| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs579435351 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90018612 | TGGATTACACACAAA[A/G]AGCACCTGAGTTCAA | 74383 |
| rs579771726 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90039781 | TAAAGGCCTGAGGCA[C/T]GACATTGGGCTACAT | 74383 |
| rs579907439 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90046732 | CACAGAGAAACCTTG[C/T]CACCAAATAAATAAA | 74383 |
| rs579983512 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90019488 | ATCACACCATGAAAC[C/T]CTGGCACAAGAAAAA | 74383 |
| rs580470489 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040394 | AGTTAGCCAGGCAGT[A/G]GTGGCGCATGCCTTT | 74383 |
| rs580845007 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90010003 | CCTCTTCTGGAGTGT[A/C]TGAAGACAGCTACAG | 74383 |
| rs580882697 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040439 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCA | 74383 |
| rs580886267 | snp | A/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90014464 | CCCACCAAAAAAACA[A/T]AGGTCTAAAGAGGTA | 74383 |
| rs581067861 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90024614 | GACAGCTACAGTGTA[A/C]TTACATAATCAATAA | 74383 |
| rs581445486 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90021544 | ACACAAGTTATGAGC[A/C]AGTGACATTGATACA | 74383 |
| rs581448054 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90024410 | AAACAAACAAACCAA[A/C]CAAACAAACAAACAA | 74383 |
| rs581536826 | snp | A/C | | | intron-variant, utr-variant-3-prime | Ubap2l | GRCm38.p3 | 3:90006437 | GAAGGTATCCACCAA[A/C]TCATTTCCCCAAGCC | 74383 |
| rs582101438 | snp | G/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90045814 | GATATTGTGTAGGGC[G/T]AGAGAGATGGCTCAG | 74383 |
| rs582177277 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ubap2l, Mir7669 | GRCm38.p3 | 3:90012438 | GCCACTATACAACTG[A/G]TTTCAACAATAACTT | 74383 |
| rs582590139 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90029265 | TAAACATATATATAC[A/C]TGGGCGTCTTTGTTG | 74383 |
| rs582884268 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90003092 | ACTTTTGGTTATGGA[C/T]TTAGAAAGAATGAAA | 74383 |
| rs582886691 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90045056 | TTTAAAAAAAAAAGC[C/T]GGGCGTGGTGGCGCA | 74383 |
| rs583149281 | snp | C/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90038202 | GCATTTACACACACT[C/G]CTGTTCAAGCAAGTG | 74383 |
| rs583160892 | snp | G/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90016597 | GAAAGAGGAAAAGCC[G/T]ACCAACCAACCAACC | 74383 |
| rs583334726 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90019810 | TCAAGTTGTGTACAT[A/G]GTCAACAAGGAACTT | 74383 |
| rs583748909 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90039783 | AAGGCCTGAGGCACG[A/G]CATTGGGCTACATAC | 74383 |
| rs583793966 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90004696 | GGAGGAAAAAAAAGC[A/G]CAGAACCACAGAAAT | 74383 |
| rs583917975 | snp | C/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040400 | CCAGGCAGTGGTGGC[C/G]CATGCCTTTAATCCC | 74383 |
| rs584301073 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040471 | GGCCAGCTGGTCTAC[A/C]GAGTGAGTTCCAGGA | 74383 |
| rs584306452 | snp | G/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90010057 | TTATAAAAAAAAAAA[G/T]ATGTCACAGGGAGCT | 74383 |
| rs584325358 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90045495 | CCAGGATAGCAAAAA[C/T]ACAGAAACTGTGCCT | 74383 |
| rs584415558 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90024414 | AAACAAACCAAACAA[A/C]CAAACAAACAAAAAC | 74383 |
| rs584874162 | snp | C/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040487 | GAGTGAGTTCCAGGA[C/G]AGCCAGGGCTACACA | 74383 |
| rs585007817 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90009914 | TAAGAGCACCGACTG[C/T]TCTTCTGAAGGTCCT | 74383 |
| rs585092732 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90045815 | ATATTGTGTAGGGCT[A/G]GAGAGATGGCTCAGC | 74383 |
| rs585364117 | snp | C/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90045075 | CGTGGTGGCGCATGC[C/G]TTTAATCCCAGCACT | 74383 |
| rs585521416 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90037523 | GACTATACAGAGAAA[C/T]CCTGTCTGAAAAACC | 74383 |
| rs585633105 | snp | A/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90032112 | AAAATCGGTTTTTTT[A/T]AAAATATTTAAACTG | 74383 |
| rs585912902 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90039529 | AGTTCTATTCAGCTC[A/G]GTAGCTCAGGTACAG | 74383 |
| rs586183390 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ubap2l, Mir7669 | GRCm38.p3 | 3:90012501 | ATTAATCCCAGCAAC[C/T]GAGGCATTAATCCGG | 74383 |
| rs586452438 | snp | A/G | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90013942 | GAGGGGGGAAAAATA[A/G]GTGCAATTTACATAT | 74383 |
| rs586749858 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040108 | AAGTGAGTTCCAGGA[C/T]AGCCAGGGCTATAGA | 74383 |
| rs587017327 | snp | A/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040486 | AGAGTGAGTTCCAGG[A/T]CAGCCAGGGCTACAC | 74383 |
| rs587028568 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90003532 | ATGGAATATATATAT[A/C]TGGGCTGCTTTTTGA | 74383 |
| rs587111753 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90005266 | AAACAACAACAAAAA[A/C]CAGGCATTGGTTTTC | 74383 |
| rs587234091 | snp | A/C | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90021169 | TCCAAATAAACCCTT[A/C]GACTATCTCATCCTG | 74383 |
| rs587276339 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90013533 | ACACAGGCAGAACAT[C/T]CCTACATGTTAAAAA | 74383 |
| rs587540312 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90022685 | AAAAAAAAAAGGAAA[C/T]CAGAAACCAGAAAAA | 74383 |
| rs587545886 | snp | C/T | | | intron-variant | Ubap2l | GRCm38.p3 | 3:90040415 | GCATGCCTTTAATCC[C/T]AGCACTTGGGAGGCA | 74383 |
| rs864268019 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Ubap2l, 4933434E20Rik | GRCm38.p3 | 3:90052903 | GACGGACTCTAGCCT[G/T]GTTTTTTTTTTTTTT | 74383 |
| rs864289281 | snp | C/G | | | intron-variant, downstream-variant-500B | Ubap2l, Gm19710 | GRCm38.p3 | 3:90001513 | TCTCCCACCACCACA[C/G]ATTAATTAATGTGAA | 74383 |
| rs864292488 | in-del | -/T | | | intron-variant, downstream-variant-500B | Ubap2l | GRCm38.p3 | 3:90006819 | ATACCCTTTAAAATA[-/T]TTGTAACTGGACCGC | 74383 |