SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6181130 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63404796 | GCCAATCACTGAGCA[A/G]AATTCCCAGCAGAGG | 12143 |
rs6275800 | snp | C/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63404187 | CCTGCCAGGTAAAGT[C/G]AAGGCGAGGATGGTC | 12143 |
rs6324518 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63412922 | CATGCTGTGCTAGAT[A/G]CCTGCTCAGCCTCCT | 12143 |
rs6325648 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413107 | CCTTGCTGCCCAGAG[A/G]NAGCCTCTGAAAACC | 12143 |
rs6325649 | snp | A/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413108 | CTTGCTGCCCAGAGN[A/T]AGCCTCTGAAAACCC | 12143 |
rs6325759 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Blk | Mm_Celera | 14:63413174 | ATAGATGACACCAGC[A/G/T]CAAGAGACCAAACTA | 12143 |
rs6326248 | snp | A/C | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413209 | TTCAGAGCACTTGAC[A/C]GCTCCNATACATACA | 12143 |
rs6326252 | snp | A/C | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413215 | GCACTTGACNGCTCC[A/C]ATACATACAACAGGA | 12143 |
rs6326813 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Blk | Mm_Celera | 14:63413342 | CCTGTATTTATTGTG[C/T]AGACCAGATGTGTCA | 12143 |
rs6328319 | snp | C/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413581 | GTGGTTGTTTGGCAC[C/T]GAGATCTCTGCTTNG | 12143 |
rs6328342 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413595 | CNGAGATCTCTGCTT[A/G]GAGGGAGCTGTGGCT | 12143 |
rs6329052 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413749 | TGTCAAAAATTCGCA[A/G]TGCNACTTCCCCTGT | 12143 |
rs6329056 | snp | C/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413753 | AAAAATTCGCANTGC[C/T]ACTTCCCCTGTCTGT | 12143 |
rs6341904 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413789 | TTCAGAGCCCACAGC[A/G]CAGGCCANGGAGACC | 12143 |
rs6341918 | snp | C/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63413797 | CCACAGCNCAGGCCA[C/T]GGAGACCCTCATGGA | 12143 |
rs6341960 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Blk | Mm_Celera | 14:63413821 | TCATGGAGATCAGCA[C/T]GGTTAGCAGTGACGT | 12143 |
rs6342506 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63413931 | CTTTCGTGCAAGAAT[A/G]GTTTGcgagcctggt | 12143 |
rs6342995 | snp | C/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63414000 | gatggacaagtctct[C/T]gtctgtctgggctac | 12143 |
rs6343537 | snp | A/C | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63414104 | ctagctcagtgcaca[A/C]aattttcctactaag | 12143 |
rs6343581 | snp | C/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63414130 | ctaagtatgagacct[C/T]aggtccaatccctag | 12143 |
rs6344113 | snp | A/G | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63414210 | aaggggggcgagaag[A/G]aagaggagagaaaga | 12143 |
rs13482220 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Blk | Mm_Celera | 14:63380943 | ACTGTGTCTCTTGTC[C/T]CCTCACTCCTGCGGT | 12143 |
rs30389842 | snp | G/T | 0.5 | 0 | intron-variant | Blk | Mm_Celera | 14:63400035 | ACTCATACCATCCCA[G/T]TTGGACACAAGCCCC | 12143 |
rs30785912 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Blk | Mm_Celera | 14:63386539 | AGAGGACACTGGAGA[A/G]CCAGGAGACTAGATT | 12143 |
rs30936895 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63412285 | TCCTCTTAAACTCCC[A/G]TTTGCAGTGAGGTCA | 12143 |
rs30936897 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63412029 | GGGGCCAGCTGACCT[C/T]TTATCTTCATAGTCT | 12143 |
rs30936899 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63411966 | CTTCTAGAAAGTGCT[C/T]AACTTGCAAGAATTC | 12143 |
rs30936901 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63411853 | CCTAGGTCACCATCT[C/T]GTCCTGTCCATATCA | 12143 |
rs30936903 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63411828 | GGCTCTTCCTCCAGT[C/T]TTAACCCTACCTAGG | 12143 |
rs30937815 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63411721 | AGTTGCCCAGCCAAG[A/G]CTACAGGCCAGAGCT | 12143 |
rs30937817 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63411590 | TAACCAGCCTTCACC[A/G]TTTGACCAAAGTGCT | 12143 |
rs30937819 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63411472 | CATCTCAGCGGTGCT[C/T]CCTCCCAGCTCTGGA | 12143 |
rs30937820 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63411304 | TGTTCTCAGCCCTCA[A/C]CTCTATGATGACCCA | 12143 |
rs30937822 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Blk | Mm_Celera | 14:63411124 | GAAGCAGACTCAGCA[A/G]GATCCTGTCCCCAGG | 12143 |
rs30937823 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63411090 | GGAAGGTGACCACAG[A/G]AATAGCCCACAGGGC | 12143 |
rs30938481 | snp | G/T | 0.152778 | 0.230321 | upstream-variant-2KB | Blk | Mm_Celera | 14:63419093 | GACAAAATTGTCAAC[G/T]AAACAAATACAAAGA | 12143 |
rs30938483 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Blk | Mm_Celera | 14:63418921 | CCATGACTCTACACC[A/G]ACCTTCTGATAACAA | 12143 |
rs30938655 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63410774 | ACAAGTGACCTGCCT[C/T]CCTTTTCTGCATTCT | 12143 |
rs30938656 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63410678 | TCATGGCCAGCCCTT[C/T]CTGCTGCTAGAGGAA | 12143 |
rs30938658 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63410527 | CACTAAAGCTACTGA[A/G]AGAGGACTGGATAGG | 12143 |
rs30938659 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63410497 | TCCTCATGAGAGCGT[A/G]AAGTCAGCTACTCCC | 12143 |
rs30938661 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63410476 | GCATCTGCGGTCCTC[A/G]TGGTATCCTCATGAG | 12143 |
rs30938663 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63410469 | TCGCCTGGCATCTGC[C/G]GTCCTCGTGGTATCC | 12143 |
rs30939384 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63380441 | CAAAGACAACATCTG[G/T]CTGAGAATGGAAGAG | 12143 |
rs30939386 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63380440 | ACAAAGACAACATCT[A/G]TCTGAGAATGGAAGA | 12143 |
rs30939388 | snp | A/G | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63380386 | GAGAGCTGGAGTTAA[A/G]AGGACCTAGTGAAAT | 12143 |
rs30939390 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63380352 | TGACTCCCAATATCT[G/T]ATGTATGGCTTGTGT | 12143 |
rs30939392 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Blk | Mm_Celera | 14:63380318 | TTCTGTTTGCAAAGA[C/T]CCTGGAGCTCCTGGC | 12143 |
rs30939444 | snp | A/C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Blk | GRCm38.p3 | 14:63418338 | CTGAGGCTGGGAGAA[A/C/T]ACGAAGGGATGACAT | 12143 |
rs30939445 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Blk | Mm_Celera | 14:63418287 | TTCTCAGACCTTGAA[C/T]AGAGAATGTTTGGAC | 12143 |
rs30939447 | snp | C/G | 0.142012 | 0.225474 | upstream-variant-2KB | Blk | Mm_Celera | 14:63417757 | CACAGCTCATGATCT[C/G]TACCCATATGGAGCA | 12143 |
rs30939449 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Blk | Mm_Celera | 14:63417633 | CCCAGAAGACATCAT[G/T]GACCACCGATCACCT | 12143 |
rs30939451 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Blk | Mm_Celera | 14:63417411 | TTGATGCTCAGTACA[C/T]ACAAATCCCTCCATG | 12143 |
rs30939453 | snp | C/T | 0.142012 | 0.225474 | utr-variant-5-prime | Blk | Mm_Celera | 14:63417067 | CTGGCTCCTCAGCCC[C/T]GGAGGTGTTTCTGAG | 12143 |
rs30939515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63385490 | GGACACTTTTCAGAT[A/G]ATCATTGTTTGACAC | 12143 |
rs30939517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63385483 | GCATGCTGGACACTT[C/T]TCAGATGATCATTGT | 12143 |
rs30939519 | snp | C/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63385443 | AGGATGTTGACAAGC[C/T]GGTGAGGCAGTAGAA | 12143 |
rs30939520 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Blk | Mm_Celera | 14:63385274 | GAATCCAACTTGCCT[C/T]TGAAGTATCCCCTCA | 12143 |
rs30939522 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Blk | GRCm38.p3 | 14:63385260 | CAGTAGCTGATCCTG[A/C/T]ATCCAACTTGCCTCT | 12143 |
rs30939523 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63385152 | ATCTTCCTTTCAGAA[C/T]TAAGGCCTAGACAAA | 12143 |
rs30939625 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Blk | Mm_Celera | 14:63410386 | GAAATGGCTTGTCTG[C/T]GGTGACTGATGAGTG | 12143 |
rs30939627 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63409652 | TCGTTTTTGAACCAC[A/C]GCTCTCTGTGTAATG | 12143 |
rs30939629 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63409620 | GCAGCTCAGATTAAC[G/T]TTGCCTGTGTGCTAT | 12143 |
rs30939631 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63409481 | AAACTCTCAGCCACC[A/G]TCGTCACCGCTTACA | 12143 |
rs30939633 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63409435 | ACTGGCCAGCAAATA[A/T]GGTTGTCAGGGAGCC | 12143 |
rs30940244 | snp | C/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63380293 | ACAGTCACACACCAG[C/T]AAATGTGACTTCTGT | 12143 |
rs30940246 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63380151 | GGCATCAGAATGGAA[A/C]TTTGAGACATGGACC | 12143 |
rs30940248 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63380128 | GATAAAGGTGTGAGG[C/T]TCCAGGAGGCATCAG | 12143 |
rs30940250 | snp | C/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63380064 | AATGGCCGGGGCTTG[C/T]TCTTCCTATGGGTGC | 12143 |
rs30940252 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63379999 | CTCAGGATGTGTTGG[G/T]GTTCATGCAGTCTGG | 12143 |
rs30940253 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63379974 | GTCTCTGAGAACCCC[A/G]CAACAGAGCCTCAGG | 12143 |
rs30940325 | snp | C/T | 0.244898 | 0.249948 | utr-variant-5-prime | Blk | Mm_Celera | 14:63416999 | CGCCATGAACAGCCC[C/T]AAGAAGCAGCTCAGT | 12143 |
rs30940327 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63416630 | ACAGTAGGATGCCTT[A/C]TTCATAGCTGTAGGA | 12143 |
rs30940329 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63416582 | ACCCTAGGTGGGTGA[A/G]CTTTTATAAATTCAA | 12143 |
rs30940331 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63416440 | TTACTTTCCTTTCTA[A/G]CAGGCTGGGGAACTT | 12143 |
rs30940333 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63416344 | CATTAAAAACCAGAG[A/T]ATCGAGAGTAATCAC | 12143 |
rs30940534 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63385111 | ACAGCCACTCTAGGA[A/G]TAGGCCGACCCTCAT | 12143 |
rs30940535 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63385088 | TCTCAGGAAGTGACA[C/T]CAGACCCACAGCCAC | 12143 |
rs30940537 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Blk | Mm_Celera | 14:63384898 | CCTGTCATTCACAGC[A/G]GCATAGTCAAACAGA | 12143 |
rs30940539 | snp | A/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63384829 | TGGGGACAGGATGCT[A/T]GAAATTTACCTCCTC | 12143 |
rs30940541 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63384647 | AGAAGGCCAGACGTG[A/G]AAACCACCTTACCAG | 12143 |
rs30940542 | snp | C/T | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63384610 | ATCCAGGGAGGTGTC[C/T]CGTTAGATTTTAACA | 12143 |
rs30940585 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Blk | Mm_Celera | 14:63409349 | CCAAAGCTCTAGGGG[C/T]TGTTTCCTTATGAGT | 12143 |
rs30940587 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63408825 | ATAAACATGCCAGTT[C/T]TAAAAGGTGACTGAT | 12143 |
rs30940589 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63408438 | TTTAGTCTAAAAAAA[C/T]GCCAACATGTTCTCT | 12143 |
rs30940591 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63408306 | CCCTTCACTCTTAGC[C/T]GATAACATTTTGGGC | 12143 |
rs30940593 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63408186 | GAAAAGGAAAGAACC[A/G]ATGCTGGCATCAGGA | 12143 |
rs30941035 | snp | A/G | 0.32 | 0.24 | intron-variant | Blk | Mm_Celera | 14:63379947 | TTCATATCTTGTATA[A/G]GATGCCAGTTTGTCT | 12143 |
rs30941037 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Blk | Mm_Celera | 14:63379823 | AGGGCGGGAGAGTGA[A/T]GGAGCCATTCAGATG | 12143 |
rs30941039 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Blk | Mm_Celera | 14:63379704 | GCCTCTCATGCTGCA[A/G]GGTTTTCATCACGTT | 12143 |
rs30941041 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Blk | Mm_Celera | 14:63379675 | TCTGGTGACCACAGC[A/G]TAGAGACGAACCAGC | 12143 |
rs30941043 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Blk | Mm_Celera | 14:63379645 | CATGTATTCAGTGAC[A/G]ATGTAAATGGGCTCT | 12143 |
rs30941244 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63416317 | CATAATACCCAAAAA[G/T]CCAAATAATTTCATT | 12143 |
rs30941246 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63415674 | GTAAGGATGAAATCA[A/G]TGACCAATTACAAAG | 12143 |
rs30941248 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63415235 | ACACCAGAACTAATA[A/C]ACTAATACTGGCACA | 12143 |
rs30941250 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Blk | Mm_Celera | 14:63414842 | CCGCTGCCTCTTTCT[C/T]TGCCTCCTGTCTCCT | 12143 |
rs30941252 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Blk | Mm_Celera | 14:63414679 | TTCCTCTCCAGCTTC[G/T]GAGGCATCGATGATC | 12143 |
rs30941384 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Blk | Mm_Celera | 14:63384405 | AAAGCTGTGTAGAAT[C/T]TAAGATCAGGGCACT | 12143 |
rs30941386 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Blk | Mm_Celera | 14:63384238 | AGTGCAGAGGAAGGG[C/T]AGATTTGCTTGTATA | 12143 |
rs30941388 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Blk | Mm_Celera | 14:63384217 | GTGACAGGCAGAAGG[A/G]GTCATAGTGCAGAGG | 12143 |