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

Gtf2h2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs261491131	snp	A/T			intron-variant, downstream-variant-500B	Gtf2h2	Mm_Celera	13:100476329	TCTTTATTATATATT[A/T]CTCTTAACTATAAAT	23894
rs261684277	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100474638	TCGGGCTTGGTGGCA[A/G]GTGCCTTTATGTACT	23894
rs261726366	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100470794	TTTACCTCTACCTTA[C/T]TGTCTTTATAGGGAA	23894
rs261880785	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100470324	TGACAGTGGGAGAAA[C/T]AGCCTTCCCAACAGG	23894
rs261907282	in-del	-/G			intron-variant	Gtf2h2	Mm_Celera	13:100471302	ACACGAGCTCTGGGG[-/G]TACTGGTTAGTTCAT	23894
rs261913631	in-del	-/A			intron-variant	Gtf2h2	Mm_Celera	13:100474428	GTCCTTCTCCTTCTC[-/A]GTCCTACTTCCTCTA	23894
rs261949674	in-del	-/C			upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493639	ACACCACAAGCCCCT[-/C]CCATTTCCCTTTTCT	23894
rs262027898	snp	C/T			upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493055	ATAGCCATAGCCCCA[C/T]CTGCCGCCCCACCCC	23894
rs262131356	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100491613	GGAAAGGGGATAACA[C/T]TGGAACTGTAAATAA	23894
rs262158927	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100477785	CTTTTCATCTCTGAC[A/G]TTATATTCTTCATTT	23894
rs262164359	in-del	-/T			intron-variant	Gtf2h2	Mm_Celera	13:100462872	CATCTTTTATTTATC[-/T]TTTCCCTACAGCACA	23894
rs262172340	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100470374	AAACCTGAAAATACA[C/T]AGCAATGCACAGAGC	23894
rs262427780	snp	A/C			intron-variant	Gtf2h2	Mm_Celera	13:100475825	GTGTGAAAAGTGATG[A/C]ATTATTATATATGAA	23894
rs262456098	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100474027	GCCCACCCCCAGGGT[A/G]CACACTGATAGGCCC	23894
rs262470562	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100479171	AAAAAAGTTATCACT[A/G]ACAATTGCTCTTTAC	23894
rs262491456	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100473071	CTATTCCTGGCAGAG[A/G]CAGGCAGATCTCTAA	23894
rs262502771	in-del	-/GTGTGTGTGTGTGTGTGTGT			intron-variant	Gtf2h2	GRCm38.p3	13:100467829	TGGTCACTTAACTCC[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	23894
rs262515402	snp	G/T			intron-variant	Gtf2h2	Mm_Celera	13:100469964	AACCAGAAAAACCAC[G/T]AACTTCATTCTAAAT	23894
rs262612501	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100466580	ACCATCTAACCCCAG[A/G]AGGGCTACCATCAGT	23894
rs262765206	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100473658	GGCACCACATGTGGT[A/G]TTTCTATATAATTAA	23894
rs262782008	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100466147	AACAAGGGCTCAGAC[C/T]TTAGTAGGCCCTGAG	23894
rs262796653	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100472647	CTACAGAAAACTATC[A/T]GAGCTGGGCGGTGGT	23894
rs262811572	snp	G/T			intron-variant	Gtf2h2	Mm_Celera	13:100479949	ACAAGATGGCTCAAC[G/T]GGTAAGAGCACTGAC	23894
rs262849764	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100478550	AACATGTATACATAA[A/T]GTGTATTATATACAT	23894
rs262872879	in-del	-/TTTG			intron-variant	Gtf2h2	Mm_Celera	13:100487962	TTGTTTGTTTGTTTG[-/TTTG]AATTATTGGAGGATT	23894
rs262886337	snp	A/C/T			intron-variant	Gtf2h2	Mm_Celera	13:100488290	CCTTCAGCCAATGAG[A/C/T]TGCCCCTTCCTGGAG	23894
rs262919055	snp	G/T			intron-variant	Gtf2h2	Mm_Celera	13:100486587	AAAACAGCAGTAGCA[G/T]ACGCCACGCCAGTGC	23894
rs262944868	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100478421	CCTTTTATTCTGAGA[A/G]GAGTCTTACTATGTT	23894
rs263006342	in-del	-/TAT			intron-variant	Gtf2h2	Mm_Celera	13:100472430	CCTATCTGATTACAG[-/TAT]TATTATTATTATTAT	23894
rs263030985	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100487610	GCTCAGGCTCATTTT[A/G]GACCTCATTTTGTAG	23894
rs263154621	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100479470	AAAAAGCAGAGGAAA[A/T]GGAGGGATGATCTTT	23894
rs263177874	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100483666	AAATGACACAATCCC[A/G]TATTTTTCTTGGGGG	23894
rs263200993	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100478073	CCTCCTTTCTCGTGC[C/G]CAAGTGCTGGCCTGT	23894
rs263265408	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100485565	ACAGCATACATAACA[A/G]AGACAAAAGAAACTG	23894
rs263294549	in-del	-/G			intron-variant	Gtf2h2	Mm_Celera	13:100465472	TAGGAGTCCTGCCCT[-/G]TTCTGAATATAAATG	23894
rs263330523	in-del	-/G			downstream-variant-500B	Gtf2h2	Mm_Celera	13:100459712	GAGTTTTGAAGTAAT[-/G]GTTTTTTTTGTTTTG	23894
rs263407565	snp	A/T			downstream-variant-500B, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100459798	AAGATTTATTTATTT[A/T]TTATATGTGAGTACA	23894
rs263445742	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100474204	AGCTCTAATCTTTCC[A/G]TGAATAGCCTAGACA	23894
rs263476975	snp	A/C			intron-variant	Gtf2h2	Mm_Celera	13:100474356	TCATCTCCACTCACC[A/C]TTGTCCTAAGCTTCC	23894
rs263634187	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100490984	GAGAAACTCTGTCTC[A/G]AAAACCAAAAAAGTA	23894
rs263725553	in-del	-/T			downstream-variant-500B, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100460220	GGATTTGCATCCTTC[-/T]TTTTTTTCTTTCTTC	23894
rs263732330	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100482549	GGCCTGGAGCAATGG[C/G]TCAGCAGCTAAGGGC	23894
rs263801666	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100465845	ACTGGCTCTGGTAAC[A/T]TTTCAAGAGGAGACA	23894
rs263913810	snp	C/T			downstream-variant-500B, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100460197	GAAGCACAGGCCAAG[C/T]GAGGTACAGGATTTG	23894
rs263950693	in-del	-/ACAC			intron-variant	Gtf2h2	GRCm38.p3	13:100460912	CCACACCCACACTAT[-/ACAC]ACACACACACACACA	23894
rs263991382	in-del	-/C			intron-variant	Gtf2h2	Mm_Celera	13:100483203	TCTCCTTTTCTTTTG[-/C]TTTGGCTCATTTGTC	23894
rs264006176	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100466928	ACCTTACCAGAGAGA[C/T]ATTTCCCACGTTTAC	23894
rs264025695	snp	A/G			downstream-variant-500B, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100460087	CCATAGCCAGCTCAG[A/G]AAAGGAAGAGCTCTT	23894
rs264176260	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100488398	TGAAACACCATGAAC[A/G]AGCAAGCCGTTTCAC	23894
rs264180103	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100462660	TGTCACTACACTGTC[A/G]TAGGACAAAATATGT	23894
rs264305910	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100461107	CCGACTCATAAATCA[A/G]GTAAATTTGTTTTTA	23894
rs264346260	snp	A/G			upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100492759	GTGGGGTGCATTTCT[A/G]TAGACCAAACAGCTA	23894
rs264382002	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100484729	GCAGTGAAATTATTT[C/T]AAGATGTTTTATATT	23894
rs264419238	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100492386	TCAGGCGGAAGCTGC[C/T]GCGCTCCCTGCACAC	23894
rs264478063	in-del	-/TT			intron-variant	Gtf2h2	Mm_Celera	13:100473534	GTTCCTTTTTTTTTC[-/TT]TTGCTTTTTTTTTTT	23894
rs264482790	snp	A/C			intron-variant	Gtf2h2	Mm_Celera	13:100482175	TCTGAAAAAATAATA[A/C]TATAAATGGTTATGG	23894
rs264506427	in-del	-/AC			intron-variant	Gtf2h2	Mm_Celera	13:100464660	CTTCCCCAAGAAAGT[-/AC]ACACTTAGTGAAAGA	23894
rs264566162	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100467973	GTGCAGGTGAAAGCA[C/G]TGACTAACCAAAAGT	23894
rs264621799	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100492221	CGCGCATGGCCACTG[C/G]GGAGGCTCTGCCTCG	23894
rs264784645	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100485778	ATAGCCCAATTCAAC[C/T]TTTATACTTTCTGCT	23894
rs264958606	snp	G/T			intron-variant	Gtf2h2	Mm_Celera	13:100470047	CTCTTTTCAAAAGAT[G/T]GAGACCATTATAGAA	23894
rs264968596	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100462276	CCTTCATGTTTCCTT[C/T]CTTGAAACAGATCTC	23894
rs265041860	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100478124	CAGCTGGCAGCCAGA[C/T]ACTTCTACATCCTGT	23894
rs265128839	in-del	-/A			intron-variant	Gtf2h2	GRCm38.p3	13:100488138	TGGGGCTGCTCCCCC[-/A]ACCCCGCCCCGGGGC	23894
rs265164745	snp	G/T			intron-variant, downstream-variant-500B	Gtf2h2	Mm_Celera	13:100476452	TTGTGACATATAAAT[G/T]AATCAAAATTCATAT	23894
rs265201138	snp	G/T			intron-variant	Gtf2h2	Mm_Celera	13:100473242	CCCCTGAAGTATCTT[G/T]AACATTTTTTTAAAA	23894
rs265258517	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100466813	TATAAAGCTGAACAG[A/G]TTCCAAAAGAGCCAG	23894
rs265427995	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100478695	ATTCTATAGCTCAGA[A/G]TGACCTCAAACTCAA	23894
rs265482891	in-del	-/AATAATAAAATTA			intron-variant	Gtf2h2	Mm_Celera	13:100486553	ATTAAAAGGCAGCAT[-/AATAATAAAATTA]AAAGGCAAAACAGCA	23894
rs265620091	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100474474	CATCTCTATTTTGCT[A/G]AGCAATTTTTATAAC	23894
rs265649582	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100481991	GACAAGGATTACAGG[C/G]AGAAACATTGTTTCA	23894
rs265862684	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100489436	GGACAGAAAGGCTTC[A/G]AGAACCTCTTTTCCT	23894
rs265896467	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100460477	GAAGGGGTCCCTCCA[C/T]TGCTGTAGCTGACAC	23894
rs265919328	in-del	-/AGTCA			intron-variant	Gtf2h2	Mm_Celera	13:100482243	GCTAGAAGAGTCAGG[-/AGTCA]AGTCATCATTGGCTA	23894
rs265926231	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100467407	AAGTGGAGGCAGTAC[A/G]ACATACAGGAAAGAA	23894
rs265969413	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100464477	AATGGACTAAGTGCT[A/T]TAATTAAAAGATAAA	23894
rs266022153	in-del	-/ATACACACACACAC			intron-variant	Gtf2h2	GRCm38.p3	13:100460910	AACCACACCCACACT[-/ATACACACACACAC]ACACACACACACACT	23894
rs266114085	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100485016	ATCTCTAACCTTTCC[C/T]AAGACTTCTTGGGGG	23894
rs266185302	in-del	-/A			intron-variant	Gtf2h2	Mm_Celera	13:100479153	ATGTACATAACATTT[-/A]AAAAAAAAGTTATCA	23894
rs266237937	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100483144	TTTTAAAGAACAGAA[A/T]GCCTTCAATTTCTGC	23894
rs266247979	in-del	-/ATA			intron-variant	Gtf2h2	GRCm38.p3	13:100491913	GCACACACAGTTCGC[-/ATA]ATATTACTTTTAAGC	23894
rs387003101	in-del	-/T			intron-variant	Gtf2h2	Mm_Celera	13:100462554	GTTTTCTTTTTTTTT[-/T]GAGACAGTCTCTCTA	23894
rs387003135	in-del	-/AA			intron-variant	Gtf2h2	Mm_Celera	13:100490418	AACCCTCTCTCAAAG[-/AA]AAAAAAAAAGTCAGA	23894
rs387367961	in-del	-/AC			intron-variant	Gtf2h2	GRCm38.p3	13:100460912	CCACACCCACACTAT[-/AC]ACACACACACACACA	23894
rs387382398	in-del	-/ATT			intron-variant	Gtf2h2	Mm_Celera	13:100472466	ATTATTATTATTATT[-/ATT]GCCTAGTCTGTTGTC	23894
rs387839963	in-del	-/GAAG			intron-variant	Gtf2h2	Mm_Celera	13:100482439	AAGGAAGGAAGGAAG[-/GAAG]AAAAGATGGAAAGAA	23894
rs578297314	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100480240	GCTACAGTGTACTCA[C/T]ATACATAAAAATAAA	23894
rs578386003	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471346	CTATAGGGTTGCAGA[C/T]CCTTCAGCTCCTTGG	23894
rs578388746	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100461348	CCTTAAGTGGTGACC[A/C]ATATCTTCAACAATT	23894
rs578394507	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100490377	TCCAGAGCAAGTTCC[A/G]GGACAGCCAAGGCTA	23894
rs578483869	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100484422	TTTTTGGAGGAACTC[A/G]CCTTCCTCAATCTCA	23894
rs578497758	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472765	AGGACAGCCAGGGCT[A/G]CACAGAGAAACCCTG	23894
rs578520466	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470472	ATAAAGCACTTTACC[A/G]TGCAAACATGAAATT	23894
rs578699398	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100469944	CTATCTCCAGCACTT[C/T]ACTAAACCAGAAAAA	23894
rs578789602	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100484218	CTGTGTGCTGGGCAC[A/C]GGGGAAATGCACACT	23894
rs578866645	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470547	TGTGTAGCCCTGGCT[A/G]TCCCGGAACTCACTC	23894
rs578941822	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473520	ATGTATCTGTATATA[G/T]TTCCTTTTTTTTTCT	23894
rs579096319	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471670	ATAGTGTCCACACTT[C/T]GGTCTTTGTTCTTCT	23894
rs579101166	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100480077	GAAGACGGCTACAGT[G/T]TACTTATATATAATA	23894
rs579109810	snp	A/G			downstream-variant-500B, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100459847	ACCCCAGAAGAGGAC[A/G]CCAGATCTCATTACG	23894
rs579350812	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471595	CCTTTCGCCTCAGCT[C/T]CAAACTTTGTCTCTG	23894
rs579465444	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100465459	TTAGTTGATATACAT[A/G]GGAGTCCTGCCCTTT	23894
rs579469077	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471717	TGCAAATTGTATCTT[A/G]GGTATTCTAAGTTTC	23894
rs579572038	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100491371	AACTAACCAGTACCC[A/C]CAGAGCTCCCAGGGA	23894
rs579639221	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473970	CCCCAGGGTGCCCCC[C/T]CCCCCCGTGTGCCCA	23894
rs579647993	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100487362	GAACAGCAGTTCTCA[A/C]CCTGTGGGACACAAC	23894
rs579701438	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470596	CGAACTCAGAGATCC[A/G]CCTGCCTCTGCCTCC	23894
rs579796684	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100463920	TCCACCTCCACACAC[A/G]ACAGACAGACAGACA	23894
rs579849436	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100470575	CTCTGTAGACCTGGC[C/T]GGCCTCGAACTCAGA	23894
rs579884111	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100486978	TGAGGCAAGGAGTCT[A/G]AAGTCAGCTGAGGAA	23894
rs579906384	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100475172	ATAAAAAAAAGTTCA[A/T]ACCATCTAGTATCAG	23894
rs579959877	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100474013	CCACCCCCCAGTGTG[C/T]CCACCCCCAGGGTAC	23894
rs580370264	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100482333	AGGAGAAAGGGAAGA[A/T]GGGGGAATGAGGGGG	23894
rs580376356	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100463918	CCTCCACCTCCACAC[A/C]CGACAGACAGACAGA	23894
rs580436440	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100462752	GTTTTGGTTTTTTTG[A/G]CACAAGATCTTACCT	23894
rs580472001	snp	C/G			intron-variant	Gtf2h2	GRCm38.p3	13:100482138	ATGTTGACATACTTT[C/G]AATACAATTTACAGA	23894
rs580508836	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100472251	TTGTTTTGATTTGCA[G/T]TTCCCTGATGATTAA	23894
rs580568749	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100484221	TGTGCTGGGCACCGG[A/G]GAAATGCACACTACC	23894
rs580741190	snp	C/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472754	AAGTGAGTTCCAGGA[C/G]AGCCAGGGCTACACA	23894
rs580837077	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100476633	ACAAAGGCTAAAAAG[C/T]CAAGAGATATACTTA	23894
rs580846713	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100490410	CACAAAGTAACCCTC[C/T]CTCAAAGAAAAAAAA	23894
rs580854742	snp	A/C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471529	AGTGTCAGCGTTTGG[A/C/T]AGCTGATTATGGGAT	23894
rs580891422	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471171	CTTACCCACCCACTT[C/T]CACTTCTTGGCCCTG	23894
rs581145934	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100478954	TTCTAACTTAGAGGA[A/G]TAAATTTTAAGTGTT	23894
rs581215649	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100471155	CTCCGCCCCCTGCTC[A/C]CTTACCCACCCACTT	23894
rs581288313	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100488393	CCCAATGAAACACCA[C/T]GAACAAGCAAGCCGT	23894
rs581390823	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100483246	AATCTCCTTATATAG[A/C]TCTGGCTGTCCTGGA	23894
rs581430102	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100472446	ATTATTATTATTATT[A/T]TTATTATTATTATTA	23894
rs581444273	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472772	CCAGGGCTACACAGA[A/G]AAACCCTGTCTCGGA	23894
rs581473466	snp	C/G			intron-variant	Gtf2h2	GRCm38.p3	13:100467651	ACTTGTACAGTCTTT[C/G]GGTCTGTTTTGTTTT	23894
rs581547355	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100483204	TCTCCTTTTCTTTTG[C/T]TTGGCTCATTTGTCT	23894
rs581610541	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100466831	CCAAAAGAGCCAGAG[A/G]GACCCTGTCTTAAAA	23894
rs581802647	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100461733	TGAACCCACAAGAAC[G/T]GTTAAGGCACTAAGA	23894
rs581805710	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470440	ACGGGTGGTTGGGTG[A/G]ATAACGAGCTCAAAG	23894
rs581852691	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100473959	AGGGTGCCCACCCCC[A/G]GGGTGCCCCCCCCCC	23894
rs581908276	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100480745	TATAATTTCATAACC[A/G]TTTTAATTATCACTT	23894
rs582057404	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471671	TAGTGTCCACACTTC[A/G]GTCTTTGTTCTTCTT	23894
rs582180691	snp	A/G			upstream-variant-2KB	Gtf2h2	GRCm38.p3	13:100494384	AGAACTAGCTCTGTA[A/G]ATTAGACTGGCCTTG	23894
rs582185459	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100480143	GCAGGTTGACCAGAG[C/T]GGGCAGGGTTGACTG	23894
rs582191489	snp	C/T			downstream-variant-500B, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100460216	GTACAGGATTTGCAT[C/T]CTTCTTTTTTTCTTT	23894
rs582247874	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100488407	ATGAACAAGCAAGCC[A/G]TTTCACGGAGCAGCT	23894
rs582473156	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471639	GGGTGTTTTGTTCCC[A/T]ATTCTAAGAAGGGGC	23894
rs582514784	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473707	ACAGCATTCACTATT[G/T]AGTTTGTTCCACATA	23894
rs582569972	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100486547	AATAAAATTAAAAGG[A/C]AGCATAATAATAAAA	23894
rs582577461	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100470562	ATCCCGGAACTCACT[C/T]TGTAGACCTGGCTGG	23894
rs582617059	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100473971	CCCAGGGTGCCCCCC[A/C]CCCCCGTGTGCCCAC	23894
rs582730696	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100482141	TTGACATACTTTCAA[C/T]ACAATTTACAGAAAA	23894
rs582866781	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100484598	GCTGGCCATAAAAAC[C/T]TGAGGCTATTGAAAA	23894
rs582872692	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100470521	TTTTTCTTTTTGAGA[C/T]AGGGTTTTTCTGTGT	23894
rs582980897	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100465469	TACATAGGAGTCCTG[C/T]CCTTTCTGAATATAA	23894
rs583088524	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472714	GGCAGGCGGATTTCT[A/G]AGTTTGAGGCCAGCC	23894
rs583144538	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100483193	TTAATAAGAAGTCTC[A/C]TTTTCTTTTGTTTGG	23894
rs583166125	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471887	GTACTCCATTGTGTA[A/G]ATGTACCACATTTTC	23894
rs583287676	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100487001	CTGAGGAAACACAGC[A/G]AGATCTCATCGTGAA	23894
rs583409426	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100482822	TTCCCAGCAACCACA[G/T]GGTGGCTCACAACCA	23894
rs583417590	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100463919	CTCCACCTCCACACA[A/C]GACAGACAGACAGAC	23894
rs583478644	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470591	GGCCTCGAACTCAGA[A/G]ATCCACCTGCCTCTG	23894
rs583524222	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100475191	ATCTAGTATCAGTAA[A/G]GTTTGGGCAAATAAT	23894
rs583537527	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471157	CCGCCCCCTGCTCAC[C/T]TACCCACCCACTTCC	23894
rs583821607	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100488399	GAAACACCATGAACA[A/C]GCAAGCCGTTTCACG	23894
rs583944618	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100487864	GGTTGCCTGGAAGAA[A/C]AACTAGTGAAAGCCA	23894
rs584026543	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471118	ACATTTCAAATGCTA[A/T]CCTGAAAGTCCCCTA	23894
rs584046120	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472308	TCTCAGCCATTCGAT[A/G]TTCATCAGTTGAGAA	23894
rs584076409	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100470443	GGTGGTTGGGTGAAT[A/G]ACGAGCTCAAAGGAT	23894
rs584202700	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100484222	GTGCTGGGCACCGGG[A/G]AAATGCACACTACCT	23894
rs584384212	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100472764	CAGGACAGCCAGGGC[A/T]ACACAGAGAAACCCT	23894
rs584461053	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100488414	AGCAAGCCGTTTCAC[G/T]GAGCAGCTGCACCAC	23894
rs584500537	snp	C/G			intron-variant	Gtf2h2	GRCm38.p3	13:100473736	TAAAATGTTTCAGCT[C/G]TGACAAGTATGTGCA	23894
rs584514820	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100484216	CACTGTGTGCTGGGC[A/C]CCGGGGAAATGCACA	23894
rs584684748	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471269	ACTAGACCATCTTCT[A/G]CTACATATGCAGCTA	23894
rs584763674	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100477525	TTAGTTCCATCCAGT[C/T]TGTTTTTTCTTTTCT	23894
rs584775768	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100480234	TGTACAGCTACAGTG[G/T]ACTCATATACATAAA	23894
rs584783909	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100461345	TCTCCTTAAGTGGTG[A/C]CCCATATCTTCAACA	23894
rs584991828	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100479739	CCAGCCTGGTCTACA[A/T]AGTGAGACCTTGTCT	23894
rs584999017	snp	A/G			downstream-variant-500B, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100459803	TTATTTATTTATTAT[A/G]TGTGAGTACACTGTA	23894
rs585017285	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100491242	TGCCAAATACAGAAG[A/T]GGATGCTCACAGCCA	23894
rs585069916	snp	C/G			intron-variant	Gtf2h2	GRCm38.p3	13:100490413	AAAGTAACCCTCTCT[C/G]AAAGAAAAAAAAAAA	23894
rs585078473	snp	A/G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471530	GTGTCAGCGTTTGGA[A/G/T]GCTGATTATGGGATG	23894
rs585088545	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100470595	TCGAACTCAGAGATC[A/C]ACCTGCCTCTGCCTC	23894
rs585274586	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473376	ATGTCAACACATAGG[G/T]GAAAATAACAAAATC	23894
rs585323744	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100483207	CCTTTTCTTTTGTTT[G/T]GCTCATTTGTCTTGT	23894
rs585330474	snp	A/G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100467286	GCAGAAAAATAGATC[A/G/T]ATCCAGAATGTATAA	23894
rs585345963	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100486909	TGAGCCGCATCAAAC[A/C]CAGCAGGCACCTGCT	23894
rs585361046	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100487008	AACACAGCAAGATCT[C/T]ATCGTGAAATTCAAA	23894
rs585507860	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473961	GGTGCCCACCCCCAG[G/T]GTGCCCCCCCCCCCC	23894
rs585654817	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471640	GGTGTTTTGTTCCCA[A/G]TTCTAAGAAGGGGCA	23894
rs585660534	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100470569	AACTCACTCTGTAGA[A/C]CTGGCTGGCCTCGAA	23894
rs585858287	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471686	GGTCTTTGTTCTTCT[C/T]GAGTTTCATGTGTTT	23894
rs585907460	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100481400	CAGGGGGAGGGTATA[A/G]GGAACTTTCAGAATA	23894
rs586021901	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100482232	TGGGAAGTAGAGCTA[A/G]AAGAGTCAGGAGTCA	23894
rs586247167	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100462686	TATGTCTTTGGGGAA[C/T]AAATATGTAAATTTT	23894
rs586370094	snp	G/T			intron-variant	Gtf2h2	GRCm38.p3	13:100473993	TGTGCCCACCCCCAG[G/T]GTGCCCACCCCCCAG	23894
rs586482057	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100484601	GGCCATAAAAACTTG[A/G]GGCTATTGAAAACAT	23894
rs586484317	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100470529	TTTGAGATAGGGTTT[C/T]TCTGTGTAGCCCTGG	23894
rs586638352	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100475882	TTCTAAAATGCTGAT[A/G]CTTTTTGAATAAAAA	23894
rs586820001	snp	A/C			intron-variant	Gtf2h2	GRCm38.p3	13:100472413	ATATTGGATATTAGT[A/C]CCCTATCTGATTACA	23894
rs586828519	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471170	ACTTACCCACCCACT[C/T]CCACTTCTTGGCCCT	23894
rs586838011	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100474404	TAGAGGCAGATCCTC[C/T]GATTCCATGTCCTTC	23894
rs586917078	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100488405	CCATGAACAAGCAAG[C/T]CGTTTCACGGAGCAG	23894
rs586950367	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100472739	CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC	23894
rs586960786	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100482840	TGGCTCACAACCATC[C/T]GTAATGAGATCTGAT	23894
rs586994919	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100483197	TAAGAAGTCTCCTTT[C/T]CTTTTGTTTGGCTCA	23894
rs587326520	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100483231	GTCTTGTTGATACAG[A/G]ATCTCCTTATATAGC	23894
rs587331669	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100467362	ATATGCAGAATACAG[C/T]CAATAATATATGTGT	23894
rs587390753	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100465941	CATATCTTACAAGGA[A/T]AAAAGACAGCAGTTA	23894
rs587469791	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100478231	GAAGTAACTTAGGTA[C/T]TTACTGATCTATTCA	23894
rs587558096	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100488389	CACCCCCAATGAAAC[A/G]CCATGAACAAGCAAG	23894
rs587563134	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471143	CCCCTATACCCTCTC[C/T]GCCCCCTGCTCACTT	23894
rs864301912	in-del	-/A			intron-variant	Gtf2h2	GRCm38.p3	13:100481455	TATCTAATAAAAAGG[-/A]AAAAACAGAAAGAAA	23894
rs864315859	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100463958	agacagacagacaga[C/T]agactgacTAttttt	23894
rs864319088	snp	C/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100463958	AGACAGACAGACAGA[C/T]TGACTGACTATTTTT	23894

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