SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8147591 | snp | C/T | | | utr-variant-3-prime | Tnk2 | Rn_Celera | 11:71348997 | AAGACCAGCCAAGCC[C/T]GAGTTCACAGTGAAG | 303882 |
rs105412973 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71381016 | AAGACAAACTAGAAC[C/T]GTGCCAATCATTTGT | 303882 |
rs196970303 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71371928 | TCCTTTGTGCCCCAT[A/G]TTCTTACAGCTGACA | 303882 |
rs197052543 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71368586 | CCTAAAACAGCTGAG[C/T]TGGAGCAGCTCAGAG | 303882 |
rs197053393 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rnor_6.0 | 11:71350055 | CCTCACCCCTGCCTG[A/G]TTCGCCACCTTTGGG | 303882 |
rs197061598 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71381872 | CTGCCATGACAGACC[A/G]CCTCACCACAGGCCT | 303882 |
rs197222098 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71379460 | CCCCAAGTGACCGGC[A/G]CTCCACCACCCTGCA | 303882 |
rs197233762 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71373118 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 303882 |
rs197236083 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71360140 | AGCAAAGGGCAGTGA[A/G]GCTGAGGCTAGGCAG | 303882 |
rs197281432 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71374269 | ACCTCTCCCACCCAT[C/T]CTACCCTCAAAGGTA | 303882 |
rs197345512 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71373644 | CACTCCCCACCCTCA[A/G]CACCCTCCCTAGCTT | 303882 |
rs197358666 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71364066 | ACCTTCTAAACAGCA[C/T]ACTCTCTTGCCCCTA | 303882 |
rs197446560 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71362674 | CAGTTTACATACTGC[A/G]CCCCTTGCCCTGCGT | 303882 |
rs197517120 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71365143 | AGTAAGCTGGGTAAT[A/G]GAGCCACCGCTGCTT | 303882 |
rs197555832 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71354889 | GATGGACAGAGTGCC[A/G]ACAAGAGCCTGCCTC | 303882 |
rs197557449 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71359282 | CAGGTAAATCCAAGA[C/T]TCCCAGGGCCCATTC | 303882 |
rs197564484 | snp | G/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71367066 | TAAGAGGTTTGTTTC[G/T]GTGCTGGGAATTAAA | 303882 |
rs197675195 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71376748 | TCACCCTTCCTTCTA[C/T]TCTACTCTACTCTAC | 303882 |
rs197700371 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71365942 | TATACCTCTGGGCAA[C/T]AGGAGAAGGCTCCTA | 303882 |
rs197720334 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71379732 | TAAGTGGCCTGTTCC[A/G]GTCTTCACATAAAAT | 303882 |
rs197802944 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rnor_6.0 | 11:71359643 | TTTCAGGCTGGCCAC[A/G]CACACAGCAGTCCTT | 303882 |
rs197835198 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71375415 | GAGCAGCTACAAGGA[C/T]CCAAAGCCCGCAGGT | 303882 |
rs197858388 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71371576 | CCTGGCTCAGACGAC[A/G]TTAATGTGTCCCTGT | 303882 |
rs197881965 | snp | A/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71362286 | CCCCTCTGTCACATG[A/T]GGCAGGAGACTAGAG | 303882 |
rs197890679 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71373170 | ACCTCCTCGATCAGG[A/G]GTGTAAGGGGAGGGG | 303882 |
rs198006449 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71361310 | CCAAGGCAGGCCAGG[C/T]ACCACCATGGATATC | 303882 |
rs198066232 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71356656 | TGCTCAGCCTAAGCT[C/T]CTCTGGGTAAGTCAG | 303882 |
rs198081091 | snp | C/T | 0 | 0 | missense | Tnk2 | Rn_Celera | 11:71351918 | GAGGGTCCAGGCCAC[C/T]GACTTGCCTCTTCCT | 303882 |
rs198103608 | snp | G/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71366299 | GGTGAGTCTCAAACT[G/T]GCTGGAGGCGTTTAC | 303882 |
rs198170118 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71365638 | AAGACCTGAAGACTC[A/G]AGAGCATGGGGGAAG | 303882 |
rs198208777 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71354553 | CGCCCCTGACCCACC[C/T]CACCCCAGCTCCTGT | 303882 |
rs198229241 | snp | G/T | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71374609 | CAGAGCCCTAAGGTC[G/T]CTCTCTCTCTCTCTC | 303882 |
rs198253023 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71372488 | TTCAGACCTAGGAGC[C/T]TGGGGTTACTGGTAA | 303882 |
rs198331500 | snp | A/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71361517 | CCTTCCAGTAACCCT[A/T]GAGAATTCCTTGGGT | 303882 |
rs198362896 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71363039 | ATAATATAATTAAGA[A/G]AAAAAAGGCTATGAC | 303882 |
rs198398637 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71387593 | ATACAATTGTATGTG[C/T]TGGGTGGGGAAGGTG | 303882 |
rs198408357 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rnor_6.0 | 11:71359825 | CGGCACCAAGGGACA[C/T]GGTCAGACTCCTTCC | 303882 |
rs198418491 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71371649 | GAGTGGGACAGTGCA[A/G]CCAAGAACTGGGGTG | 303882 |
rs198470278 | snp | A/T | 0 | 0 | utr-variant-3-prime | Tnk2 | Rn_Celera | 11:71349350 | CAGAACAGCGCTGGG[A/T]GGGTGAGCGAGGTGG | 303882 |
rs198552252 | snp | G/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71354682 | GAGGGTGCAGGCCTA[G/T]CTGCAAGGGCCTCCC | 303882 |
rs198555113 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71355409 | CAAGCCACATCCATG[C/T]CCTGCTCTTGTCTAG | 303882 |
rs198635759 | snp | A/G | 0 | 0 | upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71389264 | AACTCACTTCTACCC[A/G]TTCTCAATTGCTTCT | 303882 |
rs198647418 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71374226 | CTAACTGGCAGCTCC[C/T]TAACCCACTCCTTAT | 303882 |
rs198798184 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71365128 | CCCACAGCCCTGCAC[A/G]GTAAGCTGGGTAATG | 303882 |
rs198800056 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71374610 | AGAGCCCTAAGGTCT[C/G]TCTCTCTCTCTCTCT | 303882 |
rs198801544 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71364641 | TAGGTTACTTCTCCC[A/G]GTTTGTGAAATGAGC | 303882 |
rs198806458 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rnor_6.0 | 11:71359504 | CCAGTTCCTCAGACA[C/T]TCTGGGGAATCAGAA | 303882 |
rs198887350 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71366682 | CAGTAAGCCGCACCC[C/T]TCCATGGCTTCTGCA | 303882 |
rs198943882 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71377002 | GTAGCTATTCCAGTA[C/T]CTGCCCAGCATACAG | 303882 |
rs198969710 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | Tnk2 | Rn_Celera | 11:71373918 | TCTAGAAATCTTGGG[A/G]ACTCAAGCATCGTCC | 303882 |
rs199064692 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71380041 | CTGTAGAGATGGTTC[C/T]GCCCTAAAGGAGCAT | 303882 |
rs199078405 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71359356 | ACGCACAGATATACT[A/G]AAGGCCCCTGTGGGC | 303882 |
rs199083380 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71367794 | AGGTTCAGTATCTCT[C/T]TTTTTTTTTTTTTTT | 303882 |
rs199183697 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71363384 | CTTGAAAGAAAAAAA[A/G]AAAAAAAAAACCACT | 303882 |
rs199201941 | snp | A/G | 0 | 0 | missense | Tnk2 | Rn_Celera | 11:71352474 | AAGGTGCACAGGGCC[A/G]TGGGGTTGGGGCTAC | 303882 |
rs199266041 | snp | C/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71362583 | TCATGGTCCCCAACA[C/T]TGAGCTAACTGCTCC | 303882 |
rs199270624 | snp | A/T | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71373263 | CAGAGCACCAGCAGA[A/T]GACGAGGCCTGAGCC | 303882 |
rs199388064 | snp | A/G | 0 | 0 | intron-variant | Tnk2 | Rn_Celera | 11:71358980 | TTTAAGTCTCTGCTA[A/G]GAACCTCCAGGGAGG | 303882 |
rs199416012 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tnk2 | Rn_Celera | 11:71375485 | TTGCCCTGGCAGGCT[A/G]AATGAAGGTTCAAAA | 303882 |