SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8160204 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76349193 | TTTTTCATGATTCTC[C/T]CAAGGCTGGGCTTAC | 494338 |
rs8161422 | snp | C/T | 0.31498 | 0.241407 | utr-variant-3-prime | Trim25 | Rn_Celera | 10:76361826 | CCCCTTCGCCAGCTC[C/T]CCTCCCAATCTCCTA | 494338 |
rs13458229 | snp | C/T | 0 | 0 | missense | Trim25 | Rnor_6.0 | 10:76361508 | GGCAGCGTTTCTCCA[C/T]GTTGTTGTGCCAGGC | 494338 |
rs64916939 | snp | G/T | 0 | 0 | upstream-variant-2KB | Trim25 | Rnor_6.0 | 10:76342955 | GGTGGGGGGGTGGCA[G/T]CGGACACTTTTGTTC | 494338 |
rs65114478 | snp | C/G | 0 | 0 | upstream-variant-2KB | Trim25 | Rnor_6.0 | 10:76342901 | TCATATCGTATGGTT[C/G]TGTTTTGTTTTCCTT | 494338 |
rs65645226 | snp | A/G | 0 | 0 | upstream-variant-2KB | Trim25 | Rnor_6.0 | 10:76342948 | GATATTGGGTGGGGG[A/G]GTGGCATCGGACACT | 494338 |
rs65758349 | snp | A/C | 0 | 0 | upstream-variant-2KB | Trim25 | Rnor_6.0 | 10:76342962 | GGGTGGCATCGGACA[A/C]TTTTGTTCTTNACTN | 494338 |
rs66199585 | snp | C/G | 0 | 0 | upstream-variant-2KB | Trim25 | Rnor_6.0 | 10:76342984 | TCTTNACTNACCAAG[C/G]TTTCAGTAATTGTAT | 494338 |
rs104899904 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356879 | TCACACAGGCAGGGC[A/G]GCAGGGCTTGAAGCA | 494338 |
rs104988630 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345392 | CCAAGTGCTGGGACT[A/T]AAGGCGTGGGCCACC | 494338 |
rs105066005 | snp | A/C | 0 | 0 | upstream-variant-2KB | Trim25 | Rn_Celera | 10:76343600 | TAGGATACTCCAACC[A/C]CTGGGACAATTCATC | 494338 |
rs105241922 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76352491 | TCCTGCCTCAGTCTC[C/T]GGAGGAACCGAAGTA | 494338 |
rs105274193 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345297 | TTTTTTGACAGTCCT[A/T]TGTAGTCCTGGCTGT | 494338 |
rs105431506 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345332 | GAACTCACTCTGTAG[A/G]CCAGGCTGGCTTTGA | 494338 |
rs105603223 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346895 | TGGTCAGTGGTCTGT[C/T]GTTGCCGCCTAAGTC | 494338 |
rs105661926 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357125 | ATCATTGAACCGTTA[C/T]ATTTTCCCTTAGACC | 494338 |
rs105669411 | snp | G/T | 0 | 0 | upstream-variant-2KB | Trim25 | Rn_Celera | 10:76342507 | AACTTTGAATCTCAT[G/T]TCAGAACCTGAAGGT | 494338 |
rs105672646 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76351728 | GTGTATTTTTTTTTT[G/T]TTTGTTTGTTTGTCG | 494338 |
rs105678900 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356999 | CCAAGGACTAGAGCA[C/G]CCAGAGTGGGCGGCT | 494338 |
rs105735342 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350486 | TATGCTGGCAGAAGA[G/T]AATGCTGGGTAGTTG | 494338 |
rs105767404 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76352816 | TTGGTTTCTGGGTTT[C/T]GAGACAGGGTTTCTC | 494338 |
rs105913747 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350451 | GGTCCAGGGTTGCAC[A/G]GGCTGTACTATAGCA | 494338 |
rs105929046 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346925 | CCTTGAGCTGCCTCT[C/T]TTTGATTAGGAGTAG | 494338 |
rs105951463 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356743 | TCCATATGCCATTAG[A/G]CATTCTAGTCTTGTT | 494338 |
rs106073620 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345247 | GACACCGTGGTGTAG[C/T]CCATCTTGATTTTTT | 494338 |
rs106135420 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76351742 | TGTTTGTTTGTTTGT[C/T]GTGTTTGATTCTGAA | 494338 |
rs106159632 | snp | C/T | 0 | 0 | downstream-variant-500B | Trim25 | Rn_Celera | 10:76362514 | TTGTGTCAAGGTAAC[C/T]CAGACGTGGTTGAGA | 494338 |
rs106168249 | snp | A/G | 0 | 0 | upstream-variant-2KB | Trim25 | Rn_Celera | 10:76342381 | TTCTAACAGCTTGTG[A/G]GACAGAGCAGTTTAC | 494338 |
rs106249937 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345608 | ATGGTGCCTCTCCTT[G/T]GTCCATCTGTCAAAG | 494338 |
rs106326588 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356963 | CTCCATTTCTTCATC[C/T]TATGCAGTCCAGCAT | 494338 |
rs106327147 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356859 | CCGGGTCAGGTCACC[A/G]TCCATCACACAGGCA | 494338 |
rs106346932 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346140 | ACTACAAATGGTAAA[A/T]TGGGGGACGAGGACG | 494338 |
rs106541585 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76352859 | GCTGTCCTGGAACTC[A/G]CTCTGTAGACCAGGC | 494338 |
rs106664346 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345307 | GTCCTTTGTAGTCCT[A/G]GCTGTTCTGGAACTC | 494338 |
rs106676537 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345581 | GGATCTAGAGGTCCC[C/T]GTCTTCCCCTTATGG | 494338 |
rs106722165 | snp | A/C | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76348936 | TCCAGACCAGCCTTG[A/C]TGGGTTTCGTTTTGT | 494338 |
rs106757188 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346957 | TCAGAGTAGGTTCCC[C/T]CCCACCCCCCATCCA | 494338 |
rs106893365 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359259 | ATGGATGTAGGAGAG[C/T]TCTTGGGGATGCAGG | 494338 |
rs107202397 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76344630 | TGCTGGGCCAGAGAT[C/T]CTATATCCCACCCCT | 494338 |
rs107274205 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim25 | Rn_Celera | 10:76352701 | TGCTGGGATTATAGT[C/T]GTGAGTCACCACACT | 494338 |
rs107339786 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76345391 | CCCAAGTGCTGGGAC[C/T]AAAGGCGTGGGCCAC | 494338 |
rs107340840 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358549 | AATGTGATCCTATAC[A/G]TACACAGTATATTAT | 494338 |
rs107342227 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359177 | CATAATGTGTGAGTC[G/T]TCTTCAGCAAACCAC | 494338 |
rs107427979 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76348863 | TTCTCTCCTGAGACC[A/G]CAGAAACTGGTAGGG | 494338 |
rs107429139 | snp | G/T | 0.5 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76351471 | ATAATAAATTTAACG[G/T]TTTTTTTTTTTTTCA | 494338 |
rs197041983 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76354696 | CCAGATTGCCTGGCT[C/T]AGTACAGGAGTGATG | 494338 |
rs197115076 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350959 | GCTAGGTCACCCTCA[C/G]CTGCTTTCTCTCGCT | 494338 |
rs197156191 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357582 | CATTAGCCTAGCCTC[C/T]ACTCCACCCCAGACA | 494338 |
rs197215914 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76354061 | TCGATTAATTCTTTC[A/G]TCTGGTTGGATATGT | 494338 |
rs197241512 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358423 | AGGTTTGCGTGGCAA[C/T]TGTTTCACCCACTCA | 494338 |
rs197288754 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76352041 | ACATTTTCCTTTTTG[A/G]TAGTACTGGGGTTTG | 494338 |
rs197297908 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346339 | TAGCCAGTGGTCAGC[A/G]AGATGGCTCGACTGG | 494338 |
rs197299950 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358727 | TGTAGAGAGACCCTG[C/G]CTCAAAAAAGAAAAA | 494338 |
rs197305574 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76349946 | CGTTGAGCTGCACTT[C/T]ACCATGGCAACTGTT | 494338 |
rs197458587 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356579 | CTCAGACTCCTAAGA[A/G]ATTCCCCAGCCTCGG | 494338 |
rs197463760 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359260 | TGGATGTAGGAGAGC[C/T]CTTGGGGATGCAGGA | 494338 |
rs197529277 | snp | A/G | 0 | 0 | upstream-variant-2KB | Trim25 | Rn_Celera | 10:76342468 | GACTGGCACTTAGAC[A/G]TTCGTATTTTTGCCT | 494338 |
rs197537031 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76353739 | TATCTCCTGGTTCCC[C/T]GGGCCCAGCGTCTGG | 494338 |
rs197540305 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76351168 | TGATGATGCTCCCGC[A/G]TGCTCTCTTATTAAA | 494338 |
rs197583835 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76349305 | TCCGAGGTGGAAGGT[A/G]AGAACAGAAACACAG | 494338 |
rs197634415 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359746 | ACCCGTAAGTTGTGC[A/G]TCTGTGTATCTTTTT | 494338 |
rs197671764 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76344951 | CCTGGCAGCATGTAA[G/T]AACTGTGTGTGCTCA | 494338 |
rs197715474 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357396 | TCTTTGGGGATGTGG[A/G]TGATGGTCTTGGACT | 494338 |
rs197773434 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357417 | GTCTTGGACTCCACT[C/G]AGGCCATCCCAGTGT | 494338 |
rs197787133 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76348991 | AGCCCTGGCTGTCCA[G/T]GAACTCACTATGTGA | 494338 |
rs197866095 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358099 | TTTCACAGTTGTGTG[C/T]GCGTGCATGCTTATG | 494338 |
rs198000324 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358462 | CTGAGCCCTATGTTT[C/T]TCTCTCTTTTCCCCA | 494338 |
rs198019858 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76355207 | CCACAGTGGTCCGAC[A/G]CTGATGAGCCCTTCG | 494338 |
rs198028693 | snp | A/C | 0 | 0 | downstream-variant-500B | Trim25 | Rn_Celera | 10:76362163 | AAAAAAAAAAAAGCC[A/C]GGTGCTGTGATACAC | 494338 |
rs198041382 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356286 | GCCATGCTTCCTGCC[A/T]CAGGACCTTTGTATA | 494338 |
rs198080144 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76354522 | GTGTTGCAGAGTATG[C/G]CCCACCCCCGGTAGT | 494338 |
rs198265117 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350760 | AGAAGAAGAAGAAGA[A/G]GAAGAAGAAGAAGAA | 494338 |
rs198276010 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76348566 | AGTGTAGGGGAACTA[A/G]GACACTAGGGTAAAG | 494338 |
rs198312242 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359135 | AGGGGAGTGAGAGGG[C/T]TCAGTGTGCTTTACT | 494338 |
rs198347957 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357418 | TCTTGGACTCCACTC[A/T]GGCCATCCCAGTGTC | 494338 |
rs198443028 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358321 | GTGATGAACAGCCAT[C/T]ATCTTGCTGTAAGAC | 494338 |
rs198470172 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76354693 | GACCCAGATTGCCTG[A/G]CTCAGTACAGGAGTG | 494338 |
rs198507026 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357405 | ATGTGGGTGATGGTC[C/T]TGGACTCCACTCAGG | 494338 |
rs198573171 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356190 | AGAGCAGTCAGTGCT[C/T]TTACCCACTGAGCCA | 494338 |
rs198578970 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350912 | GATAGGTCACTTGAA[C/T]GAACTTCCTGGGTAA | 494338 |
rs198609204 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350976 | TGCTTTCTCTCGCTT[A/G]TGAAAAGAGGAACAA | 494338 |
rs198666781 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359300 | AGCATTATTGTGATA[C/G]TTAACCAGGATTGTT | 494338 |
rs198705110 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76351931 | TAGGTAAACATTCTG[C/T]CCCTGAACTGTACTC | 494338 |
rs198709117 | snp | G/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76358678 | TTTGAGGCCAGCTTG[G/T]TTTACGCAGTGAGTT | 494338 |
rs198748878 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76352644 | AGTATTGTAGCCAAA[A/G]ATGACCTTGAACTTC | 494338 |
rs198761192 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76357304 | TGGGTCCTGGGGATC[A/G]GACTCAGGTTTGGCA | 494338 |
rs198831121 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359138 | GGAGTGAGAGGGTTC[A/T]GTGTGCTTTACTTGT | 494338 |
rs198904439 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359432 | CCAGTCAGATATATT[C/T]TGACAAATGAGTTCT | 494338 |
rs198976123 | snp | A/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76353009 | AAGTACTTTCCTAGG[A/T]ATTGGAGTTGCTGGG | 494338 |
rs199059322 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76353961 | CAAGCCAGCAGAAAC[A/G]TTCCTCCCTCCAGGA | 494338 |
rs199064268 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76349867 | TTAACCACTGAGCCA[C/T]CTCTCCAGGGCCCAA | 494338 |
rs199070744 | snp | C/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76350474 | CTATAGCATGGATAT[C/G]CTGGCAGAAGATAAT | 494338 |
rs199159930 | snp | A/G | 0 | 0 | downstream-variant-500B | Trim25 | Rn_Celera | 10:76362249 | TGCGGAGAGCCTGGT[A/G]TACATAGTGGGTTTT | 494338 |
rs199198741 | snp | A/C | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76356573 | GCTGGCCTCAGACTC[A/C]TAAGAGATTCCCCAG | 494338 |
rs199201927 | snp | A/G | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76359235 | AGAACATTTGGTGAC[A/G]GTGTGCTTATGGATG | 494338 |
rs199277406 | snp | C/T | 0 | 0 | intron-variant | Trim25 | Rn_Celera | 10:76346170 | GGTCTCGGGCTATAG[C/T]GAACCTTGGGCGAAG | 494338 |