]CCCAAGTAGCTGGGA	10517
rs145723699	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18771835	AACTTGAGGCCAGGC[G/T]CAGTGGCTCGTGCTT	10517
rs145762173	in-del	-/T	0.148661	0.22854	intron-variant	FBXW10	GRCh38.p7	17:18759778	CACCACACCAGGCTA[-/T]ATTTTTTTTTGTATT	10517
rs145973790	snp	C/T	6.62877e-05	0.00575669	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744652	GACCAAGGCGAATTA[C/T]ACTCTCTTACTGCTG	10517
rs146416419	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18765570	CACACCTTGAGTCAT[C/T]GCCGGCTGTTAGTGC	10517
rs146517457	snp	A/C/T	0.000461137	0.0151777	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18770018	TTCCTCAACGGGAAC[A/C/T]GTATGAAGGTGTTAA	10517
rs146558751	snp	A/C	0.34659	0.230587	intron-variant	FBXW10	GRCh38.p7	17:18777819	AAGTGTGGGGATTAC[A/C]GGCGTGAGCCACCGC	10517
rs146665253	snp	C/T	0.0119091	0.0762411	intron-variant	FBXW10	GRCh38.p7	17:18751519	ACAGGCGTGAGCCAC[C/T]GCGCTCAGCCCGACA	10517
rs146670163	snp	C/T	0.101301	0.200969	intron-variant	FBXW10	GRCh38.p7	17:18774782	TCTGGGCAACAAGAG[C/T]GAAACTGCATCTCAA	10517
rs146781245	snp	A/G	0.02016	0.0983543	intron-variant	FBXW10	GRCh38.p7	17:18774204	TTAGTCTTGGTTTCA[A/G]TGAAGAATAGAGAGT	10517
rs146784395	snp	C/T	0.000155988	0.00883003	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778929	AGACCAAGTGACCAG[C/T]TCAATTGAAAGGGCT	10517
rs147138981	snp	A/G	0.00141998	0.0266078	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772652	ACCTCCCAAGTCCCG[A/G]GTACTCCTGAAGCCG	10517
rs147227828	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18775960	AGTCCAGGAGCTTGA[C/T]GTTACAGTGAGCTAT	10517
rs147350518	snp	C/T	1.66211e-05	0.00288275	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778878	ACCCCAGCCCATGAT[C/T]ATCCGCTCCAGGTTC	10517
rs147454197	snp	C/G	0.0532157	0.154195	intron-variant	FBXW10	GRCh38.p7	17:18750697	GAGGCTGGCGACAGT[C/G]TGACCGTCTTTACTG	10517
rs147519900	snp	C/T	0.000101588	0.00712627	stop-gained, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778780	CCTATAGATGTGAAA[C/T]GAACCAGTATTCCCC	10517
rs147719420	snp	A/C	0.130399	0.219535	intron-variant	FBXW10	GRCh38.p7	17:18756432	TATTTTTTGAAATAT[A/C]TTTATTTTGTTTTAT	10517
rs147772607	snp	C/T	0.115438	0.210697	intron-variant	FBXW10	GRCh38.p7	17:18756241	TGACCTTTGTGTACA[C/T]GGAAAGGCAAGCTCT	10517
rs147788281	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18755098	TGAAACTCCGTCGCT[A/G]CTAAAAATACAAAAA	10517
rs147788841	snp	A/C	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18773265	CAAACTTATAAGAAC[A/C]TTTGCACAGTAGATA	10517
rs147905984	snp	G/T	0.000134694	0.00820541	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756066	TACAACCTGTGGACT[G/T]CATACCAGAACGAGG	10517
rs147924107	snp	C/T	0.00318978	0.0398085	intron-variant	FBXW10	GRCh38.p7	17:18771189	TTCGGCTTGAGTGAA[C/T]GTAAGTCTAAAAGGG	10517
rs147930073	snp	A/G	0.000593903	0.017222	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768645	ATGGTGGGGAAGTAC[A/G]AGCGCTGCCTGATGG	10517
rs148015675	snp	C/T	0.0217236	0.101931	intron-variant	FBXW10	GRCh38.p7	17:18755065	GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACGT	10517
rs148027955	snp	G/T	0.000313265	0.0125114	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744512	TTCATCTATAACAGG[G/T]CCCGGATCAACCTCA	10517
rs148135561	snp	A/G	0.0252325	0.109451	intron-variant	FBXW10	GRCh38.p7	17:18767199	TCTGTAGGGCCAGGC[A/G]CAGTGGCTCACACCT	10517
rs148248453	snp	A/G	0.00597247	0.0543191	intron-variant	FBXW10	GRCh38.p7	17:18746542	TAGATCACAATATAT[A/G]TCACTTGATTTATTT	10517
rs148396663	snp	A/C	1.64882e-05	0.00287121	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768540	TTCTTGCAGACTCTC[A/C]GTGGCCATGAGGGAG	10517
rs148778764	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18777045	TAGGGAAGATTTTGA[C/T]ATCTTGATTTCACTC	10517
rs148854428	snp	A/G	0.00478085	0.0486577			GRCh38.p7	17:18741379	CCTGAGTCCCTGCTG[A/G]CTGGCCAGGCCAGGT	10517
rs148936383	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18760702	CAGCTACTCAGGAAG[C/G]CTGAGGCAGGAGAAT	10517
rs149007393	snp	C/G	0.131723	0.220251	intron-variant	FBXW10	GRCh38.p7	17:18756829	GTTTTGCAAAGTCCA[C/G]TTCTACTTTATTTTT	10517
rs149011771	snp	C/T	0.0154538	0.0865337	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743624	CTTTCTGTGAGCTGC[C/T]CAATATGTTTTGCCT	10517
rs149050467	snp	C/T	0	0			GRCh38.p7	17:18739907	ATGATGTCCCTAAAT[C/T]AAGTAGACTAAATAT	10517
rs149076818	snp	C/T	0.0490535	0.14873	intron-variant	FBXW10	GRCh38.p7	17:18778166	GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGAA	10517
rs149093897	snp	A/G	0.321292	0.23962	intron-variant	FBXW10	GRCh38.p7	17:18762443	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10517
rs149142028	snp	C/G/T	3.29485e-05	0.00405874	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769949	CTCGACGTGTCCCTT[C/G/T]TCTTCCTCCGGGTCA	10517
rs149323817	snp	C/T	0.000231302	0.0107516	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744453	ATAGCTTATATTTGT[C/T]ACACTATTTCCAAAA	10517
rs149324181	snp	C/T	6.34659e-05	0.00563284	intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744873	GCACAGAACTCAGCA[C/T]AGGTTTTTTGAACTG	10517
rs149546887	snp	C/G	6.59609e-05	0.00574248	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772634	AGAGCTCCTACCAGG[C/G]AAACCTCCCAAGTCC	10517
rs149590497	snp	A/C/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18774922	ATGATGGATATCCTA[A/C/G]TTATCTTGATCTGAT	10517
rs149594366	snp	A/G	0.0123036	0.0774623			GRCh38.p7	17:18741931	CGCCCAGGCTGGAGT[A/G]CAGTGGCACATCTCC	10517
rs149783676	snp	A/C/G	0.0012159	0.0246314	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778889	TGATTATCCGCTCCA[A/C/G]GTTCTCTGGCAGCTT	10517
rs149882032	snp	C/T	0.000708209	0.0188043	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768602	TCTCCTCTCAGGAAG[C/T]ACTGATGGCCTGGTC	10517
rs149906800	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743310	TGGTCTTTCAACATG[A/G]GCATTAGAAAGGCAC	10517
rs149915973	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18776889	TAAAAATTGTATGAT[A/G]AGGATCTGTATATAC	10517
rs149924362	snp	C/T			synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751042	CATCCGAAGTGGAAG[C/T]TGAGAACGAAGGTGG	10517
rs150006059	snp	C/T	6.59044e-05	0.00574002	synonymous-codon, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769939	CAGGGAGGTGCTCGA[C/T]GTGTCCCTTCTCTTC	10517
rs150056591	in-del	-/TCAT			intron-variant	FBXW10	GRCh38.p7	17:18752208	CGGACGGTGTGGCTG[-/TCAT]GGACTGGACAGTTCA	10517
rs150057313	snp	A/G	0.00848606	0.0645834	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750090	CAACAGGTCAAGATG[A/G]ACTTGTCAGCGCACG	10517
rs150230158	snp	C/T	0.0193772	0.0965046	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744150	ATAGAAAAGGCACAA[C/T]TGGGGTATTTATTCA	10517
rs150234775	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18751713	CCATGCCTCTGGAGG[A/C]TCCAGCATCTGCTGC	10517
rs150284688	snp	A/T	0.00358779	0.0422022	intron-variant	FBXW10	GRCh38.p7	17:18752913	TTGCTCTTTTAAGTA[A/T]AACACAAAGAATACC	10517
rs150329747	snp	C/T	0.0146839	0.0844177	missense, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772489	ATGCCGTGGAAAAAA[C/T]GAAACAAAAGAAGAA	10517
rs150381644	snp	C/T	3.3211e-05	0.00407485	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758489	CTCCTAAGCGGGAGC[C/T]ATGACCTAAGTATCA	10517
rs150425811	snp	C/T					GRCh38.p7	17:18741823	CTGGCGCCATGTCCC[C/T]GCATTGGCCTATCCC	10517
rs150445604	snp	A/G	0.00874735	0.0655527	intron-variant	FBXW10	GRCh38.p7	17:18765752	TTTTTTTTTGAGATG[A/G]AGTCTTGCTCTGTGG	10517
rs150460680	snp	C/T	0.00914312	0.0669923	intron-variant	FBXW10	GRCh38.p7	17:18771392	CAGAAAGGGGAAAGC[C/T]GCTTGCTTGTAAAAC	10517
rs150515943	snp	C/T	0.26326	0.249648	intron-variant	FBXW10	GRCh38.p7	17:18759613	TTGCATTGTTTCTAG[C/T]TTTTTGTTTTTTTTT	10517
rs150620854	snp	A/C	0.0111196	0.0737302	intron-variant	FBXW10	GRCh38.p7	17:18769829	AGGCCAGTTATGGCC[A/C]GTGCTGCTCAATCAC	10517
rs150642944	snp	A/C	1.6593e-05	0.00288031	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778864	GTCCAGTCCACCATA[A/C]CCCAGCCCATGATTA	10517
rs150697158	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768619	CTGATGGCCTGGTCA[C/T]GGCCTGGAGCATGGT	10517
rs150701378	snp	A/G	0.020391	0.0988924	intron-variant	FBXW10	GRCh38.p7	17:18747898	CATTTTCCTCAACAC[A/G]CCCGCTTCAAGAGCA	10517
rs150933603	snp	C/T	0.0154538	0.0865337	intron-variant	FBXW10	GRCh38.p7	17:18770593	AGGTGTGAGCCACCA[C/T]GCCCGGCCTGTTTTG	10517
rs150980523	snp	C/T	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18768059	TTCCTTCCTTCTTTC[C/T]TTCTTTCTTTCTTCT	10517
rs151027138	in-del	-/AT			intron-variant	FBXW10	GRCh38.p7	17:18757076	CATATACACACACAC[-/AT]ATATATATACACATA	10517
rs151034607	snp	C/T	0.000183819	0.00958518	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758482	AAACTTTCTCCTAAG[C/T]GGGAGCTATGACCTA	10517
rs151142904	snp	A/G	0.000860528	0.0207249	intron-variant	FBXW10	GRCh38.p7	17:18768515	TCTGAGTTGAAGACA[A/G]TGGTATCTTTTCTTG	10517
rs151267144	snp	A/G	0.115088	0.210473	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779796	AACTCCTAAGGAAGA[A/G]AATTAGCATATTTAT	10517
rs180700641	snp	A/C	0.00716266	0.059414	intron-variant	FBXW10	GRCh38.p7	17:18747149	GCCCGGATGGTCTCC[A/C]TCTCCTGACCTTGTG	10517
rs180706625	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18765491	AACTTCTCTATGCCT[C/T]AGTTTCCTCATCTGT	10517
rs181176474	snp	A/G	0.00398564	0.0444627	intron-variant	FBXW10	GRCh38.p7	17:18752207	GCGGACGGTGTGGCT[A/G]TCATGGACTGGACAG	10517
rs181192750	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18769514	GGGCATGGTGGCGCA[C/T]GCCTGTAATCCCAGC	10517
rs181233133	snp	G/T	0.00636936	0.0560724	intron-variant	FBXW10	GRCh38.p7	17:18761951	TATGTTTCATAATTG[G/T]TTTTTCTTTTTCTTT	10517
rs181311849	snp	C/T	0.0166325	0.0896639	intron-variant	FBXW10	GRCh38.p7	17:18747015	CTGCAAGCTCCGCCT[C/T]CCGGGTTCACGCCAT	10517
rs181347226	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18775865	AGACCCTTGTCTCTA[C/T]CAAAAATTCAAAAAA	10517
rs181396376	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18758997	ATGGTGAAACCCCGT[C/T]TCTACTAAACAAAAT	10517
rs181472390	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18752669	AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG	10517
rs181475576	snp	A/G	0.00119737	0.0244387	intron-variant, missense	FBXW10	GRCh38.p7	17:18771650	CCTCCCCATTAGAGA[A/G]CTTTCCTCATTCCCA	10517
rs181509140	snp	G/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18764937	AATGCTTTGTTTTGC[G/T]CATTTCTATAGGCAG	10517
rs181529498	snp	G/T	0.00119737	0.0244387			GRCh38.p7	17:18741562	TATGTGGGAAGGCAG[G/T]AAAAGCAAGTGCAGA	10517
rs181628913	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18761516	GTGATTCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	10517
rs181893524	snp	G/T	1.67598e-05	0.00289476	intron-variant	FBXW10	GRCh38.p7	17:18775104	AATCGAAGTATATAA[G/T]GACTACAGCTTCTTC	10517
rs181915686	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18757874	ACAGGACTTTGAACC[C/T]AATATATGCTCACTG	10517
rs181948038	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18762707	GCCTTCCAGTGCCAT[A/G]GCAGGCAGTAGCAGT	10517
rs182066235	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18765949	GGCTAGGCTGGTCTC[A/G]ATTTCCTGACCTGGT	10517
rs182111271	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18749277	AGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	10517
rs182156927	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18777729	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC	10517
rs182347432	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747673	GAGCATTCCCTGTTG[A/C]AATTCCTGACCTCGA	10517
rs182354952	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18775980	CAGTGAGCTATGATT[A/G]CACCACTGGGTGACA	10517
rs182469520	snp	A/G	0.00557542	0.0525036	intron-variant	FBXW10	GRCh38.p7	17:18767947	ATTCCTCCTTAACCC[A/G]AGAGAGAGCTCTATG	10517
rs182508390	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18770270	GGGCTTTGCACAAAA[C/G]TTAGTAATCAGGAAG	10517
rs182607413	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771773	TTCTTGGCACCCTAG[A/G]TACGTGGCACTCACT	10517
rs182607901	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759364	TTTCTTAATCATTTT[C/T]GCTTCCTTCTTATAC	10517
rs182611704	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18745872	AGGGTGGTGTCTGTT[C/T]TGCTTTGCTATAAAG	10517
rs182629310	snp	C/T	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18764233	TTTGAGACAGAGTCT[C/T]GCTCTATTGGCAGGC	10517
rs182760245	snp	A/C	0.00126787	0.0251461	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766754	CCTGAAGACGTTTAG[A/C]CACAAAGACCCCATC	10517
rs183039642	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18755441	ACGCTTGTAGTCCCA[A/G]TTACTCTGGAGGCTG	10517
rs183058274	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18773032	CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	10517
rs183073041	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759862	CCTCGTGATCCACCC[A/G]CCTCGGCCTCCTAAA	10517
rs183182349	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759470	GTACCTCATTCTTAC[A/G]TGGAACTGTTTTTGA	10517
rs183209188	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18738384	TTTTATTGAATCCCT[A/G]CGGGTTGTTGGTGCT	10517
rs183251961	snp	A/G	0.00755907	0.0610114	intron-variant	FBXW10	GRCh38.p7	17:18753590	GTAATTTAAGAAAAG[A/G]GGCCAGGCGCAGTGG	10517
rs183323649	snp	C/T	0.0023933	0.0345097			GRCh38.p7	17:18739414	GCCTCAAGCAGTGGG[C/T]GCATCTTTTTTCTTT	10517
rs183342567	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779719	AAGAATTTAAAAGGG[C/G]AAGCCCTCAGTGGGG	10517
rs183354232	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743519	GACAGGTTGCCTGCT[C/T]GAGACCATATAGCTC	10517
rs183479685	snp	G/T	0.0158469	0.0875917	intron-variant	FBXW10	GRCh38.p7	17:18763374	TGTTAGCCAGGATGG[G/T]CTCGATCTCCTGACC	10517
rs183764649	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18769515	GGCATGGTGGCGCAC[A/G]CCTGTAATCCCAGCA	10517
rs183875250	snp	C/T	0.0123036	0.0774623	intron-variant	FBXW10	GRCh38.p7	17:18747073	GGGACTACAGGTGCC[C/T]GCCACCACGCCCGGC	10517
rs183878223	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18765433	CCTAGGTCCAAATCC[C/T]GGCTCTGCCACTCAC	10517
rs183937192	snp	C/T	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18754949	GACAAATGAAAGTTG[C/T]AGATGTATGAAAACT	10517
rs183956178	snp	C/G	0.00874735	0.0655527			GRCh38.p7	17:18739578	CTTCCATTATGTAGA[C/G]TTACAAAAAAAAAAA	10517
rs184018551	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18769307	ATAAGTAAACGCTAG[G/T]AATCAAATTGCAAGA	10517
rs184019674	snp	A/G	0.00636936	0.0560724	intron-variant	FBXW10	GRCh38.p7	17:18751757	GAGGACCCGAGGGGA[A/G]GGCCAGGGCTGGTTC	10517
rs184109717	snp	C/T	5.19197e-05	0.00509482	intron-variant	FBXW10	GRCh38.p7	17:18772389	CAGTCCTTTTGTGGA[C/T]AACCCTGTTGTTTCG	10517
rs184511037	snp	C/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18752407	CAGTTTTAAAAACTA[C/T]ATAGGCCAAAGAAAA	10517
rs184670178	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760579	GAGGCTGAGGCAGGC[A/G]GATCATCTGAGGTCG	10517
rs184671160	snp	A/G	0.00993419	0.0697739	intron-variant	FBXW10	GRCh38.p7	17:18773653	AGATCTATAGAGAAC[A/G]ATGATAAATCACCCC	10517
rs184802360	snp	A/C	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18756826	AAGGTTTTGCAAAGT[A/C]CACTTCTACTTTATT	10517
rs184833953	snp	A/G	0.0520825	0.152737			GRCh38.p7	17:18740906	GCTGGGACTACAGGC[A/G]CCCACCACCACGCCC	10517
rs184835811	snp	A/G	0.0256215	0.110247	intron-variant	FBXW10	GRCh38.p7	17:18761411	GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCT	10517
rs184980670	snp	G/T	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18764465	TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGGG	10517
rs184983413	snp	C/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18746364	GCTCAGATTTAAGCA[C/G]AGGTGGGAGAAAGCT	10517
rs185055951	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18759391	ATACATCTCCAGAAG[C/T]ATTAGTTACTTGTGC	10517
rs185206017	snp	C/T	0.00874735	0.0655527	intron-variant	FBXW10	GRCh38.p7	17:18761964	TGGTTTTTCTTTTTC[C/T]TTTTCTTTTTTTTTT	10517
rs185236028	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742450	TCCACAGGTGTTTGA[A/G]GAGAACCGTGTGTGT	10517
rs185357234	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18746740	GTGGGCTGAAAACCA[C/G]GATCCCCTCCTGGGC	10517
rs185440553	snp	A/C	0.00105499	0.022943	intron-variant	FBXW10	GRCh38.p7	17:18764693	TCTACGCAGTATGAT[A/C]CTCTGGGCCCTCAGG	10517
rs185469403	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18768901	TTTTCTTGTGAAGTA[A/G]CTATAGAAACTGGGG	10517
rs185593960	snp	A/G	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18757550	ACTTTGGGAGGCTGA[A/G]GTAGGAGGATCGCTT	10517
rs185715610	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18753034	GACTGTATTGACAGA[A/G]TTGTACTGTCATCTT	10517
rs185733880	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18774664	AGCCGGTGTGGTGGC[A/G]CATGCCTGTAATTCC	10517
rs186076107	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771708	GCTGTGCTTAAAACA[A/G]ACAAAGAAACAAAAA	10517
rs186076610	snp	C/G	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18777197	CTCCTCAGTAGCTAG[C/G]ATTACAGGCGCCTGC	10517
rs186098424	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18753767	TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCAGA	10517
rs186117677	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18763180	TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	10517
rs186119518	snp	A/G/T	7.21371e-05	0.00600528	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744210	GTTGCCGTTGCAAGT[A/G/T]CGCAGGGCTAAAATG	10517
rs186187440	snp	A/G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18771940	TGGCGAAACCCTGTC[A/G/T]CTACTAAAAACACAA	10517
rs186214249	snp	C/T	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18775900	CCAGATATGGTAGCA[C/T]GCACCTCCTAGCTAC	10517
rs186216599	snp	A/C	0.00279162	0.0372561	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775259	GGCAGGAGAATTTGG[A/C]AGCAAAATCCACAGC	10517
rs186263166	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18757990	AAAAAGGTTTCCGTG[A/C]TCAATTAAATCCGGG	10517
rs186352126	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18761638	TTTACCAACTTTCAA[C/T]AAAACCTAACTAGAC	10517
rs186411840	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18759067	CCCAGCTACTCGGGA[C/T]GCTGAGGCAGGAGAA	10517
rs186608949	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18741824	TGGCGCCATGTCCCC[A/G]CATTGGCCTATCCCA	10517
rs186906770	snp	A/G	0.00318978	0.0398085	intron-variant	FBXW10	GRCh38.p7	17:18747748	ATGGGGGCGTGCTGA[A/G]AAGCTAACAGGAAGC	10517
rs186909075	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18746161	CACTCATTACTGTGG[A/G]AAGGGCACCAAGCTA	10517
rs186912090	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18764246	CTCGCTCTATTGGCA[A/G]GCTGGAGTGCAGTGG	10517
rs187048266	snp	C/T	0.0115144	0.0749975	intron-variant	FBXW10	GRCh38.p7	17:18767227	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	10517
rs187051986	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18748694	AGACACATCTGAAGA[C/T]AGAGATCAGAAAGGA	10517
rs187088899	snp	C/G	0.02016	0.0983543	intron-variant	FBXW10	GRCh38.p7	17:18771064	AAAGAGGGCAGCCTG[C/G]TAATAAGGCTCAATT	10517
rs187266678	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18752486	TTGGGAGGCCGAGGC[A/G]GGCGGATCACTAGGT	10517
rs187337412	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18755667	TAATATACATATGAC[G/T]TTCCGACTTCTGTGA	10517
rs187339404	snp	C/G	0.0205511	0.0992634	intron-variant	FBXW10	GRCh38.p7	17:18773177	ACCTCAGGTGATCCT[C/G]CCGGCTTGGCTTCCC	10517
rs187472085	snp	A/T	0.000399281	0.0141238			GRCh38.p7	17:18738526	CTTATTTTTATTTTT[A/T]AAAAAATCGAGATGC	10517
rs187474154	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18759721	AGGTTCACACCATTC[C/T]CTTGCCTCAGCCTCC	10517
rs187476268	snp	C/T	0.0429648	0.14013	intron-variant	FBXW10	GRCh38.p7	17:18778121	AGCCAGGCATGGTGG[C/T]GGACGCCTGTAGTCT	10517
rs187558828	snp	A/C	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18768091	TCTTTTTTGAGACAG[A/C]GTCTCACTCTGTCAC	10517
rs187560926	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18755053	AGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG	10517
rs187820291	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:18739476	ACAAATAGAAAAAAA[A/G]TAGAACAAGGGTTTA	10517
rs187855458	snp	A/G	0.00636936	0.0560724	intron-variant	FBXW10	GRCh38.p7	17:18750362	ATAGGGATAGAGACC[A/G]CTCAGGAGCAGAGAG	10517
rs188104376	snp	G/T	0.00557542	0.0525036	intron-variant	FBXW10	GRCh38.p7	17:18759871	CCACCCGCCTCGGCC[G/T]CCTAAAGTACTGGGA	10517
rs188212194	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747087	CCGCCACCACGCCCG[C/G]CTAATTTTTTTTGTA	10517
rs188212348	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18765434	CTAGGTCCAAATCCC[A/G]GCTCTGCCACTCACC	10517
rs188242358	snp	C/T	0.00199481	0.0315187			GRCh38.p7	17:18740807	ACTCTGTCGCCTAGG[C/T]TGGAGTGCAGTGGTG	10517
rs188258233	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18762612	CAGGCATGAGCCACC[A/G]CGCCCGGCCGACAAT	10517
rs188262588	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18760677	GCATGGTGGCACATG[A/C]CTGTAATCTCAGCTA	10517
rs188360424	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18751961	CATGGTTGATATTCC[C/T]AAAACCATTAGATTT	10517
rs188368056	snp	A/G	0.0494327	0.149241	intron-variant	FBXW10	GRCh38.p7	17:18763378	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	10517
rs188368924	snp	C/T	0.00557542	0.0525036	intron-variant	FBXW10	GRCh38.p7	17:18769463	CTTGAGAGAAGCTCA[C/T]GGTTTACTTCCACAA	10517
rs188626530	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18746569	ATTTGGTGTGTCAGG[A/G]GTATAGAAGAATGAT	10517
rs188637289	snp	C/G	0.0263992	0.111815	intron-variant	FBXW10	GRCh38.p7	17:18745563	TGGGACTACAGGTGC[C/G]TGCCACCATGTCCTA	10517
rs188744084	snp	C/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18769082	CTGGGACTACAGGCG[C/G]CCACCACCACACCCA	10517
rs188861720	snp	A/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18764510	TGACCAACGACTCTT[A/G]TTATTATTTCCATTT	10517
rs188975698	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775349	CTCTCACTCTAGTTT[C/T]GTATTGTTTTCCAGC	10517
rs189018792	snp	G/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18758016	CCGGGCAATGCCACA[G/T]ACTCCATTCTCTCTC	10517
rs189165005	snp	A/T	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18761464	TAGAGACAAGGTTTC[A/T]CTGTGCTAGCCAGGA	10517
rs189252277	snp	C/T	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18757085	ACACACATATATATA[C/T]ACACATATACACATA	10517
rs189284671	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18757561	CTGAGGTAGGAGGAT[C/T]GCTTGAGGCCAAGAG	10517
rs189555722	snp	A/G	0.00398564	0.0444627	intron-variant	FBXW10	GRCh38.p7	17:18774093	AAGGGGAGTTGCTTA[A/G]CATTCTGCTGTAAAG	10517
rs189625302	snp	C/T	0.131381	0.220067	intron-variant	FBXW10	GRCh38.p7	17:18762191	ATGGTCTCGATCTCC[C/T]GACCTTGTGATCCAC	10517
rs189630130	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18774957	ACACATTTTATGCAT[G/T]TATCAAAATATCACA	10517
rs189660259	snp	A/C/T	0.00199529	0.0315338	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743039	TTAGGGTAACGTGCT[A/C/T]GCCTTACAGATCCAA	10517
rs189852438	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18767268	ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	10517
rs189895189	snp	A/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18749003	TTTATATGGAAAATT[A/T]CAAATTTCAAAAGTA	10517
rs189915194	snp	C/G	0.00232426	0.0340107	intron-variant	FBXW10	GRCh38.p7	17:18764727	TCTCACATTCTTTTG[C/G]CCTGATTCCTGCAGA	10517
rs190020826	snp	C/T	0.00755907	0.0610114	intron-variant	FBXW10	GRCh38.p7	17:18761805	ATTTTATTACTATTG[C/T]GAATGGTATCTTAAT	10517
rs190206291	snp	G/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18746872	CATAGGAATGGGCTA[G/T]TTACACTGGAGTTGT	10517
rs190227139	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18768030	CTTCCTTCCTTTCTT[C/T]CTTCCTTCCTTCCTT	10517
rs190308992	snp	C/G	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18771503	CATTAAAGTGGGGAT[C/G]AGAGAAGTTAGAAAT	10517
rs190333032	snp	A/G	0.00119737	0.0244387			GRCh38.p7	17:18741038	AGTACTGGGATTACA[A/G]GCGTGAACCACCGCG	10517
rs190398769	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771753	ACATCTGTGTGCAGA[C/G]TACCTTCTTGGCACC	10517
rs190543476	snp	A/G/T	3.36895e-05	0.00410412	intron-variant	FBXW10	GRCh38.p7	17:18748148	ATATGGGCTAGGTGC[A/G/T]GTGGCTCATGCCTGT	10517
rs190668048	snp	C/T			intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18772050	AGGCGGAGGTTGCAG[C/T]GAGCTGAGATCATGC	10517
rs190702780	snp	G/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18752643	GTGTGAACCCGGGAG[G/T]CAGAGCTTGCAGTGA	10517
rs190810223	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759164	GACACAGCGAGACTC[C/T]ATCTCAAAAAAAACC	10517
rs190954970	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18753922	AGAGAAGCAGAGAAG[C/G]AGGTGAAACAGTATG	10517
rs191036026	snp	C/T	0.0337553	0.125452	intron-variant	FBXW10	GRCh38.p7	17:18759434	TCAACATAAAAAGAA[C/T]CATATTTTAAAAATT	10517
rs191053027	snp	G/T	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18777405	ATTCAAGATTACTTG[G/T]AGTCAAATTTGATTA	10517
rs191061286	snp	A/G	0.00716266	0.059414	intron-variant	FBXW10	GRCh38.p7	17:18775961	GTCCAGGAGCTTGAC[A/G]TTACAGTGAGCTATG	10517
rs191077894	snp	A/C	0.00517822	0.0506191			GRCh38.p7	17:18738364	GATCAGCTTGGACTG[A/C]CTTATTTTATTGAAT	10517
rs191324981	snp	A/G	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18746285	ACAAATATCCAAACT[A/G]TATCAGGAGGCAAGA	10517
rs191325153	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18764287	GCTCGCTGCAACCTC[C/T]GCCTGCCGGATTCAA	10517
rs191337818	snp	C/T	0.0532157	0.154195	intron-variant	FBXW10	GRCh38.p7	17:18745665	GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	10517
rs191502468	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18766275	AAGACAACATCTGGG[A/G]AAAATGACAACACTA	10517
rs191585893	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18763445	ACAGGTGTGAGCCAC[C/T]GTGCCCGGCTGTTAA	10517
rs191822931	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18755947	TCAGAGGAAGAATCC[A/G]TGAGCCCTGTGCCCT	10517
rs191828773	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18773444	GTTTTTAGACCTGAG[A/G]GATAATGTTTGTAGC	10517
rs191912090	snp	C/T			intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18745228	ACCATGCTCCTTGCT[C/T]ATCCATGAAATGAAA	10517
rs191939278	snp	A/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18751531	CACCGCGCTCAGCCC[A/G]ACACTTCCTCTTCTT	10517
rs191939480	snp	C/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18769087	ACTACAGGCGCCCAC[C/G]ACCACACCCAGCTAA	10517
rs191983431	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779699	GAAGCCTGATAAAAC[C/T]CATTAAGAATTTAAA	10517
rs192096918	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18755091	AACGTGGTGAAACTC[C/T]GTCGCTGCTAAAAAT	10517
rs192103802	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18773006	CAATCTTGGCTCACC[A/G]CAACCTCCGCCTCCC	10517
rs192111404	snp	A/G	0.00597247	0.0543191	intron-variant	FBXW10	GRCh38.p7	17:18747497	GGAGGCGGAGGTTGC[A/G]GTGAGCCAAGACCGA	10517
rs192197593	snp	C/T	0.00438332	0.0466095	intron-variant	FBXW10	GRCh38.p7	17:18774290	GAGCAGGAAAACAGC[C/T]GCGCTATGTGACTCA	10517
rs192334579	snp	C/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18760019	AAGGTATATTCTTAG[C/T]ATGGGAATTTCTAGG	10517
rs192596055	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18757374	TTTTTTTGTAGAGAC[A/G]GGGTTTCGTTCTCTG	10517
rs192619036	snp	A/G	0.00835141	0.0640778			GRCh38.p7	17:18740847	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCTCA	10517
rs192632808	snp	C/G	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18761400	CCTCCCGAGTAGCTG[C/G]GACTACAGGCACCCG	10517
rs192714648	snp	A/G					GRCh38.p7	17:18739556	TATTCACCCATCCTT[A/G]TCTTTTCTTCCATTA	10517
rs192846136	snp	A/G	0.00119737	0.0244387			GRCh38.p7	17:18738613	TTGATCTCCCATGTT[A/G]GAGGTGGAGCTGGGT	10517
rs193051025	snp	A/G	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18759762	AGACTACAGGGGCCC[A/G]CCACCACACCAGGCT	10517
rs193091319	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18764522	CTTATTATTATTTCC[A/C]TTTTATCAATGAGGA	10517
rs193157889	snp	C/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18746724	TTAGGTCACCCACCA[C/T]GTGGGCTGAAAACCA	10517
rs193284533	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18768193	CTGCCTCAGCCACCC[A/G]AGTGGCTGGGATTAC	10517
rs199551168	snp	C/T	0.00509884	0.0502337	intron-variant	FBXW10	GRCh38.p7	17:18749708	CCACGTACCTTTCTC[C/T]GGCTTCACTCTAGAG	10517
rs199572430	snp	A/G	0.00331757	0.0405928	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758367	CTGTGTCATCTAATC[A/G]AAAGATCCATCTTCT	10517
rs199659416	in-del	-/G	0.0158469	0.0875917	intron-variant	FBXW10	GRCh38.p7	17:18758891	ACACATACGTGGCCA[-/G]GCGCGGTGGCTCACG	10517
rs199777375	in-del	-/TAGTT			intron-variant	FBXW10	GRCh38.p7	17:18757157	ACACACATATATATG[-/TAGTT]TAAAGAACAATTATC	10517
rs199784714	snp	C/T	6.67768e-05	0.00577789	intron-variant	FBXW10	GRCh38.p7	17:18769887	AACCCAGGCATTTTA[C/T]GAGAGGATGGGTACT	10517
rs199847738	in-del	-/T	0.00835141	0.0640778	intron-variant	FBXW10	GRCh38.p7	17:18750518	TATAAGGCTGCAAAG[-/T]TTTTTTTTAAGTTAA	10517
rs199859632	in-del	-/G	0.131038	0.219882	intron-variant	FBXW10	GRCh38.p7	17:18762153	ATTTTTAGTAGAGAC[-/G]GGGTTTCACTGCGTT	10517
rs200032360	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18762512	GTATTTTAGTAGAGA[C/T]GAGGTTTCACTATGT	10517
rs200033566	in-del	-/C	0.120674	0.21395	intron-variant	FBXW10	GRCh38.p7	17:18771118	GCTAAAAAAAAAAAA[-/C]AAAACAAAACTCTGG	10517
rs200034399	snp	C/T	0.000374582	0.0136803	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750113	AGCGCACGGCTTCAT[C/T]CAGAACCAGATTACC	10517
rs200062063	snp	A/C	0.00106489	0.0230502	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778639	GGGGAATTTGCCTAT[A/C]CCTGTAGGCCCCAAA	10517
rs200120712	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18768077	CTTTCTTTCTTCTTT[C/T]TTTTTTGAGACAGAG	10517
rs200240910	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18770637	CCTAGGTGTTTGTGG[A/G]AATTGCAGTGGGTGC	10517
rs200312304	in-del	-/TTTC			intron-variant	FBXW10	GRCh38.p7	17:18772913	TTGCAAAAGCTAGAT[-/TTTC]TTTCTTTCTTTCTTT	10517
rs200360399	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18757029	AATAAGGGCAAAAAT[A/G]TCAAGAATTGCTCCT	10517
rs200464103	snp	A/T	0.0365591	0.130165	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758310	TGGCACTCAGGTGGG[A/T]TCAAAACCGAGTCAT	10517
rs200466867	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18768437	GCAGTCACAGATTGG[-/T]TGGGGGGTGGCTTTG	10517
rs200500172	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18765045	TCCATCCATTCAACA[A/G]CTGTCTGTAGAATAC	10517
rs200519240	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769936	TTCCAGGGAGGTGCT[C/T]GACGTGTCCCTTCTC	10517
rs200529554	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743046	AACGTGCTCGCCTTA[C/T]AGATCCAAAGAGTCT	10517
rs200535885	snp	A/C/G	0.366006	0.221466	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749832	AATCTATTGGTTGAC[A/C/G]TGGATGACATCAGAG	10517
rs200553727	snp	A/G	0.000164718	0.00907368	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744324	CCATCCCTCTATGCC[A/G]GAAGTGTGAGACGTG	10517
rs200654387	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18768051	TTCCTTCCTTCCTTC[C/T]TTCTTTCTTTCTTTC	10517
rs200658685	snp	C/T			synonymous-codon, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772538	AAAAGAAGAAAATAG[C/T]CTCATGGAAATTCTC	10517
rs200711350	snp	A/C	0.128877	0.218699	intron-variant, synonymous-codon	FBXW10	GRCh38.p7	17:18749963	TCCCAGACACCTCCC[A/C]TCTTGGCCCAGTTCT	10517
rs200752591	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18760843	CAGGGTTTTTTTTTT[-/T]CTTCATTTCTGTGAT	10517
rs200798926	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18768069	CTTTCTTTCTTTCTT[C/T]CTTCTTTCTTTTTTG	10517
rs200806553	snp	G/T	4.95372e-05	0.00497656	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744409	CATATCACAGAGGAG[G/T]TTTCTAGTTGGCATT	10517
rs200809443	snp	G/T	0.000218524	0.0104507	intron-variant	FBXW10	GRCh38.p7	17:18775093	TTTTATGCCCTAATC[G/T]AAGTATATAATGACT	10517
rs200843193	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18764663	CCTCCCAACTAACTA[A/C]TTATCTACATGGGTT	10517
rs200851525	snp	C/T	8.33507e-05	0.00645511	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756077	GACTGCATACCAGAA[C/T]GAGGAAACGCAGCAG	10517
rs200852537	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18771474	CAAGTTCCGGAGCTC[-/T]TTTGTCTATGGAGCA	10517
rs200883433	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757097	ATATACACATATACA[C/T]ATATGTACATGTATA	10517
rs200903982	snp	A/C			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742043	CACCACACCCGGCTA[A/C]TTTTTTGTATTTTTT	10517
rs201011941	in-del	-/CTGA			intron-variant	FBXW10	GRCh38.p7	17:18766594	AAGTCCTTCTAGAAT[-/CTGA]CTTGATGGGCTTGAT	10517
rs201055075	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18759616	CATTGTTTCTAGTTT[C/T]TTGTTTTTTTTTTTG	10517
rs201057327	snp	G/T	0.000116532	0.00763232	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778643	AATTTGCCTATCCCT[G/T]TAGGCCCCAAACAGA	10517
rs201078575	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18772928	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	10517
rs201131706	snp	A/G			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742367	TATTCTCAGGAGGCA[A/G]CCCGTTGTCATCTTC	10517
rs201137619	in-del	-/TGTT			intron-variant	FBXW10	GRCh38.p7	17:18773450	AGACCTGAGAGATAA[-/TGTT]TGTAGCTGGAAAATC	10517
rs201169182	snp	A/G			missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756054	TGTTAGAATGAGTAC[A/G]ACCTGTGGACTGCAT	10517
rs201231821	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18755392	AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT	10517
rs201275430	in-del	-/G	0.00897077	0.0663695	frameshift-variant, intron-variant, utr-variant-3-prime, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778545	GCCCAGTCACCCAAA[-/G]AAAAAGTCTTGGAAA	10517
rs201329963	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18768070	TTTCTTTCTTTCTTT[C/T]TTCTTTCTTTTTTGA	10517
rs201359995	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757077	ATATACACACACACA[C/T]ATATATATACACATA	10517
rs201382359	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18759665	TCACCCAGGCTGGAG[A/G]GCAGTGGCGCCATGT	10517
rs201398418	in-del	-/AC/C			intron-variant	FBXW10	GRCh38.p7	17:18771117	GCTAAAAAAAAAAAA[-/AC/C]CAAAACAAAACTCTG	10517
rs201649436	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18764956	TTCTATAGGCAGGCA[C/G]TCATTTATTCTTTAT	10517
rs201657571	snp	C/T	0.000752304	0.01938	stop-gained, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758318	AGGTGGGATCAAAAC[C/T]GAGTCATCCACTATT	10517
rs201848876	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18759673	GCTGGAGAGCAGTGG[C/T]GCCATGTTGGCTCAC	10517
rs201908911	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18759586	TTTATTTGTTTTTCT[C/G]TTGGTGGACATTTGC	10517
rs201935353	snp	A/G	3.30142e-05	0.00406276	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744489	TTCAGACCACACAGG[A/G]AAAGGATTTCATCTA	10517
rs202016618	in-del	-/T					GRCh38.p7	17:18740770	TTTTTCTTTTTTTTT[-/T]GAGACGGAGTCTCAC	10517
rs202018947	in-del	-/G			intron-variant	FBXW10	GRCh38.p7	17:18759910	GTGAGCCACCGCGCC[-/G]GGCCCTTGTTTCTAG	10517
rs202063654	snp	A/G	0.00199795	0.0315433	stop-gained, intron-variant, utr-variant-3-prime, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778557	AAAGAAAAAGTCTTG[A/G]AAAATCCCTATGTCA	10517
rs202111205	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18759619	TGTTTCTAGTTTTTT[G/T]TTTTTTTTTTTGAGA	10517
rs202165228	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18756891	GATAATAGAACAGTC[A/G]GTATGGGGAAGACAG	10517
rs367569739	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18746763	TCCTGGGCCCCTTCC[A/G]CTCTGGAGTGAGTGC	10517
rs367572478	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18760123	TTCTTATATATTCTC[A/G]CCAACACTTACTATT	10517
rs367784732	snp	A/G	0.000153988	0.00877328	intron-variant	FBXW10	GRCh38.p7	17:18770099	AGGTGGGTGGTAGGT[A/G]TGGAGGTCAGAACTG	10517
rs367810251	snp	C/G	0.00874735	0.0655527	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744037	CCATGTTTCCAAGGA[C/G]GTCTGTACAAAAAGC	10517
rs368003711	snp	C/G	1.66186e-05	0.00288254	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766740	GACACAGGGAAGTGC[C/G]TGAAGACGTTTAGAC	10517
rs368081015	snp	A/T			intron-variant	FBXW10	GRCh38.p7	17:18754909	TTTGTGGGGCAAGGG[A/T]TCTACTTTGTAAGGC	10517
rs368084632	snp	C/T	0.0134861	0.0810011	intron-variant	FBXW10	GRCh38.p7	17:18772932	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA	10517
rs368098797	snp	C/T			intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771776	TTGGCACCCTAGGTA[C/T]GTGGCACTCACTCCA	10517
rs368179743	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18761391	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10517
rs368197208	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742025	GGAACTACAGGCGCC[C/T]GCCACCACACCCGGC	10517
rs368213609	snp	C/T	6.6096e-05	0.00574836	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749886	TACCGAGACTTCATC[C/T]GTTACCTGCCCATCC	10517
rs368217343	snp	A/T			intron-variant	FBXW10	GRCh38.p7	17:18748381	ATGCCACTGCACTCC[A/T]GCCTGGGCAACAGAG	10517
rs368262323	snp	C/G	0.000129874	0.0080573	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766856	TGCCATGGCCCAGTT[C/G]GTAAAGGTAAGTGGG	10517
rs368351579	snp	A/G	0.000115739	0.00760631	intron-variant	FBXW10	GRCh38.p7	17:18764905	TAAGAAGTTTCCCCC[A/G]ACCCACGGGTTACCA	10517
rs368455869	in-del	-/T/TT	0.422787	0.180679	intron-variant	FBXW10	GRCh38.p7	17:18777062	CTTGATTTCACTCAG[-/T/TT]TTTTTTTTTTTTTTT	10517
rs368499866	snp	A/G	4.96372e-05	0.00498158	intron-variant	FBXW10	GRCh38.p7	17:18749687	GTTTCTACAGAGCCA[A/G]CTCAACCACGTACCT	10517
rs368567132	snp	A/G	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18776956	AAAAAAGACAAATTA[A/G]TAAACAATGAGCTCA	10517
rs368675102	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18763188	TTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC	10517
rs368798752	snp	G/T	0.00199481	0.0315187			GRCh38.p7	17:18740824	GGAGTGCAGTGGTGC[G/T]ATCTTGGCTCACTGC	10517
rs368815799	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18773005	ACAATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC	10517
rs368827263	snp	A/G	3.30994e-05	0.004068	synonymous-codon, nc-transcript-variant, missense	FBXW10	GRCh38.p7	17:18772430	GGTGGTCAACACAGA[A/G]AGCAATGTTCTCATG	10517
rs368895180	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18755644	TGCTTTGTACTATCA[C/G]GTAGATGTAATATAC	10517
rs369025810	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18767123	CAGCATGAGATATGG[G/T]CTCAGGGCCTTCTAA	10517
rs369182185	snp	A/G			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742371	CTCAGGAGGCAGCCC[A/G]TTGTCATCTTCTCAA	10517
rs369333094	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18752654	GGAGGCAGAGCTTGC[A/C]GTGAGCCGAGATTGC	10517
rs369335784	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18765047	CATCCATTCAACAGC[C/T]GTCTGTAGAATACCT	10517
rs369369715	snp	G/T	0.00248825	0.0351843	intron-variant	FBXW10	GRCh38.p7	17:18778440	TATTTTTCATAGAAC[G/T]CCGATTTTTTAAAAT	10517
rs369432962	snp	C/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18777291	CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCT	10517
rs369517876	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772472	GCACATAAAGTGGCA[A/G]TATGCCGTGGAAAAA	10517
rs369742505	snp	A/C/G	0.000161123	0.00897426	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744195	CTAGTGTTTGGTGGC[A/C/G]TTGCCGTTGCAAGTG	10517
rs369750229	snp	A/G	3.32298e-05	0.004076	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775204	GATGGTAAGAAGAGA[A/G]TTTATTCTGTTCATA	10517
rs369780198	snp	C/T	9.98735e-05	0.00706589	intron-variant	FBXW10	GRCh38.p7	17:18775125	CAGCTTCTTCCTCAA[C/T]CTCAATTTAGCAGTG	10517
rs369822793	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18753381	CCCTCCCAGATAAGC[A/G]CAACAAAGAGACACA	10517
rs369853204	snp	C/T	0.000115564	0.00760057	intron-variant	FBXW10	GRCh38.p7	17:18751091	GCAAGTAGCTGTGAG[C/T]GTCTCATTCTAATTG	10517
rs369871667	snp	A/G	0.0178098	0.0926698	intron-variant	FBXW10	GRCh38.p7	17:18755993	AGGGGCTCTGGGACT[A/G]TGGGTATTTGAAGTT	10517
rs369895576	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18760541	AGGCGCGGTGGCTCA[C/T]GCCTGTAAGCCCAGC	10517
rs369938927	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18750770	ATCTGCACACACTGC[C/G]AGAGGAACTGGCCAG	10517
rs369941747	snp	C/T	0.00676609	0.0577691	intron-variant	FBXW10	GRCh38.p7	17:18748215	ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	10517
rs369946859	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18778195	AAGGCAGAGCTTGCA[A/G]TGAGCAGAGATCATG	10517
rs369968368	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742103	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	10517
rs370045217	snp	C/G			missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18748083	AGAAAATGAACACTT[C/G]CTTGGGGCAGCATCT	10517
rs370087150	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18747488	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	10517
rs370104676	snp	G/T	0.00122042	0.0246722	intron-variant, nc-transcript-variant, missense	FBXW10	GRCh38.p7	17:18744758	ATCTCAGGTAAACAA[G/T]GCCACAGGCAGAGAC	10517
rs370118600	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18756878	CAAATTGCATCTTGA[C/T]AATAGAACAGTCGGT	10517
rs370119394	snp	C/T	3.31466e-05	0.0040709	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778599	CCTCCTGACTGTTAG[C/T]GCCCTGCAGCACGCC	10517
rs370158560	snp	A/G			intron-variant, nc-transcript-variant, missense	FBXW10	GRCh38.p7	17:18744798	CCCGAAGACCAGAAG[A/G]CAAGGCTTCAGAAAT	10517
rs370173787	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18749314	GAGGCCGAGGCGGGC[A/G]GATCACACGGTCAGG	10517
rs370227023	snp	A/G/T	6.59419e-05	0.00574172	synonymous-codon, missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769930	GTTCCCTTCCAGGGA[A/G/T]GTGCTCGACGTGTCC	10517
rs370320215	snp	C/T	1.64982e-05	0.00287208	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18748094	ACTTGCTTGGGGCAG[C/T]ATCTAACCCTGGTAA	10517
rs370339129	in-del	-/A	0.136913	0.22296	intron-variant	FBXW10	GRCh38.p7	17:18771105	TTCAGTCATGCTGCT[-/A]AAAAAAAAAAAACAA	10517
rs370476175	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18747956	GGCTCAATCAAGACA[A/T]CACAGATGTGTGTTT	10517
rs370546800	in-del	-/AA	0.00358779	0.0422022	intron-variant	FBXW10	GRCh38.p7	17:18755245	TCCAGCCTGGGTGAG[-/AA]GAGTGAAACTCCGTC	10517
rs370583951	snp	C/T	0.000223422	0.010567	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758441	CATGCTGGGAGTGTC[C/T]GGGCCCTCTTCCTGT	10517
rs370644534	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18776394	TTTTTAAGGACATTG[G/T]TAAAAATTTAAAATG	10517
rs370681362	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18772351	TGGGATGGTAACTGC[A/G]GTGCATCTTTCGGTG	10517
rs370894653	snp	C/T	0.0023933	0.0345097			GRCh38.p7	17:18740803	TCTCACTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	10517
rs370987673	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18767998	TTCTTTTTTTCTTTT[A/C]TTTTTTCTTTTCCTT	10517
rs371149617	snp	C/T	0.00037354	0.0136613	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778744	CAACGTGCAGTTGAT[C/T]GGTTGAGATTGAGCA	10517
rs371189519	snp	C/T					GRCh38.p7	17:18741441	GAGCCAGCAGAGGCT[C/T]AGGTCCTCTGGTGCA	10517
rs371194302	snp	A/G			utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744015	GTTTAGGAGATTTAC[A/G]GTAAAGCCATGTTTC	10517
rs371223372	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18748533	GATTTGAGGAACTCA[C/T]ATTCATTTAGCATCT	10517
rs371238356	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18776608	AAATTGCTAAGCCAA[A/C]GGATAAGTGCATTCA	10517
rs371264924	in-del	-/T			intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779364	TGTTGCTATTTGGCC[-/T]TTTTTTTTTTTTTTT	10517
rs371266553	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18752858	GCTGAGTGAAAGAGG[A/C]ATTCATTTGAACGTG	10517
rs371268851	snp	A/G	0.000889225	0.0210671	intron-variant	FBXW10	GRCh38.p7	17:18770114	GTGGAGGTCAGAACT[A/G]TGAGTGATTCTGTTG	10517
rs371316490	snp	C/T	0.000153988	0.00877328	intron-variant	FBXW10	GRCh38.p7	17:18764728	CTCACATTCTTTTGG[C/T]CTGATTCCTGCAGAT	10517
rs371463008	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:18741608	TGAGGAGGTTTTATC[A/G]GGATCGTGAATAAAA	10517
rs371467039	snp	A/G/T	0.000283872	0.0119103	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778956	GGCTGTGTGCAGTAC[A/G/T]GGTCCCCTGACCAGT	10517
rs371467801	snp	A/G	0.00358779	0.0422022	intron-variant	FBXW10	GRCh38.p7	17:18775791	CCAGTGCTTTGGGAG[A/G]CCAAGTTGGGAGGAT	10517
rs371478371	snp	A/G			intron-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18771777	TGGCACCCTAGGTAC[A/G]TGGCACTCACTCCAG	10517
rs371548336	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18749142	TTTTCTTGTTGGAGT[A/G]TTTTTAAGAAAATTC	10517
rs371561713	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18776820	ACTAAATGTCCATCA[A/C]TGGGCAATGGCTAAG	10517
rs371567992	snp	G/T	1.66563e-05	0.0028858	intron-variant	FBXW10	GRCh38.p7	17:18768493	TTGGTTCTTGGAGGA[G/T]TCACAGTCTGAGTTG	10517
rs371689400	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18746864	CCATTCACCATAGGA[A/G]TGGGCTATTTACACT	10517
rs371708563	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18760134	TCTCACCAACACTTA[A/C]TATTGACAGTCTAAC	10517
rs371753550	snp	A/G/T	8.23621e-05	0.00641672	missense, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769970	CTCCGGGTCATCAGC[A/G/T]CCTGTGCAGATGGCA	10517
rs371757116	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18773254	AGCTAGATTTTCAAA[C/T]TTATAAGAACCTTTG	10517
rs371774794	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751031	TGCGTGTGAAACATC[C/T]GAAGTGGAAGCTGAG	10517
rs371814695	snp	A/G	0.00358779	0.0422022	intron-variant	FBXW10	GRCh38.p7	17:18777973	CTTGTTTTATTGGCC[A/G]GCTGCGGTGGCTCAT	10517
rs371830584	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18754646	TAGAATATGGCAGGG[A/G]ATATAAATGGAACTG	10517
rs371835270	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18769037	ACCTCCTGGGTTCAC[A/G]CTATTCTCCTGTCTC	10517
rs371852621	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18777327	CCTAGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	10517
rs371870097	snp	A/G	0.0142736	0.0832652	intron-variant	FBXW10	GRCh38.p7	17:18754913	TGGGGCAAGGGATCT[A/G]CTTTGTAAGGCAGCT	10517
rs371949986	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742033	AGGCGCCTGCCACCA[C/T]ACCCGGCTAATTTTT	10517
rs371967944	snp	C/G	0.00318978	0.0398085	intron-variant	FBXW10	GRCh38.p7	17:18769691	CTGAGACAGGAGAAT[C/G]GCTTGTATCTGGTAG	10517
rs372048450	snp	A/T	3.29979e-05	0.00406175	intron-variant	FBXW10	GRCh38.p7	17:18751082	GCATCTGGGGCAAGT[A/T]GCTGTGAGCGTCTCA	10517
rs372082761	snp	C/G/T	1.86149e-05	0.00305075	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18766857	GCCATGGCCCAGTTG[C/G/T]TAAAGGTAAGTGGGC	10517
rs372134223	snp	G/T	0.000153988	0.00877328	stop-gained, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750963	AATTGATCCTAATTA[G/T]GCCAATAAGGTTTCT	10517
rs372149006	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, missense	FBXW10	GRCh38.p7	17:18772460	GTTCCAGTTTGAGCA[C/T]ATAAAGTGGCAGTAT	10517
rs372209815	snp	G/T	0.000153988	0.00877328	stop-gained, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772527	AAAGAGGAGGAAAAA[G/T]AAGAAAATAGTCTCA	10517
rs372345142	snp	G/T	1.74717e-05	0.00295559	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750081	GCCATGGCTCAACAG[G/T]TCAAGATGGACTTGT	10517
rs372375978	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18755412	ATACAAAAATTAGCT[A/G]GGCATGGTGGTGCAC	10517
rs372445387	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18773231	GGCCACCGTGCCCGG[C/T]CTGCAAGAGCTAGAT	10517
rs372486915	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18750828	CTTACCCATCCTTCA[C/G]ATTTTGCCAAGAACT	10517
rs372514251	snp	A/G	0.000251006	0.0112	intron-variant	FBXW10	GRCh38.p7	17:18750170	GAAAGGGGAATGTCT[A/G]AGACCAGCTTCATTT	10517
rs372543327	snp	A/G	0.000545576	0.0165073	intron-variant	FBXW10	GRCh38.p7	17:18749691	CTACAGAGCCAACTC[A/G]ACCACGTACCTTTCT	10517
rs372579881	in-del	-/AACCC			intron-variant	FBXW10	GRCh38.p7	17:18753058	CATCTTGGACAAACA[-/AACCC]CCGCCACTTTAAGTT	10517
rs372591983	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18748157	AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	10517
rs372593430	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18759335	TCTAATTTTATACTA[A/G]TGATTCCCTTGCATT	10517
rs372666856	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18767428	GACGTTGCAGTGAGC[C/T]GAGATCATGCGTCTC	10517
rs372776041	snp	C/T	0.000191339	0.00977921	intron-variant	FBXW10	GRCh38.p7	17:18768700	CTGTGAAGCCCGGAG[C/T]GATGAACCTGGTGTC	10517
rs372843756	snp	C/T	1.73993e-05	0.00294947	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778517	AAGGACAATTGGAAA[C/T]TCCTGGAAAACTGCC	10517
rs372890959	snp	C/T	1.66034e-05	0.00288122	stop-gained, nc-transcript-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775183	AAGTCAAAATCACCC[C/T]GAAGAGATGGTAAGA	10517
rs372926016	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18760087	ATTTACATTCCCATT[A/G]GCAGCATATGAGAAT	10517
rs372967852	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18751719	CTCTGGAGGCTCCAG[C/T]ATCTGCTGCTCAGGA	10517
rs373000642	snp	A/G/T	3.3116e-05	0.00406904	missense, stop-gained, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778627	GCCCATAATTCCGGG[A/G/T]AATTTGCCTATCCCT	10517
rs373007218	snp	A/G			intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775312	ACTTAATTCTGAATT[A/G]GTGGCAAGATCCAAA	10517
rs373096488	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18776334	GTTTAAAAAAAAAAA[-/A]GTTTCTGGACATCAT	10517
rs373122324	snp	C/T	0.00174064	0.0294498	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18756085	ACCAGAACGAGGAAA[C/T]GCAGCAGGTCCTGAT	10517
rs373192421	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760905	CTAATATTTTCTTCT[A/G]TCAACATTACAGTTT	10517
rs373196959	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18762908	TAAATTTAAAAAACC[A/C]ACCTGAAGACATATA	10517
rs373225292	snp	A/C	0.000153988	0.00877328	intron-variant	FBXW10	GRCh38.p7	17:18772700	TAAAAAACTGAAATA[A/C]CAGCAAGTTCAGTGA	10517
rs373241895	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18763882	AAAAACCACCTGACA[C/T]TGATCAAGCATTTTG	10517
rs373299198	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18747643	ATTGAAGAAAATTCA[A/G]CTTGAGCTTCCGAAG	10517
rs373305814	snp	A/G	4.95311e-05	0.00497625	intron-variant	FBXW10	GRCh38.p7	17:18751092	CAAGTAGCTGTGAGC[A/G]TCTCATTCTAATTGT	10517
rs373308289	snp	A/G			intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775234	AAGGGAACAAGTGGC[A/G]CGGATGGTGGGCAGG	10517
rs373446321	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18745984	AGAAGCATGGCACCA[A/G]CATCTCTTTCTGGTG	10517
rs373483392	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742412	TAGAAAAGGAGGTGC[C/T]GAGGGGCAACAACAT	10517
rs373487829	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18757562	TGAGGTAGGAGGATC[A/G]CTTGAGGCCAAGAGT	10517
rs373519556	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18770362	AGGCTGGAGTGCAGT[A/G]ATGTGATCTCGGCTC	10517
rs373550846	in-del	-/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742908	TGTCAGCCTCATAGA[-/T]TAAAATCCTAATTTA	10517
rs373584385	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18765377	TAGTTAGGGCTAACC[G/T]AGCAGAAATGATTAA	10517
rs373590960	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18747221	ATGAACCATCACGCC[A/G]GGCCAACAACCTTCT	10517
rs373606674	snp	G/T	1.65282e-05	0.00287469	intron-variant	FBXW10	GRCh38.p7	17:18768521	TTGAAGACAGTGGTA[G/T]CTTTTCTTGCAGACT	10517
rs373632534	snp	C/T	6.29716e-05	0.00561087	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779177	AGTCCACTGGAGTGG[C/T]TGATCCAGGAAAAGT	10517
rs373641042	snp	A/C	0.0225045	0.103662			GRCh38.p7	17:18741165	ATGATACTAATAATA[A/C]TTGTTAGCTCCTCAC	10517
rs373654877	snp	A/C/G	0.000407255	0.0142643	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758404	CATACAAGTGAAAGC[A/C/G]ATACCCGTTGAATTC	10517
rs373925015	snp	C/T	8.46647e-05	0.00650578	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778794	ACGAACCAGTATTCC[C/T]CTTGAAATCCAGAAA	10517
rs374106016	snp	A/G	0.000100398	0.00708442	intron-variant	FBXW10	GRCh38.p7	17:18766687	TTTCCCCACTCCCAT[A/G]TCTTCCTCTCTCTCC	10517
rs374109595	snp	A/G					GRCh38.p7	17:18740523	TTTCTGGCTTGCTCT[A/G]TAGTCTTGTTGGGAA	10517
rs374114257	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18774602	AGTTTGAGACCAGCC[C/T]GACAAACATGGAGAA	10517
rs374121502	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18756580	ATGTCTACCCTTCTA[A/G]AATTCTTTTCTTTGC	10517
rs374125112	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18767623	TATTCTTGCTGGATC[G/T]GAACCCCTAGCCTTA	10517
rs374206318	snp	C/T	4.94222e-05	0.00497078	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749755	CACTCCGGTGTATAT[C/T]CGAAATGAATAGGCT	10517
rs374281871	snp	A/G					GRCh38.p7	17:18741681	GGCTGCTCGTAGCCT[A/G]AATACTTGAGAGGTC	10517
rs374283633	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18757031	TAAGGGCAAAAATGT[A/C]AAGAATTGCTCCTTA	10517
rs374317959	snp	G/T	0.000399281	0.0141238			GRCh38.p7	17:18741053	AGCGTGAACCACCGC[G/T]CCCAGCCAAGCTTTT	10517
rs374320648	snp	C/T	0.00279162	0.0372561			GRCh38.p7	17:18740821	GCTGGAGTGCAGTGG[C/T]GCTATCTTGGCTCAC	10517
rs374335912	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18749104	CCATTCATTTCCCCC[A/C]CTTTCTTAAGTTGTT	10517
rs374450568	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18776021	GCCTCTTAAAGAAAA[A/G]AAAAAAAAAAAAAGT	10517
rs374611444	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, intron-variant, nc-transcript-variant	FBXW10	GRCh38.p7	17:18769954	CGTGTCCCTTCTCTT[C/T]CTCCGGGTCATCAGC	10517
rs374846355	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18755510	GCAGTGAGCTGAGAT[C/T]GCACCACTACACTCC	10517
rs375062830	snp	A/G			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742333	GCACTCACTTGCTCT[A/G]GAGCACCCCTTGTCC	10517
rs375198642	snp	C/T	4.95471e-05	0.00497705	intron-variant	FBXW10	GRCh38.p7	17:18751098	GCTGTGAGCGTCTCA[C/T]TCTAATTGTCATTGA	10517
rs375247688	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18755187	AGAATTGCCTGAACT[C/T]GGGAGGCGGAGGTTG	10517
rs375251286	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18766663	CTGTAACCTTTCCTT[G/T]TCCCCCTTTTTCCCC	10517
rs375352795	snp	A/G	6.64099e-05	0.00576199	missense, nc-transcript-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775184	AGTCAAAATCACCCC[A/G]AAGAGATGGTAAGAA	10517
rs375386762	snp	A/C/T	3.29838e-05	0.00406092	intron-variant	FBXW10	GRCh38.p7	17:18764694	CTACGCAGTATGATC[A/C/T]TCTGGGCCCTCAGGA	10517
rs375390149	snp	G/T	3.29533e-05	0.00405901	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18768613	GAAGTACTGATGGCC[G/T]GGTCATGGCCTGGAG	10517
rs375535196	snp	G/T	1.73408e-05	0.0029445	intron-variant	FBXW10	GRCh38.p7	17:18772385	TCCACAGTCCTTTTG[G/T]GGACAACCCTGTTGT	10517
rs375579501	in-del	-/AA	0.110519	0.207473	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742986	AACAAGTTAATTACG[-/AA]AAAAAAAAAAGAGCT	10517
rs375622049	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18751879	ATATAGCCCTTTCCA[C/T]TAGTTCTTGGGCAAT	10517
rs375662938	snp	A/C/G	3.39186e-05	0.00411805	synonymous-codon, missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778755	TGATCGGTTGAGATT[A/C/G]AGCAATCCTCCTATA	10517
rs375699839	snp	C/T	0.000115336	0.00759305	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749745	TGGAGGAATTCACTC[C/T]GGTGTATATCCGAAA	10517
rs375772086	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757137	AAAAATATATGTATA[C/T]ACACACACACATATA	10517
rs375801478	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18751481	GTGATCCTCCCGCCT[C/T]GGCCTCCCAAAGTGC	10517
rs375868487	snp	C/T					GRCh38.p7	17:18739230	GGGCATGGTGGTGCG[C/T]GCCTGTAATCCCAGC	10517
rs375915301	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18748235	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	10517
rs375919515	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18760948	TCAGTTTTTTAATCT[A/C]TTTGCAATTCAACCT	10517
rs375951034	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18768309	CTGACCTTGTGATCC[A/G]CCCGCCTCGGCCTCC	10517
rs375952947	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18748607	CACAGCTGGTAAGGG[A/G]AGGAGCAAGGATTAA	10517
rs375966968	snp	A/G	0.000137455	0.00828906	intron-variant	FBXW10	GRCh38.p7	17:18772712	ATACCAGCAAGTTCA[A/G]TGATAACCCACAGAG	10517
rs376006877	snp	A/G	4.94214e-05	0.00497074	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751032	GCGTGTGAAACATCC[A/G]AAGTGGAAGCTGAGA	10517
rs376019829	snp	C/G	3.3123e-05	0.00406945	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18764796	CGGTGGTCACCAGGG[C/G]ACTATCACTTGCATG	10517
rs376028839	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18752485	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACTAGG	10517
rs376056941	snp	C/T	9.88354e-05	0.00702908	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751005	TAAAATGGTAGATGA[C/T]GGGAAGAGCATGCGT	10517
rs376114266	snp	C/T	8.27493e-05	0.00643178	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18747945	CTGTGTTTCAGGGCT[C/T]AATCAAGACATCACA	10517
rs376241364	snp	C/T	3.29766e-05	0.00406045	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18748057	ACATCCCTTCCTTTG[C/T]CCAAAGCCCCAGAAA	10517
rs376553619	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18763918	GTTAGTCACTATTCC[A/G]GTGTTATCTCCACTG	10517
rs376635428	snp	A/G/T	7.65987e-05	0.00618825	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758427	TTGAATTCCGAGGCC[A/G/T]TGCTGGGAGTGTCCG	10517
rs376654494	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742074	TTTTTAGTAGAGATG[A/G]GGTTTCACCGTGTTA	10517
rs376670862	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18762279	TAATTGGTTTTTCTA[C/T]GTAGACAATCCTATC	10517
rs376761725	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18747010	CACTGCTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	10517
rs376772140	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18760178	TGATGGGTATTAAAT[A/G]AAACCCACTGTGTTT	10517
rs376789796	snp	G/T	1.93763e-05	0.00311252	intron-variant	FBXW10	GRCh38.p7	17:18766901	GGCGGAAAGGGCACT[G/T]GGGAGGAGATGGGTG	10517
rs376791823	snp	A/G	0.000355492	0.0133274	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758319	GGTGGGATCAAAACC[A/G]AGTCATCCACTATTC	10517
rs376804860	snp	A/G	8.2618e-05	0.00642668	missense, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18772651	AACCTCCCAAGTCCC[A/G]AGTACTCCTGAAGCC	10517
rs376869403	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18770592	CAGGTGTGAGCCACC[A/G]CGCCCGGCCTGTTTT	10517
rs376909141	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18758019	GGCAATGCCACATAC[G/T]CCATTCTCTCTCTTG	10517
rs376972738	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18754842	CGACTTGATAAAATT[G/T]ATTTCCTTTCCCTGA	10517
rs377050932	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18739925	GTAGACTAAATATAC[A/G]TGGCATTTATAATGC	10517
rs377068064	snp	A/C/T	0.000505276	0.0158867	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778570	TGGAAAATCCCTATG[A/C/T]CACCTGACCAATTCC	10517
rs377141244	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18767429	ACGTTGCAGTGAGCC[A/G]AGATCATGCGTCTCA	10517
rs377162869	snp	C/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742083	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	10517
rs377326035	snp	A/G	5.22634e-05	0.00511165	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778506	AGCACAAAAACAAGG[A/G]CAATTGGAAACTCCT	10517
rs377437115	snp	C/G	0.000100212	0.00707785	intron-variant	FBXW10	GRCh38.p7	17:18769878	CTACAAACAAACCCA[C/G]GCATTTTACGAGAGG	10517
rs377470335	snp	C/T			intron-variant, missense	FBXW10	GRCh38.p7	17:18771602	GCATGGAGTGTGTGG[C/T]GTCTGCGTGGAGGGT	10517
rs377476079	snp	A/G	1.6486e-05	0.00287102	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744548	AAAGAGGGGAAAGTT[A/G]TGAAGTCCTCCTTGA	10517
rs377525526	snp	G/T			intron-variant	FBXW10	GRCh38.p7	17:18756841	CCACTTCTACTTTAT[G/T]TTTGGCCATGAATCT	10517
rs377563779	snp	A/G					GRCh38.p7	17:18740792	TTGAGACGGAGTCTC[A/G]CTCTGTCGCCTAGGC	10517
rs377567516	snp	G/T			upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742582	ATTAAAACTGCTTCC[G/T]TGGCCTGGGGTGGTG	10517
rs377572808	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18757603	AGGGAGTTATTATTG[C/T]GCCCCTGTACTCCAG	10517
rs377642870	snp	A/G	0.000473789	0.0153841	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778781	CTATAGATGTGAAAC[A/G]AACCAGTATTCCCCT	10517
rs377683448	snp	C/T					GRCh38.p7	17:18740710	TCACCTGAAAGAAAG[C/T]GTGTATATATGTGCA	10517
rs377698809	in-del	-/T	0.474453	0.110094	intron-variant	FBXW10	GRCh38.p7	17:18751225	ACAAGACACTTCCTC[-/T]TTTTTTTTTTTTTTT	10517
rs377714384	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18753166	ACACAGATAAGACAT[C/G]TAGGGCACAGAGGGA	10517
rs386795990	multinucleotide-polymorphism	ACT/GCA					GRCh38.p7	17:18739378	AAAAAAAAGAGTTGG[ACT/GCA]TATTTGCCTTCTGTC	10517
rs397736684	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18770321	TTTTTTTTTTTTTTT[-/T]GAGACATAGTTTCAC	10517
rs397760475	in-del	-/A	0	0	intron-variant	FBXW10	GRCh38.p7	17:18767461	AAAAAAAAAAAAAAA[-/A]TTCTGGCATGGGGTG	10517
rs397776716	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18750638	ACTTGGATTTTTTTT[-/T]CCCCCAGCAGAGAGG	10517
rs398030480	in-del	-/TT	0	0	intron-variant	FBXW10	GRCh38.p7	17:18749387	GGCTAATTTTTTGTA[-/TT]TTTTTTTTTTTTAGT	10517
rs398030481	in-del	-/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18760795	ACATTCATATTGAGA[-/T]TTTTTTTTTTTTTTT	10517
rs527253743	snp	C/T	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18748986	ATAGATTCTAAAACA[C/T]TTTTATATGGAAAAT	10517
rs527256828	snp	A/G	0.0581099	0.160244			GRCh38.p7	17:18740910	GGACTACAGGCACCC[A/G]CCACCACGCCCAGCT	10517
rs527290895	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18748014	GTCTGCGACCTCACA[A/G]GTCTATTGGACAGCC	10517
rs527398401	in-del	-/A	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18762899	TTCTTGCATAAATTT[-/A]AAAAAACCAACCTGA	10517
rs527434565	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18756340	CCATTCTTGGCAGTG[A/G]GTAAAGGACACTTTC	10517
rs527472639	snp	C/T	1.65466e-05	0.00287628	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778602	CCTGACTGTTAGCGC[C/T]CTGCAGCACGCCCAT	10517
rs527525614	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18758087	GCCTTGTGTCTCTAG[C/T]TTTTAAATTTAACGG	10517
rs527545898	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18777733	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	10517
rs527616813	snp	A/C	0.000399281	0.0141238			GRCh38.p7	17:18741159	TCCCTAATGATACTA[A/C]TAATAATTGTTAGCT	10517
rs527639139	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18751495	TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG	10517
rs527697324	snp	C/T	1.65332e-05	0.00287512	intron-variant	FBXW10	GRCh38.p7	17:18764911	GTTTCCCCCGACCCA[C/T]GGGTTACCAAAATGC	10517
rs527698517	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18757583	GGCCAAGAGTTGGAG[A/G]TTACAGGGAGTTATT	10517
rs527730495	snp	A/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18764424	CCAGTATGGTCTCAA[A/T]CTCTTGATCTCATGA	10517
rs527766494	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18774565	TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG	10517
rs527850698	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742844	CCCTCCAGCCTGGGG[A/G]ATAGAGCGAGACTCT	10517
rs527889517	snp	C/T	0.00755907	0.0610114	intron-variant	FBXW10	GRCh38.p7	17:18750465	CAAGAAAGCCATAAA[C/T]GTGTCTCTGCATCAA	10517
rs528013240	snp	C/T	6.65713e-05	0.00576899	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18750028	TGCTGGATAGACACA[C/T]CCTGAACAAGTGCGC	10517
rs528028784	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18758995	ACATGGTGAAACCCC[A/G]TCTCTACTAAACAAA	10517
rs528254231	snp	A/C	0.0115144	0.0749975	intron-variant	FBXW10	GRCh38.p7	17:18751441	TTCACCGTGTTAGCC[A/C]AGATGGTCTTGATCT	10517
rs528313268	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18767179	TCTCCTCCAGAGTAT[C/T]GCACTCTGTAGGGCC	10517
rs528345764	snp	C/T	0.000483482	0.0155405	intron-variant	FBXW10	GRCh38.p7	17:18766692	CCACTCCCATGTCTT[C/T]CTCTCTCTCCCTCCT	10517
rs528441359	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18745421	GATTCTGTATGTCTT[G/T]TCTTTTTTTTTTGAG	10517
rs528488880	snp	C/T	1.6513e-05	0.00287336	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744410	ATATCACAGAGGAGG[C/T]TTCTAGTTGGCATTC	10517
rs528675030	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18768137	CAGTGGTGAGATCTT[G/T]GCGCACTGCAACCTC	10517
rs528711712	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18774744	AGGTTGCGGTGAGCC[A/G]AGATCGTGCCATTGC	10517
rs528825724	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18762752	TCATCTTGTTCCCCT[C/T]CTGGAAGGGAATACA	10517
rs528839933	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18754279	TGAGCAAGGGCCAAT[G/T]AATTCTCACCTGGGT	10517
rs528862309	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18761429	CGCCACCACGCCTGG[C/T]TAATTTTTTGTATTT	10517
rs528874942	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18761544	TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC	10517
rs529081835	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747293	TGGTTGGGCGCAGTG[A/G]CTCACGCTTGTAATC	10517
rs529090704	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:18739379	AAAAAAAGAGTTGGA[C/T]TTATTTGCCTTCTGT	10517
rs529193391	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18755079	ACCAGCCTGGCCAAC[A/G]TGGTGAAACTCCGTC	10517
rs529262937	snp	G/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18770138	TCTGTTGGATTTTTT[G/T]ATTTTTTTCCTCCCC	10517
rs529310221	snp	C/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18769558	AAGGTAGGTGGATCA[C/G]CTGAGGTCAGGATTT	10517
rs529349812	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18776643	CTAGAAAGATATTGC[C/T]AAGGTTGTCCTGAAA	10517
rs529470940	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18748207	AGCAGATCATGAGGT[C/T]AGGAGATCGAGACCA	10517
rs529527529	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18764275	GGCACAATCTCAGCT[C/T]GCTGCAACCTCTGCC	10517
rs529659477	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:18741793	CTATTTGCCCACCTG[C/T]CTGTTTGAGTACCAC	10517
rs529662653	snp	C/T	0.000798403	0.0199641			GRCh38.p7	17:18741244	GGTAGGACCATGGTC[C/T]CTACTTCATGGAAGA	10517
rs529713363	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18778211	TGAGCAGAGATCATG[A/C]CACTGCACTCCAGCC	10517
rs529795313	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18749260	GATTCTATTCTCGGC[C/T]GAGTGCGGTGGCTCA	10517
rs529885273	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18772193	GCCCCGATCATGTTT[A/T]TTTTTTAAAGAAAAG	10517
rs530007971	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18750548	AAATGAAATTTTCCC[C/T]AATGGCAATCTTCTC	10517
rs530044590	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759059	CCTGTAGTCCCAGCT[A/C]CTCGGGACGCTGAGG	10517
rs530179152	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18758446	TGGGAGTGTCCGGGC[C/T]CTCTTCCTGTGTGAG	10517
rs530261392	snp	A/G	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18765884	GTCGCACGCCACCAC[A/G]CCCAGCTAATTTTTT	10517
rs530276432	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18740825	GAGTGCAGTGGTGCT[A/G]TCTTGGCTCACTGCA	10517
rs530321272	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743709	CTTAAATTTACATTA[A/G]ACATTTCTGGTTTTA	10517
rs530367432	snp	C/T	0.00438332	0.0466095	intron-variant	FBXW10	GRCh38.p7	17:18751227	AAGACACTTCCTCTT[C/T]TTTTTTTTTTTTTAA	10517
rs530400237	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18766609	CTGACTTGATGGGCT[C/T]GATGAGTCTTTGCTT	10517
rs530447840	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18773943	GAAGATCCTTTAAAT[A/G]GACAAAAACAGAGGT	10517
rs530484339	snp	C/T	0.00478085	0.0486577	intron-variant	FBXW10	GRCh38.p7	17:18773014	GCTCACCGCAACCTC[C/T]GCCTCCCAGGTTCAA	10517
rs530512490	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18767248	GAGGCCGAGGCAGGC[A/G]GATCATGAGGTCAGG	10517
rs530587018	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18776685	AATTTACACTCCTAC[C/T]TGCAATATATGAGAG	10517
rs530588304	snp	C/T	1.6525e-05	0.00287441	stop-gained, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744464	TTGTTACACTATTTC[C/T]AAAATATCCTTCAGA	10517
rs530625520	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760766	CCAGGGCAACAAGAG[C/T]GAAACTCGGTCTCAA	10517
rs530694659	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18753061	TCTTGGACAAACACC[A/G]CCACTTTAAGTTCCA	10517
rs530999836	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18769434	AAGTAGCTGCAGAAT[A/G]GGAAGAGGTATGTCT	10517
rs531058653	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18745489	GGTGCGATCTTGGCT[C/T]ACTGAAACCTCCACC	10517
rs531121407	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18761556	AGGCATGAGCCACCG[C/T]GCCCGGCCTCACTTT	10517
rs531127448	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18763391	TCGATCTCCTGACCT[C/T]GTGATCTGCTTGCCT	10517
rs531179629	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747399	AACCCCATCTCTACT[A/G]AAAATACAAAAAATA	10517
rs531187185	snp	A/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18775844	GCCAGCCTGGGCCAC[A/T]TAGCAAGACCCTTGT	10517
rs531213725	snp	A/G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18755239	TTGCACTCCAGCCTG[A/G/T]GTGAGAAGAGTGAAA	10517
rs531349742	snp	A/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18762236	CAAAGTGCTGGGATT[A/T]CTGGCGTGAGCTACT	10517
rs531350313	snp	G/T	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18754461	ATCTGAGGAAGAGTC[G/T]AAAGGCATGGAGCAG	10517
rs531399998	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18777696	CTACAGGCGCCCGCC[A/G]CCATGCCGGGCTAAT	10517
rs531502682	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18756202	GGATGCTTGAGTTAC[C/G]CACACTGACATTTGG	10517
rs531503242	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:18740882	TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA	10517
rs531538102	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18752464	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	10517
rs531561948	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18774475	AGTTCCAGCGTTTGG[C/T]TGCACGGTAGGATGA	10517
rs531593970	snp	A/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18764374	GCCCAGCTAACTTTT[A/G]TATTTTTAGTAGAGA	10517
rs531602104	snp	C/T			intron-variant, synonymous-codon	FBXW10	GRCh38.p7	17:18771639	AGGAGAAGAGGCCTC[C/T]CCATTAGAGAGCTTT	10517
rs531650512	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18778067	CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	10517
rs531650623	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18770208	TGTGCAATGCCTCTC[C/T]ACAATTCTGGCTGGG	10517
rs531699302	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744613	GAAAGAGATCTTGTA[C/T]TGGTTTGCGAACAGC	10517
rs531860538	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18747286	AATGTTCTGGTTGGG[C/T]GCAGTGGCTCACGCT	10517
rs531913238	snp	C/T	0.00517822	0.0506191			GRCh38.p7	17:18741331	AGAGCCCAGTTCATT[C/T]CTTGCCCTCCTACTC	10517
rs531915116	snp	A/G	1.66499e-05	0.00288525	intron-variant, missense	FBXW10	GRCh38.p7	17:18749931	ATTCTAAGTATGCTG[A/G]GGTGTATGAGGGGAT	10517
rs531945655	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18758158	AGGCCTGTTAATTCT[C/T]GACCTTGCCTTCTGC	10517
rs531952445	snp	A/C	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18749361	GGCTAACACGGTGAA[A/C]CCCCGCCTCTACTAA	10517
rs532139220	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779652	GGATTATATCAGGGT[A/C]ATGCATTGGTGTTTT	10517
rs532177780	snp	C/T	0.000374353	0.0136761	stop-gained, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778729	AAAGGAAAATCAATC[C/T]AACGTGCAGTTGATC	10517
rs532194509	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759118	GAGCTTGCAGTGAGC[C/G]GAGATGGTGCCACTA	10517
rs532318254	snp	A/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18766576	GAGGTGCTAGGCCAC[A/G]GGAAGTCCTTCTAGA	10517
rs532345268	snp	C/T	0.00358779	0.0422022	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744045	CCAAGGAGGTCTGTA[C/T]AAAAAGCCAGACTTC	10517
rs532382829	snp	A/C	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18751382	AGGAGCCCGCCACCA[A/C]GCCCGGCTAATTTTT	10517
rs532407691	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18772279	CCCTCCAGCTGCCTA[C/T]ACTACTAGTCTGTTT	10517
rs532686532	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759658	CACTGTGTCACCCAG[C/G]CTGGAGAGCAGTGGC	10517
rs532702039	snp	G/T	0.000841064	0.0204896	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744396	GCAGGATCAATGACA[G/T]ATCACAGAGGAGGTT	10517
rs532757590	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18759213	ACAATATAACAAACA[C/T]TCATGCATCCATTAC	10517
rs532786515	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18768064	TCCTTCTTTCTTTCT[G/T]TCTTTCTTCTTTCTT	10517
rs532817965	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18767354	GCATGGTGGTGGGCG[C/T]TTGTAACCTCAGCTA	10517
rs532826564	snp	A/G					GRCh38.p7	17:18741030	CCTCCCAAAGTACTG[A/G]GATTACAAGCGTGAA	10517
rs533135456	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18746403	GTGGTCACATGGAGG[C/T]GTTTTGGAGTTTTAG	10517
rs533160721	in-del	-/T	0.000513387	0.0160134	intron-variant	FBXW10	GRCh38.p7	17:18778459	TTTTTTAAAATTTTC[-/T]TTTTTTTTGAAAAAG	10517
rs533246198	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18751921	ACCGGAAGACTCTTC[A/G]AGCTCTTTGCTTTGA	10517
rs533324916	in-del	-/TAAAGTCTATTT			intron-variant	FBXW10	GRCh38.p7	17:18752006	GCTTAAAGTCTATTT[-/TAAAGTCTATTT]AATTGGCCCCAAAAG	10517
rs533356846	snp	A/G	0.00517822	0.0506191	intron-variant	FBXW10	GRCh38.p7	17:18768997	CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT	10517
rs533412488	snp	C/T	0.00835141	0.0640778	intron-variant	FBXW10	GRCh38.p7	17:18755666	GTAATATACATATGA[C/T]GTTCCGACTTCTGTG	10517
rs533501787	snp	A/T	0.000399281	0.0141238			GRCh38.p7	17:18739327	GCACCACTGCACTCC[A/T]GCCTGGGTGACAGAG	10517
rs533546045	snp	G/T	0.00119737	0.0244387			GRCh38.p7	17:18740632	GTCAATATAGCAGTG[G/T]TCAGTCATTTTAGGT	10517
rs533680124	snp	G/T	0.000399281	0.0141238			GRCh38.p7	17:18739839	TGATGACAATGGGAT[G/T]GGCCCAATCACGGAG	10517
rs533742647	snp	A/G	0.00438332	0.0466095	intron-variant	FBXW10	GRCh38.p7	17:18752814	AGATAAAGAAACTGA[A/G]GCTCAGAGAGGTCAA	10517
rs533763506	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18770412	GGGTTCAAGCAATTC[C/T]CTGCCTCAGCCTCCC	10517
rs533767759	snp	A/C	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18762675	TTTTGTTTTTCTTTT[A/C]TTCTAACTTTGCCTA	10517
rs533801135	snp	A/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18769732	CAGTGAGCCAAGATC[A/G]CACCGTTGCACTCCA	10517
rs533825602	snp	A/G	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18776047	AAAGTGGCCGGGCGC[A/G]GTGGCTCACACCTGT	10517
rs534165717	snp	C/T	0.000486934	0.0155958	intron-variant	FBXW10	GRCh38.p7	17:18778445	TTCATAGAACGCCGA[C/T]TTTTTAAAATTTTCT	10517
rs534274091	in-del	-/TTATGGC	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18769821	CCATTTTGAGGCCAG[-/TTATGGC]CAGTGCTGCTCAATC	10517
rs534533719	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742431	GGGCAACAACATACT[A/C]TGGTCCACAGGTGTT	10517
rs534539429	snp	G/T	0.00398564	0.0444627			GRCh38.p7	17:18741515	CCTCTATCTGGCCCA[G/T]CAGCGGCCGCACCTT	10517
rs534570378	snp	C/G	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18750335	TCATTGTCAGTGCAT[C/G]TCACAAGGACAATAG	10517
rs534589207	snp	G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18766058	AGAAAACCCTGTTCT[G/T]CCACCCACCCACCCA	10517
rs534591444	snp	A/C/G	0.00185101	0.0303661	intron-variant	FBXW10	GRCh38.p7	17:18758556	CCTAGGGCCTAGAGG[A/C/G]AGCTCATGGAAGAAG	10517
rs534716374	snp	G/T	1.69298e-05	0.0029094	synonymous-codon, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778797	AACCAGTATTCCCCT[G/T]GAAATCCAGAAACTG	10517
rs534847441	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744065	AGCCAGACTTCTGCT[A/G]GCAGTTACTGAGAGA	10517
rs534871106	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759296	CTCTTCTTGCTTCTT[C/T]CTGCCAACCAGAGGT	10517
rs534879941	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760419	CAACGGTGCAGATGA[A/G]GCCCAAAGGCCATCT	10517
rs534898685	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18751749	AATTTGAGGAGGACC[C/T]GAGGGGAGGGCCAGG	10517
rs534916074	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18767473	AAAATTCTGGCATGG[C/G]GTGAGGGGATGAACA	10517
rs534916316	snp	A/G/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759905	CAGGTGTGAGCCACC[A/G/T]CGCCGGGCCCTTGTT	10517
rs534951527	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18766871	GGTAAAGGTAAGTGG[A/G]CAGTGGGCTACCTTG	10517
rs535016304	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18773208	AAAGTGCTGGGATTA[C/G]AGGTGTGGGCCACCG	10517
rs535085501	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18745662	CTCGTGATCCGCCTG[C/T]CTCGGCCTCCCAAAG	10517
rs535121474	snp	C/T	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18753197	AGTGGGGGGACAGTC[C/T]CTTGGGTAACTACCA	10517
rs535288910	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18775955	CTTTGAGTCCAGGAG[C/T]TTGACGTTACAGTGA	10517
rs535486719	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18752594	TGGCAGTGCCTCTAG[C/T]CCCATCTACTCGGGA	10517
rs535675427	snp	C/T	1.66101e-05	0.0028818	missense, nc-transcript-variant, utr-variant-3-prime	FBXW10	GRCh38.p7	17:18775139	ATCTCAATTTAGCAG[C/T]GTTAATAGAGGAACT	10517
rs535688762	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747529	CCATTGCACTCCACC[C/T]TGGGCAATAAGAGCA	10517
rs535742368	snp	C/T			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779169	GGCCAGGGAGTCCAC[C/T]GGAGTGGTTGATCCA	10517
rs535790258	snp	C/G	0.000399281	0.0141238			GRCh38.p7	17:18738464	CACTTTAGATTTCTG[C/G]TGTGGGTTAATACCA	10517
rs535832161	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18754891	GTAAAATAATGAGAA[C/T]ATTTTGTGGGGCAAG	10517
rs535833964	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18762494	GGCGGCTAATGTTTT[C/T]TTGTATTTTAGTAGA	10517
rs535871950	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18761868	CATAGAGAAATGCAA[C/T]TGATTTTTGTAAATT	10517
rs536022522	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18757610	TATTATTGCGCCCCT[A/G]TACTCCAGCCTGGGT	10517
rs536099665	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18763730	ATCTATCTCTTAGAT[A/G]TGCTCTATATGTACA	10517
rs536190025	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18747025	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	10517
rs536199636	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18755556	CGAGACTCCGTCTGA[A/G]AAAAAAAAATGCAAA	10517
rs536318685	snp	C/T	0.00159617	0.0282053	intron-variant	FBXW10	GRCh38.p7	17:18777206	AGCTAGGATTACAGG[C/T]GCCTGCCACCACGCC	10517
rs536389963	snp	C/T	0.000798403	0.0199641			GRCh38.p7	17:18740982	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA	10517
rs536392843	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18749608	ATCTAGTGGCCTAAG[C/G]TTAGAGTCTGAGGAG	10517
rs536440745	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18765508	GTTTCCTCATCTGTG[C/T]TGTGGGGAATAATAA	10517
rs536478838	snp	C/G	0.00557542	0.0525036	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18771935	CAACATGGCGAAACC[C/G]TGTCGCTACTAAAAA	10517
rs536508261	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18770928	GGTGCTATTATATGA[A/G]AATAACCAAATAGAA	10517
rs536619084	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742125	CTGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC	10517
rs536619204	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18763997	TTCTTTACTGTGGGG[C/T]CTGCCCTGTGCAATG	10517
rs536654572	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18762088	CTTCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10517
rs537026732	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18759840	CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT	10517
rs537111284	snp	A/C	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18766223	AGTGAGGGTAGATGA[A/C]CTTCTTTCATTTTGG	10517
rs537271468	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18761107	ACATTGAAATTTCCC[A/G]TATGTGCATGAGAAT	10517
rs537302393	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18768231	TGCCACCATGCCCAG[C/T]TAATTTTTGTATTTT	10517
rs537374156	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18759788	AGGCTATTTTTTTTT[C/G]TATTTTTTAGTAGAG	10517
rs537474327	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18774112	TCTGCTGTAAAGAGG[C/T]GACAATCACAAGGGG	10517
rs537513807	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18773354	CCAAATTCAAAACAT[A/G]TATTACATAACTATT	10517
rs537598372	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18745725	GACCAGGGATTCTGT[A/G]TTTCTAACAAGTTTC	10517
rs537631673	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18749548	CGAGACTCCGTCTCA[-/A]AAAAAAAAAGATTCT	10517
rs537646016	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18769676	CAGCTACTTGGGAGA[C/T]TGAGACAGGAGAATC	10517
rs537711081	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW10	GRCh38.p7	17:18760452	CAGAGAATACCCTCT[C/T]GCCAGGACTATCTAT	10517
rs537733864	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18761972	CTTTTTCTTTTTCTT[C/T]TTTTTTTTGAGACGG	10517
rs537849444	in-del	-/G	0.00279162	0.0372561	intron-variant	FBXW10	GRCh38.p7	17:18773862	GAGTGCAAAGTTTGA[-/G]GGCAGCATCCAGGGA	10517
rs537857917	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:18738565	ATTTGATACAATTTG[A/G]ATATTTGTCCCCTCC	10517
rs538079198	snp	C/T	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18769181	ACCTCATGATCCACC[C/T]GCCTCAGCCTCCCAA	10517
rs538170478	snp	G/T			intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775507	GGTTTGCGTTTCCAG[G/T]TTTTGGCTGACTGCC	10517
rs538225118	snp	A/G	0.000798403	0.0199641	intron-variant	FBXW10	GRCh38.p7	17:18756517	TGTATAGAGAAAGGC[A/G]AAGTTTTCCTGTAGT	10517
rs538247243	snp	C/T	0.00119737	0.0244387	intron-variant	FBXW10	GRCh38.p7	17:18764545	AATGAGGAAAGGAAA[C/T]GTAACACAAAAATTA	10517
rs538255492	in-del	-/A	0.00398564	0.0444627	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18742279	AAGGTGCAGGCCAGC[-/A]AGGAGGCAGGGAGGA	10517

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