SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13462636 | snp | C/T | | | utr-variant-3-prime | Sumo1 | Mm_Celera | 1:59639587 | GAAAGTTCTAATGTT[C/T]ATCAGCAGTTATTAA | 22218 |
rs30714576 | snp | A/C | 0.32 | 0.24 | intron-variant | Sumo1 | Mm_Celera | 1:59650231 | TGTTTTTAATACCAA[A/C]CAACAAAAATATCCA | 22218 |
rs31308445 | snp | A/C | 0.32 | 0.24 | intron-variant | Sumo1 | Mm_Celera | 1:59650234 | TTTTAATACCAAACA[A/C]CAAAAATATCCATTT | 22218 |
rs32821834 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59641012 | ATAGAAATAAAAATT[A/T]AAAACAAGGATTTTA | 22218 |
rs32821835 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Sumo1 | Mm_Celera | 1:59639524 | CAAAAAGTACAAACA[A/G]AATCAAAAGCAGTGT | 22218 |
rs32822075 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Sumo1 | Mm_Celera | 1:59658524 | ATAAAGATGTATACT[A/G]TAAAAGTAAGAAAAT | 22218 |
rs32822077 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sumo1 | Mm_Celera | 1:59657977 | GTCTACAAAACAACT[A/G]CCAGGCCTGACTATT | 22218 |
rs32822079 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59657636 | TCCTGGTCTACATAA[A/G]AGCTCTAGACCAGCC | 22218 |
rs32822081 | snp | G/T | 0.375 | 0.216506 | intron-variant | Sumo1 | Mm_Celera | 1:59657607 | GGCAGTGAATTCCTG[G/T]GTTATTGCAGCTATC | 22218 |
rs32822083 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59657516 | TTTTGGTTCAACATA[G/T]GACTTAATTTATTGT | 22218 |
rs32822845 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59657515 | ATTTTGGTTCAACAT[A/G]TGACTTAATTTATTG | 22218 |
rs32822847 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59657416 | ATATATGGCGTTTAA[C/T]TTAGTTTACTTAATG | 22218 |
rs32822849 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Sumo1 | Mm_Celera | 1:59657058 | CAAAAATGAAATAAA[A/G]TCCAGGGATCCAATC | 22218 |
rs32822851 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59657002 | ATGTCCAACCACTAA[A/C]GCTGCAGCCCGTGAA | 22218 |
rs32822853 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59656997 | GAAAGATGTCCAACC[A/T]CTAAAGCTGCAGCCC | 22218 |
rs32823606 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Sumo1 | Mm_Celera | 1:59669929 | AAGTGCCAAGCATCT[A/G]CTGGTTAAAGCCCAG | 22218 |
rs32823608 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Sumo1 | Mm_Celera | 1:59668924 | TCTCTTCAGGCTAAC[A/G]TGCTTTCTAGCTCTT | 22218 |
rs32823610 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Sumo1 | Mm_Celera | 1:59668325 | TTCATATGCAAATTG[C/T]TTTAATGTGTAGCTC | 22218 |
rs32823612 | snp | C/T | 0.18 | 0.24 | intron-variant | Sumo1 | Mm_Celera | 1:59667826 | TCACAGCAGCAAAAA[C/T]ACAAGTCATGTAGAA | 22218 |
rs32823635 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Sumo1 | Mm_Celera | 1:59656971 | GCAGAGGCACTAACA[A/G]TGGACAGCCAGAAAG | 22218 |
rs32823637 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59656841 | GAAAATGTCACTAAC[A/G]GTGGATAAAAGTAGC | 22218 |
rs32823639 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59656803 | AGCACCTCATTAGTC[A/T]TGTTTACTGGAACAG | 22218 |
rs32823640 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Sumo1 | Mm_Celera | 1:59656780 | ATTAACAGACTAAGT[C/T]AGCATAAAGCACCTC | 22218 |
rs32823642 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59656717 | GGGAAGATAAGGAAA[A/G]AGACTTACAAACTCA | 22218 |
rs32824124 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Sumo1 | Mm_Celera | 1:59667644 | CTAGAATACTTAAGG[A/C]ATTCAACACAAACTA | 22218 |
rs32824126 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sumo1 | Mm_Celera | 1:59667405 | ATGGGTTTGCAATAT[C/T]CACTAGCAATATCTC | 22218 |
rs32824128 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Sumo1 | Mm_Celera | 1:59667332 | TACTCTAAGCAGAAT[C/T]ATCCTACTGTTTCAA | 22218 |
rs32824130 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59667328 | TGAATACTCTAAGCA[G/T]AATTATCCTACTGTT | 22218 |
rs32824132 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59667279 | CTGTCTCAAAAAGAA[A/G]TTTTACAGTTTTGAA | 22218 |
rs32824133 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59667152 | TAGGAGTATCACAAT[A/T]TGAAAAATGGTTTAC | 22218 |
rs32824324 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59656299 | TAGTTGTACCAAGAC[A/G]TGTAAATACATCACA | 22218 |
rs32824326 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59656298 | TTAGTTGTACCAAGA[C/T]GTGTAAATACATCAC | 22218 |
rs32824327 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59656273 | GTTCTCACAGCCTAT[C/T]TTGAGACTATTAGTT | 22218 |
rs32824328 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant | Sumo1 | GRCm38.p3 | 1:59656206 | CAATTCTTCTTAATC[A/C/G]CGAGTTCATCCTCCT | 22218 |
rs32824329 | snp | C/T | 0.32 | 0.24 | intron-variant | Sumo1 | Mm_Celera | 1:59655878 | AATCTAAAACTTAAC[C/T]ATGTGTTAGTCACCT | 22218 |
rs32824330 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59655144 | TATTTTGATAATAAG[C/T]GTGTATTTCACTAAT | 22218 |
rs32824332 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59654947 | CAGAACACTTACCTG[C/G]CCAAGTGCCAGACCC | 22218 |
rs32824785 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Sumo1 | Mm_Celera | 1:59667123 | TTATAACAGAGCTAA[A/T]ATAACTAACTATATA | 22218 |
rs32824787 | snp | A/C | 0.375 | 0.216506 | intron-variant | Sumo1 | Mm_Celera | 1:59666676 | TTAACAAACAATCCT[A/C]GTGAATGGCTAAGGA | 22218 |
rs32824789 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Sumo1 | Mm_Celera | 1:59666228 | CTGGCCCTAGATAGA[A/G]CAAGAGAATGTAACT | 22218 |
rs32824791 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Sumo1 | Mm_Celera | 1:59666164 | TCTGATCTGGGTGCA[G/T]TTTACACAAATGTGT | 22218 |
rs32824793 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Sumo1 | Mm_Celera | 1:59665428 | CAGTAAAAACAGACT[A/G]GAGTGTAATATAGCA | 22218 |
rs32825284 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59654889 | CACGCACACACACCA[C/T]ACTCAGAGTAATAAA | 22218 |
rs32825285 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59654833 | TTCTCTCTGACTCCC[A/G]CTATGTGAGTGTAAG | 22218 |
rs32825286 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59654746 | ATGAATACCAGGCAC[A/G]CAGGTGCTACCAACA | 22218 |
rs32825288 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59654728 | GGCAACTCACAAACA[C/T]CCATGAATACCAGGC | 22218 |
rs32825289 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59654657 | GGACAAATAAGTCAG[G/T]GTTTTAGACCACCGG | 22218 |
rs32825291 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59654624 | ATAATGATGGTAATA[A/G]TAGTAGTGTCAGCAG | 22218 |
rs32825292 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Sumo1 | Mm_Celera | 1:59654472 | TCAAATATCCTGCAA[A/C]ATTTCCTTTTAATCC | 22218 |
rs32825293 | snp | A/G | 0.375 | 0.216506 | intron-variant | Sumo1 | Mm_Celera | 1:59654414 | TACAACTAAAAAAGA[A/G]ATTTTTCCAGTAAAT | 22218 |
rs32825475 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Sumo1 | Mm_Celera | 1:59665202 | ATCCTAACAAAAAAG[G/T]ACTATAAACAAGTAT | 22218 |
rs32825477 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59665178 | TACTTATTAATCAAT[C/T]CAAAAGCAATCCTAA | 22218 |
rs32825479 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59665176 | TCTACTTATTAATCA[A/T]TCCAAAAGCAATCCT | 22218 |
rs32825481 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sumo1 | Mm_Celera | 1:59664689 | TAATTTGGAGATATG[A/G]CAGACATTGTTAATC | 22218 |
rs32825483 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Sumo1 | GRCm38.p3 | 1:59664565 | AACTAAAAATTACAG[C/G/T]GAAAATCTGCTGCTA | 22218 |
rs32826175 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Sumo1 | Mm_Celera | 1:59664438 | ACCAATCATATATAA[C/T]TCACTTCAAAGTTTA | 22218 |
rs32826177 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Sumo1 | GRCm38.p3 | 1:59663038 | ATTCATCGTTGTGAC[A/C]ATTTTCAGTGGCTCT | 22218 |
rs32826179 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Sumo1 | GRCm38.p3 | 1:59663030 | CCTTAGCCATTCATC[A/G]TTGTGACAATTTTCA | 22218 |
rs32826181 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59662683 | AAAGGGCCTGAATAT[C/T]TATAGTTGATGACCC | 22218 |
rs32826183 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Sumo1 | Mm_Celera | 1:59662523 | TCCAAGACCTCTGCT[A/T]CCCCTCAATGATGAA | 22218 |
rs32826384 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59654304 | ATTGGTTGCTTGCTC[A/C]TTTCTTGGCCTATGT | 22218 |
rs32826385 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59654290 | TTTTCTTCCTGTTAA[C/T]TGGTTGCTTGCTCCT | 22218 |
rs32826387 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sumo1 | Mm_Celera | 1:59653951 | TCCTTGAAGATTTCC[C/T]AGGTGTTACTAATTC | 22218 |
rs32826389 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59653697 | GCACAATTATCAAAC[C/T]GTTTTTTTATATTTG | 22218 |
rs32826390 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sumo1 | Mm_Celera | 1:59653616 | GTCTGTGTCTGAGTA[C/T]TTTTCTTATTTTCAT | 22218 |
rs32826391 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sumo1 | Mm_Celera | 1:59653563 | CCCCTCCAGTTTCAC[A/G]ATGTGGTGTTATGGT | 22218 |
rs32826392 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Sumo1 | Mm_Celera | 1:59647068 | CAAGCACCTTGGACC[A/G]CAGTTTCAGAGATTG | 22218 |
rs32826393 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59645083 | TAAAATAAAATAAAA[G/T]TGAACCATCAGAAAC | 22218 |
rs32826745 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59660660 | TATGAGAACTTTACT[C/T]TCTACTAGCTGTAAT | 22218 |
rs32826747 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Sumo1 | Mm_Celera | 1:59660399 | TTCAGCCCTTTATGG[C/T]CCCAGTTTCCTTTAG | 22218 |
rs32826749 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Sumo1 | Mm_Celera | 1:59659672 | TCTCACCATTCCTTT[C/T]TGAAACCCAAAAAAT | 22218 |
rs32826751 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Sumo1 | Mm_Celera | 1:59659125 | GCAATCAAACCTCTC[C/T]TTCCTTTGAAGGAAG | 22218 |
rs32826753 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sumo1 | Mm_Celera | 1:59658870 | AGAGCAAAGGTTATC[C/T]TCTGTAATGAAGGAC | 22218 |
rs32827275 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Sumo1 | Mm_Celera | 1:59644834 | TTGTCTATCAAAGAA[G/T]GCATTCCTTTATGAC | 22218 |
rs32827277 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Sumo1 | Mm_Celera | 1:59644778 | CCCATTAAAAAAATT[A/C]GTAAAACAGATGTTT | 22218 |
rs32827279 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Sumo1 | Mm_Celera | 1:59644740 | CAGCAATCTAATCAA[A/C]TTCCAAGTAACTTTT | 22218 |
rs32827281 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Sumo1 | Mm_Celera | 1:59644725 | TAACTAGTTTCAGTA[C/T]AGCAATCTAATCAAC | 22218 |
rs32827282 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Sumo1 | Mm_Celera | 1:59644602 | CTGCTATCCTAAGGA[A/G]ATAAAAGAAACATTG | 22218 |
rs32827283 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sumo1 | Mm_Celera | 1:59643823 | CATGTAGCTGAAGAT[A/G]ATCTGGAACATTTTA | 22218 |
rs32827395 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59658844 | AGTTGCTTCTTCCTG[G/T]AAGTATCTAGAGAGC | 22218 |
rs32827397 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Sumo1 | Mm_Celera | 1:59658763 | AGTTGGACAGTACTT[C/T]ATATGATAACTAGAA | 22218 |
rs32827399 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Sumo1 | Mm_Celera | 1:59658624 | AAGAAACTTTCTACT[A/C]CAAGATTCAGTCCAG | 22218 |
rs32828114 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59643334 | TTAAACACTGTACCT[A/G]AAACAAAACCACAAA | 22218 |
rs32828115 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sumo1 | Mm_Celera | 1:59642906 | CAAAAGAGATAGCTA[A/G]TTAAGGCACAGTAAT | 22218 |
rs32828117 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Sumo1 | Mm_Celera | 1:59642819 | GAAAATAAGGACCTG[A/T]ATATGCTTTCTAGCT | 22218 |
rs32828119 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Sumo1 | Mm_Celera | 1:59642591 | AAACATGAAAGGCTT[A/T]AGGAAATCTCATGTT | 22218 |
rs32828121 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Sumo1 | Mm_Celera | 1:59641949 | CACCTAGACAGCCAC[A/C]CATTTTCAAGAACTC | 22218 |
rs32828123 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Sumo1 | Mm_Celera | 1:59641456 | GTGTTTTAATAGTGA[C/T]CTTCTAACACAGAAG | 22218 |
rs47085635 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59667001 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 22218 |
rs47249046 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59666837 | AGGCACCAGGCATGT[A/G]CATGGTACATATACA | 22218 |
rs48093985 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59642314 | ACATGGTGGCTCACA[A/G]CTATCTGTAATGGAG | 22218 |
rs48573709 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59666953 | AATCCCAGCACTTGG[A/G]AGGCAGAGGCAGGTG | 22218 |
rs48574978 | snp | C/T | | | intron-variant | Sumo1 | Mm_Celera | 1:59642312 | ATGGTGGCTCACAAC[C/T]ATCTGTAATGGAGTC | 22218 |
rs50778290 | snp | A/C | | | intron-variant | Sumo1 | Mm_Celera | 1:59666745 | AGGACCTAGGTTCAG[A/C]TCCCAGTATCCACAT | 22218 |
rs50865790 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59643083 | TCTATTTAAGGGCTA[A/G]AGAAATAGCTCAGTG | 22218 |
rs51306774 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59642496 | TGGAACTCCCTAAAA[A/G]AAGGAAAAAGAAAGT | 22218 |
rs51959999 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59666854 | ATGGTACATATACAT[A/G]CATGTAAGCAGAGCA | 22218 |
rs52391273 | snp | C/T | | | intron-variant | Sumo1 | Mm_Celera | 1:59667028 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 22218 |
rs52513312 | snp | A/C | | | intron-variant | Sumo1 | Mm_Celera | 1:59668977 | CTTAAGCATTAACCC[A/C]AAAAAAAAAGAAAAA | 22218 |
rs107910737 | snp | A/G | | | intron-variant | Sumo1 | Mm_Celera | 1:59642309 | CACATGGTGGCTCAT[A/G]TGGTAATGGAGTCTG | 22218 |