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

FEM1B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs769492587	snp	A/C			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277474	CCGGCTCAGGGGCAG[A/C]AGCAGGACCCGCACC	10116
rs769495920	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291720	GCCAAACTGCTGTAG[A/G]TAGTTTACACTCTTC	10116
rs769623041	snp	C/T	1.64751e-05	0.00287007	synonymous-codon	FEM1B	GRCh38.p7	15:68291017	TTTTTTGACCTTGCA[C/T]TCCATCATCATTAGC	10116
rs769728625	snp	C/T	1.65425e-05	0.00287593	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278585	CATCGCAGCCCGCAA[C/T]GGACACGCAAAGGTG	10116
rs769774488	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	FEM1B	GRCh38.p7	15:68290327	GCAAGACAGAGATGC[C/T]CTTCATATGGAAGGC	10116
rs769853958	in-del	-/CA			intron-variant	FEM1B	GRCh38.p7	15:68286476	GACCTCTTGGACTCA[-/CA]CACACACACACACAC	10116
rs770012854	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276056	CAGAAAAGGAAGTCA[C/T]CACACATCTGAATGT	10116
rs770012994	snp	C/G	1.64925e-05	0.00287158	synonymous-codon	FEM1B	GRCh38.p7	15:68290501	AGGTAACAGGAACAC[C/G]CACAAGGATCTTCTT	10116
rs770017372	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68279867	ATTATACACATTAAG[G/T]AGATGTTTTTTTTCA	10116
rs770485475	snp	A/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278273	TTCCCTGGGCCGCAC[A/T]GCTGCCTGGGCGCGG	10116
rs770558578	snp	A/G			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278963	GTCTGTGAACAAGCC[A/G]TTTGGAGGAGGTGGC	10116
rs770659641	snp	C/T	3.30836e-05	0.00406702	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278607	GCAAAGGTGGTACGC[C/T]TGCTCTTAGAACATT	10116
rs770691347	in-del	-/AGCC			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293780	TTTGAAAATATGTTT[-/AGCC]AGCCAGACCCTTCCC	10116
rs770819033	snp	A/G	1.67184e-05	0.00289118	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278695	AGCCAGCCTCTCTCC[A/G]ACGCGCGCGGACTCG	10116
rs770853845	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68284618	CTAGTCACTCTCTAG[A/T]TCAATGTGTAGAACA	10116
rs771003642	snp	A/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295057	ATGCCCTCCCCCAAA[A/T]AAGGGATCTGAAATA	10116
rs771011808	snp	A/G	1.64792e-05	0.00287042	missense	FEM1B	GRCh38.p7	15:68290709	ACCTTTCTGTATTTA[A/G]TGTGCATCTCTACCA	10116
rs771040816	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278068	GACCCGTAGCTCGGG[C/T]ACGCGCCTGTCGCAT	10116
rs771201983	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281294	GTCATTCACGTGCTA[A/G]CTTCATAATTTTTGG	10116
rs771300003	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68282880	CTTTAATCTGTTTAA[-/T]ATTTTGATTTAGATG	10116
rs771335626	snp	A/G	9.93164e-05	0.00704616	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289832	TGACAACACCTGCCT[A/G]ATGATTGCGGCATAT	10116
rs771427645	snp	A/G			missense	FEM1B	GRCh38.p7	15:68290281	GGAATAGAACTGAAT[A/G]TAGAAATCCTCAGGA	10116
rs771506572	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68279534	TGTATAACGATTTTG[A/C]TACATATGTTTTGGT	10116
rs771625699	snp	A/C/T	8.36402e-05	0.0064664	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278701	CCTCTCTCCGACGCG[A/C/T]GCGGACTCGTTAATT	10116
rs772156479	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68282440	TAAAATAAAGTGTGG[A/G]TCATTTATATTTAAT	10116
rs772206739	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276195	TTCAGAGACGCTACC[A/G]GTAGAATCTTACCTT	10116
rs772563011	snp	C/T	4.9476e-05	0.00497348	synonymous-codon	FEM1B	GRCh38.p7	15:68290012	AGTAGTGAATGGCCA[C/T]GGGATGACGCCATTG	10116
rs772569429	snp	C/T	3.29516e-05	0.00405891	synonymous-codon	FEM1B	GRCh38.p7	15:68290738	CAAAACACAGTGCAG[C/T]GAAGAAGATCAGTGC	10116
rs772579577	snp	G/T	1.64944e-05	0.00287175	synonymous-codon	FEM1B	GRCh38.p7	15:68290129	TTTGGAACTCTTGGG[G/T]GCCTCCTTTGCAAAT	10116
rs772772546	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288931	TTCACTACCTCTCCC[C/T]AAAAGTAACCAGTAT	10116
rs772835151	in-del	-/TTC			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291771	CAGCACATTTTAGCA[-/TTC]TTCAGGAGGATTTTT	10116
rs772972196	snp	C/G	4.94262e-05	0.00497098	missense	FEM1B	GRCh38.p7	15:68291019	TTTTGACCTTGCACT[C/G]CATCATCATTAGCCT	10116
rs773060355	snp	C/T	1.73426e-05	0.00294466	missense	FEM1B	GRCh38.p7	15:68291214	ACCAGATCCCCAGAA[C/T]TCTTGAAGAGTTTGT	10116
rs773062081	snp	G/T	1.65715e-05	0.00287845	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278540	TGGCTATGTCAGCCA[G/T]CAGGGAGGGCAGCGC	10116
rs773076788	snp	A/G	1.65414e-05	0.00287583	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278594	CCGCAATGGACACGC[A/G]AAGGTGGTACGCTTG	10116
rs773079080	snp	C/G	3.29886e-05	0.00406118	synonymous-codon	FEM1B	GRCh38.p7	15:68290195	CTATCTATATTTAGC[C/G]ATGTTAGAGAGGTTC	10116
rs773243888	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294160	CAAACCCATCCCCTC[A/G]ATTGATAAAGAAGGG	10116
rs773683829	snp	A/C	1.67947e-05	0.00289777	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278717	GCGGACTCGTTAATT[A/C]ACGGGCCCTCCCCTC	10116
rs774056725	in-del	-/AGTA			intron-variant	FEM1B	GRCh38.p7	15:68284836	TGCTGTTCTCTTGAT[-/AGTA]AGTGTCACGGGATCT	10116
rs774181670	in-del	-/GTGT			downstream-variant-500B	FEM1B	GRCh38.p7	15:68295897	TTTATTAATTATTCA[-/GTGT]GCCTTAGTTGCGATG	10116
rs774193213	in-del	-/TTTTACA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294182	AAAGAAGGGGAACAT[-/TTTTACA]TTAGAACTGACACTG	10116
rs774245168	snp	C/T	1.64836e-05	0.0028708	synonymous-codon	FEM1B	GRCh38.p7	15:68290405	TCATCCCATCATTTA[C/T]AGAGGAGCTGTTTAT	10116
rs774322241	in-del	-/AAAAAAAAAAA			intron-variant	FEM1B	GRCh38.p7	15:68283509	ATCTCTACCTAAAAA[-/AAAAAAAAAAA]AAAAAAAAAAAAAAG	10116
rs774331177	snp	A/G	1.65007e-05	0.00287229	missense	FEM1B	GRCh38.p7	15:68290541	CAAGTTTTCTCACAA[A/G]TGATACATTTGAATG	10116
rs774354567	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68284645	AACACTTTATCACTC[C/T]AAAAGTTTCCCTTGT	10116
rs774533588	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278337	AGGGCCCAGGTTTAA[A/G]GCGCTGGCGAACGCG	10116
rs774656717	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278286	ACTGCTGCCTGGGCG[C/G]GGCGGCGGCGACGGC	10116
rs774683164	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292081	TGTCACAGTGTAGTT[A/G]TACATTCTATTTTTG	10116
rs774744183	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68289114	ACTCAATTAGCTTAG[C/G]GGAAACTTACCTGCT	10116
rs774744397	snp	C/T	1.6483e-05	0.00287076	synonymous-codon	FEM1B	GRCh38.p7	15:68290696	ATGTAATCTCTATAC[C/T]TTTCTGTATTTAGTG	10116
rs774841707	in-del	-/GAGAGACAGA			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275969	GGAGTTAGAGATATG[-/GAGAGACAGA]GAGAGATAGAAAGGC	10116
rs774903303	snp	A/G	3.2994e-05	0.00406152	missense	FEM1B	GRCh38.p7	15:68289995	AAATGGCGTGCTGCT[A/G]TAGTAGTGAATGGCC	10116
rs775256769	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68287726	ATCAAGGTGCCAGTA[G/T]GTTCAGTTGTCTGGT	10116
rs775266107	snp	A/G/T	0.000115325	0.00759278	missense, stop-gained	FEM1B	GRCh38.p7	15:68290739	AAAACACAGTGCAGC[A/G/T]AAGAAGATCAGTGCA	10116
rs775340231	snp	A/G			missense	FEM1B	GRCh38.p7	15:68290556	ATGATACATTTGAAT[A/G]AAACTGTGAAGGCCC	10116
rs775418507	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294316	CCAAAGCAGACCATC[C/T]GTAAGCTTTGGTCTG	10116
rs775421523	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68284034	GGGATTACAGACATG[C/T]GCCACCACACCTGGC	10116
rs775864890	in-del	-/AAAA			intron-variant	FEM1B	GRCh38.p7	15:68286801	CAATAAAAACATAAC[-/AAAA]AAATAACAAAAGTGA	10116
rs775905482	snp	C/G	1.67114e-05	0.00289057	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278486	GACTCTGGCCGCCTT[C/G]CTTCTCAACCGGTCT	10116
rs775928993	snp	C/G	1.64939e-05	0.0028717	synonymous-codon	FEM1B	GRCh38.p7	15:68290132	GGAACTCTTGGGTGC[C/G]TCCTTTGCAAATGAC	10116
rs776077957	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277457	CAACCCCTTCCCTAA[C/T]CCCGGCTCAGGGGCA	10116
rs776079037	snp	A/G	1.64811e-05	0.00287059	missense	FEM1B	GRCh38.p7	15:68291045	AGCCTAGTTGAAGCC[A/G]GAGCTCACACTGACA	10116
rs776100984	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68287325	TGCAGAGGTCTTAAG[C/T]ATGCAGTTTGGTGAG	10116
rs776262186	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295791	CCTAATAACTCAGCT[A/G]ATTTGAAACTAACAA	10116
rs776309145	snp	C/T	1.65999e-05	0.00288091	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278520	AGCGACATCCGCTAT[C/T]TGCTTGGCTATGTCA	10116
rs776379045	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276272	TAACTCGTGTTTCTG[C/T]AGGGATCTGCAATAA	10116
rs776417687	snp	A/G	5.36812e-05	0.00518051	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278391	GCAGCGGTGGCGACC[A/G]AACGGGTGTTGGAGT	10116
rs776476475	snp	C/G	1.64746e-05	0.00287002	missense	FEM1B	GRCh38.p7	15:68290787	TACAACCTGATTCAC[C/G]TTGATCCCAGAACTC	10116
rs776498279	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	FEM1B	GRCh38.p7	15:68290999	CAACAGGCCCATCAG[C/T]GATTTTTTGACCTTG	10116
rs776743293	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292844	GAGATACCCCACAAA[A/G]TGAAATATTTTGAAG	10116
rs776781660	snp	A/G	9.88761e-05	0.00703052	missense	FEM1B	GRCh38.p7	15:68290311	AACTGGAGTCCATTC[A/G]GCAAGACAGAGATGC	10116
rs776889699	snp	A/G	0.000164919	0.00907921	synonymous-codon	FEM1B	GRCh38.p7	15:68290174	TGACATCATAAAGAC[A/G]TACCACTATCTATAT	10116
rs777112138	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279769	GCTTTTTCTTCTATT[C/T]TAGATGAGTGGAAAA	10116
rs777118460	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293869	AGCCCTCTGTGAACT[C/T]TAGGCTGTCTCCATT	10116
rs777200098	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279222	CAGACATCTCAAGAC[A/G]TGATTCTGATTCCTC	10116
rs777247568	snp	A/C			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279066	CATTGAAGAACTCCG[A/C]AAGAGTTATTTGGGC	10116
rs777251676	snp	A/G	1.6557e-05	0.00287719	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278626	TCTTAGAACATTACC[A/G]GGTGCAGACTCAGCA	10116
rs777320070	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291623	CAGCATGTTATCCAT[A/G]CAGCAGTTTTGAGGA	10116
rs777326998	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295497	GGAGTAAAATCTGAC[-/T]GGCCTAATCGATGGA	10116
rs777505284	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68285447	CCAAATAGTTTCCCC[A/G]AAGTTCAACAACCAA	10116
rs777541915	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68279361	TGATCATTTACTGTT[A/T]GTTGAGGTGGGAAGT	10116
rs777735211	snp	C/T	5.00948e-05	0.00500449	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278689	ATCCCAAGCCAGCCT[C/T]TCTCCGACGCGCGCG	10116
rs777760220	snp	C/T			missense	FEM1B	GRCh38.p7	15:68290802	CTTGATCCCAGAACT[C/T]GTGAAGGTTTCACCT	10116
rs777838629	snp	C/T	1.64982e-05	0.00287208	synonymous-codon	FEM1B	GRCh38.p7	15:68290525	TCTTCTTCGATTTGC[C/T]CAAGTTTTCTCACAA	10116
rs777899121	snp	A/G	1.71661e-05	0.00292963	intron-variant	FEM1B	GRCh38.p7	15:68289603	TTATTCTTTTCATGT[A/G]TAGGTATGTCATTGA	10116
rs777999203	snp	C/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276932	CTGTTCTTGTCACTT[C/G]TCATAGAGGTCTTGT	10116
rs778031981	snp	C/T	1.86726e-05	0.00305548	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278436	GAGGGCCTGGCTGGC[C/T]ATGTATACAAGGCGG	10116
rs778055591	snp	A/T	1.64741e-05	0.00286998	synonymous-codon	FEM1B	GRCh38.p7	15:68290927	GCTGGACTGTGGTGC[A/T]GAGGTGAATGCCGTG	10116
rs778128166	snp	A/C	1.64825e-05	0.00287071	missense	FEM1B	GRCh38.p7	15:68290695	AATGTAATCTCTATA[A/C]CTTTCTGTATTTAGT	10116
rs778162157	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68279347	GTTGTGGGGAAGCTT[G/T]ATCATTTACTGTTAG	10116
rs778795325	in-del	-/G			intron-variant	FEM1B	GRCh38.p7	15:68280655	TCAGTGCTGTTGCAA[-/G]AAGGGATTCAAGTTG	10116
rs778899859	snp	C/T	1.64751e-05	0.00287007	missense	FEM1B	GRCh38.p7	15:68290728	GCATCTCTACCAAAA[C/T]ACAGTGCAGCGAAGA	10116
rs778936422	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68288369	CTAGTGTGGTTTTTG[A/G]TGTGTATATTTAATT	10116
rs778940242	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276188	CAGCTATTTCAGAGA[C/T]GCTACCAGTAGAATC	10116
rs779033565	in-del	-/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291396	TATTTGTTTTTCTTG[-/C]CTCATGGTAATTGAT	10116
rs779235672	snp	A/G	4.96553e-05	0.00498249	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278561	AGGGCAGCGCTCCAC[A/G]CCCCTCATCATCGCA	10116
rs779248177	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68285042	GCCTTTATCAGCAGC[A/G]TGAAAATGGACTAAT	10116
rs779356612	snp	C/T	1.64933e-05	0.00287165	synonymous-codon	FEM1B	GRCh38.p7	15:68290108	CCGAAGAAGTCGGAT[C/T]GAAGCTTTGGAACTC	10116
rs779375978	in-del	-/AATA			intron-variant	FEM1B	GRCh38.p7	15:68286749	GTGTTATTTTTTGAC[-/AATA]AATAAATGTTTATTG	10116
rs779696008	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68280737	TTTGGTGATCCCTGT[A/T]TAAAGTACTAAGAGT	10116
rs779808143	snp	C/T	4.94743e-05	0.0049734	synonymous-codon	FEM1B	GRCh38.p7	15:68290090	CTCTCATGCTGATTG[C/T]GACCGAAGAAGTCGG	10116
rs779809430	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277871	CGGGGCCGTTGGCAG[C/G]GCCTGGCACTTCTGA	10116
rs779867856	in-del	-/C	1.95679e-05	0.00312787	intron-variant	FEM1B	GRCh38.p7	15:68289580	TGTGGCCTCTGTTAT[-/C]TAACTGCTTATTCTT	10116
rs779936256	snp	A/C	1.64931e-05	0.00287163	missense	FEM1B	GRCh38.p7	15:68291102	CTAGACAAAAGTACA[A/C]CTGGGGTATCTGAAA	10116
rs780026098	snp	C/T	1.65482e-05	0.00287643	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278565	CAGCGCTCCACGCCC[C/T]TCATCATCGCAGCCC	10116
rs780049127	snp	A/G	1.66763e-05	0.00288753	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278494	CCGCCTTGCTTCTCA[A/G]CCGGTCTGAAAGCGA	10116
rs780080094	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277287	AGCTCCCCTTCGCTC[C/T]CATCTTTCTCTCACA	10116
rs780106358	snp	A/G	1.6473e-05	0.00286988	missense	FEM1B	GRCh38.p7	15:68290976	GCCCTTCATATTATC[A/G]TTCAGTACAACAGGC	10116
rs780393004	snp	C/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275975	AGAGATATGGAGAGA[C/G]AGAGAGAGATAGAAA	10116
rs780585867	snp	C/T	4.94515e-05	0.00497225	missense	FEM1B	GRCh38.p7	15:68290280	GGGAATAGAACTGAA[C/T]GTAGAAATCCTCAGG	10116
rs780651243	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279697	ACATTTCTTCTTTAA[A/G]ATGACTAGGGAAATG	10116
rs780740916	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293668	AATTCTATCTTGTAA[A/G]ATCAATCCAAATGTG	10116
rs780745415	snp	C/T	0.00029758	0.0121943	missense	FEM1B	GRCh38.p7	15:68290463	ATCAAGTTGTGGCTT[C/T]ATGCCCTGCACCTCA	10116
rs780752736	snp	G/T			synonymous-codon	FEM1B	GRCh38.p7	15:68289967	GCACATAGATATTGT[G/T]AAAGAGCTGATAAAA	10116
rs780845695	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293659	TGAGAATCTAATTCT[A/G]TCTTGTAAAATCAAT	10116
rs780948964	snp	C/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291440	TAACAAAACCACATT[C/G]TTTTGGTGTAACTAT	10116
rs780968615	in-del	-/GTG	1.91569e-05	0.00309485	cds-indel	FEM1B	GRCh38.p7	15:68291270	GTAAAGTCGTTTAAT[-/GTG]GTGCTAAAAAGTAAA	10116
rs781026440	snp	A/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277990	CGGGTGGGCCGGGTC[A/T]GGAGAGACGCGCCCA	10116
rs781091505	snp	C/T			downstream-variant-500B	FEM1B	GRCh38.p7	15:68295932	TCTTTTGTTGAGTGC[C/T]TTAAAGTTGTCAAAG	10116
rs781154090	snp	C/T	1.65908e-05	0.00288012	missense	FEM1B	GRCh38.p7	15:68291169	GCCTGGCTGCCCGAG[C/T]AGTTCGGGCTAATGA	10116
rs781386396	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294892	GAGGTTTTAAGCTGT[A/G]TGTCCATTCCTACTC	10116
rs781407442	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68286695	GCATTTTTCATTAGA[G/T]TTATTACTATTTATT	10116
rs781435603	snp	G/T	1.64882e-05	0.00287121	missense	FEM1B	GRCh38.p7	15:68290670	GTCCACAATGCTATG[G/T]ACAATTATGAATGTA	10116
rs781511975	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68289373	TCAGGTTTGTTTTTT[A/G]GGGTTATATACTCTA	10116
rs781512434	snp	C/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276016	AGACAGATGGTAGAT[C/G]AGGTGCATGCTTGCC	10116
rs781737229	snp	A/G			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296282	ATGGATTGAAAATGT[A/G]TTTAACTAGATTTTA	10116
rs781773494	in-del	-/ATGAA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295329	CAAGCTTGCCAAATG[-/ATGAA]ATGAACAAGATTTTG	10116
rs796068237	in-del	-/AT			intron-variant	FEM1B	GRCh38.p7	15:68286498	CACACACACACACAC[-/AT]ATACCACACAACCTG	10116
rs796165746	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288220	CATCACCTCTTAATG[C/T]TATTCACGTTTGGCA	10116
rs796240618	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294590	AAGCAGAAGCGTTTC[-/T]TTTTTTTTTTTTGGA	10116
rs796248257	in-del	CAACAAATA/TATTTTG			intron-variant	FEM1B	GRCh38.p7	15:68285274	TTCCTATTAATTAAT[CAACAAATA/TATTTTG]TTGTTTCCAGTGTTT	10116
rs796468349	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292638	GTGAAGACCTGTAGC[-/T]TTTTTTTTTTTCTTT	10116
rs796707283	in-del	-/A			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292697	ATCAGATATAAACTT[-/A]AAAAAAAAAGGTTTC	10116
rs796792476	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279197	GCATCATGAGGGATT[A/G]TCACGCAGCCAGACA	10116
rs796803767	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68283962	GTGATCTTGGCTCAC[C/T]GCAAACTCTGCCTCC	10116

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