SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3686697 | snp | A/G | 0.5 | 0 | intron-variant | Gan | GRCm38.p3 | 8:117165434 | ATCTCTGCTGAACTA[A/G]GAAGCACCGAGGGGA | 209239 |
rs33353493 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117183380 | TTGATCTGACGCTAA[A/G]TCTTCTAACTGGAAG | 209239 |
rs36244801 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Gan | GRCm38.p3 | 8:117190721 | CTACGACCCTAACCG[A/G]CAGCTGTGGATTGAA | 209239 |
rs36271011 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117202056 | ACCGTCCTGGACAGC[A/G]GAGCCTCAAGGCTGC | 209239 |
rs36294070 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gan | Mm_Celera | 8:117180144 | AATGTTAGTTTTGTT[A/T]TTTAACCTCCAAATG | 209239 |
rs36338284 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gan | GRCm38.p3 | 8:117200722 | AGGCGAAGTCAGTCC[C/T]TGCACACTCCCATCC | 209239 |
rs36356769 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Gan | GRCm38.p3 | 8:117157491 | TCTGCTTTAAAGACC[C/T]CGATCTTAGAAACCT | 209239 |
rs36370120 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117195422 | GAGCTAGGTCAAAAC[A/G]TATATACAGGATTTG | 209239 |
rs36417156 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Gan | Mm_Celera | 8:117156986 | CTTGCTGCTTCCAGG[A/G]TGAAAACCAAGACTT | 209239 |
rs36420019 | snp | C/G | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117173843 | GCCAGACTTCAGCCA[C/G]GACGGGACCATTTAA | 209239 |
rs36434124 | snp | A/C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Gan | GRCm38.p3 | 8:117204382 | GCATCCCGTGGCTGG[A/C/T]GGCGGCAAGTGCAGT | 209239 |
rs36449903 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117184759 | GGGTGTGCACATGTG[C/T]GATTGTTAAACTAGA | 209239 |
rs36459605 | snp | A/G | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117189691 | CTTTGCCAGGCGTGT[A/G]AGACAACAGAGTCGC | 209239 |
rs36497647 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | GRCm38.p3 | 8:117198371 | CTCAGACACTTCAGA[C/T]GAGTCTTTACTTCCC | 209239 |
rs36499402 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Gan | Mm_Celera | 8:117205371 | AGGAGTATAGATGAA[C/T]TTTGCTCCAGGTAAC | 209239 |
rs36518794 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Gan | Mm_Celera | 8:117204735 | TATGCAAGCCAACAT[A/G]GCCGGCGTACGAGGT | 209239 |
rs36530666 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117189164 | CGGTGCACACTCAGA[A/C]ACCATGCTGTGGTCT | 209239 |
rs36536375 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Gan | Mm_Celera | 8:117204037 | AGGAGCCAGTATTTA[C/T]GTTATCGGAGACCTG | 209239 |
rs36571745 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117201060 | AGGCTGTATCTTTCC[A/G]TCCCAGGCCTGGCTC | 209239 |
rs36583071 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gan | GRCm38.p3 | 8:117177880 | GCGTGAAGCTGGCCT[A/G]GGTCTCTAGTTCCCA | 209239 |
rs36584351 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117181287 | TCCCGGACCCTGAAC[A/G]AAGAATTGGTCATTC | 209239 |
rs36603019 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117193407 | TCTGGAAGTTTTATC[A/G]GGTGTGGGTTCCTGT | 209239 |
rs36604862 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117176292 | ACAAGTCTCGGCTTC[C/T]CGGAAGACCACTGGT | 209239 |
rs36606033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117194555 | TCACGTCAGCAGTCA[C/T]ACATCACAGCAGGAA | 209239 |
rs36617721 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Gan | Mm_Celera | 8:117187287 | CATCCGGGACTTTGC[A/G]CTGCACTACTGCCTG | 209239 |
rs36623220 | snp | A/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117189325 | TGTGACAATTCTTTG[A/T]CCTTTGGTTAATCTG | 209239 |
rs36642150 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gan | Mm_Celera | 8:117182769 | GTACTTGTCACGTAG[C/T]TTTGTCTGTGACGAG | 209239 |
rs36646731 | snp | A/C/G | 0.260355 | 0.249785 | intron-variant | Gan | GRCm38.p3 | 8:117173847 | GACTTCAGCCAGGAC[A/C/G]GGACCATTTAACTTA | 209239 |
rs36647963 | snp | A/C | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117188083 | GTCTTCAAGTGTCTT[A/C]CTGCTGCTGTCACTG | 209239 |
rs36660531 | snp | C/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117202170 | AAAGCCTAGAATCTA[C/T]TTATCTCATATGAAG | 209239 |
rs36678962 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117194543 | GGCAGCTTGCCTTCA[C/T]GTCAGCAGTCATACA | 209239 |
rs36697311 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117187957 | TCAGGCCTAGGATAT[C/T]TGAGACGCTTGGATT | 209239 |
rs36718917 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117189261 | GCTGGGACCCTGTTC[C/G]TCCTCAGCCTGCTGG | 209239 |
rs36722636 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117200412 | CGAGCAGTCCCAGAG[C/G]TGTTGCAGGCACTGC | 209239 |
rs36757889 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117203741 | ATGCAGTGGAGACAG[C/T]TGTACTCTGTGAGAG | 209239 |
rs36778638 | snp | A/G | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117179319 | GGTGTGCTTGGGCTC[A/G]TTCCTTCAGTCCATG | 209239 |
rs36781840 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gan | Mm_Celera | 8:117174385 | GACACTAGCAGTCTC[C/T]GGTCACAGACATCTC | 209239 |
rs36790861 | snp | C/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117180719 | TTTGTTTCTAAGGTT[C/T]ATTTAGTTTTATTTT | 209239 |
rs36791452 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | Gan | Mm_Celera | 8:117205040 | TGGTGCTGTGAGATC[C/G]GAGGGAGGCATACCG | 209239 |
rs36794328 | snp | C/T | 0.5 | 0 | intron-variant | Gan | Mm_Celera | 8:117180051 | GGCCATAGGAGGGAG[C/T]AATTGAGTGTGCTCA | 209239 |
rs36796318 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117200619 | GCACACGGTCCCTGT[G/T]TTGTGTTGCCAGTGT | 209239 |
rs36800459 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Gan | Mm_Celera | 8:117188679 | GGGCTAGCTAGCTGC[G/T]TAGCTGACAGTCCTT | 209239 |
rs36800574 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117189417 | CCATACTTGATGGTT[A/G]GTTGATTAAATCTGT | 209239 |
rs36812647 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117176212 | CCCCGTGGGCCTCAT[C/T]GTCTTCAGGACAGCG | 209239 |
rs36826157 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Gan | Mm_Celera | 8:117189198 | CTGCAGTGAGACCAC[A/C]TAACTGATCACATTA | 209239 |
rs36838490 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117171864 | ATCTCCAGATGCAGT[A/G]TAAACTAAGACATTT | 209239 |
rs36839596 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117189036 | CCAATCACCTGACTG[C/T]GTTGCTTTTGGAGAA | 209239 |
rs36874931 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Gan | Mm_Celera | 8:117189612 | TTTTCTCTGTTGCCC[A/G]AGTTTTACCACACTG | 209239 |
rs36894598 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117177527 | ATCCTTTAAGACGCC[A/G]CTTGCAAACTGCAGG | 209239 |
rs36904600 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gan | Mm_Celera | 8:117171515 | TTGGGTGATTCTTAC[C/T]GTCTTCTGCATTCAG | 209239 |
rs36917920 | snp | G/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117189067 | TAGATTTGGGATGCA[G/T]AGTTGCACTGCTCAC | 209239 |
rs36925223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117190158 | AGACAGGACTGTCAG[A/G]CACGATGGTATCAGC | 209239 |
rs37019688 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117199975 | CCCAGCAGTGGGCAG[C/T]GTTCCCTCCTGGGTC | 209239 |
rs37021080 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Gan | Mm_Celera | 8:117174161 | CAATCACCATGAAAA[G/T]ATGGAGATCATCACA | 209239 |
rs37075569 | snp | C/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117194708 | TGGTTCCCTCCTGTG[C/T]ACCGCTCTCATTTAG | 209239 |
rs37081443 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117201098 | GTTGATCTAGCTGAC[A/G]TCCTCTCTTCATCTT | 209239 |
rs37097665 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gan | GRCm38.p3 | 8:117176616 | GTTCCCACTCCTGTT[A/G]TGTGCTTCAGGTCAG | 209239 |
rs37132192 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117203315 | ACTTACGTGGCACAC[A/G]CCTCTTCCCTAAAAT | 209239 |
rs37175632 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117176482 | TCTGTGGGAGGACAT[C/G]GCCGTCTGAGCACGT | 209239 |
rs37235296 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Gan | Mm_Celera | 8:117204863 | AAGACTCTTAAAAAC[G/T]ATATTCTGATGAACT | 209239 |
rs37267613 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117199927 | GGAACCCACACTCGG[A/G]CTTTGGGGCTGCAGA | 209239 |
rs37272941 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117182131 | TCCCAGGCTGAGGAG[C/T]AGTGTCTTCAGCTCA | 209239 |
rs37275108 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gan | Mm_Celera | 8:117174491 | TTCAGCATCCACCTA[C/T]AGGCTGTAACACCTT | 209239 |
rs37286191 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117203459 | AGTGTGGTAGAACTC[C/T]AGCAACGAGATGTCT | 209239 |
rs37298681 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117175935 | TAATACATGCTGAAT[G/T]CCCACAGTCTCTTTC | 209239 |
rs37310786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gan | GRCm38.p3 | 8:117199595 | AAACACATGTGAATA[C/T]AACATCATCACACAT | 209239 |
rs37328331 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Gan | Mm_Celera | 8:117156344 | TGGCACCTGGAAATC[A/G]TGCCAGGCCACAATA | 209239 |
rs37332902 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117200815 | TCCCTCCACGCAGTT[C/T]ACTTAGGAGAAACGT | 209239 |
rs37333207 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117171797 | CACTCTGCAATTAAA[C/T]GTGCATTTCATGGCT | 209239 |
rs37343574 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gan | GRCm38.p3 | 8:117169662 | AAGAAGTAGCTTGAA[A/G]CTGGAGTGTAGCGCT | 209239 |
rs37350579 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117169330 | GGCCAAACATTTTGC[C/T]CCGTGGCTGAGTATG | 209239 |
rs37380958 | snp | A/C | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117188411 | ACCAATGATGTTTGC[A/C]CTAACCTCAGGCTAG | 209239 |
rs37399120 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117200232 | GCCATAAATTCCTCC[C/T]AAGTCATGGTAAAGA | 209239 |
rs37418054 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117202012 | GTGCAGGACAGTGGA[A/G]AGGCCACGGTGTCCA | 209239 |
rs37428418 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Gan | GRCm38.p3 | 8:117157248 | CAGGGGTGCTTAGTA[C/T]CACAGCCTTGATCTG | 209239 |
rs37438738 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117183986 | ACAGTTTCTTGTAGG[A/G]CATTGCAATGAAAGG | 209239 |
rs37453668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117171480 | CACTGTCACTGGCCC[A/G]AGGCTCTCTGTTGGC | 209239 |
rs37498869 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117171825 | GCTCCACTGAACCTG[A/T]TTTTTGAAGAGCTGT | 209239 |
rs37522928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117199855 | GAGGCTCAGGCACTG[C/T]CAGCCTCCAGTCTCA | 209239 |
rs37526801 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Gan | GRCm38.p3 | 8:117188554 | ACAGTGCTTGCAGGA[G/T]CCAGAATTTGCTTTA | 209239 |
rs37532382 | snp | C/T | 0.32 | 0.24 | intron-variant | Gan | Mm_Celera | 8:117178050 | CAAATGATATGACCT[C/T]AAGTGGGAACTAGAA | 209239 |
rs37548463 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117188583 | TAGCAGCAAGCAGCC[A/G]TAGTTGCCATGCAGT | 209239 |
rs37605246 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Gan | GRCm38.p3 | 8:117203918 | GCTGTACTTCTGATT[G/T]CCTGAGTTATATCTG | 209239 |
rs37609503 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Gan | Mm_Celera | 8:117193062 | TCCTCCTCCTGTAGG[A/G]TCAGAATCAACTCAA | 209239 |
rs37611361 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Gan | GRCm38.p3 | 8:117188966 | CTCAGAGAGTGTTAG[A/C]CTTAGTCCCCATTGA | 209239 |
rs37684304 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117198859 | TGATGGGAAGGAGGG[C/T]GATGCTTTGTTTCTT | 209239 |
rs37712504 | snp | A/G | 0.5 | 0 | synonymous-codon | Gan | Mm_Celera | 8:117187257 | GGGCTGCATAGCGGC[A/G]GAGAACTGCATTGGC | 209239 |
rs37738316 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117191640 | AGGTCTTTGCAGCTC[C/T]GTGTCCGGTGTTTGC | 209239 |
rs37772441 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117200670 | TAGAGTTGCACAGGC[A/G]GGCCTGACACCTAGA | 209239 |
rs37782372 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117194589 | GCCCCTGTGCTAGGA[A/T]TTGTCTGGCTCTGAG | 209239 |
rs37786592 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Gan | Mm_Celera | 8:117193218 | GATGGAGTGTCCTGT[G/T]TGTCCCCTGTGCTTC | 209239 |
rs37869413 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gan | Mm_Celera | 8:117174754 | ACCGGCTGGCTCTCT[A/G]AAGTTCTGTCAGTAC | 209239 |
rs37894602 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117172250 | GAACAGTGGGCAGGT[A/T]TCTTCATCTGTTGTT | 209239 |
rs37906543 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117180581 | CCTTCTTTGAACAGT[A/T]CACTAAGGTGAGAAA | 209239 |
rs37924778 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gan | Mm_Celera | 8:117185701 | GAAAATGTATAGAGT[C/G]TGATAAAATGGTTTT | 209239 |
rs37931325 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gan | GRCm38.p3 | 8:117198184 | TCACTCCAGTGACGT[A/G]TTCAGATCCCCAGGG | 209239 |
rs37939024 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Gan | Mm_Celera | 8:117156471 | CCCAGAAGCACTATG[C/T]GAAAACAGGCCTGCA | 209239 |
rs38005191 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117170658 | ATCCTGGAGTCATGT[C/G]TGTGTGCTTGCTATT | 209239 |
rs38008778 | snp | A/T | 0.231111 | 0.249285 | downstream-variant-500B | Gan | Mm_Celera | 8:117205608 | GGCACACTCGGTTAT[A/T]TCATAGTGTGCAATA | 209239 |
rs38019132 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gan | Mm_Celera | 8:117203342 | AAATCCAGCAGTTCC[A/G]TAAGTCCACCCCAAA | 209239 |