SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3699516 | snp | A/T | 0.5 | 0 | intron-variant | Sptan1 | Mm_Celera | 2:29984259 | TTTATTTAATTAATT[A/T]ATTTATTTATTTATT | 20740 |
rs6218110 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sptan1 | Mm_Celera | 2:30005678 | GGCCTGGCTAGTCTA[A/G]AACTTGctacataaa | 20740 |
rs6310404 | snp | A/T | 0.5 | 0 | intron-variant | Sptan1 | GRCm38.p3 | 2:29977557 | ataaaagaaacaaaa[A/T]caaaacaaaacaaaa | 20740 |
rs6310887 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Sptan1 | Mm_Celera | 2:29977616 | TCACAGTTTCTGTGA[C/T]AAATAGGAAAGCTGG | 20740 |
rs6311948 | snp | C/T | 0.5 | 0 | intron-variant | Sptan1 | Mm_Celera | 2:29977837 | gtgacatgacacctc[C/T]ctttttaaaaaGTCA | 20740 |
rs6312067 | snp | A/G | 0.5 | 0 | intron-variant | Sptan1 | Mm_Celera | 2:29977911 | ggcagaggccagcct[A/G]gtctatagagcaagt | 20740 |
rs6324827 | snp | C/T | 0.5 | 0 | intron-variant | Sptan1 | Mm_Celera | 2:29977948 | acagccaggattaca[C/T]agaacaccngtctca | 20740 |
rs6324843 | snp | A/G | 0.5 | 0 | intron-variant | Sptan1 | Mm_Celera | 2:29977957 | attacanagaacacc[A/G]gtctcaaaaaaCTTA | 20740 |
rs13467591 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Sptan1 | Mm_Celera | 2:30025042 | CAACTGGAAGGCTGA[C/T]GTGGTAGAGTCCTGG | 20740 |
rs13467592 | snp | A/G | 0.408163 | 0.193609 | synonymous-codon | Sptan1 | Mm_Celera | 2:30020526 | GGAGCACTGGAAGGA[A/G]CTAAAGCAGCTGGCG | 20740 |
rs13467593 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Wdr34, Sptan1 | Mm_Celera | 2:30031108 | TTGATCAATCCTCTT[A/G]GCTTGTAGGCAAGCC | 20740 |
rs27180026 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Wdr34, Sptan1 | Mm_Celera | 2:30031289 | GGTGCTTCAATAAAC[C/T]GCTTCCAGTCACAAT | 20740 |
rs27180027 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Sptan1 | Mm_Celera | 2:30030762 | TGAAGAGATCGAGAG[C/T]GCTTTCCGGGCCCTC | 20740 |
rs27180028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30030251 | CTTGTTAACAAGGGA[C/T]GGGTACAGGATGGGA | 20740 |
rs27180029 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30029978 | GTCCCAGCCTCACAC[A/T]GCATTTGTCCCACCC | 20740 |
rs27180030 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30029852 | TTCCTTGGCACCTCT[A/G]TCAGCTGCCTATGAA | 20740 |
rs27180031 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30029693 | AGTGTCTCAAAGGGC[G/T]TTAGCCAGAGGCCAC | 20740 |
rs27180032 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30029510 | TAGGCCATTTCCTCA[A/G]TGAAAAGAATTTCAG | 20740 |
rs27180033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30029431 | AAATTCAGTGATCTT[C/T]AAGAGCTGAGAAGCC | 20740 |
rs27180034 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Sptan1 | Mm_Celera | 2:30029146 | ACACATCTTGGAGCA[A/G]GCTTCCCCCAAGGCC | 20740 |
rs27180035 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Sptan1 | Mm_Celera | 2:30028483 | CCATGCTTCCTCACC[C/T]GTGGCTCCTCCCAAG | 20740 |
rs27180036 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30028165 | TTACAAGGTTATAGA[A/G]ACAGGGCTTGGAGGA | 20740 |
rs27180037 | snp | C/T | 0.32 | 0.24 | intron-variant | Sptan1 | Mm_Celera | 2:30028053 | CCAGTTGAGGGGAAG[C/T]TCTGCAGCCCTCTTA | 20740 |
rs27180038 | snp | A/G | 0.32 | 0.24 | intron-variant | Sptan1 | Mm_Celera | 2:30027922 | CACCAGAACTGGATT[A/G]CCTTTCCCTCTTTGC | 20740 |
rs27180039 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30027896 | GTCTGAGGACCCTGT[C/G]CATGCCTGGTCACCA | 20740 |
rs27180040 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30027881 | GGAAGCCAGAGTCAA[A/G]TCTGAGGACCCTGTC | 20740 |
rs27180041 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30027669 | TATTGCCTTCTTTTC[C/T]GGGCTCCTGGTGTGG | 20740 |
rs27180042 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30027612 | CTACCACGGCTCCTG[A/G]ACACTTGGATCTCCA | 20740 |
rs27180043 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Sptan1 | Mm_Celera | 2:30027490 | GTTGGCAACTGTCCC[A/G]AGGGAGGTAGACCAG | 20740 |
rs27180044 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30026227 | TTCCGTAAGGTAAGG[G/T]TAGGATTGAGCTGGC | 20740 |
rs27180045 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Sptan1 | Mm_Celera | 2:30026124 | TAAGGCCATCGAGGC[C/T]CGACATGCCTCCCTC | 20740 |
rs27180046 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30025843 | GTTTATTTAAGGCCA[A/G]AGATGTAACCATTGC | 20740 |
rs27180047 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30025614 | GTCAGTTGGCCTTCC[A/G]AATCTGTGGCCATGG | 20740 |
rs27180048 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Sptan1 | Mm_Celera | 2:30025580 | TCTGTCTTCTGTCCA[A/G]ACTCTGCTCACAAAA | 20740 |
rs27180049 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30025349 | ACCAAAGGGTCAGGT[C/T]ACATGAGAACTGCTT | 20740 |
rs27180051 | snp | C/G | 0.32 | 0.24 | intron-variant | Sptan1 | Mm_Celera | 2:30024881 | AGGCAAAACTAACTT[C/G]TGCTTCTTTTCCTGG | 20740 |
rs27180052 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30024298 | GACCCGAGGTGACTA[C/T]GTTGTAATGCTCTCT | 20740 |
rs27180053 | snp | G/T | 0.32 | 0.24 | intron-variant | Sptan1 | Mm_Celera | 2:30024200 | AGAGCTTTTCTCCTG[G/T]CCTTAATCACCGCAG | 20740 |
rs27180054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30024104 | AACTTGAGATTGGGG[C/T]TAGGCTGGTGCCCTG | 20740 |
rs27180055 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30024051 | CAAGTGTGCGTGCTC[C/G/T]GTGCTCCCTACACAA | 20740 |
rs27180056 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30023947 | GTCCAGGCCTCCACA[A/T]CTTCAGCTCTAGGCC | 20740 |
rs27180057 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30023910 | CAACAGCAAAGTCTA[C/G]GTATTTTCAGAGCAG | 20740 |
rs27180058 | snp | A/G | 0.18 | 0.24 | intron-variant | Sptan1 | Mm_Celera | 2:30022731 | GGTTCTTTTGTGACA[A/G]TAGGACTTTCCAGAT | 20740 |
rs27180059 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30022547 | TAAGAAGGTGAGCCA[C/T]GATCCCAGGAGAGCC | 20740 |
rs27180060 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Sptan1 | Mm_Celera | 2:30022312 | CCGCCCTGATTGATG[A/G]CCATGGACCACCATG | 20740 |
rs27180061 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Sptan1 | Mm_Celera | 2:30021487 | TCTGGCATTCCGTCT[A/G]CATGCCCATCTGTCC | 20740 |
rs27180062 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Sptan1 | Mm_Celera | 2:30021389 | CAACACAGCCCACAG[A/C]GGAGAGTCCTTTTTC | 20740 |
rs27180063 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30020651 | CACCAGAGCCACCTC[C/T]TGGAGTCGGTTCTGA | 20740 |
rs27180064 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30020348 | TGGATGTGATGTTGA[A/C]TTCTGGCAACCTGAG | 20740 |
rs27180065 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30019874 | AGTTGCTAAACTAAC[C/T]TGGCCCCTGACATGA | 20740 |
rs27180066 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Sptan1 | Mm_Celera | 2:30018289 | TTTATTAGGCTGCAC[A/G]GCCCAGTCAGGAATT | 20740 |
rs27180067 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Sptan1 | Mm_Celera | 2:30017545 | AGAGATGTCATACAG[G/T]AAAGTGCTGGAATTG | 20740 |
rs27180068 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Sptan1 | Mm_Celera | 2:30017539 | GCGCCTAGAGATGTC[A/G]TACAGTAAAGTGCTG | 20740 |
rs27180069 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30017414 | GGTGCCTGGCTCTGT[C/T]CAAGGCTGCCATTTG | 20740 |
rs27180070 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30016753 | ACTAGGAGCTTTGTC[A/G]CTGTAGGTTGCTGTG | 20740 |
rs27180071 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30016735 | CTCATCTGTGTTATT[A/G]GTACTAGGAGCTTTG | 20740 |
rs27180072 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Sptan1 | Mm_Celera | 2:30016640 | AGTCCAAAGAATCTT[A/G]GCATGATTTAAGCAT | 20740 |
rs27180073 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Sptan1 | Mm_Celera | 2:30016438 | CTGGCAAGCAGGGCT[C/G]TAAAGTGGGTGATTT | 20740 |
rs27180074 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30016259 | TGAGTAAAGAGGTTG[A/G]GAGCGGAAACTGATT | 20740 |
rs27180075 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30016135 | TTTGGGTACTGAATG[A/G]TTTGGTCAGCCAGCC | 20740 |
rs27180076 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Sptan1 | Mm_Celera | 2:30015394 | GTTCATTTCCCTTTC[A/T]GGCCTAAACCTACCT | 20740 |
rs27180077 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30015079 | ACCTGGCAAAAGTAA[A/C]ATTCAGACTGGGTTT | 20740 |
rs27180078 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Sptan1 | Mm_Celera | 2:30015016 | AAGTGTTTCATGCAG[C/T]AGCCTTGTTTCTTAA | 20740 |
rs27180079 | snp | A/C | 0.375 | 0.216506 | intron-variant | Sptan1 | Mm_Celera | 2:30014921 | CTCCAGTAACATTAT[A/C]CCTGAGACTGTTTCT | 20740 |
rs27180080 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30014851 | TCAAATGAAACATTG[A/G]GTGCAGAATCTTGGC | 20740 |
rs27180081 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30014692 | GAAGGGAAAATAAAG[C/T]TGTAGAAGAGAATAA | 20740 |
rs27180082 | snp | A/C/T | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30014554 | GTGCATACTCTGGCT[A/C/T]GTGTCCAGCGGTGCT | 20740 |
rs27180083 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30014301 | GTCATCAGTCTAATC[C/T]CCAGTCACTCCATCC | 20740 |
rs27180084 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Sptan1 | Mm_Celera | 2:30013721 | AAAAAGGTCAAAACT[C/T]GGAGAATCTCAAACA | 20740 |
rs27180085 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30013662 | GAACACTCATATTTG[A/G]TCTTCACACTCAGGT | 20740 |
rs27180086 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30013251 | CACTTGCACACCTCA[A/G]TATGACCTTAAGTCC | 20740 |
rs27180087 | snp | C/G/T | 0.260355 | 0.249785 | intron-variant | Sptan1 | GRCm38.p3 | 2:30012204 | TCACAAACAGCGAGC[C/G/T]CTTAAATCCTTGGGT | 20740 |
rs27180088 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Sptan1 | Mm_Celera | 2:30011243 | GCCCGGGAGGCCTTC[C/T]TAAACACAGAAGACA | 20740 |
rs27180089 | snp | A/T | 0.142012 | 0.225474 | stop-gained | Sptan1 | Mm_Celera | 2:30011203 | GTTCCATCGGGACTG[A/T]GAACAAGCAGAAAAC | 20740 |
rs27180090 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Sptan1 | Mm_Celera | 2:30010624 | AATGCAGAAGAGATA[C/G]AACTGGTTCCTAGAC | 20740 |
rs27180091 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Sptan1 | Mm_Celera | 2:30010497 | GGTGTAACAGTTGGG[A/G]CTGGGCTTCATGACT | 20740 |
rs27180092 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sptan1 | Mm_Celera | 2:30009578 | TAAAAGAAGTCAGTT[C/T]TCTCTACCAATGTAT | 20740 |
rs27180093 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30009283 | CGGACAACATGATTT[A/C]TGTGGTCAGACATTC | 20740 |
rs27180094 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Sptan1 | Mm_Celera | 2:30009269 | TGAGTGGATGATCAC[A/G]GACAACATGATTTCT | 20740 |
rs27180095 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Sptan1 | Mm_Celera | 2:30009114 | GCAACTGGTATTGTT[A/G]CCTGTTGTCACCAGT | 20740 |
rs27180096 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sptan1 | Mm_Celera | 2:30008943 | TATGCATGTTCACTC[A/G]GGTTCATGTCATCTT | 20740 |
rs27180097 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Sptan1 | Mm_Celera | 2:30008264 | ATTTCCGGTAAAAAA[A/C]AAATGTCTTAGTTAT | 20740 |
rs27180098 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Sptan1 | Mm_Celera | 2:30008220 | GGCCAAATTGGGTGA[C/T]TCCCATGATCTGCAG | 20740 |
rs27180099 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30008069 | TTACAACTCTTTGCT[A/C]ATAGGTGAATTCCCT | 20740 |
rs27180100 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Sptan1 | Mm_Celera | 2:30007966 | AGGCTTTGAGAGGGA[C/T]CTTGCAGCTCTTGGT | 20740 |
rs27180101 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Sptan1 | Mm_Celera | 2:30007527 | CGGTCCCTGCAACAG[C/T]TGGCTGAGGAACGTA | 20740 |
rs27180102 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30007434 | AATTATTTTCCCAAG[C/G]TCTGGTTGTGGGTGT | 20740 |
rs27180103 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Sptan1 | Mm_Celera | 2:30007226 | GAGAAGATTCTCAGA[A/T]GTCTCCATTTGGCAG | 20740 |
rs27180104 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Sptan1 | Mm_Celera | 2:30007198 | TCCAAGACTTCATTG[G/T]TTGTCGTACTGAGAG | 20740 |
rs27180105 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Sptan1 | Mm_Celera | 2:30007124 | CCAGCACAGAGCAGG[C/G]CTGAAAACCTTCGCT | 20740 |
rs27180106 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sptan1 | Mm_Celera | 2:30006815 | AGACTCCAACCTGAG[C/T]ATGTCTTTACTTTTT | 20740 |
rs27180107 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Sptan1 | Mm_Celera | 2:30006790 | CAGGCCTACTTAAGT[G/T]TCTTGATCTAGACTC | 20740 |
rs27180108 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sptan1 | Mm_Celera | 2:30006762 | TTGTCCTCGTGCTGG[A/G]GCATGCTGTGACCAG | 20740 |
rs27180109 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30006748 | ACAACAGTAGGGGCT[C/T]GTCCTCGTGCTGGAG | 20740 |
rs27180110 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Sptan1 | Mm_Celera | 2:30006589 | CTCTGAGTGGACAGG[A/G]TCTTAATGGGTTTTC | 20740 |
rs27180111 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30006550 | TGACTGTTGGGACCT[A/G]CCTGGTGTCAGTAGC | 20740 |
rs27180112 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Sptan1 | Mm_Celera | 2:30006451 | ACCCTGCAGCCATCT[C/T]CACTTAGGTACTTGG | 20740 |
rs27180113 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30006422 | AGGGTTTCACTCTCT[A/C]CTGGGTAGGCCTCAC | 20740 |
rs27180114 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sptan1 | Mm_Celera | 2:30006401 | CTTCCTTCAGCTGCT[A/G]TCCTCAGGGTTTCAC | 20740 |
rs27180115 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Sptan1 | Mm_Celera | 2:30005939 | GACTTAGGTCTCCTT[C/G]TGACTTGTCTCCTAG | 20740 |