SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13460498 | snp | C/T | 0.231111 | 0.249285 | utr-variant-5-prime, upstream-variant-2KB | Trp53, Wrap53 | Mm_Celera | 11:69580480 | GCCCTCATCCTCCTC[C/T]TTCCCAGCAGGGTGT | 216853 |
rs13469311 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579169 | TTTCCGGAAGAGGAA[A/G]GCGGACTCCGGTCTC | 216853 |
rs13469312 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | Wrap53 | GRCm38.p3 | 11:69563338 | CTTTTCCACATCCAG[A/G]CCTGGCAGAGACTGT | 216853 |
rs26922527 | snp | G/T | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Trp53, Wrap53 | Mm_Celera | 11:69582055 | CTCTCTTGTGAATGT[G/T]AAAAGATCCCAACCC | 216853 |
rs26922528 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Trp53, Wrap53 | Mm_Celera | 11:69581987 | CAGGGATGCCTTCTT[A/G]TGCAAATAGCCTCCC | 216853 |
rs26922529 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Trp53, Wrap53 | Mm_Celera | 11:69581881 | CTAGATCCTCCAGTT[C/T]ATTGAGAAAGTATAC | 216853 |
rs26922530 | snp | G/T | 0.18 | 0.24 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Trp53, Wrap53 | Mm_Celera | 11:69581234 | CATTTCCGGTTTCTT[G/T]TTTTCGGAGCAGATC | 216853 |
rs26922532 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69580217 | CGTTCCTGCTGAGGG[C/T]AACATCTCAGGGAGA | 216853 |
rs26922533 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69580166 | TCCACCCATTTTGCC[C/T]TCACAGCTCTATATC | 216853 |
rs26922534 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69580074 | AGCTCAGAACAGTGG[C/T]GGTCCACTTACGATA | 216853 |
rs26922535 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579834 | GATACCAAGTATCTC[A/G]GAGAACACGTTAGAT | 216853 |
rs26922536 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579332 | CTCCGATTCCGAGCG[A/G]GAAGGCGGGAAGGAA | 216853 |
rs26922537 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579146 | ATTACCGTTCCCAGG[A/G]ATGCTCAGAGACCGG | 216853 |
rs26922538 | snp | C/G | 0.18 | 0.24 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579085 | CGGAAGGCAGAGGTC[C/G]GGCAAGTCTCGCTGA | 216853 |
rs26922539 | snp | A/G | 0.165289 | 0.235211 | upstream-variant-2KB, missense, nc-transcript-variant | Trp53, Wrap53 | Mm_Celera | 11:69579045 | AGTCGCTCCTCCGAC[A/G]TCTTCATTCTGTAGA | 216853 |
rs26922540 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wrap53 | Mm_Celera | 11:69578073 | AACCTCGGTATCACC[C/T]GTAGTCTATTGCTCC | 216853 |
rs26922541 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Wrap53 | Mm_Celera | 11:69577808 | GTGCGAGGGCCATGG[C/G]TAGCCTCTGAGTCCC | 216853 |
rs26922542 | snp | C/T | 0.265928 | 0.249492 | missense, nc-transcript-variant | Wrap53 | GRCm38.p3 | 11:69577708 | ACATTATCAGCACTA[C/T]TGGTCAAGATACAGG | 216853 |
rs26922543 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wrap53 | Mm_Celera | 11:69577064 | GGGTGCACTGTAGCT[C/T]GCCACAGGCTGAGGT | 216853 |
rs26922544 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69576516 | ATCTGTATGACCAAG[A/G]TAAGGCCAGACGCTT | 216853 |
rs26922545 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wrap53 | Mm_Celera | 11:69574688 | TACTTCCTTGGAACC[A/G]CAGCCATTCCCCTCA | 216853 |
rs26922546 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69574152 | TGGGAACCTTCCCAA[G/T]AAACACGTTTTGGAT | 216853 |
rs26922547 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Wrap53 | GRCm38.p3 | 11:69574119 | AAGCAGCACTGAAAG[C/G]CCCTGGTTGAAGATG | 216853 |
rs26922548 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wrap53 | Mm_Celera | 11:69574084 | AAGCAGGGCTGACAG[A/G]AGGACGCTCCTTCAG | 216853 |
rs26922549 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69573986 | CCAGGATGCTATAAA[A/G]TCACCACGGTCTTTA | 216853 |
rs26922550 | snp | A/G | 0.5 | 0 | intron-variant | Wrap53 | GRCm38.p3 | 11:69573945 | TGGTGCAGAGCCCCA[A/G]TTCCTACTTTATGGA | 216853 |
rs26922551 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wrap53 | Mm_Celera | 11:69572100 | CTGTTGTCTTTATTA[C/T]TGCTGTATGTGTCTA | 216853 |
rs26922552 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Wrap53 | GRCm38.p3 | 11:69570999 | CAAGAGCGGATCTGC[A/G]GGCGCTGGATTATGG | 216853 |
rs26922553 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Wrap53 | Mm_Celera | 11:69569893 | CTTCGCACCAAAGCA[C/T]TGCAGGCCTGGCAGG | 216853 |
rs26922554 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wrap53 | Mm_Celera | 11:69569630 | CAGGAATCAAAACCA[C/T]GTACCAAATGGTTAG | 216853 |
rs26922555 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wrap53 | Mm_Celera | 11:69569296 | CACCGTAGCGTGTGG[A/G]AATACCCACTCCAAT | 216853 |
rs26922556 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Wrap53 | Mm_Celera | 11:69569290 | GTGGCCCACCGTAGC[G/T]TGTGGGAATACCCAC | 216853 |
rs26922557 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Wrap53 | Mm_Celera | 11:69569058 | AAATTTCATATAAAA[A/C]CCTGCCTCAGCTTTT | 216853 |
rs26922558 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69568880 | GAACAAGTTCACACA[C/T]AGACTGCTAACAGCA | 216853 |
rs26922559 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wrap53 | Mm_Celera | 11:69568555 | TGAGCAAGCACACTG[C/T]CCCCCGAGACACAGT | 216853 |
rs26922560 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69568494 | AGTTGTCTAATGGTG[A/G]AAGCTCAGACAGAGG | 216853 |
rs26922561 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Wrap53 | Mm_Celera | 11:69568156 | GAAGGGCCTATAGTT[C/T]ACACAGGTATATGAA | 216853 |
rs26922562 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wrap53 | Mm_Celera | 11:69568073 | TCAGGAAATAGGATG[C/T]GGAGCTAAGAGTTCT | 216853 |
rs26922563 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wrap53 | Mm_Celera | 11:69567920 | CTCACAAGTAGGAAA[C/T]TGGAAAGACTTTGTG | 216853 |
rs26922564 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Wrap53 | Mm_Celera | 11:69567855 | CTGACTTAACTATCT[G/T]AGGCCACAAAGATGA | 216853 |
rs26922565 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wrap53 | Mm_Celera | 11:69567831 | GATTACCGGATGAGA[C/T]TCTGGCTTCTGACTT | 216853 |
rs26922566 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wrap53 | Mm_Celera | 11:69567687 | ATATGGAGACAGGCA[A/G]CACTGTTAGGAATAT | 216853 |
rs26922567 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Wrap53 | Mm_Celera | 11:69567429 | CTAGGGCAAGCTCAC[A/G]GGCTTACGTGGTTAT | 216853 |
rs26922568 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Wrap53 | Mm_Celera | 11:69567300 | CCACCTCTGAAAAGC[C/T]GTCCACACCCTCGCA | 216853 |
rs26922569 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Wrap53 | Mm_Celera | 11:69567287 | AGCCTAGGTGTTTCC[A/T]CCTCTGAAAAGCTGT | 216853 |
rs26922570 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Wrap53 | Mm_Celera | 11:69566934 | TCTATTGAGCATGTC[C/G]ATTGATAATCACAAT | 216853 |
rs26922571 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Wrap53 | Mm_Celera | 11:69566817 | TCATTCTCCTGCAGC[A/G]GTATTTTAGAGACTC | 216853 |
rs26922572 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wrap53 | Mm_Celera | 11:69566198 | TCTACTGATCCTTAG[A/C]GGACCCAGCACCTGC | 216853 |
rs26922573 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wrap53 | Mm_Celera | 11:69566172 | CTTAGATTCCCACGG[A/G]CACCTCAGACTCTAC | 216853 |
rs26922574 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wrap53 | Mm_Celera | 11:69565910 | CGTAATCCTGTTTAA[A/T]AGTCCTTCCTACAGA | 216853 |
rs26922575 | snp | A/G | 0.32 | 0.24 | intron-variant | Wrap53 | Mm_Celera | 11:69565708 | ATTGGTGAAATCAAA[A/G]AAGACCTTACAAAGG | 216853 |
rs26922576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wrap53 | Mm_Celera | 11:69565673 | GTGCACAGGGTGACA[A/G]CTTAGAAAATGAAGT | 216853 |
rs26922577 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wrap53 | Mm_Celera | 11:69565630 | GTGACTCTAGGTTCC[C/T]GTCAGGTTGGCAGCT | 216853 |
rs26922578 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wrap53 | Mm_Celera | 11:69565601 | CTTTGGCTTCATATA[C/T]GGCTCATTCATGGGT | 216853 |
rs26922579 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Wrap53 | GRCm38.p3 | 11:69565485 | GCTATGTCCGTGCCC[A/G]GCTATTCTGCTCACT | 216853 |
rs26922580 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Wrap53 | GRCm38.p3 | 11:69564236 | TTAGCCTGCTTCTGC[C/T]TGGCTGGAGAAGGAA | 216853 |
rs26922581 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Wrap53 | GRCm38.p3 | 11:69563879 | GGTGTCTGGCTGGGT[A/G]GAGGACATCAGAGAA | 216853 |
rs26922582 | snp | C/T | 0.32 | 0.24 | intron-variant | Wrap53 | Mm_Celera | 11:69563845 | AAGTGCACAGGAGGG[C/T]CATTACCACTTACTA | 216853 |
rs26922583 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Wrap53 | Mm_Celera | 11:69563665 | CGGATGCTCAGACCT[C/G]GCTCTGACTGTCAAA | 216853 |
rs26922584 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wrap53 | Mm_Celera | 11:69563613 | CCAGATGTGAATCGG[A/G]TTCTCCCGGCTGCTG | 216853 |
rs26922585 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wrap53 | Mm_Celera | 11:69563508 | AGGAGGGCTGGGCCA[C/T]GGCGAGCACAGGGCT | 216853 |
rs26922586 | snp | C/T | 0.32 | 0.24 | intron-variant | Wrap53 | Mm_Celera | 11:69563469 | CTGGAGACAGGCCTG[C/T]AAAGTTTCAGTTGTC | 216853 |
rs26922587 | snp | C/G | 0.32 | 0.24 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | Wrap53 | Mm_Celera | 11:69563413 | CGGGGAGAAACAGAG[C/G]GAGTGGGCTGCTGTC | 216853 |
rs26922588 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wrap53 | Mm_Celera | 11:69563132 | TCAGTGGTACAATGC[C/T]TGTCTAACCCAACAG | 216853 |
rs26922589 | snp | A/C | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Wrap53 | Mm_Celera | 11:69562972 | TCACAAGCAATCTGA[A/C]GATCTCGTATGGTTC | 216853 |
rs26922590 | snp | A/C | 0.124444 | 0.216185 | missense, upstream-variant-2KB, nc-transcript-variant | Wrap53, Efnb3 | Mm_Celera | 11:69562442 | GTCACTTCCCGACTC[A/C]GAGACCACAGGAGGT | 216853 |
rs26922591 | snp | C/T | 0.33241 | 0.236027 | intron-variant, upstream-variant-2KB | Wrap53, Efnb3 | Mm_Celera | 11:69562323 | GAAGCCATTCCTATG[C/T]AGTGGCCTAGACCCC | 216853 |
rs26922592 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Wrap53, Efnb3 | Mm_Celera | 11:69562308 | ATGACCCTTGGGGTA[A/G]AAGCCATTCCTATGT | 216853 |
rs26922593 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Wrap53, Efnb3 | Mm_Celera | 11:69562301 | GACAGGCATGACCCT[C/T]GGGGTAGAAGCCATT | 216853 |
rs26922594 | snp | C/T | 0.265928 | 0.249492 | intron-variant, upstream-variant-2KB | Wrap53, Efnb3 | Mm_Celera | 11:69562270 | CGCTCCTGGGAAAGA[C/T]GGGAGATTTGTAGCA | 216853 |
rs26922595 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, missense, nc-transcript-variant | Efnb3, Wrap53 | GRCm38.p3 | 11:69562195 | TGTCGTCACTAAGAG[C/T]TCCACTGATATCCCA | 216853 |
rs26922596 | snp | A/G | 0.415225 | 0.187619 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | Efnb3, Wrap53 | GRCm38.p3 | 11:69561938 | CTCCAGCTCCAGCTC[A/G]CCTTCATCCCCGCTA | 216853 |
rs26922597 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | Efnb3, Wrap53 | Mm_Celera | 11:69561830 | CTTTTCATCCTGGTC[A/G]TCAACAGGGCTACTG | 216853 |
rs26922598 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, downstream-variant-500B | Efnb3, Wrap53 | Mm_Celera | 11:69561698 | AGACCCCACAGATGC[C/T]GGACAAAGGAACCTA | 216853 |
rs26922599 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B | Efnb3, Wrap53 | Mm_Celera | 11:69561523 | TCAGGAGTGAGATTT[C/T]AAACAGGTTTGCTCC | 216853 |
rs26922600 | snp | A/G | 0.465374 | 0.126941 | upstream-variant-2KB, downstream-variant-500B | Efnb3, Wrap53 | GRCm38.p3 | 11:69561376 | CTGCAGCTGCATGAT[A/G]GTAAACAGGGCGGTG | 216853 |
rs29383587 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Trp53, Wrap53 | GRCm38.p3 | 11:69581952 | AGCTGTGAAGGTTAG[A/T]CTGGACAGCCACAGC | 216853 |
rs29385241 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wrap53 | Mm_Celera | 11:69564021 | CCTGGGGAGAGCTAA[A/G]GCCCAGGGGGAGACT | 216853 |
rs29387468 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, downstream-variant-500B | Efnb3, Wrap53 | Mm_Celera | 11:69561651 | CTGCCTGGTCCCACC[C/T]CTCAGCCCCTTGGTT | 216853 |
rs29388844 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Efnb3, Wrap53 | GRCm38.p3 | 11:69562066 | TTCAAGATAATACCC[A/G]AGAAACCCACCTTCC | 216853 |
rs29389704 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69564826 | GACAGAAGCTGTAGC[C/T]GGGGTGGGTAGGACG | 216853 |
rs29389978 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wrap53 | Mm_Celera | 11:69578212 | GTCCATGTTTGCCTG[G/T]AACTCACACATCTGC | 216853 |
rs29390357 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wrap53 | Mm_Celera | 11:69577865 | CAAGCTCGTGCAGAG[A/T]GTGGTGGCACACATC | 216853 |
rs29390583 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69569435 | CTATCTGAAGAATAA[C/T]GTCTGCCACTAAAAC | 216853 |
rs29393777 | snp | A/G | 0.5 | 0 | intron-variant | Wrap53 | GRCm38.p3 | 11:69575337 | TCAAGAGCACTGGTT[A/G]CCCTTCTAGAGGACC | 216853 |
rs29395262 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69573328 | AAAGCTGGGCGTGGT[A/G]GCACATGCCTTTAAT | 216853 |
rs29395506 | snp | A/G | 0.32 | 0.24 | intron-variant | Wrap53 | Mm_Celera | 11:69564542 | CCTAAAGAATAACAG[A/G]CAGGACTGAAAGATT | 216853 |
rs29397075 | snp | A/G | 0.5 | 0 | intron-variant | Wrap53 | Mm_Celera | 11:69569903 | AAGCACTGCAGGCCT[A/G]GCAGGCTCTCACTGG | 216853 |
rs29397753 | snp | C/T | 0.5 | 0 | intron-variant | Wrap53 | GRCm38.p3 | 11:69571480 | ATGTGTGCCTGTGCA[C/T]ACAGCGTGCACTCTC | 216853 |
rs29398035 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wrap53 | GRCm38.p3 | 11:69571368 | AAGGTGGCCTAGCCA[A/G]TAAAATGGCTGGGTG | 216853 |
rs29400649 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wrap53 | GRCm38.p3 | 11:69576124 | AGAGGACCCAAGTTC[A/G]GTCCCCAGCACCCAT | 216853 |
rs29400998 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69566974 | GCGGCATTGGCACAC[A/G]CCTTCAATCCCAGCA | 216853 |
rs29403797 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69574819 | CCGCTTCTGCCAGAC[A/G]CAGCAGCTCCTGCCT | 216853 |
rs29405251 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69567125 | AAACAAACAAACAAA[A/C]AAATCACAATAGCCA | 216853 |
rs29407257 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69570317 | CCTTATTCCCAGCCC[C/T]ACCCTCCACAAGACA | 216853 |
rs29407720 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Trp53, Wrap53 | Mm_Celera | 11:69581523 | GCGGAAGGGGCGGGC[C/T]TGGGCCCCGGGCGCC | 216853 |
rs29408625 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wrap53 | GRCm38.p3 | 11:69571392 | CTGGGTGTGCCAGCC[A/T]GAGTCAGATCCCCCA | 216853 |
rs29408750 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wrap53 | GRCm38.p3 | 11:69569980 | GCTGGGACTCTTCAA[C/T]GCCACTGTGGTAAGC | 216853 |
rs29413548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wrap53 | Mm_Celera | 11:69573334 | GGGCGTGGTAGCACA[C/T]GCCTTTAATCCCAGC | 216853 |
rs29417337 | snp | A/T | 0.5 | 0 | intron-variant | Wrap53 | Mm_Celera | 11:69565960 | GTAGAAAAATAGATT[A/T]AAAAAAAATCATGGA | 216853 |