SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4136338 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Mtf2 | Mm_Celera | 5:108084273 | TAAAGATGATTTTCG[A/G]GTTTCTTAGGCTTGT | 17765 |
rs29545572 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mtf2 | Mm_Celera | 5:108091625 | TGCTATATAGGTGTG[G/T]AGCTCATTGTTAATA | 17765 |
rs29546516 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108093498 | ATTCTTTATACCTGG[C/T]TTTTAGTTCTTTTAG | 17765 |
rs29548243 | snp | A/T | 0.5 | 0 | intron-variant | Mtf2 | Mm_Celera | 5:108094522 | TACTTGATTCTTACT[A/T]TTTTTCATTTTTCTT | 17765 |
rs29550979 | snp | C/G | 0.32 | 0.24 | intron-variant | Mtf2 | Mm_Celera | 5:108097086 | GCCTCCCAAGTGCTG[C/G]AATTAAACGCAAGTG | 17765 |
rs29551014 | snp | C/T | 0.493827 | 0.0552116 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065036 | AAAGATATAAGCATG[C/T]ATTCCATTTATCAGC | 17765 |
rs29581945 | snp | C/G | 0.375 | 0.216506 | intron-variant | Mtf2 | Mm_Celera | 5:108085821 | ATGTAGTAGGTCTAG[C/G]TGTCTTGAACTTACT | 17765 |
rs29582354 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065201 | TCGTTCATCGTCAGA[A/G]AAAAAAAAAGTGAAA | 17765 |
rs29776168 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mtf2 | Mm_Celera | 5:108101922 | TCCAGTTCTGTTTTT[A/G]AATTGAGATTCTTAG | 17765 |
rs29817914 | snp | A/G | 0.475309 | 0.108333 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065202 | CGTTCATCGTCAGAA[A/G]AAAAAAAAGTGAAAA | 17765 |
rs32057604 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Mtf2 | Mm_Celera | 5:108086358 | TATAAAAAAGATGTG[A/T]ATCTGAACCTGAGTA | 17765 |
rs32057605 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108086910 | TTTGTTGAACATTCT[A/G]ATATAGTTAACACAT | 17765 |
rs32057606 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108086981 | CTCATGACTTTAATA[C/T]TGCTTTATGTATTTC | 17765 |
rs32057607 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Mtf2 | Mm_Celera | 5:108087711 | TAAATGGCTCGTAGG[G/T]TTTTTTTTTTTGTGC | 17765 |
rs32057608 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Mtf2 | Mm_Celera | 5:108088039 | TGAATGGGATGCAGG[C/T]CATAAAACCAATGTC | 17765 |
rs32057609 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108088616 | GTCATATGCCAGATA[G/T]GCCATTATAGTAAGC | 17765 |
rs32057610 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Mtf2 | Mm_Celera | 5:108089308 | TTTAATTAGATCACG[A/T]AATTTGAGCCATTTA | 17765 |
rs32057611 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108089590 | AGTTTTGGCAGCTTT[A/T]AGCTATCTAAATCAG | 17765 |
rs32057612 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108091155 | GATGTTGGTTGTTAT[C/T]AGGAATTCAAAGCCA | 17765 |
rs32057613 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108091795 | GGATGAAATAATTGA[C/T]ATTACAAACCTTTTT | 17765 |
rs32058424 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Mtf2 | Mm_Celera | 5:108092061 | TTTTTTTTGTGGTAG[C/T]TGGTATTTAAAGATG | 17765 |
rs32058425 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mtf2 | Mm_Celera | 5:108092280 | ATACTAAATAGTAAA[C/T]ATGCTCTCTATATTT | 17765 |
rs32058426 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Mtf2 | Mm_Celera | 5:108092299 | CTCTCTATATTTTCT[G/T]TGTTTTTAAATACTA | 17765 |
rs32058427 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108092511 | ATCATGTACTTTCTG[C/T]GCCAGGATATTAAGA | 17765 |
rs32058428 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108092653 | TTGCTTTTGACTTTA[C/T]TTTATAGCTCCTTTT | 17765 |
rs32058429 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Mtf2 | Mm_Celera | 5:108093154 | GAGAATTCTCTAATC[A/G]TTAAGGAAATTGTCC | 17765 |
rs32058430 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108093268 | AGCCTTATATCACTT[C/G]ATGAGTATTGGCTGT | 17765 |
rs32058431 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108093324 | CTGTAAAACTTTTTT[C/T]CCCCATTCTTTAGGT | 17765 |
rs32058432 | snp | C/T | 0.32 | 0.24 | intron-variant | Mtf2 | Mm_Celera | 5:108093421 | GGTGAGCATGACCTG[C/T]TCTACTTTCTAAAAA | 17765 |
rs32058433 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Mtf2 | GRCm38.p3 | 5:108093549 | GGCTTCAGGATTATC[C/T]ATTTAACCATTATGG | 17765 |
rs32059124 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108093913 | TTTAGGAAGTAATTT[A/G]GGTATGTTTTAGTTT | 17765 |
rs32059125 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108093958 | TAAGTTAAGCTAGTG[G/T]TTTCCAGTTTCTTCA | 17765 |
rs32059126 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108094497 | TTTGGGAAACTTGGT[G/T]GAAATAAATTACTTG | 17765 |
rs32059127 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Mtf2 | Mm_Celera | 5:108095160 | TTTATAAAGCAATTT[A/T]AAAAACCTTATAAGA | 17765 |
rs32059128 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mtf2 | Mm_Celera | 5:108095670 | ATTGAGTGAGACACT[C/T]AGAGGTAAGCTGAAT | 17765 |
rs32059129 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Mtf2 | Mm_Celera | 5:108095942 | AACAGTAAAAGGAGG[A/G]CCTAGGATGTAGTTC | 17765 |
rs32059130 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Mtf2 | Mm_Celera | 5:108096518 | TAGTATTAAGCAGTG[A/T]TGATAACTGGATCTC | 17765 |
rs32059131 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mtf2 | Mm_Celera | 5:108096529 | AGTGATGATAACTGG[A/G]TCTCTTCTGAAAAGA | 17765 |
rs32059132 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108096811 | ACTTTTGAGGGTTGA[A/G]TGTGTGCTGCTTTTT | 17765 |
rs32059133 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108097123 | AGCCCTGCAAGCATG[C/T]GCTTTTGATGTGTGA | 17765 |
rs32059697 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108064654 | TTTTTCAGAACCTAG[A/G]TAAAGGGAACTCTTT | 17765 |
rs32059698 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065120 | AACTGCTTTGCAGGA[A/G]GGTATGCTCAAATTT | 17765 |
rs32059699 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065213 | AGAGGAAAAAAAAGT[A/G]AAAATCTCCCATTAC | 17765 |
rs32059700 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065228 | GAAAATCTCCCATTA[C/T]AGATTCCAGATAAGT | 17765 |
rs32059701 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065255 | AAGTTTGGATTTGGA[G/T]AGTATTCATTGAACG | 17765 |
rs32059702 | snp | G/T | 0.132653 | 0.220748 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065400 | AAATCACCCCATCAA[G/T]ATGTACTGAGCAATA | 17765 |
rs32059703 | snp | G/T | 0.244898 | 0.249948 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065414 | AGATGTACTGAGCAA[G/T]ATCCTATTTCTGAGG | 17765 |
rs32059794 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Mtf2 | Mm_Celera | 5:108097243 | GTTAGTACTAGCACC[A/G]AAGTGCTGATAGAAT | 17765 |
rs32059795 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108097285 | TTTAGGTTCTGGTGT[C/T]CTTTCTAATCAGGAG | 17765 |
rs32059796 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108097621 | GCGTCTTGCACTGAG[A/C]GGTGGGCATGCGTGA | 17765 |
rs32059797 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108097822 | TTAGTTTTGTGCTTT[C/T]AGGGTTTACAGCGTG | 17765 |
rs32059798 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mtf2 | Mm_Celera | 5:108098017 | GCAGACTCCTGTCTA[A/G]AAGACATTACACAAA | 17765 |
rs32059799 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108098034 | AGACATTACACAAAG[A/G]TTTCACTTATGTCCT | 17765 |
rs32059800 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108098137 | ATTCTTTTTGGCAGA[C/T]AGAGTTCTCTCTCAC | 17765 |
rs32059801 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108098169 | TGATGTGTTCTTGGG[C/T]TTCGGAACTTCAACT | 17765 |
rs32059802 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Mtf2 | Mm_Celera | 5:108099411 | GGGGACGTAGATTTA[G/T]TCTACTCTCTTGAAT | 17765 |
rs32059803 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108099512 | AATATGCAAAAAATG[A/G]AGCCTTTTATGGTTT | 17765 |
rs32060564 | snp | A/T | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Mtf2 | Mm_Celera | 5:108099903 | TGAGTAATTGTACTG[A/T]TAAAAGTATTGATGC | 17765 |
rs32060565 | snp | A/G | 0.391111 | 0.206368 | intron-variant, utr-variant-3-prime | Mtf2 | Mm_Celera | 5:108100558 | ATGAATTGGGAATCT[A/G]TTATCTATGATCTAT | 17765 |
rs32060566 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Mtf2 | Mm_Celera | 5:108100774 | TATCTGGTAGTTCTC[C/T]ATGAGTGTTATGCTA | 17765 |
rs32060567 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Mtf2 | Mm_Celera | 5:108101013 | ACAGCTCTATTTATC[A/G]CTGAATGTTTGTGTT | 17765 |
rs32060568 | snp | C/G | 0.408163 | 0.193609 | intron-variant, downstream-variant-500B | Mtf2 | Mm_Celera | 5:108101158 | GAAGGAAAGGATTTA[C/G]TGATTGACTTTTCAC | 17765 |
rs32060569 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108101479 | GGAGGCCATGAAACA[C/T]AGTCTCATAATAGAA | 17765 |
rs32060570 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Mtf2 | Mm_Celera | 5:108101614 | ATTAGGTAAACAGTT[A/T]TAATTATCTTTAAAA | 17765 |
rs32060571 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108101960 | CTAAATGGTGCTGGG[C/T]GGGACTTTGACTTTA | 17765 |
rs32060572 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108101988 | TTAGATAGGGAGTGC[A/G]CAGACAGACAGACAG | 17765 |
rs32060573 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108102025 | ACAGATGATAAGTCA[A/G]GAGAAGGAATACAAT | 17765 |
rs32060574 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065449 | TAAAAAAGACCGCAC[A/G]AAAGACTGGACACGA | 17765 |
rs32060575 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065455 | AGACCGCACGAAAGA[C/T]TGGACACGATCTCTC | 17765 |
rs32060576 | snp | C/G | 0.142012 | 0.225474 | upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108065602 | GTTCAGCGCTGGTCC[C/G]GGACGCAGGGCGCGG | 17765 |
rs32060577 | snp | C/T | 0.132653 | 0.220748 | utr-variant-5-prime, nc-transcript-variant | Mtf2 | Mm_Celera | 5:108065680 | AGAGCTGCCATTCGG[C/T]CCCGGAGTAGCTCCG | 17765 |
rs32060578 | snp | G/T | 0.132653 | 0.220748 | utr-variant-5-prime, nc-transcript-variant | Mtf2 | Mm_Celera | 5:108065758 | GGCTGTTGCGAAGTG[G/T]TCTGTGTTTGAGGCC | 17765 |
rs32060579 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108066457 | TGGTAGGGGAATCTA[A/G]TGGTGGGCTAGATAG | 17765 |
rs32060580 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Mtf2 | GRCm38.p3 | 5:108066646 | ATTACAACTTAGTTA[C/G/T]TTACGGCACTAAGGG | 17765 |
rs32060581 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108066674 | GGGGTTTAACCAAAA[A/T]TTTCCAGGATTTCTT | 17765 |
rs32060582 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Mtf2 | Mm_Celera | 5:108067543 | GGCTGTTATTACTTT[A/G]CTTGAGTTCACATCA | 17765 |
rs32060583 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mtf2 | Mm_Celera | 5:108067586 | GGGTATGCAACTATA[C/T]TTAAATGTGTACTGT | 17765 |
rs32061214 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108102049 | ATACAATGATCTAGT[A/G]TAATAAATGAACAAG | 17765 |
rs32061215 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Mtf2 | Mm_Celera | 5:108102264 | TAATGAGTTGAAGTA[C/T]GATTGAATCCATACT | 17765 |
rs32061216 | snp | G/T | 0.429688 | 0.173817 | intron-variant | Mtf2 | Mm_Celera | 5:108102284 | GAATCCATACTTTGT[G/T]ATTTATGTATTAAGA | 17765 |
rs32061217 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108102380 | TTAAAGGGTACAAAA[A/G]GAATCCTAGTTAGAC | 17765 |
rs32061218 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108102635 | GCCTCAGTCTGAGAA[A/T]AACTTTTGGTAGCAG | 17765 |
rs32061219 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Mtf2 | Mm_Celera | 5:108102713 | TTGTAGAAATTAGAA[A/G]CTTTAGGTTATTGTT | 17765 |
rs32061220 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mtf2 | Mm_Celera | 5:108102928 | TTTCTGCCATTTTGC[A/G]GTTTGATCTAATCCT | 17765 |
rs32061221 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mtf2 | Mm_Celera | 5:108103007 | TCACATTGCTGTGAT[A/C]TTAGGAGTGTACTTG | 17765 |
rs32061222 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108103100 | CCACTTCCTTGTGGA[C/T]CCCGTGCATGCTCAG | 17765 |
rs32061223 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108103276 | CTGTAGTTGTGGTCC[C/T]TTTCTTTTTCTTTCA | 17765 |
rs32061414 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mtf2 | Mm_Celera | 5:108067910 | AATAGACATGTTCAG[A/T]GCTCATGTAGAGTAT | 17765 |
rs32061415 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108067989 | ACAAACGTGTACATG[A/G]GTGCACAGGCATACG | 17765 |
rs32061416 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108067995 | GTGTACATGGGTGCA[C/T]AGGCATACGTGGCAA | 17765 |
rs32061417 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108068037 | CACCTTCAAGTTACA[C/T]AATTGATATTTGATG | 17765 |
rs32061418 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mtf2 | Mm_Celera | 5:108068412 | GATATTTTTCACCAG[C/T]TATAGTGGTTTTAAA | 17765 |
rs32061419 | snp | C/T | 0.32 | 0.24 | intron-variant | Mtf2 | Mm_Celera | 5:108069631 | ATTGCTTGGCCTCAC[C/T]TGGCACTCCTGTGTT | 17765 |
rs32061420 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108069710 | CCAGTGAGTTGCAAT[A/G]AGGACTGAGATATTT | 17765 |
rs32061421 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mtf2 | Mm_Celera | 5:108069858 | AGCAATCCCAGATTG[A/G]TGCAGAAACATTGTG | 17765 |
rs32061422 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mtf2 | Mm_Celera | 5:108071272 | CTAGATTCTCTATGG[A/T]GTTTTAATGAAGTAA | 17765 |
rs32061423 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Mtf2 | Mm_Celera | 5:108072807 | AAGAGAATTACTTTC[C/T]CATAGGTTTGGTGCA | 17765 |
rs32061844 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mtf2 | Mm_Celera | 5:108103383 | AGAAGCCTCTTTGTC[C/T]CTTTTATACCTTTCT | 17765 |
rs32061845 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108103503 | CAGCTTTTTACTACT[C/T]GGTAGGTACATAAAT | 17765 |
rs32061846 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mtf2 | Mm_Celera | 5:108103870 | TTGTTATTTTTTAAA[A/G]TCTTGAAATGATAAT | 17765 |