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

Pafah1b1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs259338538	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74718775	ATAAGAAGTTAAAGG[A/G]CAGCTAAGTTATATA	18472
rs259397255	in-del	-/AA			intron-variant	Pafah1b1	GRCm38.p3	11:74690306	GAAAAAGTAAGATTT[-/AA]AAAAAAAAAAAATGG	18472
rs259463834	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74707128	AACTCAGTTGTATTT[C/T]CCAGCACCCATGCTA	18472
rs259509721	in-del	-/AGAA			intron-variant	Pafah1b1	Mm_Celera	11:74720166	TCATGTACTCCAACT[-/AGAA]AGAAAGTGCTACCTT	18472
rs259588530	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74678101	ATTGATTTACTGAAT[A/G]TTGTGCTTCAGGCTT	18472
rs259756618	in-del	-/A			intron-variant	Pafah1b1	Mm_Celera	11:74680835	ACAGGAATATGTCAT[-/A]AAACCCTGTCTCAAA	18472
rs259828957	in-del	-/GCC			intron-variant	Pafah1b1	Mm_Celera	11:74710635	GAGCATCGGTTGTGA[-/GCC]GCCGCCATGTGGTTG	18472
rs259833288	in-del	-/TGCACGCACACGCGCACG			intron-variant	Pafah1b1	GRCm38.p3	11:74695519	ATGCGCGCGCGCACA[-/TGCACGCACACGCGCACG]CACACACACACAGAG	18472
rs259856035	in-del	-/AAAAAAAAAC			intron-variant	Pafah1b1	Mm_Celera	11:74699711	AAAAAAAAAAAAAAA[-/AAAAAAAAAC]CCAAACCAACCAAAC	18472
rs259904631	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74677973	TCTAAAATTACTGAG[C/G]TTACCAACTGGATTA	18472
rs259942701	in-del	-/GT			intron-variant	Pafah1b1	Mm_Celera	11:74693893	GGGCAGATCCCAGGA[-/GT]GTGAGCTAGCCAGTG	18472
rs260005769	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74719552	ACAAGCTAGTGCAGC[C/T]ATACAACCAACTAAG	18472
rs260015564	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74717659	TTTGTAGAATTTTGA[A/T]TCTCAAAGTTCAAAC	18472
rs260016471	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74697451	AGCCACACCACTTGG[A/G]TTTTAGGGACACAGG	18472
rs260023432	in-del	-/A			intron-variant	Pafah1b1	Mm_Celera	11:74722892	TCCCAATTGTCTCTT[-/A]AAGGGGGGGGGGGGT	18472
rs260068543	snp	G/T			intron-variant	Pafah1b1	Mm_Celera	11:74706961	AGCTACAGAGCAAGT[G/T]TGAGGCCAGCCTGGG	18472
rs260299044	in-del	-/TTTTTTG			upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74726162	TTCTTTTTTTTTTTT[-/TTTTTTG]TCTTCATCAACACAA	18472
rs260317109	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74679337	CACTGGCAGGAACCC[A/G]TAATGTTGAAACAGG	18472
rs260452335	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74716897	CATCATATGCTGCAC[A/T]GGCAAAGTGATGATG	18472
rs260518318	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74715228	AACAAACAAACAAAC[A/C]AAAAAAAAAAAAAAA	18472
rs260523498	in-del	-/C			intron-variant	Pafah1b1	Mm_Celera	11:74686300	GAAGTTACAGAAAGT[-/C]AGCATACACTAGTTG	18472
rs260728274	in-del	-/AACAAAAC			intron-variant	Pafah1b1	GRCm38.p3	11:74683982	AACCCAGATAAGAAA[-/AACAAAAC]AAAAAAAAAATAACA	18472
rs260838292	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74704240	ACGCTTGGCACACTG[C/T]TTTAAACACTCTGGA	18472
rs260853021	in-del	-/GTTTTT			intron-variant	Pafah1b1	Mm_Celera	11:74710542	TTTTTTAAACTCAGG[-/GTTTTT]TTTTTTTTTTCTAGA	18472
rs260889996	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74716832	ATTAAGATAAAAAAG[A/G]TTAAAGAAAAGAAAG	18472
rs260942886	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74707301	acagacacacagaca[C/T]acacacacacacaAC	18472
rs261019188	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74700321	CACTTTGCTGCAAGG[C/T]CTAACAACCTAAATC	18472
rs261133617	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74676302	TCTCTTAAACCTACT[A/G]TAGAAACTCTGGATC	18472
rs261146103	snp	A/T			intron-variant	Pafah1b1	Mm_Celera	11:74686859	ACATGAATGAATATT[A/T]CAGATATCACTCAGG	18472
rs261211260	in-del	-/C			intron-variant	Pafah1b1	Mm_Celera	11:74678311	AGTGCATTTTTTTTT[-/C]CCTTTCTTTCTTAAA	18472
rs261250076	snp	G/T			intron-variant	Pafah1b1	Mm_Celera	11:74703163	GCCAAAGCTGCAGAA[G/T]GAGACACTGTCTCAT	18472
rs261272741	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688490	TTCAGGTAGCCTAGG[C/T]TAACCTCAAATTTGC	18472
rs261357912	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74715865	AAAATTTCCTAGTCG[A/G]AGTTAACTGCCAATT	18472
rs261587491	in-del	-/AG			intron-variant	Pafah1b1	Mm_Celera	11:74694472	GCTGACCTCAAACTC[-/AG]AGATCTGCTTGCCTC	18472
rs261783952	in-del	-/C			intron-variant	Pafah1b1	Mm_Celera	11:74721244	AGAGAAACCCTGCCT[-/C]CCAAAAAAAAAAAAA	18472
rs261806028	in-del	-/CAAAAC			intron-variant	Pafah1b1	GRCm38.p3	11:74683984	CCCAGATAAGAAAAA[-/CAAAAC]AAAAAAAAAATAACA	18472
rs261915890	in-del	-/AC			intron-variant	Pafah1b1	Mm_Celera	11:74714797	GGTATAAAAAAAAAT[-/AC]TCAGTTTCTAATTAG	18472
rs261918423	snp	A/T			intron-variant	Pafah1b1	Mm_Celera	11:74710062	AAAGAAATAAATCTT[A/T]AAAAAAAAAAATAAA	18472
rs262021036	snp	G/T			intron-variant	Pafah1b1	Mm_Celera	11:74720024	TGGAGGGAGAGTTCA[G/T]TGGTTAAGAGCATTT	18472
rs262053540	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74707642	CAAGAGGTGGAGTAA[C/G]TAACCAGTTGAGAGG	18472
rs262103031	in-del	-/ATTT			intron-variant	Pafah1b1	Mm_Celera	11:74710348	AAACTTTTTTAAAAA[-/ATTT]ATTTATTTTATATGT	18472
rs262262068	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74696807	TTTCTTTTTTGTTTT[G/T]TTTAAAGATTAATTG	18472
rs262305467	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74701504	AGATACTCTAAAAAA[A/G]GGCTACTATAATAAC	18472
rs262341067	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74708782	CAATACAGTTAAAAG[A/C]TAGAAGGCTAGGGAT	18472
rs262481895	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74696178	GGGAATCTAAGTCCC[C/T]GCTGGGCATGAGGCA	18472
rs262711179	in-del	-/TT			intron-variant	Pafah1b1	Mm_Celera	11:74721768	GTATTCTTAACTAGA[-/TT]TTTTTTTTCACTATA	18472
rs262828155	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74718802	TATAGAATTCAAAAC[C/G]TAGGCTATGTGAGAC	18472
rs262912233	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74693685	TTACAGTATTAGAAG[A/C]CCCAATTAATATAGG	18472
rs262953847	in-del	-/G			intron-variant	Pafah1b1	Mm_Celera	11:74714032	AAGAAACCCCGTCTC[-/G]GAAAAAAAAAAAAAA	18472
rs263114596	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74679673	GAACACATTTTAATA[A/C]TAAAACCAGTCCTTT	18472
rs263129814	snp	A/T			intron-variant	Pafah1b1	Mm_Celera	11:74722524	TAATACCAAATCAAA[A/T]TTTAAAGTTAAAGCT	18472
rs263155690	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74721375	AAGCTCCTGGGTGGC[A/C]GTGGGCTTGGGGTGG	18472
rs263162879	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74690897	tagcctggtctacag[A/C]gtgagttccaggaca	18472
rs263308886	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74681144	CAGAGATCCTCCTGC[C/G]TCTGCCTCTTGAGTA	18472
rs263309560	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74681495	AGTATACTTTAAGGC[A/G]TTGCTAACATTCTAT	18472
rs263315795	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74692943	CACCTAAAACCTATA[A/G]TGTTTTTAGATTCTG	18472
rs263374660	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74694795	TCTAAATATAGGTTC[C/G]ATTTGTTGACAGAAC	18472
rs263404711	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74691874	TCACACATGCACCAT[A/G]AAAATATATCTCAGG	18472
rs263413781	in-del	-/ATTATTATTATTATTATTATT			intron-variant	Pafah1b1	Mm_Celera	11:74710159	CTTACCCATTAAGCC[-/ATTATTATTATTATTATTATT]ATTATTATTATTATT	18472
rs263425399	snp	A/T			intron-variant	Pafah1b1	Mm_Celera	11:74687675	GGTTATTTTTTATTT[A/T]TTTATTttttggttt	18472
rs263535936	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74678542	TGTGGGATGTGGAGA[C/T]TAAGCATGGGTTTTC	18472
rs263594732	in-del	-/TAA			intron-variant	Pafah1b1	Mm_Celera	11:74709040	GTGTTATCTGTACTC[-/TAA]TAAATTCCAGAAGGT	18472
rs263678365	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74688208	TACAGTATGTGCCCA[C/G]CCAGAATTTTTTTTT	18472
rs263797868	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74696415	TGTAACGAGATCTGA[C/T]GCCCTCTTTCTGGTG	18472
rs263804089	in-del	-/AG			intron-variant	Pafah1b1	Mm_Celera	11:74707288	CACACACACACACAC[-/AG]ACACACAGACACACA	18472
rs263817406	in-del	-/A			intron-variant	Pafah1b1	GRCm38.p3	11:74690689	TAAAATCTTTAGGGG[-/A]GGGGGTAGTGGTGGT	18472
rs263860239	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74678177	TCACCATAAGGTCCA[C/T]CCATCATACCCTAGT	18472
rs263867226	snp	A/T			intron-variant	Pafah1b1	Mm_Celera	11:74679919	TCTTTGCTTCCACCT[A/T]GGATGCCGGAATCAT	18472
rs263921619	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695512	CACACCTATGCGCGC[A/G]CGCACATGCACGCAC	18472
rs263927752	in-del	-/AAC			intron-variant	Pafah1b1	GRCm38.p3	11:74701275	AAAAGAAACAACAAC[-/AAC]AACAAAATTATAAAG	18472
rs263945329	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74713356	GCAGCAGCTGATGCA[A/G]AGGCCATGAAGGGGT	18472
rs264086040	snp	G/T			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74677209	ACCCTTAAAGATTTA[G/T]TAAGCACACTTAAGT	18472
rs264178767	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74691891	AAATATATCTCAGGC[A/C]CATCACTCCCCACCC	18472
rs264185797	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74715705	ATAAGACTTTTTACA[A/G]TACTTCAAAAGTTAA	18472
rs264231425	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74717175	CTTGAGCCATGACTG[A/G]TTTGAAAGAGAATAA	18472
rs264263522	snp	G/T			intron-variant	Pafah1b1	Mm_Celera	11:74714602	CAACCAGTATACATG[G/T]AAGGAGTTTCCATGC	18472
rs264278774	snp	A/T			upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74726313	GCCAAGAAACATTCA[A/T]TAAATTAAATTGTCC	18472
rs264360965	snp	C/T			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74674443	TTTGCCCATGTTGCT[C/T]GTCTACCATGACATT	18472
rs264406543	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74710591	atgtacatgagtaca[A/C]tttttactctcttca	18472
rs264437980	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74687806	GCCTTCCAAGTGCTG[A/G]GATTAAAGGCGTGCG	18472
rs264523552	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74683989	ATAAGAAAAACAAAA[A/C]AAAAAAAAAATAACA	18472
rs264532394	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74714798	GTATAAAAAAAAATA[C/T]TCAGTTTCTAATTAG	18472
rs264533077	in-del	-/AG			intron-variant	Pafah1b1	GRCm38.p3	11:74715247	AAAAAAAAAAAAAAA[-/AG]AAAACCCAACCATCT	18472
rs264567587	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74701803	ACTAGCTGAAGTTAA[A/C]TCCTGGCTAAATTAT	18472
rs264712907	in-del	-/AGTAGA			intron-variant	Pafah1b1	Mm_Celera	11:74683071	ATCCAGTCTGCCTTT[-/AGTAGA]TGATCTCCAACTTAT	18472
rs264749141	in-del	-/ACAT			intron-variant	Pafah1b1	GRCm38.p3	11:74695516	CCTATGCGCGCGCGC[-/ACAT]GCACGCACACGCGCA	18472
rs264829068	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74698465	TCAGAAATCTGCCTG[C/T]CTCTGCCTCCCAAGT	18472
rs264865472	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74711436	AAGGTCAGGAAATGA[A/G]GGGGGGAAAGGAGAA	18472
rs264881639	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74708138	AGACCAGGCTGGCCT[C/G]GAACTCAGAAATCTG	18472
rs264917389	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74721118	AAATATAGAATTGTG[A/G]GCCGGGCGCACGCCT	18472
rs264995030	in-del	-/A			intron-variant	Pafah1b1	Mm_Celera	11:74699736	CAAACCAACCAAACC[-/A]AAAAAAACCCAAAAA	18472
rs265033966	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74709969	TGGCTCACAACCATC[C/T]GTAACAAGATCTGAC	18472
rs265038319	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74687207	AAAAAAATGCCTAGG[C/G]AATACATTAAAGAGC	18472
rs265074746	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74700147	GGGTCTCATTACATC[A/G]TAGCCCTGGTTGACC	18472
rs265091070	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74697400	CTGATGTTAGAGGCA[C/T]TGGATCCTCTGGAGT	18472
rs265117535	in-del	-/TG			intron-variant	Pafah1b1	Mm_Celera	11:74697277	AAGACAGGGTTTCTC[-/TG]TGTGTAACATTACTC	18472
rs265160535	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74683911	AATAAAACTTTAAAA[C/T]CTCAAGTCTAATAAA	18472
rs265215314	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74694676	TCATATCCCATCCCC[C/T]TTTTTTGAGACAGGG	18472
rs265508795	snp	A/G			intron-variant, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74723566	GGGGACTGCGGGTTC[A/G]CTTCCGCGGCCCAGG	18472
rs265525594	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74719750	TCAAGGGAAAGGCAT[A/G]TTTTTGTTTGTTTGA	18472
rs265525787	in-del	-/G			intron-variant	Pafah1b1	Mm_Celera	11:74713838	TAAAATTTAAAAAAA[-/G]AAAAAAAAAAAAGAA	18472
rs265548331	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74676204	GATTTTCTTAAAAAG[-/A]AAAAAAAAGTTGATT	18472
rs265663690	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74690430	GGCAAAATTCGAATA[A/G]CTGAATTGACCTAAC	18472
rs265714256	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74679776	GTACTGGGAACTAAA[A/C]CCAGGGTTTTTATGC	18472
rs265731424	snp	A/G			intron-variant	Pafah1b1	Mm_Celera	11:74692851	AGCCCTACTCAATAG[A/G]GCCATATGTGCCACT	18472
rs265813468	in-del	-/TACAGTACTTACTTGCCTAATGTATACAAGGCCATGAG			intron-variant	Pafah1b1	Mm_Celera	11:74705631	GGAGTACGGCTCACT[lengthTooLong]GTTTGATCCTCAGCA	18472
rs265855708	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74705513	ATAAAAATAAATTAA[C/G]AGAAAGCAGTATAAA	18472
rs265857396	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74716489	cgccctcttctgatg[C/T]gtctgaagatagcca	18472
rs265872816	snp	C/T			intron-variant	Pafah1b1	Mm_Celera	11:74678617	CCCTATTTCTTTTTC[C/T]CCCCCCTCCAAACAG	18472
rs266018230	snp	A/C			intron-variant	Pafah1b1	Mm_Celera	11:74716455	ATGGTGGCTCACAAC[A/C]ACCTGTAATGAGATC	18472
rs266025076	in-del	-/AA			intron-variant	Pafah1b1	Mm_Celera	11:74716765	AAGAACAAAGGTAAC[-/AA]ATGCCAAATTAAACA	18472
rs266089103	snp	C/G			intron-variant	Pafah1b1	Mm_Celera	11:74713404	GTGTGAGTTCCTGTC[C/G]TGACTTCCTTTGGCG	18472
rs266102672	snp	A/T			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74675430	CAGCAGGCTGTGGCA[A/T]TCTCCCAAGTAAGGA	18472
rs266186439	in-del	-/A			intron-variant	Pafah1b1	Mm_Celera	11:74687164	CACACACACACACAC[-/A]AAAATTTGGAGAAAT	18472
rs266230228	in-del	-/AAAA			intron-variant	Pafah1b1	Mm_Celera	11:74696254	AAAAATAAGCAAAGC[-/AAAA]AAAAAAAACAAAAAC	18472
rs386896614	in-del	-/A			intron-variant	Pafah1b1	Mm_Celera	11:74682343	TTTTTTAGTCTATTA[-/A]AAAAAAAAAAAACAT	18472
rs386911663	in-del	-/CAGTCACCAATTTTTTTTTTTTCATAAGATCTTTTCCTCTTTCTTTTATTCTTTCTTTTTTTTTTTTTTTTTTTTATTATTATATGTAAGTACATTGTAGCTGTCTTCAGACACACCAGAAGAGGGAGTCAGATCTTGTTACGGATGGTTGTGAGCCACCATGTGGTTGCTGGGATTTGAACTCTGGACCTTCGGAAGAGCAGTAAGAGCAGTCGGGTGCTCTTACCCACTGAGCCATCTCACCAGCCC			intron-variant	Pafah1b1	GRCm38.p3	11:74718031	TCCTGTTTTAACCAA[lengthTooLong]CAGTCACCAATTTTT	18472
rs387344936	in-del	-/GCT			intron-variant	Pafah1b1	Mm_Celera	11:74681286	TATGTGCTGCTGCTG[-/GCT]CCACCACTTCCGACT	18472
rs387508850	in-del	-/AA			intron-variant	Pafah1b1	Mm_Celera	11:74721723	GATGTTCATCAAGAG[-/AA]AAAAAAAAAACTATT	18472
rs387756223	in-del	-/GGTTAAAGAAAAGAAAGCAGAGAAACAAGTTTACACACTTGATCTCATTCTCATCATATGCTGCACT			intron-variant	Pafah1b1	GRCm38.p3	11:74716831	AATTAAGATAAAAAA[lengthTooLong]GGCAAAGTGATGATG	18472
rs387787362	in-del	-/TT			intron-variant	Pafah1b1	Mm_Celera	11:74706538	AGACAGGGTTTCTGT[-/TT]AATCCTAGAACTCAC	18472
rs387789344	in-del	-/CACACACACACACACACACACACACACA			intron-variant	Pafah1b1	GRCm38.p3	11:74702149	TCTCTCTCTCTCTCA[-/CACACACACACACACACACACACACACA]CACACACACACACAC	18472
rs578264198	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688060	CCCAGATTTATATCT[C/T]ATACCACAACAATGT	18472
rs578338112	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74698817	CCACACACACACACA[C/T]GTATGCATGTATGTA	18472
rs578518244	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695078	CAGATTTCTGAGTTT[A/G]AGGCCAGCCTGGTCT	18472
rs578569603	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74682946	AAATAAATTAAAAAA[C/T]CCCAAAACTTTAAAA	18472
rs578654420	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695514	CACCTATGCGCGCGC[A/G]CACATGCACGCACAC	18472
rs578861384	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74708099	TTCTCTTTATAGCCC[C/T]GGCTGTCCTGGAACT	18472
rs578879040	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695532	CATGCACGCACACGC[A/G]CACGCACACACACAC	18472
rs579104474	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74698905	ACAATAATATAGCAG[A/G]TGCTGGTAAAAATAC	18472
rs579205936	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688039	CCACTGAGCCATCTC[G/T]CCAGCCCCAGATTTA	18472
rs579250395	snp	C/T			downstream-variant-500B	Pafah1b1	GRCm38.p3	11:74673683	TCTCTGGAATTGAGT[C/T]TGTATCTCTAAGAGA	18472
rs579471609	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74703023	ATATCCCATTTGATT[A/C]TAGGGGTTTAGACTA	18472
rs579561824	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74691335	GAAGAGGGCGTCAGA[C/T]CTCGTTACAGATGGT	18472
rs579616830	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74719639	AAAAAAAAAAACCCT[A/G]TATCACAGCCTTAGA	18472
rs579643517	snp	C/G			intron-variant	Pafah1b1	GRCm38.p3	11:74696405	CACAACCATCTGTAA[C/G]GAGATCTGACGCCCT	18472
rs579644359	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74684963	ATACCAGATAATCGT[A/T]TTGTTTTGCTTCTTT	18472
rs579997254	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74711866	AAAAAACACACACAC[A/T]CTCTACTAGGTGAAG	18472
rs580113335	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74717918	TGGTCTACAGAGTGA[A/G]TTCCAGGACAGCCAG	18472
rs580278477	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688546	TCATTCTTTCTTATT[C/T]ATTTAGTTATTTATT	18472
rs580430050	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688554	TCTTATTTATTTAGT[C/T]ATTTATTTAATGTAT	18472
rs580623429	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74680833	AGACAGGAATATGTC[A/C]TAAAACCCTGTCTCA	18472
rs580821277	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74695079	AGATTTCTGAGTTTG[A/T]GGCCAGCCTGGTCTA	18472
rs580957070	snp	C/G			intron-variant	Pafah1b1	GRCm38.p3	11:74707289	ACACACACACACACA[C/G]ACACACAGACACACA	18472
rs580960435	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74698819	ACACACACACACACG[C/T]ATGCATGTATGTATG	18472
rs581061897	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74721756	TAGTGAAAACTAGTA[C/T]TCTTAACTAGATTTT	18472
rs581127625	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74687693	TATTTTTTGGTTTTT[C/T]GAGACAGGGTTTCTC	18472
rs581221649	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688035	TTAACCACTGAGCCA[C/T]CTCTCCAGCCCCAGA	18472
rs581291096	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74723168	CTTGGGAGACGAAAT[A/C]AGCCCACCGTCTCAA	18472
rs581506910	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74695068	CAGAGACAGGCAGAT[C/T]TCTGAGTTTGAGGCC	18472
rs581724210	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74682999	TATGTAGGGGGTTTT[A/T]TGGAGGAGGGGTCTG	18472
rs581774334	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74704584	TGTGTGTGTGTTTGT[G/T]TTTTGTTTTTCAAGA	18472
rs581837293	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74709288	AAAACAACAACAAAA[A/C]TTTTTCCCTATATTT	18472
rs582094329	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695524	CGCGCGCACATGCAC[A/G]CACACGCGCACGCAC	18472
rs582207166	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74713836	CATAAAATTTAAAAA[A/G]AGAAAAAAAAAAAAG	18472
rs582289208	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688550	TCTTTCTTATTTATT[C/T]AGTTATTTATTTAAT	18472
rs582679113	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74688042	CTGAGCCATCTCTCC[A/C]GCCCCAGATTTATAT	18472
rs582867377	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74687662	CTTTTTTTGGGGGGG[G/T]TATTTTTTATTTTTT	18472
rs583106359	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74696466	GTACTTACATATAAT[A/T]AATAAATAAATCTTT	18472
rs583124546	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74721165	GAGGGGCAGAGGCAG[G/T]CGGATTTCTGAGTTC	18472
rs583231761	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74697488	GCAAGAATAAACACT[C/T]CACACTCAGTAACCA	18472
rs583303755	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74703387	ATCTGCCTGCCTCAG[C/T]TTACCAAGTACTGGG	18472
rs583499666	snp	G/T			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74676097	TTTTTAAAAAATCTA[G/T]TATACAAACGAATAA	18472
rs583598423	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74691352	TCGTTACAGATGGTT[A/G]TGAGCCACCATGTGG	18472
rs583639961	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74679213	AATACCAGCCAGTCA[A/G]TAGGAGTGATCATTA	18472
rs583822307	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74704675	CCCAAGTGCTGGGAT[C/T]AAAGGCGTGCGCCAC	18472
rs583874242	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74718294	CCAGTCACCAATTTT[A/T]AAAAAGAAGCAACCA	18472
rs583977117	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74689383	TTACATTTATTAATA[A/G]AGATGATCATAACAC	18472
rs584062875	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74684147	ATGAATGTATGTATG[A/T]ATGTATGTATGTATG	18472
rs584384393	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74698596	TTTTTTTTTAAATTA[A/G]AAGAGCTACCTATAG	18472
rs584390622	snp	C/G			intron-variant	Pafah1b1	GRCm38.p3	11:74688044	GAGCCATCTCTCCAG[C/G]CCCAGATTTATATCT	18472
rs584403324	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74705417	CCTAGCATTCCAGAG[A/G]TCAAGGCAGACTTGT	18472
rs584420451	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74698831	ACGTATGCATGTATG[C/T]ATGTATGAAGTAATT	18472
rs584505896	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74687712	ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC	18472
rs584639291	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74693310	GTATGTGGGGTAAGG[A/T]CAGGTGGGTGAAAGT	18472
rs584670772	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74681044	GAACCTAGAATACAA[C/T]AGTTTTTTTTCTGAG	18472
rs584852219	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74682918	TAAATAGATGGATAG[A/G]TAAATAAAATAAAAA	18472
rs585014771	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74708043	GGGGAAGGTTTTGTT[G/T]TTGGTTTTGTTTTTT	18472
rs585082007	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74695077	GCAGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC	18472
rs585152104	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74703005	TTATAGTTACTGTAA[A/C]ATATATCCCATTTGA	18472
rs585226911	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688037	AACCACTGAGCCATC[A/T]CTCCAGCCCCAGATT	18472
rs585520875	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74710486	GACCTCTGGAAGAGC[A/C]GTCAGTACTCAAGCT	18472
rs585730538	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74696780	CTCCAGCCCCTTATC[A/G]TTGTTTTTTTGTTTC	18472
rs585737061	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74704150	GTCACATTTTTTTTT[A/T]ATTTACTTTAGTGTT	18472
rs585761999	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74695530	CACATGCACGCACAC[A/G]CGCACGCACACACAC	18472
rs585770898	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688537	AACTTGAATTCATTC[A/T]TTCTTATTTATTTAG	18472
rs585894487	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74684118	TACAGTGCAGTGTGT[A/G]TATGAATGGATGGAT	18472
rs586103985	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74717916	CCTGGTCTACAGAGT[A/G]AGTTCCAGGACAGCC	18472
rs586107550	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74684139	ATGGATGGATGAATG[G/T]ATGTATGTATGTATG	18472
rs586441402	snp	A/T			intron-variant	Pafah1b1	GRCm38.p3	11:74696239	TATACATAAAATTTT[A/T]AAAATAAGCAAAGCA	18472
rs586441981	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74688552	TTTCTTATTTATTTA[G/T]TTATTTATTTAATGT	18472
rs586487702	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74691384	TGCTGGGATTTGAAC[G/T]CTGGACCTTTGGAAG	18472
rs586673165	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74721238	GATACACAGAGAAAC[C/T]CTGCCTCCAAAAAAA	18472
rs586771916	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74690699	TAGGGGGGGGGTAGT[A/G]GTGGTCCAAGACAGT	18472
rs587013178	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74706887	ATTAAACCCAAATAG[A/G]TTATTGTTGGTGAAT	18472
rs587090725	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74684762	TTAGCTGTTTTCTGG[A/G]AAAAAAAAAACTCAT	18472
rs587123772	snp	G/T			intron-variant	Pafah1b1	GRCm38.p3	11:74704580	TGTGTGTGTGTGTGT[G/T]TGTTTTTTGTTTTTC	18472
rs587125736	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74677160	CATTACACAGATGGA[A/G]CAAAGATTCTGAATT	18472
rs587146398	snp	C/T			intron-variant	Pafah1b1	GRCm38.p3	11:74695059	CTTGGGAGGCAGAGA[C/T]AGGCAGATTTCTGAG	18472
rs587423163	snp	A/G			intron-variant	Pafah1b1	GRCm38.p3	11:74721762	AAACTAGTATTCTTA[A/G]CTAGATTTTTTTTTT	18472
rs587429422	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74688030	TGCTCTTAACCACTG[A/C]GCCATCTCTCCAGCC	18472
rs864299439	snp	A/C			intron-variant	Pafah1b1	GRCm38.p3	11:74719621	AAACAAACAACCAAA[A/C]AAAAAAAAAAAAACC	18472

Page 1 | 2