SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6158348 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75041988 | TTCCGAGGAGTCTAC[C/T]AGACAGAGCTGAGAG | 21968 |
rs6158851 | snp | A/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042079 | AGTGATCTGACCTTA[A/T]TGCTGGGCAAGGAAC | 21968 |
rs6158939 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042132 | GTCCCAGAAGAATTG[C/T]GCATGTTCAAAAGTC | 21968 |
rs6172223 | snp | A/G | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042258 | GCCAAACTCCAGGAA[A/G]CCAGGACACTAGATT | 21968 |
rs6172669 | snp | A/C | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042292 | ACTGAAGGTACCTAC[A/C]ACAGCACAGCCACNC | 21968 |
rs6172690 | snp | C/G | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042306 | CNACAGCACAGCCAC[C/G]CTGTAGGAAAGCCAG | 21968 |
rs6173324 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042414 | AGCCTGAGCCTTGCA[C/T]ATGTTTACCTATTAA | 21968 |
rs6173400 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042459 | ggagagatggctcag[C/T]gggtaagagcactga | 21968 |
rs6173942 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042555 | atctgatgccctctt[C/T]tggtgtgtctgaagt | 21968 |
rs6174994 | snp | A/G | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042711 | GACGCAACTTTCCAC[A/G]GACTGGCAGCTCATT | 21968 |
rs6175047 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75042737 | TCATTAATGTCCTTC[C/T]CACAGGTCTTCCTTG | 21968 |
rs6213155 | snp | A/G | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75050568 | CCCTAAAAAATGAAC[A/G]TAAAACAAATGCCTG | 21968 |
rs6213317 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tom1 | Mm_Celera | 8:75050663 | TGTCTTCAGAGCAAC[A/G]TGGCTGGANAATAGG | 21968 |
rs6213688 | snp | A/C | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75050672 | AGCAACNTGGCTGGA[A/C]AATAGGCAGGAGAAC | 21968 |
rs6213710 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75050689 | ATAGGCAGGAGAACA[C/T]CCTATCCCAGCCTCT | 21968 |
rs6348588 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75038153 | GGCCACACAGTAAAT[C/T]CTCAAGACTTCAGAG | 21968 |
rs6361631 | snp | A/C | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75038317 | GTGTCATTAAACATT[A/C]TTCTTCTcaggtgtg | 21968 |
rs30828202 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75061610 | CAGCCCAGAGGCCTC[C/T]GGCCTAGCAGCTTAC | 21968 |
rs32665047 | snp | A/G | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75050063 | TGGCCAGGGAAAGAC[A/G]GGGAGCCGTCTGAGG | 21968 |
rs32676417 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Tom1 | Mm_Celera | 8:75063663 | GGTCAGATAGGCCCT[C/T]AGCAGCTTGCACACT | 21968 |
rs32831600 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75051096 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 21968 |
rs32878225 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Tom1 | Mm_Celera | 8:75058144 | CTCAAATGTAGAGTA[A/G]GTAACTAGACAGTTG | 21968 |
rs33056520 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Tom1 | Mm_Celera | 8:75057987 | AGAACAGAAAATGAA[A/T]TCAAAAGTGATGTCC | 21968 |
rs33094547 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Tom1 | Mm_Celera | 8:75066753 | GCACATGCCAGATTG[A/G]CACTGTTGAAACTGT | 21968 |
rs33113514 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tom1 | Mm_Celera | 8:75057871 | CCAGTTCTCTAGCAT[C/T]AGGCCCCTAATTTAC | 21968 |
rs33116116 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Tom1 | Mm_Celera | 8:75058316 | TAGTGATAGCATGAG[A/C]ACAGCGAGCATGCGC | 21968 |
rs33226975 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tom1 | Mm_Celera | 8:75065642 | CATTCACTCCCCCCA[C/T]CCTTTATTCGGGCAA | 21968 |
rs33349855 | snp | C/T | 0.5 | 0 | intron-variant | Tom1 | Mm_Celera | 8:75065765 | TGTGGGATGGTATTG[C/T]AAAATCAAAATCCAG | 21968 |
rs33461705 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Tom1 | Mm_Celera | 8:75065657 | TCCTTTATTCGGGCA[A/G]CCACCTGTTGGATAT | 21968 |
rs36247621 | snp | C/T | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75044380 | TCACATGACTTCAGA[C/T]AGTTGACTGCTGAGG | 21968 |
rs36255826 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75054701 | TACTACAGGTGAGCA[A/T]ACAGCCTGCCTCCAG | 21968 |
rs36283011 | snp | A/G | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75052648 | CTTTATCTATGTGCT[A/G]GTAGGCTCACATAGA | 21968 |
rs36288632 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75068992 | AGGGTCAGCTTAAGG[A/G]CAACAGCAACACTGG | 21968 |
rs36292608 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75060261 | TTTAGAAGTGAGCAC[A/G]CTCAGCAGAAATGAA | 21968 |
rs36293072 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75048328 | GATGAAAAACTTAGA[A/G]ATGTAAAGTTCAAAG | 21968 |
rs36294159 | snp | C/T | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75056618 | CACCCTCCTCACTCT[C/T]CTGTTTTCCCCTTAG | 21968 |
rs36295987 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75057500 | CTCCTTGTGTCTATT[G/T]TGTGTTCCCCACTTG | 21968 |
rs36297223 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75066485 | TCTCCCATAGTGAGG[C/T]ACCCTAGGTAGCTTA | 21968 |
rs36306630 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Tom1 | GRCm38.p3 | 8:75053243 | AACAAAGAGAAGCTT[C/G/T]GTGCTGTCTTATACC | 21968 |
rs36325951 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75051838 | GGAAAGCACTCTGTC[C/T]TCTGTCTAGGTGCCA | 21968 |
rs36338497 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Tom1 | Mm_Celera | 8:75070248 | CCATGCTCAGATACA[A/G]TCCCTGCTTCACCCC | 21968 |
rs36345134 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75048498 | AAAGACGTAGTGTGT[A/G]TGCAGCTGGCCACTA | 21968 |
rs36347412 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75046753 | GTGTGACAAGTGACA[A/C]TAGCATCCAAACTGG | 21968 |
rs36349237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75063887 | TTTGGTCACATGTTG[C/T]CTCTAGATATTCTCT | 21968 |
rs36352867 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75054774 | TTTCCTCCCTGTCTA[C/T]ATTGCAGTCCTTTGT | 21968 |
rs36353088 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75046895 | AAATGTTAACCTGTC[A/G]CATGCTTACATGTGA | 21968 |
rs36355722 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75063081 | ACCTGCTCTTCATGT[A/G]ATCAGGAGCTGTGTG | 21968 |
rs36358980 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75048796 | CCTAATGTTTGCTCA[A/G]AAAGGTGATTCCAGC | 21968 |
rs36360266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75052341 | AAGATCCAGGGAGGT[A/G]TCAGAGATGGCCCCT | 21968 |
rs36360280 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75047484 | CTGCACAGCCATTCT[A/G]AGAGAGGGCCACTTG | 21968 |
rs36368312 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75053817 | ATTTAAATTCTGAAG[G/T]TTATTGTCACTCAAT | 21968 |
rs36373158 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75064319 | CAGGCTCACCTGATA[C/T]CCTCAGTCCTTACGC | 21968 |
rs36378798 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75066839 | GTTTGAGCTCAGAGT[C/T]AAATACTCCCATCTA | 21968 |
rs36381948 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75046728 | CCCAGCTATGAAGAC[A/T]GTCTTCCTTGTGTGA | 21968 |
rs36390436 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75044574 | CAACACAGGACTAGC[C/T]GCTGATCCCAGGACT | 21968 |
rs36390505 | snp | C/T | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75049354 | TGAACACTTTAGGTG[C/T]TCCAGACTCTGCCCA | 21968 |
rs36393583 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75053739 | CCCACCTGTGATGGC[A/G]CATGTTCAGTGCTTG | 21968 |
rs36399691 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75053989 | AGTATTCAAAGTGAA[C/T]ACAGTGTCCTCCGAG | 21968 |
rs36399818 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75047285 | AAGTGGTTCCACAGC[A/G]TTATGACGGAACCAG | 21968 |
rs36402171 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75061656 | AAGGATGCTGCTGAG[A/G]CTGCTGTGCAGATGA | 21968 |
rs36405002 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | GRCm38.p3 | 8:75068237 | TGGTCTGTGCTTAGC[A/G]TCCCACATCCATGAG | 21968 |
rs36407388 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75043842 | AAGGATGACCTTCCC[A/G]ACAGCACTCAGGGAT | 21968 |
rs36422151 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Tom1 | Mm_Celera | 8:75070300 | CTGTGCACAAGACAG[C/T]CATCTACCTGATTGG | 21968 |
rs36428101 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Tom1 | Mm_Celera | 8:75057184 | CTGCCGTGCCATGCA[A/G]CAGCGGATCCTGGAG | 21968 |
rs36443307 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75053168 | ATGATACAAATGAGA[A/G]ACACTTAATTCCCAA | 21968 |
rs36448668 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tom1 | Mm_Celera | 8:75046790 | AGCAGGTGTATGTGT[A/G]TGTACATGACATCTT | 21968 |
rs36467828 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75045606 | TTATTAGGAGTTTTG[A/G]TCCGTTGGTTAATTG | 21968 |
rs36471729 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75057927 | GCTACTCAGTGCCTC[A/G]ACTCAGTCATCACCT | 21968 |
rs36489576 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75064685 | GTTCACATTCCACTT[C/T]ATCACCTGCCAGCTA | 21968 |
rs36495316 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75044186 | ACAGAATGATTCCAA[A/G]GGACAGGAGAGCAGG | 21968 |
rs36505898 | snp | G/T | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75055800 | AGGGTTTGTGACTTG[G/T]AGCAACGACTTCAGT | 21968 |
rs36506262 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75065305 | ACAGAACACTTTTGG[A/G]CAGGCAGACTTCATA | 21968 |
rs36508373 | snp | A/G | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75053208 | CCTGACCACTTGTGT[A/G]TAGTGCATGGTCTCA | 21968 |
rs36517929 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75045117 | ACATCTCAGGGCAAG[C/T]CAGAAGAGACTGCAA | 21968 |
rs36526883 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75044082 | AGCCCTAGCAGCTTC[C/T]GGCCTGTGCAGGCAA | 21968 |
rs36527170 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75060736 | AGGAAGGGATACCAA[A/C]ATCTGACCAGAACCA | 21968 |
rs36532747 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tom1 | Mm_Celera | 8:75056710 | CGAAGTAAGAGATCA[A/G]CCTTAGGGAGCCAGC | 21968 |
rs36551563 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75054171 | AAGAATCTGAAGGTA[A/C]AGACACAGACAAAAC | 21968 |
rs36556295 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75057329 | GCCGTGGCCTCGGCT[A/G]CTCAGTCATTTTCCC | 21968 |
rs36559096 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75057061 | GTGATCTTGAGAACA[C/G]GCTTGTGGAGCCATG | 21968 |
rs36560954 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75065116 | GTGGGAAGAGGTCTA[C/T]GAGGTGTCTAGGACC | 21968 |
rs36580425 | snp | C/T | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75066102 | TGTTAACTATAAAAC[C/T]GGTGGACAAAGCAGT | 21968 |
rs36602136 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75043957 | GAGCTACAGATAATT[A/T]ATCAACAGAAAAGAG | 21968 |
rs36604730 | snp | A/C | 0.32 | 0.24 | intron-variant | Tom1 | Mm_Celera | 8:75044312 | TACCCAAATACATGA[A/C]TTTTGGCCAAGGCTT | 21968 |
rs36608597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75058571 | TCCTTGTAAAGGATA[C/T]TGGTGCTTCTTTTTA | 21968 |
rs36608603 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75045057 | GTTTAAAAACAAAAC[A/C]TGACAATCCTGTTCT | 21968 |
rs36630550 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75050737 | TCCAGATGGCCCTGC[C/G]ACCCTGCAAAGCACA | 21968 |
rs36639083 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Tom1 | GRCm38.p3 | 8:75065798 | TGGAGCTGGTGGGCA[A/C/G]TGCCTTGTCCAAGGC | 21968 |
rs36660785 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75048290 | CTTTAGACCCTTATA[C/T]AATATAGTGCCTTCA | 21968 |
rs36670136 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75042837 | CACACCTGGCAGCCT[A/G]GAGACTCAGTACACT | 21968 |
rs36672488 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75043813 | TTCGTACTGTGCCCA[G/T]CGAGCATGTATGTAA | 21968 |
rs36673636 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75049823 | ATAGTGCCCTTCAAA[G/T]TCACATCTCTGACAA | 21968 |
rs36675307 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75045096 | ACACTTACACGATAC[A/C]TTGACACATCTCAGG | 21968 |
rs36677372 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tom1 | Mm_Celera | 8:75053644 | GCACTGTGGGGTGTG[C/T]TCTTGGTCAGCTTCA | 21968 |
rs36683663 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tom1 | Mm_Celera | 8:75043505 | AGGAAGTTCCAGGAT[A/G]TCCATATCTACAGAG | 21968 |
rs36704770 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tom1 | Mm_Celera | 8:75066018 | TAGACAGAGGGGTCA[A/G]TGCATAATGGGTAGG | 21968 |
rs36705826 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tom1 | GRCm38.p3 | 8:75067646 | ATAGAAGGGCCTTGT[A/C]AGTGACTGGAGGAGA | 21968 |
rs36709193 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75053900 | AGATTTATGAGCCAT[C/T]CCATTATAAGAGGAT | 21968 |
rs36713850 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tom1 | Mm_Celera | 8:75065367 | GCACACCTGCTCTGG[C/G]CCTCTCTTCTGCATG | 21968 |
rs36735988 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tom1 | Mm_Celera | 8:75065879 | CTTGGTGCTGCGGTA[A/G]GCTAAGCCTACACTG | 21968 |