| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs581985068 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32670752 | GCCGTCCCTTTGACC[C/T]TTGTTTTTTTTTTTT | 51789 |
| rs582375694 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32661767 | TGTGTGTGTGTGTGT[A/G]TTAGGGTCTGGGTGG | 51789 |
| rs582473527 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32648090 | CTGGAACTCACTCTG[G/T]AGACCAAGCTGGCCT | 51789 |
| rs582635228 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Tnk2 | GRCm38.p3 | 16:32672471 | TGATGCAGAAGGGGA[C/T]TCCCTGTACTCCCTC | 51789 |
| rs582714854 | snp | C/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643180 | CAGCATCTTTTCCTT[C/T]CTTCCTATCTTTCTT | 51789 |
| rs582869629 | snp | C/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32677558 | CACTCAGCTTCCTCT[C/G]AGATATGTCTTAGTC | 51789 |
| rs582944122 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32655144 | CTCAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAAA | 51789 |
| rs582958955 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32650292 | GCTCTTACCCACTGA[A/G]CCATCTCACCAGCCC | 51789 |
| rs582960732 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32662292 | AGGTGGGAAGGGAGG[G/T]AAGCCTGCCGGCTGC | 51789 |
| rs583024829 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32678434 | CCCTCCCTCTCTCCC[G/T]TTCTCTCTCTTTCCC | 51789 |
| rs583041138 | snp | C/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643192 | CTTTCTTCCTATCTT[C/T]CTTTCTTTCTTTCTT | 51789 |
| rs583281928 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649785 | AGACAGGATTTCTCT[G/T]TATAGCCCTGGCTGT | 51789 |
| rs583509048 | snp | C/T | | | intron-variant, downstream-variant-500B | Tnk2 | GRCm38.p3 | 16:32681607 | ATACACATACATAGA[C/T]GGAATTTTTTTTTTA | 51789 |
| rs583548583 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649861 | CCACCTGCCGGGCTA[G/T]CAAGATGGCTCAGTG | 51789 |
| rs583602744 | snp | A/G | | | intron-variant, downstream-variant-500B | Tnk2, Tnk2os | GRCm38.p3 | 16:32665013 | GGATCAGTAGCTCAA[A/G]GTCATCCAGGCCAGG | 51789 |
| rs583714830 | snp | C/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643401 | CTTTCTTTCTTTCTT[C/T]CTTTCTTCCTTCCTT | 51789 |
| rs583791943 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32653386 | CTGAGCCTTCTCGAT[A/G]GCCCAGTTTTTGATA | 51789 |
| rs584120306 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32654360 | TCCCCCTCCTCTCCA[C/T]ACACACACACACACA | 51789 |
| rs584193531 | snp | A/C | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32647211 | AGCTCAGCAAACAAA[A/C]AGCACCCCCCCAAAA | 51789 |
| rs584372162 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649886 | TCAGTGGTTAAGAGC[A/G]CTGACTGCTCTTCCG | 51789 |
| rs584444188 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649904 | GACTGCTCTTCCGAA[A/G]GTCCTGAGTTCAAAT | 51789 |
| rs584486560 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32647700 | TGTGTGTGTGTGTGT[G/T]ATGCCAGAGAAGAAC | 51789 |
| rs584602267 | snp | A/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32656218 | ATTGGAGTAGCTACC[A/T]ATCAGGAATAGTGTG | 51789 |
| rs584667203 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32671514 | CTTTGTCCTGGGCTG[A/T]GCAGTGACCTGTTTC | 51789 |
| rs584803018 | snp | C/T | | | intron-variant | Tnk2, Tnk2os | GRCm38.p3 | 16:32667535 | TTCTCCAAAACAGGC[C/T]TTGGAGACCCCTCTA | 51789 |
| rs584832645 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tnk2, Tnk2os | GRCm38.p3 | 16:32669863 | CATTGGAGCTATGGT[C/T]GACCTCCAGAAAGAG | 51789 |
| rs584866997 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649951 | TGGCTCACAACCATC[C/T]ATAACGAAATCTGAT | 51789 |
| rs585001688 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32645239 | ACACACATACACACA[C/T]GTACGCACGCACGCG | 51789 |
| rs585274312 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32682000 | CACAGAGAAACCCTG[C/T]CTCGAAAAACCAAAA | 51789 |
| rs585352128 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32658026 | CACACAACACACACA[C/T]ACACATGTTACCTTA | 51789 |
| rs585370281 | snp | A/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32656279 | GGTGGCACTCTAGGT[A/T]GGGCTGTGCAGATTA | 51789 |
| rs585442973 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32653296 | GGTACTCTTCTTCCA[C/T]TGTGTTTCCTGGGGA | 51789 |
| rs585462400 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649128 | TTCTCCTCTCTTTGA[A/G]CCAGTTATATTACAA | 51789 |
| rs585722054 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32661957 | GGGGCTGGGGGGGAG[A/G]CTTAGGGGGGAGTCA | 51789 |
| rs585934031 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Tnk2 | GRCm38.p3 | 16:32672729 | GTGGAGATAGAAAGG[A/C]GAGAATTGTTAGGTA | 51789 |
| rs585973325 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32677586 | GTCTTTGTATCTTTG[C/T]ATTATCCCCTGGACA | 51789 |
| rs585979620 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32653987 | ACTCTTGAATTTGAG[C/T]ATTTTTAGCTTTCTC | 51789 |
| rs585991394 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32662100 | GGGCTGAGGAGCAGG[A/G]AAGGGAGCTGAGCTG | 51789 |
| rs586391610 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32650775 | TTTTTTTTTTTTTGA[C/T]ATAAGGTTTCTTTGT | 51789 |
| rs586449399 | snp | A/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643187 | TTTTCCTTTCTTCCT[A/T]TCTTTCTTTCTTTCT | 51789 |
| rs586618530 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32655382 | TAGGGGGAAGATGAT[C/T]TGACTTGTTCCTGGT | 51789 |
| rs586736228 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649888 | AGTGGTTAAGAGCGC[C/T]GACTGCTCTTCCGAA | 51789 |
| rs586744836 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32662293 | GGTGGGAAGGGAGGG[A/G]AGCCTGCCGGCTGCT | 51789 |
| rs586919040 | snp | C/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643405 | CTTTCTTTCTTTCTT[C/T]CTTCCTTCCTTCCTT | 51789 |
| rs586923903 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649856 | GAAATCCACCTGCCG[A/G]GCTAGCAAGATGGCT | 51789 |
| rs587063272 | snp | A/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32679071 | CGGGTGGGGATGTAA[A/T]TGTGTGCTGCAGTAC | 51789 |
| rs587071252 | snp | C/T | | | upstream-variant-2KB | Tnk2 | GRCm38.p3 | 16:32643365 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 51789 |
| rs587172230 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tnk2, Tnk2os | GRCm38.p3 | 16:32668670 | GGGCTGCAGCGCCCC[C/T]TCCTGCCACCCCAAC | 51789 |
| rs587318198 | snp | G/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32681867 | CAAGAAAGTTCCCTC[G/T]GAGCCAGGCGTGGTG | 51789 |
| rs587407133 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32682029 | AAAAAAAAAAAAAGT[C/T]TCCTCTGATCTCTGC | 51789 |
| rs587408942 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32646957 | GTGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 51789 |
| rs587434584 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32649863 | ACCTGCCGGGCTAGC[A/G]AGATGGCTCAGTGGT | 51789 |
| rs587449012 | snp | C/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32654652 | GACAGAGATACAGGA[C/G]CATGATAGGATGCTG | 51789 |
| rs864273417 | snp | A/G | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32673988 | GCAGGTTCTTGGCCT[A/G]GCCTGGCCTGCAGCC | 51789 |
| rs864295705 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32678562 | TCCTCCCTCCTTTCT[C/T]TATCTAAACCCTTCC | 51789 |
| rs864303768 | snp | C/T | | | intron-variant | Tnk2 | GRCm38.p3 | 16:32675139 | GAGGAAGGGAATAGG[C/T]GCATTGTGGACCATG | 51789 |