SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3662056 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | GRCm38.p3 | 4:105105757 | CCATACTGGGTGGTA[A/G]TAGAAAGCGGGAGGC | 108079 |
rs6254985 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042237 | tctagacatatctaa[A/G]gagagggaatgttga | 108079 |
rs6255481 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042313 | tgattaacaattgat[A/G]ggagagggcctagcc | 108079 |
rs6255559 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042363 | tctggacaagtggtc[C/T]taacttgtaaaagaa | 108079 |
rs6256036 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042387 | aaaagaaagtaggcc[A/G]agtaagtcattagga | 108079 |
rs6256083 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042424 | caataaccagctcta[C/T]tccatggcctctacc | 108079 |
rs6256157 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042461 | tcctgcctccaggtt[C/T]ctgccctgacttccc | 108079 |
rs6256616 | snp | C/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042497 | gaaggaagtcacctg[C/G]aagtataggatgaaa | 108079 |
rs6257127 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042579 | gaaagcctaaGATAC[C/T]TAGCAATTCCTGAAG | 108079 |
rs6257649 | snp | G/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042693 | aaaaaaaaaaaTCAG[G/T]GCCTATTGTTTAATA | 108079 |
rs6257676 | snp | G/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105042714 | TTGTTTAATATTCCA[G/T]CTATCTGGAATGGCA | 108079 |
rs6302007 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105095970 | ttgagcagcaaccat[A/G]acacanactgaacga | 108079 |
rs6302012 | snp | A/G | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105095976 | agcaaccatnacaca[A/G]actgaacgatactcc | 108079 |
rs6302990 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105096131 | attgccagctccaga[C/T]agtcnttgttcacct | 108079 |
rs6302994 | snp | C/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105096136 | cagctccaganagtc[C/T]ttgttcacctctgac | 108079 |
rs6303026 | snp | G/T | 0.5 | 0 | intron-variant | Prkaa2 | Mm_Celera | 4:105096158 | acctctgacatttca[G/T]gatcgaggcctcctt | 108079 |
rs28133268 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105032884 | GTCTTAATGTTTCTG[C/T]TTAGCTTAGGCTCCT | 108079 |
rs28133269 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105032860 | ATACCCAATTCCCTA[A/G]CACAGAGGGTCTTAA | 108079 |
rs28133270 | snp | G/T | 0.165289 | 0.235211 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032810 | AATATTCTTGAATAC[G/T]TACTTGCATAAAGTA | 108079 |
rs28133271 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032761 | TTCCCTGAGTACAAA[C/G]TAGCTAAGAAAAGAG | 108079 |
rs28133272 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105032690 | ATAAAAATCTGATTC[A/G]GTTGTTTACGATTAT | 108079 |
rs28133273 | snp | G/T | 0.459184 | 0.136902 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032576 | GCTGTGGTATCTGTG[G/T]TAGGTATGTTCCAGG | 108079 |
rs28133274 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032569 | AGGCAGAGCTGTGGT[A/G]TCTGTGTTAGGTATG | 108079 |
rs28133275 | snp | G/T | 0.497041 | 0.0383476 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032563 | GTGACCAGGCAGAGC[G/T]GTGGTATCTGTGTTA | 108079 |
rs28133276 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105032418 | AACAGAGTTGCCAAG[A/T]ACTACTAAGCCATAA | 108079 |
rs28133277 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032339 | AGCTCTGTGTCCATC[C/T]CTTTCATTTTAGGGT | 108079 |
rs28133278 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032299 | GTAGTAAACAAGGCA[G/T]GACTTCAGAGCTCAG | 108079 |
rs28133279 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105032275 | GAACACTCACACTGA[C/T]GCTCTGAAGTAGTAA | 108079 |
rs28133280 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032256 | AAACAAATACATAAA[A/G]TGTGAACACTCACAC | 108079 |
rs28133281 | snp | C/T | 0.486111 | 0.0821678 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105032234 | AGGAAAAAACACTCA[C/T]ACTAGCAAACAAATA | 108079 |
rs28133282 | snp | A/C | 0.486111 | 0.0821678 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105031749 | CCAAATCATATAAAT[A/C]CAATTTCAGAAAAAA | 108079 |
rs28133283 | snp | C/T | 0.497041 | 0.0383476 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031643 | GGACTTTCAGAATCA[C/T]GTAGAGGGCCAGGGG | 108079 |
rs28133284 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105031614 | GGGCTAATTTTCCTC[G/T]ACAAAGAGCGCCTGG | 108079 |
rs28133285 | snp | G/T | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031529 | CACAAAATTAAAAAT[G/T]GCCAAAATGAAATTT | 108079 |
rs28133286 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031499 | CTGTATAAAAACAGT[A/G]TCATCTCATTTATGC | 108079 |
rs28133287 | snp | A/G | 0.473373 | 0.11227 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031412 | ATTAACTTAAGTTAC[A/G]TTTCCAAGTTTAAAA | 108079 |
rs28133288 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031261 | GGGGCCTGTTCCTCA[C/T]GGTATTACTGTTCAG | 108079 |
rs28133289 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031167 | CTGCAGTCTGATAAC[G/T]TCTGGATTGGACCTG | 108079 |
rs28133290 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105031133 | AGTAAACATTAATGT[C/T]GGCTCACAAAATACA | 108079 |
rs28133291 | snp | A/C | 0.152778 | 0.230321 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105030943 | TTTTTAAAACTGGAA[A/C]GAATATTATACCCTA | 108079 |
rs28133292 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105030767 | AAATAACAATGCAAC[A/T]CTTTCCTAGGAGGCT | 108079 |
rs28133293 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105030697 | AATGTGGTAACAAAC[C/T]TTATTTACAAGTGAC | 108079 |
rs28133294 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105030600 | GAAGGCACCAGGTAC[G/T]CTTTCTTTCTTTGTG | 108079 |
rs28133295 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105030558 | GCAGACTTGGAACAC[A/G]TTCACTTTGACTCTA | 108079 |
rs28133296 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105030444 | CTGTGAGGTTTGGTC[A/G]AGTAGAACTGAAAGG | 108079 |
rs28133297 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105030313 | ATATAAACACTGCTA[A/G]TAATTGCATTCATTT | 108079 |
rs28133298 | snp | A/C | 0.165289 | 0.235211 | utr-variant-3-prime | Prkaa2 | GRCm38.p3 | 4:105030241 | AACACACAGGGAATT[A/C]GATCCAATTAAGAGT | 108079 |
rs28133299 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105030082 | GTCTAGTAAAAAAGG[A/G]AGGATTGACACTGAG | 108079 |
rs28133300 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Prkaa2 | Mm_Celera | 4:105029913 | CAAAAGACAGATTCG[A/G]TATTTAAACATTTGA | 108079 |
rs28133301 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029825 | GAATATAGTTGTGAA[A/C]AGTTTTGACAGTTGT | 108079 |
rs28133302 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime, downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029721 | AAAAAAAACCACAAC[C/T]ATTCCTACCAAAATA | 108079 |
rs28133303 | snp | C/G | 0.142012 | 0.225474 | utr-variant-3-prime, downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029657 | CCTAGTATCTGCCAA[C/G]TTTCAGTTTTATTTT | 108079 |
rs28133304 | snp | G/T | 0.142012 | 0.225474 | downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029625 | AGTAATACACTACGT[G/T]ATGATCATGGACACA | 108079 |
rs28133305 | snp | A/C | 0.32 | 0.24 | downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029476 | ATTATAAAAAGTAGT[A/C]CCAATTTCAATAATT | 108079 |
rs28133306 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Prkaa2 | Mm_Celera | 4:105029207 | TGTGGAAAATGCAGA[C/T]GCGCAATTAGACAGG | 108079 |
rs28152753 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105101018 | TTTAACTAATTTTTC[G/T]GCAAAATATTTTCCC | 108079 |
rs28152754 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Prkaa2 | Mm_Celera | 4:105100875 | TCTTGTATTTGGATC[A/G]ACATATGGTAAGCTG | 108079 |
rs28152755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105100825 | CATCTCATTTGCTTA[A/G]ACAGAAAAGGTACAA | 108079 |
rs28152756 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105100670 | CACTTAAGCAAGGAG[A/G]CTGCTCCCTTGAAAG | 108079 |
rs28152757 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105100640 | ATCAGAGGCCAGCAC[C/T]ACCTAACAAGTCCCC | 108079 |
rs28152758 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Prkaa2 | Mm_Celera | 4:105100491 | TAACATTTGGGATTT[A/T]AAAAAAATGCAACTT | 108079 |
rs28152759 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Prkaa2 | Mm_Celera | 4:105100475 | TACTAACTAAGCACA[A/T]TAACATTTGGGATTT | 108079 |
rs28152760 | snp | C/G | 0.32 | 0.24 | intron-variant | Prkaa2 | GRCm38.p3 | 4:105100245 | TGTACCAATAGAACT[C/G]TACAAGCAAAGTAAG | 108079 |
rs28152761 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prkaa2 | GRCm38.p3 | 4:105100229 | GAAAACCAAAACAAC[A/G]TGTACCAATAGAACT | 108079 |
rs28152762 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105100051 | AAATTAGTAAGTCAG[C/T]TGTGTGTAGTAGTGT | 108079 |
rs28152763 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105099991 | AGACATTAACTATGC[A/G]TCAAGAATCATTTAA | 108079 |
rs28152764 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105099949 | CGACTCTGAGAGACG[A/G]TGGGCTCATCAGATG | 108079 |
rs28152765 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105099902 | AGCAGTCCACAGAGC[A/G]CTGAAACAGACTATA | 108079 |
rs28152766 | snp | A/C | 0.32 | 0.24 | intron-variant | Prkaa2 | Mm_Celera | 4:105099832 | ACCATGAAAAAACGT[A/C]AATTTTTGTAGCTGC | 108079 |
rs28152767 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105099771 | AAGGACAGTTGTTCA[C/G]CAGTGATAAACCATC | 108079 |
rs28167468 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105099760 | CTAACTTCTTTAAGG[A/G]CAGTTGTTCAGCAGT | 108079 |
rs28167469 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105099255 | AGTTGTCTCAAATAG[C/T]TTTTTGCCATCCTAA | 108079 |
rs28167470 | snp | C/T | 0.32 | 0.24 | intron-variant | Prkaa2 | Mm_Celera | 4:105098979 | TAATGTGTCTCTGCA[C/T]ATCTATTTTCCAGCT | 108079 |
rs28167471 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105098824 | ATGCGGTCACACGGC[A/G]CACCTTCAGACCTCT | 108079 |
rs28167472 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Prkaa2 | Mm_Celera | 4:105098771 | TTCCAAATGCATTTT[A/C]AGCTGCATCCCTGTC | 108079 |
rs28167473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098749 | GTTATGGCGACTTTT[C/T]TTTTTTTTCCAAATG | 108079 |
rs28167474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098707 | CCCACACTGTGGTTC[C/T]GTGCAGCCATCCCCA | 108079 |
rs28167475 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098703 | CTGACCCACACTGTG[C/G]TTCCGTGCAGCCATC | 108079 |
rs28167476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098621 | ACAACCACCAAACCC[A/G]AGTAAATGAGTCAAT | 108079 |
rs28167477 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098619 | GTACAACCACCAAAC[A/C]CGAGTAAATGAGTCA | 108079 |
rs28167478 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105098561 | TGATCAAGTTGGCAA[A/G]AGCATCATCATAGGG | 108079 |
rs28167479 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105098516 | GACATGTCAATAACA[C/T]GAGGAAAAAATGTAT | 108079 |
rs28167480 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Prkaa2 | Mm_Celera | 4:105098038 | GCTGAACACTGTATA[G/T]GAACACCTGTAGAGA | 108079 |
rs28167481 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prkaa2 | Mm_Celera | 4:105097778 | GGATATTTACCTCTG[A/G]CCTGCATCATTCACT | 108079 |
rs28167482 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105097293 | CCACATAATATTAGT[C/T]CAATGGCAATAAGCT | 108079 |
rs28167483 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105097161 | GAGTGTATGCAGTTA[G/T]TTTTCATTCTTTCAA | 108079 |
rs28167484 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Prkaa2 | Mm_Celera | 4:105097149 | TTTTCATCATGTGAG[A/T]GTATGCAGTTATTTT | 108079 |
rs28167485 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105097067 | GTTCAGTATATTCAC[A/G]TTCACATTGAGTATA | 108079 |
rs28167486 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105097005 | ACACTCAAATTGAAA[C/T]TGGAGACATAAAAGC | 108079 |
rs28167487 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prkaa2 | GRCm38.p3 | 4:105096660 | ACTAAATCCTATCAC[A/G]TGCATGCTTCTCATT | 108079 |
rs28167488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prkaa2 | Mm_Celera | 4:105094409 | CATATTTAACTCTCC[A/G]AGCTCTATAGGGCAG | 108079 |
rs28167489 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105094338 | AAGATACTTCTAACA[C/T]GGAAGCAGAGAGTTT | 108079 |
rs28167490 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Prkaa2 | Mm_Celera | 4:105092257 | TGACTACCAGCACTC[A/G]TATAAGGAAGGACTA | 108079 |
rs28167491 | snp | C/G | 0.32 | 0.24 | intron-variant | Prkaa2 | GRCm38.p3 | 4:105092184 | TGACCACAGGATGCT[C/G]CCGGGATGCCAATAC | 108079 |
rs28167492 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Prkaa2 | Mm_Celera | 4:105092138 | AATTATAGCGGGGAG[A/G]AGGTTCAGTTGGAAT | 108079 |
rs28167493 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prkaa2 | Mm_Celera | 4:105091789 | GAGATGGTCTTAATG[A/G]CAAACTCTGAAATAG | 108079 |
rs28167494 | snp | A/T | 0.375 | 0.216506 | intron-variant | Prkaa2 | Mm_Celera | 4:105090051 | AAAGGTATTTAATAA[A/T]CTTGAACATCTCTTA | 108079 |
rs28167495 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prkaa2 | Mm_Celera | 4:105087357 | ATAAAATACCCTGCC[A/G]TTGAAATGTTATGGT | 108079 |
rs28167496 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Prkaa2 | Mm_Celera | 4:105087000 | ATAGTTATCACTGAA[A/G]AATGAACTTGCATTT | 108079 |
rs28167497 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Prkaa2 | Mm_Celera | 4:105085669 | CTCAATCACCCTACA[C/G]CTACTTACCTACCTT | 108079 |