SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs17739 | snp | C/T | 0.456214 | 0.141336 | utr-variant-3-prime | TP53BP2 | GRCh38.p7 | 1:223780251 | TCTAATTACTGGTAC[C/T]GTAGCTTAGTTTCAA | 7159 |
rs720757 | snp | C/T | 0.475702 | 0.107512 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223835404 | AAGAACAAATACATT[C/T]AGTTAATTCCTCCCC | 7159 |
rs898878 | snp | A/T | 0.416871 | 0.186156 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223820097 | AGAAGGAGATTAACA[A/T]TTTAGCTGCAATCCA | 7159 |
rs1003061 | snp | C/T | 0.411242 | 0.191052 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223840297 | ACTGCAATATAACTA[C/T]ACATTTCATACATAG | 7159 |
rs1124943 | snp | G/T | 0.290201 | 0.246747 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223805922 | GCAAAGCCCAAAATA[G/T]TTACTATGTAGCCCT | 7159 |
rs1153927 | snp | C/T | 0.265453 | 0.249522 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223808433 | ataatcccagctact[C/T]gggaagctgaggcag | 7159 |
rs1153928 | snp | C/T | 0.470521 | 0.117772 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223808386 | tctctactaaaaata[C/T]aaaaactagctgggc | 7159 |
rs1153929 | snp | A/G | 0.322245 | 0.239334 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223806599 | GAGGCCGAAGTGGGC[A/G]GATCACCTGAGGTCA | 7159 |
rs1153930 | snp | A/C | 0.336245 | 0.234652 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223805417 | AAATGCAGAAGCTCA[A/C]ACCTCAACTCACCTA | 7159 |
rs1153931 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223803586 | GTCCTGGAAGCAACC[A/G]ACTTCTTTTAGAAGC | 7159 |
rs1153932 | snp | C/T | 0.00398253 | 0.0444455 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223803244 | CTGTTTGCCAAAAGC[C/T]GTACAACCTCCTTTC | 7159 |
rs1153933 | snp | C/T | 0.213998 | 0.247394 | synonymous-codon | TP53BP2 | GRCh38.p7 | 1:223802264 | CCGAGGCATAGTAGA[C/T]GACTGGATATAGGGA | 7159 |
rs1153934 | snp | C/T | 0.293294 | 0.246223 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223797702 | AGGCGTGAGCCACTG[C/T]GCCCAGCCACAGTTA | 7159 |
rs1153935 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223794735 | AAGCCTCAGAACTTA[C/T]GAGGCACAGGGTTGT | 7159 |
rs1153936 | snp | C/G | 0.21572 | 0.247639 | synonymous-codon | TP53BP2 | GRCh38.p7 | 1:223792505 | GCCTTCATCATTGGG[C/G]AGGCTTGGGTCATCA | 7159 |
rs1153937 | snp | C/T | 0.38934 | 0.207568 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223791542 | ATGAGTACACAGTCA[C/T]GCGGTAGAGTAATAC | 7159 |
rs1153938 | snp | A/T | 0.389715 | 0.207315 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223791291 | AAAAATAAAAAATAA[A/T]TTTTTTTTAAAAAGA | 7159 |
rs1153939 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223785159 | AAAGTGAAAATAATA[A/T]TTCTGAATTGCTGAG | 7159 |
rs1153940 | snp | A/G | 0 | 0 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223783617 | CCTGGAGTATTTTCA[A/G]GGGAAGGCTGGCGTA | 7159 |
rs1153941 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223783560 | AGCTTACTGCAAAGC[C/G]CTGGAATCTGTTATT | 7159 |
rs1153942 | snp | A/C | 0.229723 | 0.249176 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223783043 | ACTTTCAATGGGATT[A/C]CTTGAAATGACTTCA | 7159 |
rs1153943 | snp | A/C | 0.376791 | 0.215463 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223782809 | TAACTTTAAAGAATA[A/C]TGAAAGTGAAAAACA | 7159 |
rs1153944 | snp | A/G | 0.46137 | 0.133501 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223782623 | TCTACTAAAAATACT[A/G]TAATCCCAGCTACTC | 7159 |
rs1153945 | snp | C/T | 0 | 0 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223781626 | ttttaaattttttaa[C/T]tGGGATGTAATTAAA | 7159 |
rs1153971 | snp | A/T | 0.29278 | 0.246313 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223811886 | GATTATATTTCTCAC[A/T]TTACTGACACTGAAA | 7159 |
rs1153972 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | TP53BP2 | GRCh38.p7 | 1:223809864 | agagtgtcactcttg[C/T]tgcccaggctggagt | 7159 |
rs1153973 | snp | A/G | 0.266 | 0.249487 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223808498 | gtgagccgagatcgc[A/G]ccactgcactccagc | 7159 |
rs1222081 | snp | A/G | 0.470034 | 0.11868 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223790954 | ATTAAAAAGCATGCA[A/G]TGAAAAAATCTATAG | 7159 |
rs1222120 | snp | A/C | 0.321769 | 0.239477 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223789642 | ATAAAAGTAGTTCAT[A/C]TATGCAACTTAATTC | 7159 |
rs1222121 | snp | A/G | 0.277067 | 0.24853 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223789425 | TTTATTCACGTCCTT[A/G]ATTCTTCTCACCCTT | 7159 |
rs1222122 | snp | C/T | 0.125182 | 0.216612 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223786197 | TCCTATAACTAatat[C/T]tgcagttttgcttgt | 7159 |
rs1222123 | snp | C/T | 0.439224 | 0.163383 | downstream-variant-500B | TP53BP2 | GRCh38.p7 | 1:223779535 | ATTCTAAAGATGCCC[C/T]GCACCCCCATCCCTG | 7159 |
rs1222124 | snp | A/G | 0.335559 | 0.234904 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223812307 | CCCCTCAGCTAACCC[A/G]TACTATAAATTTAAT | 7159 |
rs1222125 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223812643 | cggctcactgcaacc[G/T]ccaactccctgattc | 7159 |
rs1222126 | snp | G/T | 0.470521 | 0.117772 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223812815 | gatcctcccgcctcg[G/T]cctcccaaagtgctg | 7159 |
rs1222127 | snp | C/T | 0.460252 | 0.135255 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223814636 | CACGCTGGCCACAGG[C/T]GCACCATTTAACTTC | 7159 |
rs1222128 | snp | C/T | 0.281049 | 0.248064 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223815108 | TTAAAATCAATGAAA[C/T]TCCAGTAATGTCAAC | 7159 |
rs1222158 | snp | A/G | 0.469839 | 0.119042 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223800999 | CTTCCACTTTACTCA[A/G]GCAATTTAAAATTAG | 7159 |
rs1228475 | snp | C/G | 0.469937 | 0.118861 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223786855 | actttgggaggccga[C/G]gtgggcagatcacga | 7159 |
rs1415583 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223820662 | TCCTACACAGGCTGG[A/G]TGAACTCCTGCTGGT | 7159 |
rs1538140 | snp | C/T | 0.454423 | 0.143914 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223842796 | AACTGCCTCCCTTTA[C/T]ATGAAAATCAAATAC | 7159 |
rs1675992 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223786582 | acacacacacacaca[C/T]gcacacacgcacaca | 7159 |
rs1675993 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223799602 | AAGCATTTTGTAACT[C/T]TGAAGAAATAAGATA | 7159 |
rs1802941 | snp | G/T | | | utr-variant-3-prime | TP53BP2 | GRCh38.p7 | 1:223780224 | TAGATGTAGAATCTT[G/T]TTTGTAGGCTGAATT | 7159 |
rs1890119 | snp | C/T | 0.0905309 | 0.192535 | | | GRCh38.p7 | 1:223838296 | ATGTTAACTAAATAT[C/T]TGTTGAGCAGATGTT | 7159 |
rs1890120 | snp | C/T | 0.498693 | 0.0255257 | | | GRCh38.p7 | 1:223838435 | AGGTATCTGACTACA[C/T]TGAATTACTGCTCCC | 7159 |
rs1981171 | snp | A/G | 0.256619 | 0.249912 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223831635 | GTTTGTATTAACTAT[A/G]CTTTTAAATTATACA | 7159 |
rs1982610 | snp | A/T | 0.291235 | 0.246576 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834371 | TGCTCAAAACCCTCT[A/T]ATGCAGTGGTTCTTA | 7159 |
rs1982611 | snp | C/T | 0.460702 | 0.134554 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834223 | GAGAATTGCATGTTG[C/T]AAATCACTACTCTAG | 7159 |
rs1982612 | snp | A/G | 0.291235 | 0.246576 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834182 | CTTGCAATAAAGTCC[A/G]TACTCCTTATTCTTG | 7159 |
rs1982613 | snp | C/T | 0.291235 | 0.246576 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834142 | GCCCTGCCTGAGCTA[C/T]CCCCTGTTCTCCCTG | 7159 |
rs2045733 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223833757 | TAACGGGTGAATGAA[C/T]GAAACTTCTTGTTGA | 7159 |
rs2242188 | snp | A/T | 0.256897 | 0.249905 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223788493 | CTAGGTACAGATCTG[A/T]TGTTAGCAATCAGAA | 7159 |
rs3051220 | in-del | -/ATAAA | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223788080 | ctctaaaaaaataaa[-/ATAAA]aTAATCACAAATATC | 7159 |
rs3058420 | in-del | -/AC/ACACAC/ACACACACA/ACACACACAC/ACACACACACACA | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223825054 | CACACACACACACAC[lengthTooLong]CCTAGCCCATTCTTC | 7159 |
rs3217725 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223783776 | GTAGAGAGCTTCAGC[-/A]GGGCATTAAGGACAA | 7159 |
rs3738370 | snp | C/T | 0.206086 | 0.246113 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223821211 | GGCTCTGGTGAGAGA[C/T]GCTGACAGCCTCGTG | 7159 |
rs3753048 | snp | A/G | 0.0500175 | 0.150023 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223814202 | CAGCACAAAATAAAA[A/G]CTTAAATATCTGTCA | 7159 |
rs3753049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223814443 | CATGCAAATTATACA[C/T]TATGGATACAACAAA | 7159 |
rs3767709 | snp | A/G | 0.25634 | 0.24992 | intron-variant, upstream-variant-2KB | TP53BP2 | GRCh38.p7 | 1:223811131 | TTTTTAGCCAAAAAA[A/G]CAGAATATATAGTGT | 7159 |
rs3767710 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223784945 | ATTTTTCCCTTCCTA[A/G]TTTGAGGATTTCGAC | 7159 |
rs3835623 | in-del | -/AG | 0.5 | 0 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223782041 | AATTTTCTAACACAG[-/AG]GTCCTGTGGTTAATG | 7159 |
rs3835624 | in-del | -/TAGAGCCGATTTACA | 0.0379877 | 0.132479 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223781193 | TAGAGCCGATTTACA[-/TAGAGCCGATTTACA]GCTCAACAAGCTGTG | 7159 |
rs3856162 | snp | A/G | 0.497445 | 0.0356514 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223830303 | atctgaaatgctcca[A/G]aattgaaaactttct | 7159 |
rs3885657 | snp | A/G | 0.170408 | 0.236992 | intron-variant, upstream-variant-2KB | TP53BP2 | GRCh38.p7 | 1:223810121 | AATGCAAAATTggcc[A/G]ggtgcagtggctcac | 7159 |
rs5781333 | in-del | -/T | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834818 | AGGTGAGTGTGTGGG[-/T]TAGGGATGGATGGAT | 7159 |
rs6604724 | snp | G/T | 0.180383 | 0.240111 | intron-variant, upstream-variant-2KB | TP53BP2 | GRCh38.p7 | 1:223810869 | CTAGTCATCTATTTA[G/T]CTACTCAGTAGTTAA | 7159 |
rs6604725 | snp | A/G | 0.257176 | 0.249897 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223814627 | AGTGGGCTCCACGCT[A/G]GCCACAGGTGCACCA | 7159 |
rs6604726 | snp | A/G | 0.416382 | 0.186593 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223831361 | tatgatcatgccact[A/G]cactccagcttgggc | 7159 |
rs6604727 | snp | C/T | 0.152667 | 0.230274 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223831391 | cgacagagcaagacg[C/T]tgtctcccaaaaaaa | 7159 |
rs6604728 | snp | A/G | 0.153665 | 0.230694 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223835132 | CAACAAGAACATGAC[A/G]AAGAGGATGTTCACA | 7159 |
rs6604729 | snp | C/T | 0.142272 | 0.225598 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223835556 | TTACTCACTAAGCAC[C/T]ACATTTTTAAGATCT | 7159 |
rs6658724 | snp | A/G | 0.460813 | 0.134379 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223828818 | ttgataactgccaag[A/G]actgaggaaggggga | 7159 |
rs6658954 | snp | A/T | 0.140919 | 0.224948 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223829072 | tggctcacacctata[A/T]tcccagcactttggc | 7159 |
rs6661816 | snp | C/T | 0.417196 | 0.185864 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223828855 | agtgactgataaagg[C/T]atggggtttctttct | 7159 |
rs6662031 | snp | G/T | 0.140919 | 0.224948 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223829070 | ggtggctcacaccta[G/T]aatcccagcactttg | 7159 |
rs6663152 | snp | C/T | 0.266273 | 0.24947 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223806598 | GGAGGCCGAAGTGGG[C/T]GGATCACCTGAGGTC | 7159 |
rs6667215 | snp | C/G | 0.460589 | 0.13473 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223832266 | CCTAAGAGGAAGAAA[C/G]AGAAAATTATGAAAT | 7159 |
rs6678365 | snp | C/T | 0.143959 | 0.226396 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223836032 | CTAGGGAGAGAAACA[C/T]TGTGTATAAAGACAC | 7159 |
rs6680204 | snp | A/G | 0.461481 | 0.133325 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223819693 | tccatctcaaaaaaa[A/G]aaaaaagaaaaCTGA | 7159 |
rs6682353 | snp | A/G | 0.499999 | 0.000599041 | upstream-variant-2KB | TP53BP2 | GRCh38.p7 | 1:223846090 | CGGGCCCGGCTGGGT[A/G]GACGGGGAGCGGCGG | 7159 |
rs6682964 | snp | C/T | 0.180702 | 0.240204 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223787614 | aggcatggtggctca[C/T]acctgtaatgccagc | 7159 |
rs6685557 | snp | A/C | 0.18134 | 0.240387 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223781811 | ACTTTCCTTTAAAAA[A/C]AAAGATCAGGAAAAC | 7159 |
rs6686421 | snp | A/C | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223818791 | accatgttggccagg[A/C]tggtctcaaactcct | 7159 |
rs6691138 | snp | A/G | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223818799 | ggccaggctggtctc[A/G]aactcctaaactcag | 7159 |
rs6691139 | snp | A/T | | | intron-variant | TP53BP2 | GRCh38.p7 | 1:223818801 | ccaggctggtctcaa[A/T]ctcctaaactcaggt | 7159 |
rs6691315 | snp | A/T | 0.180702 | 0.240204 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223812322 | GTACTATAAATTTAA[A/T]CATTCCTAATGGTCA | 7159 |
rs6694214 | snp | C/T | 0.236434 | 0.249632 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223785666 | TGCTGGGATTACAGG[C/T]ATGAGCCACTGCACC | 7159 |
rs6694471 | snp | A/G | 0.417034 | 0.18601 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223819681 | acagagtgagactcc[A/G]tctcaaaaaaagaaa | 7159 |
rs6694960 | snp | C/T | 0.180702 | 0.240204 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223813571 | CCCACTGAACTCCCA[C/T]TGAATTTGTCTAGAA | 7159 |
rs6698919 | snp | C/T | 0.460813 | 0.134379 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223827695 | ggaaaatggtgttga[C/T]aggaaaCTAACTATA | 7159 |
rs6700366 | snp | C/G | 0.141596 | 0.225274 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223825378 | gagcccCTTCCTTGA[C/G]AGCATACAGGTAAAG | 7159 |
rs7517765 | snp | A/G | 0.261056 | 0.249755 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223794268 | AGGTGTGATATATGT[A/G]CTCCACATAATTCTT | 7159 |
rs7517814 | snp | C/G | 0.497151 | 0.037632 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223841150 | CGGGAGGCTGAGGCA[C/G]AGAACTGCTTTAACC | 7159 |
rs7528455 | snp | C/G | 0.153665 | 0.230694 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223834365 | TAAGTTTAAGAACCA[C/G]TGcattagagggttt | 7159 |
rs7530328 | snp | A/T | 0.180383 | 0.240111 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223803850 | ATTCTCAGTCAAAAA[A/T]TATTAAGGGGAAAAA | 7159 |
rs7533551 | snp | A/C | 0.169435 | 0.236663 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223804879 | gtgaagattaaatga[A/C]gtgtgaaatgtaaat | 7159 |
rs7536779 | snp | C/T | 0.335788 | 0.23482 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223817843 | aggcagcagaatcac[C/T]tgaacataggaggca | 7159 |
rs7543815 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223817651 | ataatttaaaaataa[C/T]gtggtggctcatgtc | 7159 |
rs7547098 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | TP53BP2 | GRCh38.p7 | 1:223818830 | gtgatcaaccctcct[C/T]ggcctcccaaagtgc | 7159 |