SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6161600 | snp | C/T | 0.5 | 0 | intron-variant | Trp53bp2 | Mm_Celera | 1:182456174 | ATAAAGACAGCAGAT[C/T]GCATGGTTTGGAGTT | 209456 |
rs6163096 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Trp53bp2 | Mm_Celera | 1:182456431 | TGGCCTGAGAGAATA[G/T]GAAATCAGAAGGTCT | 209456 |
rs6163134 | snp | A/G | 0.5 | 0 | intron-variant | Trp53bp2 | Mm_Celera | 1:182456458 | GTCTCAGGAGTATAG[A/G]TTGCTCAAGCTCTCC | 209456 |
rs30462184 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182435767 | TTAAAAATATATTTC[A/G]TAGGTCTCTCCCAGA | 209456 |
rs30572084 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182443045 | CAGGGTAAAATCTAA[A/G]TTATTTTAGAAATGA | 209456 |
rs30700022 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182420235 | TACACAGAGAAACCC[C/T]GTCTCAAAAACAAAA | 209456 |
rs30894848 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182435962 | TGTATATGCATTGAT[A/G]TACCTTTGAAGGTGT | 209456 |
rs31126093 | snp | C/T | 0.5 | 0 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182426118 | TAGAGGTAGTGGCTT[C/T]GTGGGGGGCGGGGGG | 209456 |
rs31282277 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Trp53bp2 | Mm_Celera | 1:182441545 | GGTTGGTCCTAGGAC[A/G]TTTTCAGAGAGCTCT | 209456 |
rs31300144 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182410732 | AGGAAAAGAATAGGT[A/G]GTTTTAATTGCAGGA | 209456 |
rs31320127 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182424036 | TGATTGTTTCAGTTG[G/T]TTCTTGACTAAAGTT | 209456 |
rs31330240 | snp | C/T | 0.5 | 0 | intron-variant | Trp53bp2 | Mm_Celera | 1:182436498 | GGGGTTGGAAGCCTG[C/T]ACTGCCAGGCCCAGC | 209456 |
rs31425646 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182427029 | AGTGTGTTTAGTAAA[G/T]GTTCTTCTATCTAGT | 209456 |
rs31728534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182449772 | TATTTTTCATTTTAT[A/G]TACATTAGTGTTTTG | 209456 |
rs31765479 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182454880 | TTGCCTAAAATAGAT[C/G/T]GGGGGGGGGGGGGGG | 209456 |
rs31901645 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182460577 | AAATAAAATCTGTTA[A/G]CGAGTTTTCAATTAG | 209456 |
rs31928811 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182439382 | TTGCATATGTGTGCT[C/T]GTGCACACATCTCTA | 209456 |
rs31931177 | snp | A/G/T | 0.5 | 0 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182450306 | AAATAGGTGGGAGAC[A/G/T]ACCATAATCTCTAGC | 209456 |
rs31996548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182411076 | CTTCATCATCTGTAT[C/T]TTGGGGGTGATACAA | 209456 |
rs32095425 | snp | A/T | 0.5 | 0 | intron-variant | Trp53bp2 | Mm_Celera | 1:182450433 | GCACTTTTAAAAAAA[A/T]TTTTTAATATTTTTT | 209456 |
rs32427924 | snp | A/C | 0.32 | 0.24 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182435775 | ATATTTCATAGGTCT[A/C]TCCCAGATTCTTATA | 209456 |
rs32636433 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182417087 | CTCTTAAACAGAGCC[A/G]TCTCTCCAGCCTCAT | 209456 |
rs32700609 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182425186 | TGGGCCTTTATTCTC[C/T]ATGTGGCATACTTGT | 209456 |
rs45646694 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182437313 | CACTGTGCCAGACCC[A/G]GTCTTTGGTTTGGTA | 209456 |
rs45674256 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182418381 | GAGAGCACAGCAGCG[C/T]TAACCTTACAGAGGA | 209456 |
rs45763400 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Trp53bp2 | Mm_Celera | 1:182438329 | ATCCTGGGGTGCAGC[A/G]CTTCTCTAGCTAGAC | 209456 |
rs45779775 | snp | C/T | 0.277778 | 0.248452 | missense | Trp53bp2 | Mm_Celera | 1:182448926 | TGGGGAGTGCCAGTA[C/T]GGAGAACAGTGACGT | 209456 |
rs45792564 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182420733 | TGACCTTCTGAGAAC[C/T]GTATTACAGCTGGAA | 209456 |
rs45810071 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182435543 | GGTGACCCCTTTTAA[A/G]GGCTTTTTCTTAAAA | 209456 |
rs45825326 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182415810 | ATAAACCTGCAGTGG[A/T]ACTTGTAAACAGGGT | 209456 |
rs45831657 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Trp53bp2 | Mm_Celera | 1:182447878 | GTGGTTTAAAGCTAT[C/T]ATAACAGATATTAAA | 209456 |
rs45832881 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trp53bp2 | Mm_Celera | 1:182431808 | ACATTAGAGCAACAG[C/T]GCGGGGTTCTTAGTC | 209456 |
rs45851449 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182416042 | CAGGTCTGATTTGGA[A/T]GGAATCCTAATTGGC | 209456 |
rs45861052 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182457047 | GACCTCGCGGATACA[A/G]TATTACTGCTTTGTA | 209456 |
rs45896859 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182455899 | AATGTGTTGGTTGCC[A/G]TATTTATTTGCCCTG | 209456 |
rs45904311 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182443227 | TCTGAATGAAAGCTT[A/G]GTCTGGTGTTTAACA | 209456 |
rs45935540 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182454000 | TTTGTTCAATTTTGG[A/G]AAGCAATGGAGTTTA | 209456 |
rs45956431 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182461575 | AGCTCAGTGCCTTCC[C/T]GAGTTGGTTTCCTGT | 209456 |
rs45956932 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182455599 | TTGTGAGGCTGGTAG[A/G]TAAGAGCCTGAGGAA | 209456 |
rs45985735 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182415727 | TCCCTTACTACTGTA[C/G]AGAGCACCTCAGAGC | 209456 |
rs46026124 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182412191 | TGGCACATGAAGTGA[A/T]AATTGGCTACAGACC | 209456 |
rs46096136 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Trp53bp2 | Mm_Celera | 1:182461889 | GGCGTGAGCAGAGGC[A/G]TTGCTGCTGAGCCCG | 209456 |
rs46099115 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182417824 | TCTTTTGGTATGTTG[A/T]CCGTTGATCTGTAGA | 209456 |
rs46120450 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182457039 | AAGAAAGTGACCTCG[A/C/T]GGATACAGTATTACT | 209456 |
rs46211080 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182427344 | GGTGCATTCTGTTCA[C/T]ACTAGGAATCTTGAC | 209456 |
rs46218124 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182437585 | TTGGCTCCTCAGAGC[G/T]CCATAGTAAAGCCTT | 209456 |
rs46356353 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182453960 | CGTGTTACTCTTGGA[A/G]GGCCTGGCCTCTTGT | 209456 |
rs46400525 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182427110 | AGTTTATGTGGGTGA[A/G]GACTATGGAGCAGTA | 209456 |
rs46402605 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182427632 | GTTTCAGCCTGCAAG[A/G]GAGGTCAAGTGACTT | 209456 |
rs46403189 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182432252 | TCTAGTGGTGCCCTG[C/T]AGCTCAAGGTTGTGC | 209456 |
rs46403954 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182443531 | TGTAATGGAAGGGTA[A/G]CTGACAGGAGAGTGT | 209456 |
rs46461482 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trp53bp2 | Mm_Celera | 1:182426979 | GATAGACGTGTACAG[A/G]GGTCTGTTGTGTAAC | 209456 |
rs46477008 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182438388 | TCTACTTAAGAATGA[A/G]TTTGTGAATCAAAGT | 209456 |
rs46479126 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182459989 | TGTCTGTCACATGTC[C/T]GTTAAAAGGCATTTG | 209456 |
rs46480262 | snp | A/G | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182413410 | TATAAAAGGTAGTGT[A/G]TGTTGGGTTTCATTC | 209456 |
rs46501058 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182434781 | GTGCTCATTCCATGG[C/T]GTGCATATTGTTGTA | 209456 |
rs46521267 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Trp53bp2 | Mm_Celera | 1:182422293 | CCTCCAGTGAATATA[C/T]ACGTCCGTACATACG | 209456 |
rs46547476 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182428434 | TGTGTGTGTGTGACA[G/T]TCACTCCTGAGGTCA | 209456 |
rs46549802 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Trp53bp2 | Mm_Celera | 1:182452367 | AAACAGTCTTATCTG[G/T]TTGTGGACCTCAATC | 209456 |
rs46555099 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182416285 | GCTCCTTTGTATTGA[A/G]TAGTCAGGGAACTGA | 209456 |
rs46556379 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182415554 | AGTTCTCTCCAGAAT[A/G]CAACTAACATTTGAG | 209456 |
rs46568435 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Trp53bp2 | Mm_Celera | 1:182433895 | CTTTTTACTCTAATT[A/G]TGTAACTGCCTATAA | 209456 |
rs46577851 | snp | A/G/T | 0.197531 | 0.244432 | intron-variant | Trp53bp2 | GRCm38.p3 | 1:182422117 | CTTCACATGGCTTTT[A/G/T]AAACCAAATGAACAG | 209456 |
rs46649076 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | Mm_Celera | 1:182441856 | TCCCTAGAAACACAA[A/G]CTGTCCGTAGAAAGT | 209456 |
rs46655066 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182455638 | ACAGGTAACTCACTA[C/T]GCGGAGGTCCTTGAG | 209456 |
rs46659609 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182413892 | AACACGGAGAGCCCT[A/T]GTGAAGTCTGCAGAT | 209456 |
rs46694866 | snp | A/G | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182430586 | TCTTTCTAACTCAGG[A/G]TACACTGTTTCTACT | 209456 |
rs46716099 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Trp53bp2 | Mm_Celera | 1:182450331 | TCTAGCCTACTTTTG[C/T]ATAGCTTAGTCAGAA | 209456 |
rs46725118 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | Mm_Celera | 1:182427378 | ATTTTAGCTTCTTCT[A/G]TATGATTGACTTACT | 209456 |
rs46730983 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trp53bp2 | Mm_Celera | 1:182428654 | TGTCTTGATCTAGCT[C/T]CGTTTTTGCTGAACA | 209456 |
rs46737717 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Trp53bp2 | Mm_Celera | 1:182441731 | GGAGATGCTGAAGAA[C/T]GGCAGGATCGATGGC | 209456 |
rs46783723 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Trp53bp2 | Mm_Celera | 1:182442270 | GTGGAAGAAGAAGGC[A/G]GCACTGCAGCAGAAA | 209456 |
rs46784860 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trp53bp2 | Mm_Celera | 1:182422015 | GTAAGCATGAGTTTT[C/T]GCAAATGGCAACTCT | 209456 |
rs46828851 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182418020 | TGGTCTTTCTGAGCA[A/G]CAGTTTTTCCCTCTC | 209456 |
rs46831585 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trp53bp2 | Mm_Celera | 1:182454303 | CTGTAAGAGACACAA[A/G]TTCTTTCTGTGGAGG | 209456 |
rs46889526 | snp | A/T | 0.18 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182431840 | GGATGTGACTGACAG[A/T]GGAGAAAAGGAGACA | 209456 |
rs46899444 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182432988 | TGGGCGGCTAGTGCT[C/T]TAGACACTGAGATGG | 209456 |
rs46902753 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182417301 | AGCATGCCTGGACAA[C/T]CTTGTAAGTGCTTTA | 209456 |
rs46908579 | snp | A/T | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182412271 | CAGCGGAGCTAATGA[A/T]AGGGTGCTGTGCAAG | 209456 |
rs46935882 | snp | A/G | 0.18 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182449608 | CCTCTCTTCTCTCTC[A/G]CTGAAGGTGCGCTAG | 209456 |
rs46959307 | snp | A/G | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182421814 | GTTCTTTACTGAAGC[A/G]TAGAAAACCGGTCAG | 209456 |
rs46963873 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Trp53bp2 | Mm_Celera | 1:182442480 | ACTTGCAGCAAGGTT[A/G]TAGCAGAGTTCCATG | 209456 |
rs47004691 | snp | A/G | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182411921 | ATCAGGAAAAGCGTC[A/G]CACTAATGAAAAGAC | 209456 |
rs47007375 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182460302 | ATGAAGCATGACTTT[C/T]TAATCATTTTTAAAA | 209456 |
rs47056635 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182446747 | AAGTGGTAAGGTTCC[A/G]TTGTTTGTATTTTTA | 209456 |
rs47061647 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182412741 | CATTTGCCTGTATGG[A/G]AGCGAGCACTTGGCA | 209456 |
rs47098509 | snp | A/G | 0.32 | 0.24 | intron-variant | Trp53bp2 | Mm_Celera | 1:182410739 | GAATAGGTGGTTTTA[A/G]TTGCAGGATGATTTC | 209456 |
rs47114564 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Trp53bp2 | Mm_Celera | 1:182425221 | CCTTAGCTGGACTTG[G/T]GCCTCATTTCCTTTA | 209456 |
rs47128758 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182410978 | TGTAGTGTGCATGCT[A/T]TTCTAGCTTTGAAAT | 209456 |
rs47132572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182414913 | AAAAGATGGCTAGGA[C/T]ACTTTATTGGTCTTC | 209456 |
rs47188189 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182435098 | AAGTAAAAGGTGTGA[A/G]TTGGTTGGAGTCAGA | 209456 |
rs47189166 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182414892 | TTAAGCTACTGATGA[C/T]AATAAAAAAGATGGC | 209456 |
rs47211077 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182441029 | GTGTAACTCGTGGAA[C/T]GGCCACATTTGGAAT | 209456 |
rs47221635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trp53bp2 | Mm_Celera | 1:182434329 | TGTTGTGCATTGAGT[A/G]GTGCTGAGATACCTG | 209456 |
rs47221969 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trp53bp2 | Mm_Celera | 1:182430539 | TTCAGCTTTCTCTCC[C/T]GAAGTAGGAAATCCT | 209456 |
rs47234709 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Trp53bp2 | Mm_Celera | 1:182416166 | TCTCATGGATACAGA[A/T]CAGGACAACTTTCAG | 209456 |
rs47252264 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182455411 | CAGACAGAACCAGAT[C/G]CACTTTTTTCTGTTC | 209456 |
rs47256456 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Trp53bp2 | Mm_Celera | 1:182420959 | AGAGTGACCACAGGA[A/G]CAGGAGGCTGACTGG | 209456 |
rs47269550 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trp53bp2 | Mm_Celera | 1:182415294 | CAGTTGGTGTGCTAT[C/T]TTGGCTAATGGCTAA | 209456 |
rs47278772 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trp53bp2 | Mm_Celera | 1:182448139 | TAGACAGATTCCCAA[C/T]CACGGGTGTGGTTTC | 209456 |