SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6370710 | snp | A/T | 0.5 | 0 | intron-variant | Gtf2h2 | Mm_Celera | 13:100466190 | ctgactccatgatag[A/T]agtgccattcgggtc | 23894 |
rs13466278 | snp | G/T | 0.497778 | 0.0332592 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100492489 | GGCTGGAGTGAGGCG[G/T]ACAGGAGAAGAAGCC | 23894 |
rs29228276 | snp | C/G | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100464072 | AAGTGCCTGCATCTA[C/G]TCACAGCTTGAGGCC | 23894 |
rs29229040 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483681 | GTATTTTTCTTGGGG[A/G]AAGCAAACAAGAACT | 23894 |
rs29229155 | snp | A/G/T | 0.49827 | 0.0293608 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100485514 | TCATTTAAGGAATAG[A/G/T]CTATTTTACAAAAAG | 23894 |
rs29230283 | snp | C/T | 0.493827 | 0.0552116 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493916 | GTAGTCTCAGTATAA[C/T]TATGACTAATATTCC | 23894 |
rs29232899 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100493840 | TGCTGGAACAGGGGG[G/T]TTTTATTAAAACTTT | 23894 |
rs29233052 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473074 | TTCCTGGCAGAGGCA[C/G]GCAGATCTCTAAGCT | 23894 |
rs29238759 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487566 | ATAAACCAAGACAAC[C/T]ACTTTTTCAAGTTCT | 23894 |
rs29239067 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Gtf2h2 | Mm_Celera | 13:100464894 | TTATGCTGAGAAACA[C/T]ACCCAGCTTCTACTT | 23894 |
rs29241000 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480792 | CTCAATGTCTCTAGA[C/T]ATAATAGTAACAAAA | 23894 |
rs29242052 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487037 | AAACCAAAAAAATTA[A/G]TGGATCCATTTGGAG | 23894 |
rs29242782 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | Mm_Celera | 13:100463959 | GACAGACAGACAGAC[A/T]GACTGACTATTTTTC | 23894 |
rs29244850 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100461929 | CAGGATGCTGCTTCA[C/T]GGTGTAAATTTTCTA | 23894 |
rs29246967 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100494114 | TGGCCTGGGCTGTAT[C/T]ATAAGACCTCGTGTA | 23894 |
rs29247358 | snp | G/T | 0.5 | 0 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487793 | GTGTTGGACTTTCTA[G/T]AACAGGAGTTCCTGA | 23894 |
rs29495269 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491694 | TGGAGCACACCTTTA[A/G]TCCCAGCACTCGGAA | 23894 |
rs29495560 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480804 | AGATATAATAGTAAC[A/T]AAAAAATTAAAGCCA | 23894 |
rs29509999 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461413 | GCTCCTCCCTTGGAT[A/T]AATGCCATCGCCATT | 23894 |
rs29511010 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488343 | TTATACAATCCCTGG[A/T]TCACCCAGAACAAAG | 23894 |
rs29511395 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486361 | TACCAAAAATAGGTA[C/T]ATAATCTGGTTCCCT | 23894 |
rs29516623 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100494192 | TGTGTGTGTGTCCAT[A/G]GCTGGCTGGCACAAT | 23894 |
rs29528018 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491779 | TTCCAGGACTGCCAA[A/C]ACTACACAGAGAAAC | 23894 |
rs29534817 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100485153 | CACTGTGGCAGTGGG[G/T]TTTGAGGTCTTCTCT | 23894 |
rs29548950 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100460679 | ACATCGTGTCTCTCT[C/G]TGTGTGTGTGTGTGT | 23894 |
rs29549238 | snp | A/T | 0.5 | 0 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473254 | CTTTAACATTTTTTT[A/T]AAAAGATAGCTCAGC | 23894 |
rs29570180 | snp | C/G | 0.375 | 0.216506 | intron-variant | Gtf2h2 | Mm_Celera | 13:100480718 | CTACCAAAGTTTCTA[C/G]AGATGAAAATATATA | 23894 |
rs29582841 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461201 | TAAAGCCAACCCATA[A/G]TTTTCCTTATTTTAA | 23894 |
rs29626228 | snp | C/T | 0.32 | 0.24 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100465336 | ACATCTATACATGAC[C/T]ACAGGGCAAGCTGAT | 23894 |
rs29721134 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487488 | GGGGTCACCACAACA[C/T]GAGGAACTGTATTAA | 23894 |
rs29725123 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476150 | CATAGAATCTCCTAG[A/G]GCTGGAAGTGCAGGC | 23894 |
rs29725922 | snp | C/T | 0.493827 | 0.0552116 | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100459987 | TTTAACACCACTTTC[C/T]TAAGCAAGATGTGTA | 23894 |
rs29762567 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491852 | TTTCTGTTCAGGATG[A/G]GCATAGTGGAATACA | 23894 |
rs29776868 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100472670 | GCGGTGGTGGCGCAT[A/G]CCTTTAATCCCAGCA | 23894 |
rs29777127 | snp | A/C | 0.487535 | 0.077957 | downstream-variant-500B | Gtf2h2 | GRCm38.p3 | 13:100459707 | CGCCTCGAGTTTTGA[A/C]GTAATGTTTTTTTTG | 23894 |
rs29804283 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491856 | TGTTCAGGATGGGCA[G/T]AGTGGAATACACCTG | 23894 |
rs29806169 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100477363 | CAGCCAGGACTACAC[A/T]GTAGTACCCTGTCTC | 23894 |
rs29829638 | snp | C/G | 0.493827 | 0.0552116 | downstream-variant-500B | Gtf2h2 | GRCm38.p3 | 13:100459570 | ACTGGAGCCACAGAC[C/G]AGGGTCTGAGGTAAA | 23894 |
rs29858779 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461524 | GTATCCCTACTGCTT[C/T]AACTCTTGATGTACA | 23894 |
rs29859613 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472904 | GATGCCTGTGGCTTT[G/T]TTTTTTCAGGACGGG | 23894 |
rs29864172 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487500 | ACACGAGGAACTGTA[A/T]TAAAAGTTCACAGCA | 23894 |
rs29865345 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487914 | CAAACCTTAAAGCAC[A/G]GAGCCATCCTGTCAG | 23894 |
rs29897091 | snp | C/T | 0.5 | 0 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100477992 | ACTACCACCCATCTT[C/T]CTTCTTCCTCCTCTC | 23894 |
rs29910570 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463008 | CCTTTCGTCAGCCAT[C/T]ATCCTTTTCTGGATG | 23894 |
rs29956618 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472855 | ACGGTATGTACCCTA[A/G]ATGAGTACACCAAGG | 23894 |
rs29959104 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100462801 | AACTGGAGGCAACTG[C/T]CTTGTCTCAGCTTTC | 23894 |
rs29962375 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100494452 | GTTAAAAAAGATTTA[A/T]TTAGGGCTGGTGAGA | 23894 |
rs30011036 | snp | A/T | 0.32 | 0.24 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470571 | CTCACTCTGTAGACC[A/T]GGCTGGCCTCGAACT | 23894 |
rs30011550 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100492094 | ACCGGGGAGAAGTTA[A/G]AAGTCCCCACGCCGC | 23894 |
rs30065524 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100460677 | TAACATCGTGTCTCT[C/G]TCTGTGTGTGTGTGT | 23894 |
rs30079034 | snp | A/G | 0.32 | 0.24 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100466938 | AGAGACATTTCCCAC[A/G]TTTACTATTGCTTTA | 23894 |
rs30093608 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484359 | CTGACATCTCGACAA[A/G]AAATTTGATGACAAG | 23894 |
rs45632553 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471600 | CGCCTCAGCTCCAAA[C/G]TTTGTCTCTGTAACT | 23894 |
rs45784298 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100465446 | TGAAATGCTAAGTTT[A/G]GTTGATATACATAGG | 23894 |
rs45862824 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486437 | TATATTTGACAGCAA[A/C]ATAGGAATCTAGTTC | 23894 |
rs45923861 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490656 | TTCCTATCTGAAACC[A/G]CAGACAGGGAACTAA | 23894 |
rs46107415 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491796 | CTACACAGAGAAACC[A/G]TCTCCAAATTAATTA | 23894 |
rs46139245 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100459943 | GCTCTTAACCAATGA[A/G]CCATCTCTCCAGCCC | 23894 |
rs46287394 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461352 | AAGTGGTGACCCATA[C/T]CTTCAACAATTTCCC | 23894 |
rs46311585 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471586 | ATGGTCCATCCTTTC[A/G]CCTCAGCTCCAAACT | 23894 |
rs46476130 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471916 | TCTGTATCCATTTCT[C/T]TGTTGAGGAACATCT | 23894 |
rs46513567 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490672 | CAGACAGGGAACTAA[A/G]GCCAGAACGTTATTC | 23894 |
rs46547215 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100474334 | CTCCCTGAAACAGAC[A/G]TCATCATCATCTCCA | 23894 |
rs46576434 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467552 | ATGTGCATAAAAATG[A/C]TTTCAAGAGTTAAAT | 23894 |
rs46582440 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | Mm_Celera | 13:100486785 | GATTGTAGGTATGTA[G/T]GTAACTCCAGCTCTC | 23894 |
rs46608877 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490279 | CAGTGTATTCAGTAA[A/C]TATTCTATGAAAATA | 23894 |
rs46638226 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100462870 | ATCATCTTTTATTTA[C/T]CTTTTCCCTACAGCA | 23894 |
rs46762020 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Gtf2h2 | Mm_Celera | 13:100472917 | TTGTTTTTTCAGGAC[A/G]GGCTGGTATATACCT | 23894 |
rs46825392 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100484138 | GTACCAACACCCAAA[C/T]GTCAGTCTCCTGGTT | 23894 |
rs46866097 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100464295 | AGGAAAAATTTAGAA[A/C/T]GTTTAAAAATACAAT | 23894 |
rs46893124 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493926 | TATAACTATGACTAA[C/T]ATTCCAATCACATAT | 23894 |
rs46983253 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100485886 | GATGAAGAATGTGTA[C/T]TTAAATAAGCATATT | 23894 |
rs46993797 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467553 | TGTGCATAAAAATGA[A/T]TTCAAGAGTTAAATA | 23894 |
rs47059268 | snp | G/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493251 | AGACGAAGGGCACCA[G/T]TCTCTGACTTTTTTT | 23894 |
rs47090194 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471656 | TTCTAAGAAGGGGCA[A/T]AGTGTCCACACTTCG | 23894 |
rs47137869 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100488664 | AGCTGTGTCCAGATA[C/T]AACCAGCAGAGAGGC | 23894 |
rs47172508 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468099 | TGTGGATGACTTGGT[A/G]GCTGAAATCACTCCA | 23894 |
rs47243128 | snp | C/T | 0.32 | 0.24 | intron-variant | Gtf2h2 | Mm_Celera | 13:100489403 | AGTTAAAAAGAAATA[C/T]GAAGGACGGTCACAG | 23894 |
rs47267312 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461602 | TGTTTCTAGGATCCT[A/G]CTGTGAGGTGTGACT | 23894 |
rs47473006 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486400 | CAAAGAATATATGTC[C/T]CATTTTAAAAGAAAA | 23894 |
rs47501953 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461709 | AATGAGTCCTCTGTC[C/T]TGTAAATCTGAACCC | 23894 |
rs47522121 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491577 | GGGGTAGGAAATAGG[A/G]GGTTTTCGGAGGGGA | 23894 |
rs47535026 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492710 | AGTGGTGCCCAAGAG[C/T]GTAACTGCCTTCCAG | 23894 |
rs47765990 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468120 | AATCACTCCAAAAGG[C/T]AGAGCCCTGGTACCT | 23894 |
rs47811480 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100468952 | AATACAGCCAGGACA[A/G]CAATGGAGAGAGTCA | 23894 |
rs48038280 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Gtf2h2 | Mm_Celera | 13:100483401 | CATATCCATTAATAT[A/C]CACTTAAAATGAATA | 23894 |
rs48053410 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471655 | ATTCTAAGAAGGGGC[A/G]TAGTGTCCACACTTC | 23894 |
rs48078881 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490827 | CTGATGGGAGGTGAC[G/T]CGGAAATAAAAGATA | 23894 |
rs48129644 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461385 | TGCCATAACCTGAGT[C/T]GGACCCAGCACAGCT | 23894 |
rs48131566 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486729 | GAGCAGACCGACACT[A/G]AACTTGGCGAGATGT | 23894 |
rs48227727 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100467964 | AACAAAGATGTGCAG[A/G]TGAAAGCACTGACTA | 23894 |
rs48278015 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100468982 | ATGAACAAAGACATC[A/G]CAGTCCACACAAAAA | 23894 |
rs48374668 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493751 | CCACCTTAATAAAAC[A/C]CTTTTCTCTGTCATT | 23894 |
rs48424100 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468148 | CCTGACAGTGTAAAG[A/G]AGGAACTCCTACAGA | 23894 |
rs48430764 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100481798 | TTTTTCTTAGTTCTA[C/T]GTACTGCTGTGGATT | 23894 |
rs48472378 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493117 | AATAAGAGGATTCCC[C/T]CAATAAAATAAAAAT | 23894 |
rs48483158 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461729 | AATCTGAACCCACAA[A/G]AACGGTTAAGGCACT | 23894 |
rs48501402 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480487 | CAAATGAAAGCAGAA[C/T]GCCTGACTTGAAGCA | 23894 |
rs48573948 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100467324 | TGAGGCCACATGACC[G/T]CAGAAAAAGGTGCAT | 23894 |
rs48737507 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471809 | CTCACTCAGGATGAT[A/G]CCCTCCAGATACATC | 23894 |
rs48875349 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461681 | TAACCTCTCCCCAGA[A/G]AAGAGTTAAACAAAT | 23894 |
rs48949459 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Gtf2h2 | Mm_Celera | 13:100479557 | AAAAAAATAGTTCAC[A/G]TTTTATATAGCTCCT | 23894 |
rs48996685 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471769 | GTGAGTACATATCAT[A/T]TGAGTTCTTTTGTGA | 23894 |
rs49165353 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100484150 | AAATGTCAGTCTCCT[C/G]GTTCTCTGTCCACTT | 23894 |
rs49212468 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100469245 | GTGGAATAAGGAATG[C/G]CTCTTAGAGAACGGC | 23894 |
rs49263737 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461140 | ATATATAGCAACAGG[A/G]ACAACATTCCCAGAA | 23894 |
rs49277111 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100463466 | GAGGGAAGCTCCTGA[C/T]GCCGCCTTCTCGATC | 23894 |
rs49371444 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471629 | CTTCTTCCATGGGTG[C/T]TTTGTTCCCAATTCT | 23894 |
rs49429744 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Gtf2h2 | Mm_Celera | 13:100490660 | TATCTGAAACCGCAG[A/G]CAGGGAACTAAAGCC | 23894 |
rs49456072 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100460557 | AGACCCAGCTTACTC[A/G]CTTTAAAATTAGTTT | 23894 |
rs49479133 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100482151 | TTCAATACAATTTAC[A/G]GAAAAAAATCTGAAA | 23894 |
rs49624286 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100460516 | AGCCATCCGACTGCC[A/G]GAAATGTGCCACAGC | 23894 |
rs49661906 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461341 | ACAGTCTCCTTAAGT[G/T]GTGACCCATATCTTC | 23894 |
rs49751347 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493814 | GCGTGGCCAGACAAG[C/T]CTGCTAGGACTGCTG | 23894 |
rs49784571 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100462011 | AATCTTGCAAAAATG[C/T]TTACTGCTCTTTTTA | 23894 |
rs49810303 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100465883 | TCTTTCTTCTAAGCA[C/T]GGTAGGAGTAGGAGA | 23894 |
rs49889922 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467184 | CAGGACAGCAAACCC[A/G]CCACCCCTACTACCC | 23894 |
rs49921332 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490701 | TCCCTGAGCCTCTCA[C/T]GCTGATGCACCCTTC | 23894 |
rs49925796 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100481151 | AAAATTAATGAATAA[C/T]CTTGAAAATTACTGT | 23894 |
rs49955049 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486738 | GACACTGAACTTGGC[A/G]AGATGTTCCTCTCGC | 23894 |
rs49983495 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461660 | AGCCCACAGTCCATC[A/T]TGTAATAACCTCTCC | 23894 |
rs50023476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461274 | CAAAAGACACAAGCA[A/G]GTGTGAAGCAAAAAT | 23894 |
rs50051960 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493252 | GACGAAGGGCACCAT[C/T]CTCTGACTTTTTTTT | 23894 |
rs50053541 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100489993 | TATATTGAATTTTAA[C/T]ACACATGAAACACAC | 23894 |
rs50249784 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100490144 | CATGGTGCTTATAAT[A/G]ATATATATGCTTATT | 23894 |
rs50328616 | snp | C/T | 0.5 | 0 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490856 | TAAAAGACAGGTATC[C/T]GTAGAAGCAGGACTG | 23894 |
rs50373350 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491919 | ACAGTTCGCATAATA[C/T]TACTTTTAAGCTTTT | 23894 |
rs50413461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100461478 | CTCCTTTATGGGTCT[C/T]CCACTGGCACTGACA | 23894 |
rs50422503 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471957 | CAGCTTCTGGCTATT[A/T]TAAATAAGGCTGCTA | 23894 |
rs50434177 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467152 | AAGTTCAAGGCCAGC[C/T]TAGTCTATGTGAATT | 23894 |
rs50498204 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471616 | TTTGTCTCTGTAACT[C/T]CTTCCATGGGTGTTT | 23894 |
rs50573405 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490286 | TTCAGTAACTATTCT[A/G]TGAAAATACAAAATT | 23894 |
rs50611137 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486751 | GCGAGATGTTCCTCT[C/T]GCTGCCTCCTGGGCA | 23894 |
rs50766604 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483386 | GATAGATATAAAATC[C/T]ATATCCATTAATATA | 23894 |
rs50926169 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486581 | AAAGGCAAAACAGCA[A/G]TAGCAGACGCCACGC | 23894 |
rs50942393 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493816 | GTGGCCAGACAAGTC[G/T]GCTAGGACTGCTGGA | 23894 |
rs50985808 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490687 | AGCCAGAACGTTATT[C/T]CCTGAGCCTCTCATG | 23894 |
rs50999324 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486629 | TATTTATGGAGCAGG[A/G]CTTCTCATGACTTTG | 23894 |
rs51206194 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100474408 | GGCAGATCCTCCGAT[C/T]CCATGTCCTTCTCCT | 23894 |
rs51256188 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100462393 | TCTGCCTCTCCAATG[C/T]TGGGATTGAAGGAGT | 23894 |
rs51387174 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Gtf2h2 | Mm_Celera | 13:100483402 | ATATCCATTAATATA[C/T]ACTTAAAATGAATAT | 23894 |
rs51532103 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486651 | ATGACTTTGGGGGAC[A/T]CAAGGGTGTGAGCTG | 23894 |
rs51598152 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471587 | TGGTCCATCCTTTCG[C/T]CTCAGCTCCAAACTT | 23894 |
rs51614585 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486590 | ACAGCAGTAGCAGAC[A/G]CCACGCCAGTGCCCT | 23894 |
rs51708801 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100489127 | CTAACAGAAAAATTC[C/T]TAACATACCATTCCA | 23894 |
rs51843490 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gtf2h2 | Mm_Celera | 13:100469128 | GCTCCCTATATTCTT[C/T]AATGTTTCCCTACCC | 23894 |
rs51888596 | snp | C/T | 0.5 | 0 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486398 | TTCAAAGAATATATG[C/T]CCCATTTTAAAAGAA | 23894 |
rs51901343 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100491988 | TTACTCTTCTATTAC[G/T]CTCTTAAATTCAGAG | 23894 |
rs51949429 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Gtf2h2 | Mm_Celera | 13:100480869 | ACCTTTTTGAAAGTT[A/T]TAACTCTAAAACACT | 23894 |
rs52079445 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gtf2h2 | Mm_Celera | 13:100487659 | CAGAGGACCACTTTC[C/T]AGAGGTAATGGGTTT | 23894 |
rs52230519 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491628 | TTGGAACTGTAAATA[A/T]AAAAAAAATAATAAT | 23894 |
rs52243696 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491627 | ATTGGAACTGTAAAT[A/T]AAAAAAAAATAATAA | 23894 |
rs52410644 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491571 | GGGGAAGGGGTAGGA[A/G]ATAGGGGGTTTTCGG | 23894 |
rs52567111 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491646 | AAAAAATAATAATTT[A/T]AAAAAATAACAAAAC | 23894 |
rs211840962 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460165 | TCAAAGCAGGTGCCT[A/G]GAGGCAAGAACTGAA | 23894 |
rs211898357 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482356 | TGAGGGGGGAGGGAG[A/G]GAGAGAGAGAGAGAG | 23894 |
rs211970631 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483561 | TACAAAAAGTTCCCA[G/T]AAAGATTACTGATAT | 23894 |
rs211984277 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475230 | CCTCTTTAAAGGACA[A/C]ATTTACAACATCTAC | 23894 |
rs212104749 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479719 | GGATCTCAGTGAGTT[C/T]GAGGCCAGCCTGGTC | 23894 |
rs212110209 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489021 | ATATTCTAGGCATAA[A/G]TTTTAAATCTATTCG | 23894 |
rs212190310 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480462 | TTAAATGTGAAAATG[A/G]TAACTTGCACAAATG | 23894 |
rs212215867 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487869 | CCTGGAAGAAAAACT[-/A]GTGAAAGCCAGGTTG | 23894 |
rs212247127 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488082 | AGCCCAGCATAAGAA[A/C]AAGTGAGGCGTGCTC | 23894 |
rs212261019 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466594 | GGAGGGCTACCATCA[A/G]TAAATCTAACAAATG | 23894 |
rs212367305 | snp | C/T | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459562 | CTGGGACCACTGGAG[C/T]CACAGACGAGGGTCT | 23894 |
rs212379787 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473840 | TTTTAATTACTCCAT[C/T]TTATTTTTGTTTTGT | 23894 |
rs212412681 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467214 | CCAACACAAACAGCC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 23894 |
rs212500969 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477018 | TATAATAAGCAAGAT[C/T]CAACACTTATGTTTA | 23894 |
rs212512456 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485146 | AGTGTGTCACTGTGG[A/C]AGTGGGTTTTGAGGT | 23894 |
rs212558169 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474296 | TTAGAGAATTCTAAC[C/T]TTCCAAAACAAGATT | 23894 |
rs212589469 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477653 | TCAGATCCCCTGAAG[C/G]CGGAGTCACAGGCAG | 23894 |
rs212604735 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467059 | CTATTCAGCTCTAAA[A/T]GAAAATATGATTACG | 23894 |
rs212606328 | snp | G/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493490 | CCTCGCCATAAACAG[G/T]CTGCCTCGGAGTAAT | 23894 |
rs212653750 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484653 | TGGATAAAACCAAGA[C/T]CCCTAGAAACAGCTA | 23894 |
rs212712501 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463636 | AGAGCTGTATACAAT[A/G]CCACACTATTAAAAT | 23894 |
rs212713972 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470655 | CCACACCCAACTAAT[A/T]CTATATTTTTAATAC | 23894 |
rs212751570 | in-del | -/TT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470499 | AATTTTGTTTTTTGG[-/TT]TTTTTTTTTTCTTTT | 23894 |
rs212829911 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478184 | ACTAATTTTTTTTTC[C/T]TCCATAAATATTTAG | 23894 |
rs212913352 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469436 | GGAGGGGAGCAAAAA[A/C]CCAAATACAAGAGTA | 23894 |
rs212969083 | in-del | -/A | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468326 | CAGTTTTCAGTTTTT[-/A]AAAAAAAAAAAAAAG | 23894 |
rs212991230 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467678 | TTTTGTTTTGTTTTT[A/G]GAGGGGGTATTTATT | 23894 |
rs213053087 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475912 | AGTCATTTCCTAAAA[A/T]AACCAACCGAGACCA | 23894 |
rs213058936 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462547 | TTTTGTCTGTTTTCT[C/T]TTTTTTTGAGACAGT | 23894 |
rs213175651 | in-del | -/CTT | | | downstream-variant-500B, cds-indel | Gtf2h2 | Mm_Celera | 13:100460067 | GTTCCTGTGATAAAA[-/CTT]AACCATAGCCAGCTC | 23894 |
rs213202850 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470188 | AGTGTGTCGTGAGAT[C/T]GTGTCTCCCAAGAAT | 23894 |
rs213213534 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461804 | TCTTCATATAGCCTA[C/G]GAACCCAAAACTCCC | 23894 |
rs213326831 | snp | C/T | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468398 | TTTGCTGCTCTTGCA[C/T]AGGTCCTGGGTTCAG | 23894 |
rs213360265 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461300 | AAAATGGCAGCTTCC[C/T]TCCTATCATGCTCAG | 23894 |
rs213365995 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484408 | TGATCTTCTCTTCTT[C/T]TTTGGAGGAACTCAC | 23894 |
rs213539921 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462106 | ATATTCACCACATAC[C/T]CCTCCCAGATCCATC | 23894 |
rs213590524 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477558 | TCTAAGATTTAGTTT[A/C]GTTTTAATTCTGTGT | 23894 |
rs213630463 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470153 | AGGGATCATAGATTG[C/T]AAAAGCCAGAGAAAT | 23894 |
rs213762009 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467640 | GAAGTTCACTGACTT[A/G]TACAGTCTTTGGGTC | 23894 |
rs213980012 | snp | C/T | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468210 | TAATGTAAGGGTGGA[C/T]TAGAATGTGCTGTTC | 23894 |
rs213992995 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474372 | TTGTCCTAAGCTTCC[A/T]TTGGCTTGTTCGCAG | 23894 |
rs214019737 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469678 | CCCTGAAGACTAGCT[C/T]TGACGGAACCAGAAG | 23894 |
rs214101111 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465011 | ATCAAGCATGGAAAT[A/G]AAATCTAAAACTGGG | 23894 |
rs214156228 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476937 | GTGATGCTATGCTTA[C/T]TTTTAGAAATTAATT | 23894 |
rs214167550 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478806 | TGATGGGTAACACTA[C/T]GCACATGTACCTTGC | 23894 |
rs214239874 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475155 | GCCAGTTTGAACCAA[C/T]TATAAAAAAAAGTTC | 23894 |
rs214421032 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482270 | ATTGGCTACATTGGA[A/G]GGCAGCCTGGGCAAC | 23894 |
rs214552552 | in-del | -/TT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478946 | TTAAGACCTTCTAAC[-/TT]AGAGGAATAAATTTT | 23894 |
rs214572984 | in-del | -/TA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100492048 | CACTTTTTGGCTGGG[-/TA]TACGGGGCCTCTTTA | 23894 |
rs214574317 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462454 | CTTTAAAGGGAAAGG[A/G]ATGCTGAGGTCAAAC | 23894 |
rs214588500 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488532 | TGGAATCTTGCTTGT[-/C]CCAGGCCCTGATTTC | 23894 |
rs214702733 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487012 | CAGCAAGATCTCATC[G/T]TGAAATTCAAAACCA | 23894 |
rs214777093 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494553 | GGCTCACAACCATCT[A/G]TAGTGGGATCGGACG | 23894 |
rs214853497 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470759 | GAATGACAAAACTAT[G/T]TAAATTATTTTGTTC | 23894 |
rs214900391 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470727 | TTTAAAATCTCTCAG[C/T]AGTAAAATAAGAATG | 23894 |
rs214926595 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100469484 | AAGAATATAAGAATT[-/A]AAAAAAAATACATTA | 23894 |
rs215112655 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465508 | GATGTGAATTGGGGG[G/T]GGGTGGGGGGGGACT | 23894 |
rs215132516 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463775 | AAGATGGCTCAGCAG[A/G]TAAAGGAGTTTGCTG | 23894 |
rs215242223 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478295 | TAGCTACTAATCTAA[C/T]CAAGTCTCATTATTG | 23894 |
rs215339263 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469565 | GATTTTAAAGTGACT[A/T]TATTTCAAATGTGTA | 23894 |
rs215424987 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485911 | CATATTTACTTCCAG[C/T]ACATCTACTACTTCA | 23894 |
rs215441555 | snp | A/C | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493591 | TGCCTTGACCAGATC[A/C]CCTGACCAGACCACA | 23894 |
rs215560937 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478338 | AATGTCTTTTGTGCA[A/G]CTGAGAATTGAACCT | 23894 |
rs215627672 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460127 | AGCTAACAGTCCATC[A/G]CTGGGGGCGCCAAGG | 23894 |
rs215661712 | in-del | -/GCAACTGCCTTGTCTCA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100462794 | GACCCTGAACTGGAG[-/GCAACTGCCTTGTCTCA]GCTTTCCAAATGCTG | 23894 |
rs215688764 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466308 | CAAAATACACTATTT[C/T]GTTTCTCCAGTTCTG | 23894 |
rs215701973 | in-del | -/AAAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475889 | TGCTGATACTTTTTG[-/AAAT]AATAAAAAGTCATTT | 23894 |
rs215769228 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490054 | ACAGTATCTACAGCA[C/T]GGCCAATTACATCTA | 23894 |
rs215834111 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490748 | CTGGGCTACACAATG[A/G]GACTCAAGCCCCTCA | 23894 |
rs215916375 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477725 | TTCTGAGGAGGACAT[C/T]ATATGAGCTTAACCA | 23894 |
rs216221767 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465725 | TCTGTATAGGCCTGG[A/C]TGTCCTGGAACTTAT | 23894 |
rs216228639 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471520 | ATATGCAATAGTGTC[A/T]GCGTTTGGAAGCTGA | 23894 |
rs216233994 | in-del | -/TTT | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493259 | GCACCATTCTCTGAC[-/TTT]TTTTTTTTTTAAAAA | 23894 |
rs216309743 | in-del | -/T | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459769 | TTAAGAAGACAGTTG[-/T]TTTTTTTTTTTTAAA | 23894 |
rs216444006 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473315 | CATGGGTCACAACCT[C/T]CAGGTCCAAAGCCTC | 23894 |
rs216574497 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485203 | TGGGACAGTCTCCTG[C/G]TGCCTGCAGTTCAAG | 23894 |
rs216592478 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481731 | TCTGCAGTACTAGAA[G/T]TACTAACATGCAATA | 23894 |
rs216873724 | in-del | -/CG | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482377 | AGAGAGAGAGAAGGA[-/CG]GAAGGAAGGAAGGAA | 23894 |
rs216879380 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478850 | AATATATCTTGATGA[C/T]CACAGCATATGCATA | 23894 |
rs216957851 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473021 | GAATTTATTACAAAA[C/T]AGCAATCTTAGCTGG | 23894 |
rs216957984 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479571 | CGTTTTATATAGCTC[C/G]TAATACAACCAAATA | 23894 |
rs217019358 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473424 | TGACACTCTTGTGAG[C/T]GTGCAGTTTTATTCA | 23894 |
rs217172332 | in-del | -/TTCTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461498 | GGCACTGACACTGTC[-/TTCTT]TTCATTATGTGTATC | 23894 |
rs217200964 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476051 | TTAGGTATTCATAAA[A/T]TTTGGGGGTGGTTGT | 23894 |
rs217239894 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487234 | GAAAAAACTAAATAA[A/C]TAAATAAATAAATAA | 23894 |
rs217263945 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476856 | CATGACCCAAAAAGT[A/G]CCTATTAAAATTATC | 23894 |
rs217264823 | snp | A/G | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468465 | TTAATTCCACTTCCA[A/G]GAAATCTGATGCCCT | 23894 |
rs217336295 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479658 | TTAAGTGCTAGGCAT[A/G]GTGACTCACACCTTC | 23894 |
rs217438243 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480369 | ATCAACAAACAGGAT[A/G]GGTGGCTTTAATTTC | 23894 |
rs217472629 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465637 | TACCACAGTCTCTAA[C/T]ACATCCTGGTGACTT | 23894 |
rs217526761 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473792 | TGCATGTGCAGGTAC[A/G]TGTGGAGGCCATGGC | 23894 |
rs217526967 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474332 | CTCTCCCTGAAACAG[A/G]CATCATCATCATCTC | 23894 |
rs217591992 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477813 | TTTCTAGAAGCTTCA[-/T]TTGAGTTCTTTTTAT | 23894 |
rs217663599 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489377 | ATTGTGGTAAGCTTC[C/T]CTAAGCACACAGTTA | 23894 |
rs217719117 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466275 | TCCATCAAACTCCAT[A/T]TAGTCCTGGGAAAGT | 23894 |
rs217761198 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474969 | TATCCTAACAGTGGG[A/C]CTTTTATATAAACTC | 23894 |
rs217761269 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467075 | GAAAATATGATTACG[C/T]CAGGCAATGATGGTG | 23894 |
rs217783481 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488383 | CCAATCCACCCCCAA[G/T]GAAACACCATGAACA | 23894 |
rs217817295 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474399 | GCAGTTAGAGGCAGA[C/T]CCTCCGATTCCATGT | 23894 |
rs217818890 | in-del | -/GT | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467903 | ATGCATGTTTGTTTG[-/GT]TTTTTTTAAAGAGCA | 23894 |
rs217905843 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489110 | AACTAGTTCTGCACA[A/C]ACTAACAGAAAAATT | 23894 |
rs217961274 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481870 | AAATTAAAGATAACC[A/C]ACACCACGGGGCAGT | 23894 |
rs217986977 | in-del | -/TGTTTTGTTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467655 | TACAGTCTTTGGGTC[-/TGTTTTGTTT]TGTTTTGTTTTGTTT | 23894 |
rs218177635 | in-del | -/AG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486317 | ACATGTTTAACATTT[-/AG]AGTTATTTTGCTCTT | 23894 |
rs218283373 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479814 | ATTTTCTACTCCTTG[-/A]AAAAAAAATCAGAGT | 23894 |
rs218331336 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479298 | TTAATTTCTTTTATA[A/G]GCAAAAACCAGAATT | 23894 |
rs218375179 | in-del | -/GC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470485 | CGTGCAAACATGAAA[-/GC]TTTTGTTTTTTGGTT | 23894 |
rs218544919 | in-del | -/CAAGTTACA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480817 | CTAAAAAATTAAAGC[-/CAAGTTACA]CAATCTTTACAAAGT | 23894 |
rs218597150 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487084 | AAATAAGAAAAATAT[C/T]CAGTGAGGAGAGAGG | 23894 |
rs218678171 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476320 | TACTATTATTCTTTA[C/T]TATATATTTCTCTTA | 23894 |
rs218706437 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491070 | TTAAAGAGACAAAGT[G/T]CGGAGCAGAGACTGA | 23894 |
rs218754796 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491714 | AGCACTCGGAAGGCA[A/G]AAGCAGGCAGATCTC | 23894 |
rs218962623 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484354 | ATTCACTGACATCTC[C/G]ACAAAAAATTTGATG | 23894 |
rs219006356 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460438 | AAAGGGAAGCAGAGA[A/G]GGGGTAAGAGCTCCT | 23894 |
rs219065750 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483658 | ATTCATAAAAATGAC[A/T]CAATCCCGTATTTTT | 23894 |
rs219104236 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483054 | GTTTCCTAAAGTAAA[A/G]TGAAATATCTTTTAG | 23894 |
rs219124426 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481455 | ATATCTAATAAAAAG[A/G]AAAAACAGAAAGAAA | 23894 |
rs219133381 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475652 | CTCCTGTCTCTACCT[C/T]ACAACACTGAAATTA | 23894 |
rs219146765 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483820 | CTCCTAGAACAGCTG[A/G]CAGACATCATCGTAA | 23894 |
rs219251804 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461463 | GCACTTTCACATGAA[C/T]TCCTTTATGGGTCTT | 23894 |
rs219315261 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489972 | TCACTGGGTTGTCAA[C/T]TGAGATATATTGAAT | 23894 |
rs219344668 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460967 | GCACACTTAAAGAAA[C/G]AAAAATTACCAGGTT | 23894 |
rs219382414 | in-del | -/TGTG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460675 | TTAACATCGTGTCTC[-/TGTG]TGTGTGTGTGTGTGT | 23894 |
rs219389770 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482745 | TTTTAAATTACTGGG[A/G]GCTGGAGAGATGGCT | 23894 |
rs219431658 | in-del | -/TAGA | | | intron-variant, splice-acceptor-variant | Gtf2h2 | Mm_Celera | 13:100461963 | TTACAGAGATGGACC[-/TAGA]TGGACATGGGTATAA | 23894 |
rs219439814 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460656 | ATATTTAGTGTGACT[G/T]AATTTTAACATCGTG | 23894 |
rs219494585 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480530 | AAAGCAACACGGGAG[A/C]GACACATACCCATGC | 23894 |
rs219516746 | in-del | -/AG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482652 | TAGCTCCAAGGGATC[-/AG]AGACTCTGGCCTGAT | 23894 |
rs219544586 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482152 | CAATACAATTTACAG[-/A]AAAAAAATCTGAAAA | 23894 |
rs219564332 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460201 | CACAGGCCAAGCGAG[A/G]TACAGGATTTGCATC | 23894 |
rs219587968 | in-del | -/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467508 | TCCAACTGACAGGGA[-/T]TTTTTTTTTTTAAGT | 23894 |
rs219609173 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100459807 | TTATTTATTATATGT[A/G]AGTACACTGTAGCTG | 23894 |
rs219641447 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460317 | AGTGACCATATGGGA[A/G]GGCCAAGTTCATGTT | 23894 |
rs219702574 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466113 | TATAAAAACAAAAAC[-/A]AAAAAAAGTGGCCAT | 23894 |
rs219703810 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466731 | AAAGAAGCCTGACGT[G/T]GTGGTACACGCCTTT | 23894 |
rs219837234 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491120 | CTGCCCCACCTGGGG[A/G]TCCATCCCATATACA | 23894 |
rs219920341 | in-del | -/AATATTA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464415 | GTACTAAGTATATTT[-/AATATTA]ATATGTACTACATAT | 23894 |
rs219950225 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463804 | TGCCAAACCTGACAC[A/C]CTGAGTTCCATGCCT | 23894 |
rs220002987 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467193 | AAACCCGCCACCCCT[A/C]CTACCCCAACACAAA | 23894 |
rs220071986 | snp | A/C | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492910 | ACCATGTTCGTGCCT[A/C]GTTGGGGCAGGGGAC | 23894 |
rs220113378 | in-del | -/TAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463100 | TCTTTTATTTAGACT[-/TAA]TGATTTGTACTAGTT | 23894 |
rs220133854 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484838 | CCTACAGACCAGAAG[A/G]CACTATCATATCTGC | 23894 |
rs220149259 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490184 | AAAAAAAAAAAAAAA[A/T]TAGATCACCAATTAA | 23894 |
rs220166939 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466841 | CAGAGAGACCCTGTC[A/T]TAAAAAAAATAAAAA | 23894 |
rs220198005 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478551 | ACATGTATACATAAT[A/G]TGTATTATATACATA | 23894 |
rs220199902 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100492175 | GGGAGATGCTCACGG[G/T]GAGCTCCTCGCGTGC | 23894 |
rs220205381 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487401 | GGCCTGAATGATCTT[C/T]TCACAGGGGTCGCCT | 23894 |
rs220261839 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473469 | GAACCTTCAACTATG[C/T]AAGAAATTGTCTTTT | 23894 |
rs220369656 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485322 | ACCAATAAATGTTGT[C/T]CTTTAGAAGAGTTAT | 23894 |
rs220405225 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474072 | GTGCTGGGGATCTAA[A/G]CTGCAGACCTACTGT | 23894 |
rs220457211 | in-del | -/ATGAGGACCCGA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460694 | TGTGTGTGTGTGTGT[-/ATGAGGACCCGA]GTTCATGTCCTAAAA | 23894 |
rs220527868 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465826 | AAGGTGTGTGTCATC[A/G]CAGACTGGCTCTGGT | 23894 |
rs220561944 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465271 | TCAAGCTAATTCAGA[A/C]CTCCATGCCAGAGAA | 23894 |
rs220621766 | snp | A/G | | | missense, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100468917 | TGGTATTAAATACCT[A/G]AAGGAGTTGGGATCT | 23894 |
rs220678892 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462219 | AATGTGGTCCGCCTA[A/G]CAGTGGACATACTCC | 23894 |
rs220679041 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470220 | TTAAAGACAACCATC[A/G]AGCCTGATTTTCTGA | 23894 |
rs220759800 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462674 | CATAGGACAAAATAT[G/T]TCTTTGGGGAATAAA | 23894 |
rs220830293 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469843 | ATTGGATTTAAAGTC[C/T]AGTCAACAGGAAGGA | 23894 |
rs221112345 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492763 | GGTGCATTTCTATAG[A/G]CCAAACAGCTAAAAC | 23894 |
rs221113406 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469783 | AGGACACCCTAAGGG[C/T]ATAATAGTGGCTCAC | 23894 |
rs221212755 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488306 | TGCCCCTTCCTGGAG[A/C]CTCTCACCACCATCC | 23894 |
rs221418753 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100489148 | TACCATTCCAAGTCG[A/G]ACTTGTCCATGGTGC | 23894 |
rs221448435 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462182 | ATTTGTACTACCATA[G/T]ACTCCTGGTAACACC | 23894 |
rs221519097 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472592 | CTTATTTTCATTATA[C/T]ACGTGCTTTCTGAAC | 23894 |
rs221541478 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474001 | CCCCCAGGGTGCCCA[-/C]CCCCCAGTGTGCCCA | 23894 |
rs221580022 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491492 | CTTGGTCGTGTGAAG[A/G]CTCTAAGCCCCAGTA | 23894 |
rs221589694 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465160 | CTTAACAGCAAGGAG[A/G]TCACCAGTTGGGAAG | 23894 |
rs221616749 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460773 | GGGGAAGGCTGGGGA[G/T]TCCTAGGATAACTGT | 23894 |
rs221647208 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475584 | AAGGTCTTTCACTGA[A/T]CCTGGAGCTCACTGA | 23894 |
rs221675271 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464259 | AAAGAATAAAAACAA[C/T]ATACAAGTTTCTAAC | 23894 |
rs221694746 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473061 | ACACATACCTCTATT[C/G]CTGGCAGAGGCAGGC | 23894 |
rs221774462 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467945 | GATGTCAGTTAGCAA[A/G]ATGAACAAAGATGTG | 23894 |
rs221801527 | in-del | -/ATGCACCC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465227 | ATCAGACAGAAATAA[-/ATGCACCC]ATGCTCCTGCTAGCT | 23894 |
rs222151514 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470814 | TTTATAGGGAACAAA[A/C]TTCTTATGGTGTCAC | 23894 |
rs222298302 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476211 | GTTCTAAGAGCAGTG[C/T]ACACTCCTAACCATT | 23894 |
rs222306863 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470418 | GTATTTAGGTACAGA[C/T]GGACAGACGGGTGGT | 23894 |
rs222307222 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478413 | CTCCTTTCCCTTTTA[C/T]TCTGAGAGGAGTCTT | 23894 |
rs222402029 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474466 | CCCTAAAGCATCTCT[A/T]TTTTGCTAAGCAATT | 23894 |
rs222507011 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467805 | GAAAAACATCCAGTA[C/G]ACTGGGCTCTGGTCA | 23894 |
rs222527523 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479367 | CAACAAAGTTGTATA[A/G]AAGCTCTTTCCTGCC | 23894 |
rs222533128 | snp | C/T | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468642 | GTGTGTGTGTGTGTA[C/T]ACACACACACACTAA | 23894 |
rs222569039 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479849 | TGGCAAACTTTGCTG[A/T]AACTTTCTGTTTTTG | 23894 |
rs222675919 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467410 | TGGAGGCAGTACAAC[A/G]TACAGGAAAGAAGAA | 23894 |
rs222676230 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475421 | ATATAATCCAAGAAA[A/G]ATGATGTAATTTGAG | 23894 |
rs222864489 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481992 | ACAAGGATTACAGGC[A/G]GAAACATTGTTTCAA | 23894 |
rs223179466 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480068 | GGTGCGTCTGAAGAC[A/G]GCTACAGTGTACTTA | 23894 |
rs223249661 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487755 | TGCATGTATATCTGT[A/G]CATATACGTGCCTGA | 23894 |
rs223296283 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479555 | TTAAAAAAATAGTTC[A/C]CGTTTTATATAGCTC | 23894 |
rs223403414 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470009 | TCACAAAAAGTAGTC[C/G]TCATCTCTAATCAAG | 23894 |
rs223489126 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473914 | AACCTGGAGCTCATT[A/G]ACTAGCTATTCTAGT | 23894 |
rs223636156 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477308 | GCAGGTGGATGTCTG[G/T]GAGTTCAAGCCCAGC | 23894 |
rs223640571 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473593 | GCTATCCTGGAACTT[A/G]CTTGATAGACCAGGG | 23894 |
rs223657040 | in-del | -/TC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469932 | TTGGAGTAGAAACTA[-/TC]TCCAGCACTTCACTA | 23894 |
rs223716658 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477897 | TATTTTAATACTGTC[A/G]TCTATTAATTCTAGC | 23894 |
rs223788075 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470335 | GAAATAGCCTTCCCA[A/G]CAGGTTACCCAATAT | 23894 |
rs224094952 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485580 | AAGACAAAAGAAACT[A/G]AGATTAATGTTGTTT | 23894 |
rs224194261 | in-del | -/AA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491627 | ATTGGAACTGTAAAT[-/AA]AAAAAAAATAATAAT | 23894 |
rs224217321 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483618 | CAAAGATAAAAGCAG[C/T]GAGGTATATATTTTA | 23894 |
rs224326406 | in-del | -/TTGT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487938 | TGTCAGCCCATTTGC[-/TTGT]TTGTTTGTTTGTTTG | 23894 |
rs224419253 | in-del | -/TCTC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464747 | AAGTTTGATTACCAT[-/TCTC]TCTCTCTCTGTGTCT | 23894 |
rs224449623 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484730 | CAGTGAAATTATTTC[A/G]AGATGTTTTATATTT | 23894 |
rs224490535 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100477195 | CCCTGGCTCAGTGCT[A/G]TTGTTATCCAAATGC | 23894 |
rs224524655 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476337 | ATATATTTCTCTTAA[C/T]TATAAATATGTGAGT | 23894 |
rs224690276 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483941 | AACACCTCAAACTCA[A/C]TAGACCAGGGTGGCC | 23894 |
rs224752376 | in-del | -/AAA | | | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100493270 | CTGACTTTTTTTTTT[-/AAA]AAACAATTTTCCTGC | 23894 |
rs224815906 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473640 | GACAGCAGCCTGCCA[C/T]GTGGCACCACATGTG | 23894 |
rs224876115 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460135 | GTCCATCGCTGGGGG[C/T]GCCAAGGCAAGGACT | 23894 |
rs224884990 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467447 | AGTCTTAGAGGATGC[A/G]GAAGGACTGCAAGTA | 23894 |
rs224931049 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478055 | CTTAAATTTGCCGTG[-/A]ACCCTCCTTTCTCGT | 23894 |
rs224974784 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479968 | AAGAGCACTGACTGC[A/T]CTTCTGAAGGTCCTT | 23894 |
rs224984546 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460523 | CGACTGCCAGAAATG[C/T]GCCACAGCCAGGACT | 23894 |
rs224992457 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480720 | ACCAAAGTTTCTAGA[G/T]ATGAAAATATATAAT | 23894 |
rs225014168 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478433 | AGAGGAGTCTTACTA[C/T]GTTACTCAAGCACCC | 23894 |
rs225062791 | in-del | -/TTATT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461208 | AACCCATAATTTTCC[-/TTATT]TTAAATACTTTATTC | 23894 |
rs225064617 | snp | A/G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466961 | TTGCTTTATTCGCTA[A/G/T]AGCAAAGAATTAGAA | 23894 |
rs225105675 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474022 | AGTGTGCCCACCCCC[A/G]GGGTACACACTGATA | 23894 |
rs225145079 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490782 | ACCACTGTGAACATA[A/C]AAGTAAAGTTCTGCC | 23894 |
rs225227108 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474824 | CACCTGGTGTGGCTA[A/G]TAGTGTAAATGTTTT | 23894 |
rs225298112 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481412 | ATAGGGAACTTTCAG[A/G]ATAGCATTTGAAATG | 23894 |
rs225335427 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478965 | AGGAATAAATTTTAA[A/G]TGTTAAAATGTTATT | 23894 |
rs225338402 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482028 | CAAAACAAAACAAAC[A/G]AACAAACAAAAAACA | 23894 |
rs225338521 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474325 | TTGACTACTCTCCCT[A/G]AAACAGACATCATCA | 23894 |
rs225367303 | in-del | -/AAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479761 | ACCTTGTCTCAAAAA[-/AAG]AAGATTATTTAAAAT | 23894 |
rs225428400 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484216 | CACTGTGTGCTGGGC[-/A]CCGGGGAAATGCACA | 23894 |
rs225453519 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100476650 | AAGAGATATACTTAG[-/A]AAAAAATGCTTTCAA | 23894 |
rs225468017 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482443 | AAGGAAGGAAGGAAG[A/G]AAAGATGGAAAGAAA | 23894 |
rs225549260 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480129 | AGGGACTGAGCAAGC[-/G]AGGTTGACCAGAGCG | 23894 |
rs225906640 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465117 | AAAGCAAAACAAAGG[A/G]GGGAAGGGTTTGGCT | 23894 |
rs225978883 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493873 | TAACAGGGTACCAAA[A/G]CAAAACAAAATGTGC | 23894 |
rs226022168 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488176 | GCCTGCTCTGGAACA[C/T]GTAACCACGACCCCT | 23894 |
rs226105197 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488807 | TACATATGTATATAC[C/T]CTTTCCCTACATTTA | 23894 |
rs226120921 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464058 | GCACATTTGCCAGGA[A/G]GTGCCTGCATCTACT | 23894 |
rs226163670 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489855 | TGTGTACAGGTGGTG[A/G]GGACGGAATGAGTAT | 23894 |
rs226276400 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483490 | TCTCTGAAACAGGAA[A/G]ATTACAAGTTCTAGG | 23894 |
rs226316344 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471291 | ATGCAGCTAGAGACA[C/T]GAGCTCTGGGGTACT | 23894 |
rs226330270 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482568 | GCAGCTAAGGGCCCA[A/C]ACTGTTCTTGCAGAG | 23894 |
rs226341301 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493057 | AGCCATAGCCCCACC[C/T]GCCGCCCCACCCCCA | 23894 |
rs226367340 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489579 | AAAGCAATATTTATT[A/C]GTTTGAAATAAGCTA | 23894 |
rs226423638 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484975 | TTTTAGTATTGGTGA[G/T]CAAACCCAGGGCTTT | 23894 |
rs226429441 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478131 | CAGCCAGATACTTCT[A/G]CATCCTGTGAGAGAT | 23894 |
rs226434506 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487377 | CCTGTGGGACACAAC[-/T]TTTTTGGGGGCCTGA | 23894 |
rs226466227 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463268 | AGTGGTAAATACATT[A/T]CATCTTAACAAACAG | 23894 |
rs226492884 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485084 | ACAGGGAGTGGCACT[A/G]TTAAGAGGAGTGGCC | 23894 |
rs226550499 | in-del | -/AA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472787 | GAAACCCTGTCTCGG[-/AA]AAAAAAAAAAAAAGA | 23894 |
rs226553376 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485725 | TGAGAACCAAACTCA[C/T]GTCTTCTGCAAGAAC | 23894 |
rs226737744 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465859 | CTTTTCAAGAGGAGA[C/T]ATTCAAAGTCTTTCT | 23894 |
rs226758305 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481973 | AGAGTAAGTTCTAGG[A/C]CAGACAAGGATTACA | 23894 |
rs226884869 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462265 | ACTGACTCTCCCCTT[C/T]ATGTTTCCTTTCTTG | 23894 |
rs227043951 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460803 | TTCAACCATTTTAAC[C/T]TCATTAATGATTTCC | 23894 |
rs227256296 | in-del | -/AAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465598 | GATATAAAAGAGAAT[-/AAG]AAGAAAAAATTTTAA | 23894 |
rs227273910 | snp | C/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492388 | AGGCGGAAGCTGCCG[C/G]GCTCCCTGCACACGC | 23894 |
rs227306114 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466661 | CTGTTGGTAATGGTG[C/T]AAACTAATACAGACA | 23894 |
rs227312830 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465521 | GGTGGGTGGGGGGGG[A/G]CTCGAGGAGAGAATT | 23894 |
rs227373932 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486956 | AATCTGAAACAGGAG[A/G]GTCTCCTGAGGCAAG | 23894 |
rs227424943 | in-del | -/GA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482352 | GAATGAGGGGGGAGG[-/GA]GAGAGAGAGAGAGAG | 23894 |
rs227457552 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474973 | CTAACAGTGGGCCTT[C/T]TATATAAACTCATGT | 23894 |
rs227468874 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462742 | TTCTTGTTTTGTTTT[-/G]GTTTTTTTGGCACAA | 23894 |
rs227552159 | in-del | -/TTTTT | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468320 | GAATACAGTTTTCAG[-/TTTTT]TTTTTAAAAAAAAAA | 23894 |
rs227597812 | snp | A/G | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468153 | CAGTGTAAAGGAGGA[A/G]CTCCTACAGAGAACA | 23894 |
rs227598319 | in-del | -/TTTTG | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468857 | ATTTACAGTTACAAC[-/TTTTG]TTTTGTTTTTAAACC | 23894 |
rs227598981 | snp | A/G | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459693 | CAGAGACCCTGTCCC[A/G]CCTCGAGTTTTGAAG | 23894 |
rs227602102 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462426 | GCCACCATACCCAGC[C/T]CATACTGTGTCTCTT | 23894 |
rs227604641 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470459 | ACGAGCTCAAAGGAT[A/G]AAGCACTTTACCGTG | 23894 |
rs227666288 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469123 | GCCTTGCTCCCTATA[A/T]TCTTCAATGTTTCCC | 23894 |
rs227754325 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475789 | CATCTGTATATTAAA[A/T]TTGTTCTACACTATC | 23894 |
rs227757313 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470106 | TGGTCCCAGCTGACA[A/C]ATTTACAATACAACT | 23894 |
rs227775271 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473670 | GGTATTTCTATATAA[C/T]TAAATCATCAACTTG | 23894 |
rs227812824 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494474 | CTGGTGAGATAGCTC[C/T]GTGATTAAAAGCACT | 23894 |
rs227912351 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463567 | TCCTTTGCTGACAGG[A/G]GTCCAACCTGAAGTC | 23894 |
rs228047304 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466093 | AACAGAAAGGACAGT[C/T]TGAAATATAAAAACA | 23894 |
rs228163932 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466210 | CCATTCGGGTCATAC[A/C]CTCAGCACTTAAGAC | 23894 |
rs228218683 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464321 | ACAATTCAGAAGATG[A/C]AATGGTTTAAACCAA | 23894 |
rs228234855 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461061 | CTTGTATCCAGGAGT[C/T]TGAGAGCAATCTGGG | 23894 |
rs228470194 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472766 | GGACAGCCAGGGCTA[A/C]ACAGAGAAACCCTGT | 23894 |
rs228491293 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473095 | TCTCTAAGCTTAAGG[C/T]CAGTCTGATCTATAG | 23894 |
rs228493173 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472657 | CTATCAGAGCTGGGC[A/G]GTGGTGGCGCATGCC | 23894 |
rs228511686 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478207 | ATATTTAGAGCTTTA[G/T]TTTAGAATGAAGTAA | 23894 |
rs228513136 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477327 | TTCAAGCCCAGCCTG[A/G]TCTAATAGTGAGTTC | 23894 |
rs228532541 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478591 | TACATATACATCTAC[A/T]CATATCTACATTTTA | 23894 |
rs228533406 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470666 | TAATACTATATTTTT[A/T]ATACTTCTAAACTAA | 23894 |
rs228569411 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470066 | ACCATTATAGAAAAC[G/T]ACAACCAATCAAAAT | 23894 |
rs228600248 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492319 | GGGCTGCAAACTCGC[C/T]TCGGGCCACACAGAC | 23894 |
rs228613271 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484273 | CAATGGTCTGACTGT[A/G]AGGACAGAAGCTGTC | 23894 |
rs228657042 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476722 | AGGGCCTCACACACA[C/T]TAGAAAAGCTGCCAC | 23894 |
rs228924768 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474127 | CCCATCTCCTCAGCC[C/T]CTAATTTTCCTTTGG | 23894 |
rs228927909 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466291 | TAGTCCTGGGAAAGT[C/T]TCAAAATACACTATT | 23894 |
rs228959965 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466937 | GAGAGACATTTCCCA[C/T]GTTTACTATTGCTTT | 23894 |
rs228984942 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460602 | AATAATTTTCTTATA[C/T]TTTAAATATGTCAGT | 23894 |
rs229029518 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473766 | ATGTGTGTGGTATGA[A/G]TGTGTGATGGTGCAT | 23894 |
rs229239075 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490683 | CTAAAGCCAGAACGT[C/T]ATTCCCTGAGCCTCT | 23894 |
rs229265406 | in-del | -/AAAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491824 | TAATTAATTAATTAA[-/AAAT]AAATAAATAAAATTT | 23894 |
rs229315185 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489895 | TACTGCCCTCATTTA[A/C]TGTTCTAAAAGTAGT | 23894 |
rs229562175 | in-del | -/T | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459714 | AGTTTTGAAGTAATG[-/T]TTTTTTTGTTTTGTT | 23894 |
rs229606657 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467520 | GGGATTTTTTTTTTT[A/T]AGTTTGAGTAGTGGA | 23894 |
rs229626438 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474488 | TAAGCAATTTTTATA[A/G]CATTTCATTTATCTA | 23894 |
rs229713480 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478822 | GCACATGTACCTTGC[C/T]ATTTTATTTAGTAAT | 23894 |
rs230226746 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478341 | GTCTTTTGTGCAACT[A/G]AGAATTGAACCTCAG | 23894 |
rs230313420 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485336 | TTCTTTAGAAGAGTT[A/G]TTGTGGTCACAATGT | 23894 |
rs230375423 | in-del | -/CTG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484107 | GAAAGACACAGACCT[-/CTG]ACCTCTGGTGGGAGT | 23894 |
rs230494406 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480408 | AACATGTTTCAATAT[A/G]TATTTTTATTATAAT | 23894 |
rs230536001 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481333 | TACATCCCAGCACAG[A/G]GGAACGAACGCCAGG | 23894 |
rs230579415 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475242 | ACAAATTTACAACAT[C/T]TACCAAAACTCATAT | 23894 |
rs230582037 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474223 | ATAGCCTAGACAGCC[C/T]CTAAATACATTTAAC | 23894 |
rs230633303 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493366 | CATCCTTATGACGTG[A/G]AACCGAGACTACTCC | 23894 |
rs230641605 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481880 | TAACCAACACCACGG[A/G]GCAGTGGTAGAGTAT | 23894 |
rs230661923 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100479419 | TCATAGTATAATGAA[A/T]CATAGTATAATGAAA | 23894 |
rs230734999 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482360 | GGGGGAGGGAGAGAG[A/G]GAGAGAGAGAGAAGG | 23894 |
rs230735201 | in-del | -/CAAA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487125 | ATCAAAAACAGGCAT[-/CAAA]CAAACAAGGCACTGA | 23894 |
rs230740453 | in-del | -/TTAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479910 | TAAAGATTTTGTGGC[-/TTAT]TTAAGAAATTTCTTG | 23894 |
rs230771965 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487128 | AAAAACAGGCATCAA[A/T]CAAACAAGGCACTGA | 23894 |
rs230811799 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470626 | CCGAGTGCTGGGATT[A/G]AAGGCGTGCACCACC | 23894 |
rs230828944 | in-del | -/TTTTG | | | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100494309 | AACAACCCAATACTT[-/TTTTG]TTTTGTTTTGTTTTT | 23894 |
rs230905452 | in-del | -/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493835 | AGGACTGCTGGAACA[-/G]GGGGTTTTTATTAAA | 23894 |
rs230913234 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479779 | AAGATTATTTAAAAT[A/G]ATCATTTTTATGACC | 23894 |
rs231006356 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476462 | TAAATTAATCAAAAT[C/T]CATATACCTTTCTCC | 23894 |
rs231084904 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473884 | AGGTTATTTTTAAGA[C/T]AATGTTTCTTACTGA | 23894 |
rs231086875 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494125 | GTATTATAAGACCTC[A/G]TGTAAGTCCCTCTCT | 23894 |
rs231149263 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477620 | CATGAGTACAGGTGT[C/G]CTCAGAGAGCAGAGG | 23894 |
rs231178905 | in-del | -/TA | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459781 | TTGTTTTTTTTTTTT[-/TA]AAGATTTATTTATTT | 23894 |
rs231259089 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475833 | AGTGATGCATTATTA[C/T]ATATGAAAAATATAA | 23894 |
rs231283497 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469303 | AGCTGGGAGGGTAAG[C/T]ACGCACTTATAATTC | 23894 |
rs231294014 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481795 | TTTTTTTTCTTAGTT[C/T]TACGTACTGCTGTGG | 23894 |
rs231304007 | snp | A/G | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468306 | GTTTTTTGTATGATA[A/G]AATACAGTTTTCAGT | 23894 |
rs231370931 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489210 | GTTAATTGAACATCA[C/T]AGCTACCAAAACTCA | 23894 |
rs231423736 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100490104 | AGCCTCCTTCCCACC[G/T]CTTGGTTCTCTCAGG | 23894 |
rs231460674 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461647 | CACAGGTCAACAGAG[C/T]CCACAGTCCATCTTG | 23894 |
rs231517264 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485047 | TTGTGATAGTTTGAA[A/T]GCAATTGGCCCCCAC | 23894 |
rs231570912 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477508 | TCTTGATGACTAATC[A/T]GTTAGTTCCATCCAG | 23894 |
rs231655322 | in-del | -/TGGA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481641 | TCTCAAAAAGGTGGG[-/TGGA]TGAATGGGTAGATAG | 23894 |
rs231659892 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465732 | AGGCCTGGCTGTCCT[A/G]GAACTTATACTCTGT | 23894 |
rs231690255 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466539 | AAAGTGTTCAATATC[C/T]CTAGCCATCAGGCAA | 23894 |
rs231757802 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483218 | GTTTGGCTCATTTGT[C/T]TTGTTGATACAGAAT | 23894 |
rs231825058 | in-del | -/ATT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463029 | TTCTGGATGTTAGTA[-/ATT]ATTTGGTCTTCTATT | 23894 |
rs231831394 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487922 | AAAGCACAGAGCCAT[C/T]CTGTCAGCCCATTTG | 23894 |
rs231865302 | in-del | -/CATAGTATAATGAAA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100479405 | TCGATATGTGCCTAT[-/CATAGTATAATGAAA]CATAGTATAATGAAA | 23894 |
rs231940409 | in-del | -/GTGTGTGT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467830 | TGGTCACTTAACTCC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 23894 |
rs232013692 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462128 | AGATCCATCCTTAAC[A/C]CTCAACTTTGTGTCT | 23894 |
rs232025750 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487242 | TAAATAACTAAATAA[A/C]TAAATAAGTTGGAAT | 23894 |
rs232044904 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462474 | TGAGGTCAAACAACT[G/T]ACACAACTAAAAAGG | 23894 |
rs232084349 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478708 | GAGTGACCTCAAACT[C/T]AAAGCTATCACCTTG | 23894 |
rs232172353 | in-del | -/AAC | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493274 | CTTTTTTTTTTAAAA[-/AAC]AATTTTCCTGCTAAG | 23894 |
rs232223168 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482195 | AATGGTTATGGTTGC[A/G]CATGCCTGTAATCTC | 23894 |
rs232259392 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482280 | TTGGAGGGCAGCCTG[A/G]GCAACATGGGAAAAT | 23894 |
rs232272351 | in-del | -/GAAGG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483779 | ACTGGAAGACTATCT[-/GAAGG]GACGGCCTATGCCTG | 23894 |
rs232346797 | in-del | -/AA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485530 | CTATTTTACAAAAAG[-/AA]AGTGTGATGCAATTT | 23894 |
rs232364920 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490727 | CCTTCCCTCTTCAAG[C/G]CCAGACTGGGCTACA | 23894 |
rs232400180 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484409 | GATCTTCTCTTCTTT[C/T]TTGGAGGAACTCACC | 23894 |
rs232499957 | in-del | -/ATCTAGT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475176 | AAAAAAGTTCATACC[-/ATCTAGT]ATCAGTAAAGTTTGG | 23894 |
rs232547117 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492556 | AGACCCACCAGCCTC[A/G]ACGAGACGACCCTCA | 23894 |
rs232549504 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483706 | AGAACTCACAAAGAT[A/C]TAAACAGGAGGGAGG | 23894 |
rs232712765 | in-del | -/ATAAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480747 | AATTTCATAACCATT[-/ATAAG]TTAATTATCACTTAA | 23894 |
rs232742738 | snp | C/G | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468500 | TGACCCCTGTGGGTA[C/G]CTATACTTAGGGTAA | 23894 |
rs232743534 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479507 | ACAACCTCACACTCC[A/G]AAATTTATATCTTTA | 23894 |
rs232772077 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469667 | GGAAGCTTCCTCCCT[A/G]AAGACTAGCTCTGAC | 23894 |
rs232773966 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461398 | GTCGGACCCAGCACA[C/G]CTCCTCCCTTGGATA | 23894 |
rs232943913 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494338 | TTTGTTTGGTGTACA[C/T]GGGGTTTCTTTGTGT | 23894 |
rs232993551 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467281 | CATTTGCAGAAAAAT[-/A]GATCAATCCAGAATG | 23894 |
rs233026278 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464600 | GCACTCAAGGAAAAG[A/G]AAGGAAAATGTGCAC | 23894 |
rs233093782 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473178 | CACACAAACAAAAAA[A/C]CAAAAATTCCCCAGC | 23894 |
rs233259515 | in-del | -/TTTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473539 | CTTTTTTTTTCTTGC[-/TTTT]TTTTTTTTGAGACAG | 23894 |
rs233346537 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478091 | AGTGCTGGCCTGTGG[C/T]GATGTACAGCAGCAG | 23894 |
rs233360574 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461231 | AATACTTTATTCTAA[C/T]TTTTGAGCAAATGTC | 23894 |
rs233447269 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491731 | AGCAGGCAGATCTCT[A/T]AAGTTCAAGGCCACC | 23894 |
rs233457962 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478245 | CTTACTGATCTATTC[-/A]AAAAAAATGTTTAAG | 23894 |
rs233481970 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462291 | TCTTGAAACAGATCT[C/T]GTATACAGTAGCTCT | 23894 |
rs233491688 | in-del | -/GCACTCAGCACTCT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488476 | ACCCCTCTGCACTCA[-/GCACTCAGCACTCT]GCACTCTGCACTCAC | 23894 |
rs233606810 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463202 | ACTATGATTAAAATT[-/A]TAAAAAAAGAGAAAT | 23894 |
rs233652421 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491071 | TAAAGAGACAAAGTT[C/T]GGAGCAGAGACTGAA | 23894 |
rs233698988 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460483 | GTCCCTCCATTGCTG[C/T]AGCTGACACACCTAC | 23894 |
rs233751807 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461986 | GGGTATAAGGAGGAA[C/G]CTGTGTCATAATCTT | 23894 |
rs233763824 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493503 | AGTCTGCCTCGGAGT[A/G]ATGACATCACTAGCA | 23894 |
rs233836020 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486399 | TCAAAGAATATATGT[C/T]CCATTTTAAAAGAAA | 23894 |
rs233878004 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492848 | GGTTTTGTTTTGTTG[A/G]GTTTTGTTTAGTATC | 23894 |
rs234009885 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466711 | TAGTCCTCAAAAAGT[G/T]ACAAAAAGAAGCCTG | 23894 |
rs234060605 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467091 | CAGGCAATGATGGTG[C/T]ACAATTTAACCCTAG | 23894 |
rs234107802 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479607 | TAAATGATACAGTAT[A/C]TCTTTAAGCACATAT | 23894 |
rs234148057 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477483 | TTTCTCTTAGAGTTA[-/T]TTTTTTCTTTCTTGA | 23894 |
rs234151397 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469462 | GAGTATGTCAAATGA[C/T]ACACATAAAGAATAT | 23894 |
rs234165341 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473946 | GGCCAACAAGCCCAG[G/T]GTGCCCACCCCCAGG | 23894 |
rs234195909 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461809 | ATATAGCCTAGGAAC[C/T]CAAAACTCCCTGACT | 23894 |
rs234241455 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487801 | CTTTCTAGAACAGGA[A/G]TTCCTGACAATTAGG | 23894 |
rs234383935 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470790 | CCATTTTACCTCTAC[C/T]TTACTGTCTTTATAG | 23894 |
rs234404599 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472616 | TCTGAACTAGAACTC[-/T]ATGAGAATTTGATGC | 23894 |
rs234444030 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470742 | TAGTAAAATAAGAAT[A/G]AGAATGACAAAACTA | 23894 |
rs234451692 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463856 | AAACTGTTAGCTCTA[A/T]GTTGTCTTCTGACCT | 23894 |
rs234484012 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463781 | GCTCAGCAGATAAAG[C/G]AGTTTGCTGCCAAAC | 23894 |
rs234497045 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475934 | CCGAGACCACTTCCA[C/T]TTCAGCTTTTACTAC | 23894 |
rs234562263 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470279 | CATGCTAACATGGTT[A/T]TGGGGAAGCCCACAG | 23894 |
rs234676301 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480168 | TGACTGGAGTGAGCA[A/G]AGGTCCTAAAAATTC | 23894 |
rs234760583 | snp | C/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493839 | CTGCTGGAACAGGGG[C/G]TTTTTATTAAAACTT | 23894 |
rs234776507 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464908 | ACACCCAGCTTCTAC[G/T]TCTGTAATCTTTAAA | 23894 |
rs234915657 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473340 | AGCCTCTAGCCTCTA[A/C]CAGCATCTATACTCA | 23894 |
rs234955584 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465683 | TTTTTTGTTTGTTTG[G/T]TTGGTTTTACTTTTT | 23894 |
rs234974776 | snp | A/C | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460109 | AGAGCTCTTTTGGTT[A/C]ACAGCTAACAGTCCA | 23894 |
rs235169063 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465363 | TGATCTAGATAACTC[C/T]CCAAATGAGGCTCTC | 23894 |
rs235242506 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477698 | GGGTAGGTGCTAAGA[A/G]CCAGACTCTGGTTCT | 23894 |
rs235242516 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469795 | GGGCATAATAGTGGC[A/T]CACATATTTTAGTGG | 23894 |
rs235376731 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477024 | AAGCAAGATCCAACA[C/T]TTATGTTTAATTCGG | 23894 |
rs235382500 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488419 | GCCGTTTCACGGAGC[A/G]GCTGCACCACAGGGA | 23894 |
rs235410187 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490890 | TTTTTACTCAGAAAC[A/C]GGAGGGCAGAGGCAG | 23894 |
rs235430355 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473028 | TTACAAAATAGCAAT[C/T]TTAGCTGGGTGGTGG | 23894 |
rs235482057 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470199 | AGATCGTGTCTCCCA[A/G]GAATGTTAAAGACAA | 23894 |
rs235488756 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478415 | CCTTTCCCTTTTATT[C/T]TGAGAGGAGTCTTAC | 23894 |
rs235491252 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473493 | GTCTTTTAACCCTCT[A/T]GATCCAATAATATGT | 23894 |
rs235519434 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478868 | CAGCATATGCATACA[C/T]AAAGAGGGCCATTTC | 23894 |
rs235613522 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489030 | GCATAAGTTTTAAAT[A/C]TATTCGTTTAAAAGG | 23894 |
rs235665419 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467066 | GCTCTAAATGAAAAT[A/G]TGATTACGCCAGGCA | 23894 |
rs235680657 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477853 | ACTTCTCCTTCACTT[-/A]AGAGACTAGAGAGTG | 23894 |
rs235702935 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460191 | CTGAATGAAGCACAG[A/G]CCAAGCGAGGTACAG | 23894 |
rs235854412 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465060 | GAGTTTAGGTCTTTG[C/T]TCTGATTTCACTTCT | 23894 |
rs235957095 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484867 | GCTGGAAATGGGGTT[A/G]AAGATGGTTATAGGC | 23894 |
rs235988918 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472977 | AAAGCCCTAAAAGCA[A/G]TAACATCATCCCTGT | 23894 |
rs236095486 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484254 | AGTGTCAGGGTGGCT[C/T]ACACAATGGTCTGAC | 23894 |
rs236132422 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471753 | AATATCCACTTATCA[-/G]GTGAGTACATATCAT | 23894 |
rs236207763 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477309 | CAGGTGGATGTCTGT[A/G]AGTTCAAGCCCAGCC | 23894 |
rs236264060 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479096 | CTATAACTCCTGCTC[A/C]AGGGTATCTGACACC | 23894 |
rs236286052 | in-del | -/TA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464808 | CTATCTGTCTCTGTC[-/TA]TCTCTCTGTCTCTGT | 23894 |
rs236289175 | in-del | -/TCTA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464793 | GTCTCTGTCTATGTC[-/TCTA]TCTGTCTCTGTCTCT | 23894 |
rs236296956 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477942 | TGTTTCCATTCTGTA[A/G]TTTTTCTGTTATTCT | 23894 |
rs236431451 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464011 | AGAGATGTTTCCTTG[-/T]GGCCCTCTTTATAAC | 23894 |
rs236460437 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473804 | TACGTGTGGAGGCCA[C/T]GGCCATTACCCTGAT | 23894 |
rs236507258 | in-del | -/TCATTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488404 | CCATGAACAAGCAAG[-/TCATTT]CCGTTTCACGGAGCA | 23894 |
rs236513448 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480070 | TGCGTCTGAAGACGG[C/T]TACAGTGTACTTATA | 23894 |
rs236620208 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474123 | AACACCCATCTCCTC[A/C]GCCTCTAATTTTCCT | 23894 |
rs236676134 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494554 | GCTCACAACCATCTG[C/T]AGTGGGATCGGACGC | 23894 |
rs236706027 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474406 | GAGGCAGATCCTCCG[A/G]TTCCATGTCCTTCTC | 23894 |
rs236856365 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490241 | AGTTTAAAATATCAG[A/G]ATGCAAGGTCATTTT | 23894 |
rs236939515 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476943 | CTATGCTTATTTTTA[A/G]AAATTAATTACTAGG | 23894 |
rs236976966 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469682 | GAAGACTAGCTCTGA[C/T]GGAACCAGAAGGATC | 23894 |
rs237069706 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467642 | AGTTCACTGACTTGT[A/G]CAGTCTTTGGGTCTG | 23894 |
rs237080445 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487436 | CCATTAGAGCAAAAT[G/T]ACAGTTATGAAGTGA | 23894 |
rs237082842 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478578 | CATATGTATCTTATA[C/G]ATATACATCTACACA | 23894 |
rs237182356 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475159 | GTTTGAACCAACTAT[A/C]AAAAAAAGTTCATAC | 23894 |
rs237340530 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487660 | AGAGGACCACTTTCT[A/G]GAGGTAATGGGTTTT | 23894 |
rs237388753 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488133 | CAGGACTGGGGCTGC[C/T]CCCCCACCCCGCCCC | 23894 |
rs237508181 | in-del | -/TAAAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478320 | TTATTGTGGGCTCTC[-/TAAAA]TGTCTTTTGTGCAAC | 23894 |
rs237531650 | in-del | -/TTAAGAAGTCTC | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490520 | ATATTTCCCACGGAG[-/TTAAGAAGTCTC]TCATCATTTGCCTCA | 23894 |
rs237540770 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466639 | GACAGAAAGAAACCC[A/T]TACTCACTGTTGGTA | 23894 |
rs237805628 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483663 | TAAAAATGACACAAT[C/T]CCGTATTTTTCTTGG | 23894 |
rs237866364 | snp | A/G | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476080 | GTTAAACTACTGACT[A/G]CTGAAAACTGGCCAT | 23894 |
rs237966241 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465168 | CAAGGAGGTCACCAG[A/T]TGGGAAGCTTGAGCC | 23894 |
rs238035836 | in-del | -/CCC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473965 | CCCACCCCCAGGGTG[-/CCC]CCCCCCCCCGTGTGC | 23894 |
rs238065946 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481460 | TAATAAAAAGGAAAA[A/C]CAGAAAGAAAAAAAA | 23894 |
rs238116033 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460668 | ACTTAATTTTAACAT[C/T]GTGTCTCTGTGTGTG | 23894 |
rs238192937 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479333 | GAATAAGAATCTTAA[A/G]ATATTCTTATCAGAA | 23894 |
rs238318334 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460974 | TAAAGAAACAAAAAT[G/T]ACCAGGTTTTGAAAT | 23894 |
rs238426489 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477762 | TATCCCTTCAGCCCT[C/G]CAGTGCACTTTTCAT | 23894 |
rs238535716 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479673 | GGTGACTCACACCTT[C/T]AATTGCAACACTTGG | 23894 |
rs238579713 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473425 | GACACTCTTGTGAGC[A/G]TGCAGTTTTATTCAT | 23894 |
rs238670506 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476260 | CCACCCCAGCTTCCA[C/T]TCCCCACCAAACCAA | 23894 |
rs238706407 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466141 | CATTGAAACAAGGGC[C/T]CAGACCTTAGTAGGC | 23894 |
rs238849098 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474468 | CTAAAGCATCTCTAT[C/T]TTGCTAAGCAATTTT | 23894 |
rs238912073 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470169 | AAAAGCCAGAGAAAT[G/T]AGGAGTGTGTCGTGA | 23894 |
rs238940864 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485224 | GCAGTTCAAGATGTA[C/G]AACTGTTGGCTCCAT | 23894 |
rs239045542 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474179 | CTTTCCTACATAACT[A/G]GCACAATTTAGCTCT | 23894 |
rs239096678 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460821 | ATTAATGATTTCCAA[A/G]CCAATAAAAGACCCT | 23894 |
rs239102077 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482076 | AATAACATTTTAGGG[-/T]TTTTTTCTATTTAAC | 23894 |
rs239149496 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474384 | TCCTTTGGCTTGTTC[A/G]CAGTTAGAGGCAGAT | 23894 |
rs239173945 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467445 | TAAGTCTTAGAGGAT[A/G]CGGAAGGACTGCAAG | 23894 |
rs239211152 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467811 | CATCCAGTAGACTGG[A/G]CTCTGGTCACTTAAC | 23894 |
rs239238124 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484698 | CTACCTCTAAATATA[C/T]GCCAATTCCTTTTTT | 23894 |
rs239437341 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482789 | CACTGACTTTTCTTC[C/T]GGAGGTCCTGAGTTC | 23894 |
rs239451920 | in-del | -/ATGTGT | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468620 | GTAATATCTATATAT[-/ATGTGT]GTGTGTGTGTGTGTG | 23894 |
rs239467037 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462574 | CAGTCTCTCTAGATA[A/G]ACGCTGGCTGTGCTG | 23894 |
rs239550650 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482608 | TCAAGTCTCAGCACC[C/T]GTTGTTGGGCAGTTC | 23894 |
rs239671286 | snp | G/T | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468427 | AGTTCCCAGCACCCA[G/T]ACTGGCAGTTTACAA | 23894 |
rs239772716 | in-del | -/AC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486994 | AAGTCAGCTGAGGAA[-/AC]ACAGCAAGATCTCAT | 23894 |
rs239784525 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492741 | TTCACCAATATTTCT[A/G]CTGTGGGGTGCATTT | 23894 |
rs239785934 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460359 | CTCCATCTTCATCCA[A/C]TAAGGAGAAAACTTC | 23894 |
rs239816091 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476896 | TTAAAGAAAACATTT[A/G]CCAAAGAGAGAATCA | 23894 |
rs239858533 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466740 | TGACGTGGTGGTACA[C/T]GCCTTTAATCTGAGC | 23894 |
rs239895301 | snp | A/C | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100459834 | GCTGTCTTCAGACAC[A/C]CCAGAAGAGGACGCC | 23894 |
rs239905255 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475473 | GCTTATTTGAAATTA[C/T]TTCTTTTGCATATGT | 23894 |
rs240011711 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482011 | ACATTGTTTCAAAAA[A/G]CCAAAACAAAACAAA | 23894 |
rs240149296 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480666 | ACAGGCAAAGGCAAA[A/G]CACAGCAGGTTAAAG | 23894 |
rs240265630 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490385 | AAGTTCCGGGACAGC[A/C]AAGGCTACACACAAA | 23894 |
rs240315907 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488227 | CCCAGTCACACAGCA[C/T]GGCACCTAGAACACC | 23894 |
rs240471363 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460263 | TTCCATCAGAGTAAA[A/G]ATTCTGGGATATCCT | 23894 |
rs240561764 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462679 | ACAAAATATGTCTTT[-/G]GGGGAATAAATATGT | 23894 |
rs240638994 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465125 | ACAAAGGGGGGAAGG[A/G]TTTGGCTAAAATTCC | 23894 |
rs240651797 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486164 | TATTTTAATATAACA[A/T]ATTATTTCCTCTTGA | 23894 |
rs240665404 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473607 | TACTTGATAGACCAG[A/G]GTGGACTTGAACTCA | 23894 |
rs240667081 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465418 | CAAGGTGACAATTGG[A/G]GGTGCCTAGTCTTGA | 23894 |
rs240730752 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478297 | GCTACTAATCTAACC[A/T]AGTCTCATTATTGTG | 23894 |
rs240831166 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494135 | ACCTCGTGTAAGTCC[C/T]TCTCTATTCCTCTCT | 23894 |
rs240982610 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462687 | ATGTCTTTGGGGAAT[A/G]AATATGTAAATTTTG | 23894 |
rs241053501 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469892 | CTAGCCAACTAGTTT[A/G]CTAAAGCTTATAAAG | 23894 |
rs241082805 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462247 | TCCATACGCTTAAGG[A/G]AAACTGACTCTCCCC | 23894 |
rs241161760 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485619 | TATTGACTTTATGCC[C/T]ACTGACTGTTTTCCC | 23894 |
rs241276059 | snp | G/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494021 | CGTAAAGAAAGAATT[G/T]AATAAAACCTGGGTG | 23894 |
rs241398615 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100492211 | CGAGCCGCAGCGCGC[A/G]TGGCCACTGCGGAGG | 23894 |
rs241512161 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462267 | TGACTCTCCCCTTCA[C/T]GTTTCCTTTCTTGAA | 23894 |
rs241617764 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478007 | CCTTCTTCCTCCTCT[C/T]TCTTCCCAGTGTTTC | 23894 |
rs241702632 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470037 | AAGGAAACTTCTCTT[C/T]TCAAAAGATGGAGAC | 23894 |
rs241709520 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471523 | TGCAATAGTGTCAGC[A/G]TTTGGAAGCTGATTA | 23894 |
rs241773224 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477333 | CCCAGCCTGGTCTAA[A/T]AGTGAGTTCAAGGCC | 23894 |
rs241773931 | snp | C/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476323 | TATTATTCTTTATTA[C/T]ATATTTCTCTTAACT | 23894 |
rs241882026 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470433 | TGGACAGACGGGTGG[G/T]TGGGTGAATAACGAG | 23894 |
rs241917508 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463709 | CAAGTATACACCCTC[A/G]GGTTTCATTCCCAGC | 23894 |
rs241920819 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470831 | TCTTATGGTGTCACT[A/G]TTTCAGTATTTCTTG | 23894 |
rs242252540 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475691 | TGAGGCCACATCCAG[C/T]ATTCTTTATGTGGGC | 23894 |
rs242260697 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467707 | TTTGCAATGCTCTTT[G/T]ATAATAAAAAAAATT | 23894 |
rs242313262 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460783 | GGGGATTCCTAGGAT[A/C]ACTGTTCAACCATTT | 23894 |
rs242441473 | in-del | -/ACCCACAAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461720 | GTCTTGTAAATCTGA[-/ACCCACAAG]ACCCACAAGAACGGT | 23894 |
rs242467234 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483539 | TGTCAAAAACCAAAA[A/T]TAACAGTACAAAAAG | 23894 |
rs242471343 | in-del | -/AAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490169 | CTTATTCAACTCTGT[-/AAA]AAAAAAAAAAAAATA | 23894 |
rs242573191 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465834 | TGTCATCGCAGACTG[A/G]CTCTGGTAACTTTTC | 23894 |
rs242583323 | in-del | -/GG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482354 | ATGAGGGGGGAGGGA[-/GG]GAGAGAGAGAGAGAG | 23894 |
rs242632806 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473125 | GAGCATGCTCTAGGA[C/T]AGCTGGGGCTACACA | 23894 |
rs242748370 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473688 | AATCATCAACTTGGA[C/G]AAAACAGCATTCACT | 23894 |
rs242781233 | in-del | -/GCACCAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486911 | GCCGCATCAAACACA[-/GCACCAG]GCAGGCACCTGCTAC | 23894 |
rs242891694 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489116 | TTCTGCACAAACTAA[A/C]AGAAAAATTCCTAAC | 23894 |
rs242905749 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473313 | CACATGGGTCACAAC[C/T]TCCAGGTCCAAAGCC | 23894 |
rs242949820 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474024 | TGTGCCCACCCCCAG[G/T]GTACACACTGATAGG | 23894 |
rs243165005 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480775 | TAAAATAATTTAAAT[C/T]TCTCAATGTCTCTAG | 23894 |
rs243234762 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485093 | GGCACTGTTAAGAGG[A/C]GTGGCCTTGTTGGAG | 23894 |
rs243292861 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478094 | GCTGGCCTGTGGTGA[C/T]GTACAGCAGCAGCAC | 23894 |
rs243352810 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478823 | CACATGTACCTTGCT[A/G]TTTTATTTAGTAATA | 23894 |
rs243445063 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487150 | AGGCACTGAGGCAGA[C/T]GATCTCTTGAGTCTC | 23894 |
rs243488798 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485770 | ATTCATAAATAGCCC[A/G]ATTCAACTTTTATAC | 23894 |
rs243490609 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477632 | TGTGCTCAGAGAGCA[A/G]AGGTGTCAGATCCCC | 23894 |
rs243525621 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478169 | TGTGTTGTTCTGGGT[A/G]CTAATTTTTTTTTCC | 23894 |
rs243572817 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473066 | TACCTCTATTCCTGG[A/C]AGAGGCAGGCAGATC | 23894 |
rs243597754 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486957 | ATCTGAAACAGGAGA[C/G]TCTCCTGAGGCAAGG | 23894 |
rs243694042 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462999 | CCTCTGAGCCCTTTC[A/G]TCAGCCATTATCCTT | 23894 |
rs243765337 | in-del | -/CTC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474419 | CGATTCCATGTCCTT[-/CTC]CTTCTCAGTCCTACT | 23894 |
rs243880800 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463491 | TCGATCCCCTTGAGC[C/G]CTGTCTTCTCAGAGC | 23894 |
rs243902870 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475592 | TCACTGAACCTGGAG[A/C]TCACTGAATGACTAG | 23894 |
rs243954769 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470150 | CTCAGGGATCATAGA[C/T]TGTAAAAGCCAGAGA | 23894 |
rs244032951 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462438 | AGCTCATACTGTGTC[C/T]CTTTAAAGGGAAAGG | 23894 |
rs244048916 | snp | C/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494503 | CTGGCTGCTCTTCCA[C/G]AGATCCTGAGTTCAA | 23894 |
rs244106108 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486190 | CTTGATAAAAATACA[C/T]GGAATATCAATTAGT | 23894 |
rs244300090 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492963 | GGAACTGAAGTTACA[A/G]ATGTTTGCTATCTGC | 23894 |
rs244339721 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470361 | AATATCAATGGTCAA[A/G]CCTGAAAATACATAG | 23894 |
rs244341281 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468608 | TTAATCATTACAAGT[-/A]ATATCTATATATGTG | 23894 |
rs244401339 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460144 | TGGGGGCGCCAAGGC[A/G]AGGACTCAAAGCAGG | 23894 |
rs244457359 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482297 | CAACATGGGAAAATA[C/G]TGACATGAAGAAAAG | 23894 |
rs244478454 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491647 | AAAAATAATAATTTT[A/T]AAAAATAACAAAACT | 23894 |
rs244604619 | in-del | -/CT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467498 | TGTCTCTAGTTCCAA[-/CT]CTGACAGGGATTTTT | 23894 |
rs244667004 | in-del | -/AGGAAC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460691 | GTGTGTGTGTGTGTG[-/AGGAAC]TGTGTTCATGTCCTA | 23894 |
rs244714890 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488387 | TCCACCCCCAATGAA[A/G]CACCATGAACAAGCA | 23894 |
rs244777069 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473247 | GAAGTATCTTTAACA[-/T]TTTTTTAAAAAGATA | 23894 |
rs244850140 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460037 | TCAAATGCACACTGC[C/T]CTAGTTTGTTTTCTG | 23894 |
rs244937160 | in-del | -/CA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463912 | CACCACCTCCACCTC[-/CA]CACACACGACAGACA | 23894 |
rs244937883 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464968 | TAAATTCCCTTTGAA[A/G]CATTGCGACAATATT | 23894 |
rs244974614 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481977 | TAAGTTCTAGGACAG[A/C]CAAGGATTACAGGCA | 23894 |
rs244990388 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477808 | CTTCATTTCTAGAAG[-/C]TTCATTTGAGTTCTT | 23894 |
rs245015075 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465490 | CTGAATATAAATGGA[A/G]TAGATGTGAATTGGG | 23894 |
rs245031301 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473771 | TGTGGTATGAGTGTG[G/T]GATGGTGCATGTGCA | 23894 |
rs245043115 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466898 | TTACTCCTCACTATA[C/G]CCAGAGAACTCTGGA | 23894 |
rs245097634 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465308 | TTCCTGCATCAATTA[A/G]CAAGATAATTCTACA | 23894 |
rs245106448 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466304 | GTCTCAAAATACACT[A/C]TTTCGTTTCTCCAGT | 23894 |
rs245173459 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490030 | AAAACTGAAGTTAAA[A/G]AGAAAGAGACAGTAT | 23894 |
rs245269998 | in-del | -/TTTTCTTTTC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477530 | TCCATCCAGTCTGTT[-/TTTTCTTTTC]TTTTCTAAGATTTAG | 23894 |
rs245280321 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473085 | GGCAGGCAGATCTCT[A/G]AGCTTAAGGCCAGTC | 23894 |
rs245402541 | snp | A/T | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459782 | TGTTTTTTTTTTTTT[A/T]AAGATTTATTTATTT | 23894 |
rs245426125 | in-del | -/AG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482510 | GAGGGAAGGAGGGAA[-/AG]GAAGGGAGGGAGGAA | 23894 |
rs245483238 | in-del | -/TT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483238 | TGATACAGAATCTCC[-/TT]ATATAGCTCTGGCTG | 23894 |
rs245536878 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473421 | AGCTGACACTCTTGT[A/G]AGCGTGCAGTTTTAT | 23894 |
rs245631418 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473722 | AGTTTGTTCCACATA[-/T]AAATGTTTCAGCTCT | 23894 |
rs245694765 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463477 | TGACGCCGCCTTCTC[-/A]GATCCCCTTGAGCCC | 23894 |
rs245816408 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488837 | AGCACAAACTTAGGG[A/G]GTCTACTATACCTTT | 23894 |
rs245879693 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469674 | TCCTCCCTGAAGACT[A/G]GCTCTGACGGAACCA | 23894 |
rs245880338 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480001 | TTCAAATCCCAGCAA[C/T]CATCCCATGGTGGCT | 23894 |
rs245986198 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473644 | GCAGCCTGCCATGTG[C/G]CACCACATGTGGTAT | 23894 |
rs246021322 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472595 | ATTTTCATTATACAC[A/G]TGCTTTCTGAACTAG | 23894 |
rs246060291 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489860 | ACAGGTGGTGGGGAC[A/G]GAATGAGTATAAAGG | 23894 |
rs246064108 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480453 | AAACAATTCTTAAAT[A/G]TGAAAATGGTAACTT | 23894 |
rs246097899 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481375 | GGAGTGAGTGGGTAG[C/T]GGAGCAGGGCAGGGG | 23894 |
rs246124930 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490746 | GACTGGGCTACACAA[G/T]GAGACTCAAGCCCCT | 23894 |
rs246215789 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478536 | ATGAATAATATGTAA[A/G]CATGTATACATAATG | 23894 |
rs246266052 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471406 | CCTGTGATCCATCCA[A/T]TAGCTGACTGTGAGC | 23894 |
rs246358849 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465667 | TTTATTTCTTCTTCC[-/T]TTTTTTGTTTGTTTG | 23894 |
rs246553123 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474513 | TATCTATCTGTGCGT[C/G]TATGTGTGTGAGCAT | 23894 |
rs246603832 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476022 | CTCTCCAGTAATATT[C/T]AAGAAGGCCAGCGTT | 23894 |
rs246809276 | snp | C/T | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468721 | AATTTTAATGCATAT[C/T]GGTGATAGAATCCAA | 23894 |
rs246829634 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483953 | TCACTAGACCAGGGT[A/G]GCCGGGAACTTTTAA | 23894 |
rs246912797 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491732 | GCAGGCAGATCTCTA[A/G]AGTTCAAGGCCACCC | 23894 |
rs246924840 | in-del | -/ATGTAGCAG | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491439 | TGGCTCTAGCTGCAT[-/ATGTAGCAG]AGGATGGCCTAGTTT | 23894 |
rs246929481 | snp | C/G | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476380 | ACAGATTGCTAGACA[C/G]AGTGTTCTACATCTC | 23894 |
rs246966120 | in-del | -/TG | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468619 | AGTAATATCTATATA[-/TG]TGTGTGTGTGTGTGT | 23894 |
rs246982313 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492401 | CGCGCTCCCTGCACA[C/T]GCCCCCACCCCCTCC | 23894 |
rs246982808 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461542 | CTCTTGATGTACAAT[A/G]TCTAAGGTCTGGTGA | 23894 |
rs247205342 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494444 | CTGTTAGGGTTAAAA[A/G]AGATTTAATTAGGGC | 23894 |
rs247261230 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485055 | GTTTGAATGCAATTG[A/G]CCCCCACAGGCCCAC | 23894 |
rs247296698 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493101 | TGCTCTTTAACCCAA[A/G]AATAAGAGGATTCCC | 23894 |
rs247386140 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489348 | CTTGCTAGCTCTTTA[-/C]CCCTAGTCAGACAAT | 23894 |
rs247478366 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480881 | GTTTTAACTCTAAAA[C/T]ACTGACCTATTGAGA | 23894 |
rs247495878 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461159 | ACATTCCCAGAATAT[A/G]GCAGGGAGTTGTGGA | 23894 |
rs247500511 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470067 | CCATTATAGAAAACG[A/G]CAACCAATCAAAATG | 23894 |
rs247535400 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464734 | AATTAAAGACCCAAG[-/T]TTTGATTACCATTCT | 23894 |
rs247568497 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467559 | TAAAAATGATTTCAA[A/G]AGTTAAATATAAATC | 23894 |
rs247578744 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476830 | GATAGAATTCAATCT[A/G]TCACTAAATACATGA | 23894 |
rs247591909 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460451 | GAAGGGGTAAGAGCT[C/T]CTGCATTAGGGAAGG | 23894 |
rs247650119 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460673 | ATTTTAACATCGTGT[C/G]TCTGTGTGTGTGTGT | 23894 |
rs247653323 | snp | C/T | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468167 | AACTCCTACAGAGAA[C/T]AGAATATCCCTTGTT | 23894 |
rs247661792 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469524 | TATTACATATATGGG[C/T]TAATATTCTAGAGCA | 23894 |
rs247778599 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460509 | CCTACACAGCCATCC[G/T]ACTGCCAGAAATGTG | 23894 |
rs248000612 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483104 | ATGGAAAAGCATATT[A/G]TTTCCAAACTGTACA | 23894 |
rs248044996 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486768 | CTGCCTCCTGGGCAC[C/T]GGATTGTAGGTATGT | 23894 |
rs248069752 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481130 | AAAGATTTCAGGAGG[-/A]AAAAAAAAATTAATG | 23894 |
rs248109737 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481433 | ATTTGAAATGTAAAT[A/G]AAGAAAATATCTAAT | 23894 |
rs248196769 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479890 | GACATACTTTGATTG[A/T]ACAATAAAGATTTTG | 23894 |
rs248269686 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489649 | TGTATATGTATGTTC[A/G]CAGCAGCACAATCCA | 23894 |
rs248334418 | snp | A/C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100474331 | ACTCTCCCTGAAACA[A/C/G]ACATCATCATCATCT | 23894 |
rs248418299 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474957 | TTCTTTTCACATTAT[C/T]CTAACAGTGGGCCTT | 23894 |
rs248482651 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484984 | TGGTGATCAAACCCA[A/G]GGCTTTATTAAGCTA | 23894 |
rs248495652 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478227 | GAATGAAGTAACTTA[G/T]GTACTTACTGATCTA | 23894 |
rs248656455 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464640 | GAGTCCCTAATACAT[G/T]ACCCCTTCCCCAAGA | 23894 |
rs248737468 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470701 | AATGTTGCTTGAAAA[A/T]CCGAAAAGTATTTAA | 23894 |
rs248765043 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463308 | AAAGCATATTAATGT[C/G]TTGTGTAACAGAAAA | 23894 |
rs248829708 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472776 | GGCTACACAGAGAAA[C/T]CCTGTCTCGGAAAAA | 23894 |
rs248913489 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481780 | TAATTCTCAATTAAA[-/T]TTTTTTTCTTAGTTC | 23894 |
rs248934405 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492590 | GAAGTACCGGCAGTC[C/T]GAGTGCGCCGCCAAA | 23894 |
rs248996544 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485370 | TTCACAGCAAGAAAA[C/T]CCCAACTACTGTTAA | 23894 |
rs249073823 | in-del | -/CC | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100494165 | TCTTTCCCTCTCCCT[-/CC]CTGAGTGTGGTGTGT | 23894 |
rs249138757 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470181 | AATTAGGAGTGTGTC[A/G]TGAGATCGTGTCTCC | 23894 |
rs249187353 | snp | A/T | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468307 | TTTTTTGTATGATAG[A/T]ATACAGTTTTCAGTT | 23894 |
rs249276266 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477983 | TATTTTCTCACTACC[A/C]CCCATCTTCCTTCTT | 23894 |
rs249290436 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475871 | GTGATCAAAAGTTCT[A/C]AAATGCTGATACTTT | 23894 |
rs249307576 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476944 | TATGCTTATTTTTAG[A/T]AATTAATTACTAGGG | 23894 |
rs249311326 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492428 | CTCCGCCCTCCAGGT[-/C]CCCCCCGAGGCCAAC | 23894 |
rs249314050 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478403 | GACCACAGCCCTCCT[A/T]TCCCTTTTATTCTGA | 23894 |
rs249346167 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490835 | AGGTGACTCGGAAAT[-/A]AAAGATAAAAGACAG | 23894 |
rs249360192 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483747 | GTGCAGCTGCTACCT[A/C]ATCAACATCTGAGAA | 23894 |
rs249416052 | snp | A/G | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476285 | AACCAATATAATATT[A/G]CTCTTAACTTACTCT | 23894 |
rs249418561 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484636 | TTTCTTGAGAAGGAA[A/G]TTGGATAAAACCAAG | 23894 |
rs249455839 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477231 | GGTGGAAAAGTTATT[C/T]TTAAAAGATGAAAAG | 23894 |
rs249494738 | in-del | -/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492632 | GCGCGCTGGAGCCAC[-/G]GGAAAAAAAAAATGT | 23894 |
rs249653020 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484734 | GAAATTATTTCAAGA[G/T]GTTTTATATTTATGT | 23894 |
rs249690991 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465512 | GAATTGGGGGTGGGT[-/G]GGGGGGGGACTCGAG | 23894 |
rs249700270 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460730 | ATAAAAACACTGGGT[A/G]TGGTGCACACAGCCA | 23894 |
rs249708453 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462546 | TTTTTGTCTGTTTTC[-/T]TTTTTTTTGAGACAG | 23894 |
rs249795969 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473525 | TCTGTATATAGTTCC[-/T]TTTTTTTTCTTGCTT | 23894 |
rs249808724 | snp | C/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492881 | GATGTTTTTGCCTGC[C/G]TGCATGTCTGTGCAC | 23894 |
rs249818604 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460382 | AAAACTTCTTTAGTT[C/G]AGCAGTTTGTTTTCA | 23894 |
rs249821247 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466236 | AAGACAGCACCATCT[A/G]CCAAAACTGAAACAA | 23894 |
rs249831127 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461987 | GGTATAAGGAGGAAG[C/T]TGTGTCATAATCTTG | 23894 |
rs249903236 | in-del | -/TAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466842 | GAGAGACCCTGTCTT[-/TAA]AAAAAAAATAAAAAT | 23894 |
rs249931543 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485318 | CAGCACCAATAAATG[C/T]TGTTCTTTAGAAGAG | 23894 |
rs250060114 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462204 | GGTAACACCCAATGG[A/C]ATGTGGTCCGCCTAA | 23894 |
rs250077658 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484819 | CATGTGTTTGCCTGG[C/T]GTCCCTACAGACCAG | 23894 |
rs250077682 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493798 | TTTGGCAAACTGAGA[C/T]GCGTGGCCAGACAAG | 23894 |
rs250112414 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464326 | TCAGAAGATGCAATG[A/G]TTTAAACCAATACCA | 23894 |
rs250162820 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487789 | TTAGGTGTTGGACTT[C/T]CTAGAACAGGAGTTC | 23894 |
rs250183827 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489240 | AATAAAACAATCTGT[A/G]TCTTTTTCATTAATT | 23894 |
rs250221955 | snp | A/C | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459463 | CTTTTCCAAGATAAA[A/C]TCTGAGACCACTACA | 23894 |
rs250313981 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472081 | GTCCAATTTTCTGAG[G/T]AACCGCCAGACTGAT | 23894 |
rs250388347 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479541 | TAATAAACCACATTT[A/T]AAAAAAATAGTTCAC | 23894 |
rs250423776 | in-del | -/T | | | downstream-variant-500B | Gtf2h2 | GRCm38.p3 | 13:100459727 | GTTTTTTTTGTTTTG[-/T]TTTTTTTTGTTTTGT | 23894 |
rs250461752 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480787 | AATCTCTCAATGTCT[A/C]TAGACATAATAGTAA | 23894 |
rs250472309 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478315 | TCTCATTATTGTGGG[C/T]TCTCTAAAATGTCTT | 23894 |
rs250486721 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483830 | AGCTGGCAGACATCA[C/T]CGTAACACTGCTATA | 23894 |
rs250570611 | in-del | -/AA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467713 | ATGCTCTTTTATAAT[-/AA]AAAAAATTGTTTTTA | 23894 |
rs250637947 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473232 | ATTTCTACCTCCCCT[A/G]AAGTATCTTTAACAT | 23894 |
rs250659990 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100489186 | CTCTGTTAAAATTAT[-/A]AAAAAACAGTTAATT | 23894 |
rs250835557 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465172 | GAGGTCACCAGTTGG[G/T]AAGCTTGAGCCAGCC | 23894 |
rs250867438 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465733 | GGCCTGGCTGTCCTG[C/G]AACTTATACTCTGTA | 23894 |
rs250920268 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470551 | TAGCCCTGGCTATCC[C/T]GGAACTCACTCTGTA | 23894 |
rs250934050 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463783 | TCAGCAGATAAAGGA[A/G]TTTGCTGCCAAACCT | 23894 |
rs250960780 | in-del | -/GACAGACAGACAGACAGACAGACAGATAGACTGACT | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463932 | CACGACAGACAGACA[lengthTooLong]ATTTTTCTCTCCCTT | 23894 |
rs250984576 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465719 | CATTTCTCTGTATAG[C/G]CCTGGCTGTCCTGGA | 23894 |
rs251144856 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486648 | CTCATGACTTTGGGG[A/G]ACACAAGGGTGTGAG | 23894 |
rs251239345 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467034 | GTGATACACAAATAA[A/C]AATGGACTACTATTC | 23894 |
rs251332999 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479447 | AAACTCTAATGCCAA[A/G]GTATAAGAAAAAGCA | 23894 |
rs251434104 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462003 | GTGTCATAATCTTGC[-/A]AAAAATGCTTACTGC | 23894 |
rs251497320 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465139 | GGTTTGGCTAAAATT[A/C]CAGTCCTTAACAGCA | 23894 |
rs251530425 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461345 | TCTCCTTAAGTGGTG[-/A]CCCATATCTTCAACA | 23894 |
rs251531678 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461560 | AAGGTCTGGTGAGTA[-/C]ATTAATAAATAACAA | 23894 |
rs251551792 | snp | A/C | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493909 | AATCATGGTAGTCTC[A/C]GTATAACTATGACTA | 23894 |
rs251560143 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472545 | AAATTATACAATATG[C/T]CCCAGGTCATCACAT | 23894 |
rs251594192 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473046 | AGCTGGGTGGTGGTA[A/G]CACATACCTCTATTC | 23894 |
rs251654740 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485548 | GTGTGATGCAATTTG[A/T]AACAGCATACATAAC | 23894 |
rs251792113 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474271 | TTTTCATCCCCTCAA[G/T]ACATCTTTCTTAGAG | 23894 |
rs251915716 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467904 | ATGCATGTTTGTTTG[G/T]TTTTTTAAAGAGCAT | 23894 |
rs251946895 | snp | A/G | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468566 | TAAAAATCTAAAATG[A/G]AAAAAAACTGAGATT | 23894 |
rs252032475 | in-del | -/TA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100476979 | ATGAAAAAAGCAATC[-/TA]TTTTTCTTTATACAA | 23894 |
rs252087946 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487926 | CACAGAGCCATCCTG[C/T]CAGCCCATTTGCTTG | 23894 |
rs252120401 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479681 | ACACCTTCAATTGCA[A/G]CACTTGGGAGGCAGA | 23894 |
rs252216844 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460111 | AGCTCTTTTGGTTCA[C/T]AGCTAACAGTCCATC | 23894 |
rs252218210 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487331 | TCAGTTGGGGAGAGG[G/T]GAGTAACTAGCCTCA | 23894 |
rs252255386 | snp | C/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493436 | CATGAGGGCAACTAC[C/G]TATGGTGGGGAGGCT | 23894 |
rs252390299 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470636 | GGATTAAAGGCGTGC[A/G]CCACCACACCCAACT | 23894 |
rs252560022 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467744 | AATTTAAAAGCAATT[A/T]AAAAAAAGAACCACT | 23894 |
rs252589296 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480302 | ACCACAAGTATTTTT[A/C]ATTATATAAAGTATC | 23894 |
rs252633974 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475301 | AATTTGTCCTGCATA[C/T]TCTTGTACAACTATT | 23894 |
rs252723989 | in-del | -/GT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480349 | TTAACAAGACCAGAA[-/GT]GTTATCAACAAACAG | 23894 |
rs252767453 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476587 | CCTAATGCAGAAAGA[C/T]AGAGACATTAACAAG | 23894 |
rs252868912 | in-del | -/TTTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465608 | GAGAATAAGAAAAAA[-/TTTT]AAAAACTAGCTACCA | 23894 |
rs253118970 | in-del | -/TTTTTT | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473538 | CTTTTTTTTTCTTGC[-/TTTTTT]TTTTTTTTTTTTGAG | 23894 |
rs253130906 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484373 | AAAAATTTGATGACA[A/G]GAGGGAAAGAGAAGA | 23894 |
rs253173748 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476902 | AAAACATTTACCAAA[A/G]AGAGAATCAGGAAAG | 23894 |
rs253257457 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475123 | AACCTGAAACAATGC[A/G]ACTTTAGTTTTGATT | 23894 |
rs253279788 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469405 | CCAGCCTGGGCTACA[A/C]GACTATGGGAGGAGT | 23894 |
rs253306406 | snp | A/C | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468456 | AACTGCCTTTTAATT[A/C]CACTTCCAGGAAATC | 23894 |
rs253361312 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482203 | TGGTTGCGCATGCCT[A/G]TAATCTCAACATTTG | 23894 |
rs253393256 | in-del | -/AAAGAG | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490027 | AATAAAACTGAAGTT[-/AAAGAG]AAAGAGACAGTATCT | 23894 |
rs253400241 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491115 | AGAAACTGCCCCACC[C/T]GGGGATCCATCCCAT | 23894 |
rs253431181 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462617 | CCAGGCCTGCCTTTG[-/T]TTCCCAAGTGTTAGG | 23894 |
rs253563702 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465546 | AGAATTCGGGGGTGG[A/G]GCTGGGAGGAGAGAA | 23894 |
rs253622104 | in-del | -/AA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485485 | CTTATGTGTATTAAC[-/AA]AAGATTGAGAACCTC | 23894 |
rs253635223 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460980 | AACAAAAATTACCAG[A/G]TTTTGAAATCAAGCT | 23894 |
rs253685022 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475082 | ATCCATCTACTAGAC[-/T]TTTCATTAAGTTCAC | 23894 |
rs253693125 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467128 | GGAGGCAGAAGCAGG[C/T]AGATCTCTAAGTTCA | 23894 |
rs253697718 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460617 | TTTTAAATATGTCAG[C/T]ACTTTGTCAGATATT | 23894 |
rs253734010 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460599 | TACAATAATTTTCTT[A/T]TATTTTAAATATGTC | 23894 |
rs253765195 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474012 | CCCACCCCCCAGTGT[A/G]CCCACCCCCAGGGTA | 23894 |
rs253794496 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466728 | CAAAAAGAAGCCTGA[C/T]GTGGTGGTACACGCC | 23894 |
rs253813496 | in-del | -/ACACAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473366 | CTCACATTCATGTCA[-/ACACAT]ACACATAGGGGAAAA | 23894 |
rs253870681 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491711 | CCCAGCACTCGGAAG[A/G]CAGAAGCAGGCAGAT | 23894 |
rs253890905 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490449 | AAGATTAGAGACTAG[C/T]CCTAAGGGGCTTTTT | 23894 |
rs253906064 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460295 | AATTGGCTTGTTGGG[G/T]TTTTTCAGTGACCAT | 23894 |
rs253931040 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483637 | GTATATATTTTATTA[A/G]TAAATATTCATAAAA | 23894 |
rs253936154 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461639 | GCAATTCACACAGGT[-/C]AACAGAGCCCACAGT | 23894 |
rs254129047 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489956 | ATTTTTCAAAAGAAT[C/T]TCACTGGGTTGTCAA | 23894 |
rs254170873 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467527 | TTTTTTTTAAGTTTG[A/G]GTAGTGGATATGTGC | 23894 |
rs254361590 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463600 | CAAGCCTACCTGTCC[C/T]GATTTGTCACTGTAC | 23894 |
rs254470457 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485181 | TCTATGCTCAAGCCA[C/T]ACTCAGTGGGACAGT | 23894 |
rs254518713 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473913 | GAACCTGGAGCTCAT[C/T]AACTAGCTATTCTAG | 23894 |
rs254598561 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479793 | TAATCATTTTTATGA[C/T]CAATAATTTTCTACT | 23894 |
rs254638562 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473505 | TCTAGATCCAATAAT[A/G]TGTATCTGTATATAG | 23894 |
rs254640435 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480514 | AGCAAAGGTGCACAG[A/T]AAAGCAACACGGGAG | 23894 |
rs254646599 | in-del | -/CTT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474585 | GGAGTCAATTCCCTC[-/CTT]CTATCATGGGGGTCC | 23894 |
rs254651395 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478673 | TATTTATGGCTTTTA[C/G]AAATATATTCTATAG | 23894 |
rs254652838 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484874 | ATGGGGTTGAAGATG[A/G]TTATAGGCTGGCAAT | 23894 |
rs254669943 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100476687 | TCATTTCTCTTTTTC[C/T]AGTGATGGGGATCCA | 23894 |
rs254678815 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471556 | GGATGGATCCCTGGA[C/T]ATGGCAGTCTCTGGA | 23894 |
rs254700572 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477318 | GTCTGTGAGTTCAAG[C/T]CCAGCCTGGTCTAAT | 23894 |
rs254728985 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463764 | CTCACACCAGCAAGA[C/T]GGCTCAGCAGATAAA | 23894 |
rs254749326 | in-del | -/TT | | | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100492816 | ATGCGTTTAGGGAGG[-/TT]TTTTTTTTTGTCCGT | 23894 |
rs254751807 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487038 | AACCAAAAAAATTAA[A/T]GGATCCATTTGGAGT | 23894 |
rs254765221 | snp | C/T | | | intron-variant, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100461876 | ATTCCACTAACATAT[C/T]TCCCAAACGGCTGGT | 23894 |
rs254768406 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484261 | GGGTGGCTTACACAA[C/T]GGTCTGACTGTAAGG | 23894 |
rs254856671 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472906 | TGCCTGTGGCTTTGT[G/T]TTTTCAGGACGGGCT | 23894 |
rs254948889 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470212 | CAAGAATGTTAAAGA[C/T]AACCATCGAGCCTGA | 23894 |
rs254992584 | snp | A/C | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493544 | AAACCCTTGCGAAAC[A/C]AGGCCTTTGTTGGCA | 23894 |
rs254995304 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478754 | TCCTAGAAATGCAGA[A/T]GTGAGCCAGCATGCC | 23894 |
rs255028808 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477037 | CACTTATGTTTAATT[C/T]GGCAGCTACATAATT | 23894 |
rs255066090 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477715 | CAGACTCTGGTTCTG[A/T]GGAGGACATTATATG | 23894 |
rs255066106 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469817 | TTTTAGTGGTAATCA[A/T]CAGCTCTCTAATTGG | 23894 |
rs255117394 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478120 | GCACAGCTGGCAGCC[-/T]AGATACTTCTACATC | 23894 |
rs255201980 | snp | A/T | | | utr-variant-3-prime, intron-variant | Gtf2h2 | Mm_Celera | 13:100468762 | TCTATTTTCATAGTT[A/T]AAAGTTTCTTAAATC | 23894 |
rs255395507 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462478 | GTCAAACAACTTACA[C/T]AACTAAAAAGGATTA | 23894 |
rs255465143 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100492127 | CCAGATCACCCGTTT[C/T]TTAGACTTTCCGTCA | 23894 |
rs255609361 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491634 | CTGTAAATAAAAAAA[A/T]AATAATAATTTTAAA | 23894 |
rs255650914 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467187 | GACAGCAAACCCGCC[A/G]CCCCTACTACCCCAA | 23894 |
rs255711278 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491488 | GGCCCTTGGTCGTGT[A/G]AAGACTCTAAGCCCC | 23894 |
rs255747741 | in-del | -/AA | | | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100492634 | CGCTGGAGCCACGGG[-/AA]AAAAAAAAAATGTTC | 23894 |
rs255750106 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491134 | GATCCATCCCATATA[C/G]AGTCACCAAACCAAG | 23894 |
rs255815618 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475603 | GGAGCTCACTGAATG[A/G]CTAGGCTAGCTGGCC | 23894 |
rs255871316 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488359 | TCACCCAGAACAAAG[C/T]CTATGCAGCCAATCC | 23894 |
rs255895100 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479544 | TAAACCACATTTTAA[A/T]AAAATAGTTCACGTT | 23894 |
rs255941960 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480058 | ACTCTCTTCTGGTGC[A/G]TCTGAAGACGGCTAC | 23894 |
rs256011380 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472981 | CCCTAAAAGCAATAA[C/T]ATCATCCCTGTCCAT | 23894 |
rs256032110 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487664 | GACCACTTTCTAGAG[G/T]TAATGGGTTTTCTCC | 23894 |
rs256060470 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467461 | CGGAAGGACTGCAAG[C/T]AGGAAATGAATTGAA | 23894 |
rs256093725 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465071 | TTTGTTCTGATTTCA[C/T]TTCTGTTGAGGTGAT | 23894 |
rs256125629 | in-del | -/AAAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491634 | CTGTAAATAAAAAAA[-/AAAT]AATAATTTTAAAAAA | 23894 |
rs256127638 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489881 | AGTATAAAGGCACTT[A/T]CTGCCCTCATTTACT | 23894 |
rs256165522 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488138 | CTGGGGCTGCTCCCC[A/C]ACCCCGCCCCGGGGC | 23894 |
rs256257374 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482017 | TTTCAAAAAGCCAAA[A/C]CAAAACAAACGAACA | 23894 |
rs256290586 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482912 | CACATAAAAAATAAA[C/T]AAATCTTTAAAAGAA | 23894 |
rs256354935 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463520 | GCTGAGGCTTACCTT[C/T]TCTACTCCAGCACTG | 23894 |
rs256365697 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481390 | TGGAGCAGGGCAGGG[A/G]GAGGGTATAGGGAAC | 23894 |
rs256400524 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464320 | TACAATTCAGAAGAT[A/G]CAATGGTTTAAACCA | 23894 |
rs256631188 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478582 | TGTATCTTATACATA[C/T]ACATCTACACATATC | 23894 |
rs256651140 | in-del | -/GC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462336 | TTGCTATATAGACAG[-/GC]TAGCCTCAAACTAAG | 23894 |
rs256670200 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479343 | CTTAAGATATTCTTA[C/T]CAGAAAGTCAACAAA | 23894 |
rs256670470 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472706 | GAGGCAGAGGCAGGC[A/G]GATTTCTAAGTTTGA | 23894 |
rs256751356 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473818 | ATGGCCATTACCCTG[A/G]TGTCTTTTTTAATTA | 23894 |
rs256756454 | in-del | -/TC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484763 | TCTTTTGGTTTTTTT[-/TC]CACATATATGGCTGT | 23894 |
rs256895493 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470751 | AAGAATGAGAATGAC[A/G]AAACTATTTAAATTA | 23894 |
rs257194130 | in-del | -/ACT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467040 | CACAAATAAAAATGG[-/ACT]ACTATTCAGCTCTAA | 23894 |
rs257251824 | snp | A/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493364 | AACATCCTTATGACG[A/T]GGAACCGAGACTACT | 23894 |
rs257276348 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470081 | GACAACCAATCAAAA[C/T]GCAGAGTCCTGGTCC | 23894 |
rs257311340 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462262 | GAAACTGACTCTCCC[C/T]TTCATGTTTCCTTTC | 23894 |
rs257315718 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477276 | TGTTATTCAAACCCA[A/G]CAGTCAGGAGGCAGA | 23894 |
rs257324379 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470458 | AACGAGCTCAAAGGA[A/T]AAAGCACTTTACCGT | 23894 |
rs257347468 | in-del | -/AA | | | downstream-variant-500B, intron-variant | Gtf2h2 | Mm_Celera | 13:100468325 | CAGTTTTCAGTTTTT[-/AA]AAAAAAAAAAAAAAA | 23894 |
rs257374926 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485707 | GAGCCCCTATGTGAG[C/T]GCTGAGAACCAAACT | 23894 |
rs257507388 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485062 | TGCAATTGGCCCCCA[C/T]AGGCCCACAGGGAGT | 23894 |
rs257637621 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463436 | AACTTTGGTTGTCGT[A/G]CTGTATGATGATCAG | 23894 |
rs257676665 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464215 | GCCTTATGTTATTTT[C/T]TAGGGAACTCAAGTT | 23894 |
rs257703765 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487836 | TCCATATGGGTGCTG[A/G]AAATTGAGCCAGGGT | 23894 |
rs257711205 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466957 | ACTATTGCTTTATTC[A/G]CTAGAGCAAAGAATT | 23894 |
rs257742540 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474385 | CCTTTGGCTTGTTCG[A/C]AGTTAGAGGCAGATC | 23894 |
rs257749548 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467446 | AAGTCTTAGAGGATG[C/T]GGAAGGACTGCAAGT | 23894 |
rs257777393 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479626 | TTAAGCACATATAAA[A/G]GAAAACCAAAATCCC | 23894 |
rs257795404 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470016 | AGTAGTCGTCATCTC[-/T]TAATCAAGGAAACTT | 23894 |
rs257866010 | in-del | -/TTAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463202 | TACTATGATTAAAAT[-/TTAA]AAAAAGAGAAATCTT | 23894 |
rs257920805 | in-del | -/AGATAAAAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477382 | GTACCCTGTCTCAAA[-/AGATAAAAT]AGATAAAATTTTATT | 23894 |
rs257949968 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479265 | AATCCTTAATAGGTT[-/A]AAAAAAAAATTACAG | 23894 |
rs258105528 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460879 | TATTATTGTCCTCTG[A/G]CCTACACAGACACAT | 23894 |
rs258114733 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477538 | GTCTGTTTTTTCTTT[A/T]CTTTTCTAAGATTTA | 23894 |
rs258200285 | in-del | -/A | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493893 | ACAAAATGTGCACAG[-/A]AATCATGGTAGTCTC | 23894 |
rs258215919 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473438 | GCGTGCAGTTTTATT[C/T]ATAAGTACTAGCCAT | 23894 |
rs258337423 | in-del | -/TTTTG | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459732 | TTTTTGTTTTGTTTT[-/TTTTG]TTTTGTTTTGTTTTG | 23894 |
rs258342471 | in-del | -/CAGAGCGAGCTCTAGAGTGAGCTC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490340 | AGCCAGCATGGTCTA[-/CAGAGCGAGCTCTAGAGTGAGCTC]CAGAGCAAGTTCCGG | 23894 |
rs258465941 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481463 | TAAAAAGGAAAAACA[A/G]AAAGAAAAAAAAAGA | 23894 |
rs258577972 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480841 | ACAAAGTATTACATA[C/G]AGTGAGATTGCTACC | 23894 |
rs258577982 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473753 | GACAAGTATGTGCAT[A/G]TGTGTGGTATGAGTG | 23894 |
rs258616833 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474125 | CACCCATCTCCTCAG[C/T]CTCTAATTTTCCTTT | 23894 |
rs258679417 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475792 | CTGTATATTAAATTT[C/G]TTCTACACTATCTTT | 23894 |
rs258697635 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480084 | GCTACAGTGTACTTA[G/T]ATATAATAATAAGTA | 23894 |
rs258705508 | in-del | -/AAAAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100480271 | TGATAAATAAATCTT[-/AAAAA]AAAAAGAAATTTCTT | 23894 |
rs258737015 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487172 | TTGAGTCTCTGGTCT[A/G]CAGAGCTAGTTCTGA | 23894 |
rs258941487 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473129 | ATGCTCTAGGACAGC[C/T]GGGGCTACACAGAAA | 23894 |
rs258967168 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461098 | AGGGAGACCCCGACT[A/C]ATAAATCAAGTAAAT | 23894 |
rs258974638 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473629 | TTGAACTCACAGACA[A/G]CAGCCTGCCATGTGG | 23894 |
rs258976700 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465441 | AGTCTTGAAATGCTA[A/T]GTTTAGTTGATATAC | 23894 |
rs259004330 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478882 | ATAAAGAGGGCCATT[G/T]CTTTTCATGGCTATG | 23894 |
rs259065886 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482620 | ACCCGTTGTTGGGCA[A/G]TTCCTAACTGCCTGT | 23894 |
rs259076405 | in-del | -/AT | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476378 | AACAGATTGCTAGAC[-/AT]ACAGTGTTCTACATC | 23894 |
rs259099910 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475566 | TACCTTGTTTTAAGA[A/G]CCAAGGTCTTTCACT | 23894 |
rs259109236 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484315 | CAGAATCCCTAAAGG[A/G]CAGTTCATCTTTTCA | 23894 |
rs259214681 | in-del | -/AAA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490418 | AACCCTCTCTCAAAG[-/AAA]AAAAAAAAGTCAGAA | 23894 |
rs259220196 | snp | G/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492354 | GGCAAACGGCAGCCC[G/T]GCAGCGAGAACTTTC | 23894 |
rs259343996 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489108 | CAAACTAGTTCTGCA[C/T]AAACTAACAGAAAAA | 23894 |
rs259603031 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487219 | AGAAACTTTGTCTTG[-/A]AAAAAACTAAATAAC | 23894 |
rs259719228 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467073 | ATGAAAATATGATTA[C/T]GCCAGGCAATGATGG | 23894 |
rs259778216 | in-del | -/ACACAC | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100460911 | CCACACCCACACTAT[-/ACACAC]ACACACACACACACA | 23894 |
rs259948457 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481921 | ACTTGGGAATCAGAG[A/G]CAGACAGATCTCAAG | 23894 |
rs259950964 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485907 | TAAGCATATTTACTT[C/T]CAGTACATCTACTAC | 23894 |
rs260003827 | in-del | -/CACACACTCACACG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460931 | ACACACACACACACA[-/CACACACTCACACG]CACATGTGCACACTT | 23894 |
rs260090950 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466081 | AACTGGCAAATAAAC[A/T]GAAAGGACAGTCTGA | 23894 |
rs260166799 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489838 | TCTGTAGGTCATGAC[A/T]GTGTGTACAGGTGGT | 23894 |
rs260300765 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488691 | AGGCAGAACACGGGA[C/G]CAACATTTCTACTCA | 23894 |
rs260393487 | in-del | -/GTA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465962 | CAGCAGTTACCTGTA[-/GTA]ACAGGAGAAACTTTT | 23894 |
rs260528722 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466656 | ACTCACTGTTGGTAA[G/T]GGTGCAAACTAATAC | 23894 |
rs260530879 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462295 | GAAACAGATCTCGTA[C/T]ACAGTAGCTCTAGTT | 23894 |
rs260595096 | snp | A/G | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459637 | ATAAGCCAATGGAGC[A/G]AAGGCCCTAGTTCCA | 23894 |
rs260651826 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462211 | CCCAATGGAATGTGG[C/T]CCGCCTAACAGTGGA | 23894 |
rs260772211 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473088 | AGGCAGATCTCTAAG[C/T]TTAAGGCCAGTCTGA | 23894 |
rs260837968 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469683 | AAGACTAGCTCTGAC[A/G]GAACCAGAAGGATCC | 23894 |
rs260911256 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462153 | GTGTCTTTTTTAAAA[A/G]TAATTCAAGTCTAAT | 23894 |
rs260941018 | in-del | -/TACT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467376 | TCAATAATATATGTG[-/TACT]TATAAACAAATGTAT | 23894 |
rs260988194 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460800 | CTGTTCAACCATTTT[A/G]ACCTCATTAATGATT | 23894 |
rs261025014 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475215 | AAATAATATATAAAG[C/T]CTCTTTAAAGGACAA | 23894 |
rs261055986 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467669 | TCTGTTTTGTTTTGT[C/T]TTGTTTTTAGAGGGG | 23894 |
rs261065621 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483876 | ACTTCTCGGCTTTCC[C/T]ACCTTCTGTTTTGCT | 23894 |
rs261124352 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491848 | AAAATTTCTGTTCAG[A/G]ATGAGCAGAGTGGAA | 23894 |
rs261325826 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467474 | AGTAGGAAATGAATT[C/G]AAAGCTAACTGTCTC | 23894 |
rs261336044 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100463893 | TGCAAGGGAAGGCAA[A/G]CATGCACCACCTCCA | 23894 |
rs261377952 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100491660 | TTAAAAAATAACAAA[A/G]CTATGAGCCTGGCTG | 23894 |
rs261452363 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461518 | TTATGTGTATCCCTA[A/C]TGCTTTAACTCTTGA | 23894 |
rs261457755 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475743 | CTTCACTCTTGCATA[A/G]TAAGTATCCTTACCC | 23894 |