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 |