SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27353568 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151509479 | CCTTGTTTCTTTCTA[C/T]ACTGCCCTGATGTTC | 386649 |
rs27353569 | snp | A/G | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151509461 | CTTGTACCTCTGTGA[A/G]GACCTTGTTTCTTTC | 386649 |
rs27353570 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151509294 | GCCATGTCAGTGAAG[C/T]TGAGCCATCCTGATC | 386649 |
rs27353571 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151509207 | GGGTGCCTGCCTGAA[A/G]AACATAACACAGCCA | 386649 |
rs27353572 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Nsfl1c | GRCm38.p3 | 2:151508929 | ATAAAATAAATGCCC[A/C/G]TGTGAGTTCATTAGT | 386649 |
rs27353573 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151508809 | TGTGAGCACAAATAA[C/T]TGGCAGAAGCTCCAT | 386649 |
rs27353574 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151508547 | GGCTCCACTTTTAAT[C/T]CTCTCAGCCCCTATC | 386649 |
rs27353575 | snp | A/G | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151508509 | AAAGCAGCTTCTCAC[A/G]GGTGTATGGTTGGTA | 386649 |
rs27353576 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151508465 | CCACTGTCCCAGGCT[C/T]GGGTCTTACAGGCCA | 386649 |
rs27353577 | snp | A/G | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151506796 | TTCCTGTCCAGCACC[A/G]TCTCCCAGGAGTGCT | 386649 |
rs27353578 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nsfl1c | Mm_Celera | 2:151506209 | TAATCAGGTTTCCAT[C/T]CATCTCAAAATAAAC | 386649 |
rs27353579 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nsfl1c | Mm_Celera | 2:151505611 | TTTTAGCTGTTTTCC[A/T]TGAGGCATAGCTAAG | 386649 |
rs27353580 | snp | C/T | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151505575 | TAAAGATTCACAGAT[C/T]ACTCCAAAAACCTTG | 386649 |
rs27353581 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nsfl1c | Mm_Celera | 2:151505516 | TGAGCTGTCAGGTGG[A/G]AAAGGAAGAAAAGTT | 386649 |
rs27353582 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsfl1c | Mm_Celera | 2:151505161 | CTTCTCCTAACCTGC[A/G]TCATAGCATGTCCCT | 386649 |
rs27353583 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nsfl1c | Mm_Celera | 2:151504588 | CACACCCTCCAGGCA[G/T]TGATACTATATAATT | 386649 |
rs27353584 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Nsfl1c | Mm_Celera | 2:151504496 | AGAACCTTGAAAATG[C/G]CAAAGAAGGCCTGAA | 386649 |
rs27353585 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Nsfl1c | Mm_Celera | 2:151504476 | GGTATTTTGGGGATA[C/G]TTGAAGAACCTTGAA | 386649 |
rs27353586 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Nsfl1c | Mm_Celera | 2:151504357 | GTTTTCACTTGGTGG[A/T]TAGAGGGCCAGGGCA | 386649 |
rs27353587 | snp | A/T | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151503899 | TGAGTTTATACTGAG[A/T]ATAGTAGCTATTCCC | 386649 |
rs27353588 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Nsfl1c | Mm_Celera | 2:151503261 | TCTAGCAGAGATTGG[C/T]TCCTTTGTTTCTTCA | 386649 |
rs27353589 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Nsfl1c | Mm_Celera | 2:151503176 | AGAGACCAGTAAACC[A/G]AGAGTGAGCATAAGG | 386649 |
rs27353590 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nsfl1c | Mm_Celera | 2:151502897 | CTGCTTGCACCCTTA[C/T]GTGTTTTTCTAGCTA | 386649 |
rs27353591 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nsfl1c | Mm_Celera | 2:151502886 | TTGCATCATATCTGC[C/T]TGCACCCTTATGTGT | 386649 |
rs27353592 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsfl1c | Mm_Celera | 2:151502317 | CATCTCTTGAGGCTC[C/T]CAATGTACATCATAA | 386649 |
rs27353593 | snp | C/G | 0.5 | 0 | intron-variant | Nsfl1c | Mm_Celera | 2:151502310 | TCTAGTGCATCTCTT[C/G]AGGCTCCCAATGTAC | 386649 |
rs27353594 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151502308 | CTTCTAGTGCATCTC[C/T]TGAGGCTCCCAATGT | 386649 |
rs27353595 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nsfl1c | Mm_Celera | 2:151501023 | TTTCTCTCTCTAATT[A/G]TTACAGGGAGGTATT | 386649 |
rs27353596 | snp | G/T | 0.18 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151500934 | GAGCAGTTTGCTCTC[G/T]GTAGGTTAGCAGTAA | 386649 |
rs27353597 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nsfl1c | Mm_Celera | 2:151500913 | CATAGGGGTATAATA[G/T]CCTAAGAGCAGTTTG | 386649 |
rs27353598 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nsfl1c | Mm_Celera | 2:151500541 | TATTCTCAGTCCTGT[A/G]TGACCTTAACAGACA | 386649 |
rs27353599 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nsfl1c | Mm_Celera | 2:151500096 | TATAGTAGATAGTTG[C/T]TTATCTGTGCCACTA | 386649 |
rs27353600 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Nsfl1c | Mm_Celera | 2:151499985 | TTGGTAATGGTCCAA[A/T]TGTGCCTTTTTGTAG | 386649 |
rs27353601 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nsfl1c | Mm_Celera | 2:151499964 | AGTCTCCTGTTCACC[A/G]GTTCCTTGGTAATGG | 386649 |
rs27353602 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151499597 | CTGCTGAAGCCAGAG[A/C]TAACCCCTCAAACTT | 386649 |
rs27353603 | snp | A/G | 0.42 | 0.183303 | intron-variant | Nsfl1c | Mm_Celera | 2:151499573 | AGAGTTTTTGCACTA[A/G]CCATCTGTCTGCTGA | 386649 |
rs27353604 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsfl1c | Mm_Celera | 2:151499506 | CTCTCATGTTGTCTT[A/G]AACCCTTTTCCTGAT | 386649 |
rs27353605 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nsfl1c | Mm_Celera | 2:151498884 | TATACTTTGGCAGGT[A/G]TCTTCTGGCAAGAGA | 386649 |
rs27353606 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nsfl1c | Mm_Celera | 2:151498682 | AGCTGTTACAGGACA[C/T]TTAGCCTGCTGCTGA | 386649 |
rs27353607 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151498505 | CTTTGACTGTGGGCT[G/T]CTGTGAAGGACAAAA | 386649 |
rs27353608 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nsfl1c | Mm_Celera | 2:151498408 | GCTACAGCTTAACAT[C/T]AGCATTAAACGTGAA | 386649 |
rs27353609 | snp | C/T | 0.5 | 0 | intron-variant | Nsfl1c | Mm_Celera | 2:151498268 | CTATGACTGACACTG[C/T]ACCCTGCCTCATTCC | 386649 |
rs27353610 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nsfl1c | Mm_Celera | 2:151497806 | TCCTCTCTTCTTCCA[C/T]AGTCCAGAATAACCC | 386649 |
rs27353611 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nsfl1c | Mm_Celera | 2:151497753 | AGTACCAAGGAGGAG[A/G]AATTGAAATGTAGCC | 386649 |
rs27353612 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nsfl1c | Mm_Celera | 2:151497333 | TCTCTCTACAGAAGC[A/G]TCTGAGCTCCCACAC | 386649 |
rs27353613 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Nsfl1c | Mm_Celera | 2:151497214 | TTCTGAAGTTGACAC[C/G]GGGAGTTAACTAACA | 386649 |
rs27353614 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nsfl1c | Mm_Celera | 2:151497209 | ACCTCTTCTGAAGTT[A/G]ACACGGGGAGTTAAC | 386649 |
rs27353615 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Nsfl1c | Mm_Celera | 2:151497162 | TGAGGTTAATGGCCT[A/G]TCACACTAGTAAGAT | 386649 |
rs27353616 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsfl1c | Mm_Celera | 2:151497150 | CCATAGTAGAGATGA[A/G]GTTAATGGCCTGTCA | 386649 |
rs27353619 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nsfl1c | Mm_Celera | 2:151495965 | GGACTCATATGAAGG[A/G]CTTTCACATGTGTAA | 386649 |
rs27353620 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nsfl1c | Mm_Celera | 2:151495919 | AATCAATGCCTTCTC[A/G]TTGAGTTGGCGACAG | 386649 |
rs27353621 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsfl1c | Mm_Celera | 2:151495846 | CAGGAGGTGCCTCCT[C/T]CATCTCCGTGGGACT | 386649 |
rs27353622 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nsfl1c | Mm_Celera | 2:151495672 | TAACTTGACTAGCAG[C/T]GCCAGGACTTGAATG | 386649 |
rs27353623 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nsfl1c | Mm_Celera | 2:151495668 | GTGGTAACTTGACTA[A/G]CAGTGCCAGGACTTG | 386649 |
rs27353624 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsfl1c | Mm_Celera | 2:151495319 | AAAGACTAACCCTAT[C/T]TTATGGATAAGGAAT | 386649 |
rs27353625 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Nsfl1c | Mm_Celera | 2:151494364 | GGTGACTGGCACTGA[A/G]GAGGACAGGGCCCGT | 386649 |
rs27353626 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Nsfl1c | Mm_Celera | 2:151494273 | GGGCTGTTGCAGTGT[C/T]CGCCGGAGCGGTTTG | 386649 |
rs27353627 | snp | A/G | 0.375 | 0.216506 | utr-variant-5-prime | Nsfl1c | Mm_Celera | 2:151494199 | TGGGCGGAGCCTACG[A/G]GCAGGCGCCCAGCGG | 386649 |
rs27353628 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151494136 | GCCACCAGAGGGCGC[A/G]AGGCGGCTAGGTTTC | 386649 |
rs27353629 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151494032 | AGGATCTGATTTCGG[A/G]ACTACTTCATCCTGT | 386649 |
rs27353630 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493941 | CAAGCCATAGACAGC[C/G]TAATGCTTCAAGAAG | 386649 |
rs27353631 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493745 | AGCCTGCCAGTGGCA[A/G]TGCAATGGTGATTTG | 386649 |
rs27353632 | snp | A/G | 0.4032 | 0.19756 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493516 | TCAATAAGTTCTGGT[A/G]GAATAATTGCTGGTC | 386649 |
rs27353633 | snp | A/G | 0.497041 | 0.0383476 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493470 | AGAAAAACAAAGCAT[A/G]TAATCAGCTGACAGG | 386649 |
rs27353634 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493407 | ATTCATTAGTAGTGG[C/T]TTCATGCACAGTGAA | 386649 |
rs27353635 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493273 | GCTCTTCATTCTCAT[A/G]GTATGACTCTGTGGA | 386649 |
rs27353636 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492761 | TAAATATGCTCTGCA[A/G]GGTCACTCTTTCAGT | 386649 |
rs27353637 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492694 | GCATCCTCTGCCTTT[G/T]AGCATGGATTCACTT | 386649 |
rs27353638 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492574 | GACAGCGAAGATAGA[A/G]GCTTGGTCAGTCTTT | 386649 |
rs27353639 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492507 | AGCTTTAAATTGAAA[A/C]CAGAACTTGACCACA | 386649 |
rs27353640 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492392 | CTGGAAGCCATGAGT[A/G]TTGTGTGGAGTGCCC | 386649 |
rs27402538 | snp | C/G | 0.32 | 0.24 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511701 | GGTATGTATAGTTAA[C/G]GTGTAGCTTTGGGAC | 386649 |
rs27402539 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511685 | GAAGCAATTTTATTT[C/G]GGTATGTATAGTTAA | 386649 |
rs27402540 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511603 | GCAGCAGATACACAT[A/T]TGGGAATGAATGTCT | 386649 |
rs27402541 | snp | A/G | 0.152778 | 0.230321 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511545 | AGTGGGTTCAGGTAG[A/G]TGTCTTTTTCTAGGA | 386649 |
rs27402542 | snp | C/T | 0.197531 | 0.244432 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511542 | CTTAGTGGGTTCAGG[C/T]AGGTGTCTTTTTCTA | 386649 |
rs27402543 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511505 | ATAGAGGGGTTTTCT[A/T]TTGGATGTGGCACAT | 386649 |
rs27402544 | snp | A/C | 0.32 | 0.24 | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511428 | AAGTCACTGTGTACA[A/C]ATAATCATCTCCTGC | 386649 |
rs27402545 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Nsfl1c | Mm_Celera | 2:151511173 | CCCTTCCAGTGCCAC[A/G]TCTCGTCCGTAGCTC | 386649 |
rs27402546 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Nsfl1c | Mm_Celera | 2:151511114 | TGTCTCCCATGACTG[C/T]GGCCATGCCCGTGGG | 386649 |
rs27402547 | snp | A/T | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151510380 | TCCCAGGTGCAAGAA[A/T]GTGCCTGGAGGAGGG | 386649 |
rs27402548 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151510336 | GGTATAAGGAAGAAT[C/T]CTGTTGCCAGTGGCT | 386649 |
rs27402549 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsfl1c | Mm_Celera | 2:151510127 | ACCAAATGTTCCTAA[C/T]GTTGGTGCTTCCCTC | 386649 |
rs27402550 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsfl1c | Mm_Celera | 2:151510104 | AGGTAGGCAATCTTT[A/G]AGTGCTGACCAAATG | 386649 |
rs27402551 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Nsfl1c | Mm_Celera | 2:151510051 | GTTTCATCCATAGTG[G/T]GCTAGCTAAGCCAGG | 386649 |
rs27402552 | snp | A/G | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151510008 | TAAAGATACTTGGCA[A/G]CTCCTTTCTCTCAAA | 386649 |
rs27402553 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nsfl1c | Mm_Celera | 2:151509967 | TGAAGAGACTAGCAG[A/G]AGAGGTGCTAGGGGC | 386649 |
rs27402554 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nsfl1c | Mm_Celera | 2:151509869 | TAGGTCTCATTCCTC[A/C]TCATTAGGATTAAGC | 386649 |
rs27402555 | snp | C/T | 0.32 | 0.24 | intron-variant | Nsfl1c | Mm_Celera | 2:151509683 | CCACAGGTACCTTCT[C/T]TATCTGGACTACCTT | 386649 |
rs27402556 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon | Nsfl1c | Mm_Celera | 2:151509536 | GGTATTAAACACCAG[C/T]TCTCCAGCCCAACAA | 386649 |
rs45947017 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496383 | TCTTTGTTTCCCTTG[A/G]TGGGTGGATTTCCCC | 386649 |
rs46427525 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496327 | GATAAATAATAGTTG[A/G]TGGTCTTCCTTTATG | 386649 |
rs47166990 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496349 | TCCTTTATGTTTTTC[A/G]TATTAATTTTATTTA | 386649 |
rs48897904 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496365 | TATTAATTTTATTTA[A/G]TATCTTTGTTTCCCT | 386649 |
rs50446547 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496326 | GGATAAATAATAGTT[C/G]GTGGTCTTCCTTTAT | 386649 |
rs50850311 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496376 | TTTAGTATCTTTGTT[C/T]CCCTTGGTGGGTGGA | 386649 |
rs107677296 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496975 | AGTTAATACATGATT[G/T]TGGGCCACCATGTGG | 386649 |
rs107954411 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496949 | GAAGGCATTGGATTT[C/T]CTGAAACTGGAGTTA | 386649 |
rs108547543 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496887 | TTGTTTTGAATGTGA[A/G]TGGGTGTTCTGCCTG | 386649 |
rs211718042 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505485 | GAAAAGCCCATGTTA[C/G]TCTCACTTTCGTGAA | 386649 |
rs212059907 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492777 | GGTCACTCTTTCAGT[C/T]TCAGGCACCTGAGAA | 386649 |
rs212155497 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503941 | ATTCCAGCTTTCACC[A/T]CTTATCCTGCCCCTG | 386649 |
rs212829027 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151502320 | CTCTTGAGGCTCCCA[A/G]TGTACATCATAAGAA | 386649 |
rs213113478 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499414 | CCTTCATCCTTGCTC[C/T]TCTGCTGAGCAGCAC | 386649 |
rs213516975 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504264 | CCATTTCAAAAGGGA[C/T]TAGTTACGTGTGTGA | 386649 |
rs213538992 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151502819 | TCTCCCCATCTCCAT[G/T]CTGCCACCACCATTG | 386649 |
rs213790690 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500340 | AGTTACAGATATTTG[G/T]GAGCTACTATGTGTG | 386649 |
rs214652816 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510068 | CTAGCTAAGCCAGGA[C/T]TCAGATGTGGGCCAC | 386649 |
rs214717723 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509219 | GAAGAACATAACACA[A/G]CCAGTCACTTGCAGT | 386649 |
rs214742244 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496831 | GTTTTTTTGTGGCTT[G/T]GTTTGTTTGTTTGTT | 386649 |
rs214989398 | in-del | -/TC | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505705 | CCTGGTGACAGAGAG[-/TC]TCTCTCCTCTCAGGC | 386649 |
rs215386904 | in-del | -/ATA | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509143 | ACAACATGAGGTACT[-/ATA]ATATTAAAGGGTTGC | 386649 |
rs215604618 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492852 | CCTACTGAACCTCTG[A/G]TTTCTGTCTTTACCT | 386649 |
rs216049627 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498115 | GACTCAAAAGCAAAA[A/G]GCCAGACCTCAGAGC | 386649 |
rs216288610 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508740 | GAACTTGGTTTGCCC[A/G]AGGCCACCCAGCTAA | 386649 |
rs216347114 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510128 | CCAAATGTTCCTAAT[A/G]TTGGTGCTTCCCTCT | 386649 |
rs216377900 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509969 | AAGAGACTAGCAGAA[A/G]AGGTGCTAGGGGCCT | 386649 |
rs216788043 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507052 | ATATAAAACAAACCT[C/G]AGATTTGGGGGGTTT | 386649 |
rs216845972 | in-del | -/TTGTTTGC | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496846 | GGTTTGTTTGTTTGT[-/TTGTTTGC]TTGCTTGCTTCCTTG | 386649 |
rs217538393 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496488 | CAGGTGTAGGAACCA[A/G]AGTATGGGTTTTGTC | 386649 |
rs217899347 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504411 | AAGGTTTCTTGAGTG[G/T]TCTTTGGATCACACA | 386649 |
rs218068967 | in-del | -/GTGGTGGTGGTA | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151492311 | GTGGTGGTGGTGGTG[-/GTGGTGGTGGTA]GTGGTGGAGTGTGTG | 386649 |
rs218447942 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503424 | TTAAGGAGGGAGGAA[A/T]TTTTTGTTGTTAACA | 386649 |
rs218528112 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500686 | CTTTAACTCTTCCTG[A/T]TATAATTTTTGCTCC | 386649 |
rs218536561 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509057 | AAACACAGGTATTTT[A/T]CAATTCATACCAGTA | 386649 |
rs218958174 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505265 | GTAGTAATGTAAGAT[A/C]GTGAAAACTCACTCA | 386649 |
rs219111037 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510245 | AGTGTGGATGAGGGG[-/T]CTAGGCTGCATCTTA | 386649 |
rs219175658 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151502209 | AAATTTTAAAAAGTG[A/C]TGGTTTAATCTCAAG | 386649 |
rs219206554 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492504 | GTCAGCTTTAAATTG[A/G]AACCAGAACTTGACC | 386649 |
rs219313054 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500518 | CCTCACAGTAGCATT[C/T]GCTAATTTATTCTCA | 386649 |
rs219519316 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497154 | AGTAGAGATGAGGTT[-/A]ATGGCCTGTCACACT | 386649 |
rs219668921 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498478 | TTTCTTACTGTTTTG[C/G]TTAAGCCCTAGCTTT | 386649 |
rs220115484 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497378 | AGTCTAATTGCACTT[-/A]ACTCCAGGGTATATG | 386649 |
rs220145416 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507918 | TCAGCCTGCTCTCTT[A/G]TAGAACCAAGACTAC | 386649 |
rs220149175 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510431 | CTGGCATACAGTTGA[A/G]AAGTGCCCCCTCTGA | 386649 |
rs220199790 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506107 | CTTAGAGAGATGGCC[A/G]CAAGCCATTCTGGGA | 386649 |
rs220216996 | snp | A/C | | | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511765 | CGGACCTTTGACTTG[A/C]AGCAGCTTCAGGCAT | 386649 |
rs220231676 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497265 | CTAGACCTTTGGCCA[C/T]AGTCAATCACTTTTG | 386649 |
rs220259523 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151494469 | ACGGAGTGCGGCGTC[A/G]GCTCTGCGATCCCTA | 386649 |
rs220809933 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493375 | TTTCATCCATTCACT[C/T]ATTCATTCATTCACA | 386649 |
rs220891111 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495175 | GACGATGACTAATAT[G/T]TCTTGAGTACCTACA | 386649 |
rs221231816 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495524 | CCAGGAGTAAATAGT[C/T]CCTCTTTCAAAAACA | 386649 |
rs221370462 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499791 | GCAGTAGAAATAGGC[A/T]GAGAGCTCTATGCTC | 386649 |
rs223448134 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503974 | ACAAGGGGCAAACAC[A/G]AGCAAACCTTGTCCC | 386649 |
rs223500901 | in-del | -/TTTCTTGCTTGTTTGC | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496845 | GGTTTGTTTGTTTGT[-/TTTCTTGCTTGTTTGC]TTGTTTGCTTGCTTG | 386649 |
rs223855376 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510739 | AGAGGAGGAAATGAG[A/G]TTGATGTGCTTCCAG | 386649 |
rs224011001 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510809 | AAGCAGGCATGGTAA[A/G]AAGGAGCCTTCAGAA | 386649 |
rs224065102 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498545 | AAGGGGGTGTGGCTT[G/T]TCATTGTCTTTGTTT | 386649 |
rs224133265 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499637 | ACCCTGTGGGGTTCA[C/T]CCAACCCCACCCCCT | 386649 |
rs224175910 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507086 | TTTCAAGTTATATAT[-/A]AAAAAAACCTTTTTA | 386649 |
rs224348325 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508075 | CTGTGTCAAGTTGAC[A/G]CAAAACTAGCCAGTA | 386649 |
rs224501054 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500214 | TTCAGTAGTAAAAAA[A/T]ATTTTTTAATTTTAT | 386649 |
rs224532302 | in-del | -/CT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500378 | ATCCAAATGTTGGTC[-/CT]CTGCAAGAGCATCAA | 386649 |
rs224584225 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501218 | GTGTCCTCCCAACAC[C/T]ATCATACTGTTTTTA | 386649 |
rs224977601 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499146 | CTCTTCTGCTTCCTG[A/C]GTCTCAGTTTTCTGT | 386649 |
rs225303648 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505600 | ACCTTGTCCATTTTT[A/T]GCTGTTTTCCTTGAG | 386649 |
rs225890434 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504870 | TTTTATGTGAAGGGG[A/G]CAGGGGATATGCACA | 386649 |
rs226047968 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507482 | CCAAAATAGCAATGG[A/C]CCTGAAAAGAGTCTC | 386649 |
rs226146569 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493026 | GTCAGGCTGGGCAGA[A/G]GGCTGACTATGAATC | 386649 |
rs226202222 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504970 | TGGCATAAGTGCTAG[A/G]AACTAGGAACCAAAG | 386649 |
rs226421016 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496310 | AGACGACCTGACACA[C/T]GGATAAATAATAGTT | 386649 |
rs226483887 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509769 | TGTTCTCCTTCATGT[A/T]CACTATCCAGCAATC | 386649 |
rs226568037 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505836 | AGAGATGGAGACAAA[A/G]AGGAAGAAGTGCTTG | 386649 |
rs226739359 | in-del | -/CT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498330 | TGAGAGAGAGAGAGA[-/CT]AAGAGAGAGAGAGAG | 386649 |
rs228168973 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501573 | TTGAATTATTTCCTT[A/C]CAGTAATTTCTCTAA | 386649 |
rs228278945 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503611 | CCTCTCCTGAGGGAG[A/G]AATTTGGGGGTTTTG | 386649 |
rs228477573 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497622 | ATTATTTGCAGTGAG[A/G]TACTGATGAAATACT | 386649 |
rs228539110 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508306 | TCCTTTGAGCTACTT[C/T]CTCAACTTTTCTGGG | 386649 |
rs228881656 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496496 | GGAACCAAAGTATGG[C/G]TTTTGTCTTCATGTT | 386649 |
rs228912586 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499080 | CAGACACAAGAGCTG[G/T]GCTTCTTCCCTAGAT | 386649 |
rs229675378 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497502 | GAGCTTTAAACTACA[-/T]TTTTTTCCCTTTGAG | 386649 |
rs229911350 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500841 | CACAGTGGTGTTTAA[A/G]TCACCTAGGATAAGG | 386649 |
rs229979576 | snp | A/G | | | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511693 | TTTATTTGGGTATGT[A/G]TAGTTAACGTGTAGC | 386649 |
rs229989895 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151502659 | TTGCCTCCTGGAAAG[C/G]GGCTTGCAGAAGGAT | 386649 |
rs230030896 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499463 | AGAACTCCAGTTGCA[A/G]CTCTAAATCTGTTTA | 386649 |
rs230934604 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507508 | GTCTCTAATTTTCCT[C/T]CTGAAATTTCACAAG | 386649 |
rs231048882 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509163 | ATTAAAGGGTTGCAG[C/T]ATTAAAGGTTAAGAA | 386649 |
rs231413314 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496421 | AATATATCCCCATCT[C/T]CACTTCCAGGCTAAC | 386649 |
rs231553950 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500461 | ACAGTGAATAACTCA[-/T]TTCCCCCATTTCCAG | 386649 |
rs231694653 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151494970 | TAGGACTTACTGTCT[G/T]GTTCACTGGCATGTA | 386649 |
rs231773609 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496849 | TTGTTTGTTTGTTTG[C/T]TTGCTTGCTTGCTTC | 386649 |
rs232033064 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497436 | TTCAACTCCAGTATG[C/T]AGAAAAAATGTCTCT | 386649 |
rs232314045 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506458 | TGAGGATCTCAGTGA[A/G]AGTAGTGGCAGAGTA | 386649 |
rs232470404 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492800 | CCTGAGAAGCTGGGA[C/T]GGCAAGGCCCAGGTT | 386649 |
rs232534838 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506920 | CTCAGCATCCTCCTG[C/T]CACAAAGTGCTAGGG | 386649 |
rs233050506 | snp | A/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493637 | CCCCACTTTCACTTG[A/T]GGGGCAGCACTGTTG | 386649 |
rs233175099 | in-del | -/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510241 | ACAGAGTGTGGATGA[-/G]GGGTCTAGGCTGCAT | 386649 |
rs233404645 | in-del | -/ACCCATCTT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510156 | TCTGAGAGAGTTGTA[-/ACCCATCTT]ACCAACCAGTTACTG | 386649 |
rs233503828 | snp | A/C | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492865 | TGGTTTCTGTCTTTA[A/C]CTGTAAAATGGGAAT | 386649 |
rs233632299 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151494162 | GTTTCCCACACGGAG[A/G]GCTTTTCCTGTGGCA | 386649 |
rs233715134 | in-del | -/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498212 | CAAACAAACAAACAA[-/C]CCCAACTTTATGTAG | 386649 |
rs233958003 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506677 | TGCATGTAGAACTGT[C/T]TGGCATGAGCTGTGA | 386649 |
rs234243004 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499325 | TCTGTCTTTGTTGGT[A/G]TCCTCTAAATTGCTG | 386649 |
rs234393352 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509052 | TGGAAAACACAGGTA[-/T]TTTTTCAATTCATAC | 386649 |
rs234873596 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498440 | GGAATGTAAGACTGG[A/C]CAGGAGTTGAGGCCT | 386649 |
rs234984972 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500353 | TGTGAGCTACTATGT[A/G]TGTTCTGGGATCCAA | 386649 |
rs235671451 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500093 | CCTTATAGTAGATAG[C/T]TGCTTATCTGTGCCA | 386649 |
rs235682261 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499821 | CCCTGCCACCCACAC[A/G]TTGATTCTGCAGGAC | 386649 |
rs235696220 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499099 | TCTTCCCTAGATCAC[A/T]CAAGCCAGCAAATGG | 386649 |
rs235780360 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151494440 | GGCGGGCCGCTTCGG[A/G]CGGGCTGGGGAATAC | 386649 |
rs236867576 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505919 | TGCTTTCTGTTGCTG[G/T]GATTAAACCCAGAAT | 386649 |
rs237540591 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493102 | CAATGTGTTAGGTTC[C/T]AAATGGCCTCTGTGG | 386649 |
rs237758024 | snp | A/C | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493345 | TGAGATCCTCATTGT[A/C]TGATCCATGTGTTAT | 386649 |
rs237768401 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508006 | AATGCCTTACAGTTG[C/G]ATCTCATGGAGGCAT | 386649 |
rs237845725 | in-del | -/GA | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505827 | AGAAAGGGAGAGATG[-/GA]GAGACAAAGAGGAAG | 386649 |
rs237910157 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508321 | TCTCAACTTTTCTGG[A/G]AAATGTTTGTTTGTT | 386649 |
rs238242593 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507214 | TTTGAGCCACTTACC[A/T]GACAGTTTGATAAAG | 386649 |
rs238528731 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508858 | AACCACTCCACTACC[-/A]GGCTCATAGCTGACC | 386649 |
rs238592762 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504286 | CGTGTGTGAACGAGC[A/G]GCCTCTAAAAGACGA | 386649 |
rs238833318 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498516 | GGCTTCTGTGAAGGA[A/C]AAAAGAGGACGGAAA | 386649 |
rs239257015 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505325 | CCTGTCATTGTAACT[C/T]CGTGCTTATTACCTC | 386649 |
rs239667055 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500017 | AAGCCTTTCCCTCAC[A/G]GGAGACAAGAGGCTT | 386649 |
rs239968913 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501262 | TGTAATAGAATTATT[A/G]TTTCATTGTAGAAAA | 386649 |
rs240109659 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503509 | CCCTATACACTCCCC[C/G]CGCCCTGCTCCCCAA | 386649 |
rs240292740 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499646 | GGTTCACCCAACCCC[A/G]CCCCCTGAATATTAG | 386649 |
rs240443379 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505604 | TGTCCATTTTTAGCT[A/G]TTTTCCTTGAGGCAT | 386649 |
rs240481455 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497148 | TGCCATAGTAGAGAT[G/T]AGGTTAATGGCCTGT | 386649 |
rs240497953 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510260 | TCTAGGCTGCATCTT[A/C]TATCTCCAGCCTCTC | 386649 |
rs241129386 | in-del | -/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497574 | CTGCCTCCCACAGAA[-/G]GGGGGGGGGGTCACA | 386649 |
rs241817224 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504370 | GGTTAGAGGGCCAGG[C/G]CAGGAATGGGGAAGA | 386649 |
rs241981309 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497671 | GGGTGGGTTGTAAGT[A/G]TATGGGCTGCTGGCA | 386649 |
rs242153535 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495554 | ATAACAAACAGAAAG[A/T]TGCTCTTAAAGGCGC | 386649 |
rs242180624 | in-del | -/AGAGAGAGAGAGAA | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498318 | GGGTGGGTGGATGTG[-/AGAGAGAGAGAGAA]AGAGAGAGAGAGAGA | 386649 |
rs242286316 | in-del | -/TT | | | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511497 | TCCTAGAATAGAGGG[-/TT]GTTTTCTTTTGGATG | 386649 |
rs242831101 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509807 | TCCCTGGAGGAAGCA[A/G]TGGGTTGGGATGATT | 386649 |
rs243001023 | in-del | -/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496980 | ATACATGATTGTGGG[-/C]CACCATGTGGGTGCT | 386649 |
rs243414129 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498156 | TAATCCCAGCACTGC[A/C]TAGGCAGAAGCAGGT | 386649 |
rs244046750 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506696 | CATGAGCTGTGAATG[G/T]AGCATAGCTGCTGCT | 386649 |
rs244108553 | snp | G/T | | | synonymous-codon | Nsfl1c | Mm_Celera | 2:151505409 | AGACAATGGTGACCT[G/T]AGAAGCTACCAAGAC | 386649 |
rs244532939 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505022 | CATGCTCTTGACCAC[C/T]GAGTCATCTCTCCAG | 386649 |
rs244574423 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504243 | CTTGTGGACTGTTCA[C/T]TGTGCCCATTTCAAA | 386649 |
rs244658948 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506958 | AATGTACACCCATCA[C/T]ACCTAGGCTCATTAT | 386649 |
rs244768777 | snp | A/C | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151494036 | TCTGATTTCGGGACT[A/C]CTTCATCCTGTGGGA | 386649 |
rs244818727 | snp | A/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492836 | TTTCATTAGGTGTGG[A/T]CCTACTGAACCTCTG | 386649 |
rs244844809 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496335 | ATAGTTGGTGGTCTT[C/T]CTTTATGTTTTTCAT | 386649 |
rs245175994 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508211 | CTCCTTCTAGTCTCT[G/T]TTCTTACTGCCAACA | 386649 |
rs245225327 | snp | A/C | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492474 | GGGTACATTTCATAC[A/C]TGAATGACAAGAAAG | 386649 |
rs245241659 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504894 | ATGCACATGAGTACA[A/G]AGGCCAGAAGAGGGT | 386649 |
rs245589017 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504740 | AGACAGTAAAACTTT[C/T]ATAGACTTGTAGCAG | 386649 |
rs245605397 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498356 | GAGAGAGAGACTGAG[-/A]ATCTGTGTGTTTTAC | 386649 |
rs245672285 | in-del | -/C | | | utr-variant-3-prime | Nsfl1c | Mm_Celera | 2:151511138 | CCGTGGGGATTTCCT[-/C]CCACCCCGTACACAC | 386649 |
rs245783654 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510449 | GTGCCCCCTCTGATA[C/T]CAAAATAAGATGTGT | 386649 |
rs245869519 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500215 | TCAGTAGTAAAAAAA[A/T]TTTTTTAATTTTATA | 386649 |
rs245925543 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499493 | ATAAGTAACATCTCT[C/G]TCATGTTGTCTTGAA | 386649 |
rs246294011 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499224 | CCTGAATCTGCCTTT[C/T]TCATCTTAACCCCTT | 386649 |
rs246349394 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497900 | AGACTCATGACTTGC[G/T]ACAGAGTATTTATCT | 386649 |
rs246949802 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503309 | CTGTGTAGAAGACTA[A/G]TGTGTCTGTGAGCTA | 386649 |
rs247190077 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501000 | GTCATGTACTGGGGC[-/T]TTTTTTATTTCTCTC | 386649 |
rs247975372 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503622 | GGAGGAATTTGGGGG[G/T]TTTGTTTATTTGTTT | 386649 |
rs248112221 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497482 | AAATTCTCACAGAGG[A/G]TCTCTGAGCTTTAAA | 386649 |
rs248163063 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510751 | GAGGTTGATGTGCTT[A/C]CAGGTGACAGCTTTG | 386649 |
rs248377682 | snp | A/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493390 | TATTCATTCATTCAC[A/T]CATTCATTAGTAGTG | 386649 |
rs248386449 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509165 | TAAAGGGTTGCAGCA[C/T]TAAAGGTTAAGAACC | 386649 |
rs248447982 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507607 | TCTTAACAACGAATG[A/G]ATCTTCTAGCCCAAA | 386649 |
rs249209942 | in-del | -/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498464 | AGGCCTCTTAGCCTT[-/G]TCTTACTGTTTTGCT | 386649 |
rs249256480 | in-del | -/CTGTGGGCTT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498496 | AAGCCCTAGCTTTGA[-/CTGTGGGCTT]CTGTGAAGGACAAAA | 386649 |
rs249455310 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496693 | CTAGGTAAGGACCAA[C/T]TTCAGTTGCTACATG | 386649 |
rs249614293 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510383 | CAGGTGCAAGAATGT[A/G]CCTGGAGGAGGGTTC | 386649 |
rs249863095 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498514 | GGGCTTCTGTGAAGG[-/A]ACAAAAGAGGACGGA | 386649 |
rs249939429 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503937 | GGGTATTCCAGCTTT[C/T]ACCTCTTATCCTGCC | 386649 |
rs250067409 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504389 | GAATGGGGAAGAAGA[C/T]GGACACAAGGTTTCT | 386649 |
rs250130548 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503332 | GTGAGCTAGATCAGA[A/G]CTCAGAAACCTACCT | 386649 |
rs250169036 | in-del | -/TC | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503689 | GTCTGTTTTTAGAAT[-/TC]TCTCTGTAGACCATG | 386649 |
rs250205782 | in-del | -/CTC | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499613 | TAACCCCTCAAACTT[-/CTC]CTCCACACCCTGTGG | 386649 |
rs250317169 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151502767 | AACCTCATCCTCAAG[A/C]GATCCCAGGAAATAG | 386649 |
rs250384453 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500904 | ACTGCTGTGCATAGG[A/G]GTATAATATCCTAAG | 386649 |
rs250618630 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501124 | CCACAACATAGAAAT[A/T]GCCAAGTATCTTCTT | 386649 |
rs250782448 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500215 | CAGTAGTAAAAAAAA[-/T]TTTTTTAATTTTATA | 386649 |
rs251049705 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498668 | CCAGCCTTTGACCTA[A/G]CTGTTACAGGACACT | 386649 |
rs251361157 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509462 | TTGTACCTCTGTGAG[A/G]ACCTTGTTTCTTTCT | 386649 |
rs251584471 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504529 | ATGGATGGATTTGGT[C/T]GGTTTTGTTTTGTTT | 386649 |
rs251622111 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495325 | TAACCCTATCTTATG[C/G]ATAAGGAATTGGACC | 386649 |
rs252080044 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498447 | AAGACTGGCCAGGAG[C/T]TGAGGCCTCTTAGCC | 386649 |
rs252104783 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505237 | GTGTATTTGTCTGAT[A/T]GTTGATGTTTTTGTA | 386649 |
rs252135597 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497213 | CTTCTGAAGTTGACA[A/C]GGGGAGTTAACTAAC | 386649 |
rs252211486 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495069 | GATCCCTAGAGCAAC[A/G]CCCATCTCTTATTGC | 386649 |
rs252497224 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501734 | ACAAGAATAATCTGG[C/T]TATAGCCTCATTTCT | 386649 |
rs253275170 | in-del | -/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509141 | CTACAACATGAGGTA[-/C]TATAATATTAAAGGG | 386649 |
rs253362136 | in-del | -/AA | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493291 | ATGACTCTGTGGAAC[-/AA]AAAGACTGAAAGGGG | 386649 |
rs253492377 | in-del | -/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498637 | ATTTGGTGGTAGTCA[-/G]GGGAGCAGCTGCTCT | 386649 |
rs253608521 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498542 | GGAAAGGGGGTGTGG[C/T]TTTTCATTGTCTTTG | 386649 |
rs253955875 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504924 | TGTTTAGATTTTCAG[G/T]AATGAGAGTTAAAGA | 386649 |
rs254085942 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506084 | GCACTTGTCAATGAA[A/T]ACAGTCTCTTAGAGA | 386649 |
rs254180876 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493874 | CATAAGCAACAAGAA[A/G]ACAGGATACTTTGTT | 386649 |
rs254406731 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509033 | CAGAATTCACCTAAG[A/G]TCATTGGAAAACACA | 386649 |
rs255322410 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505104 | TTGAGTCATTTCTTA[C/T]ATAGTCACCTCGATA | 386649 |
rs255718535 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493103 | AATGTGTTAGGTTCC[A/G]AATGGCCTCTGTGGG | 386649 |
rs255901696 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493876 | TAAGCAACAAGAAGA[C/T]AGGATACTTTGTTTT | 386649 |
rs255903664 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509767 | GCTGTTCTCCTTCAT[A/G]TACACTATCCAGCAA | 386649 |
rs255909722 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499120 | CAGCAAATGGAGGGT[A/G]GAAGTCCGAGCTCTT | 386649 |
rs255914943 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508446 | ACAAGTAGCATGATA[A/G]TTGCCACTGTCCCAG | 386649 |
rs256029104 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495567 | AGATGCTCTTAAAGG[C/T]GCTGTGAAGCCTCTG | 386649 |
rs257273405 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506634 | GTCCTTGCCCTCGGG[A/G]TTCTATAGGGAGGAA | 386649 |
rs257290048 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500430 | TTCTCTCCAGCTCTC[A/G]GTAGTTTTCTTTAAA | 386649 |
rs257807052 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503596 | TTGCAAGACCAAGGT[C/T]CTCTCCTGAGGGAGG | 386649 |
rs257820320 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501545 | CACCGTTTATGTTAA[C/T]CTTTGACCAGTTTTG | 386649 |
rs258323045 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493355 | ATTGTCTGATCCATG[C/T]GTTATTTCATCCATT | 386649 |
rs258540840 | snp | C/T | | | downstream-variant-500B | Nsfl1c | Mm_Celera | 2:151511467 | TCCTGCTGCAGGTGG[C/T]TGTGTGGAGGATTCC | 386649 |
rs258609210 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510782 | GCCACTCTGTAGAGA[A/T]GGGACACAGGGAAGC | 386649 |
rs258736709 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499633 | CCACACCCTGTGGGG[C/T]TCACCCAACCCCACC | 386649 |
rs259457488 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499411 | TTGCCTTCATCCTTG[A/C]TCCTCTGCTGAGCAG | 386649 |
rs259533199 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508035 | ATTTCCTCAACTGAA[C/G]CTCCTTTCTCTGTGA | 386649 |
rs259783071 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497413 | CAGAAAATTTTGCTG[A/G]GTTTGAATTCAACTC | 386649 |
rs259950845 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151496478 | TCTTTGGTTCCAGGT[A/G]TAGGAACCAAAGTAT | 386649 |
rs260286527 | snp | A/C | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500646 | TCAAGTGTGCAACTC[A/C]CCAGTTGATACAGGC | 386649 |
rs260397247 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151498289 | GCCTCATTCCACAAC[A/T]GGCAGGTGGGTGTGG | 386649 |
rs261068452 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505827 | GAGAAAGGGAGAGAT[A/G]GAGACAAAGAGGAAG | 386649 |
rs261237089 | snp | G/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151494457 | GGGCTGGGGAATACG[G/T]AGTGCGGCGTCGGCT | 386649 |
rs262015515 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500214 | TCAGTAGTAAAAAAA[-/T]ATTTTTTAATTTTAT | 386649 |
rs262171638 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151501179 | TAACTTACACAATAA[A/G]TAGAAAAATAGGGTT | 386649 |
rs262324103 | in-del | -/TGG | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151492236 | TGATGATGATGATGA[-/TGG]TGATGGTGATGATGG | 386649 |
rs262840857 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504329 | CTCAATGGGGACTTA[C/G]ATAAAAATGACAGTT | 386649 |
rs263025798 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500074 | TACAGCCCCTGTTGT[A/G]CATCCTTATAGTAGA | 386649 |
rs263476977 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509443 | GAACCCAGAGATTTC[A/G]GCCTTGTACCTCTGT | 386649 |
rs263507023 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510541 | TACAACCACTTCTGT[A/G]GCAAGATGGGAGCAA | 386649 |
rs263555995 | in-del | -/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493637 | CCCACTTTCACTTGA[-/T]GGGGCAGCACTGTTG | 386649 |
rs263677504 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499764 | CTAAGGAAACTTTTT[A/T]AAAATTATCCTGCAG | 386649 |
rs263765508 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151510286 | CTCTCATGGGCCACT[A/G]CTACATAGTGGCAGA | 386649 |
rs263996230 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504441 | CAAGGGGGCAGTGTG[-/T]GTGGGGGGAGTGATT | 386649 |
rs264037131 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495428 | GCTTCCCAAACATTA[A/G]GGATCTTTATTCCTT | 386649 |
rs264365435 | snp | A/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506672 | GCCAGTGCATGTAGA[A/T]CTGTTTGGCATGAGC | 386649 |
rs264418780 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492881 | CTGTAAAATGGGAAT[A/G]CTAACCTCTACCTAG | 386649 |
rs264453656 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151507332 | TCTCTTCTTAATCAC[C/G]GCTAATTTCTTAGCT | 386649 |
rs264511129 | in-del | -/GT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497577 | CTCCCACAGAAGGGG[-/GT]GGGGGGGTCACAGGA | 386649 |
rs264524713 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151503896 | TTATGAGTTTATACT[A/G]AGAATAGTAGCTATT | 386649 |
rs264745779 | in-del | -/CCCGG | | | intron-variant | Nsfl1c | Mm_Celera | 2:151494607 | TGGAGGCGGGCGGGC[-/CCCGG]CCTGCTTTGCAGGGC | 386649 |
rs264932309 | snp | C/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500122 | CACTAGCCTGTAATA[C/G]CAGTGTCTAATTTTT | 386649 |
rs264944258 | in-del | -/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504350 | AATGACAGTTTTCAC[-/T]TGGTGGTTAGAGGGC | 386649 |
rs265406226 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151500946 | CTCGGTAGGTTAGCA[A/G]TAATTCCCATCTCAT | 386649 |
rs265612005 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151499286 | CTAGTTCCTTTGATG[A/G]CCCATCTCTGTGATA | 386649 |
rs265624925 | in-del | -/TA | | | intron-variant | Nsfl1c | Mm_Celera | 2:151505962 | GGAGAATGGGGTTTG[-/TA]TAACAAGCTGCTTGT | 386649 |
rs265664407 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151509864 | ATCTGTAGGTCTCAT[C/T]CCTCCTCATTAGGAT | 386649 |
rs265734696 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151506223 | TCCATCTCAAAATAA[A/G]CCCACCATTGCCTTT | 386649 |
rs265874706 | snp | A/G | | | intron-variant | Nsfl1c | Mm_Celera | 2:151497526 | CTTTGAGAAACACTA[A/G]CACCAAATCTCATTG | 386649 |
rs265949892 | snp | A/T | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493408 | TTCATTAGTAGTGGC[A/T]TCATGCACAGTGAAT | 386649 |
rs266141023 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151508230 | TTACTGCCAACACTA[C/T]AGGAATCCTAGATAA | 386649 |
rs266220774 | snp | C/T | | | intron-variant | Nsfl1c | Mm_Celera | 2:151504777 | CCAGTGCATTAGCTG[C/T]TAGCCTTTCAAACTT | 386649 |
rs387090881 | in-del | -/AGAG | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493919 | CCACAGCCCTTGGAA[-/AGAG]ATCAAGCCATAGACA | 386649 |
rs387434617 | in-del | -/TTTGT | | | upstream-variant-2KB | Nsfl1c | Mm_Celera | 2:151493884 | AGAAGACAGGATACT[-/TTTGT]TTATCTCTGTTATTT | 386649 |
rs387780700 | in-del | -/ATT | | | intron-variant | Nsfl1c | Mm_Celera | 2:151495293 | AGAGCTAACTACTAA[-/ATT]AACAGGTAAAGACTA | 386649 |
rs387845200 | in-del | -/A | | | intron-variant | Nsfl1c | Mm_Celera | 2:151494981 | TCTTGTTCACTGGCA[-/A]GTAGTAAATAGTCAC | 386649 |
rs578588510 | snp | G/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495810 | GCTCATTTCCTCCTA[G/T]ACAGTTGGTTACCTT | 386649 |
rs578775834 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493087 | CTTACTGCTTCTCTG[C/T]AATGTGTTAGGTTCC | 386649 |
rs578834403 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507872 | AGGCCATAGAAGGAT[A/G]TTCTTTACTGGCTTG | 386649 |
rs579019131 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493526 | CTGGTAGAATAATTG[C/T]TGGTCACCAACTTAG | 386649 |
rs579040823 | snp | C/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507703 | CTGGTACCAATTTGT[C/G]TTAGTCAGGGTTTCT | 386649 |
rs579161157 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507735 | TTCCTGCACAAACAT[C/T]ATGACCAAGAAGCAG | 386649 |
rs579201224 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492635 | AAAACTGGGATTGAA[A/G]CTATAGCCTCTCCCA | 386649 |
rs579432932 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496107 | AGCATCTGTCCCTAT[A/G]CTCTTCTTCCTCTTA | 386649 |
rs579590158 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496173 | GGTTGAACCTGACCC[A/C]ACTTCTTACCTCCAG | 386649 |
rs579773774 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496212 | TTCATTTTGCAGTCC[A/G]TTTGTGCCAGCTATA | 386649 |
rs579920518 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151494454 | GACGGGCTGGGGAAT[A/G]CGGAGTGCGGCGTCG | 386649 |
rs580106294 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151504333 | ATGGGGACTTACATA[A/G]AAATGACAGTTTTCA | 386649 |
rs580202313 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151494792 | GTCGCGGTGGCCTTC[C/T]GATTCCGCTTCTGCA | 386649 |
rs580282409 | snp | G/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507901 | TGCTTCCCTTGGCTT[G/T]CTCAGCCTGCTCTCT | 386649 |
rs580309583 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507949 | CAGCCCCGAGATGGT[A/C]CCACCCACAAGGGGA | 386649 |
rs580424791 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151494110 | GCCATTAAGGTGAGG[C/T]TCACATAGGGGCCAC | 386649 |
rs580522526 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495632 | TCCCAGTAGATCATC[C/T]GAACTGAGGCTCTTA | 386649 |
rs580652140 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151509140 | ACTACAACATGAGGT[A/C]CTATAATATTAAAGG | 386649 |
rs580756422 | snp | A/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507614 | AACGAATGAATCTTC[A/T]AGCCCAAAGTTCCAA | 386649 |
rs580943910 | snp | C/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492196 | TATTCGAGGAGTAGA[C/G]TGCCATGGACGCCAT | 386649 |
rs581045933 | snp | A/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507677 | AGGTTGTCAAGGGAT[A/T]CCCCACTATGCTGGT | 386649 |
rs581114769 | snp | A/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492330 | TGGTGGTAGTGGTGG[A/T]GTGTGTGTGTGTGTG | 386649 |
rs581650490 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495036 | AGCTCCACCAGGCAT[A/G]AAATGTTGCACACTT | 386649 |
rs581704829 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496175 | TTGAACCTGACCCCA[C/T]TTCTTACCTCCAGAA | 386649 |
rs582004416 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507838 | ACTCAAGCAGGTCAG[A/G]AAGCAGGAGCTGATG | 386649 |
rs582036026 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151494154 | GCGGCTAGGTTTCCC[A/G]CACGGAGGGCTTTTC | 386649 |
rs582162939 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493088 | TTACTGCTTCTCTGC[A/G]ATGTGTTAGGTTCCA | 386649 |
rs582265616 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507884 | GATGTTCTTTACTGG[C/T]TTGCTTCCCTTGGCT | 386649 |
rs582467187 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493529 | GTAGAATAATTGCTG[A/G]TCACCAACTTAGCAG | 386649 |
rs582659650 | snp | A/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495815 | TTTCCTCCTAGACAG[A/T]TGGTTACCTTTTAGA | 386649 |
rs582827941 | snp | G/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496133 | TCTTAGAACATAAGC[G/T]TGAGGGCCTGAGCAT | 386649 |
rs583216538 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151508003 | GAAAATGCCTTACAG[C/T]TGGATCTCATGGAGG | 386649 |
rs583374370 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507940 | CAAGACTACCAGCCC[A/C]GAGATGGTCCCACCC | 386649 |
rs583476171 | snp | A/G | | | utr-variant-3-prime | Nsfl1c | GRCm38.p3 | 2:151511125 | ACTGTGGCCATGCCC[A/G]TGGGGATTTCCTCCC | 386649 |
rs583616487 | snp | A/C | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492201 | GAGGAGTAGAGTGCC[A/C]TGGACGCCATAGGTG | 386649 |
rs583644305 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151494927 | GGTCTCTGCACATTT[C/T]GTAGTTAACTGTAAA | 386649 |
rs583823006 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496243 | AAGTGAGACAATAAT[A/G]ATACTAATTACGAAA | 386649 |
rs583999172 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507616 | CGAATGAATCTTCTA[A/G]CCCAAAGTTCCAAAG | 386649 |
rs584038187 | snp | G/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151504344 | CATAAAAATGACAGT[G/T]TTCACTTGGTGGTTA | 386649 |
rs584298836 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493058 | GACCAGCATCAAAAG[C/T]AGATAGGGTTCTCCT | 386649 |
rs584481166 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495343 | AAGGAATTGGACCCT[C/T]AAAGGGACACCGAAT | 386649 |
rs584598323 | snp | G/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495691 | AGGACTTGAATGCAG[G/T]TTCTCTAAATGTCAG | 386649 |
rs584881049 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495969 | TCATATGAAGGGCTT[C/T]CACATGTGTAAAGCT | 386649 |
rs585073706 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507685 | AAGGGATTCCCCACT[A/C]TGCTGGTACCAATTT | 386649 |
rs585098758 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507864 | TGATGCAGAGGCCAT[A/G]GAAGGATGTTCTTTA | 386649 |
rs585205474 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507713 | TTTGTCTTAGTCAGG[A/G]TTTCTATTCCTGCAC | 386649 |
rs585220123 | snp | C/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492593 | TGGTCAGTCTTTCTC[C/G]AAACTTCCAGGCTAG | 386649 |
rs585308192 | snp | C/T | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493436 | AATGTGGCTCTGAGT[C/T]AGGCATAGGAAGAAG | 386649 |
rs585550083 | snp | C/T | | | utr-variant-5-prime | Nsfl1c | GRCm38.p3 | 2:151494276 | CTGTTGCAGTGTCCG[C/T]CGGAGCGGTTTGGGA | 386649 |
rs585640982 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507894 | ACTGGCTTGCTTCCC[C/T]TGGCTTGCTCAGCCT | 386649 |
rs585790819 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496191 | TTCTTACCTCCAGAA[A/G]CTGTCTTCATTTTGC | 386649 |
rs585868671 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151496168 | CCTGGGGTTGAACCT[A/G]ACCCCACTTCTTACC | 386649 |
rs586420701 | snp | A/C | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151494781 | GCCCCACCGAGGTCG[A/C]GGTGGCCTTCCGATT | 386649 |
rs586498663 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151493756 | GGCAATGCAATGGTG[A/G]TTTGCTAGATGCTGT | 386649 |
rs586664517 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495382 | TGTGTGAGCTTTCTG[A/G]TGTAACCATGTCTAC | 386649 |
rs586985040 | snp | A/T | | | utr-variant-3-prime | Nsfl1c | GRCm38.p3 | 2:151511134 | ATGCCCGTGGGGATT[A/T]CCTCCCACCCCGTAC | 386649 |
rs587016158 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507526 | GAAATTTCACAAGCC[A/G]GGCCTCCATTTTCTG | 386649 |
rs587022239 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507674 | GTCAGGTTGTCAAGG[A/G]ATTCCCCACTATGCT | 386649 |
rs587157091 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492186 | TAAGCTGGGCTATTC[A/G]AGGAGTAGAGTGCCA | 386649 |
rs587211848 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151498331 | TGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 386649 |
rs587217294 | snp | A/G | | | upstream-variant-2KB | Nsfl1c | GRCm38.p3 | 2:151492298 | TGTTGTTGTTCTGGT[A/G]GTGGTGGTGGTGGTG | 386649 |
rs587394814 | snp | C/T | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151507948 | CCAGCCCCGAGATGG[C/T]CCCACCCACAAGGGG | 386649 |
rs587509851 | snp | A/G | | | intron-variant | Nsfl1c | GRCm38.p3 | 2:151495017 | GAATTAATTTAGAAG[A/G]CAAAGCTCCACCAGG | 386649 |