SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs46897151 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089331 | TGTCCGGATTGTGGG[C/T]GGCACCTTCTGGTAG | 432649 |
rs47278267 | snp | C/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091407 | TGATGTAATGACTTG[C/T]TCCATGTGACTGGCG | 432649 |
rs47534500 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088725 | GGTAATAGACTTATG[C/T]AAACTGATGCTCTGG | 432649 |
rs47745437 | snp | C/G/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089321 | TGAGAAGCCCTGTCC[C/G/T]GATTGTGGGTGGCAC | 432649 |
rs48226144 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091168 | CCTAGTCCTGCGACC[A/G]TGCTGTCCTGAAGAA | 432649 |
rs48233167 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089740 | TCTTATCCTGGCGTC[A/G]GGGAGGATTAGCCAC | 432649 |
rs48449324 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089305 | CTGGTCTTGATTGAT[A/G]TGAGAAGCCCTGTCC | 432649 |
rs49221716 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089023 | TATCAGTTAAAAGCA[C/T]TGGTTCCTCTTGCAG | 432649 |
rs49262507 | snp | C/T | | | upstream-variant-2KB | Gm5434 | GRCm38.p3 | 12:36088768 | TCTTCCTGGCTATTT[C/T]CCCCCCCCCCCCCCC | 432649 |
rs49332198 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091199 | GATCCTCCTGACTGC[C/T]CACTGTAGGTGGCGA | 432649 |
rs49339694 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090994 | GCAGGACAAGGAGGA[C/T]TTTCGGGACAAAGTG | 432649 |
rs49393179 | snp | C/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091187 | TGTCCTGAAGAAGAT[C/G]CTCCTGACTGCCCAC | 432649 |
rs49662945 | snp | C/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091395 | GTCCTGCACAGGTGA[C/T]GTAATGACTTGTTCC | 432649 |
rs49998835 | snp | A/C | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091011 | TTCGGGACAAAGTGG[A/C]TGAATACATCAGACG | 432649 |
rs50904288 | snp | C/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091485 | TCTTAGCTTCTTCCA[C/G]GAACGCTGACCGAAC | 432649 |
rs51187317 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091329 | CTCCGAAGTTGTAAC[A/G]AACTCACCCCTGAGG | 432649 |
rs51235083 | snp | A/G | | | utr-variant-3-prime, intron-variant | Bzw2, Gm5434 | GRCm38.p3 | 12:36091989 | TAAAAAAAGGGGTGT[A/G]CTGAGTTTTGAGCTT | 432649 |
rs51510995 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089203 | CTCCCCCTCCCTCTC[A/G]GAATATCACATTGAG | 432649 |
rs51641043 | snp | C/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090854 | CTAAGAGAACATTCC[C/G]CTGATGGCACTGGCT | 432649 |
rs51805905 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090981 | CAGAACATCATTTGC[A/G]GGACAAGGAGGATTT | 432649 |
rs51889249 | snp | A/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091149 | GTCAGCCCCTTGGGA[A/T]TGTCCTAGTCCTGCG | 432649 |
rs51953073 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091186 | CTGTCCTGAAGAAGA[C/T]CCTCCTGACTGCCCA | 432649 |
rs52009749 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089375 | AAAAGGCTGCTGAGT[A/G]GATTTGTGCCAACCC | 432649 |
rs107594952 | snp | G/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091470 | ATGGGATGCACACTC[G/T]CTTAGCTTCTTCCAG | 432649 |
rs107623995 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090907 | GGATGTCGTTTGGGG[A/G]TTAAACTCTTTATTT | 432649 |
rs107766701 | snp | C/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091456 | CGCTATAAACAGTGA[C/T]GGGATGCACACTCTC | 432649 |
rs108017670 | snp | A/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091598 | TTTGGRACAGATTTG[A/T]AATTTGTACCAAAAA | 432649 |
rs108038610 | snp | G/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091541 | AGTCACTTACTGTAG[G/T]AGATCTTACTGAAAT | 432649 |
rs108071331 | snp | A/C | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091232 | ATTATASAGCAAGAA[A/C]GTGTGTCTGGGTCTC | 432649 |
rs108094727 | snp | C/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091622 | CCAAAAAAWTGTAAC[C/T]GTTTAATGTTTGGAT | 432649 |
rs108115320 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090812 | CACCCCAACATCACA[A/G]AAACGGGGGAAATAT | 432649 |
rs108158370 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091258 | GTCTCGAGAGAGGTG[C/T]CTGCTTCCCTTAACG | 432649 |
rs108167825 | snp | G/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091497 | CCAGGAACGCTGACC[G/T]AACCTAAATGTGACA | 432649 |
rs108235069 | snp | A/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091512 | GAACCTAAATGTGAC[A/G]CTTCCCAGAATGCAG | 432649 |
rs108244436 | snp | A/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091615 | ATTTGTACCAAAAAA[A/T]TGTAACYGTTTAATG | 432649 |
rs108261745 | snp | G/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091457 | GCTATAAACAGTGAT[G/T]GGATGCACACTCTCT | 432649 |
rs108304804 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090509 | GCAAGCAAGTTGAAG[C/T]GGGATGAAGATCTCA | 432649 |
rs108322053 | snp | A/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091164 | TTGTCCYAGTCCTGC[A/G]ACCGTGCTGTYCTGA | 432649 |
rs108338102 | snp | A/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091713 | GGGGCCCATGAGATG[A/G]CTTAGCAGGTAAAAG | 432649 |
rs108341278 | snp | C/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091175 | CTGCRACCGTGCTGT[C/T]CTGAAGAAGAYCCTC | 432649 |
rs108370714 | snp | A/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091192 | TGAAGAAGAYCCTCC[A/T]GACTGCYCACTGTAG | 432649 |
rs108393628 | snp | C/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091223 | GTGGCGAACATTATA[C/G]AGCAAGAAMGTGTGT | 432649 |
rs108400622 | snp | G/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091524 | GACACTTCCCAGAAT[G/T]CAGTCACTTACTGTA | 432649 |
rs108479520 | snp | C/T | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091781 | CCCAGGCCTGTTCTC[C/T]CAGACCCCACAACAC | 432649 |
rs108500075 | snp | A/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090721 | CTACCAGGGTGGAAA[A/T]TTTCAGTTTGAAATT | 432649 |
rs108850937 | snp | A/C | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | GRCm38.p3 | 12:36091759 | TGGGAACCCTCTGAC[A/C]GCCATGCCCAGGCCT | 432649 |
rs108919115 | snp | A/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091588 | GTGAGTATATTTTGG[A/G]ACAGATTTGAAATTT | 432649 |
rs212230801 | snp | G/T | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36091255 | TGGGTCTCGAGAGAG[G/T]TGTCTGCTTCCCTTA | 432649 |
rs212321400 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089390 | GGATTTGTGCCAACC[C/T]CGCTGCCGATTCCTT | 432649 |
rs212386097 | snp | A/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090047 | CAGAACAGAACTGTA[A/T]GTTTACTTCTTTAAC | 432649 |
rs212880428 | snp | A/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091792 | TCTCCCAGACCCCAC[A/G]ACACACTATGCTAAT | 432649 |
rs213788273 | snp | A/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088475 | TAACACTTGTCAAAT[A/T]TGTTGACCAAATTTA | 432649 |
rs214265917 | in-del | -/A | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091609 | TTTGAAATTTGTACC[-/A]AAAAAATGTAACCGT | 432649 |
rs214327307 | in-del | -/CT | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089176 | TGAAACTCCCATACA[-/CT]CACACACAACTCTCC | 432649 |
rs215049991 | snp | A/T | | | utr-variant-3-prime, intron-variant | Bzw2, Gm5434 | Mm_Celera | 12:36092244 | AGTGTGGCGTTTTAA[A/T]TTTTTTTTTCTTTTT | 432649 |
rs215383358 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090152 | AAAAGAATGGAGTAA[A/G]GTTGTTTTTCCCTCA | 432649 |
rs216349295 | in-del | -/CCCCCCC | | | upstream-variant-2KB | Gm5434 | GRCm38.p3 | 12:36088768 | TCTTCCTGGCTATTT[-/CCCCCCC]CCCCCCCCCCAAAGG | 432649 |
rs216720126 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090295 | TGTAATACTGGGATT[A/G]TAGGTTTGAGTGACC | 432649 |
rs217167669 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088386 | TCCAAAATGTTTTTA[A/G]AATCCGTGTATTGGA | 432649 |
rs217178738 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088541 | GTAGCCCAGGCTGGC[C/T]TCAAATTCACAATTC | 432649 |
rs217646233 | in-del | -/G | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091696 | AACCAACCAACCTCT[-/G]GGGGGCCCATGAGAT | 432649 |
rs217845353 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089825 | ACCTTCCCATGGCCT[C/T]GACAGCAAGAGAACT | 432649 |
rs217900000 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090362 | GCAGACTTCCGGTTC[C/T]GCCGCCGAGAGCCAG | 432649 |
rs220069973 | in-del | -/AC | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089173 | AGGTGAAACTCCCAT[-/AC]ACACACACACAACTC | 432649 |
rs221387912 | snp | A/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089008 | GCAGCTGAGATGACT[A/T]ATCAGTTAAAAGCAT | 432649 |
rs221427296 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089737 | TTTTCTTATCCTGGC[C/G]TCGGGGAGGATTAGC | 432649 |
rs222290435 | in-del | -/AATTAG | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089258 | TTAATGGTGGTGACA[-/AATTAG]AATCACCTGAGTAGG | 432649 |
rs222898625 | snp | C/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090396 | GGCTCTGAAGGGCTG[C/G]GCAACTCGGTGCCGC | 432649 |
rs223251396 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088442 | GAAGCATGCCTGCTA[C/T]GAATCCTAACTAGCA | 432649 |
rs223312660 | snp | A/C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089185 | CCATACACACACACA[A/C/G]CTCTCCCCCTCCCTC | 432649 |
rs223399613 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Bzw2, Gm5434 | Mm_Celera | 12:36092241 | AAAGTGTGGCGTTTT[-/A]AATTTTTTTTTTCTT | 432649 |
rs223576369 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089577 | CAAGTGTGATTTGGC[C/T]CTGGCTACCATTTGG | 432649 |
rs225577420 | in-del | -/AG | | | upstream-variant-2KB | Gm5434 | GRCm38.p3 | 12:36089655 | CATCCCCTTGGATCT[-/AG]GTTCTTCTAGGTGAT | 432649 |
rs226240034 | in-del | -/TCCTGA | | | cds-indel | Gm5434 | Mm_Celera | 12:36090449 | GTGCCGGCTCACCTC[-/TCCTGA]TTCGTGGTGCTCAGA | 432649 |
rs227239890 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088783 | CCCCCCCCCCCCCCC[C/T]CAAAGGACAATCTAA | 432649 |
rs228771249 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088683 | ATCATTTAAGTTCTC[C/T]TTTTCACGTAGGTGG | 432649 |
rs228875928 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090034 | AGGAAAACAGAGGCA[C/G]AACAGAACTGTAAGT | 432649 |
rs229574252 | snp | A/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090055 | AACTGTAAGTTTACT[A/T]CTTTAACAGCTGTTA | 432649 |
rs230670528 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089967 | CAATATATACAAATA[C/G]AAATAGATCCTTTAG | 432649 |
rs230909220 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089507 | CAGCTGCTCTGGAAC[C/G]ACTCCAGTTGTTGAC | 432649 |
rs231658621 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091975 | CCTGAAAATACAGCT[-/A]AAAAAAGGGGTGTAC | 432649 |
rs231949472 | in-del | -/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090816 | CAACATCACAGAAAC[-/G]GGGGGAAATATGTCT | 432649 |
rs234325514 | snp | A/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090338 | AGTAGTTTTTAATAG[A/G]TAAGAAATGCAGACT | 432649 |
rs235824155 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088593 | GCTGAGAGTAGCATG[C/T]GCCACTATGTTGTTT | 432649 |
rs237291301 | snp | C/T | | | utr-variant-3-prime, intron-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091932 | AGTGGCCCTGTAACA[C/T]AGACACCAGTGGGGC | 432649 |
rs238021947 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36090208 | TCTTACACTTAACTC[C/G]AAGCTAGCCTGAAGC | 432649 |
rs238084741 | in-del | -/TTATTATTA | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088487 | ATATGTTGACCAAAT[-/TTATTATTA]TTATTATTATTATTA | 432649 |
rs240072642 | snp | G/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089668 | CTAGGTTCTTCTAGG[G/T]GATGTGATTGAAGCA | 432649 |
rs241982872 | snp | A/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089887 | TCCCAAATGGTCAGA[A/T]GCATTTCAATGCTAC | 432649 |
rs242781090 | snp | C/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088456 | ACGAATCCTAACTAG[C/T]AGTTAACACTTGTCA | 432649 |
rs243454616 | in-del | -/TCCCC | | | upstream-variant-2KB | Gm5434 | GRCm38.p3 | 12:36088767 | TTCTTCCTGGCTATT[-/TCCCC]CCCCCCCCCCCCCAA | 432649 |
rs243663346 | in-del | -/A | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089631 | ATCTATAGCATACAT[-/A]TATATTTTCATCCCC | 432649 |
rs244145239 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088884 | CCTGGGACCCACATT[C/G]GTGAAAGGAGAGGCC | 432649 |
rs244398534 | in-del | -/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089451 | TTCTGGATCCACCTT[-/G]TAGACTAAATGACTA | 432649 |
rs244610467 | in-del | -/ATGGGAACCCTCTGACCGCC | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091743 | GTACTGGAGAAGAGA[-/ATGGGAACCCTCTGACCGCC]ATGCCCAGGCCTGTT | 432649 |
rs244813237 | in-del | -/AA | | | intron-variant, nc-transcript-variant | Bzw2, Gm5434 | Mm_Celera | 12:36091641 | AATGTTTGGATAGGG[-/AA]AAAAAAATGATGACA | 432649 |
rs244885997 | snp | A/C | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090409 | TGCGCAACTCGGTGC[A/C]GCTGCTCGCCGGGCA | 432649 |
rs244895426 | snp | C/G | | | nc-transcript-variant | Gm5434 | Mm_Celera | 12:36090385 | AGAGCCAGTGCGGCT[C/G]TGAAGGGCTGCGCAA | 432649 |
rs248072570 | snp | A/G/T | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36088476 | AACACTTGTCAAATA[A/G/T]GTTGACCAAATTTAT | 432649 |
rs249074397 | snp | C/G | | | upstream-variant-2KB | Gm5434 | Mm_Celera | 12:36089388 | GTGGATTTGTGCCAA[C/G]CCCGCTGCCGATTCC | 432649 |