SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31097134 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078345 | ATTAAAGGCGTGCGC[C/T]ACCACGCCCGGCTGT | 66394 |
rs31153364 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45071539 | TTGGAGCTTTGCTTT[C/G]TTTGAAGAACACAGA | 66394 |
rs31158750 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064318 | CACCCCCAGTTCTTG[A/G]CAGTCTCTAAACTCG | 66394 |
rs31179735 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nosip | Mm_Celera | 7:45069516 | TTGTGAGCCACCATG[C/T]CAGTGCTGGAAGTTG | 66394 |
rs31207243 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45064811 | TTGTTTTTGAGCAGG[G/T]TTTCTCTGTGCAGAC | 66394 |
rs31237463 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Nosip | Mm_Celera | 7:45066730 | GCTTAGACTTACAGT[A/C]CCTCTGAGAAAATGA | 66394 |
rs31336198 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070563 | TCTGAGACAGGGTCT[C/T]TCTCAGTTCTTACTG | 66394 |
rs31345396 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Nosip | Mm_Celera | 7:45070778 | AGAGGATTCCACCCC[A/T]TTGGGCCCTGCCTAC | 66394 |
rs31377748 | snp | C/G | 0.5 | 0 | intron-variant | Nosip | Mm_Celera | 7:45067124 | AGAGTCTTGGGGAAA[C/G]GGTGGTAAGGTGCTA | 66394 |
rs31383397 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Nosip | Mm_Celera | 7:45066880 | CTCAAATAGGAAACA[A/G]ACTTTTTTTTTATAA | 66394 |
rs31388296 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070120 | GGGCATCAGATCCCA[A/T]TGCAGATGGTTATGA | 66394 |
rs31432176 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45066891 | AACAAACTTTTTTTT[A/T]ATAATTTAAGTGACT | 66394 |
rs31441324 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061077 | CTCTGCCTCCCAAGC[A/G]CTGGGATTAAAGGTG | 66394 |
rs31486074 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070763 | GATAGAGGGAGGGAG[A/G]GAGGATTCCACCCCT | 66394 |
rs31525488 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062954 | TCTAGAACTCGCTAT[A/G]TAGTTAGCCTCAAAC | 66394 |
rs31591839 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070043 | TAAATCTTTTTTTTT[A/T]AAGATTTATTTATTT | 66394 |
rs31598675 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063660 | GCACTGTCTACAGAG[C/G]CCAGAAGGCCATTAG | 66394 |
rs31653574 | snp | A/G | 0.375 | 0.216506 | intron-variant, missense | Nosip | Mm_Celera | 7:45076237 | AACACAGGTGACAAG[A/G]AATACCTGCCCTTGG | 66394 |
rs31689137 | snp | A/C | 0.375 | 0.216506 | synonymous-codon | Nosip | Mm_Celera | 7:45077320 | TCTCTAGGGCGGCAC[A/C]GGCTTTGCGGGCTCC | 66394 |
rs31701846 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062971 | AGTTAGCCTCAAACT[A/C]ACAAAGATCCGCCAA | 66394 |
rs31706287 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077838 | ACCCTCATCCCTGCC[G/T]CCAAGTAAAAATAGC | 66394 |
rs31711374 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063085 | GTTTTTGTTTTTTGG[C/T]TTTTCGAGACAGGGT | 66394 |
rs31730498 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45075886 | GGAGGAGGACTGGGT[C/T]CCATATTGAGTAGGA | 66394 |
rs31760746 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Nosip | Mm_Celera | 7:45070444 | ATACATGTAGAGAGC[A/G]GACAATTCTTCCATG | 66394 |
rs31762319 | snp | A/G | 0.265928 | 0.249492 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077524 | CCAGGCAGAAACCCC[A/G]GCGTGAACCTGTGGG | 66394 |
rs31769138 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45064923 | GGTGAAAGCTATGTA[C/T]CATGCCTGGCTGTAC | 66394 |
rs31769310 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Nosip | Mm_Celera | 7:45071413 | AAATCAGGTTAAAAT[A/G]GGAACCAATGAAAAT | 66394 |
rs31776630 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nosip | Mm_Celera | 7:45065912 | AGTCACGTGTGGGGA[A/G]CAGGTTCCCTACCGT | 66394 |
rs31783193 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064425 | TTATGGCCTGTTTGC[A/G]GATGAACAGTCTGTT | 66394 |
rs31815415 | snp | A/T | 0.255 | 0.24995 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063855 | TTTCTTGAGATGCAC[A/T]ACCTGGTACTGAAAT | 66394 |
rs31840602 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nosip | Mm_Celera | 7:45071505 | TGTATGTATGTGTTT[C/T]ACATGGGTAGTGACA | 66394 |
rs31894656 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Nosip | Mm_Celera | 7:45064979 | CACCTTCCTAACTGA[G/T]CTGGGCCGCAGGCTT | 66394 |
rs31901058 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45069712 | TTGGCACCAGGCACA[C/T]ATGTTGTGTATAGAC | 66394 |
rs31935039 | snp | A/G | 0.255 | 0.24995 | intron-variant | Nosip | Mm_Celera | 7:45076435 | GAAAAGCCGGTGAGG[A/G]CCCAATGTCCAGGAT | 66394 |
rs32029051 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070234 | TGGCTCCAAAGTTAA[A/T]TACACCGGGCTTGGT | 66394 |
rs32058838 | snp | A/G | 0.32 | 0.24 | intron-variant | Nosip | Mm_Celera | 7:45076477 | CAGTCCGTTCTCCCC[A/G]CCCCTCATGCCCCTT | 66394 |
rs32076582 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nosip | Mm_Celera | 7:45066943 | CTGTGAGTTGTGGCT[A/G]AAGCCCCTGCAGCTC | 66394 |
rs32092666 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nosip | Mm_Celera | 7:45066784 | AGTCCTGTCTTCGCA[A/G]CCCTTAGAAGGCTGA | 66394 |
rs32101165 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45067326 | TGTGGCTCAGAGGCA[A/G]AGCCCCTAGAATCCT | 66394 |
rs32156322 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Nosip | Mm_Celera | 7:45066201 | TTCTTCTCTCCTGTG[G/T]TGGTCTCCTCTGACT | 66394 |
rs32176447 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070469 | TCCATGGCACAGGAG[A/G]TTGAACTCAGGTTAT | 66394 |
rs32203984 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077387 | ATGCAGGCCTGAGCC[G/T]TGGCCTAATAAACGT | 66394 |
rs32233831 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070353 | GAGGCCAGCCTAGCC[C/T]TTTTGAGACCTGTTG | 66394 |
rs32279047 | snp | A/G | 0.255 | 0.24995 | intron-variant | Nosip | Mm_Celera | 7:45065859 | GCTGGTTAGCTTTTG[A/G]TGGTAGACTGACAAT | 66394 |
rs32295611 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45069723 | CACACATGTTGTGTA[C/T]AGACATCCATGCAGG | 66394 |
rs32321721 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45075935 | CAGGGCCACCTTAGC[A/G]AAAGAACACGAAAGT | 66394 |
rs32369475 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime | Nosip, Prrg2 | Mm_Celera | 7:45062414 | GCGACTAGGGGCAGA[A/G]TTATTTCCGGTCTCC | 66394 |
rs32381615 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077479 | TGCGGTGTGGGCCTG[A/G]GCTCCTGGGATTTAC | 66394 |
rs32382775 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nosip | Mm_Celera | 7:45071232 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGACAG | 66394 |
rs32397927 | snp | C/T | 0.387812 | 0.208586 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062663 | AGCGCTCTTGAACGC[C/T]TAGGTTGGAAGACGA | 66394 |
rs32401407 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077839 | CCCTCATCCCTGCCT[C/G]CAAGTAAAAATAGCT | 66394 |
rs32440945 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nosip | Mm_Celera | 7:45070369 | TTTTGAGACCTGTTG[C/T]GGAAACCATTGGGTG | 66394 |
rs32444111 | snp | C/T | 0.32 | 0.24 | intron-variant | Nosip | Mm_Celera | 7:45071647 | ATGATTTGCCTTGTG[C/T]CCTAGCAGAGGTGTA | 66394 |
rs36243007 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45073632 | TGGCTTTCTAATTCT[A/G]CCCTGTTGTCCTGTT | 66394 |
rs36262509 | snp | G/T | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062494 | TTCCGGTTCGGGACG[G/T]AGTTGAAGCAACGAC | 66394 |
rs36266967 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45075971 | CAACTGTTGCCAGTT[A/C]TGCCAGAGCTGCCCA | 66394 |
rs36275742 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075313 | GGCACCCGGGCTTCA[C/T]AGGCCAAGCACCTGC | 66394 |
rs36301613 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nosip | Mm_Celera | 7:45074184 | CAGGCAGCTCACCTC[C/T]ACCACAGGTGCAGTT | 66394 |
rs36331368 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Nosip | Mm_Celera | 7:45076173 | GAAGGAGGCGGCCAT[C/T]GTGAGCCGGCCCCTC | 66394 |
rs36351829 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064291 | CCACATTCTTTGCCA[C/T]TTAGTCTTTCTCACC | 66394 |
rs36395487 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075146 | CCTGTGCTTGGTCTT[A/C]CGCTGTACAATGGCC | 66394 |
rs36428750 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nosip | Mm_Celera | 7:45068925 | CCATGCCCGTGAAAC[A/G]GGAACTTCATCTTGA | 66394 |
rs36429432 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45067790 | GAGGAGACATATAGG[A/T]GAGTGTGACTGTGGC | 66394 |
rs36431943 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063315 | TTAAGATTTATTAGC[C/T]GGGCAGTGGCAAAAA | 66394 |
rs36480189 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nosip | Mm_Celera | 7:45066704 | GTCATCACCACCACT[A/G]TGTTACCCAAGCTTA | 66394 |
rs36508521 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45068515 | GTGGACATAAATTGA[C/G]TACACTCCGTAGATG | 66394 |
rs36543664 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078704 | CAGATGTCCACCTGC[C/G]GCCACTAGAGGGCAG | 66394 |
rs36566831 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45068846 | TTTTATTTCTTGTTG[C/T]GCTCTGCTAGAATTC | 66394 |
rs36624351 | snp | A/C | 0.244898 | 0.249948 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078960 | CACACAGGGACACAC[A/C]AAATACAGATGTTAC | 66394 |
rs36643967 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45067011 | CCAGTCTCCATAGGC[C/T]TCTCTCTCAGTGGCA | 66394 |
rs36646969 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45066515 | AATTATCCAGGTGGT[A/T]ACAGCTTGTTTTTTC | 66394 |
rs36676612 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075492 | ACCTCAGCTGGGTGA[C/T]CCAGGGAGTCTCCAG | 66394 |
rs36680693 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nosip | Mm_Celera | 7:45076963 | ACCGCAGCCCTCACC[A/G]CAGCCCGCACCCCAT | 66394 |
rs36726102 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nosip | Mm_Celera | 7:45074443 | AAAGAGAGGACTGAA[A/G]GGAGTGCTGTGAAGA | 66394 |
rs36774951 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075185 | GAAGCTAGAGGGTGC[A/G]CAGAGCAAGTGCAAG | 66394 |
rs36778793 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45070969 | TCTCACTAAGTTACT[C/T]AGGCCAGGACACTAA | 66394 |
rs36786690 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078406 | CACTGGCCATGCAGT[A/G]ATGAGAAGATGTGTT | 66394 |
rs36801561 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45067537 | CACCACAAGTCAAGG[A/G]CACATCAATCAATTG | 66394 |
rs37000550 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078597 | TGGGTCTTTCCTGTG[C/T]GCGTAGTTTGCTGCT | 66394 |
rs37004280 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45066356 | GCAACAGACCAAACC[A/T]CGGCTAGTTGGCTTC | 66394 |
rs37082874 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45068401 | CTCAGTATTGAGTCT[A/G]TGTAAATGTACTGAA | 66394 |
rs37125465 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45074854 | GGCAGGGCAGTTTCT[A/G]CAATGGTGGCGTCTG | 66394 |
rs37162593 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nosip | Mm_Celera | 7:45073372 | GACTGCTGTGGTTTA[A/G]GGCTGTGTTTTCGGC | 66394 |
rs37179324 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45077092 | GTTGGCTCTTCTATG[A/G]CACTGTTTTCTTTCT | 66394 |
rs37190410 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | GRCm38.p3 | 7:45071132 | TGGAAGAGCAGTGAC[C/T]GCTGGAAGAGCAGTC | 66394 |
rs37209184 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45069865 | CTGGAGGTGGCTAGC[C/T]CAGCTGGTCCTTGCT | 66394 |
rs37233658 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45076803 | GGGGCTGACTTTTGG[C/T]ACTGTCTTCCACTGT | 66394 |
rs37237238 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45073070 | TGCAGTTCCGCATGC[A/G]CACACTTGCCTAGCA | 66394 |
rs37257687 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45073404 | ACCTGAACAGGCTTC[A/T]GGAGCAGGCTACTGA | 66394 |
rs37296873 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078718 | CGGCCACTAGAGGGC[A/G]GAACGTCACTGCCGA | 66394 |
rs37318155 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078553 | TTTCACTGCCCTTGT[C/T]GCACATTACCGGAGT | 66394 |
rs37327208 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45067761 | GCCTCAACGTCCTGG[A/G]CAAAGGAGACCCTGA | 66394 |
rs37387748 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45075101 | CCAGGCACTTAGCAG[A/G]GGCTTGAGATGTAAA | 66394 |
rs37403962 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063252 | TTTTGAGGCAAGGTG[A/G]CATGTAGTCCAGGCT | 66394 |
rs37460934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45069893 | GCTTGGTGACAGTCA[C/T]AGGAAACCCTGTGGT | 66394 |
rs37486489 | snp | A/C | 0.391111 | 0.206368 | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077441 | GCGCCTCATTGTAGG[A/C]CCGGCGACAGAAGGA | 66394 |
rs37598419 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Nosip | Mm_Celera | 7:45074034 | CCGGGACGCTGTGAA[A/G]GACTTTGACTGCTGC | 66394 |
rs37634098 | snp | A/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062699 | ATTTCCCAGGATGCC[A/T]TGTACTGTCTCCCTC | 66394 |
rs37753649 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Nosip | Mm_Celera | 7:45074937 | AGCATCCGCATAGAC[C/G]TCCTGCGGGCCAGGC | 66394 |
rs37755133 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45069291 | GCCCTGAGTCACTCC[C/T]TTCCGTTGTTTGTTT | 66394 |
rs37785325 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45068918 | TTCCTTTCCATGCCC[A/G]TGAAACGGGAACTTC | 66394 |
rs37805698 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078766 | AAACAGGCTGGGGCT[A/G]AGAGTCCACAGACTG | 66394 |
rs37859254 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nosip | Mm_Celera | 7:45073040 | AGAGATGAGAAACAT[A/G]GGGAAGGCTGGGGAT | 66394 |
rs37881924 | snp | C/T | 0.32 | 0.24 | intron-variant | Nosip | Mm_Celera | 7:45071479 | TTTCTGGTGAAACCT[C/T]TTCTTTAGTTTGTAT | 66394 |
rs37898081 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45076995 | CTAGCCTGCACTGCA[A/G]ACTGTCCCCTGGTGT | 66394 |
rs37932243 | snp | A/C | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078648 | ATACTGTCAAGGACA[A/C]AACCTTTCAAAGATT | 66394 |
rs37969885 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078723 | ACTAGAGGGCAGAAC[A/G]TCACTGCCGATGAGA | 66394 |
rs38048805 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078515 | AGGCATAGTGGTGTG[C/T]GCCTGTAACACTGAC | 66394 |
rs38144386 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075708 | GCACTTTAGAAACTT[C/G]GCCTTGTGGCTGGGG | 66394 |
rs38149293 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075215 | GACACAAATAGATAA[C/T]CTAAGTGCCCAGCAG | 66394 |
rs38365198 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075423 | GCTAGACTCTCCCTG[A/T]CCTTGGTTCCCTCAT | 66394 |
rs38374104 | snp | A/T | 0.231111 | 0.249285 | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062471 | AGAGTTTAAAAACAG[A/T]ACTCTTTTTCCGGTT | 66394 |
rs38422029 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078777 | GGCTGAGAGTCCACA[C/G]ACTGGAAGGTGTGAG | 66394 |
rs38423642 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Nosip | Mm_Celera | 7:45078984 | ATGTTACCCAAGTAC[A/G]TAAAGTAACCAGAAA | 66394 |
rs38445674 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45074168 | GAGCCCTCACCAGAG[A/G]CAGGCAGCTCACCTC | 66394 |
rs38472869 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078436 | TCAATGTGTGGCAAC[G/T]TGTGTATTTATAATT | 66394 |
rs38591119 | snp | C/T | 0.260355 | 0.249785 | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078490 | AATATTTAAACAAAA[C/T]GTATATTCCAGGCAT | 66394 |
rs38746536 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45073920 | CTACACACTTCTCTG[C/T]GACATTTGGTGGAGG | 66394 |
rs38917422 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063275 | TCCAGGCTGCATCGA[A/G]TTTCACTAAATATCT | 66394 |
rs39041630 | snp | G/T | 0.32 | 0.24 | intron-variant | Nosip | Mm_Celera | 7:45073881 | TGACCTAGCCATTGT[G/T]GACTCTCTCAGACTC | 66394 |
rs39113931 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45073847 | TGAGCCTCTTCACCC[C/T]GCTTCTGGGGAAAAA | 66394 |
rs39237361 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45074884 | GCCTGGAATGCCATC[C/T]ACCTCCCGCTTCTCT | 66394 |
rs39431109 | snp | A/C | 0.408163 | 0.193609 | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078385 | TCTTGATGGAAAAAA[A/C]CAAAACACTGGCCAT | 66394 |
rs39568677 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nosip | Mm_Celera | 7:45075419 | GCTAGCTAGACTCTC[A/C]CTGACCTTGGTTCCC | 66394 |
rs39604997 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nosip | Mm_Celera | 7:45073597 | TCACTGTCACCTTCA[A/G]TTTCACCCTTTGTGA | 66394 |
rs45870789 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072397 | CTCACAGCCACCTGT[A/T]ACTCTGGCTTCAGAG | 66394 |
rs46002966 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062940 | GTAGCCCTTGCTGTT[A/C]TAGAACTCGCTATGT | 66394 |
rs46208191 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45074376 | CCTTCAAGGCAAGCC[C/T]CAGCTACATAGTAGT | 66394 |
rs46791439 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071884 | GGGAGCTTGATGCCC[A/G]TAATGAGCAGGAGGT | 66394 |
rs46895224 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45068098 | GTGGCCCACAACCAC[A/G]TGGTGGCTCACAACC | 66394 |
rs47027117 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45071731 | GTTTTCAGAGGGTCT[A/C]TAAATGCTAGGGCCC | 66394 |
rs47570536 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061259 | ATAAGCACACAGTTG[C/G]TGAGGCTTGCTTTCT | 66394 |
rs47582994 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45077295 | ACCTCCAGCTTGTTC[C/T]TTTCTCTCCTCTCTA | 66394 |
rs47910596 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45074279 | ATGCAGGAACCTCTG[G/T]TCCATCCCAGCACCA | 66394 |
rs48036773 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074413 | CTAGCCTGAGCTCCA[A/G]TACATTGTCTCTCTA | 66394 |
rs48102731 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45074255 | CTCGGGGTACAGTGC[G/T]TGCCTCGCATGCAGG | 66394 |
rs48238965 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45068632 | TTTTTTTAAAGATTT[A/G]TTTTTTATGTGCATT | 66394 |
rs48344835 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45073198 | GAGTTTTTTTTTTTT[G/T]TTTTTGTTTTTAAAG | 66394 |
rs48746788 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45073169 | AAGATCAGCCTGGGC[A/C]ATAGAGGAAGACAGA | 66394 |
rs48905901 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45077259 | AACCCCCACTGCTGC[C/T]GGGAGCCCAGCCTGT | 66394 |
rs49028662 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067143 | GGTAAGGTGCTAAAC[C/T]GGTACCCTACCATTA | 66394 |
rs49202095 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45072438 | CCTCTTCTGGTCTTG[G/T]CAGGCATTGCTGCAC | 66394 |
rs49204564 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074188 | CAGCTCACCTCCACC[A/G]CAGGTGCAGTTGGGC | 66394 |
rs49277713 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071929 | TCCGCCCCCTTCCCA[A/G]CCCTTTTCTTCCCAT | 66394 |
rs49888303 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45073220 | TTTTTAAAGTGGTTC[A/C]GGCCTTTAAACCAGC | 66394 |
rs49941284 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073343 | GTGTTCTGTCCTCCC[C/T]GCTGAGACCCACGGA | 66394 |
rs49953750 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45071957 | CATCCTTTTTCCTCT[C/T]TCTAGTGTTGGGGGT | 66394 |
rs50472194 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45073099 | CACAGACGTGGTGGC[A/T]CAGCCTGTCTTCCCA | 66394 |
rs50558990 | snp | A/C | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078958 | CACACACAGGGACAC[A/C]CCAAATACAGATGTT | 66394 |
rs50786945 | snp | C/G/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45071883 | AGGGAGCTTGATGCC[C/G/T]ATAATGAGCAGGAGG | 66394 |
rs50990496 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074117 | GGCAAAGGGGCAGCT[A/G]GTGTGTGTGGGTTTA | 66394 |
rs51085300 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072199 | ACAAACACAAAAAAC[A/G]AAACAACCCAAGTGA | 66394 |
rs51142095 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45067144 | GTAAGGTGCTAAACT[G/T]GTACCCTACCATTAA | 66394 |
rs51577025 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073239 | CTTTAAACCAGCTCT[C/T]AGGGGGCAGAGGTAG | 66394 |
rs52192869 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071133 | GGAAGAGCAGTGACT[A/G]CTGGAAGAGCAGTCA | 66394 |
rs52210972 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072955 | CTTAACCCCTGAGTC[A/G]TCTCCCTACCCCCTC | 66394 |
rs52332233 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072133 | CAAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 66394 |
rs52371720 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071062 | AAGAACATGATACTA[A/G]GTTTTATTTATTTAT | 66394 |
rs52562057 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072154 | GTTCCAGGACAGCCA[A/G]GGCTGTCTCAAAAAC | 66394 |
rs108508704 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067436 | GAGGTAGAGCCTCTA[C/T]CTTGCAACCTTGCAG | 66394 |
rs211756474 | in-del | -/G | | | intron-variant | Nosip | Mm_Celera | 7:45074243 | GGCTGAGGCTGACTC[-/G]GGGTACAGTGCGTGC | 66394 |
rs211973637 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061668 | TGTGCAAAGGGGTAG[C/G]CAAGAGGGGAGGGGA | 66394 |
rs212065661 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060655 | GAATCTAGGAAGTCT[C/T]CTGGCTAGGGAGAGG | 66394 |
rs212145171 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45069584 | GAAGAGGACTCCTCC[A/G]GTTCTCTTTCAGAGG | 66394 |
rs212159087 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072327 | TGGAGAGATGGCTCA[A/T]CCATTAGTAATGATG | 66394 |
rs212175912 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45066483 | TGTGGCTCAGTGGGT[-/A]GAATGGACCAGGATC | 66394 |
rs212213919 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063291 | TTTCACTAAATATCT[C/T]TAAGGAGATTAAGAT | 66394 |
rs212348253 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078474 | CTGTAAGTCTGTTGC[C/T]AATATTTAAACAAAA | 66394 |
rs212364702 | snp | A/C | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45078025 | AGCCTAGTCTAGATG[A/C]TGGGGGCCAGGCTTG | 66394 |
rs212412349 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062711 | GCCTTGTACTGTCTC[C/T]CTCATCCTGGCTGGT | 66394 |
rs212605260 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45066846 | CCTGAGCTATATGCA[G/T]TATGAGACACAGACA | 66394 |
rs212644767 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071290 | GATCCATCCCCTGGG[A/G]CTGTGTCTATAGGAG | 66394 |
rs212662945 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45067350 | GAATCCTCCAATGAG[A/G]GGTAGGGAATGTGGC | 66394 |
rs212731906 | in-del | -/GGG | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078570 | ACATTACCGGAGTGT[-/GGG]GTGGGGGCACCTGGG | 66394 |
rs212751733 | in-del | -/GAGTT | | | intron-variant | Nosip | Mm_Celera | 7:45073184 | ATAGAGGAAGACAGA[-/GAGTT]GTTTTTTTTTTTTGT | 66394 |
rs212891596 | snp | G/T | | | synonymous-codon | Nosip | Mm_Celera | 7:45076092 | GAAGCAGCGAGGAGC[G/T]AGGAGAGAAGAGCAG | 66394 |
rs213151477 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062783 | AGTGAGGGGGAACTT[-/G]GGGGTTCCCTGTGTT | 66394 |
rs213194946 | in-del | -/AAAAA | | | intron-variant | Nosip | GRCm38.p3 | 7:45071822 | ACAAAGAAGGAAAGG[-/AAAAA]AAAAAAATGAGATAT | 66394 |
rs213588532 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45074561 | GGGGACCCGACCCTG[C/T]GGCTGAGCCCACGCC | 66394 |
rs213708177 | snp | G/T | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077573 | AGGACTTGGAAGAGG[G/T]TGCCCTGAACAAGAA | 66394 |
rs213771467 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45070282 | TCTAGGACTCCAGAG[A/G]TGGATGCAGGAGGAT | 66394 |
rs213776599 | snp | A/C/T | | | intron-variant | Nosip | Mm_Celera | 7:45077032 | CACCTGTCTTCCACC[A/C/T]GGCCCCCTTTTGCCC | 66394 |
rs213881259 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068278 | GTTCGAGCCCAGCCT[C/T]GTCTATAGAACTACT | 66394 |
rs213916864 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nosip, Prrg2 | Mm_Celera | 7:45060854 | CCAGATGACAAATGC[C/T]GCAGCGGAGTTAGGA | 66394 |
rs214045359 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45069668 | GATTCCAGGGGATCC[A/G]ATACCCTCACCCCCA | 66394 |
rs214437837 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45073800 | CCGAGAGCCACAGTG[A/G]TGGTCCCCACCCCGG | 66394 |
rs214736656 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45073117 | GCCTGTCTTCCCAGC[A/G]TTGAAGAGGCTGAGG | 66394 |
rs214815348 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45064625 | AAACAAACAAACAAA[A/C]TATATATATATATTT | 66394 |
rs214886545 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45066792 | CTTCGCAGCCCTTAG[A/G]AGGCTGACGTAGGGA | 66394 |
rs214917872 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45073878 | AGCTGACCTAGCCAT[G/T]GTGGACTCTCTCAGA | 66394 |
rs215146826 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45065670 | GCTGGCCAGACTGTC[A/T]TTGGCTTTTTTTGTT | 66394 |
rs215917375 | in-del | -/TT | | | intron-variant | Nosip | Mm_Celera | 7:45064637 | AACTATATATATATA[-/TT]TTTTTATGTATGAGT | 66394 |
rs216211463 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073037 | AGGAGAGATGAGAAA[C/T]ATAGGGAAGGCTGGG | 66394 |
rs216236890 | snp | A/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078896 | ACCTCCTCTCCCTAC[A/G]TAATGTAAGCAGTGG | 66394 |
rs216287788 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45072511 | ATGGTTTTGAAAAAG[G/T]CAAGGTTTTAGTTGT | 66394 |
rs216401989 | in-del | -/AA | | | intron-variant | Nosip | GRCm38.p3 | 7:45067276 | CCCTATCTTAATATT[-/AA]AAAAAAAAAAAAAAT | 66394 |
rs216674049 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062602 | TTTGCAGTTCTGAGG[A/G]AGGTAGGATAAGGTT | 66394 |
rs216808488 | in-del | -/TT | | | intron-variant | Nosip | Mm_Celera | 7:45064635 | CAAACTATATATATA[-/TT]TATTTTTATGTATGA | 66394 |
rs216945747 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065402 | AGATTAGATTATATT[A/G]AAGGCAGGGTTCATT | 66394 |
rs217021881 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45064578 | AGCCAGGGCTATACA[C/G]AGAAACCCTGTCTCG | 66394 |
rs217088301 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061764 | ACTGATTACCTTCTT[G/T]GGGAGGGACTCAGGT | 66394 |
rs217104822 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45065234 | TTCTCTCCCCCCCCA[-/C]ACCCCCCCCACCCCG | 66394 |
rs217157974 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060568 | TTCTGAAGCAGGGGG[C/T]GACCATGTGGATCTG | 66394 |
rs217252797 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45069184 | TCCAATTCCAGTAGA[A/G]GTCAGCTTTCAAGAA | 66394 |
rs217269640 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45076000 | CAGGGCTCTGTCCCC[A/C]CACTGGTGGGGTGGG | 66394 |
rs217309262 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45068471 | CGCTCACTCCTCTAT[G/T]TGAGGCAAGGCTTTC | 66394 |
rs217517017 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063353 | ATTTATTTAAAGTAA[C/T]GAGGGGGGGGATGGG | 66394 |
rs217615467 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061830 | GGTCTTCAGTGCCAC[C/G]GCCCCACACAGAAGA | 66394 |
rs217674012 | snp | C/T | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078943 | CTGGCCTGTGGGTGT[C/T]ACACACAGGGACACA | 66394 |
rs217754137 | in-del | -/TAG | | | intron-variant | Nosip | Mm_Celera | 7:45067687 | CTTCTGAAAGGAAGT[-/TAG]TAGTCTCGGCAATCA | 66394 |
rs217762946 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45072612 | TGTGCTTGCTAGGCA[A/C]GCACTCTACCACTGA | 66394 |
rs218241318 | in-del | -/TTG | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063806 | TGTTTTTTGTTTTTT[-/TTG]TTTGTTTTTTGTTTT | 66394 |
rs218386537 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061325 | TTTAAACAAGCTCAT[C/T]ATCAACCCTCTTCCC | 66394 |
rs218410994 | in-del | -/CCCCCC | | | intron-variant | Nosip | GRCm38.p3 | 7:45077225 | GGACTTATTTCTCTG[-/CCCCCC]CCCCCCCCAACAGAA | 66394 |
rs218441105 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062096 | GATCTTTGAAAATTG[C/T]TTTTTCTATAATAGG | 66394 |
rs218506681 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073090 | CTTGCCTAGCACAGA[C/T]GTGGTGGCACAGCCT | 66394 |
rs218708790 | in-del | -/T | | | intron-variant | Nosip | Mm_Celera | 7:45071030 | CTTTTTCTTTTTTTC[-/T]TTTTTTTTTTTTTAA | 66394 |
rs218736856 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45064956 | GGTTTAGACCTGGGG[A/G]CAGCAAGCACCTTCC | 66394 |
rs218748915 | in-del | -/CAGA | | | intron-variant | Nosip | Mm_Celera | 7:45067531 | ACACACACCACAAGT[-/CAGA]CAAGGACACATCAAT | 66394 |
rs218797188 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065993 | CACCTCGATCTTTCC[A/G]TTCCCAGATAAAAGA | 66394 |
rs218819016 | in-del | -/GG | | | intron-variant | Nosip | Mm_Celera | 7:45072048 | GATACAAGTGAATGT[-/GG]GGGGGGGGGGGGACG | 66394 |
rs218966582 | in-del | -/AAACAAAC | | | intron-variant | Nosip | Mm_Celera | 7:45072165 | CCAAGGCTGTCTCAA[-/AAACAAAC]AAACAAACAAACAAA | 66394 |
rs219133633 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45070041 | ATAAATCTTTTTTTT[-/A]TAAAGATTTATTTAT | 66394 |
rs219268849 | in-del | -/CAA | | | intron-variant | Nosip | Mm_Celera | 7:45065233 | TGTTCTCTCCCCCCC[-/CAA]CCCCCCCCACCCCGT | 66394 |
rs219486898 | snp | A/G | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077814 | AACTTGCTCAAAGAG[A/G]CGCAGACCACCCTCA | 66394 |
rs219710260 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45077266 | ACTGCTGCTGGGAGC[A/C]CAGCCTGTGAGGCAC | 66394 |
rs219782905 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075736 | GGGAGAGCTTGGTTA[A/G]TAGCATGAAGCCCTA | 66394 |
rs219858354 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45071558 | GAAGAACACAGAAAT[-/A]TTATAAGAATATGAT | 66394 |
rs219907335 | snp | C/T | | | intron-variant, synonymous-codon | Nosip | Mm_Celera | 7:45076578 | GACCTGCCCGATGTC[C/T]GGGAAGCCACTGCGC | 66394 |
rs220100799 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074106 | AGCAGGGGAGGGGCA[A/G]AGGGGCAGCTGGTGT | 66394 |
rs220161981 | snp | A/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078669 | TTCAAAGATTTGGAA[A/G]GGCCTCTTGGCCAGT | 66394 |
rs220518759 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45069788 | GGGTGCTTTGATAAG[A/G]GGCTGTGGTCTTCTA | 66394 |
rs220771300 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45064785 | CATTGAGCCATCTCC[C/T]CAGCCAGTTGTTGTT | 66394 |
rs220771809 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45070486 | TGAACTCAGGTTATA[C/G]GGTTTGTAAGGCAAG | 66394 |
rs220800023 | snp | A/G | | | synonymous-codon | Nosip | Mm_Celera | 7:45074636 | GTATGAGAGGGAAGC[A/G]ATCCTGGAGTACATC | 66394 |
rs220862895 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45066984 | TGTTCACTTTGTATA[C/G]CACATGGCTTCCCAG | 66394 |
rs220886764 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072822 | TTATTTTATGTGCAC[C/T]GGTGTTTTGCCTGCA | 66394 |
rs221150763 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45069980 | GGCACCAGACACACA[G/T]GAGGGGCACAAACAT | 66394 |
rs221154353 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078256 | GGGTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG | 66394 |
rs221239165 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45077280 | CCCAGCCTGTGAGGC[A/T]CCTCCAGCTTGTTCT | 66394 |
rs221269612 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075685 | GCCATGTGGTCATCA[A/G]AGTCTAAGCACTTTA | 66394 |
rs221647850 | in-del | -/GCTGGAAGAGCAGTGACT | | | intron-variant | Nosip | Mm_Celera | 7:45071115 | CGTAAGTACACTGTA[-/GCTGGAAGAGCAGTGACT]GCTGGAAGAGCAGTC | 66394 |
rs221780636 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063007 | GCCGCCCAAGTGTTG[A/T]GATTAAAAGTGTGCA | 66394 |
rs221952604 | snp | A/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078719 | GGCCACTAGAGGGCA[A/G]AACGTCACTGCCGAT | 66394 |
rs221991497 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45074736 | GAGGGCATCGGATCC[C/T]GTTACAGATGGTTGC | 66394 |
rs222234218 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063483 | GATCCCAGAACTGGG[C/T]GCAGAGGTAGATGGA | 66394 |
rs222257934 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068809 | AGCCGAGCCATTATT[C/T]TTCCAGCCTCCAGAT | 66394 |
rs222523309 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066309 | ACCTGGTGCCAGCCC[C/T]TCCCCATACACACTT | 66394 |
rs222614228 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067709 | CGGCAATCAGCAATC[C/T]ACAGTCCTCTGCTCT | 66394 |
rs223010147 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063581 | AAAGAAAAGAAATGC[C/T]TTCCTTTTATTTTAT | 66394 |
rs223098806 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45072653 | CAACCCCAGTAACTT[C/G]TTTTGTTTGCTGAGC | 66394 |
rs223566036 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061195 | TAAAGTCATTTGCCT[A/G]TTGTACCAGGTTTTC | 66394 |
rs224100863 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063769 | CTTTTAGCCACTGCC[C/T]CATCTCTCCAGCTTC | 66394 |
rs224164707 | in-del | -/AAAAAAAAAA | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063325 | TAGCTGGGCAGTGGC[-/AAAAAAAAAA]AAAAAAAAAAAGATT | 66394 |
rs224386615 | in-del | -/ATGCTAGC | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078807 | GTTCAGATCCCTGTA[-/ATGCTAGC]ATCAGAGACGAGGGT | 66394 |
rs224702047 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45065410 | TTATATTAAAGGCAG[C/G]GTTCATTGGGAAGCT | 66394 |
rs224928789 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064078 | GCACTCCCCTCAGTC[C/T]TGAGGAATTGAATGC | 66394 |
rs225398203 | in-del | -/C | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078530 | CGCCTGTAACACTGA[-/C]CCCCTGCTTTCACTG | 66394 |
rs225440020 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074289 | CTCTGGTCCATCCCA[A/G]CACCACAGAAAGCCG | 66394 |
rs225595412 | snp | A/C | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062269 | CGCTCTGGGTAATGC[A/C]TAGAACAGGCTAGGG | 66394 |
rs225659413 | in-del | -/TG | | | intron-variant | Nosip | Mm_Celera | 7:45073197 | AGAGTTTTTTTTTTT[-/TG]TTTTTGTTTTTAAAG | 66394 |
rs225810762 | in-del | -/TTTGTTTTTTTTGTTTGTTTTTTG | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063796 | CTTCTTAATTTGTTT[-/TTTGTTTTTTTTGTTTGTTTTTTG]TTTTGTTTTGTTTTG | 66394 |
rs226056375 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078304 | AGGCTGGCCTCGAAC[A/T]CAGAAATCCACCTGA | 66394 |
rs226354082 | snp | C/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078824 | GCTAGCATCAGAGAC[C/G]AGGGTCCCTGGGGTT | 66394 |
rs226568278 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078328 | CACCTGACTCTGCTG[A/G]GATTAAAGGCGTGCG | 66394 |
rs226672616 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45072716 | TCACTTTGTAGATTC[-/A]AAGTAGTTCAAATTC | 66394 |
rs226716455 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45072447 | TCTTGGCAGGCATTG[-/C]CTGCACATGACGTCA | 66394 |
rs226958613 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45065310 | TACTCTCTAGTCTAG[A/T]CTGGCCTTGAACTCC | 66394 |
rs227010148 | snp | C/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45077225 | GGACTTATTTCTCTG[C/T]CCCCCCCCCCCCCAA | 66394 |
rs227331138 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45069019 | CCCTCCCTGTAGGGA[A/T]CCACACTCACCCACA | 66394 |
rs227450789 | snp | C/T | | | synonymous-codon | Nosip | Mm_Celera | 7:45076677 | ACGCAGTGAGCGCTA[C/T]GTTTGCGCAGTGACC | 66394 |
rs227527994 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45075161 | ACGCTGTACAATGGC[C/T]ACCAGGGTGAAGCTA | 66394 |
rs227730034 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068235 | GAAACTCTCTGCGCC[C/T]AGCAGGCATAGGTCA | 66394 |
rs227965765 | in-del | -/AGA | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061420 | GATCAGAGACTACAC[-/AGA]GACAGATCAGGTCGT | 66394 |
rs227991415 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45069435 | TGGTCTCTAGAGCTC[-/A]ATGTACTTAATGTCT | 66394 |
rs228071341 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061589 | ATGCACCCACTTACC[A/T]GGCCAGGGCTGGGAG | 66394 |
rs228137726 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45071092 | TTAAGATTTATTTAT[C/T]TATTATACGTAAGTA | 66394 |
rs228210906 | snp | C/T | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077574 | GGACTTGGAAGAGGG[C/T]GCCCTGAACAAGAAG | 66394 |
rs228212426 | in-del | -/CCCC | | | intron-variant | Nosip | Mm_Celera | 7:45065235 | TCTCTCCCCCCCCAA[-/CCCC]CCCCCCCCACCCCGT | 66394 |
rs228239155 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45069196 | AGAGGTCAGCTTTCA[A/C]GAATCTCCTTCTCTT | 66394 |
rs228564895 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45072193 | AACAAACAAACACAA[-/C]AAAACAAAACAACCC | 66394 |
rs228591516 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063270 | TGTAGTCCAGGCTGC[A/T]TCGAATTTCACTAAA | 66394 |
rs228937177 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45075052 | CAGGCGCGCAGCCCA[C/T]GGCCCACAGGAGCAG | 66394 |
rs228947996 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45067250 | AAAAGCCAAACTAAG[G/T]TATAGATGATACCCT | 66394 |
rs229094586 | in-del | -/TTCCATGT | | | intron-variant | Nosip | Mm_Celera | 7:45070452 | GAGAGCGGACAATTC[-/TTCCATGT]TTCCATGGCACAGGA | 66394 |
rs229345697 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45073763 | TCTTAACCATTCCTG[G/T]CCAGCTCTGCCGAAA | 66394 |
rs229537024 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45067900 | ATGGCCTGTAACTGT[A/G]GGGCTCTCTTCTGAG | 66394 |
rs229570870 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074239 | TAGTGGCTGAGGCTG[A/G]CTCGGGGTACAGTGC | 66394 |
rs230423877 | in-del | -/ACACACACACACACACACACACACAC | | | intron-variant | Nosip | GRCm38.p3 | 7:45067485 | CCACTGCACACACAT[-/ACACACACACACACACACACACACAC]ACACACACACACACC | 66394 |
rs230442558 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063484 | ATCCCAGAACTGGGC[A/G]CAGAGGTAGATGGAT | 66394 |
rs230780111 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070928 | TGCAAGAGCTCTGCC[C/T]CAGCTCTCGGCTCGA | 66394 |
rs230793090 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062522 | GACAAGCCGGATAAC[C/T]GCTCTTGAGGTAAGC | 66394 |
rs230944978 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064237 | TGAACTACCCTCTCA[A/C]ACTGGACATGGTTAA | 66394 |
rs231001045 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061686 | AGAGGGGAGGGGAGG[A/G]GAGGAGGGGAGCTCC | 66394 |
rs231037418 | snp | C/G/T | | | intron-variant | Nosip | Mm_Celera | 7:45072964 | TGAGTCATCTCCCTA[C/G/T]CCCCTCCCTTGAACT | 66394 |
rs231076899 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45064622 | ACAAAACAAACAAAC[A/T]AACTATATATATATA | 66394 |
rs231100354 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070240 | CAAAGTTAAATACAC[C/T]GGGCTTGGTGCTACC | 66394 |
rs231311819 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45065127 | ACTCTGTAAAGTAGG[A/C]TGGCCTTGAACTCAG | 66394 |
rs231497071 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45074573 | CTGCGGCTGAGCCCA[C/T]GCCAGTGCGTCCCTC | 66394 |
rs231500970 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072338 | CTCATCCATTAGTAA[A/T]GATGGCTGCTCTTCC | 66394 |
rs231520419 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063121 | TGTGTAGCTCTGGCT[A/G]TCCTGGAACTAGCTC | 66394 |
rs231842037 | in-del | -/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45073185 | TAGAGGAAGACAGAG[-/T]TTTTTTTTTTTTGTT | 66394 |
rs231862107 | snp | C/T | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45078093 | GAGCCATCTTCACCC[C/T]GTGTTTCCATCCCAT | 66394 |
rs232058604 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062650 | GTCAATCATTAACAG[C/G]GCTCTTGAACGCCTA | 66394 |
rs232079052 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060713 | TCCAAACACTCACCT[G/T]CAAACTTGAAGAGAC | 66394 |
rs232120326 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061396 | ACCTGTTGCCTCATC[A/G]AGCCTCAGAGATCAG | 66394 |
rs232133879 | in-del | -/AAAC | | | intron-variant | Nosip | Mm_Celera | 7:45072166 | CCAAGGCTGTCTCAA[-/AAAC]AAACAAACAAACAAA | 66394 |
rs232263620 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45068280 | TCGAGCCCAGCCTCG[G/T]CTATAGAACTACTTC | 66394 |
rs232500008 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078487 | GCTAATATTTAAACA[A/C]AACGTATATTCCAGG | 66394 |
rs232687814 | snp | A/C | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060499 | CCTGAGCAAGAGGGG[A/C]CAGAGTTTTCACCAT | 66394 |
rs232965474 | in-del | -/TAA | | | intron-variant | Nosip | GRCm38.p3 | 7:45067276 | ACCCTATCTTAATAT[-/TAA]AAAAAAAAAAAATGA | 66394 |
rs233094859 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063451 | TTTATTTAAAGGGGT[A/G]TGGTAGACACATCTT | 66394 |
rs233105670 | in-del | -/TTTC | | | intron-variant | Nosip | Mm_Celera | 7:45071008 | CCTGCCTTTGTTTCT[-/TTTC]TTTTCTTTTTCTTTT | 66394 |
rs233114845 | in-del | -/GG | | | intron-variant | Nosip | Mm_Celera | 7:45073189 | GGAAGACAGAGTTTT[-/GG]TTTTTTTTGTTTTTG | 66394 |
rs233174536 | in-del | -/CTC | | | intron-variant | Nosip | Mm_Celera | 7:45066206 | CTCTCCTGTGTTGGT[-/CTC]CTCTGACTTCCAAGC | 66394 |
rs233180122 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072018 | GATAAAGAACCTACA[A/T]AGCAGCAAAGACTGT | 66394 |
rs233221206 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072520 | AAAAAGTCAAGGTTT[C/T]AGTTGTTTCTAGAGT | 66394 |
rs233567231 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075853 | CACAGTGAGTTTCAG[A/G]CCGAGGAGGCCCTCC | 66394 |
rs234090689 | snp | C/T | | | synonymous-codon | Nosip | Mm_Celera | 7:45076737 | CGCAGTGCTGCGTCC[C/T]TCGTGAGTGCGGGGT | 66394 |
rs234178371 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072907 | TGGGTGCTGGGAATT[A/G]AACCCAGGTTCTCTG | 66394 |
rs234182256 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060595 | TCTGAGGGGAGAAGC[C/T]GGGGCACAGACCCTA | 66394 |
rs234194146 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45068497 | TTTCTAGGCAGTCAG[-/A]AGGTGGACATAAATT | 66394 |
rs234416209 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078443 | GTGGCAACTTGTGTA[C/T]TTATAATTTTACATC | 66394 |
rs234481261 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067360 | ATGAGGGGTAGGGAA[C/T]GTGGCTCAGAGGCAG | 66394 |
rs234679095 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073968 | TCTTCATTCCCACCT[C/T]GTTCTGTCCCCAGCG | 66394 |
rs234717375 | in-del | -/CAATAATTTTT | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063405 | AAATTCACAAAGAAC[-/CAATAATTTTT]GTAGGACATTTGAAA | 66394 |
rs234754512 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45067277 | CCCTATCTTAATATT[-/A]AAAAAAAAAAAAATG | 66394 |
rs234754858 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45069612 | AGGACTGGGGTTCAA[C/T]TCCCAACACCCACAT | 66394 |
rs234845130 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070302 | TGCAGGAGGATAAGA[C/T]GTTCAAGGCTATCCT | 66394 |
rs234988939 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45069669 | ATTCCAGGGGATCCA[A/G]TACCCTCACCCCCAT | 66394 |
rs235023430 | snp | A/G | | | missense | Nosip | Mm_Celera | 7:45076342 | CCCAGTGTGGGTCCC[A/G]TAGGCAAGGACAAGG | 66394 |
rs235129410 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072615 | GCTTGCTAGGCACGC[A/G]CTCTACCACTGAGCT | 66394 |
rs235269428 | in-del | -/ACAAACAAAC | | | intron-variant | Nosip | Mm_Celera | 7:45072180 | AAAACAAACAAACAA[-/ACAAACAAAC]ACAAAAAACAAAACA | 66394 |
rs235286572 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45067712 | CAATCAGCAATCTAC[A/T]GTCCTCTGCTCTAGG | 66394 |
rs235734951 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061848 | CCCACACAGAAGAAA[C/T]AAGGCTTTCCGACAC | 66394 |
rs235873101 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45064637 | AAACTATATATATAT[A/T]TTTTTATGTATGAGT | 66394 |
rs236056684 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074530 | CTGAATATGCTTGGT[A/G]GTACCCCATGTGGAG | 66394 |
rs236060307 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45066808 | AGGCTGACGTAGGGA[A/G]ATTGCTGGGAGTTCA | 66394 |
rs236071040 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066871 | CAGACACACCTCAAA[C/T]AGGAAACAAACTTTT | 66394 |
rs236189208 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065910 | GAAGTCACGTGTGGG[A/G]AACAGGTTCCCTACC | 66394 |
rs236246371 | in-del | -/GCGC | | | intron-variant | Nosip | Mm_Celera | 7:45075040 | CACACTGGACCGCAG[-/GCGC]GCAGCCCACGGCCCA | 66394 |
rs236314368 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063032 | TGTGCACCACCACAC[C/T]TAGCACTTATTACCC | 66394 |
rs236332831 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45068680 | TATCTGTATGAGGGT[A/G]CCAGATCCCCTGAAA | 66394 |
rs236412335 | in-del | -/CCTGGACCCCCGGACCCCCTGGTGCC | | | intron-variant | Nosip | Mm_Celera | 7:45074979 | CACCTGCTAACCCCA[-/CCTGGACCCCCGGACCCCCTGGTGCC]CTCGTACTCACTGCT | 66394 |
rs236487973 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062456 | GGAAGTAGGAGGAGT[A/G]GAGTTTAAAAACAGT | 66394 |
rs236510138 | snp | A/C | | | synonymous-codon | Nosip | Mm_Celera | 7:45076093 | AAGCAGCGAGGAGCG[A/C]GGAGAGAAGAGCAGA | 66394 |
rs236869191 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45073091 | TTGCCTAGCACAGAC[A/G]TGGTGGCACAGCCTG | 66394 |
rs237266162 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45071363 | TGCTGAGATATATGA[A/G]TGATTACCTAAATAG | 66394 |
rs237277071 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062759 | CGCAGTAGAGGAGTG[A/T]TGCGGACCAAGTGAG | 66394 |
rs237497427 | snp | A/T | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078523 | TGGTGTGCGCCTGTA[A/T]CACTGACCCCCTGCT | 66394 |
rs237650987 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45065780 | ACTTCAGGCTCTCTG[C/T]TTTCCAGGACTTGCA | 66394 |
rs237805317 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073421 | GAGCAGGCTACTGAC[C/T]ACAAGCCCAGGAGGC | 66394 |
rs238010407 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45077267 | CTGCTGCTGGGAGCC[C/T]AGCCTGTGAGGCACC | 66394 |
rs238199691 | snp | A/G | | | missense | Nosip | Mm_Celera | 7:45076633 | TTCACGCAGCTGGAC[A/G]ACTCTGTGGACCGCG | 66394 |
rs238518655 | in-del | -/CCTC/CCTCC/GC | | | intron-variant | Nosip | Mm_Celera | 7:45072783 | CCCTCCCTCCCTCTG[-/CCTC/CCTCC/GC]CCCCCCCCCAAGTAA | 66394 |
rs238673433 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063045 | ACCTAGCACTTATTA[-/C]CCCCCCCCCCCCGCC | 66394 |
rs238753133 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061815 | GGACCATAGGATCAA[C/G]GTCTTCAGTGCCACG | 66394 |
rs238821032 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45070612 | AACCTCCTGCCTCAG[A/G]CTTCTGTGTCCTGGG | 66394 |
rs238930313 | in-del | -/A | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077599 | AGAAGTGCAAGTCTC[-/A]GTGATAGCACTCCCA | 66394 |
rs239045184 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070034 | ACATCAAAATAAATC[C/T]TTTTTTTTAAAGATT | 66394 |
rs239050432 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078278 | CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT | 66394 |
rs239473992 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070493 | AGGTTATAGGGTTTG[C/T]AAGGCAAGCAAGCAT | 66394 |
rs239596190 | snp | A/C/G | | | downstream-variant-500B | Nosip | GRCm38.p3 | 7:45078935 | ACCCAGCTCTGGCCT[A/C/G]TGGGTGTCACACACA | 66394 |
rs240416870 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45076044 | TGGGCCCTGGTACTG[C/T]TAACCCAGGTCCCTC | 66394 |
rs240438512 | in-del | -/T | | | intron-variant | Nosip | Mm_Celera | 7:45075383 | TTGCTCCACAGACTC[-/T]TGTGTCTCCCACACA | 66394 |
rs240963844 | in-del | -/AGGAGGAAGACTGG | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060524 | CACCATTGGGCATGA[-/AGGAGGAAGACTGG]AGTCTGGAACTCTAC | 66394 |
rs241003318 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066024 | ACACAACTTTTATTA[C/T]TTACAATAAACCTTT | 66394 |
rs241455411 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067762 | CCTCAACGTCCTGGG[C/T]AAAGGAGACCCTGAG | 66394 |
rs241467339 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45067819 | GCACCACAGCCAGCC[A/G]GCACTTCTGGCTGGA | 66394 |
rs241533350 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068810 | GCCGAGCCATTATTT[C/T]TCCAGCCTCCAGATC | 66394 |
rs241591226 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45074944 | GCATAGACCTCCTGC[C/G]GGCCAGGCCCTCTGG | 66394 |
rs241594169 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45066987 | TCACTTTGTATACCA[A/C]ATGGCTTCCCAGTCT | 66394 |
rs241654476 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45075763 | CCTAGGTCCCAACCC[C/T]AGCACGGATAACCAG | 66394 |
rs241773358 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45066358 | AACAGACCAAACCAC[A/G]GCTAGTTGGCTTCCT | 66394 |
rs241870098 | in-del | -/TTGT | | | intron-variant | Nosip | Mm_Celera | 7:45069297 | AGTCACTCCCTTCCG[-/TTGT]TTGTTTCTTTGTTGA | 66394 |
rs241992055 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078313 | TCGAACTCAGAAATC[C/T]ACCTGACTCTGCTGG | 66394 |
rs242189563 | in-del | -/CTTC | | | intron-variant | Nosip | Mm_Celera | 7:45072768 | TCCCTCTCTCTCCCT[-/CTTC]CCCTCCCTCCCTCTG | 66394 |
rs242286941 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061268 | CAGTTGCTGAGGCTT[G/T]CTTTCTCTACCTATC | 66394 |
rs242334591 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062641 | GAATCCCTGTCAATC[-/AT]ATTAACAGCGCTCTT | 66394 |
rs242349895 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45071163 | AGTGCTCTTAATTGC[G/T]GAGCCATCTCTCCAA | 66394 |
rs242409996 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45068883 | CCACTGTGCTATAAT[A/G]CTTGTTTTGAAGATG | 66394 |
rs242478117 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063800 | TTAATTTGTTTTTTG[-/T]TTTTTTTGTTTGTTT | 66394 |
rs242726167 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Nosip | Mm_Celera | 7:45069387 | TGTTTTGCAGAGGTG[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 66394 |
rs242786039 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45072823 | TATTTTATGTGCACT[A/G]GTGTTTTGCCTGCAT | 66394 |
rs242907791 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060611 | GGGGCACAGACCCTA[C/G]GATCTGAGGGAGAAG | 66394 |
rs242976180 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061624 | GCCTCTCTTCTTTAA[C/T]GAAGGCCCTCTGGGT | 66394 |
rs243010640 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063107 | AGACAGGGTTTCTCT[C/G]TGTAGCTCTGGCTGT | 66394 |
rs243091134 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45075469 | CCTCAGGCATTGTTA[A/C]TGTCACCACCTCAGC | 66394 |
rs243187090 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065182 | CTGGGATTGAGGGCT[A/G]CACCCCCACCACCAT | 66394 |
rs243633574 | in-del | -/T | | | intron-variant | Nosip | Mm_Celera | 7:45074459 | GAGTGCTGTGAAGAC[-/T]GTTGCCTAAAGGTAC | 66394 |
rs243983502 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072990 | GAACTCTTCTCCTGC[C/T]TCCCCTGACCCCCAA | 66394 |
rs244188053 | snp | C/T | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078849 | GGGGTTTGCTGATGA[C/T]CCACACCATCCCATT | 66394 |
rs244364558 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064217 | AATCCGAGGCCTGGA[C/T]TACATGAACTACCCT | 66394 |
rs244380776 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45067049 | ACAGGCATTGCCTGA[A/G]CCAGCTCTTCCAGGA | 66394 |
rs244483473 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062710 | TGCCTTGTACTGTCT[C/G]CCTCATCCTGGCTGG | 66394 |
rs244666917 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061336 | TCATCATCAACCCTC[C/T]TCCCTTCCAGCCCAG | 66394 |
rs244802814 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062282 | GCCTAGAACAGGCTA[A/G]GGTGTCTCCCAGAGT | 66394 |
rs244816694 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45071616 | GGCTGCTTCAGACCG[C/T]CCACAGCAGCTGACT | 66394 |
rs245050283 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45069086 | ACTTGTCTGTGGAGC[C/T]ATGACACACATTGTT | 66394 |
rs245113131 | in-del | -/GGGAATTGAACCCTGGTC | | | intron-variant | Nosip | Mm_Celera | 7:45068735 | TCTCACGTGGGTACT[-/GGGAATTGAACCCTGGTC]AGCAGGTCCTCTGGA | 66394 |
rs245136370 | snp | C/T | | | synonymous-codon | Nosip | Mm_Celera | 7:45076683 | TGAGCGCTACGTTTG[C/T]GCAGTGACCCGAGAC | 66394 |
rs245155436 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062625 | ATAAGGTTTCGCACT[-/C]CGAATCCCTGTCAAT | 66394 |
rs245247581 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45075998 | CCCAGGGCTCTGTCC[C/G]CACACTGGTGGGGTG | 66394 |
rs245369387 | in-del | -/T | | | intron-variant | Nosip | Mm_Celera | 7:45071337 | CTCCAGCCCTCTGTA[-/T]TTTTTTCTATTGCTG | 66394 |
rs245436673 | in-del | -/T | | | intron-variant | Nosip | Mm_Celera | 7:45072048 | TGATACAAGTGAATG[-/T]GGGGGGGGGGGGACG | 66394 |
rs245632445 | in-del | -/TA | | | intron-variant | Nosip | Mm_Celera | 7:45066891 | ACAAACTTTTTTTTT[-/TA]ATAATTTAAGTGACT | 66394 |
rs245736769 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063606 | TTTTATGTAAACGAG[G/T]GTTTTGCCTGTTTTT | 66394 |
rs245836253 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072786 | CTCCCTCCCTCTGCC[C/T]CCCCCCAAGTAATTA | 66394 |
rs246025514 | in-del | -/A | | | intron-variant | Nosip | GRCm38.p3 | 7:45067499 | TACACACACACACAC[-/A]CACACACACACACAC | 66394 |
rs246060992 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066316 | GCCAGCCCCTCCCCA[C/T]ACACACTTAGCATTC | 66394 |
rs246173264 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062475 | TTAAAAACAGTACTC[-/T]TTTTTCCGGTTCGGG | 66394 |
rs246683580 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45070303 | GCAGGAGGATAAGAC[A/G]TTCAAGGCTATCCTC | 66394 |
rs246786472 | in-del | -/TTTTTTT | | | intron-variant | Nosip | Mm_Celera | 7:45072554 | TACATAGTAACTTGG[-/TTTTTTT]GTTTTTTGTTTTTTT | 66394 |
rs246928338 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074343 | CAGCACTCAGGCAAT[A/G]CAGACAGGAAGACGA | 66394 |
rs247067822 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073877 | AAGCTGACCTAGCCA[C/T]TGTGGACTCTCTCAG | 66394 |
rs247077933 | in-del | -/GC | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061089 | GCGCTGGGATTAAAG[-/GC]GTGTGCCACCACTGC | 66394 |
rs247079458 | in-del | -/G | | | intron-variant | Nosip | Mm_Celera | 7:45072049 | GATACAAGTGAATGT[-/G]GGGGGGGGGGGACGC | 66394 |
rs247180142 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062183 | ATATTTGGGGAACTG[A/G]ATATCAGTCTCTTCG | 66394 |
rs247365149 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061435 | CGACAGATCAGGTCG[C/T]ATATTTCTAGGTCTT | 66394 |
rs247603545 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45065311 | ACTCTCTAGTCTAGA[C/G]TGGCCTTGAACTCCT | 66394 |
rs247684048 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064454 | TTGTATGAGATATGC[C/T]GTGCCTTATTTCTCC | 66394 |
rs247821853 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45066843 | TAGCCTGAGCTATAT[A/G]CAGTATGAGACACAG | 66394 |
rs247925711 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45076497 | TCATGCCCCTTCCAC[C/T]GCCCACATGGCGGAC | 66394 |
rs248267880 | in-del | -/CCCAGCAC | | | intron-variant | Nosip | GRCm38.p3 | 7:45072071 | GGGGACGCCTTTAAT[-/CCCAGCAC]CCCAGCACCCGGGAG | 66394 |
rs248418605 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45067744 | AGCTGCTTCCCCCGT[-/A]AGCCTCAACGTCCTG | 66394 |
rs248574810 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074694 | CAGGTGAAGGTGATG[A/G]AGGCTGAGGGGAGGA | 66394 |
rs248768058 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062651 | TCAATCATTAACAGC[A/G]CTCTTGAACGCCTAG | 66394 |
rs248833018 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063222 | TGCGCCACCACCCCA[A/G]CGATTATTGTATTTT | 66394 |
rs248871179 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068572 | TGCCTCAGAACCCTC[C/T]CAGGTAGCTGGGGTG | 66394 |
rs249153726 | snp | C/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45067510 | acacacacacacaca[C/T]acacacacacacacc | 66394 |
rs249323562 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45066659 | CAAGACCCTGCCTCA[A/G]AGGACAGCCATCTGC | 66394 |
rs249408655 | snp | A/C | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45078201 | TACATTTGAGTCCTT[A/C]AATCTGGCCAAATTC | 66394 |
rs249714437 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075873 | GGAGGCCCTCCCAGG[A/G]GGAGGACTGGGTTCC | 66394 |
rs249851340 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45076751 | CCTCGTGAGTGCGGG[A/G]TGTGGGGAGAAGAGG | 66394 |
rs249870977 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063574 | GAAAGGAAAAGAAAA[-/G]AAATGCTTTCCTTTT | 66394 |
rs249968058 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45075145 | CCTGTGCTTGGTCTT[-/C]ACGCTGTACAATGGC | 66394 |
rs250087880 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45071402 | ACAAAGACATGAAAT[C/T]AGGTTAAAATAGGAA | 66394 |
rs250132900 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078467 | TTACATCCTGTAAGT[C/T]TGTTGCTAATATTTA | 66394 |
rs250597680 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062079 | GAACAGTTTAGTCTC[C/G]AGATCTTTGAAAATT | 66394 |
rs250619419 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062153 | AAGATGCAATGGGGG[-/AA]AAAAAATAAGTAATA | 66394 |
rs250662875 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45070241 | AAAGTTAAATACACC[A/G]GGCTTGGTGCTACCC | 66394 |
rs250683044 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061319 | TAGGCATTTAAACAA[A/G]CTCATCATCAACCCT | 66394 |
rs250723552 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061725 | TACTAGGCCCGAGCC[A/G]GCTACTGGCGAGGGG | 66394 |
rs250864164 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063326 | TAGCTGGGCAGTGGC[A/T]AAAAAAAAAAGATTT | 66394 |
rs251201743 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066950 | TTGTGGCTAAAGCCC[C/T]TGCAGCTCAGCTAGG | 66394 |
rs251213241 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067613 | ATTAAACTGCATATG[C/T]GTAAAGGAGTAAAAA | 66394 |
rs251334067 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45068250 | CAGCAGGCATAGGTC[A/G]GTGGATCTCTGAGTT | 66394 |
rs252040347 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074578 | GCTGAGCCCACGCCA[A/G]TGCGTCCCTCATCCC | 66394 |
rs252056671 | in-del | -/ACCCCCC | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063044 | CACCTAGCACTTATT[-/ACCCCCC]CCCCCCCGCCCCATT | 66394 |
rs252079628 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45071033 | TTTCTTTTTTTCTTT[-/C]TTTTTTTTTTAATAA | 66394 |
rs252095657 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060560 | AACTCTACTTCTGAA[A/G]CAGGGGGTGACCATG | 66394 |
rs252135132 | in-del | -/GT | | | intron-variant | Nosip | Mm_Celera | 7:45072555 | ACATAGTAACTTGGG[-/GT]TTTTTTGTTTTTTTC | 66394 |
rs252350121 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075722 | TGGCCTTGTGGCTGG[A/G]GAGAGCTTGGTTAAT | 66394 |
rs252446768 | snp | C/T | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077652 | CTAGACATGGACCTG[C/T]CCCCACCAAGTGCCC | 66394 |
rs252657672 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45067760 | AGCCTCAACGTCCTG[C/G]GCAAAGGAGACCCTG | 66394 |
rs252669733 | in-del | -/AGGCCC | | | intron-variant | Nosip | Mm_Celera | 7:45065572 | GCTGGGAGAACCTGG[-/AGGCCC]AGTCTGCTTTGATGT | 66394 |
rs252892750 | in-del | -/TTTATTTA | | | intron-variant | Nosip | Mm_Celera | 7:45071064 | AACATGATACTAGGT[-/TTTATTTA]TTTATTTATTTATTA | 66394 |
rs253022866 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45069710 | CCTTGGCACCAGGCA[C/T]ACATGTTGTGTATAG | 66394 |
rs253161929 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45077178 | CTGTCCAGACTCTTC[C/G]ATGTTCTGAATGCCC | 66394 |
rs253163597 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068836 | AGATCTGAATTTTTA[C/T]TTCTTGTTGTGCTCT | 66394 |
rs253334077 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45073786 | TGCCGAAAGGAAGGC[C/G]GAGAGCCACAGTGGT | 66394 |
rs253397577 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45073204 | TTTTTTTTTGTTTTT[G/T]TTTTTAAAGTGGTTC | 66394 |
rs253462701 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065501 | GCAGGAGGGGAGGGG[A/G]AGAAGAGAAAAAGTT | 66394 |
rs253500247 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072530 | GGTTTTAGTTGTTTC[C/T]AGAGTGTCTTACATA | 66394 |
rs253522297 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072812 | AATTATTTGTTTATT[A/T]TATGTGCACTGGTGT | 66394 |
rs253554394 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063468 | GGTAGACACATCTTT[A/G]ATCCCAGAACTGGGC | 66394 |
rs253706737 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063077 | CATTGTTCGTTTTTG[G/T]TTTTTGGCTTTTCGA | 66394 |
rs253752490 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45075074 | CAGGAGCAGCTTCCC[A/C]TGCTCTCAGCTCCAG | 66394 |
rs253923747 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45070144 | GTTATGAGCCACCAT[A/G]TGGTTGCTGGGGATT | 66394 |
rs254196793 | snp | C/T | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078800 | GGTGTGAGTTCAGAT[C/T]CCTGTAATGCTAGCA | 66394 |
rs254227271 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45065226 | TTGTTGTTGTTCTCT[-/C]CCCCCCCAACCCCCC | 66394 |
rs254347402 | snp | A/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078941 | CTCTGGCCTGTGGGT[A/G]TCACACACAGGGACA | 66394 |
rs254578707 | in-del | -/AG | | | intron-variant | Nosip | Mm_Celera | 7:45065141 | GATGGCCTTGAACTC[-/AG]AGATCTGGCTGCCTC | 66394 |
rs255025076 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062524 | CAAGCCGGATAACCG[C/T]TCTTGAGGTAAGCTG | 66394 |
rs255076165 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063326 | TAGCTGGGCAGTGGC[-/A]AAAAAAAAAAGATTT | 66394 |
rs255112970 | snp | A/G | | | synonymous-codon | Nosip | Mm_Celera | 7:45076653 | TGTGGACCGCGTGGG[A/G]CTCATCACACGCAGT | 66394 |
rs255162355 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45077279 | GCCCAGCCTGTGAGG[C/T]ACCTCCAGCTTGTTC | 66394 |
rs255299471 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45075950 | AAAAGAACACGAAAG[C/T]GTCAACAACTGTTGC | 66394 |
rs255409343 | snp | A/G | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078667 | CTTTCAAAGATTTGG[A/G]AGGGCCTCTTGGCCA | 66394 |
rs255810076 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062152 | TAAGATGCAATGGGG[-/A]GAAAAAATAAGTAAT | 66394 |
rs255837725 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45064624 | AAAACAAACAAACAA[A/T]CTATATATATATATT | 66394 |
rs255853124 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064365 | CGGCTGGGCTTTTGT[-/GA]CTGGCTTCTCTCCCG | 66394 |
rs255976696 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067373 | AATGTGGCTCAGAGG[C/T]AGAGCCTTGCCTAGA | 66394 |
rs256067266 | in-del | -/TTTA | | | intron-variant | Nosip | Mm_Celera | 7:45068621 | ATCTTGATTTTTTTT[-/TTTA]AAGATTTATTTTTTA | 66394 |
rs256389698 | in-del | -/CCGA | | | intron-variant | Nosip | Mm_Celera | 7:45076513 | CCCACATGGCGGACC[-/CCGA]CTCTCCCTCTCCCCT | 66394 |
rs256656684 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45077261 | CCCCCACTGCTGCTG[A/G]GAGCCCAGCCTGTGA | 66394 |
rs256674596 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45069750 | CAGGCACAGCTGTAG[C/T]CCTAGCTGGCCTGAA | 66394 |
rs257440349 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45070504 | TTTGTAAGGCAAGCA[A/C]GCATCTTCACCCTGA | 66394 |
rs257453486 | snp | A/C | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062238 | TCAAACTTGAAGAGA[A/C]TCAAAGCAACTGCCC | 66394 |
rs257483532 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063356 | TATTTAAAGTAACGA[-/G]GGGGGGGATGGGTGG | 66394 |
rs257660375 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078351 | GGCGTGCGCTACCAC[A/G]CCCGGCTGTTGGGCA | 66394 |
rs257702245 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078378 | GCAAATTCTTGATGG[-/A]AAAAAACCAAAACAC | 66394 |
rs257785957 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45069444 | AGAGCTCATGTACTT[-/A]ATGTCTCTGGAGGTC | 66394 |
rs257842309 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074538 | GCTTGGTGGTACCCC[A/G]TGTGGAGGGGGACCC | 66394 |
rs258034258 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064449 | TCTGTTGTATGAGAT[-/A]ATGCTGTGCCTTATT | 66394 |
rs258043631 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45068797 | TCTTAACTGCTGAGC[C/T]GAGCCATTATTTTTC | 66394 |
rs258220631 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45066336 | ACTTAGCATTCCAAT[A/T]CATAGCAACAGACCA | 66394 |
rs258246852 | snp | A/G | | | synonymous-codon | Nosip | Mm_Celera | 7:45073527 | GAACTGCACTGCAGG[A/G]GCCGTCTACACCTAC | 66394 |
rs258313766 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45074157 | TCAGAGCCTCAGAGC[C/T]CTCACCAGAGGCAGG | 66394 |
rs258799624 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45065238 | CTCCCCCCCCAACCC[-/A]CCCCCACCCCGTGTG | 66394 |
rs258812759 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074984 | GCTAACCCCACCTGG[A/G]CCCCCGGACCCCCTG | 66394 |
rs258823829 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061188 | CAGGTAGTAAAGTCA[C/T]TTGCCTATTGTACCA | 66394 |
rs258932065 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45074434 | TGTCTCTCTAAAGAG[A/C]GGACTGAAAGGAGTG | 66394 |
rs259068862 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45065853 | CTGCCTGCTGGTTAG[C/T]TTTTGATGGTAGACT | 66394 |
rs259187244 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45066507 | CAGGATCCAATTATC[A/C]AGGTGGTTACAGCTT | 66394 |
rs259227694 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45076054 | TACTGCTAACCCAGG[C/T]CCCTCTTCCCCCAGG | 66394 |
rs259231244 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45066995 | TATACCACATGGCTT[C/T]CCAGTCTCCATAGGC | 66394 |
rs259482998 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067150 | TGCTAAACTGGTACC[C/T]TACCATTAAGCTAAG | 66394 |
rs259484629 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075769 | TCCCAACCCCAGCAC[A/G]GATAACCAGGAATGG | 66394 |
rs259492939 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45067841 | CTGGCTGGAGAGATG[C/T]CTCAGCTTGTTTTTA | 66394 |
rs259497297 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Nosip, Prrg2 | Mm_Celera | 7:45062399 | AGGCGAAGCGCCTCC[C/G]CGACTAGGGGCAGAA | 66394 |
rs259626359 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070116 | AAGAGGGCATCAGAT[C/T]CCAATGCAGATGGTT | 66394 |
rs259637095 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061549 | CAGGACACCAGATCC[C/T]CTGCCCAGGAGTTTC | 66394 |
rs259637425 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45070740 | CTTTTCATCTGTCAG[C/T]ACACTCAGATAGAGG | 66394 |
rs259856105 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45071043 | TTCTTTTTTTTTTTT[A/T]AATAAGAACATGATA | 66394 |
rs260096233 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45076949 | GTTGCCATTCGCTCA[-/C]CGCAGCCCTCACCGC | 66394 |
rs260106399 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45073884 | CCTAGCCATTGTGGA[C/G]TCTCTCAGACTCCAC | 66394 |
rs260223856 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45070043 | TAAATCTTTTTTTTT[-/A]AAGATTTATTTATTT | 66394 |
rs260595681 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063505 | GTAGATGGATTTTCC[C/T]GAGTTTGAGACCAGC | 66394 |
rs260611089 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45072885 | GAACTGGGTGTGAGC[A/C]ACCATGTGGGTGCTG | 66394 |
rs260616002 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063916 | TGTTCTTATTTTCAA[C/T]GAGGTTTATTGGGAT | 66394 |
rs260676890 | in-del | -/TG | | | intron-variant | Nosip | Mm_Celera | 7:45071216 | GCAGTTTATTACATT[-/TG]TGTGTGTGTGTGTGT | 66394 |
rs260705539 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078288 | ACTCACTTTGTAGAC[C/T]AGGCTGGCCTCGAAC | 66394 |
rs260708604 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45072635 | ACCACTGAGCTAAAT[A/C]CCCAACCCCAGTAAC | 66394 |
rs261091983 | in-del | -/CCCACAACCACATGGTGG | | | intron-variant | Nosip | Mm_Celera | 7:45068069 | ACCCTGAGTTCAATT[-/CCCACAACCACATGGTGG]CCCACAACCACATGG | 66394 |
rs261275081 | in-del | -/TGA | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078843 | GTCCCTGGGGTTTGC[-/TGA]TGATCCACACCATCC | 66394 |
rs261352073 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45072005 | GTGAAAGGTGGAAGA[A/T]AAAGAACCTACAAAG | 66394 |
rs261392118 | in-del | -/A | | | intron-variant | Nosip | Mm_Celera | 7:45067596 | CTCATGTGACCTCAG[-/A]AATTAAACTGCATAT | 66394 |
rs261452374 | snp | A/C | | | utr-variant-3-prime | Nosip | Mm_Celera | 7:45077449 | TTGTAGGCCCGGCGA[A/C]AGAAGGAGTGGGCCT | 66394 |
rs261588917 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45073374 | CTGCTGTGGTTTAGG[G/T]CTGTGTTTTCGGCGA | 66394 |
rs261662542 | in-del | -/CCC | | | intron-variant | Nosip | Mm_Celera | 7:45065236 | TCTCTCCCCCCCCAA[-/CCC]CCCCCACCCCGTGTG | 66394 |
rs261791900 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45068229 | TTTCAGGAAACTCTC[G/T]GCGCCCAGCAGGCAT | 66394 |
rs261816185 | in-del | -/TTTGTTTTTTGTTTTTTTTG | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063789 | TCTCCAGCTTCTTAA[-/TTTGTTTTTTGTTTTTTTTG]TTTGTTTTTTGTTTT | 66394 |
rs261836412 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45075883 | CCAGGAGGAGGACTG[A/G]GTTCCATATTGAGTA | 66394 |
rs261992273 | snp | A/G | | | upstream-variant-2KB, missense, utr-variant-5-prime | Nosip, Prrg2 | Mm_Celera | 7:45060816 | AGAGCAGGGAAGGAC[A/G]GCCCCTCATACTGTG | 66394 |
rs262139754 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45062765 | AGAGGAGTGATGCGG[A/G]CCAAGTGAGGGGGAA | 66394 |
rs262222292 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45060464 | TGGGGTCCTAGGGGT[A/G]CGGACCAGGCCTGGA | 66394 |
rs262268380 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45069001 | CCTGAGATAGCCCCA[C/T]TCCCCTCCCTGTAGG | 66394 |
rs262475269 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45069646 | AGCTCTCAATGTCTG[A/T]AACTGCGATTCCAGG | 66394 |
rs262544708 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45067775 | GGCAAAGGAGACCCT[G/T]AGGAGACATATAGGA | 66394 |
rs262648040 | in-del | -/C | | | intron-variant | Nosip | Mm_Celera | 7:45072379 | CCAGTCCCCACATGG[-/C]AGCTCACAGCCACCT | 66394 |
rs262725197 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063058 | TACCCCCCCCCCCCC[C/G]CCCCATTGTTCGTTT | 66394 |
rs262763032 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45065092 | AGACAGGGTTTCTCT[A/G]TGTAGTCCTGCTGAA | 66394 |
rs262928205 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061822 | AGGATCAAGGTCTTC[A/G]GTGCCACGGCCCCAC | 66394 |
rs263226209 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45064770 | AACAGTGTTCTTAAC[C/T]ATTGAGCCATCTCCC | 66394 |
rs263658212 | in-del | -/ACAGACAGACAGACAGACAGAC | | | intron-variant | Nosip | Mm_Celera | 7:45071241 | GTGTGTGAGAGAGAG[-/ACAGACAGACAGACAGACAGAC]AGACAGACAGACAGA | 66394 |
rs263736784 | snp | A/T | | | intron-variant | Nosip | Mm_Celera | 7:45073247 | CAGCTCTTAGGGGGC[A/T]GAGGTAGAGTTTGAG | 66394 |
rs263777919 | in-del | -/TT | | | intron-variant | Nosip | GRCm38.p3 | 7:45068612 | GACACCAGATCTTGA[-/TT]TTTTTTTTTTTAAAG | 66394 |
rs263843855 | snp | A/G | | | intron-variant | Nosip | Mm_Celera | 7:45074710 | AGGCTGAGGGGAGGA[A/G]GACACCAGGAGAGGG | 66394 |
rs264424527 | snp | C/T | | | synonymous-codon | Nosip | Mm_Celera | 7:45076722 | CAATGCCACGCCGTG[C/T]GCAGTGCTGCGTCCC | 66394 |
rs264428999 | in-del | -/AGACAGACAGACAGAC | | | intron-variant | Nosip | Mm_Celera | 7:45071242 | GTGTGTGAGAGAGAG[-/AGACAGACAGACAGAC]AGACAGACAGACAGA | 66394 |
rs264587395 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Nosip | Mm_Celera | 7:45071215 | GCAGTTTATTACATT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 66394 |
rs264624600 | snp | G/T | | | intron-variant | Nosip | Mm_Celera | 7:45070889 | GTTGACCAGGCCTTG[G/T]GTGCTAGGCAAGTGC | 66394 |
rs264651084 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | Mm_Celera | 7:45078326 | TCCACCTGACTCTGC[C/T]GGGATTAAAGGCGTG | 66394 |
rs264680320 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45064225 | GCCTGGACTACATGA[A/G]CTACCCTCTCAAACT | 66394 |
rs264704039 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45072962 | CCTGAGTCATCTCCC[C/T]ACCCCCTCCCTTGAA | 66394 |
rs264783852 | snp | C/G | | | intron-variant | Nosip | Mm_Celera | 7:45076516 | CACATGGCGGACCCT[C/G]TCCCTCTCCCCTATT | 66394 |
rs264957029 | snp | A/C | | | intron-variant | Nosip | Mm_Celera | 7:45068906 | TGAAGATGCAAGTTC[A/C]TTTCCATGCCCGTGA | 66394 |
rs265169751 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45061381 | AGTCAGCCTCCCTCT[A/G]CCTGTTGCCTCATCG | 66394 |
rs265554951 | in-del | -/AAACA | | | intron-variant | Nosip | Mm_Celera | 7:45064599 | CCTGTCTCGAAAAAC[-/AAACA]AAACAAAACAAAACA | 66394 |
rs265691260 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | Mm_Celera | 7:45063114 | GTTTCTCTGTGTAGC[C/T]CTGGCTGTCCTGGAA | 66394 |
rs265765604 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45065186 | GATTGAGGGCTGCAC[C/T]CCCACCACCATTAGG | 66394 |
rs266027654 | snp | C/T | | | intron-variant | Nosip | Mm_Celera | 7:45073738 | ACCATCCCACGTCTG[C/T]TCCCCTTCCTCTTAA | 66394 |
rs266191081 | snp | A/C | | | downstream-variant-500B | Nosip | Mm_Celera | 7:45078755 | GCTTAGAATTTAAAC[A/C]GGCTGGGGCTGAGAG | 66394 |
rs266222484 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | Mm_Celera | 7:45062154 | AAGATGCAATGGGGG[-/A]AAAAATAAGTAATAT | 66394 |
rs387095023 | in-del | -/A | | | intron-variant | Nosip | GRCm38.p3 | 7:45071822 | ACAAAGAAGGAAAGG[-/A]AAAAAAAAAAATGAG | 66394 |
rs578814136 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072063 | TGGGGGGGGGGGGAC[A/G]CCTTTAATCCCAGCA | 66394 |
rs578955018 | snp | A/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45068487 | TGAGGCAAGGCTTTC[A/T]AGGCAGTCAGAGGTG | 66394 |
rs579163600 | snp | A/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45071234 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACAGAC | 66394 |
rs580075921 | snp | C/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072113 | CGGATTTCTGAGTTT[C/G]AGGCCAAGCCTGGTC | 66394 |
rs580443730 | snp | A/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45072383 | GTCCCCACATGGAGC[A/T]CACAGCCACCTGTAA | 66394 |
rs580513411 | snp | A/T | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | GRCm38.p3 | 7:45062166 | GGGAAAAAATAAGTA[A/T]TATATTTGGGGAACT | 66394 |
rs580842278 | snp | G/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45067695 | AAGGAAGTTAGTCTC[G/T]GCAATCAGCAATCTA | 66394 |
rs580854797 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063843 | TGTTTTGTTTTGTTT[C/T]TTGAGATGCACAACC | 66394 |
rs581091639 | snp | C/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072779 | TCCCTCCCTCCCTCC[C/G]TCTGCCCCCCCCCAA | 66394 |
rs581233358 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Nosip | GRCm38.p3 | 7:45078391 | TGGAAAAAACCAAAA[C/T]ACTGGCCATGCAGTG | 66394 |
rs581999782 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072099 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTTGA | 66394 |
rs582855280 | snp | G/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45069538 | TGGAAGTTGAGTCCA[G/T]GTCCTCTGTAGAAGC | 66394 |
rs582898819 | snp | A/C/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45070443 | CATACATGTAGAGAG[A/C/G]GGACAATTCTTCCAT | 66394 |
rs583169704 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45074437 | CTCTCTAAAGAGAGG[A/G]CTGAAAGGAGTGCTG | 66394 |
rs583196925 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072549 | GTGTCTTACATAGTA[A/G]CTTGGGTTTTTTGTT | 66394 |
rs583555774 | snp | A/C | | | intron-variant | Nosip | GRCm38.p3 | 7:45072203 | ACACAAAAAACAAAA[A/C]AACCCAAGTGAATGG | 66394 |
rs583705154 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | GRCm38.p3 | 7:45061016 | CTGGCTGTCCTGGAA[C/G]TCACTCTGTAGAGCA | 66394 |
rs583755901 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45062780 | ACCAAGTGAGGGGGA[A/C]CTTGGGGTTCCCTGT | 66394 |
rs584204025 | snp | A/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45065225 | TTTGTTGTTGTTCTC[A/T]CCCCCCCCAACCCCC | 66394 |
rs584860869 | snp | A/G | | | downstream-variant-500B | Nosip | GRCm38.p3 | 7:45078828 | GCATCAGAGACGAGG[A/G]TCCCTGGGGTTTGCT | 66394 |
rs584939568 | snp | C/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45067728 | GTCCTCTGCTCTAGG[C/T]AAGCTGCTTCCCCCG | 66394 |
rs585453944 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45072059 | AATGTGGGGGGGGGG[A/G]GACGCCTTTAATCCC | 66394 |
rs586182012 | snp | C/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45072112 | GCGGATTTCTGAGTT[C/T]GAGGCCAAGCCTGGT | 66394 |
rs586384905 | snp | A/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45072204 | CACAAAAAACAAAAC[A/T]ACCCAAGTGAATGGT | 66394 |
rs586602813 | snp | C/T | | | intron-variant | Nosip | GRCm38.p3 | 7:45072767 | TCTCCCTCTCTCTCC[C/T]TCCCTCCCTCCCTCT | 66394 |
rs586766510 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nosip, Prrg2 | GRCm38.p3 | 7:45063170 | CCAACTCAGAAATCC[A/G]CCTGCCTCTGACTCC | 66394 |
rs586773209 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nosip, Prrg2 | GRCm38.p3 | 7:45061029 | AACTCACTCTGTAGA[A/G]CAGGCTGGCCTCAAA | 66394 |
rs586818122 | snp | A/C | | | intron-variant | Nosip | GRCm38.p3 | 7:45076938 | GCAGCGGGTGAGTTG[A/C]CATTCGCTCACCGCA | 66394 |
rs587000315 | snp | A/G | | | intron-variant | Nosip | GRCm38.p3 | 7:45066479 | GGGATGTGGCTCAGT[A/G]GGTAGAATGGACCAG | 66394 |