SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8266471 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711108 | ACCCCCTTCTCACAA[C/T]NTTCCTCCCCGNCCC | 17246 |
rs8266472 | in-del | -/CC | 0.124444 | 0.216185 | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711107 | CCCCCTTCTCACAAN[-/CC]TTCCTCCCCGNCCCA | 17246 |
rs8266473 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Mdm2 | GRCm38.p3 | 10:117711097 | ACAATTTCCTCCCCG[C/T]CCCACTCCACCCTCT | 17246 |
rs8266474 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mdm2 | GRCm38.p3 | 10:117709610 | GATTATCGCACAGTC[A/G]TTTTAAGTATTTACC | 17246 |
rs8266475 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117709573 | CTCTTAACTTTCTCG[A/G]TTGCAATTGCATTAG | 17246 |
rs8266476 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mdm2 | GRCm38.p3 | 10:117709469 | TGCTGCTGGTTGTGA[A/C]ATGATGTTCTATCAC | 17246 |
rs8266477 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117701310 | TGGTCTACTTTTTAC[A/G]TGGGTTCTGGTATCC | 17246 |
rs8266478 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117701233 | ACATCTTACCAGTCC[C/T]CTAATCATGTTTTAA | 17246 |
rs8266479 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117703681 | GTGCAGTAGGTCAGC[A/T]GTCCTCCTGCTCTCT | 17246 |
rs8266480 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117703650 | GCGGGGAGTTGGCTT[C/T]AGGACACTGCCTGCC | 17246 |
rs8266481 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117703619 | AAGTCTCTTACTTAA[A/G]CCNTGAAACTGTCTC | 17246 |
rs8266482 | snp | A/G | 0.18 | 0.24 | intron-variant | Mdm2 | GRCm38.p3 | 10:117703616 | TCTCTTACTTAANCC[A/G]TGAAACTGTCTCTGT | 17246 |
rs8266500 | snp | A/G | 0.32 | 0.24 | intron-variant | Mdm2 | GRCm38.p3 | 10:117703368 | AAGATCTTTATTCTA[A/G]GACACTTGAGAATGT | 17246 |
rs8266501 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692555 | TGTCTGTCAGCCTTT[C/T]AGTAAGATGAAGAGG | 17246 |
rs8266502 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692537 | TAAGATGAAGAGGCC[A/G]TCTANTCAGAGTCTC | 17246 |
rs8266503 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692532 | TGAAGAGGCCNTCTA[G/T]TCAGAGTCTCTGNAA | 17246 |
rs8266504 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Mdm2 | Mm_Celera | 10:117692519 | TANTCAGAGTCTCTG[C/G]AAAGNCTTGCTTTTT | 17246 |
rs8266505 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692514 | AGAGTCTCTGNAAAG[G/T]CTTGCTTTTTCATTT | 17246 |
rs8266506 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692454 | TGAGGTGAAATTTTA[G/T]AGtttctttgcttga | 17246 |
rs8266507 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117692351 | cactagatatggtta[C/T]tagccaccatgtggt | 17246 |
rs8266508 | snp | G/T | 0.165289 | 0.235211 | missense | Mdm2 | GRCm38.p3 | 10:117696043 | TGTACTTAGGATCCT[G/T]TGCAAGCGCCACCAG | 17246 |
rs8266509 | snp | A/G | 0.152778 | 0.230321 | missense | Mdm2 | GRCm38.p3 | 10:117696001 | TCATCTTCTGATTTA[A/G]TTTCTAGACTGTCTA | 17246 |
rs8266510 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695882 | gtcaaatgacccttt[G/T]acagaggtctgagac | 17246 |
rs8266511 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695844 | cactgaaaaccacat[A/G]gttgcattatgattc | 17246 |
rs8266512 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695807 | ttagcaaaactatgg[C/T]tatgaagtagcaatg | 17246 |
rs8266513 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695790 | atgaagtagcaatga[A/G]aatagttttatgctt | 17246 |
rs8266514 | snp | A/G | 0.235537 | 0.249581 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695726 | tcacagtgccgggcg[A/G]tggtggctctcatct | 17246 |
rs8266515 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117695705 | gctctcatctttaat[C/G]cagcacttgggaggc | 17246 |
rs8266516 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695665 | cggatttctgagttc[A/G]aggccagcctggtct | 17246 |
rs8266517 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695633 | cagagtgagttccag[A/G]acagccaggggtata | 17246 |
rs8266518 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695565 | tcacagtgttaggaa[A/G]gttaagagctgctAC | 17246 |
rs8266519 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695399 | CTCTGCTGCTCTTAA[C/T]CACTGAGCNGTTTCA | 17246 |
rs8266520 | snp | C/T | 0.32 | 0.24 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695390 | TCTTAANCACTGAGC[C/T]GTTTCACCAGCCCAG | 17246 |
rs8266521 | snp | A/G | 0.18 | 0.24 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695327 | ATCGTGTACTGTTGA[A/G]TCAGTAAAAGCACTA | 17246 |
rs8266522 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695272 | GAGGTAACGTCCACA[A/G]AGAAGGTTGCAAGCT | 17246 |
rs8266523 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Mdm2 | Mm_Celera | 10:117695248 | GCAAGCTTAGAAGTA[A/G]AGCTTATGTGTAGCT | 17246 |
rs8266524 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Mdm2 | GRCm38.p3 | 10:117695109 | AATCTCAAATCAGTC[A/C]CAGTACAGGGAGTTT | 17246 |
rs8266525 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Mdm2 | Mm_Celera | 10:117688761 | aacagatggttgtga[C/G]ccnccatgtggtggc | 17246 |
rs8266526 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Mdm2 | Mm_Celera | 10:117689399 | GGCACAAGTGTTGCA[G/T]TTTGTCCCAGGTAAA | 17246 |
rs8266527 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | Mdm2 | Mm_Celera | 10:117689194 | TACTCTCCTGGTTCA[A/T]AATACGCCTCTTCCC | 17246 |
rs8266528 | in-del | -/T | 0.132653 | 0.220748 | frameshift-variant | Mdm2 | Mm_Celera | 10:117690559 | TCCTCGCTGTCCTCC[-/T]NAGCACATGGCTCTT | 17246 |
rs8266529 | in-del | -/C | 0.132653 | 0.220748 | frameshift-variant | Mdm2 | Mm_Celera | 10:117690560 | CCTCGCTGTCCTCCN[-/C]AGCACATGGCTCTTT | 17246 |
rs13473213 | snp | A/G | 0.231111 | 0.249285 | missense | Mdm2 | Mm_Celera | 10:117690549 | TGCTGAGGAGGACAG[A/G]GAGGAGAAGGCCGAA | 17246 |
rs16794342 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Mdm2 | GRCm38.p3 | 10:117693162 | GCTTCAGATAATAGT[A/G]GGTGTGCATATAATC | 17246 |
rs29337394 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Mdm2 | GRCm38.p3 | 10:117689582 | CGTGTGTGTGCGTGC[A/G]TGCGTGCATCCATTT | 17246 |
rs29365202 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Mdm2 | Mm_Celera | 10:117700767 | CAGAACTGCACTCTA[C/T]GAAGAAGTATACATC | 17246 |
rs29382981 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Mdm2 | GRCm38.p3 | 10:117711558 | CTATTGGGTCCATCT[C/T]TAGGGACATTCCATT | 17246 |
rs45637694 | snp | A/G | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711490 | CAAGTGAGTTTGCAG[A/G]CCTGACATAAAGCAT | 17246 |
rs45708621 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mdm2 | Mm_Celera | 10:117697396 | TGATTCAGTGGAGGA[A/G]GCCTCAGTTAGCATG | 17246 |
rs45916336 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117702006 | CAGCTGGTACTTCTT[G/T]AAGATGTTTTTTATG | 17246 |
rs45917585 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711966 | ACAGCCGTCTGGGTC[C/T]ACCTTTTAAGGTACA | 17246 |
rs46305730 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Mdm2 | Mm_Celera | 10:117698604 | AAAGAGCCTTAGCAG[A/G]TCCCAGTAACCTCAG | 17246 |
rs46481751 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Mdm2 | Mm_Celera | 10:117695716 | GCTGGATTAAAGATG[A/T]GAGCCACCATCGCCC | 17246 |
rs46490015 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117701978 | CTGACAGAGGTGAGA[A/C]ACAGTGACCGCCCAG | 17246 |
rs46680695 | snp | A/C | 0.444444 | 0.157135 | utr-variant-5-prime | Mdm2 | Mm_Celera | 10:117710653 | GCTCGAGCGACGAGA[A/C]GGCGGCGGCTCCTCA | 17246 |
rs46716377 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117704070 | TTAACCTAAGTGAGC[A/C/G]AGAGAAACACTTATA | 17246 |
rs46944025 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Mdm2 | GRCm38.p3 | 10:117690774 | ATTGCATGAGGTACA[C/T]TTCCAATAGTCCTTC | 17246 |
rs46967389 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mdm2 | Mm_Celera | 10:117693786 | GTATGCCTTTAATCC[C/T]AGCATTCATTCAGGA | 17246 |
rs47016137 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mdm2 | Mm_Celera | 10:117696469 | AGAAAGTAAAAAGTG[A/G]ATCAAAACAAAGAAA | 17246 |
rs47148639 | snp | A/G | | | intron-variant | Mdm2 | Mm_Celera | 10:117696276 | CAGCTCCAGGTGAGC[A/G]TCACCTCTTTCTTTT | 17246 |
rs47150143 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117708816 | GGAAAGGAAGAGCGA[C/G]AGTAAATAGAGAGAG | 17246 |
rs47228018 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117706306 | CCAGCTTTCCCAGTA[A/G]TGAGACAATAGTTGA | 17246 |
rs47425383 | snp | C/T | 0.21875 | 0.248039 | synonymous-codon | Mdm2 | Mm_Celera | 10:117694911 | AAGCACTACCTGATG[C/T]GAGGGCGTCTCTGTG | 17246 |
rs47457385 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Mdm2 | GRCm38.p3 | 10:117689456 | TGCTGGAAAATAAGG[C/T]GTGTGTTTTCACTTA | 17246 |
rs48075269 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117706625 | TGGCAGCCTGACAAC[A/G]GATACCAAGGAACAC | 17246 |
rs48146064 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Mdm2 | Mm_Celera | 10:117690112 | TATGTGGACTAAGAC[A/T]GTTTTCTGGCTTTAA | 17246 |
rs48316848 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117703957 | AAAGGACACTTGGGT[C/T]CCTCCAACAAAGTGT | 17246 |
rs48467683 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mdm2 | Mm_Celera | 10:117691540 | CTATTGGACACTGTT[C/T]GTTGCATGCTTTACA | 17246 |
rs48607587 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117702956 | AAGACAGGACATCAT[C/G]AGTAACATCTCCCAA | 17246 |
rs48612029 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mdm2 | Mm_Celera | 10:117693047 | ACTAACTTTTTCTCA[A/G]TAAGATAATCTGAGT | 17246 |
rs48811512 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mdm2 | Mm_Celera | 10:117695505 | ATATAGAAGCCCTGT[C/T]CCAAAACAAAGAACA | 17246 |
rs48847820 | snp | C/T | | | intron-variant | Mdm2 | GRCm38.p3 | 10:117705732 | AGCACTGACTCCTTC[C/T]TACAGCTCCATCATC | 17246 |
rs48977510 | snp | A/C | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711274 | TGCAGGGTACTCAAC[A/C]CACTCTTCTGGTCTC | 17246 |
rs49174226 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Mdm2 | Mm_Celera | 10:117692785 | ATTGCCTCTGGGCCT[C/G]ATTTAGAGCTCCCGG | 17246 |
rs49221941 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mdm2 | Mm_Celera | 10:117698186 | ATCCAAGTTCCAGAA[C/T]TGGAATGGACAAAAT | 17246 |
rs49461624 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Mdm2 | Mm_Celera | 10:117689040 | ACCCACCGCCTCCTA[G/T]TCAAATGCTGTCACG | 17246 |
rs49496215 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117712227 | TGGGGCTTGCCACTT[C/T]TTACTGACAGCCTTC | 17246 |
rs49633859 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mdm2 | Mm_Celera | 10:117698849 | AACGGTAAGGATTAC[A/G]GGGTTTCAGAGCCCA | 17246 |
rs49852794 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mdm2 | Mm_Celera | 10:117701844 | CACACACACACAATC[A/G]AAACTAAGATTCCAG | 17246 |
rs50011600 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117703696 | AGCTGACCTACTGCA[C/T]ACAGCTTAGCATAAG | 17246 |
rs50016811 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711203 | GCTCCATGGTCAAGA[A/G]TGCATACAGCTCCTT | 17246 |
rs50234729 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117708408 | AAGCAAGAAGTTCTA[C/T]ATTTTTGCATATTAA | 17246 |
rs50250342 | snp | C/T | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711241 | TTTCAGTCACTCACG[C/T]CACACAAATTCTGTC | 17246 |
rs50256766 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117704118 | TTCTGTCTACAACTG[A/C]CCAACCTCTAGCTGA | 17246 |
rs50306476 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117691524 | AAGAGATACTCGGGT[C/T]CTATTGGACACTGTT | 17246 |
rs50404571 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117706572 | ACTGTCACCTACCTA[A/G]CAAGGTGTCACCCAC | 17246 |
rs50439978 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mdm2 | Mm_Celera | 10:117693317 | CCTTAGTTGGCCTGG[A/G]GCCTCATGTGACACT | 17246 |
rs50440159 | snp | A/G | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711136 | GGTGTCCCAGAAGGG[A/G]ACGGAGAGCGGGGTG | 17246 |
rs50695747 | snp | A/G | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711285 | CAACACACTCTTCTG[A/G]TCTCCATGAGCAACC | 17246 |
rs50796237 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Mdm2 | GRCm38.p3 | 10:117689095 | CTCTGAAGCTTTAAC[A/G]CAACATTAATACAAA | 17246 |
rs50843733 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mdm2 | Mm_Celera | 10:117701708 | ACACCCACAGACTAA[C/T]GACTCGACCTGTCTC | 17246 |
rs51228165 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mdm2 | Mm_Celera | 10:117701346 | GCCAAGCTGTTTTTT[C/G]ACTTCCAGGTATACA | 17246 |
rs51276817 | snp | A/T | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711343 | ATTAAAGTTAAAATT[A/T]AAAAAAAAAATTCAA | 17246 |
rs51908959 | snp | A/G | | | upstream-variant-2KB | Mdm2 | Mm_Celera | 10:117711133 | GGGGGTGTCCCAGAA[A/G]GGAACGGAGAGCGGG | 17246 |
rs52683103 | snp | A/T | | | intron-variant | Mdm2 | Mm_Celera | 10:117706071 | CTCTCTCTCTCTCTC[A/T]CTCACACACACACAC | 17246 |
rs52683105 | snp | A/T | | | intron-variant | Mdm2 | Mm_Celera | 10:117706073 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 17246 |
rs211846890 | snp | C/T | | | intron-variant | Mdm2 | Mm_Celera | 10:117703773 | ACTACTAAATCCATA[C/T]TTGTTTATCATTTGT | 17246 |
rs211852694 | snp | A/G | | | intron-variant | Mdm2 | Mm_Celera | 10:117702904 | TAGTGACATGTCACA[A/G]ACGTATACTTCTACA | 17246 |
rs211909950 | snp | A/G | | | synonymous-codon | Mdm2 | Mm_Celera | 10:117692630 | GTCACTCAGGCTGTA[A/G]TCTTCCGAGTCCAGA | 17246 |
rs212084329 | snp | C/T | | | intron-variant | Mdm2 | Mm_Celera | 10:117693270 | GTGACGACACACAAA[C/T]ACCAAGCTGGCATCT | 17246 |