SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3661541 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28806524 | GGATTCTACTACTGG[A/G]TCAAATTGTAATGTG | 380752 |
rs3699185 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28756473 | CCCAGGATGGCCTTG[A/G]CCTCATGGCCTCTGT | 380752 |
rs3699186 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28756476 | AGGATGGCCTTGACC[G/T]CATGGCCTCTGTGCC | 380752 |
rs3700242 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Tssc1 | Mm_Celera | 12:28756609 | ATGTGTTTGTGACTG[C/T]AGCACAAGGGTGAAT | 380752 |
rs3704142 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808938 | AAATAGTCCCTGCCT[G/T]CCTTCCCACAGTGTA | 380752 |
rs3705361 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809142 | TCCTTCTGGGGTCAC[A/G]CTGCCTCTTTTTTGG | 380752 |
rs3718064 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28806085 | CATTCTTCTGAGTCC[G/T]GTCTCCTGCATCTGT | 380752 |
rs3718666 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806167 | TTAGTTGTAGAGCAT[C/G]TAGGAAGGAATGCGC | 380752 |
rs3718688 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806173 | GTAGAGCATGTAGGA[A/G]GGAATGCGCAGCCTG | 380752 |
rs3719250 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806235 | CCCTGTATGTGTTTT[C/T]TGTTTGTTTTCTTTT | 380752 |
rs3719285 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806252 | GTTTGTTTTCTTTTG[C/T]TTTTGTTTTTGTCTT | 380752 |
rs3720409 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806393 | GACAACACACAGCTG[C/G]TATAAATTGGTCTTG | 380752 |
rs3720429 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806401 | ACAGCTGGTATAAAT[C/T]GGTCTTGCCAGTTGA | 380752 |
rs3720473 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28806425 | CAGTTGAGCAGAAGC[C/T]CAGGTGGACTGAGGA | 380752 |
rs3720534 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28806459 | GGGCTCAGATATTTG[C/T]GGGATTCATCTTCTC | 380752 |
rs3723495 | snp | C/T | 0.290657 | 0.246672 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751421 | GCTGTATGTCACTGC[C/T]CACTTACACCATCAC | 380752 |
rs3724299 | snp | C/T | 0.290657 | 0.246672 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751599 | TAATGCCAAGTTAAC[C/T]GTTCTCTTTAGGGCT | 380752 |
rs3724873 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751668 | GCGCCGCCCTGATGG[A/C]CGTCCATTCCCGCTG | 380752 |
rs3724874 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751669 | CGCCGCCCTGATGGA[C/T]GTCCATTCCCGCTGC | 380752 |
rs3724894 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751682 | GACGTCCATTCCCGC[A/T]GCTTTTGCTCCGGGC | 380752 |
rs3724896 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751685 | GTCCATTCCCGCTGC[C/T]TTTGCTCCGGGCCCG | 380752 |
rs3724932 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751700 | TTTTGCTCCGGGCCC[C/G]GCCTTCCAACCCAGG | 380752 |
rs3724935 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751704 | GCTCCGGGCCCGGCC[C/T]TCCAACCCAGGATCT | 380752 |
rs3725381 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751724 | ACCCAGGATCTCCTG[C/T]AGCTGCTGGGTCTCA | 380752 |
rs4156875 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28820151 | ATTCAAAGTGAGGCT[C/G]GAGAGATAGCTCCGC | 380752 |
rs4156876 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28820146 | AAGTGAGGCTCGAGA[A/G]ATAGCTCCGCAGATA | 380752 |
rs4156877 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28820102 | TTCTTGCAGAGGACC[C/T]GAGTTTGGTTTAAGA | 380752 |
rs4156878 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28819962 | ACAGGCACACACACA[C/T]ATACACACACATAAA | 380752 |
rs6292845 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28845938 | TTCTCTATTGATCGT[G/T]GTGCGttttactttt | 380752 |
rs13472941 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime | Trappc12, Tssc1 | Mm_Celera | 12:28751936 | ACTCGAGCTCTGAGG[C/T]GTGAGTAGCTGGGTA | 380752 |
rs13472942 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Trappc12, Tssc1 | Mm_Celera | 12:28751859 | GGAGCCGGTCTGGGT[G/T]CTCGTAGTCCATTTT | 380752 |
rs13481366 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Tssc1 | Mm_Celera | 12:28861603 | TGCACCTGTACTCAC[A/G]TACCTGAATGCACAT | 380752 |
rs29122274 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28768980 | GTTGGGGAAGGGGGT[A/G]GCTCTGCGGGCCCAT | 380752 |
rs29122924 | snp | C/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28847369 | ATTGTATCTATCATG[C/G]TAGGTCACAGCTTTG | 380752 |
rs29122955 | snp | A/C | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28828394 | CAGGCAAACTATGGC[A/C]GAACAGTTGACAAAT | 380752 |
rs29123534 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28835043 | CTCTAACTTTATTGG[G/T]TTTTACTTATAGTCA | 380752 |
rs29125406 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28811094 | ACTGCCTGTAACTTC[A/T]GGAGCATCTGACCCA | 380752 |
rs29125457 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28866538 | CCAGTCCCAGTCCCA[A/G]ATTGGCCGCACACCT | 380752 |
rs29125635 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28833831 | GGCTGGACTCCTATG[C/T]GGAGAGTGTAGAGGA | 380752 |
rs29125732 | snp | A/G | 0.455 | 0.143091 | intron-variant | Tssc1 | Mm_Celera | 12:28775945 | ACAGGGCATGAGGAC[A/G]ACATAGAGCCTGCTT | 380752 |
rs29125890 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tssc1 | Mm_Celera | 12:28792465 | GACATGGAGTTGGTG[C/T]GCATTCACATAGCCT | 380752 |
rs29129034 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844581 | CCCTTCTGGATGTGT[A/G]CCACATTTTCATTAG | 380752 |
rs29129121 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28805122 | GCATATTCAGAGCCA[A/G]TGTGGGTGGAGACAT | 380752 |
rs29129296 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28805754 | CCAAGCATTTATCTG[G/T]TAACTCAAGTAATGC | 380752 |
rs29129624 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Tssc1 | Mm_Celera | 12:28818238 | ATCTCTTGTGCCATG[C/T]CAAGGCTTTGTTTTA | 380752 |
rs29129769 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28824787 | AGGGATATAAAACTG[A/T]CATATCATTTGAGGA | 380752 |
rs29130172 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28791210 | GAAGCATGAGTGAGC[C/G]CTGGTAGAAACGCCT | 380752 |
rs29130460 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28766696 | AGTTTGCACTTGGTT[C/T]TTTATAGTCATGGTG | 380752 |
rs29131694 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28755546 | AATTCAGGATGCAGG[C/T]TGCTGTGGACAGTGG | 380752 |
rs29131784 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28796301 | CATGAAGAATAATTT[C/T]GTTTGTTTGTTTGTT | 380752 |
rs29132100 | snp | A/G | 0 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28767085 | GTTGCTGTTCCAGGA[A/G]CACTGCACCCGAGGG | 380752 |
rs29132279 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28845027 | TGTTTAGATCCCCAA[C/G]TCCCCTAGTTTCTTT | 380752 |
rs29132376 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28788536 | GTCTTGCTCACAGGG[A/G]TCCTGTGGACCCTAT | 380752 |
rs29132694 | snp | A/G | 0.255 | 0.24995 | intron-variant | Tssc1 | Mm_Celera | 12:28854962 | GTCATGATGCTGGCA[A/G]GACAGCTGCAACAGT | 380752 |
rs29132960 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28802906 | GATTTTATACTGCTC[G/T]GCTCCCCCTTTACAA | 380752 |
rs29134069 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28795183 | TCGAATTGTTCTTTT[C/T]GCCGCTCCCAGACAC | 380752 |
rs29134133 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28824948 | TTTGCCTTGTAAATC[A/G]CCCCATTTTGCTTTC | 380752 |
rs29134627 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28843058 | ATAGCTATAGACAGA[A/C]AAGGGTATACATAGA | 380752 |
rs29134661 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28769667 | TTGACAGTCCCGCTG[C/T]GGGTGCATGAAGGTG | 380752 |
rs29135112 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28793538 | TGTTCTGACCTAGCT[C/G]TTCTCTATGGCATAC | 380752 |
rs29135121 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28784955 | TTGGAAACCTCAGGC[C/T]GCCCAGGGAGTATTC | 380752 |
rs29135437 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28866454 | CTTGGGAATGTGTAC[A/G]GCCCTGGATTCTCTA | 380752 |
rs29136220 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28790373 | GGAGTTCGAGGAAAG[A/G]AAGACTTGATTAAGA | 380752 |
rs29136317 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28788519 | ATCTGCTTGCTGGAC[A/G]GGTCTTGCTCACAGG | 380752 |
rs29136345 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Tssc1 | Mm_Celera | 12:28865203 | GTGTTGACCATGTCC[G/T]TATAGCCTTCAGCTC | 380752 |
rs29136515 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28846858 | TTCAGATCCATGGTT[A/G]CAGTAGTTGGGTTGC | 380752 |
rs29136548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28812400 | CCTAGAGGCAGGAGC[C/T]GAGGCAGAGGCCATG | 380752 |
rs29136618 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28759635 | GCTGGGATTAAAGGC[A/G]TGTGCCACCACTGCC | 380752 |
rs29137298 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28804970 | GCTGCTAGCCTATGC[C/T]GCTCCGTGGTTGTTG | 380752 |
rs29137456 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809398 | GAATGCACTGCTCTA[C/G]ACTGCCCTGTTCCTC | 380752 |
rs29137653 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844549 | TATGAATCATAATGT[A/G]AATATATGAATAGTA | 380752 |
rs29139523 | snp | A/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28798568 | ACCTGGAGCTCTGCC[A/T]TTAAACAGTCAAAAC | 380752 |
rs29140095 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28802911 | TATACTGCTCTGCTC[C/T]CCCTTTACAAAAGAC | 380752 |
rs29140859 | snp | A/G | 0.455 | 0.143091 | intron-variant | Tssc1 | Mm_Celera | 12:28793431 | ATCTGTGTTTTAGAA[A/G]ACCTCTGGGTGAGTT | 380752 |
rs29140994 | snp | C/G | 0 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28767101 | CACTGCACCCGAGGG[C/G]TTCTGAGAGGGGAGG | 380752 |
rs29140996 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Tssc1 | Mm_Celera | 12:28757317 | TTGAGGGCTAGGTTT[C/T]GGCATGAGAGCTTAG | 380752 |
rs29141024 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28845089 | ATGTATTCTTTTATG[C/T]ATTCTTTGTTATATG | 380752 |
rs29141150 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28780670 | GCAATCTCCCTGGCT[C/T]TTGGAGGCTTGGACT | 380752 |
rs29142337 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28865183 | TTTCAGTGAATAGTT[C/T]AGTAGTGTTGACCAT | 380752 |
rs29142496 | snp | A/T | 0.188366 | 0.242283 | intron-variant | Tssc1 | Mm_Celera | 12:28755552 | GGATGCAGGTTGCTG[A/T]GGACAGTGGTGAGCT | 380752 |
rs29142588 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28766680 | GGTATAGCAGCCATT[A/G]AGTTTGCACTTGGTT | 380752 |
rs29143514 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28798405 | TGTTTAAATGAACCA[A/C]TCATATGAAATCCTG | 380752 |
rs29143774 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28759638 | GGGATTAAAGGCGTG[C/T]GCCACCACTGCCCTG | 380752 |
rs29144887 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28794566 | TATGAATTATGATGG[G/T]CTTCATGAGTCTAAA | 380752 |
rs29144956 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28853413 | CAATTTTCAGGTTGC[A/C]TCTGTAAGAAGAGCA | 380752 |
rs29145027 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Tssc1 | Mm_Celera | 12:28847506 | GCTGTTGGGCTATAG[C/T]CTTGGCAGTCCCCAT | 380752 |
rs29145369 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844266 | TGCAATAGTGGTGTG[C/T]ATACTTTGGGAATAA | 380752 |
rs29146022 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28759760 | CCTGCATTGCATCGC[C/T]GGAAGCCCTTTCTGT | 380752 |
rs29146279 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Tssc1 | Mm_Celera | 12:28835137 | TGCTACTGTATTCTT[C/G]ACTTGTTAATATTGT | 380752 |
rs29148373 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28811597 | GGAAATCCCCTGTAC[C/T]ATAGTGGAGAAAACA | 380752 |
rs29148662 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28824941 | ACTGACGTTTGCCTT[A/G]TAAATCACCCCATTT | 380752 |
rs29149036 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28787937 | GGACATTTGGTATGA[C/T]TGGTTTAAAATAACT | 380752 |
rs29149081 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28831716 | GTTCTCCTTGAGTTC[A/G]TGGCTACACTGATAC | 380752 |
rs29149590 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Tssc1 | Mm_Celera | 12:28819153 | AGTGAGAAATGCTGA[A/T]TTGCAACATTTGGAA | 380752 |
rs29149997 | snp | C/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28855112 | CTTAAGGCTGGGAAG[C/G]GGGTTAGGGTAGGAT | 380752 |
rs29150512 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Tssc1 | Mm_Celera | 12:28779878 | ATAAAGTTCTAGGGA[C/T]GCAAGTATTGTCCAG | 380752 |
rs29151640 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Tssc1 | Mm_Celera | 12:28835102 | TTATATAGGGACAGA[A/G]CACATTTCTACTGGC | 380752 |
rs29152463 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28855030 | TGAGAAGGCTGAGTC[A/C]TCTGTCCAGGTGTCA | 380752 |
rs29152551 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28833957 | TAAGACAGAACAGGC[G/T]CTAGCATAGAGCTCT | 380752 |
rs29152792 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Tssc1 | Mm_Celera | 12:28839857 | ATTACTTTGTTAACA[A/T]GACTTGTTAGATGTT | 380752 |
rs29153375 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844770 | TTCCTTTTGATGGCT[C/T]TCCTCACTGATTTCT | 380752 |
rs29153457 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tssc1 | Mm_Celera | 12:28818559 | CATCCCTCCTGTATT[C/T]CCTGCTTAGCTCTGT | 380752 |
rs29155159 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tssc1 | Mm_Celera | 12:28788256 | TACAAGTGTTAGTCA[C/T]CTTTGGATTTGGGTG | 380752 |
rs29155528 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Tssc1 | Mm_Celera | 12:28847743 | TTCCTGATGCTCACA[C/T]TGGTAATTTCAAAAT | 380752 |
rs29156070 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28831345 | TTCTGCAGCCTGGGG[C/T]GTGAAGCAGAGTGCA | 380752 |
rs29157139 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Tssc1 | GRCm38.p3 | 12:28842977 | TATCTTCATCTGTTA[A/C/G]AAGGAGAAACTTTTT | 380752 |
rs29157749 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Tssc1 | Mm_Celera | 12:28780231 | TCTGGGTCCCATTTG[C/T]GTCATTTCTCTGTCC | 380752 |
rs29157819 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Tssc1 | Mm_Celera | 12:28792652 | TATTTGAAGCTGACA[C/T]GTGCTTCCCTGTGTC | 380752 |
rs29158295 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28771221 | CCGAGCTCTTCTCAG[C/T]GCAGCCAGCAGGGGC | 380752 |
rs29159147 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28819563 | GCCAGCCTGGTCTAT[A/G/T]AAGTGAGTTCCAGGA | 380752 |
rs29159190 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28759621 | TCTGCCTCCCAAGTG[C/G]TGGGATTAAAGGCGT | 380752 |
rs29159585 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28818386 | CCAATCAATGCCTCC[C/T]TGCTTATTAGAGCCC | 380752 |
rs29160110 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Tssc1 | Mm_Celera | 12:28824779 | TTCTTCATAGGGATA[C/T]AAAACTGTCATATCA | 380752 |
rs29160499 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28780403 | GGTGTTCTGCCATTT[A/G]TCAGTGTGCTTTGTT | 380752 |
rs29160554 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Tssc1 | Mm_Celera | 12:28855475 | AGAGACATTTCATCT[A/G]AAAGCGTTTGCTAGA | 380752 |
rs29160992 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844135 | GTTATTGAGGACTAG[C/T]TTCATAGTATCAGAA | 380752 |
rs29161035 | snp | A/G | 0.277778 | 0.248452 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Trappc12, Tssc1 | Mm_Celera | 12:28750288 | CTCTGTGGGAAGGTC[A/G]AGGGTACCGGCGACC | 380752 |
rs29161310 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Tssc1 | Mm_Celera | 12:28837553 | TCTTCCCTGTTTCTG[C/G]GGAATTTTTGCTTGT | 380752 |
rs29161775 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tssc1 | Mm_Celera | 12:28757185 | TCCAGGTACACACAC[C/T]GTAAGGTTAGAACCT | 380752 |
rs29162343 | snp | A/G | 0.444444 | 0.157135 | missense | Tssc1 | Mm_Celera | 12:28864803 | GTGGACGACGGTGAC[A/G]TCAGTGATCCAGAAG | 380752 |
rs29163036 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28755494 | ATAACTAAATAAATT[A/G]TAAAAAAATATAAGG | 380752 |
rs29163417 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28847303 | TGCTCTCTCCTCTTA[C/T]GGGGACTTAGGTCCC | 380752 |
rs29164329 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28864524 | TGCTAGGTCGGAAAA[A/G]AATATTTTGGATCTA | 380752 |
rs29164388 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trappc12, Tssc1 | Mm_Celera | 12:28750441 | GCTTGTGCGTCTGCG[C/T]GTGCTGGCCACGGAG | 380752 |
rs29164715 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28836651 | TGGGACATGAATGTG[A/G]CTGGGCCTTGATTAC | 380752 |
rs29165044 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28824863 | TCAAGTGACTGTCTT[A/G]ACAGAAGTCCTTTCT | 380752 |
rs29165257 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tssc1 | Mm_Celera | 12:28854611 | ACTGTTGCCACTGTG[C/T]GTTTGAGTTACATTA | 380752 |
rs29165409 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28847714 | TACAGCTTTTGGCTG[A/G]ATGCAGAATACACTT | 380752 |
rs29165414 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28843128 | TAGAGTGTAGTTTAT[A/G]GTATAGTGCTGTGGT | 380752 |
rs29165650 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28794680 | ACAGATCGAGGAGGT[G/T]AGGCCCAGGTGTGGT | 380752 |
rs29166462 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28837336 | AATCAAGGTAGACAG[A/G]TCATCATCTCAGAGA | 380752 |
rs29167625 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28817884 | TGATGCCGGGAATAT[A/C]ACGAACCTTGTGAAC | 380752 |
rs29168349 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844385 | GCAGCCATGGATCTC[C/T]GGAAGAACCCACAAT | 380752 |
rs29168547 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28837264 | GTAAGCCCAAATTTA[A/G]TCCCCAGACTTTGTA | 380752 |
rs29168553 | snp | A/G | 0.444444 | 0.157135 | missense | Tssc1 | Mm_Celera | 12:28864798 | ACCTGGTGGACGACG[A/G]TGACATCAGTGATCC | 380752 |
rs29168690 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28866426 | CTCCTGATACTGGCC[A/T]GGAGGCCTGCTCCTT | 380752 |
rs29168756 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28795914 | CACCCCAAAGTAACC[A/G]ACTTGTTCCAACAAT | 380752 |
rs29168931 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28811629 | ACTGCTGCAATAGCA[A/G]TAACCCCAAACAAAG | 380752 |
rs29169450 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28788385 | GTAGAAGGACATGAG[C/T]CAGGGTTAGGCTGCT | 380752 |
rs29169454 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844854 | TTCTCTACGTTTTCT[C/T]CAGCATTTGTTGTTA | 380752 |
rs29169609 | snp | A/C | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28769030 | CTGAGTGACTAGCCA[A/C]ATGACAGTATAGCGT | 380752 |
rs29170168 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28854777 | AGATGGTATTACAGG[C/T]AGCATTTGCACTCGG | 380752 |
rs29170796 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Tssc1 | Mm_Celera | 12:28846878 | AGTTGGGTTGCAACA[A/G]CAGGGACACTGGCTG | 380752 |
rs29172726 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28847700 | GTTGTCTTTGGAATT[A/G]CAGCTTTTGGCTGAA | 380752 |
rs29172727 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28819109 | GTTGCTCCTGTGTAC[G/T]GTTTCAGGGCTGGCA | 380752 |
rs29172899 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809278 | AGCCTAAGCTGCCTG[A/G]GAACGCCTGTCTTTG | 380752 |
rs29173017 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28793114 | AACTGTGAGAGTCCT[C/T]CCAGCATGCACTTCA | 380752 |
rs29174630 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28788182 | TGCTCTGTGGAGGGA[C/T]TGAGGGCTCTTGCCT | 380752 |
rs29176058 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28776838 | GTGGCCTGACTGAAG[C/T]GGCTATGAGAAGCTC | 380752 |
rs29176122 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28769300 | GGTAACTGGGACAGA[A/G]CCTAGACTAAATGCC | 380752 |
rs29176757 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tssc1 | Mm_Celera | 12:28866112 | TCCTGGTATTTGTCA[C/T]AAAGTATTCTTTGAC | 380752 |
rs29177493 | snp | A/C/T | 0.34 | 0.28 | intron-variant | Tssc1 | GRCm38.p3 | 12:28835053 | ATTGGTTTTTACTTA[A/C/T]AGTCAGCCCTTGCTT | 380752 |
rs29177658 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28798052 | AGGATGTCCTCAGAG[A/T]TTCCCTGCCTCTGCA | 380752 |
rs29178162 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tssc1 | Mm_Celera | 12:28863969 | TGTAGGAAAGTCTGG[C/T]TGAGAGATCCACTTT | 380752 |
rs29179300 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28794380 | ATGTTAATGATGCTA[C/T]GATAATCTGACAGCA | 380752 |
rs29179989 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28769606 | TGTAGGCAGGTGGGT[A/G]CTCTTTGTGATTAGC | 380752 |
rs29180098 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Tssc1 | Mm_Celera | 12:28834103 | TGTACTCAGACTCTG[A/G]CCCTCTCTGCTCTTG | 380752 |
rs29180903 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28802667 | TTATGTGTGTGTATG[C/T]ATGAATGTGTGCGAT | 380752 |
rs29181318 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28835030 | CAAAGGACCTCAGCT[A/C]TAACTTTATTGGTTT | 380752 |
rs29182951 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28770630 | TGTTTCTCAATTGTT[A/G]GGATTTGGAGCAGCT | 380752 |
rs29183288 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28853493 | CATCCCTGTGAGCCC[A/T]TGGGATCTGTCCAGT | 380752 |
rs29183622 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Tssc1 | Mm_Celera | 12:28836128 | CATAGTCGATGTGCA[C/T]TGGAGCACCTGGGAC | 380752 |
rs29184844 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28768615 | CCCTCCACTTTCTCT[C/G]CTTATATGTGTTTGG | 380752 |
rs29185041 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28819122 | ACTGTTTCAGGGCTG[A/G]CAGTTTGGTGTTGGG | 380752 |
rs29185068 | snp | C/T | 0.255 | 0.24995 | intron-variant | Tssc1 | Mm_Celera | 12:28861875 | GCTACTGTCCACCTG[C/T]ACTGAGCATGTCACT | 380752 |
rs29185843 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Tssc1 | Mm_Celera | 12:28864796 | TCACCTGGTGGACGA[C/T]GGTGACATCAGTGAT | 380752 |
rs29186051 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28779783 | TTTCATGTTTTGTTT[A/G]TAGTAACTTTTACTA | 380752 |
rs29187219 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Tssc1 | Mm_Celera | 12:28775504 | TATATACTTGGAAAC[A/G]GCAGGGCTAGCTTTT | 380752 |
rs29187358 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28834050 | GTTGAGTTTGTGCGT[C/T]TCTTGCATGGTTAAT | 380752 |
rs29187980 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28797159 | CCTTTCAGAGAGTTC[C/T]GCTCCCTGTTTACTA | 380752 |
rs29188359 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28793387 | GGGATTACTGTTGAG[G/T]TGTTTCCAAATTTTG | 380752 |
rs29190018 | snp | A/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28784304 | TGTCCCTTGCTGTGG[A/T]CCCTCAGAGCCTCCC | 380752 |
rs29190463 | snp | A/C/T | 0.475309 | 0.108333 | intron-variant | Tssc1 | GRCm38.p3 | 12:28790364 | GATACACGTGGAGTT[A/C/T]GAGGAAAGGAAGACT | 380752 |
rs29190548 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28818191 | GTCCAGAGGCTGTGC[C/T]TGGGATGCTGTCTCG | 380752 |
rs29190714 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28798482 | GCACCAATTCCTCCC[C/T]CAGTCCCCGCCCCTT | 380752 |
rs29191252 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Tssc1 | Mm_Celera | 12:28835602 | GACAAGAGCAGAGGG[A/C]AAGCCTGTGCACAGG | 380752 |
rs29191526 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Tssc1 | Mm_Celera | 12:28818536 | AACCAATTTGTGTGT[C/G]TCTGTGGCATCCCTC | 380752 |
rs29192211 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28802698 | TGCTTGGTGTGTGTG[G/T]GAGGGTGCAGGCAGT | 380752 |
rs29192815 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Tssc1 | Mm_Celera | 12:28834286 | GTTAGCTTTCTGTCT[C/G]CCTGAAAGTGGAATT | 380752 |
rs29193237 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Tssc1 | Mm_Celera | 12:28836316 | CTGGCCTCTGCTCCG[G/T]GCTTTCTCCCTTAAA | 380752 |
rs29194044 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28772498 | CTGCGTCCCCAGCCC[C/T]TGTACTGATGACTCC | 380752 |
rs29194108 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Tssc1 | Mm_Celera | 12:28864317 | GGAGAAATGGCACCA[A/G]TATCAGACCTGATAC | 380752 |
rs29196143 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28837476 | TCACAGCGATCCACC[A/C]GTCTTTGCCTCCAGA | 380752 |
rs29196794 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28787846 | AATGTAGAGGGCCCC[A/C]GGGAAAGGCAGTGAC | 380752 |
rs29196827 | snp | A/G/T | 0.5 | 0 | intron-variant | Tssc1 | GRCm38.p3 | 12:28810969 | ACATCTAAGGTGGTG[A/G/T]ACCTGTAAACTTAGG | 380752 |
rs29197242 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28805301 | GGACTTGGAGTCAAG[C/G]TTTAGAGATGTCCTG | 380752 |
rs29197667 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28802829 | ACCCAGCTTCATTAT[G/T]ATTTTTTTATAGAGA | 380752 |
rs29197868 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28750682 | TTCTCCACGTTTCCC[A/C]CCTTGTGTCTGTGGC | 380752 |
rs29198403 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Tssc1 | Mm_Celera | 12:28865870 | GCTGTTCTTCCAGGG[C/T]GCCATGCAGACGGGC | 380752 |
rs29199005 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28831822 | CATGCCCAGCTGGTA[C/T]ATCCCAGCATGTTTG | 380752 |
rs29199453 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28797828 | TATCTCTAGACATTC[C/T]GGAGCCATTATCAGG | 380752 |
rs29199870 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28844596 | GCCACATTTTCATTA[G/T]GCATTCCTCAGTTCA | 380752 |
rs29200051 | snp | A/C/T | 0.290657 | 0.246672 | intron-variant | Tssc1 | GRCm38.p3 | 12:28837651 | CTTTCATTGAAATTC[A/C/T]TTACTCAGTGTTGAA | 380752 |
rs29200257 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28796666 | GGAATTACTACTGTA[C/T]CAGGATTCTACATTG | 380752 |
rs29200843 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Tssc1 | Mm_Celera | 12:28757223 | AGAGACTGGGCCATC[A/G]GACTTTCTGCCCTTT | 380752 |
rs29201707 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Tssc1 | Mm_Celera | 12:28836372 | TATTTGTATAAACAG[C/T]TGTGTTCATTGACAA | 380752 |
rs29201966 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28805713 | CATGGGCCGGTTGTC[C/T]CTTTTCCCATAAGCA | 380752 |
rs29202160 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28819258 | AATTCACCTTCCAGC[C/T]GTGTCTCTGCTAACT | 380752 |
rs29202459 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Tssc1 | Mm_Celera | 12:28755263 | TACACTATCAGTTGA[A/G]TTTTGTGTTGCTGTC | 380752 |
rs29203239 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28864846 | AAAAGTAAGAGACAC[C/T]GCTTCGAGCAACGCT | 380752 |
rs29203614 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809349 | GTTTCTTGAATGTCT[A/T]GCTCTGCTGACTGGA | 380752 |
rs29204304 | snp | A/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28828390 | ATTTCAGGCAAACTA[A/T]GGCCGAACAGTTGAC | 380752 |
rs29204706 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Tssc1 | Mm_Celera | 12:28847669 | GTGGTGAGTAAGAAG[A/G]GAGAAACTCTCACCG | 380752 |
rs29205056 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28855381 | TTTTCTGAAATGCAT[C/T]GTGTGAGGCTCCAGA | 380752 |
rs29205327 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28794284 | GGCTCCACTAGTGTC[A/G]ATGGCTGCTGTGGGT | 380752 |
rs29205539 | snp | A/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28866606 | GCTGAGATCCCAGAC[A/T]CTGGCTACTCTGTAG | 380752 |
rs29205597 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28847940 | TATGTCAGCTTAATG[C/G]CACATTGCTGGCTAT | 380752 |
rs29206282 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28847134 | ACTGCAGTCATCCTG[A/G]ATTGCTCTTGTGGCT | 380752 |
rs29206757 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28788205 | TCTTGCCTGGCTGTT[C/T]CCAATTCATTACAGG | 380752 |
rs29207155 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28819233 | CACAGTGTTGTCCTC[C/T]AGCCCTAGGAATTCA | 380752 |
rs29207902 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28844178 | GCTTCCAAAAGAGTG[A/G]AGCAACCAATAAATC | 380752 |
rs29207934 | snp | A/C | 0.455 | 0.143091 | intron-variant | Tssc1 | Mm_Celera | 12:28861662 | GATAATTGAAAATGC[A/C]ATCAGGCTGGGGAAG | 380752 |
rs29208026 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28815479 | ATATGAGGGCTTGGC[C/T]CCCTGCTGGTCTGTG | 380752 |
rs29208784 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28757263 | TTTCCTTCTTCTGCC[C/T]CTGTGGTTTTGTCTT | 380752 |
rs29210050 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28802700 | CTTGGTGTGTGTGTG[A/G/T]GGGTGCAGGCAGTGT | 380752 |
rs29210357 | snp | A/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28837334 | GTAATCAAGGTAGAC[A/T]GATCATCATCTCAGA | 380752 |
rs29211861 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28794378 | TAATGTTAATGATGC[C/T]ACGATAATCTGACAG | 380752 |
rs29212647 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime, downstream-variant-500B | Tssc1, Gm31209 | Mm_Celera | 12:28867162 | CTACGAGGTAATTCC[C/T]TTCACAGACAGATTC | 380752 |
rs29212687 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Tssc1 | Mm_Celera | 12:28812360 | TGCCACTGAGGGAAG[C/G]CAGGGCAGAAGCTCA | 380752 |
rs29212713 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Tssc1 | Mm_Celera | 12:28865497 | GTTGTGAGAGAAGGC[G/T]GCAGGGCCCATAGCT | 380752 |
rs29213347 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28770469 | CTTCATACCGCAGGC[C/T]AAGGCAGAGGCAGCC | 380752 |
rs29213412 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28804975 | TAGCCTATGCCGCTC[C/T]GTGGTTGTTGAATCC | 380752 |
rs29213538 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28837470 | TCAAACTCACAGCGA[C/T]CCACCCGTCTTTGCC | 380752 |
rs29214056 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Tssc1 | Mm_Celera | 12:28780769 | CGAGGCTCTGTGCTC[C/G]TCCTCTCTGCTGTGC | 380752 |
rs29214624 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28785913 | TTCCTTCCTTCCTTT[C/T]TTTTTTTTTTTTTTT | 380752 |
rs29214874 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28813858 | ACTCCTTCATCCTGG[C/T]GGATTCTGGGGCAAC | 380752 |
rs29215621 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28756151 | CTAGGTCAACTAAGC[C/G]TCGTAATTCAGTTCT | 380752 |
rs29215665 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28824546 | GGACTAAAGGCGTGT[A/G]CCACCACGCCTGGCG | 380752 |
rs29215895 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28843280 | TAAGTAAATGAGTGG[A/G]CCAAGAAAAGATCAT | 380752 |
rs29216749 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28798778 | TACTACATGCTTGAC[C/T]GGTGGCCTTGGAGGT | 380752 |
rs29217364 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809276 | GTAGCCTAAGCTGCC[C/T]GAGAACGCCTGTCTT | 380752 |
rs29218736 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28854779 | ATGGTATTACAGGCA[A/G]CATTTGCACTCGGAG | 380752 |
rs29220360 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28826483 | GGAAAGATTTGTGGT[A/G]TAAATAGTTGAGCTT | 380752 |
rs29221339 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28788694 | CAGGAGTGGGGCTGC[A/G]GGACAATATGAGCTT | 380752 |
rs29221988 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28766593 | CTGTGGAGGCACTGC[A/T]CGGGGACTTGCCACT | 380752 |
rs29222626 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28828282 | GGTCCTGGCTGCTCT[C/T]CTGCCACACACTAGC | 380752 |
rs29222876 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28775874 | GGTGATCTCGTCATA[A/G]CATCACAGAGAGTGC | 380752 |
rs29223303 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28843076 | GGGTATACATAGATA[A/G]GACCTATGCTTACCT | 380752 |
rs29223429 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28795145 | TAGAACACAGGTCAT[C/T]AGCTTGGATCCACAA | 380752 |
rs29484463 | snp | C/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28787954 | GGTTTAAAATAACTC[C/G]TTTAAACAAGACAGT | 380752 |
rs29485377 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28769420 | CTAGGGGCCAGTGAA[C/T]TTGCCCAAGAGCAGC | 380752 |
rs29486781 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28756003 | TAAGAAATGGAGGAA[C/T]ATCCATGTCTTTTCT | 380752 |
rs29488703 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28861147 | TATAGGAGCTAGCTG[A/G]AGATGTAAATGTATA | 380752 |
rs29488945 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28793156 | GATGTCACATATATG[C/T]ACCTCTGCCCTCACC | 380752 |
rs29489107 | snp | A/C | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28861481 | CACATCCCCAGGCCC[A/C]AGCCACATAAAAGCC | 380752 |
rs29489327 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28834484 | GTAAAGGCCCTGCAC[C/T]TCTGCAGAGAGATCA | 380752 |
rs29489861 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28798665 | TACATCAAGATGGTC[A/G]TCTGTTCATGATTCT | 380752 |
rs29489905 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Tssc1 | Mm_Celera | 12:28780679 | CTGGCTCTTGGAGGC[C/T]TGGACTCTGCATTAG | 380752 |
rs29491119 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28818270 | ACAGCGTCTGTGCCT[A/G]ATGCCCTCTGCAAGC | 380752 |
rs29491699 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Tssc1 | Mm_Celera | 12:28791400 | CACGTGCTTCACCAC[A/G]CTGCCTTAGAGACTA | 380752 |
rs33843547 | snp | C/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28788535 | GGTCTTGCTCACAGG[C/G]GTCCTGTGGACCCTA | 380752 |
rs33843602 | snp | A/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28790374 | GAGTTCGAGGAAAGG[A/T]AGACTTGATTAAGAG | 380752 |
rs33843966 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Tssc1 | Mm_Celera | 12:28836240 | AGGGCTTCATGTGTA[C/T]AGGAAAGCAAAACAC | 380752 |
rs33844485 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28788379 | GAGGAAGTAGAAGGA[C/T]ATGAGCCAGGGTTAG | 380752 |
rs33845204 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28831816 | TTCATACATGCCCAG[C/T]TGGTACATCCCAGCA | 380752 |
rs33846018 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28756936 | ACTTTATGCTGGCCT[A/T]AGTTTCCTAGACTTC | 380752 |
rs33847486 | snp | C/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28755659 | AAGCCCCACACTAAA[C/G]CCAATTCACTGGGGT | 380752 |
rs33857990 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28770540 | CCACTGGGTCTTGGT[A/T]CTTGATGTAGACTAA | 380752 |
rs33881829 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28838013 | TCAGGATGCAGCCCC[C/T]AGGAGGCCCCTTCCT | 380752 |
rs45651071 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28780884 | AGCAGTTCATGTCTC[C/T]CATGGCCTTCTCTGT | 380752 |
rs45657158 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28787087 | CAAGCAGGGGAACCT[A/G]TGTTTTCCATGTAGC | 380752 |
rs45668342 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809770 | GGATTTTCTGAATTT[C/T]TGTTAAATTGCCAAG | 380752 |
rs45676926 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28865087 | AGGCTACTGTTGTCA[C/T]CAGATTGAACACTGG | 380752 |
rs45679310 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28860296 | CAAAATGCAAGATTC[A/G]CACAGCACTGGCTGG | 380752 |
rs45682504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | GRCm38.p3 | 12:28753710 | CCTGAATACTGGGAC[A/G]GAATTCCAATGCTAG | 380752 |
rs45683885 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28837175 | CTTGTGTGTATGTAC[A/G]TGCATGGACGTGTTT | 380752 |
rs45705617 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Tssc1, Gm31209 | Mm_Celera | 12:28867977 | TACTATTGCTGTGTT[A/G]AAACACCCTGGCCAA | 380752 |
rs45707391 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28810592 | GGAATGTATTACTCA[G/T]GGTCAGGATTCAAAC | 380752 |
rs45711564 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28857338 | TGTGGATATCATTCC[G/T]TCTGCCCTGGGCTTT | 380752 |
rs45722429 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28813224 | TTAATGGTTCCAGTA[A/G]CAGCCGAGAGTCGTC | 380752 |
rs45722461 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28808116 | ATGTTTGAGGAAAGT[A/T]GTGTTTAATTCTTGT | 380752 |
rs45724665 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813229 | GGTTCCAGTAACAGC[C/T]GAGAGTCGTCCTTCC | 380752 |
rs45743745 | snp | C/G | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809470 | TCAGATTTTGTCGTT[C/G]TTGGAGGTCTGCACT | 380752 |
rs45748273 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | GRCm38.p3 | 12:28782875 | GAGCCTCCAGGCAGT[A/C/G]TAAGGCAAGGTAGTG | 380752 |
rs45761014 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28803148 | GCTTGGCCCCTGGAA[A/G]TGGCATTATTAGGAG | 380752 |
rs45769696 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801519 | TCAGGCATTTGGACA[C/T]CAAGATATAAAGCTA | 380752 |
rs45776279 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28820255 | GGATGATGATGGAAA[A/G]CATTAAAAGTCTTTG | 380752 |
rs45783462 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28824746 | GTTTGGGATTGTTAC[G/T]GAAGGGAGAAGGGTG | 380752 |
rs45796657 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28787018 | GCTGAGGCACAGCTG[C/T]AGTGGATAAATAGTT | 380752 |
rs45801008 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28814417 | CCTGTCCAGCAGGTC[C/T]AGTTATTCGAGGGGA | 380752 |
rs45801531 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28757427 | TTGCGAGCATGCAGT[G/T]TCAGGGTGCGCCAGC | 380752 |
rs45801797 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28767932 | AATTTCCCTGTCTTA[G/T]TTATTGTTCTGTTGC | 380752 |
rs45802445 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28842759 | ACATTGGTGAGACTT[A/C]ATGGGTGTAGCTTCA | 380752 |
rs45802962 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28829391 | CCACACAGTGGCCAT[A/G]GCTTCAGACACCACT | 380752 |
rs45807294 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813958 | AGTGAAGCAGGGCTT[C/T]CTGGGGCCTGCTGTG | 380752 |
rs45812671 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trappc12, Tssc1 | Mm_Celera | 12:28750459 | GCTGGCCGCGGAGAC[C/T]CGACTTCCGCACATG | 380752 |
rs45824895 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813834 | GGCCTCCTCACCCAG[C/T]ATGTCAGGACTCCTT | 380752 |
rs45833760 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28763146 | CACCTCTAAATAGTG[C/T]TGCTCACTCCCTGGC | 380752 |
rs45837711 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845907 | CCACATTCTTCCTTT[C/T]CTTATCTTCAGCATC | 380752 |
rs45839214 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28763299 | AGGATTTCCCAGCAG[C/T]CTGTCCCATCAGGAC | 380752 |
rs45847125 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751543 | TTGGGCAGTGCTCTG[G/T]TGCTCAGGACCACGG | 380752 |
rs45851537 | snp | A/C | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28805320 | AGAGATGTCCTGAGG[A/C]ATACTGCAGCTGCTG | 380752 |
rs45870266 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28782123 | TGATGGTTATCCAGT[A/G]CTGTGCACTATACAC | 380752 |
rs45872106 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Tssc1 | Mm_Celera | 12:28817014 | TCTGCTGGCACCTGC[A/T]GTGAATCGTGTGGTG | 380752 |
rs45872511 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28786529 | CCCTACTGCCTGGCT[C/T]ATTGAGTATCGTGTG | 380752 |
rs45873974 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tssc1 | Mm_Celera | 12:28822826 | CCCTGGGTGGCTGCA[C/T]CTCCTGCCCTTGAGG | 380752 |
rs45875657 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28848039 | CTTAAGTCTTTCTTT[C/T]CTAAGATGTGTATCA | 380752 |
rs45879238 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28836954 | TTAAACCTTTACTTA[C/T]AACTTTGCCATGTTT | 380752 |
rs45884516 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28842895 | CATGTTGTGTATCTG[G/T]CAGTTGGGGCTGGGT | 380752 |
rs45896873 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28852035 | TCTCTCAGTCCAGTG[C/T]GTTGTGGGACTTGGG | 380752 |
rs45902472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28760008 | GCAGATGAGATAAGC[C/T]GACTTTTCTGTGTTT | 380752 |
rs45903867 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28783740 | CCTAGGGTTTTACAT[G/T]CTAGCAAGGTCTGCC | 380752 |
rs45904149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28835366 | CACAAACATGATGAC[A/G]GGAGAGTAACCTATA | 380752 |
rs45906166 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845855 | CCATCGGGGTTCAGA[G/T]CTCAGCTCGACTGGA | 380752 |
rs45908933 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28841235 | TGTCCATCAAAGTCT[A/T]CATGGCTTTAATAAC | 380752 |
rs45912114 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28838156 | GCATGCTCTCTCCTC[C/G]CAGGTGCTTGTCTGT | 380752 |
rs45915888 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28839813 | AATGCCCAGAGGAGA[A/G]CTCCTTTAGTGCCCA | 380752 |
rs45929631 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28794761 | GCTTCAAAAAGGCAG[A/G]CATATCTCTGAATTG | 380752 |
rs45931855 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28783657 | CACCAGGGATAGGCA[G/T]CATGCCCTCCTAGGA | 380752 |
rs45942407 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28848702 | GGAGAGCCAGTGCCC[A/G]GACTAGCTGTGGACA | 380752 |
rs45949283 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28858607 | TCACCAATAGTGGGT[C/T]CAGGATGTTGGAGGA | 380752 |
rs45949953 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28864094 | TGTGTCTGTGAAGCC[C/G]TAGGGCCCTCCCTGT | 380752 |
rs45951117 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28786173 | CAAAGCCTATGAGAG[G/T]GAGTGAGTGTACATT | 380752 |
rs45972937 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28817068 | GTAGAACTGCTGACA[A/G]TACCCTTTCTCTGTC | 380752 |
rs45974104 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28855135 | GGTAGGATGGTCAGA[A/G]TTGTCACATAAGCTG | 380752 |
rs45976893 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28774512 | AGCGTAGGGGCCAGA[C/T]CCATAGGGTAGATCT | 380752 |
rs45977791 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28811729 | CTCTCACTGCATCTG[C/T]AGTCAGAAAGCAGAG | 380752 |
rs45979347 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28754212 | ATTTTCCTAGTGGGT[C/T]TATTCATTATTCAGT | 380752 |
rs45994160 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28829634 | ACCTGATCTTCAGGA[A/G]TCATGCTCCCCTAGA | 380752 |
rs45995692 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28824505 | TCGAGCTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 380752 |
rs46006299 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866391 | GCATTTTGCAGACGG[A/G]AAACCCTGGAGTTTC | 380752 |
rs46007638 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28848606 | TATTTAAGAGAAACA[A/G]ATCATGTTCAGAAGA | 380752 |
rs46009148 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28834250 | ACCTTTGGTTTGCCT[C/G]ACCTCCAGGCTGTGT | 380752 |
rs46014320 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28754887 | TTAGGTGGAGCCCAT[C/T]CCCTGCTTTCTTCCC | 380752 |
rs46016454 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28768278 | GAGTTCCATGTACTG[C/T]GGACAAGCACTCATA | 380752 |
rs46019985 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28787571 | GGAGGCTGGCTCCGA[C/T]CTACATACGACCTTT | 380752 |
rs46028472 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28764142 | TATTTAAGTTCACAG[A/C]TGAAGGATGCAAACT | 380752 |
rs46028950 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28764419 | GCGCTAGCCCAGGAC[A/G]GCTGCCATAATCACT | 380752 |
rs46039477 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28815197 | CTGACTCTGTGGATG[C/T]CAGTATGATAGCTGC | 380752 |
rs46052488 | snp | C/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821380 | GGGGTGGCCTAAAAG[C/G]AAATGTTGGTCGAAA | 380752 |
rs46069268 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28852777 | GCTGTGTATCCTATA[A/C]AACTCAAAAAACAAA | 380752 |
rs46069351 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28761091 | GAACAGGTCATGATC[A/G]CATCGCAATAAGAAA | 380752 |
rs46078120 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28863624 | AAAGAAAGAATGAGA[C/T]GCAGACTAGTATATA | 380752 |
rs46083862 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28841424 | ACGTGTAAGAAGCAG[A/T]GAGCAGCCTCACCTC | 380752 |
rs46085982 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28839592 | CCTCCAGGAACCTTT[G/T]TAATGTGCTATTTGT | 380752 |
rs46088764 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28836958 | ACCTTTACTTATAAC[G/T]TTGCCATGTTTTAGA | 380752 |
rs46098316 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28764986 | TCGGGTGTGGTGAAA[C/T]CTATGAACCATCTTG | 380752 |
rs46111598 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28848172 | AGGCAGGGGGATTTC[A/T]GAGTTCGAGGCCAGC | 380752 |
rs46116316 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28789335 | CGTGGCTCTGCTCTA[A/C]GCTCTCATCCCATCC | 380752 |
rs46125155 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28850644 | AGAACCCGAGGAACC[C/T]TGGATTCTGAAGGCT | 380752 |
rs46134502 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866651 | CTTTCAGTGTCCTTC[C/G]GGCTCACTTGCTAGT | 380752 |
rs46138121 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28862601 | AGGATTTGGCTCTTT[C/T]ACAGTCTTGGTCCCT | 380752 |
rs46138939 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28816489 | GATTCTGCCCTGGGG[C/T]TGGGAAAGAAGGCAG | 380752 |
rs46145478 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28848539 | AGTGCTTAAAAACTC[C/G]GGCCCCGCTGTCTGA | 380752 |
rs46146201 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28775379 | ATGCCTGGCTGCACG[C/T]GGGGCCCTGCTGCAT | 380752 |
rs46152723 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28814523 | TAGCATCAAGGTCTC[C/T]CTGTATTCAGCAAGG | 380752 |
rs46157346 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28856584 | GACATCAAACCTAAG[C/G]TGCCATCATTTAATG | 380752 |
rs46170416 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28836498 | CAAGGGAGTGCAGGT[A/C]ACATGCAGTCAGCTC | 380752 |
rs46171856 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28761614 | TCAGAAATGGTCAGA[A/C]TATGAAAATGTACAA | 380752 |
rs46172577 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28790143 | CATACCAGCACTCAG[A/G]TCTACAAGGTTACCC | 380752 |
rs46179416 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28761395 | AGATAACATTAGCAG[C/T]TGCTGACAAATAGTG | 380752 |
rs46179731 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28838755 | CTGGTCATTTCTCTC[A/G]TCCCGTAATTCCTCA | 380752 |
rs46180378 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28811807 | TTTCATATGTTTGAA[G/T]ACTTGGTTGTCAGTT | 380752 |
rs46186648 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28841366 | GAGCTGTGCCCGACA[C/T]GGGATCTACTCGGTT | 380752 |
rs46195854 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Tssc1 | Mm_Celera | 12:28763220 | AGTTGGGATGCAGTG[C/G]AACATGATGGGTCTG | 380752 |
rs46198639 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tssc1 | Mm_Celera | 12:28848469 | AAAACGTGGCTGATG[A/G]TGCATCGTTGTGACA | 380752 |
rs46204547 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28830817 | CCTTGAGCAGTCACA[C/T]GCCTGCTTTTGTTTG | 380752 |
rs46205576 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28814205 | ATATCTCTGAAAGCT[C/G]AGGGAGGGTTCCTTC | 380752 |
rs46210799 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28772974 | ATCACAAGGTCCATG[C/T]CCATGACAAGGTTCA | 380752 |
rs46213247 | snp | A/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28767325 | CAGCATTTCTGTCAG[A/G/T]CAGTCAGTGAGCGAC | 380752 |
rs46220397 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28794794 | TTACAATGTTAAGAA[A/G]AAAAACATATACTTC | 380752 |
rs46221452 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tssc1 | Mm_Celera | 12:28817350 | TCTCAGGTGCCAGGG[C/T]ACTCAATGTACAGCA | 380752 |
rs46235961 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28827631 | CCTGACCTAGAGGAT[C/T]CCACAGAACAACTGC | 380752 |
rs46237470 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28816404 | AGCTGTGGCACACCT[A/G]GACTGCACACCCTGC | 380752 |
rs46244109 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28826805 | TTCTAAGCATCTTTA[A/C]TATGAACCCTAACAT | 380752 |
rs46244305 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28811792 | GAGTGGCCCCCATAA[G/T]TTCATATGTTTGAAG | 380752 |
rs46244812 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801796 | TGCAGAACCCAGATC[C/T]TGGGTACATAGCTGA | 380752 |
rs46247918 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28860766 | ATCTATAGGAGCTAG[C/T]TGAAGATGTAAATCT | 380752 |
rs46248584 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28804307 | CCTTGTGTCAATCTC[A/G]TCTGCTTCATGTGCC | 380752 |
rs46260474 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28790925 | ATTGAATATTTTTTT[C/T]CTCACAAAACTCAAA | 380752 |
rs46260822 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28789493 | AACTTACCCTGCTCA[C/T]CCCTGGTCCATAACA | 380752 |
rs46264799 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783267 | GGACTTCAGGAAGAG[C/T]AAAGATGGGCTATGT | 380752 |
rs46276200 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28857020 | CAAGCCCAGCTCCCC[A/T]CATGCCCTTGTGCTG | 380752 |
rs46281272 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28820211 | AAGCAGCAGTTTTCA[G/T]AGTCAAGCAGTGAAA | 380752 |
rs46284760 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28815893 | ACTGAGTAGACCAAA[A/G]CAGAGGGTACAGAGA | 380752 |
rs46286969 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28832901 | GACAGTTCTATGATG[C/T]CAAAGAATACTATAA | 380752 |
rs46291809 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28765754 | TGTTCCTCTCTCCTT[A/C]AATCTACATTATGGA | 380752 |
rs46293730 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28851772 | ATTGGCCTGCTTATT[C/G]CAGCAGTGGAGATTC | 380752 |
rs46302092 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28753156 | CCCCAGTAGTCAGTG[G/T]AAACCTTAAAGTGGA | 380752 |
rs46309898 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Tssc1 | Mm_Celera | 12:28763682 | AACTCTAGTCCTGGG[A/G]TAGCCATTGCCCTCT | 380752 |
rs46323168 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28851669 | GCTATGGGTTTGTTG[A/G]CCCTCTGACTTGGCA | 380752 |
rs46329921 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28831977 | AGGGTGATTCTGCCA[C/T]TCCCTGTCTCCTTCT | 380752 |
rs46334733 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28811399 | TTCTGTAAAATTCAA[A/T]TTTAATTGGGCATTA | 380752 |
rs46337431 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28810955 | TAGAGATGATGAAAA[C/T]ATCTAAGGTGGTGGA | 380752 |
rs46340146 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28801837 | TGGTGGCGAGAGGCG[A/C]CATCTGCCCTGGAAT | 380752 |
rs46343793 | snp | C/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28812015 | CCATGGACTTCAACC[C/G/T]TCGAGACTATAAATC | 380752 |
rs46350283 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28802783 | CCTAGATACTGAACT[A/C]CAGTCATCAGATTTG | 380752 |
rs46360799 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tssc1 | GRCm38.p3 | 12:28821296 | GTAACAAGGCAAATA[C/T]AGAACAGTTCTGCAG | 380752 |
rs46367759 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28811881 | AGAAGGTGTATCACT[G/T]AGGGCAGTCTTTGAG | 380752 |
rs46388197 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28762264 | TTCTCTACTGTGATA[C/T]GCACTGGGCATTTTC | 380752 |
rs46391394 | snp | G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28785051 | CCCCATTAAAAAGTC[G/T]CCTACATTCTGCCTC | 380752 |
rs46392244 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28833311 | CAGCTTTTAATGGCA[A/G]AATTTCATTCCCATC | 380752 |
rs46401618 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28762507 | GTACATGCTCTTAAT[A/G]ACTGAGCCATCTTTC | 380752 |
rs46407202 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28852586 | CTAAGTACAAATTCT[G/T]CTGTGACTGAGTAGC | 380752 |
rs46411680 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784518 | TGGTGTGCCAAGGCC[C/T]GGGAATCCCCCTAGT | 380752 |
rs46411788 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28856138 | GGGTCAATTGCCCAG[A/G]AAAGTGAGTTGCTGA | 380752 |
rs46421254 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28785297 | TTCTATATTGCACCT[C/T]TCAGTTTGTCACCTG | 380752 |
rs46426310 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784328 | GCCTCCCTTCTACCT[C/T]ACTTTTGGCTATTAA | 380752 |
rs46427131 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime | Trappc12, Tssc1 | Mm_Celera | 12:28751876 | TCGTAGTCCATTTTT[C/T]AGGCGGGGAATGAAT | 380752 |
rs46467686 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28815780 | AGAAGCTTGGGAACC[C/G]CCTGGCAGCCACCAG | 380752 |
rs46473998 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28799951 | TTTGAGTGCGGACTA[C/G]AGACGTGGTGGAAGA | 380752 |
rs46479365 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28826908 | GAAACAGGACCTTCT[A/G]TATAGCACATGGTGT | 380752 |
rs46482382 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28841662 | CTGGGCCAGTGAAGA[A/G]CAGTGATGATTAGAT | 380752 |
rs46487936 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28789321 | ATGCTAGGTGGGGCC[A/G]TGGCTCTGCTCTACG | 380752 |
rs46496437 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28846008 | GCAAATGGCATCCTA[A/C]CCACAAACGCCTTCC | 380752 |
rs46506254 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28778173 | GAATATGGAGATCCT[A/G]AGTACTACCCCAGTC | 380752 |
rs46513914 | snp | A/C | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28777349 | TAAGCTCCTTGGGTA[A/C]TTTCTCTAGCTCCTC | 380752 |
rs46517109 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28861319 | AGCTGAAGATGTAAA[C/T]GTATAGGAGCTAGCT | 380752 |
rs46542417 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28769326 | ATGCCAACATCTTCT[C/T]TTTTCTCTCTTTTCT | 380752 |
rs46548637 | snp | A/C | 0.444444 | 0.157135 | intron-variant, missense | Tssc1 | Mm_Celera | 12:28859245 | TGAACAATACCCGTT[A/C]TACCAGCTGGCCAGC | 380752 |
rs46564133 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28831116 | CTTGCAGCCCAGCGT[A/G]TGAAAAGATGCAAAT | 380752 |
rs46565184 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28841377 | GACACGGGATCTACT[C/T]GGTTCTCCTTTGTAC | 380752 |
rs46567978 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28785393 | AAGACCAGGTGTATC[C/T]TCTCAAAGTTGTTTT | 380752 |
rs46572900 | snp | A/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28777348 | TTAAGCTCCTTGGGT[A/G]ATTTCTCTAGCTCCT | 380752 |
rs46579495 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28784727 | TCAGGAGGAAGAGTC[A/G]ACAATCTAGTTTCAA | 380752 |
rs46589483 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28815207 | GGATGTCAGTATGAT[A/G]GCTGCCTGCTAAGAT | 380752 |
rs46592065 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28803827 | TCCTTTGATAGCCAC[G/T]TGGACCTTCTTGATG | 380752 |
rs46602035 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28764192 | TAGAAATCAAATTCT[C/G]TAAACTTATAAATGC | 380752 |
rs46618569 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28767341 | CAGTCAGTGAGCGAC[C/T]TCACTTCTCCCTCAG | 380752 |
rs46620784 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28763399 | TGTCATCTCGGATCA[C/G]GAGAGACCGACCAAG | 380752 |
rs46644429 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28855172 | CCTTGCCTTTCACAC[A/C]GCTTTCACAGGTTGC | 380752 |
rs46644733 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28817169 | GAGAGATGTCTGTGC[C/T]CTGTTACGTCTTCCT | 380752 |
rs46647792 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28810722 | TTCCAGCACATTTTT[A/T]AAAAATTAAAATTAG | 380752 |
rs46653575 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tssc1 | Mm_Celera | 12:28811754 | GCAGAGTGATGAGTG[C/T]TCAGCTCAGGTGGTT | 380752 |
rs46659159 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28841065 | GGCTGCATCTGGTAC[C/G]TAGGAGTTCCAGGTG | 380752 |
rs46659528 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813941 | TAGGCACAGCTGGCA[G/T]CAGTGAAGCAGGGCT | 380752 |
rs46670337 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28855296 | AGTGCTTGCTCCTGA[A/G]CGCTTTCTGGCTCAG | 380752 |
rs46672966 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28820248 | TGCTGAGGGATGATG[A/G]TGGAAAGCATTAAAA | 380752 |
rs46675449 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28785052 | CCCATTAAAAAGTCT[C/T]CTACATTCTGCCTCA | 380752 |
rs46685554 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28752988 | CAGTGTATTTACTTG[A/C]AAAATGAGAAGAAAT | 380752 |
rs46686400 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28770769 | TATGCTGGTGGCTTA[A/G]TGGGTCCCCTGCTGA | 380752 |
rs46704520 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28764590 | GGGGACACCACTGGA[C/G]CCTAGCCGCTCTTAA | 380752 |
rs46707881 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28764424 | AGCCCAGGACAGCTG[C/T]CATAATCACTGAACT | 380752 |
rs46708036 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28848847 | AGGATACTCCTCCCC[A/G]GCAGGCTTTGCTGTG | 380752 |
rs46718838 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28852119 | TTACACTTAGGACAG[C/T]TGTGCTGGGTGTAGT | 380752 |
rs46729207 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28781273 | GTTTCTAACTAGAAG[C/T]GGCATCCTGCAGGCA | 380752 |
rs46729951 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28765132 | GTTCCTACCTCCCAA[A/G]TGTGGATTAAAAGCA | 380752 |
rs46734350 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Tssc1 | Mm_Celera | 12:28764608 | TAGCCGCTCTTAAGA[A/G]GGTAGCTTTTGGTGG | 380752 |
rs46735730 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28822441 | ACATGGGGCACGTGT[C/T]GACCCATGTCCTGGA | 380752 |
rs46736773 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28781109 | TTGTTATTTATGGAG[C/T]GGTTTGGGTAGGGCC | 380752 |
rs46745838 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28836806 | ATCACAAGCCTTTCC[A/G]TTCAGACCACGTCCT | 380752 |
rs46745912 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28753270 | TTGCTCTGTGTACTA[C/T]CAGTTCAGTGGGAAC | 380752 |
rs46747276 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28803333 | TCCTGGTTGCCTTCA[C/G]ATCAAGATGTAGAAC | 380752 |
rs46758564 | snp | A/C | | | synonymous-codon | Tssc1 | Mm_Celera | 12:28828862 | CCAAGGCAACGTGGC[A/C]TGGTAGGATGCTACA | 380752 |
rs46758850 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28804109 | TGAGTGCCCGAGTAG[A/T]GCTCTGATCAGTGTA | 380752 |
rs46761788 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28802365 | GTGGAGGCTAACCTG[A/G]TCCTGAGCTCCTCCC | 380752 |
rs46763976 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801942 | AAACCTTTGATGGAA[A/T]TGAAGAAGAGCATCC | 380752 |
rs46791743 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28765782 | GGACAACTTTCCATG[A/C]TGCTAAGCAGTCTAC | 380752 |
rs46794290 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28803732 | TTTTGCAGGCAAAGG[C/T]ACCAAAGCCTATGAA | 380752 |
rs46807144 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tssc1 | Mm_Celera | 12:28862264 | ACCCCAGCTTCTTCA[C/T]CTTTCTCACAGGTTT | 380752 |
rs46815503 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28764452 | ACTATGAGTTGAAAG[C/T]GGGCTGTAGTGAGAG | 380752 |
rs46818479 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28835833 | TGTCAGAAACTCTGA[A/G]AAGCCTGACTCTGAG | 380752 |
rs46824017 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28832907 | TCTATGATGTCAAAG[A/G]ATACTATAAATGTCC | 380752 |
rs46826552 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28857080 | AAAAGAAATGCGCTC[C/T]GGTAGCAGAATTGAA | 380752 |
rs46834489 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783058 | TTCCAGGGTACTGGT[G/T]AGGGTCAGGAAAGGT | 380752 |
rs46837985 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28766577 | ATTCTGCAGCTTGGT[A/T]CTGTGGAGGCACTGC | 380752 |
rs46848325 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28826414 | CCTCTGTAAGTGCTG[A/G]GGTTATAGGTAGGAA | 380752 |
rs46849906 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28766237 | TTGCCTATCATAGAG[A/G]GACTAGGCATAGCTC | 380752 |
rs46850512 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28764102 | ATTGGAAAAAGTGTG[A/T]TGTATTTAATAATGT | 380752 |
rs46861522 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28769366 | CATCCTTCTCCAGCC[C/T]CCCCCCGCCCCCCCC | 380752 |
rs46861991 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28777373 | GCTCCTCCATTGGGG[A/G]CCGTGTGATCCATCC | 380752 |
rs46863214 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28851729 | AGGAGCCTTCTGCAG[A/G]GGACTCGATATGAGT | 380752 |
rs46868028 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28769981 | CCAGGGTCTCCTGGG[C/T]TTTATTATCACCTCA | 380752 |
rs46878436 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28856014 | GACCTGGGTGTGAGC[A/C]AATTGTCCCTCCACA | 380752 |
rs46882108 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28805909 | GGATTTTCCCTAGAG[C/T]TAGAGTTAGAGTCTG | 380752 |
rs46895270 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28850441 | TCTCTCTGTTCTCTT[C/T]GTGTTCTTCTTGCCT | 380752 |
rs46896329 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28765831 | CTGGGGTTCTGCCGC[A/G]GCCAAGTGCTAGCTG | 380752 |
rs46925328 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28863386 | GGAAACGTGAATGTG[C/T]GCAGATGTTCACACA | 380752 |
rs46933777 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808402 | TCTAGTGGATTGAAA[C/T]TTTGATCATGCCCTA | 380752 |
rs46942652 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28802364 | CGTGGAGGCTAACCT[C/G]GTCCTGAGCTCCTCC | 380752 |
rs46945963 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28811503 | TGTGCTTTATTGATG[C/T]CATTTCTCACTGTGC | 380752 |
rs46949413 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28827010 | GTTCCTTTGTTTACC[A/G]CGCTTCTGTAGGCAG | 380752 |
rs46955731 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28826527 | TAAGAATTAATTCTT[C/G]ATTCATTCATTTATT | 380752 |
rs46955993 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28765159 | AGCATGTGCCATGGT[C/G]TGTGACTGAAAAATT | 380752 |
rs46958531 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28816256 | ACCCAAGGATTGATA[C/T]AGTCTGTAGCAGGAC | 380752 |
rs46966748 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783282 | TAAAGATGGGCTATG[C/T]CCTTAAAATTAACAG | 380752 |
rs46967456 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28819298 | TTCACATCCATCTGG[A/G]GGAAAGGTTGCTGTA | 380752 |
rs46968684 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783126 | GACAAGCCCCCAGAC[C/T]GAAGCTAAGGTTGCC | 380752 |
rs46971247 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28825765 | GTGGCCTTGGCAGTG[C/T]GAAGCTGCCCCTCCC | 380752 |
rs46979933 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28832333 | TCTGAATAACTGTGG[C/T]GCTGCACAGCCAACT | 380752 |
rs46981028 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28753132 | ATAATTTTTAAGTGA[A/G]ATGCATAGCCCCAGT | 380752 |
rs46991731 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28839300 | GGGTTCGATTCCTAG[C/T]GCTCACGCGGCAGCT | 380752 |
rs46995935 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28783030 | CAGCTAGGGTCTTTG[A/G]GATCAGGCTTGTTTC | 380752 |
rs46996374 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tssc1 | Mm_Celera | 12:28823388 | CCTGCAGTGATTATG[A/G]TGGTGTATACTGTTC | 380752 |
rs46999191 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28833312 | AGCTTTTAATGGCAG[A/T]ATTTCATTCCCATCA | 380752 |
rs47024867 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28771042 | AAGGACCGATGAGAG[A/G]CTAGCTCTTTCCACT | 380752 |
rs47040076 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28830327 | GGGTATGAAAGTGCT[C/T]GCCTGGTTATGTTCT | 380752 |
rs47064534 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28834544 | TCAAAACTGCCTTTT[A/C]AATCCTTATAGCACG | 380752 |
rs47065197 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28755028 | GTTACTAATAGGCCC[A/C]AATTTTGGCATGTGT | 380752 |
rs47067501 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28766458 | TGCAACCATAGATCC[A/G]AGAATCTGACAGGTT | 380752 |
rs47069151 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28819861 | AGCAGAAGCACATTC[A/G]GGATTTTCTCTAAAA | 380752 |
rs47077727 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28769941 | TTTCAAGTGTTCACT[C/G]GGTGTCTGTCTGGAG | 380752 |
rs47078809 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28807266 | TAAGGCTATGGATTA[C/T]TGGAGGAAAGGAGAT | 380752 |
rs47094944 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28782756 | AAGGGCTGTGTGGAC[A/G]TGGTTGGGTAACTTG | 380752 |
rs47097381 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28838685 | TGATTAATGTTGTGA[A/G]TATTTTAATGGTTTT | 380752 |
rs47100854 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28804370 | ATAGTTTGGTCCAGG[C/G]CATGGCATCCCTGTT | 380752 |
rs47103055 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28812083 | GTTTTATAAAAGGAA[A/C]TGAGACACCTCATTG | 380752 |
rs47103714 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28789276 | CTAATTATAAAAACC[C/T]GAGCTCTTGTCCTCT | 380752 |
rs47107178 | snp | C/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28861131 | GCTGTAGATGTAAAT[C/G]TATAGGAGCTAGTTG | 380752 |
rs47111371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28824671 | TAAATGCGTGCCTGG[C/T]GCACCCTGCTGTCCT | 380752 |
rs47113728 | snp | A/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28769346 | CTCTCTTTTCTGAGC[A/G/T]TATCCATCCTTCTCC | 380752 |
rs47116162 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28774496 | CTCTTAGGGCAGCTG[C/T]AGCGTAGGGGCCAGA | 380752 |
rs47133269 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808335 | GTTACATCATGATGC[C/T]GTCTCACAATGAAAT | 380752 |
rs47134581 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28832679 | AAGCTGCTTAAGGGA[A/G]GGTTTCAGAAGTTTG | 380752 |
rs47168099 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28807415 | GAGGCCTGTGCACTG[C/T]GTACCTGTCATCACA | 380752 |
rs47169057 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tssc1 | Mm_Celera | 12:28823197 | CTTCTGTAAGTAAAA[C/T]CCAGGACTTTACTTG | 380752 |
rs47174556 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28771617 | CATCTTTCAGTCAAG[A/G]CTGAGGCTTTCAAGA | 380752 |
rs47181884 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Tssc1 | Mm_Celera | 12:28763963 | TCACAGTGCTAAGGC[A/G]TCCTGGGATTTAGGC | 380752 |
rs47182239 | snp | C/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28830123 | GCCATGGTTGTCATG[C/G/T]GTATATGTGTCTCTA | 380752 |
rs47187927 | snp | A/G | 0.18 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28815202 | TCTGTGGATGTCAGT[A/G]TGATAGCTGCCTGCT | 380752 |
rs47201845 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28774678 | TCCAGAGCATGTGGT[C/G]CAGAGGGACAGACAG | 380752 |
rs47232934 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28831805 | CTTCCTAGAACTTCA[A/T]ACATGCCCAGTTGGT | 380752 |
rs47240771 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | GRCm38.p3 | 12:28753388 | TTCCTGAGGAAGCCT[A/G]TGTGCTTGGGGCATC | 380752 |
rs47244873 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28850147 | TGTGTTTCAAAATAA[G/T]AAGTTAAAAGGGCAG | 380752 |
rs47248348 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28856420 | AGTAGGCAGAATGAA[C/T]CGACCCTGCTTACTG | 380752 |
rs47249377 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28823442 | TGGGCTGCTGTCTCT[C/G]TAGTCAGTGGGGTCC | 380752 |
rs47259574 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28768305 | CATATGAATGACCCT[A/G]TGGGAGTCATTGTTA | 380752 |
rs47262195 | snp | A/C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28848155 | CCCAACACTTGAGGC[A/C/T]GAGGCAGGGGGATTT | 380752 |
rs47264046 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28804667 | TACAAGAAGATGCAC[C/T]CACAGAGGATCCAGG | 380752 |
rs47271520 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28850235 | CAGAGACAAGATAGG[C/T]GATATCCCAGCTCCC | 380752 |
rs47271566 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28856541 | AAACCCTGAGAAGAC[A/T]CTGAGGGAAGAATTT | 380752 |
rs47277239 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28754121 | AACCTAGGTTCTCTG[G/T]AAGTGCAACAGGTAT | 380752 |
rs47296512 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28856099 | AAGCTCAGTGCGGTT[A/G]GTCCCTGAGGTGGGG | 380752 |
rs47300670 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28767375 | CCCTGCTCTGTCTGT[C/G]ACTTTCCTCATGGTG | 380752 |
rs47309853 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28856709 | TAGCATCGATGTTGT[A/G]CCTCCTCTTTAGTAA | 380752 |
rs47312893 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28823874 | AGTTGTCTCTTTTGC[A/G]TTAGGCATTTGCTGT | 380752 |
rs47324900 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28781166 | AGCTGTGAGGCAACC[C/T]GTCTCTCAACATTTC | 380752 |
rs47326573 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28864518 | CTTGTTTGCTAGGTC[C/G]GAAAAGAATATTTTG | 380752 |
rs47327880 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28763093 | CCGCACAGTGACACA[C/T]TTTCTCCAATAAGGC | 380752 |
rs47332454 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28781563 | TAGCTTGAGGAAGGA[A/G]ATCTCTGTTCATGAA | 380752 |
rs47334635 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28764374 | GGAAAAATAGTCAGA[C/T]ACGACCATGAAAATG | 380752 |
rs47341560 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28856530 | TGGCTCTGTGTAAAC[C/T]CTGAGAAGACACTGA | 380752 |
rs47343724 | snp | A/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28807416 | AGGCCTGTGCACTGC[A/G/T]TACCTGTCATCACAG | 380752 |
rs47344608 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28760688 | GAGATCTGCCTGCCT[C/T]TGCCTCCTGAGTGCT | 380752 |
rs47347640 | snp | C/T | | | missense | Tssc1 | Mm_Celera | 12:28828843 | GTCACCTTGACAACT[C/T]GGCCCAAGGCAACGT | 380752 |
rs47356621 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28761998 | CACAGAAACACATTC[A/G]GGCAAAAACACTCAT | 380752 |
rs47357684 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Tssc1, Gm31209 | Mm_Celera | 12:28867419 | TGTTGTCATGAGATT[A/G]CAAACTGAAATAAAG | 380752 |
rs47357730 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28848271 | AAACAAAAAAGAAGA[A/G]AACTCTGGAGCCCTG | 380752 |
rs47359050 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28760719 | GAGGTTAGAGGTGCA[C/T]CGCCATGCCAGGCAG | 380752 |
rs47360093 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28763327 | GACTGCTAGAGCACC[C/T]CCAGGATTGGCTGTG | 380752 |
rs47360780 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809796 | CCAAGTGAGATTTTT[A/T]AAAAATAACTGTCAT | 380752 |
rs47361436 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | GRCm38.p3 | 12:28802488 | GAACAGACTTTGCCA[A/G]TGCGCTAAACAGGCT | 380752 |
rs47365357 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28822988 | AAGACTGTACCTTCC[G/T]TTTTGTTTTTCTGGG | 380752 |
rs47367086 | snp | C/T | | | synonymous-codon | Tssc1 | Mm_Celera | 12:28859296 | GGGACAGCTGAAGTT[C/T]ACCGCGGGGCGGTGG | 380752 |
rs47370785 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28771426 | TGACTGCATATAACA[A/G]CCTTCTCAGGAAGAA | 380752 |
rs47371903 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28856759 | CTGGCTCTTAGCACC[C/T]TCCTGTCTCAGAGCC | 380752 |
rs47373682 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28829640 | TCTTCAGGAGTCATG[C/G]TCCCCTAGAGGAGAC | 380752 |
rs47386909 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28775934 | GGCATCAGGCTACAG[A/G]GCATGAGGACGACAT | 380752 |
rs47388762 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28822445 | GGGGCACGTGTCGAC[C/T]CATGTCCTGGAGACC | 380752 |
rs47392051 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28784823 | ACCAGTGTAGAAGTC[A/G]GCAAGCAGGGCTTGG | 380752 |
rs47403111 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28765278 | GCAGCCTTACCAAGT[C/T]GGTCTCTGTTACCTT | 380752 |
rs47405521 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28805755 | CAAGCATTTATCTGG[C/T]AACTCAAGTAATGTC | 380752 |
rs47406969 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845204 | GGAAAAGGGGTCACA[C/T]GTCCAGCCAGAGTTC | 380752 |
rs47411456 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28802344 | AGGAGGAGGGAAGAG[C/T]GCCACGTGGAGGCTA | 380752 |
rs47411563 | snp | C/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28861158 | GTTGTAGATGTAAAT[C/G]TATAGGAGCTAGCTG | 380752 |
rs47413785 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28812587 | TCTCTCCTCAGGCCC[C/T]CAGAGTAGCTCAGCT | 380752 |
rs47417015 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28762802 | CTTGAAGCCAATACC[C/T]CAGAGCTTTCCGTAG | 380752 |
rs47418219 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28829993 | CTGCAGGCGCGAACA[C/T]TTGTGTGCTGTCACT | 380752 |
rs47422359 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28858735 | AAGTGGAGTGGCCTT[C/T]TATCCCAGGCTTGGA | 380752 |
rs47422745 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28825650 | CTGCTCCTGACAGTG[C/T]GAGCAGAGTCATGTG | 380752 |
rs47425932 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28767320 | ACCTTCAGCATTTCT[A/G]TCAGTCAGTCAGTGA | 380752 |
rs47434673 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771469 | CTTTGCAAGTGAATG[C/T]TTATATCTTTTTTTT | 380752 |
rs47438959 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28832585 | GTCTCTTTCCTTTCT[C/G]AGTTTGGTTTATATT | 380752 |
rs47441132 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28815063 | AGGTGTCTGTTGCCA[C/T]GTCTGGCTTGGACCG | 380752 |
rs47442594 | snp | A/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821619 | CGGTTTCTAATAACT[A/G]AAAGTAAAGATGCTA | 380752 |
rs47456717 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28831928 | ATATAATGTAGCCGC[A/G]TCACCATGGTTCTAA | 380752 |
rs47457898 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28787127 | TGAAGTTGGTTGGAC[C/T]TAGTAATGTAGTAGG | 380752 |
rs47470826 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845923 | CTTATCTTCAGCATC[G/T]TCTCTATTGATCGTG | 380752 |
rs47477369 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771529 | CCATGAACTACTAGG[C/T]TTCCATGTGATCATT | 380752 |
rs47478905 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28864015 | CTAGGTGAGGAGGCC[C/T]CTCCAGGGCTTTCCC | 380752 |
rs47487979 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28773534 | AGAAGGAAAGCACAC[A/G]TGCCAGTGAAAAGAC | 380752 |
rs47495921 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28839235 | TTAAAGACACAGAAT[C/T]CTGGGGCTCGGTCGG | 380752 |
rs47502002 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28811708 | GGCAGGAGTGTGAGG[C/T]GCCTGCTCTCACTGC | 380752 |
rs47516692 | snp | A/G | 0.18 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28816161 | CTGCCCTTTTGACCA[A/G]TCTTAACTTATGGAC | 380752 |
rs47516906 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28852504 | TCAGAGCTGTGCTTG[A/C]ACTTATATGTGAAGC | 380752 |
rs47528646 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28846614 | ACTTAACAAACTGCA[G/T]CTTCTCTGGGCTCAG | 380752 |
rs47532646 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28828109 | ATGAGTTTATTTTCT[C/T]TATCTATTCATGACT | 380752 |
rs47535120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28842353 | CAAAATACTAAGAAA[C/T]GTGAGCTTTTTCTCA | 380752 |
rs47539880 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28862793 | CTATAGGGGGAGAAA[C/T]GTGGATGAGCCCAGG | 380752 |
rs47542994 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Tssc1 | Mm_Celera | 12:28851671 | TATGGGTTTGTTGGC[C/T]CTCTGACTTGGCAGA | 380752 |
rs47546359 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Tssc1 | GRCm38.p3 | 12:28780640 | TTCCGCTTTGGAGAT[A/G/T]CAGAGTAGGAGCATG | 380752 |
rs47554235 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28813163 | TTTAAGTTACACTTC[C/T]TCAGAATAGAAAATG | 380752 |
rs47569694 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28837093 | AGAACTCGAAGGCCT[C/T]AGCCCACTGCAGACA | 380752 |
rs47569831 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28839519 | TTGACCTAGAATGAC[C/T]GGGATAATTTTAAGA | 380752 |
rs47583965 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28764667 | GGAGTGGTAGACGGT[A/G]GATGTCCCCTTTAAC | 380752 |
rs47585092 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28841166 | CACAGGGCTGTACTG[C/T]AGTTTACAACTGGGA | 380752 |
rs47596465 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28762303 | GAGGACTGTTTAATG[C/T]CCGTCACCCTGTCAC | 380752 |
rs47638562 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28811206 | ACTCAGATTTTGGGA[C/T]GTTTCTGCTCTAATT | 380752 |
rs47639013 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808241 | AAACATGTAAACTAA[A/G]GTTAAGCTGAGAAAC | 380752 |
rs47645711 | snp | A/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28832404 | CTCCCCTAGGGCTAG[A/T]GTAAATATCACACTG | 380752 |
rs47645752 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28760255 | AACATTTAAAAAAAA[C/T]TTAATGCCACACAAA | 380752 |
rs47649482 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28812102 | GACACCTCATTGTCT[C/T]CTTTTTTATTCAGTC | 380752 |
rs47660246 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28849573 | AGCATGGTTTAGAGA[C/T]GCAGTCCGGCCTGAA | 380752 |
rs47660587 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28811502 | GTGTGCTTTATTGAT[A/G]TCATTTCTCACTGTG | 380752 |
rs47680265 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28826882 | TTCCCCTCAAGATTC[G/T]TGTCTGTGCCGAAAC | 380752 |
rs47682231 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28832863 | TTGTCTCTTAGATTG[C/T]TGCTTAGTTTGCTGA | 380752 |
rs47682494 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28846598 | GTCTTTGTTCACAGC[C/T]ACTTAACAAACTGCA | 380752 |
rs47686696 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28784155 | CTGAAAGCGAAAAGT[A/G]TATTCAACATCAGGC | 380752 |
rs47689498 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28850143 | AGACTGTGTTTCAAA[A/T]TAATAAGTTAAAAGG | 380752 |
rs47692498 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28839637 | AGATGACATAGAGAG[C/G]ATGTGACCCAAGCAG | 380752 |
rs47699851 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28828084 | AGAGCTGTGAGTCTA[C/T]TCTTTCAAGATGAGT | 380752 |
rs47703959 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808409 | GATTGAAACTTTGAT[C/T]ATGCCCTAAAACATC | 380752 |
rs47706010 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28814425 | GCAGGTCCAGTTATT[C/T]GAGGGGACCTTCTCC | 380752 |
rs47706552 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28856327 | ATAAAAATAAATCTT[A/C]AAAAACCTGATATGA | 380752 |
rs47717456 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28829507 | GAGGAGACATGGGTC[C/T]ACAACAAGCGGTCAG | 380752 |
rs47730674 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28759721 | TGCTTTTCCAGTTCT[C/T]TGCAGGGAAATTGGC | 380752 |
rs47745688 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28766066 | CATTGAGATGGCATC[A/G]TTAGCTTTCTCTCTT | 380752 |
rs47746757 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28857003 | TGTCTGCCACTGAGC[C/T]GCAAGCCCAGCTCCC | 380752 |
rs47753125 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28803922 | AGATTTTTTTAGGTG[C/T]AAATTGTATCAAGTG | 380752 |
rs47754745 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28754660 | GCTGTCTTTAATGTC[C/G]GTCTAAGTGTGCGGA | 380752 |
rs47756288 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28810037 | AGGCTCCTGTTTGTT[C/T]GTGAGTTTTATCGCG | 380752 |
rs47765602 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28850288 | TTCCTGGTGTTGGCC[A/G]TGCATGTTGCATCGC | 380752 |
rs47766047 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28864077 | CTTACCGGAAGTGGT[A/G]CTGTGTCTGTGAAGC | 380752 |
rs47767083 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28784194 | GATCCCCAAATTGGC[A/G]TTCTATAAAATTGTG | 380752 |
rs47769504 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28754511 | GTAGACCCGGCTGGC[C/T]GAAAGTTGTCTCAAA | 380752 |
rs47779969 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28801343 | TTTCGGCCTTGAGGT[A/G]AGAAACTCCACCACC | 380752 |
rs47781558 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28811577 | GACTGAATACCCTCC[C/T]TGAAGGAAATCCCCT | 380752 |
rs47786800 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tssc1 | Mm_Celera | 12:28850756 | CACATCTTGGACTCT[A/G]CCCAGAGGGATAATG | 380752 |
rs47787623 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28804147 | ATCTCTCAGATCTGA[C/T]GCTTCAGCTCATGCT | 380752 |
rs47788017 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime | Trappc12, Tssc1 | Mm_Celera | 12:28751839 | AAACAGGAAGTGAGC[C/G]GTCAGGGAGCCGGTC | 380752 |
rs47790135 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28856062 | TGTGGGCTAGTGACC[A/G]ACAGGAGGCTTACCT | 380752 |
rs47793722 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866085 | GAAAATGGGATTCCC[C/T]GTGGAGATGCTTCCT | 380752 |
rs47794914 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28829093 | GAACACATTTCCCAC[C/T]CTTTCCCTCTTCTAA | 380752 |
rs47801642 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28855740 | GCCTGATCAGGAGTC[A/G]GTCCTGCTTTCCCTC | 380752 |
rs47811665 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Tssc1 | Mm_Celera | 12:28859353 | GGCCACAGCAAGTGA[C/T]ACGACCCTCCGAGGA | 380752 |
rs47822940 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28800186 | ATTAGTGGGTAGCCA[C/T]GCAGCCTTTTTGTCA | 380752 |
rs47839578 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28856944 | TTTTATTGTTGATTT[C/T]GATGTTGGGGATACC | 380752 |
rs47840488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28763199 | TGCAATTGCACCACA[A/G]CCGTCAGTTGGGATG | 380752 |
rs47849269 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tssc1 | GRCm38.p3 | 12:28821909 | AGTAGGTGTTGGTTA[C/T]AGTGAGAATTGAGAG | 380752 |
rs47859860 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28823123 | CTGCTTTTCTTGTGG[A/T]TCTCGTTTTATATGT | 380752 |
rs47862679 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783642 | GAGAGGGATTGTATG[C/T]ACCAGGGATAGGCAG | 380752 |
rs47862720 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28764494 | AGGAAAGCTAGTGAG[A/T]GGCTGGAGGAGTCTC | 380752 |
rs47866016 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28773046 | ATCACAGGTCCATGT[C/T]CATCACAAGGTCCAT | 380752 |
rs47868553 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28865554 | AGATGCTCTCATCCC[C/T]TACAGTGGTTTTACC | 380752 |
rs47872329 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28786592 | ACTGAGTGGTCTGAA[C/T]TATTCATTGTGTTTG | 380752 |
rs47875307 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28848713 | GCCCAGACTAGCTGT[A/G]GACAACACTGGGAAC | 380752 |
rs47877351 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28815228 | CTGCTAAGATTCAAG[A/C]GTAGCTACCAGCTTT | 380752 |
rs47878913 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28757350 | GTTCCCTTCCTGTGG[C/T]GGACTTACTGCTGGC | 380752 |
rs47887193 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28841453 | TCTCCCCAGGGCTCT[C/T]CTGGGCAGGGCTCTT | 380752 |
rs47891559 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28811343 | GGTCTTGCCTGTTTT[A/G]CTTTTATGACTGTTT | 380752 |
rs47901484 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28786971 | GGGTGGATGCTCACA[G/T]TATCTTTCGGTGTTT | 380752 |
rs47904390 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28789431 | CAGTGTCCAGTACAT[A/G]TCCTCATCACTCTGC | 380752 |
rs47917752 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Tssc1 | Mm_Celera | 12:28763721 | CCATAGGCACTGCAT[A/G]CATGTGGTTGTAGCC | 380752 |
rs47918395 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809843 | TTCATTTAATTCTAG[C/T]AAACAAACAAAAATC | 380752 |
rs47919980 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28763678 | TTGTAACTCTAGTCC[C/T]GGGGTAGCCATTGCC | 380752 |
rs47931146 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28807740 | GTGGTATCAGCTAAC[A/G]TCTGGCTAGGGCTCT | 380752 |
rs47938520 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28763475 | AGGCCTGCTCTTTGC[A/T]GTCAGAGAACATTGA | 380752 |
rs47940976 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28842011 | TATGCAGACTCTGCG[A/G]CTCCAGAGTAGGGCA | 380752 |
rs47941255 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28845949 | TCGTGGTGCGTTTTA[C/G]TTTTATGAAGTTACA | 380752 |
rs47955548 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28856716 | GATGTTGTACCTCCT[C/G]TTTAGTAACTGCATT | 380752 |
rs47956406 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866838 | CTGGCCACACATAGG[C/T]TGCATATGGTCCTTG | 380752 |
rs47958268 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809932 | CACTCACTTGAATGT[C/T]TTTAAGATTGTGGTG | 380752 |
rs47965005 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28804687 | GAGGATCCAGGTTCC[A/G]TTCCCAGTACCCATG | 380752 |
rs47965688 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28849647 | CTTCCCTTTCCCAGA[A/G]CTGGATGTAGTTCGG | 380752 |
rs47966160 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28825886 | ATCCCCTTGTCTTTT[C/T]CTTCCCCGTGAATAA | 380752 |
rs47969522 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28816972 | AGCAAAAGGCCATGG[C/T]TGTTCCCTGACCACT | 380752 |
rs47977683 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trappc12, Tssc1 | Mm_Celera | 12:28750422 | AAGATCCAAGGTCCC[C/G]CGCGTTTGTGCGTCT | 380752 |
rs47979618 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821374 | GTGTCTGGGGTGGCC[C/T]AAAAGCAAATGTTGG | 380752 |
rs47983729 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28857656 | GCTGCTACATGTTTC[C/T]GTGCGAGCAGACTGC | 380752 |
rs47991863 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28802341 | AGCAGGAGGAGGGAA[A/G]AGCGCCACGTGGAGG | 380752 |
rs47992702 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28842962 | TGTAGTGTTCTGCAA[G/T]ATCTTCATCTGTTAC | 380752 |
rs47996553 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28772818 | GACTTTTAAGCCTTA[C/T]GAGGATTTTGCCTCT | 380752 |
rs47996956 | snp | A/C | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821431 | GAGAGGGAAAGGTTC[A/C]TGGTGACCAATAGAT | 380752 |
rs48011086 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28802236 | TTGACAACACAATGT[C/T]CCCTTTCTCCTAGGC | 380752 |
rs48028524 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28807513 | TCATCAAGGAAGCAT[C/T]TTGTAAATCTCATGT | 380752 |
rs48036742 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28854376 | GGTTAGTCTGCCCTT[C/T]TTAAACCCAGGCTCC | 380752 |
rs48037759 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28786552 | ATCGTGTGGCTTCGA[A/T]GTTATGTTGAAGAGT | 380752 |
rs48044200 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Tssc1 | Mm_Celera | 12:28817098 | CACACTCACTTCCCA[A/G]CCAGTCTTTGCACTG | 380752 |
rs48044531 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28826668 | AGGCTTGAGGCCCAG[C/T]GCCTTCACCAACTGA | 380752 |
rs48054278 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28812104 | CACCTCATTGTCTCC[C/T]TTTTTATTCAGTCTA | 380752 |
rs48061004 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28813008 | AAATGTGTGCAGAGG[A/G]CAGAGGACAACTTGT | 380752 |
rs48062435 | snp | A/C | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28827011 | TTCCTTTGTTTACCG[A/C]GCTTCTGTAGGCAGC | 380752 |
rs48065477 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28841101 | GCGACATTGCCAGTA[A/G]TGTAGTTGGCAAGGC | 380752 |
rs48075613 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Trappc12, Tssc1 | Mm_Celera | 12:28752261 | TTGAGTTGTGTGTTG[G/T]ATACTGCTCAGTACA | 380752 |
rs48086588 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28865553 | GAGATGCTCTCATCC[C/T]TTACAGTGGTTTTAC | 380752 |
rs48092097 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tssc1 | Mm_Celera | 12:28817136 | GAACTTGTGCACCTG[C/T]CACCTGCACAGAAAC | 380752 |
rs48092352 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809554 | TGTCCTACTCTCCGA[C/T]CCAGAGAATTTGTAT | 380752 |
rs48094577 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trappc12, Tssc1 | Mm_Celera | 12:28750427 | CCAAGGTCCCGCGCG[C/T]TTGTGCGTCTGCGTG | 380752 |
rs48101787 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28766177 | CAAAAATGTGCTAAA[A/G]CACAGGCTCATCCCA | 380752 |
rs48102259 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28845373 | ACACCCTGTAGCCCC[A/G]GGGTTATAGGAGAGA | 380752 |
rs48103994 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28845334 | GTGGAGAAGGGGCAG[A/C]CCCCGACCGGGGACC | 380752 |
rs48108124 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Tssc1 | Mm_Celera | 12:28810870 | AGGCAGGCGTTCAGT[C/T]TTGAGCTTTCTCATT | 380752 |
rs48109528 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28807174 | TTAGAACAGTTGATG[A/T]GAAGCAGGGATTGGG | 380752 |
rs48111492 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28787306 | GTCTCATTCTCATGT[G/T]GTTGAGAAGCCTGAC | 380752 |
rs48111839 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28816158 | CTCCTGCCCTTTTGA[C/T]CAATCTTAACTTATG | 380752 |
rs48116448 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28829020 | GCTTGTCACTTTTAG[C/T]CCTAGGTGTTTTTAG | 380752 |
rs48121083 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Tssc1 | GRCm38.p3 | 12:28817177 | TCTGTGCCCTGTTAC[A/G/T]TCTTCCTGGAGAGGG | 380752 |
rs48123465 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28804108 | CTGAGTGCCCGAGTA[A/G]TGCTCTGATCAGTGT | 380752 |
rs48131559 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28762850 | TTAAGGTTTCCATTG[C/T]TGTGAAGAGACACCA | 380752 |
rs48131779 | snp | G/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809946 | TTTTTAAGATTGTGG[G/T]GTCTGAGGTCATTGT | 380752 |
rs48137978 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28856336 | AATCTTAAAAAACCT[C/G]ATATGACCTATGCGT | 380752 |
rs48142348 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tssc1 | GRCm38.p3 | 12:28808512 | AAGAAACTTTCACTG[A/G]CTTTTTTAAAAACAT | 380752 |
rs48143113 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28864259 | TTCGGTGGTCTTAGA[A/G]GGGTCAGGAGGCCAA | 380752 |
rs48144305 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28822459 | CCCATGTCCTGGAGA[C/G]CACCTTTGGCCCAGC | 380752 |
rs48160264 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28760830 | ACCTCTCTAGTGCTA[C/G]GATCATAGGTTTGTG | 380752 |
rs48163376 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28807227 | ACCTGGTAGAGGACA[C/G]TGTTTTGCGTGTGCT | 380752 |
rs48163739 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28822404 | CTGCCTTGCTTCGGA[A/G]CTGGTGCTGGTCTCA | 380752 |
rs48180479 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | GRCm38.p3 | 12:28842145 | GTGACAGAGAACTTG[C/G/T]GTCTGGGGCATAAAG | 380752 |
rs48180912 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28841757 | CTTGTCACCTGCTGG[A/G]CACTATTTCACAGAG | 380752 |
rs48198028 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28772670 | TTGCTCATCCTAAAA[A/G]TGGTGTTATTGCCAT | 380752 |
rs48198700 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28767832 | CCTAAACCTCCCACA[C/T]TCTTGGGTTATAGAT | 380752 |
rs48201538 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28819831 | CAGCTTTGAAAAAAC[A/T]ACATAGTATAGAAGA | 380752 |
rs48204193 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28857740 | CACTGCCACATTCCC[A/T]CCAGGTGCAAGGGAC | 380752 |
rs48208235 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28851288 | TGGCTTCACAGTGAA[A/G]ATGGCAGGCATTGCT | 380752 |
rs48217289 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28861347 | GCTGTAGATGTAAAT[C/G]TATAGGAGCTAGCTG | 380752 |
rs48217845 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28826424 | TGCTGGGGTTATAGG[C/T]AGGAACTATTGTACC | 380752 |
rs48227462 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28862714 | TTGTCCACTTGTCCA[A/G]TTGGCCCAGGGAACT | 380752 |
rs48233283 | snp | A/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28802506 | CGCTAAACAGGCTTA[A/G]CAGGAGTTTGCAGCA | 380752 |
rs48246551 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28762385 | AACAATTTAGTTTTT[C/T]TTTTCTATTTATTTT | 380752 |
rs48248329 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801634 | AGACTGGCTTAAGGA[G/T]CAAGGTTCAGTAGGG | 380752 |
rs48255664 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28829961 | TCACAGGCAAGGGAA[A/G]CCAGTGTGTCCTTAA | 380752 |
rs48266691 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28787435 | ACATGTCCTGGACAC[A/G]GGCAGGCACAGAGTA | 380752 |
rs48277262 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28841643 | GTCCTTTCTGGTGTC[A/G]GTTCTGGGCCAGTGA | 380752 |
rs48301882 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808789 | GATATTATGTGAGCT[C/T]TGTTATTCTGGTTTC | 380752 |
rs48303966 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28850218 | TTTCATCTCCAGAAC[A/C]GCAGAGACAAGATAG | 380752 |
rs48304833 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28755224 | GTGTCACCCTGGACA[C/T]GTAGTTCTTCTATTT | 380752 |
rs48306456 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28811153 | ATACAGCTCCTCCCC[A/T]ATACACATAATTAAA | 380752 |
rs48312970 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28753788 | AGCATGTGATTGTCT[C/T]CATAGGACAGCATCG | 380752 |
rs48315401 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28786984 | CAGTATCTTTCGGTG[C/T]TTTCGCTGCAGTGAC | 380752 |
rs48322340 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28858342 | CCAGGACGTCCTGTG[C/T]CCCACCTGCCTGTGA | 380752 |
rs48327804 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tssc1 | GRCm38.p3 | 12:28822031 | TGACTATCCCGCCGG[A/G]CTGTCAGTCATACCT | 380752 |
rs48332625 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Tssc1 | GRCm38.p3 | 12:28755159 | GACATGCGTCCTTAG[A/C]CTGCTCTGCCTGTTG | 380752 |
rs48333409 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28762228 | GGTTCTTTTCTGTAT[C/G]TGATTTTCCCTGTTT | 380752 |
rs48338285 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28838204 | TGCCATGTCTCTGAG[C/G]GCTCCACGCCTGTTC | 380752 |
rs48340603 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28790042 | TAGGAGGCTGCAGTA[C/G]TCCTGCCATTGTACC | 380752 |
rs48340818 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28864095 | GTGTCTGTGAAGCCC[C/T]AGGGCCCTCCCTGTG | 380752 |
rs48347721 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28848455 | CCTAGGTTAAAGAGA[A/G]AACGTGGCTGATGGT | 380752 |
rs48353204 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801565 | CGGCCCAGGCAGCCT[C/T]CTTTCTCTGCTTGGT | 380752 |
rs48354037 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28852611 | AGTAGCTATCTGTGC[A/C]CTTGGATTTTGTAAA | 380752 |
rs48354903 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28767833 | CTAAACCTCCCACAT[G/T]CTTGGGTTATAGATG | 380752 |
rs48369747 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28768261 | TCCTAATCGTTTTCA[A/G]TGAGTTCCATGTACT | 380752 |
rs48374965 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28839044 | GGAAGCACCTCTGTG[A/G]GGAAGATCTGCAAGC | 380752 |
rs48376760 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28787109 | CCATGTAGCAAGGTT[A/G]ACTGAAGTTGGTTGG | 380752 |
rs48383431 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28846066 | CGTTCTCCTCTAGCA[A/G]TTTCAGTGCTTTAGG | 380752 |
rs48385003 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28771377 | AGATGCCTCTAGAAA[A/G]CCTTGGCTCTACAGG | 380752 |
rs48390651 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28855716 | CTTGCCTTAGGAGTC[C/T]GTACACTAGCCTGAT | 380752 |
rs48395701 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28783420 | GAGGGTGGCCAGCAT[A/C]CATCTCCTGCCTTAT | 380752 |
rs48399868 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771324 | TGATCTGTGGTGACA[G/T]TCACCATCATGGGGA | 380752 |
rs48401306 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28794884 | AGGAGATGAGCTATC[C/T]AGAGATTTCTTTTTA | 380752 |
rs48401695 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Tssc1 | Mm_Celera | 12:28857609 | TGGCTTCTCACCAAG[A/C]CCCTGACTCCTCACA | 380752 |
rs48418513 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28817255 | AGCGTCAGTCTGTGC[A/G]TCCCTCATACTTATT | 380752 |
rs48419226 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28765405 | AAGAGGACTGTAGCT[A/G]CGTGTGCTAACTGGC | 380752 |
rs48420465 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28831627 | AGAATAGACTTTGAG[C/T]GCTCTTGACCACTGA | 380752 |
rs48422106 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28754815 | TTTTTGGGTACTCTA[A/G]TCCTTGTATCATTTG | 380752 |
rs48437873 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751646 | GAGGGAGCAGCGCAG[A/G]ATAAGAGCGCCGCCC | 380752 |
rs48438565 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771865 | ATGCACTTAGACAGG[A/T]GTGCCCTTGTGTAAG | 380752 |
rs48442717 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28772639 | ACAGTGGTGACAAAT[A/G]ACAGGTCTTGATTGT | 380752 |
rs48449307 | snp | G/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28813710 | CTTAGACACAGCCCA[G/T]TCGAACCATCCTCTG | 380752 |
rs48451332 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28840071 | GATTGCTCCAGGTGA[C/T]TCCCAACCACCATGC | 380752 |
rs48451967 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784393 | ACAGCCACGTTGGAA[C/T]AGCTGTTGGCCAACC | 380752 |
rs48464171 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808272 | ACACACCTGTAACCC[C/T]GGTATGTGGGAGGCA | 380752 |
rs48467912 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tssc1 | GRCm38.p3 | 12:28848341 | GGTCACCTTCACAGC[A/G]TGTGGGTTCCTCAGG | 380752 |
rs48476676 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771417 | TGCCATGTCTGACTG[C/T]ATATAACAGCCTTCT | 380752 |
rs48487084 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28831499 | GAGAAGGCTTCCAGT[A/G]TTTTGCCTTCATATG | 380752 |
rs48492013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28848021 | TTTCTTCATGGTTGG[C/T]TCCTTAAGTCTTTCT | 380752 |
rs48496503 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28828196 | CAGGATCTGAGAATG[A/G]TAGGAAGCCCCTGCA | 380752 |
rs48509286 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28856452 | GCTTATGTTTTTAGT[A/G]TATTCTGTCACCAGC | 380752 |
rs48511405 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28785089 | CTGGCAGCTCCCTCT[A/C]CCCAAGTCTTCCTGT | 380752 |
rs48516985 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28807501 | ATTTCCAATAAATCA[C/T]CAAGGAAGCATTTTG | 380752 |
rs48523867 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28839542 | TTTTAAGAAAGAACA[C/G]AGATTACACAGTGAT | 380752 |
rs48527233 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28858728 | AGGGGGAAAGTGGAG[G/T]GGCCTTCTATCCCAG | 380752 |
rs48530136 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28763040 | CACAGGAGCAGACTG[A/G]CTTCCAGGCAGCTAG | 380752 |
rs48535829 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821322 | TGCAGTATCCTGTTT[C/T]ATCGAGCCATACAGC | 380752 |
rs48539255 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28763245 | GGTCTGCTTATGCTT[C/T]TGATGGAAAAACCAT | 380752 |
rs48544551 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28828545 | GTCAAAGAACAGGAG[G/T]AAACTGAGTTTGAGG | 380752 |
rs48547735 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28811940 | GTTTCTCAGCCTCTT[A/G]CTTGTAGATTTAAGA | 380752 |
rs48551943 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28850571 | TAAGGTCCCCATGTC[G/T]TCTTATATCCCTGTC | 380752 |
rs48559690 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28832756 | AGGTCATCGTTAGAT[C/T]AGCCACGACTGTAGA | 380752 |
rs48562113 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28846378 | CCACCTCAGCTCTCT[A/G]AGATGTTTGCCTCTT | 380752 |
rs48594358 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28785422 | TTGTTTCTAACACAG[C/T]TCTGGTCTGTTAGGC | 380752 |
rs48595865 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28832839 | CCTGACTATTGCTCA[A/G]TACCAAACTTGTCTC | 380752 |
rs48606022 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784537 | AATCCCCCTAGTGGC[C/T]ATCACGATGAGTACA | 380752 |
rs48613605 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28816836 | CAAGTCTGTAGGAAT[G/T]GGCAGAGTCCGTGGT | 380752 |
rs48621761 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28770754 | CCAGGCTCCAGAGTA[C/T]ATGCTGGTGGCTTAA | 380752 |
rs48624258 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28836484 | AGATGTGATGTCAGC[A/G]AGGGAGTGCAGGTAA | 380752 |
rs48624801 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28825825 | CATGCTTACATTTCT[A/G]TAGGACTTTCCTTTT | 380752 |
rs48634910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28859534 | TTCACCCCAAAATAA[A/G]CTAGCAGGCCCATTG | 380752 |
rs48635116 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28785296 | TTTCTATATTGCACC[G/T]TTCAGTTTGTCACCT | 380752 |
rs48635356 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784379 | ATTGTGCTATGGGTA[C/T]AGCCACGTTGGAACA | 380752 |
rs48637107 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28838747 | AAGAAAGACTGGTCA[C/T]TTCTCTCATCCCGTA | 380752 |
rs48641091 | snp | G/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28765869 | CCCAGGCATCAAGGT[G/T]GCTTTGACTCTTTCA | 380752 |
rs48645251 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28784010 | TACAGTGGGCTTGTG[C/T]AGACCCCAGGCTCTG | 380752 |
rs48653113 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28835504 | CCCCATGTCTTTTTC[A/G]AGTACATATTACAGG | 380752 |
rs48660184 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28807476 | TGGGGTCTGAAGGAG[A/G]AGGTACTGTATTTCC | 380752 |
rs48667017 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28782931 | GGGTTGGAGCTTTCA[C/T]AGTGTGAGACTGGGC | 380752 |
rs48667363 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28856419 | GAGTAGGCAGAATGA[A/G]CCGACCCTGCTTACT | 380752 |
rs48668991 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28782937 | GAGCTTTCACAGTGT[A/G]AGACTGGGCATGATA | 380752 |
rs48672074 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28843859 | CTGAGGGGCCAACTC[C/T]TCCCCTGAGCTAAGG | 380752 |
rs48680032 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845281 | TTGGCCCTGGGTGGG[C/T]ATCTAAGCCTCTAAC | 380752 |
rs48699160 | snp | C/T | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28835564 | CATCATTTACAACCT[C/T]CTCCCAGCAGAGACC | 380752 |
rs48701136 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28852985 | GACTTGGGCCGCCGT[A/G]TGCCTATGGCCTGGC | 380752 |
rs48703525 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28830476 | AGTGCCATCCTTGCA[C/T]ACTTTTCTCACATTT | 380752 |
rs48707090 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28838844 | TTAGCAAGCTCCTGT[A/G]ATGGGTGCCTTTTAG | 380752 |
rs48716367 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28767434 | ACAGAGTGCATCACT[G/T]TTCTGATGGGTGGCT | 380752 |
rs48720568 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Tssc1 | Mm_Celera | 12:28757448 | GTGCGCCAGCCTTCT[C/T]GTTACAATTCTGCTC | 380752 |
rs48729456 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28788046 | CCAATAATGTGATGT[C/G]TATTTTGTACTTTGG | 380752 |
rs48731184 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28853412 | ACAATTTTCAGGTTG[C/T]CTCTGTAAGAAGAGC | 380752 |
rs48736691 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28827303 | AGGATGGTATGATAA[A/G]TGAAGCAGGTGTATA | 380752 |
rs48746242 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28830017 | TGTCACTCTGCTGCC[C/T]GAGTACAGAGTCTGC | 380752 |
rs48746783 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28835440 | GAAACTCTGCCAGCT[A/G]TGCCCAGTGTTGCAG | 380752 |
rs48757752 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28755104 | TGGTTTAAGGCTGTC[C/T]AAATGTCCATCCAAG | 380752 |
rs48767786 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28824492 | GACCAGGCTGGCCTC[A/G]AGCTCAGAAATCTGC | 380752 |
rs48768381 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28845863 | GTTCAGATCTCAGCT[C/T]GACTGGATACCAGCC | 380752 |
rs48773720 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28833293 | CAAGTGCTGCAGACT[A/G]GGCAGCTTTTAATGG | 380752 |
rs48775354 | snp | A/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28851820 | CCAGGCCCTGTCTCT[A/G]TCCTTCAGGAAGGGA | 380752 |
rs48777721 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813240 | CAGCCGAGAGTCGTC[C/T]TTCCTAGCTCGGGCT | 380752 |
rs48780507 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28848179 | GGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 380752 |
rs48784577 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Tssc1 | Mm_Celera | 12:28783791 | CACCAAGAGCACATT[A/T]TCTCCCATTTCCTTC | 380752 |
rs48786304 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28848570 | AGTTTGACTTGGCCC[A/G]TTTTCCTAGAGCACG | 380752 |
rs48790127 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28857300 | AAAGTTGGCTGATAC[A/G]ACCAGTATGACCTGC | 380752 |
rs48792147 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28838790 | CTCAGGCCTCTGCTC[A/C]CTGAGAAGAGTGAAA | 380752 |
rs48794453 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28847484 | CAGTGTGAGGAGTCT[A/G]GGTAAAAGCTGTGGG | 380752 |
rs48828977 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28763882 | TGGCTAAGTCAGCTG[C/T]TTTCCTAGCCTTGGC | 380752 |
rs48834328 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28854885 | TTGGTTCAGTTTCTC[A/G]ACAGCATGAAGTCTC | 380752 |
rs48839580 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28851563 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 380752 |
rs48845661 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28783179 | CTGCCTGTCACTCTG[G/T]ACCCTTGTCTCAGCA | 380752 |
rs48847554 | snp | A/G | | | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28751067 | TTTCATAGCTTTGGG[A/G]TCGGTGGAAGCTAGT | 380752 |
rs48851243 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28813046 | AGTTGTCTTCTACCA[C/T]GTGGGTTTCAGGGAT | 380752 |
rs48854463 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tssc1 | Mm_Celera | 12:28764044 | GTAGAAGACTCAAGG[A/G]TATTCATATACATAG | 380752 |
rs48855177 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28770441 | CTGTTGCTTACCAGT[G/T]TTGAGGGACCAGCTT | 380752 |
rs48857552 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28811011 | ATCTAGTTGTTAAGA[A/G]CATGTACTGCTTGCT | 380752 |
rs48859535 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28847153 | GCTCTTGTGGCTTGT[A/G]AGGCAGGATGGCCAA | 380752 |
rs48862387 | snp | C/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28845273 | TTTTCCACTTGGCCC[C/G/T]GGGTGGGTATCTAAG | 380752 |
rs48875586 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Tssc1 | Mm_Celera | 12:28822502 | GCTGTGCTCCAAAGG[A/G]TGTGAGCCTCTGCTG | 380752 |
rs48884082 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B, nc-transcript-variant | Tssc1, Gm31209 | Mm_Celera | 12:28867881 | CGTCCCTTAGGCAAG[A/G]CTCCTGTGGACCATT | 380752 |
rs48884257 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28757157 | TCTGTAGCAAATGCC[C/T]GAGTTCTACTTTTCC | 380752 |
rs48886975 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28856224 | AACTCCATTCCCAGG[A/G]GATTCAATGCATTCT | 380752 |
rs48887173 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28803766 | GCTGGAGTAGCTTGC[A/C]TGTGGTCAGACAGCT | 380752 |
rs48897813 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Tssc1 | GRCm38.p3 | 12:28763119 | AAGGCCACACCTACC[A/C/G]TAACAAGACCACACC | 380752 |
rs48898749 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Tssc1 | Mm_Celera | 12:28813837 | CTCCTCACCCAGCAT[C/G]TCAGGACTCCTTCAT | 380752 |
rs48904116 | snp | G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821344 | CCATACAGCCAAGGG[G/T]ATGGTGGTTAAGCAG | 380752 |
rs48913188 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28857113 | CCCCATTCTGCCAAA[C/G]TAAGGAAAAACAAGG | 380752 |
rs48918005 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28830128 | GGTTGTCATGGGTAT[A/G]TGTGTCTCTAGAGGC | 380752 |
rs48927204 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Tssc1, Gm31209 | Mm_Celera | 12:28867338 | TGCCCAGTCTCTGTT[C/T]GGTTTCTGGTTTCTG | 380752 |
rs48934572 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771124 | TGTCTCTAGGAAGGG[G/T]GTAGTTTGACAGCAT | 380752 |
rs48939691 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28771821 | AGAACCATGGGAAGG[A/G]AGCTTCTAAGAAGAG | 380752 |
rs48941915 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28836466 | AAGGCATGATGGAGC[A/T]GCAGATGTGATGTCA | 380752 |
rs48952819 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28858608 | CACCAATAGTGGGTT[C/T]AGGATGTTGGAGGAG | 380752 |
rs48956469 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28841208 | ACGTTTGGCTGAGGG[C/T]CTAAGAGTCTGTGTC | 380752 |
rs48960302 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28761055 | CCATTTCTCACTGCT[C/T]CTATTACTTTGTGTA | 380752 |
rs48961941 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | GRCm38.p3 | 12:28808480 | TATGTCCTTACGTTT[C/T]AGGGTTAATTTTCGA | 380752 |
rs48962352 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28753073 | AATGGAAGTTACTGG[A/G]AGATGTTCCAATTTA | 380752 |
rs48962860 | snp | C/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28839290 | CAAAGGACCTGGGTT[C/G]GATTCCTAGTGCTCA | 380752 |
rs48973347 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28801752 | TGAGTGGATAGGTGA[A/G]TGGAGATGAGAGGAG | 380752 |
rs48973770 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28848178 | GGGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 380752 |
rs48978871 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Tssc1 | Mm_Celera | 12:28850588 | CTTATATCCCTGTCG[A/C]TACTTGTACCCAGTG | 380752 |
rs48984459 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28766316 | AACCTATACAGTTAT[C/T]CTCAGATCTCACTGG | 380752 |
rs48992523 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28765100 | CAGGCTGTCTTTGAA[A/C]TCACAAAAAGCTATC | 380752 |
rs48999465 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tssc1 | GRCm38.p3 | 12:28825200 | TCTACTCCCCATAAA[G/T]TTTGCACAGTGCTGA | 380752 |
rs49007571 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809981 | TCTGAGATCACTGGG[C/T]TGCAGTTCTGTTCTG | 380752 |
rs49015552 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28787166 | TCCCACACCTACCTC[A/G]GATACAGAAGGGACT | 380752 |
rs49016963 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28861050 | GCTGAAGATGTAAAT[C/G]TATAGGAGCTAGCTG | 380752 |
rs49022671 | snp | C/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28830392 | GTGTGGTTGTTGGCT[C/G]TCCTGAGTGCTCTTG | 380752 |
rs49030360 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28820419 | TTATTTATTGTGTGT[C/T]TGAGAGTGTGAGTGG | 380752 |
rs49031477 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28862651 | CAAGTTTGGTGGCAG[A/G]TACCTTTACCCACTG | 380752 |
rs49036966 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28771705 | GAGGCCAGCAGGCTT[A/T]GGGAACCACTTTTTA | 380752 |
rs49038483 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28850768 | TCTACCCAGAGGGAT[A/G]ATGGGGCCTCCTAAC | 380752 |
rs49045676 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28861309 | TATAGGAGCTAGCTG[A/T]AGATGTAAACGTATA | 380752 |
rs49055403 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Tssc1 | Mm_Celera | 12:28779321 | GGATGGGGTTTGTTC[A/G]TCATGGCTTTCATGG | 380752 |
rs49065244 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783113 | CCAAGGCAACCGAGA[C/T]AAGCCCCCAGACTGA | 380752 |
rs49071340 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28765648 | GGCTATGGCCCCCAC[C/G]TTGGGAATGAGTCCT | 380752 |
rs49077417 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28815488 | CTTGGCCCCCTGCTG[A/G]TCTGTGTGTTCTGGT | 380752 |
rs49081952 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28801664 | GTCAGGCAGGTGATT[C/T]ATAGAAATAACCATG | 380752 |
rs49105385 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28829004 | TATAGTGTTTACACT[C/T]GCTTGTCACTTTTAG | 380752 |
rs49106026 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28825018 | CATGCAGGTACTTTG[C/T]TTTGCTTTGCTGAGA | 380752 |
rs49107772 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28784131 | AGGCTCATATTGTAC[A/G]GATTATTGCTGAAAG | 380752 |
rs49109950 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tssc1 | Mm_Celera | 12:28841064 | GGGCTGCATCTGGTA[C/T]GTAGGAGTTCCAGGT | 380752 |
rs49125070 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB, intron-variant | Trappc12, Tssc1 | Mm_Celera | 12:28752384 | GCCTTTTTCCTTATG[A/G]ACTTTTTATTTCAAT | 380752 |
rs49125284 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tssc1 | Mm_Celera | 12:28811665 | TTCCACTCGGAGGTT[C/T]AGCCCTTGGTGATGG | 380752 |
rs49130253 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28788127 | TAAGATTTTCTGAGT[A/T]CTAGAATCTATTACA | 380752 |
rs49136875 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28750786 | TGGTTGGTTGAGAAT[C/T]GTCCTCAAGTCAAGA | 380752 |
rs49145253 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28761333 | AAAGGTTTGTAAGGC[C/T]ATGTTAGTCATGGTA | 380752 |
rs49162261 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28765110 | TTGAAATCACAAAAA[A/G]CTATCTGTTCCTACC | 380752 |
rs49162341 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28811380 | TCACCATAACAGCCA[A/G]TAGTTCTGTAAAATT | 380752 |
rs49164585 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28761571 | TTTGTATATAAATAA[C/T]AGTAACTACAGTGGT | 380752 |
rs49176384 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28801658 | AGTAGGGTCAGGCAG[A/G]TGATTTATAGAAATA | 380752 |
rs49196961 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28822832 | GTGGCTGCACCTCCT[G/T]CCCTTGAGGCCTTCT | 380752 |
rs49199564 | snp | C/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28762315 | ATGCCCGTCACCCTG[C/G/T]CACTAAAGACTTGTC | 380752 |
rs49200472 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28763080 | TCTCAAAGCCCACCC[A/G]CACAGTGACACATTT | 380752 |
rs49201031 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28811791 | AGAGTGGCCCCCATA[A/C]TTTCATATGTTTGAA | 380752 |
rs49217206 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28753767 | CAGAAGCCTCTTGTT[C/T]GTGTCAGCATGTGAT | 380752 |
rs49233873 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28770546 | GGTTTTGGTTCTTGA[A/T]GTAGACTAACCCCTG | 380752 |
rs49240524 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Tssc1 | Mm_Celera | 12:28775597 | TGAGGACCTGTCACT[A/C]TGGAGACCCTTGGGG | 380752 |
rs49257004 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28788922 | GGACCACTCTTTTAC[A/G]GACTCATTGTATCAC | 380752 |
rs49270903 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28784385 | CTATGGGTACAGCCA[C/T]GTTGGAACAGCTGTT | 380752 |
rs49272386 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28803234 | AGGAAGTGTGGCACT[A/G]TGGGTGTGTGTTTTT | 380752 |
rs49278168 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28760803 | ATGAGCTCCAGAGAT[C/T]TGTCTGTCTCCACCT | 380752 |
rs49281204 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Tssc1 | GRCm38.p3 | 12:28811456 | AGTATTTCCTTTTCC[A/T]TGTTTTCCATCTGAT | 380752 |
rs49289508 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28829516 | TGGGTCCACAACAAG[C/T]GGTCAGCTCACCCCA | 380752 |
rs49291008 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tssc1 | Mm_Celera | 12:28838064 | TGGGCCATTTTGAAT[C/T]CCTCTGAACTCCTGG | 380752 |
rs49295483 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28826934 | GGTGTTTCTGCCTCA[A/G]CCTCCCTGATGGAGG | 380752 |
rs49296427 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28782844 | TTGACTGGCAGTTTG[G/T]TGAGCACCTCAGGTT | 380752 |
rs49302782 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28850379 | ATGCACAGTGGTGGG[A/G]CTCCTGCAGGGTCTC | 380752 |
rs49313269 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28787156 | GGCACAAGTATCCCA[C/T]ACCTACCTCAGATAC | 380752 |
rs49323267 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28753985 | TTTTCTGTGTATCAG[G/T]GTTTCGCTTGCTTTT | 380752 |
rs49337468 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28820136 | CAAGTGCTCTTATCT[G/T]CGGAGCTATCTCTCC | 380752 |
rs49343954 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28843946 | ACTTAGTTCTCTACT[C/G]TTCTTAGCCATTTCC | 380752 |
rs49364092 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28841086 | GTTCCAGGTGAAGAA[A/G]CGACATTGCCAGTAG | 380752 |
rs49366529 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tssc1 | Mm_Celera | 12:28852518 | GCACTTATATGTGAA[A/G]CTATCTTCTTCTAAA | 380752 |
rs49367848 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tssc1 | Mm_Celera | 12:28784290 | GGTCATAGGGCCTGT[A/G]TCCCTTGCTGTGGAC | 380752 |
rs49375151 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28835439 | AGAAACTCTGCCAGC[C/T]GTGCCCAGTGTTGCA | 380752 |
rs49376678 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28848768 | GCTGGGCGCTGGGCT[A/G]CAGTCGGCCAGCACG | 380752 |
rs49387844 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tssc1 | Mm_Celera | 12:28813582 | GATAACTAAAATAAA[C/T]TGTTGAGCACACTAA | 380752 |
rs49393966 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28858737 | GTGGAGTGGCCTTCT[A/C]TCCCAGGCTTGGAAC | 380752 |
rs49399117 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28750650 | TTTTCCTAGGATTTT[A/G]TCTTTGTGCTAGTTG | 380752 |
rs49403219 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28841136 | AAGCTGGCTATGTGT[A/G]AGCTTTGACTTCAGC | 380752 |
rs49416041 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tssc1 | Mm_Celera | 12:28786549 | AGTATCGTGTGGCTT[C/T]GAAGTTATGTTGAAG | 380752 |
rs49418847 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28764250 | GACTCACTTATGGTA[A/T]CATAACCAGGAAGTG | 380752 |
rs49431867 | snp | A/G | 0.32 | 0.24 | intron-variant | Tssc1 | Mm_Celera | 12:28762142 | AGCTTGGAAGCAGCT[A/G]TTGGCTCTGCTCTTC | 380752 |
rs49435259 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28803888 | GGAACAACTTTCCTC[A/G]TATTTACTTAGAAAA | 380752 |
rs49441718 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28753298 | AACTTCAGAAGCACT[A/G]GGAGGACTCGGGGAA | 380752 |
rs49442425 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28754132 | TCTGGAAGTGCAACA[A/G]GTATTCTTCACCCCT | 380752 |
rs49447582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28865713 | CTCTGCGCTGGTTTG[C/T]GTCCACACACACTCC | 380752 |
rs49455941 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28857931 | CTCTCTTCCCTCATG[C/T]TGTCCTCTTGTTTGG | 380752 |
rs49468408 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tssc1 | Mm_Celera | 12:28813312 | ACTGTCTCTGTGTGC[C/T]TGCAGCTTAATTTAC | 380752 |
rs49477679 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28803122 | GTTCCCTTCTTTGGT[A/G]GTTTGAATATGCTTG | 380752 |
rs49483540 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Tssc1 | Mm_Celera | 12:28813628 | AATCCTTTGCATGTG[C/T]CCCTAGCCTTCAGCT | 380752 |
rs49485548 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866357 | GGAAGTTGCCTGTGT[C/G]TGTGGAGCAGGTTGG | 380752 |
rs49492369 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28852972 | TTGAAGGCCAGAGGA[C/T]TTGGGCCGCCGTGTG | 380752 |
rs49506066 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tssc1 | Mm_Celera | 12:28852102 | CGTGCAGACCAGCTG[A/G]CTTACACTTAGGACA | 380752 |
rs49508285 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28808248 | TAAACTAAGGTTAAG[C/T]TGAGAAACACACACC | 380752 |
rs49513140 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28830003 | GAACATTTGTGTGCT[A/G]TCACTCTGCTGCCTG | 380752 |
rs49538648 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28816483 | CCAACAGATTCTGCC[C/T]TGGGGCTGGGAAAGA | 380752 |
rs49539627 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tssc1 | Mm_Celera | 12:28855902 | TGAACGTCCTGATAT[C/G]TCAGCTTAGGACTTC | 380752 |
rs49553321 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28855771 | AGCTGACCGCTTGGC[C/T]GTGAGTGAGTTCCTC | 380752 |
rs49556713 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28772779 | CTTTTTGTAGTCTGT[A/C]TTTCTCAAAATATGT | 380752 |
rs49556838 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28804382 | AGGGCATGGCATCCC[C/T]GTTAGACCAGGCCAG | 380752 |
rs49561616 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | GRCm38.p3 | 12:28782845 | TGACTGGCAGTTTGG[C/T]GAGCACCTCAGGTTG | 380752 |
rs49576059 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28761612 | AGTCAGAAATGGTCA[C/G]AATATGAAAATGTAC | 380752 |
rs49579053 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28841454 | CTCCCCAGGGCTCTC[C/G]TGGGCAGGGCTCTTC | 380752 |
rs49595467 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28761818 | AAATTTTCTAAAGTG[A/T]GTGGGTAAGGGATAT | 380752 |
rs49597597 | snp | A/T | 0.297521 | 0.245442 | upstream-variant-2KB | Trappc12, Tssc1 | Mm_Celera | 12:28750520 | GGAAGCCGGGCGCAT[A/T]TCCGGCTCAAGAGCT | 380752 |
rs49606601 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28810744 | TAAAATTAGTTAAAA[G/T]GTCAACAGATCACAC | 380752 |
rs49608773 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28768443 | TCCTTCCCTGATGCC[G/T]GATCGAGCAGTAATG | 380752 |
rs49611283 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28785072 | ATTCTGCCTCACTGC[A/G]TCTGGCAGCTCCCTC | 380752 |
rs49613980 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | GRCm38.p3 | 12:28753677 | TCACAGGCACAGTTC[C/T]CCAGATTTTGGGTAA | 380752 |
rs49615473 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28848668 | ACCCACAGGGGTGTT[C/T]ACAGTAAAAGGTCAG | 380752 |
rs49617616 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28855684 | CAGGATGTTTCTAAG[C/G]TTTACCTTCTCCCTT | 380752 |
rs49624674 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28857873 | CTCCCAAATGATGTT[C/G]CTAATCCCTTCGCAA | 380752 |
rs49627554 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28774499 | TTAGGGCAGCTGTAG[A/C]GTAGGGGCCAGATCC | 380752 |
rs49630764 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28813325 | GCTTGCAGCTTAATT[G/T]ACTGCTGTGTTTGAG | 380752 |
rs49631407 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Trappc12, Tssc1 | Mm_Celera | 12:28751859 | GGGAGCCGGTCTGGG[G/T]CTCGTAGTCCATTTT | 380752 |
rs49635825 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28774702 | CAGACAGATGTGACC[A/G]GCAGCAATGGTGTGA | 380752 |
rs49645297 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28856084 | GGCTTACCTGCTTCC[A/G]AGCTCAGTGCGGTTA | 380752 |
rs49650192 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Tssc1 | GRCm38.p3 | 12:28852059 | ACTTGGGGATCATGA[A/C]AGCATCACCTGTACA | 380752 |
rs49651757 | snp | C/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28777375 | TCCTCCATTGGGGGC[C/T]GTGTGATCCATCCGA | 380752 |
rs49657703 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tssc1 | Mm_Celera | 12:28809972 | ATTGTGGGGTCTGAG[A/G]TCACTGGGCTGCAGT | 380752 |
rs49658984 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28783145 | GCTAAGGTTGCCTAG[C/G]CTTTCTCCTCAGGCT | 380752 |
rs49661285 | snp | G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28804025 | CTGCAAATCGTTAGA[G/T]TTTCAAAGAATGAAG | 380752 |
rs49668924 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28802947 | TGAAAGTTTAGCTAT[A/G]CGCTAAGGCTGCAGC | 380752 |
rs49670318 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Trappc12, Tssc1 | Mm_Celera | 12:28752168 | GGCTGGCATAGACAG[C/T]AGAGGGTGAGCACTC | 380752 |
rs49680035 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28838115 | TCTGTAGAGGCTGGC[C/T]GTGTGGCCTGATAGC | 380752 |
rs49690693 | snp | A/G/T | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28849581 | TTAGAGATGCAGTCC[A/G/T]GCCTGAAGTTCACCA | 380752 |
rs49697009 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28829262 | AGTGTCCTCAGTTCC[C/T]TCCATCTCTCTGTCC | 380752 |
rs49706690 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28783736 | AGACCCTAGGGTTTT[A/G]CATGCTAGCAAGGTC | 380752 |
rs49713022 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Tssc1 | Mm_Celera | 12:28753805 | ATAGGACAGCATCGT[C/T]ACACTGGGGAGCTCC | 380752 |
rs49722824 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28845145 | TTCTGTGTTCTTCTT[C/G]TGTTGGGAACAAAAA | 380752 |
rs49742345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28856821 | CTCTCTCCTATGCAG[C/T]GCCACAGTAGCTTCC | 380752 |
rs49747502 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28839407 | TATTTGCAGGCAAAA[A/C]ACCCATGCACAGAAA | 380752 |
rs49753658 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28822723 | CTGTAGAGTAGGGCC[A/G]CCCAGCTCTGTGTCT | 380752 |
rs49764454 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28860266 | GACAAGAAGCTCAAA[A/G]ACTGGCTCACACACC | 380752 |
rs49764955 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28864064 | AGTTTGTGAATTTCT[C/T]ACCGGAAGTGGTACT | 380752 |
rs49780597 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28845294 | GGTATCTAAGCCTCT[A/G]ACCCCCCACTCGGCT | 380752 |
rs49791453 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28775577 | AAGAATCAAGAGCTT[A/G]CTGCTGAGGACCTGT | 380752 |
rs49796909 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28763202 | AATTGCACCACAACC[C/G]TCAGTTGGGATGCAG | 380752 |
rs49801103 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Tssc1 | Mm_Celera | 12:28823655 | CCTCTGGTCCATCAC[C/T]GTGCTCAGGCCTTTC | 380752 |
rs49810105 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28814962 | CACTCACCATGTGAC[A/G]TGGTCCTCCCTGTGT | 380752 |
rs49827110 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28802761 | GGCGCTCTTTCATCA[C/T]GTGGGTCCTAGATAC | 380752 |
rs49837126 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28789062 | TTTTGAAATATCTGG[C/T]ATCACTTTTGAAATG | 380752 |
rs49849477 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28772798 | CTCAAAATATGTTTT[C/T]GGTAGACTTTTAAGC | 380752 |
rs49851606 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tssc1 | Mm_Celera | 12:28823699 | GCAGCAGTCTACACA[C/T]GGCCACTAGAGGAAG | 380752 |
rs49858169 | snp | A/G | 0.5 | 0 | intron-variant | Tssc1 | Mm_Celera | 12:28832763 | CGTTAGATCAGCCAC[A/G]ACTGTAGAAGAGTCA | 380752 |
rs49858197 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | GRCm38.p3 | 12:28841843 | AGCGCCATGACTATT[C/T]CTAGGCTCGTTTGTA | 380752 |
rs49865815 | snp | C/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28816812 | ACAGACTTATGTGTA[C/G]TCTGTGCTCAAGTCT | 380752 |
rs49878942 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Tssc1 | Mm_Celera | 12:28775565 | TGAAAAAGAGAGAAG[A/T]ATCAAGAGCTTACTG | 380752 |
rs49879499 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28803551 | GCTGTGGTCAGTTTG[C/T]TTGCACAGGCTTGGC | 380752 |
rs49883019 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28852866 | CAGGAAGACAGCAAT[A/G]AAAGATTGGACCAAA | 380752 |
rs49887030 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28771659 | GCACAGCTGGTAGGG[A/C]GGACAGGCCTGGAAA | 380752 |
rs49891509 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28839321 | CGCGGCAGCTTGCAA[C/T]TGTCTGTAACTCCAG | 380752 |
rs49891718 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28825865 | TCTCTCTTCCCCCAC[A/G]TTTTGATCCCCTTGT | 380752 |
rs49892309 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28759473 | CTCAGACTTAAACCT[C/G]CAGGGACAAAGTAGC | 380752 |
rs49894875 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28766061 | AAAAGCATTGAGATG[G/T]CATCGTTAGCTTTCT | 380752 |
rs49899231 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tssc1 | Mm_Celera | 12:28759655 | CCACCACTGCCCTGC[A/G]ATCCTGGGCTTGTCA | 380752 |
rs49904556 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28848103 | AAGAAGAAAGAAGAA[C/T]ACTCTGAAGCCGGGC | 380752 |
rs49922102 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tssc1 | Mm_Celera | 12:28848513 | ACACTTAGAATACTA[A/T]GTGACATTTCAGTGC | 380752 |
rs49924602 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tssc1 | Mm_Celera | 12:28866738 | AGAATACTCCAGACA[A/G]ATGATCACCCCAGGA | 380752 |
rs49925648 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28783773 | TTTCTCATCTCCTCA[C/T]CCCACCAAGAGCACA | 380752 |
rs49926925 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28777402 | CCGATAGCCGACTGT[A/G]AGCATCCACTTCTGT | 380752 |
rs49934821 | snp | A/G | | | intron-variant | Tssc1 | Mm_Celera | 12:28784084 | TGGCCCCTTCCTTCC[A/G]TCACCTCCCTCCATA | 380752 |
rs49941340 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Tssc1 | Mm_Celera | 12:28793578 | CAGTCTCTTATCCAT[A/C]CCTGAGAGACAGCGC | 380752 |
rs49947688 | snp | A/C | | | intron-variant | Tssc1 | Mm_Celera | 12:28795107 | CCAGAGAGAAAGCAG[A/C]ACATATCAAGAAAAG | 380752 |
rs49949630 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Tssc1 | Mm_Celera | 12:28838632 | AGCAACTCCTAACTT[G/T]GAGATTTTCACATTT | 380752 |
rs49956462 | snp | G/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28788076 | GTTTTTTTGTGGGGG[G/T]GTGTGGCAAAATATT | 380752 |
rs49957546 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tssc1 | Mm_Celera | 12:28837067 | CAGGAAAGACAGACA[A/G]TTGTAAGGCAAGAAC | 380752 |
rs49959307 | snp | A/G | | | intron-variant | Tssc1 | GRCm38.p3 | 12:28821605 | GTCATAAATACATGC[A/G]GTTTCTAATAACTGA | 380752 |
rs49961116 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28828604 | TGAGTTCCCTGCTAC[C/T]CAGGTTGGGCGGACT | 380752 |
rs49961658 | snp | C/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28851664 | TCATGGCTATGGGTT[C/T]GTTGGCCCTCTGACT | 380752 |
rs49964424 | snp | C/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Trappc12, Tssc1 | Mm_Celera | 12:28752148 | TGTGGCCAAGTGAGG[C/G]CCAGGGCTGGCATAG | 380752 |
rs49968808 | snp | C/T | 0.5 | 0 | intron-variant | Tssc1 | GRCm38.p3 | 12:28840084 | GATTCCCAACCACCA[C/T]GCTCAACAGAACAAG | 380752 |
rs49973558 | snp | A/T | | | intron-variant | Tssc1 | Mm_Celera | 12:28781035 | TTTCCATACGTGGTC[A/T]CCTGGGACTTGGGGC | 380752 |