SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3152487 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Tsg101 | Mm_Celera | 7:46895066 | TAATTCCAACGGAAC[C/T]GTGGATGTAGCTCTC | 22088 |
rs3152488 | snp | C/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46912554 | CTGAACTGTTAAAAC[C/G]TAAGCACAGAATGTT | 22088 |
rs3152489 | snp | C/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46912869 | agttaagagcactga[C/G]tgctcttgcagaggt | 22088 |
rs3152490 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46913043 | TTAAAAAAATAATTC[C/T]CTCTATGGGCTGGAT | 22088 |
rs3152491 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Tsg101 | GRCm38.p3 | 7:46913454 | GACGGTTAGATCTCT[A/G]TATTTGTACTGAAAA | 22088 |
rs3152492 | snp | A/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46913914 | AACTCTAACAGCCCA[A/T]AACTTCAGTACTCTC | 22088 |
rs3152493 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46914199 | GCCCTGGCTGTCCTG[G/T]AACTCACTCTGTAGA | 22088 |
rs3152494 | snp | A/C | | | intron-variant | Tsg101 | Mm_Celera | 7:46914808 | CACTGCAAACCTGTT[A/C]ATCTAGCCTATCAAA | 22088 |
rs3152495 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Tsg101 | Mm_Celera | 7:46895390 | GATCCCTGCTAGCTT[A/T]CGAACTAGGCATGGT | 22088 |
rs3152556 | snp | C/T | 0.5 | 0 | intron-variant | Tsg101 | GRCm38.p3 | 7:46892335 | AGCCGGGCGTGGTGG[C/T]ACACGCCTTTAATCC | 22088 |
rs3152557 | snp | C/T | | | intron-variant | Tsg101 | GRCm38.p3 | 7:46892221 | tacacagagaaaccc[C/T]gtctcgaaagaaaaa | 22088 |
rs3152558 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Tsg101 | GRCm38.p3 | 7:46890811 | TTTGTTTTTAGTCCC[A/G]TAATGGTCTTAGAGT | 22088 |
rs3152559 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tsg101 | GRCm38.p3 | 7:46890293 | TGTAGGTAGGTGGGG[A/G]CTGGAGAGATGGCTC | 22088 |
rs3152560 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tsg101 | GRCm38.p3 | 7:46890275 | GGAGAGATGGCTCAG[C/T]GGGTAAGAGCACTGA | 22088 |
rs3152561 | snp | C/T | | | intron-variant | Tsg101 | GRCm38.p3 | 7:46889741 | TCATGACTGGATCAA[C/T]GCGTTTCTGAGATGT | 22088 |
rs3152562 | snp | C/T | 0.42 | 0.183303 | utr-variant-3-prime, nc-transcript-variant | Tsg101 | Mm_Celera | 7:46889613 | GTGACCTCTACTGAC[C/T]TGTGCTGTCAGCTGG | 22088 |
rs3152563 | snp | A/T | 0.375 | 0.216506 | downstream-variant-500B | Tsg101 | Mm_Celera | 7:46889026 | ATAGATACATACTTT[A/T]AAAAAAAAAAAAAAC | 22088 |
rs3152564 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Tsg101 | GRCm38.p3 | 7:46888945 | GGGTGATTTAAAGGA[A/G]GTACTCTTTGCAAAC | 22088 |
rs3152643 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46896520 | AACTATGGGCTTTTC[C/T]ACCAGTGCCCCCAAT | 22088 |
rs3152644 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46896738 | TCTATCTCAGAGTTC[C/T]TCTCTCCCTATCAGA | 22088 |
rs3152645 | snp | A/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46897270 | tgtgctgagaatgaa[A/T]cctgggtcctctgga | 22088 |
rs3152646 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tsg101 | Mm_Celera | 7:46897827 | TGTGCCAGCTTTATG[C/T]AAGCAATAGGCTCTA | 22088 |
rs3152647 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Tsg101 | Mm_Celera | 7:46898386 | aaacttgtcttctga[C/G]cacactagtgctgag | 22088 |
rs3152648 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46898438 | GTAACAAATGTTTAA[A/G]TATTCACAAATGAGA | 22088 |
rs3152649 | snp | A/C | | | intron-variant | Tsg101 | Mm_Celera | 7:46898440 | AACAAATGTTTAAAT[A/C]TTCACAAATGAGATC | 22088 |
rs3152650 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46899042 | TTACAGATTAAAGAC[C/T]CCCAGCattttttat | 22088 |
rs3152651 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46899053 | AGACTCCCAGCATTT[C/T]TTATTCAAATAATTT | 22088 |
rs3152652 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46899176 | ggttatacaatgaga[C/T]ctggtctcaaaaTTA | 22088 |
rs3152653 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46899354 | CCGATCTCATGACAT[C/T]GGAAAACATAAAAGA | 22088 |
rs3152654 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46899503 | TGACAATACAAAGGA[A/G]ATAACCAACCCAACA | 22088 |
rs3152655 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Tsg101 | Mm_Celera | 7:46899574 | agaaacaacgaggag[C/G]aggatcaacaagacc | 22088 |
rs3152656 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46900008 | CATTTAAAGCTCTAT[C/T]GCTAGAGTGAGGAAG | 22088 |
rs3152657 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46900070 | CATAAgagaaggagc[C/T]tgtggagactgagca | 22088 |
rs3152658 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tsg101 | Mm_Celera | 7:46900084 | cttgtggagactgag[C/T]acaagcacctgagct | 22088 |
rs3152659 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46900642 | TGTGACACCATCTTA[C/T]TGACCCTTTCATGCT | 22088 |
rs3152660 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Tsg101 | Mm_Celera | 7:46900777 | AGGCCCTAGTGACTC[A/C]AAACATGTGAGATCC | 22088 |
rs3152661 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46893877 | AAACAAAAAAGCCTC[C/T]CCCCCAAAACAAAAC | 22088 |
rs3152662 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tsg101 | Mm_Celera | 7:46902160 | CTCTGATTATATGAG[A/G]TTACTTTCAGAGAGG | 22088 |
rs3152663 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tsg101 | Mm_Celera | 7:46903625 | TGAAAGTCATATGCA[C/T]AGTCCTGAATATAAA | 22088 |
rs3152664 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46894206 | TTTATACTTGTCTTT[A/G]AAAGACCCCAGTCTA | 22088 |
rs3152665 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tsg101 | Mm_Celera | 7:46903651 | ATAAAGGCTATAGAG[C/T]AATATGAACCACTAT | 22088 |
rs3152666 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46904389 | aggagaagagagaag[A/G]gaagagaagagaaga | 22088 |
rs3152667 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46905376 | aaTGAGGTTTGGATA[C/T]GATGTTGGCtttaat | 22088 |
rs3152668 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46905615 | ATGTCTCACTATGCC[A/G]CCTAGACAGACCCTG | 22088 |
rs3152669 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Tsg101 | Mm_Celera | 7:46905785 | GTTCTGAGCAATGAT[G/T]TCTCAACTATTAAAT | 22088 |
rs3152670 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Tsg101 | Mm_Celera | 7:46905886 | GTTCACAGTCGTACC[C/T]GATGATGATGATGGC | 22088 |
rs3152671 | snp | A/G/T | 0.345679 | 0.230967 | intron-variant | Tsg101 | GRCm38.p3 | 7:46905990 | AGCTAGCTCTTCAGT[A/G/T]CTTGATGCGACGGTG | 22088 |
rs3152672 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tsg101 | Mm_Celera | 7:46906318 | ACTCAAGAATCAAGA[C/T]AGTCTTCATGAGAAA | 22088 |
rs3152673 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Tsg101 | Mm_Celera | 7:46906816 | TAGCTCGATTTGGCA[C/T]CTTCTCTTCCACTCT | 22088 |
rs3152674 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46907343 | gggtgtgtgctgagg[C/T]cagaaataagtatgg | 22088 |
rs3152675 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Tsg101 | Mm_Celera | 7:46907548 | AATCTTCTTTACCTA[A/T]ACATAGCTCTCTCTT | 22088 |
rs3152676 | snp | G/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46907639 | AGTAACAGGAGCTAG[G/T]GAACAATAAAAAGGA | 22088 |
rs3152677 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tsg101 | Mm_Celera | 7:46908130 | GAGGCTCAGCAGTTA[A/G]GAGCACAGGCTACTT | 22088 |
rs3152678 | snp | A/C | | | intron-variant | Tsg101 | Mm_Celera | 7:46894660 | CAGAATAATGGAACA[A/C]AGTGGAGAAGCCAGA | 22088 |
rs3152679 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tsg101 | Mm_Celera | 7:46908228 | TGATGCCATCTTCTG[A/G]CTTCCACAGACACCA | 22088 |
rs3152680 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tsg101 | GRCm38.p3 | 7:46894716 | GATTTTTACTAAAGA[C/T]GAAAGTCATGAAAAC | 22088 |
rs3152681 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46909086 | AAGAGAGAAGAAGAA[A/G]CCTCAATTACTCTAC | 22088 |
rs3152682 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Tsg101 | Mm_Celera | 7:46909179 | CACTAGGGCTATTTT[A/T]AATTCAAGATGCTTC | 22088 |
rs3152683 | snp | A/C | 0.5 | 0 | intron-variant | Tsg101 | Mm_Celera | 7:46894782 | cctatctcttatctg[A/C]aaaaaatctaataaa | 22088 |
rs3152684 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tsg101 | Mm_Celera | 7:46910207 | AACTGACTGCTTCAG[A/G]GACTAGTCATCCAAA | 22088 |
rs3152685 | snp | C/G | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46911021 | GCATGGTTTTAAGCT[C/G]ATTTAAAAATCACCC | 22088 |
rs3152686 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46911729 | atttgtttttacttt[A/G]tgtgttcatgtgcgc | 22088 |
rs3152851 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46913138 | GAAGAACAAATATCC[C/T]CAGCCTAACTCCGTG | 22088 |
rs3152852 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46913984 | ACATGGACATACATG[C/T]AGGCATTAAGAAAAA | 22088 |
rs3152853 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46914129 | TCAAACTCTATGCTG[C/T]CTGCCTGCCTGCCTG | 22088 |
rs3152854 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tsg101 | Mm_Celera | 7:46914599 | ACCCACAGGCCTATG[C/T]TCAATTCCTTTAGTA | 22088 |
rs3152855 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46915091 | AGACAGTGAGATGTG[A/G]TCAGATTTGGATATG | 22088 |
rs3152856 | snp | A/C | | | intron-variant | Tsg101 | Mm_Celera | 7:46915453 | gacctccacatgctc[A/C]ctgctgcatgtgcAA | 22088 |
rs3152857 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tsg101 | Mm_Celera | 7:46915622 | TCTCTTCTAGAATCA[A/G]TTATTTTTGAGCCAC | 22088 |
rs3152858 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46915841 | GGAGAGAACTGACTT[C/T]AGTGACTTCTGAACT | 22088 |
rs3152859 | snp | A/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46915846 | GAACTGACTTTAGTG[A/T]CTTCTGAACTTGAAA | 22088 |
rs3152860 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46917304 | CAACTCGGCTGGGTG[C/T]TATGGATCATGCCTT | 22088 |
rs3152861 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46917685 | tgtagccttggccag[C/T]ctggacctcaatatg | 22088 |
rs3152862 | snp | C/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46917894 | AAGCTCAATGTCAAA[C/G]AGCACTACTTCCTGT | 22088 |
rs3152863 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46919496 | ATGCAAACAATGGAA[C/T]GCAACTGCAGAGTTC | 22088 |
rs3152864 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46919602 | CCGAGCTCCGGTGGG[A/G]TGTGCCGGGTTGGGC | 22088 |
rs3152865 | snp | A/C | | | intron-variant | Tsg101 | Mm_Celera | 7:46919659 | CTGAGCAGGGCCGGG[A/C]TCCGGCCGGCGGGGA | 22088 |
rs3152866 | snp | A/G | | | upstream-variant-2KB | Tsg101 | Mm_Celera | 7:46920059 | AGGTCCGGTCCACGG[A/G]TGCCCGTGGTGCGGT | 22088 |
rs3152867 | snp | A/T | | | upstream-variant-2KB | Tsg101 | Mm_Celera | 7:46920206 | AGACACTTTTAGGTG[A/T]CTGCGCCCGAGGCAC | 22088 |
rs3152868 | snp | C/T | | | upstream-variant-2KB | Tsg101 | Mm_Celera | 7:46920312 | AAGGAGATTTTTTTT[C/T]CCCCGTTAGGAAGCT | 22088 |
rs3154432 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46913239 | TACTCTCCTGTTTCC[C/T]GACAGCTGTTAGGTG | 22088 |
rs3154433 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46895158 | atgggttagggtcct[C/T]ggctgaaTAACGAgc | 22088 |
rs3154434 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46913610 | CTCACAGAGATCCAC[A/G]TGCCTACCTCCCAAG | 22088 |
rs3154435 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tsg101 | Mm_Celera | 7:46913808 | CCACTATTTTAGTGC[A/G]TTTCTTCAAGTTAAA | 22088 |
rs3154436 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46895452 | ggttcccagtaccca[C/T]atcaggtggctcctg | 22088 |
rs3154438 | snp | C/T | | | intron-variant | Tsg101 | Mm_Celera | 7:46895497 | catttccaggagttt[C/T]catgtctgcttctgg | 22088 |
rs3154499 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tsg101 | GRCm38.p3 | 7:46892820 | TCAGGCTTTTTACTT[A/G]GGTTCCAGAAATTGA | 22088 |
rs3154500 | snp | A/G | | | intron-variant | Tsg101 | GRCm38.p3 | 7:46892623 | TGAGGAAGTCCAAGG[A/G]TTCTGAATGGCGAAC | 22088 |
rs3154501 | snp | A/G | | | intron-variant | Tsg101 | GRCm38.p3 | 7:46892220 | acacagagaaaccct[A/G]tctcgaaagaaaaaa | 22088 |
rs3154502 | snp | A/G | 0.5 | 0 | intron-variant | Tsg101 | GRCm38.p3 | 7:46892199 | AAAGAAAAAAAAACA[A/G]AAACAAAAAGTAGTA | 22088 |
rs3154503 | snp | A/G | 0.32 | 0.24 | intron-variant | Tsg101 | GRCm38.p3 | 7:46891725 | TCCAGCACCCATATC[A/G]GGGTACACACACGCA | 22088 |
rs3154504 | snp | C/T | 0.32 | 0.24 | intron-variant | Tsg101 | GRCm38.p3 | 7:46890494 | TCTACCACTGCCTTC[C/T]GGCTGGGTGGCAAGG | 22088 |
rs3154505 | snp | C/T | | | intron-variant | Tsg101 | GRCm38.p3 | 7:46889859 | tcagcactgcaaaGG[C/T]AAAGCCAGGCCCTGC | 22088 |
rs3154506 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tsg101 | GRCm38.p3 | 7:46889730 | TCAATGCGTTTCTGA[A/G]ATGTTAACATTTTCC | 22088 |
rs3154507 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Tsg101 | GRCm38.p3 | 7:46888846 | TTCCTCAGATTCCAC[C/T]GTCACTGCCAACTCT | 22088 |
rs3154590 | snp | C/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46897209 | gccagaagaggatgt[C/G]agatttcccggaact | 22088 |
rs3154591 | snp | A/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46898611 | attttattttatttt[A/G]ttttgtttttttcaa | 22088 |
rs3154592 | snp | C/G | 0.32 | 0.24 | intron-variant | Tsg101 | Mm_Celera | 7:46899203 | ATTAACAAATCCTTT[C/G]TTACTTAAAGGAAGC | 22088 |
rs3154593 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tsg101 | Mm_Celera | 7:46900463 | GAAATGATAACCCAG[A/T]GTGAGTTAGAAGACA | 22088 |
rs3154594 | snp | C/G | | | intron-variant | Tsg101 | Mm_Celera | 7:46893876 | CAAACAAAAAAGCCT[C/G]TCCCCCAAAACAAAA | 22088 |