SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8144702 | snp | G/T | | | utr-variant-3-prime | Sumo1, RGD1562029 | Rn_Celera | 9:66453433 | GGAGCTTTAGTACGG[G/T]TTTTACAAATATTGT | 301442 |
rs65656586 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66481214 | AAGTCAAGCACATTA[C/T]CGAACCCCCCAACTT | 301442 |
rs104920524 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66459179 | ACTGAGCTAAATCCC[C/T]AGCCCCAAAACTAAA | 301442 |
rs104955316 | snp | A/C | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66460769 | GTGTTTCAAAGAATG[A/C]ATTCCTTCATGACAG | 301442 |
rs105011772 | snp | A/C | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66470006 | AGCAAACCTAGTCTA[A/C]CAAAGTAAGTTCAAG | 301442 |
rs105262197 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66471576 | TCTTCTGGTGTATCT[A/G]AAGACAGTGTATTCG | 301442 |
rs105390100 | snp | C/T | 0 | 0 | upstream-variant-2KB | Sumo1 | Rn_Celera | 9:66483788 | AGGGAATGCGGGAGA[C/T]GAAATCGTCAAGGTT | 301442 |
rs105800915 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66457078 | CTTAATCTGGATCTC[A/G]GGAGGTAGAAAGATC | 301442 |
rs106025779 | snp | A/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66476426 | AAAATCTCTTTATAT[A/T]CTCCTGGCTGTCCTG | 301442 |
rs106053231 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66464668 | CAAACTTCACAAAAT[A/G]AAACACATCCATTTG | 301442 |
rs106327869 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66481024 | AATCCCAGGACTCAG[G/T]AAAGTAAAAACAGAA | 301442 |
rs106456804 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66468309 | GAGGAATTCCCAGGT[A/G]TTATCAAATCTGATG | 301442 |
rs106954634 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66462590 | TGTGGTTCCTTTCAG[G/T]ATTGGCGGTTCCATT | 301442 |
rs106972110 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66462474 | ATTTATCTGCCAGTC[A/G]GTGGTTTCCATTTTG | 301442 |
rs106982878 | snp | A/G | 0.5 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66464151 | TCGGAGCTGGGGACC[A/G]AACCCAGGGCCTTGC | 301442 |
rs107396683 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66477834 | TGGAATAGAACCAAT[C/T]AGATATAACTCACCT | 301442 |
rs197042181 | snp | C/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66469425 | AGATAAAAGCCAGAC[C/G]AAACTCTGGTGCTAT | 301442 |
rs197071600 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66467741 | TTAATTTGTTTCACA[C/T]AGGGTAAGTACAAAT | 301442 |
rs197184108 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66481211 | TTCAAGTCAAGCACA[C/T]TATCGAACCCCCCAA | 301442 |
rs197283841 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66457714 | TGAGTTCCAACAAGG[C/T]AGGGCTATGTTACAC | 301442 |
rs197459126 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66472778 | TATTACATCCAAAAG[G/T]CAATCACTATCTAGT | 301442 |
rs197483855 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66472147 | TTTCATTTTAGAAAT[A/G]CAATTGTATTTAATA | 301442 |
rs197501906 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66461387 | AGCCAGAGTTACATG[A/G]AGCTATCCTGTCTAT | 301442 |
rs197639821 | snp | A/C | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66482679 | AAAAAAAAAAAAAAA[A/C]CAACAAAAAAAATTT | 301442 |
rs197752638 | snp | C/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66464799 | GACTATTTAACATTC[C/G]TTGTGGAAGAACTTT | 301442 |
rs197820649 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66464127 | TTTTTTTTTTTTTGG[G/T]TCTTTTTTTCGGAGC | 301442 |
rs197850104 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66468120 | ATTAAAGATAAAATA[C/T]GGGTCACCAGACTGA | 301442 |
rs197873221 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66455690 | TGCCCTGAGGATCCA[C/T]TCCTAAGTGGAATTT | 301442 |
rs197928027 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66479481 | AGAGGAGGAAGAGAA[A/G]GGGATCACACATAAC | 301442 |
rs198025713 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66469456 | GAGAAAGAGGAGGAA[A/G]CCCTGAAAATTGCTG | 301442 |
rs198261081 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66458438 | CGTCATGAGGTTCTT[A/G]ACAAGGACTCAGGAA | 301442 |
rs198505095 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66467012 | TTAGTCCAATGCTGG[C/T]ACTGGACACACCTTC | 301442 |
rs198688381 | snp | C/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66461484 | AGAGCGCTTGCCTAG[C/G]AAGCGCAAGGCCCTG | 301442 |
rs198690183 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66455964 | GCGCTCTACCACTGA[A/G]CTAAATCCCCAACCC | 301442 |
rs198720270 | snp | C/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66472597 | GGCAGTAAACTGAAA[C/G]TGAAACTACTAAATT | 301442 |
rs198755443 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66480410 | CAAGACCAGCAGACA[G/T]TAATAACAAGCTATA | 301442 |
rs198764956 | snp | C/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66464013 | AATCTTAATTGTATC[C/T]ATAGCTTTTCTTCTC | 301442 |
rs198776098 | snp | A/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66479274 | TTCTCAAAAAAAAAA[A/T]TTTTTTTTAATCAGT | 301442 |
rs198796145 | snp | A/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66480298 | TAGATGGTAAAGTTA[A/G]CTGCTATAGTTCAAT | 301442 |
rs199057132 | snp | A/C | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66468458 | TTTCGGAGCTGGGGA[A/C]CGAACCCAGGGCCTT | 301442 |
rs199311973 | snp | A/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66479275 | TCTCAAAAAAAAAAT[A/T]TTTTTTTAATCAGTA | 301442 |
rs199338855 | snp | C/G | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66460880 | CTAAAGTGTCCCGAA[C/G]GTGGTCACACTAGAA | 301442 |
rs199400290 | snp | G/T | 0 | 0 | intron-variant | Sumo1 | Rn_Celera | 9:66477291 | AAGAACACAACAACT[G/T]GTTATCCAATACCAA | 301442 |