SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs331440 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | RAG1 | GRCh38.p7 | 11:36526684 | aatggttgaactaat[C/T]tacactcccaccaac | 5896 |
rs331441 | snp | A/C/T | 0.0894459 | 0.191631 | intron-variant | RAG1 | GRCh38.p7 | 11:36525613 | atcctttacatgttt[A/C/T]gtacgtgttttgtta | 5896 |
rs331442 | snp | A/G | 0.040671 | 0.13668 | intron-variant | RAG1 | GRCh38.p7 | 11:36523845 | tctaccaatggtaac[A/G]tcatgcaaaactgta | 5896 |
rs331443 | snp | C/G | 0.039522 | 0.134904 | intron-variant | RAG1 | GRCh38.p7 | 11:36523120 | ggcatgattcatttt[C/G]aaatgtgaagatacg | 5896 |
rs331444 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | RAG1 | GRCh38.p7 | 11:36521754 | ttcaatggctttgac[C/T]aaaatgctgataatg | 5896 |
rs331449 | snp | C/T | 0.120674 | 0.21395 | upstream-variant-2KB, intron-variant | TRAF6, RAG1 | GRCh38.p7 | 11:36511020 | ATCCGGTTTTTCCTA[C/T]AATAAATGTGTGATT | 5896 |
rs331450 | snp | C/T | 0.126564 | 0.217402 | intron-variant | RAG1 | GRCh38.p7 | 11:36513198 | gcaagataccagccc[C/T]ttgagtttggacttc | 5896 |
rs331451 | snp | A/G | 0.093417 | 0.194889 | intron-variant | RAG1 | GRCh38.p7 | 11:36514757 | cagctgatgtggcag[A/G]aggtggagctcaggc | 5896 |
rs331452 | snp | C/G | 0.093417 | 0.194889 | intron-variant | RAG1 | GRCh38.p7 | 11:36516302 | GTGTGGTAAAAATCA[C/G]TGTTGTGTTTTTTGT | 5896 |
rs331453 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RAG1 | GRCh38.p7 | 11:36518230 | cacattttcttaatc[C/T]agtctatcattgttg | 5896 |
rs331454 | snp | C/T | 0.361894 | 0.223562 | intron-variant | RAG1 | GRCh38.p7 | 11:36518548 | ctaacaggtgtgaga[C/T]ggtatctcattgtgg | 5896 |
rs331455 | snp | C/T | 0.366473 | 0.221211 | intron-variant | RAG1 | GRCh38.p7 | 11:36518999 | GAGCTAATGATACTA[C/T]TTTCCTGAAGAAGAT | 5896 |
rs331456 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | RAG1 | GRCh38.p7 | 11:36519180 | TTGTTGTTTTCTGCA[C/T]CAGTAAGGTAGGGAT | 5896 |
rs550292 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RAG1 | GRCh38.p7 | 11:36519668 | AAAGGCTGTGAATAT[G/T]TATGACTCCTGTTAC | 5896 |
rs587682 | snp | C/T | | | intron-variant | RAG1 | GRCh38.p7 | 11:36548817 | cctgcatagccaaga[C/T]aatcctaagcaaaaa | 5896 |
rs748974 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TRAF6, RAG1 | GRCh38.p7 | 11:36509504 | GCTTTCCCATGACAG[G/T]GACAGCCGGAGTCGC | 5896 |
rs872052 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant | RAG1 | GRCh38.p7 | 11:36568023 | AAACAAGAGGGCAAG[A/G]AGAGAGCAGAGAACA | 5896 |
rs872053 | snp | A/G | 0.114387 | 0.210022 | utr-variant-5-prime, intron-variant | RAG1 | GRCh38.p7 | 11:36568072 | GTATTGAGTAATATC[A/G]ACCAAATTGCAGACA | 5896 |
rs962353 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | RAG1 | GRCh38.p7 | 11:36543058 | ATGGGGGAAGAAGAT[C/T]CAGTAGTGACTCGTT | 5896 |
rs1056403 | snp | C/T | 0.474634 | 0.109726 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36579620 | CATTTGACATGGAAA[C/T]ACAGGTCCCCTGAAT | 5896 |
rs1356049 | snp | C/T | 0.262985 | 0.249663 | intron-variant | RAG1 | GRCh38.p7 | 11:36543277 | TGAGAGGCAACCTCA[C/T]ACTTCCAAAGAGAAG | 5896 |
rs1399601 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36566341 | GGAAGTTATGTAAAA[C/G]TAAAGTGACAAAATG | 5896 |
rs1399602 | snp | C/T | 0.264632 | 0.249571 | intron-variant | RAG1 | GRCh38.p7 | 11:36544306 | CAGTAGTCTCCTTGT[C/T]GACCCTTCTATGTTA | 5896 |
rs1515060 | snp | C/T | 0.259674 | 0.249813 | intron-variant | RAG1 | GRCh38.p7 | 11:36564772 | ACCCTGCACTGGCGG[C/T]GGAGAGACAGCGTCT | 5896 |
rs1515061 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RAG1 | GRCh38.p7 | 11:36572417 | TTTTTACCAGAAGAG[A/T]AACATTACTCCCACC | 5896 |
rs1515062 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | RAG1 | GRCh38.p7 | 11:36541058 | GAAAACAACAGACCA[G/T]CATATCATGTCATGT | 5896 |
rs1801203 | snp | C/T | 1.64836e-05 | 0.0028708 | RAG1 | 11 | allele_origin=T(germline)/C(germline) | 11:36573771 | GGCCGGACCTCATTG[C/T]CAAGGTTTTCCGGAT | 5896 |
rs1980131 | snp | A/G | 0.126448 | 0.217336 | synonymous-codon | RAG1 | GRCh38.p7 | 11:36576184 | CATTGGGGCATGGGC[A/G]AGTGAGGGAAATGAG | 5896 |
rs2056094 | snp | C/G | 0.114387 | 0.210022 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36567521 | AAACAATCTCAGAAC[C/G]TTTCAACCTGGTCAA | 5896 |
rs2133165 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | RAG1 | GRCh38.p7 | 11:36530697 | gaacgcacttgatat[A/G]ctttgattctttgaa | 5896 |
rs2173394 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | RAG1 | GRCh38.p7 | 11:36561687 | TAATTTCCCAGCTCC[A/C]GCTTcagcaatcagg | 5896 |
rs2173395 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | RAG1 | GRCh38.p7 | 11:36547174 | GCCCACAGGAGAAAG[C/T]GGGGAAGATCTAAAA | 5896 |
rs2201845 | snp | A/G | 0.250168 | 0.25 | intron-variant | RAG1 | GRCh38.p7 | 11:36534708 | AATTGTGACTGTTTT[A/G]CAATCAATGTGTCTA | 5896 |
rs2227973 | snp | A/G | 0.303558 | 0.244196 | missense | RAG1 | GRCh38.p7 | 11:36575763 | TAGGGGAAGTGTATA[A/G]GAATCCCAATGCTTC | 5896 |
rs2422294 | snp | C/T | 0.230017 | 0.2492 | intron-variant | RAG1 | GRCh38.p7 | 11:36544153 | ATATCAGGGCTTAAT[C/T]CCTGGGACCTATAAA | 5896 |
rs2422295 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | RAG1 | GRCh38.p7 | 11:36550851 | ctctattgttcatat[A/C/T]aatcccacagaagta | 5896 |
rs2554015 | snp | C/T | 0.0551013 | 0.156571 | | | GRCh38.p7 | 11:36529415 | TTATGTCAATAGGTA[C/T]AGAAAAGGTCTTCGA | 5896 |
rs2554016 | snp | C/G | 0.0551013 | 0.156571 | | | GRCh38.p7 | 11:36529438 | GTCTTCGACAAAATT[C/G]AACAGCACTTCATGC | 5896 |
rs2554017 | snp | A/G | 0.25045 | 0.25 | | | GRCh38.p7 | 11:36529532 | ACAAACTCACAGCCA[A/G]TATCATACTGAATGG | 5896 |
rs2554018 | snp | A/G | 0.0551013 | 0.156571 | | | GRCh38.p7 | 11:36529623 | ACTCCTATTCAATAT[A/G]GTATTGGAAGTTCTG | 5896 |
rs2673017 | snp | C/T | 0.0543475 | 0.155628 | downstream-variant-500B | RAG1 | GRCh38.p7 | 11:36579767 | AGAAATTATAATACA[C/T]ACCATTTTCAAATCT | 5896 |
rs2673019 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | RAG1 | GRCh38.p7 | 11:36529404 | AAACCACATGATTAT[C/G]TCAATAGGTATAGAA | 5896 |
rs3740955 | snp | A/G | 0.494385 | 0.0526865 | RAG1 | 11 | allele_origin=G(germline)/A(germline) | 11:36574050 | GACAAGCCCGTCAGC[A/G]CAAGAGAAGAGCTCA | 5896 |
rs3758873 | snp | A/C | 0.475613 | 0.107697 | intron-variant | RAG1 | GRCh38.p7 | 11:36565467 | GCCTGTCGGCACTTC[A/C]AGGACTAACCACAGC | 5896 |
rs3841219 | in-del | -/GAG | | | upstream-variant-2KB, intron-variant | TRAF6, RAG1 | GRCh38.p7 | 11:36510599 | CCCCTCTCCAAGCAG[-/GAG]AAAACCCCAGCTGGG | 5896 |
rs4150996 | snp | C/G/T | 0.0387552 | 0.1337 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36566853 | AAGTAGGTCCAAATG[C/G/T]GAAAGAGTGGGAGAT | 5896 |
rs4150997 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36567371 | GTTGCAGGTGATGAG[A/G]TTGAAGTTCCTAAAG | 5896 |
rs4150998 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36567397 | TAAAGTTTAAGTAAT[A/G]AATCAAAGGCCTGAG | 5896 |
rs4150999 | snp | C/G | 0.0494327 | 0.149241 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36567643 | TTTCCTATAATAACT[C/G]TCATTGTATAACATT | 5896 |
rs4151000 | snp | C/T | 0.101658 | 0.201233 | upstream-variant-2KB, intron-variant | RAG1 | GRCh38.p7 | 11:36567791 | CAACCCAAACATTCT[C/T]AGGGAGGGAACTGGC | 5896 |
rs4151001 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RAG1 | GRCh38.p7 | 11:36568568 | CTAAGTAGGAGACCA[A/G]TGTTTCTCAAAATAT | 5896 |
rs4151002 | snp | A/G | 0.182933 | 0.240836 | intron-variant | RAG1 | GRCh38.p7 | 11:36568663 | GACTCTTTGGGACCT[A/G]ATGATCTGCATTTCT | 5896 |
rs4151003 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RAG1 | GRCh38.p7 | 11:36568847 | GTTGTCTGAAGGAAG[A/G]GCAAGAATTGTAGTG | 5896 |
rs4151004 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | RAG1 | GRCh38.p7 | 11:36569311 | GAGATGGCAGTGGCC[A/G]GTGGGGACAGGGCTG | 5896 |
rs4151005 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | RAG1 | GRCh38.p7 | 11:36569907 | TGCTATTGTCATTCT[A/G]TTCTCTGCTTTTTCA | 5896 |
rs4151006 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAG1 | GRCh38.p7 | 11:36570211 | CAAAGATAATATATT[C/T]AAAAATTTTAAAGAT | 5896 |
rs4151007 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAG1 | GRCh38.p7 | 11:36570226 | CAAAAATTTTAAAGA[C/T]ATTGCTAAATTGTCT | 5896 |
rs4151008 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RAG1 | GRCh38.p7 | 11:36570370 | GAATAGATAAAAAAT[A/G]TCTAATCTAAGTCTA | 5896 |
rs4151009 | snp | A/G | 0.00345422 | 0.0414147 | intron-variant | RAG1 | GRCh38.p7 | 11:36570457 | AAATCACAAGTAAGG[A/G]TAAAAAATAGTGCAG | 5896 |
rs4151010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAG1 | GRCh38.p7 | 11:36570531 | ACTTCCTTTGGATAA[A/T]TACCCAGTAGTAGGA | 5896 |
rs4151011 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | RAG1 | GRCh38.p7 | 11:36570532 | CTTCCTTTGGATAAA[C/T]ACCCAGTAGTAGGAC | 5896 |
rs4151012 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RAG1 | GRCh38.p7 | 11:36571461 | ATTTTGAGGTGTTCG[C/T]TGGGCTGCAGTTGAA | 5896 |
rs4151013 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RAG1 | GRCh38.p7 | 11:36571614 | AATTTTTATGAAAAA[C/T]GCCCATTTCTTTGTT | 5896 |
rs4151014 | snp | A/T | 0.0722614 | 0.17581 | intron-variant | RAG1 | GRCh38.p7 | 11:36571812 | tggtacagatggagt[A/T]tcaccatgttggcca | 5896 |
rs4151015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAG1 | GRCh38.p7 | 11:36571881 | CCTTGACCTCCCAAA[A/G]TGTTGGGATCACAGG | 5896 |
rs4151016 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAG1 | GRCh38.p7 | 11:36571956 | GTGATGCATGTAAGA[C/T]AGAACAAACTTCAGT | 5896 |
rs4151017 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RAG1 | GRCh38.p7 | 11:36571993 | GGGACTTGAAAAGAG[A/G]CTTTGGTAACAGCTG | 5896 |
rs4151018 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RAG1 | GRCh38.p7 | 11:36572141 | TTGATCAATTGAGGG[A/G]AAAACATATGTTACT | 5896 |
rs4151019 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAG1 | GRCh38.p7 | 11:36572238 | TTGAAAATACAGCTG[C/T]TCTCTTTCCAATCAT | 5896 |
rs4151020 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RAG1 | GRCh38.p7 | 11:36572338 | CTTTTTTTCTGCATC[A/G/T]CTAGCGATCTGTGCA | 5896 |
rs4151021 | snp | A/C | 0.00333889 | 0.0407222 | intron-variant | RAG1 | GRCh38.p7 | 11:36572461 | TTACAAACTATAGTG[A/C]TAATGACCATCGACC | 5896 |
rs4151022 | snp | C/T | 0.0119756 | 0.0764486 | intron-variant | RAG1 | GRCh38.p7 | 11:36572597 | GCAGGTTTAGAGTTC[C/T]GTGTTTTTTGTTTCT | 5896 |
rs4151023 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RAG1 | GRCh38.p7 | 11:36572867 | TGTCCAGCTAGTACA[A/G]TGAGGCTAATACAAT | 5896 |
rs4151024 | snp | G/T | 0.029116 | 0.117091 | intron-variant | RAG1 | GRCh38.p7 | 11:36572910 | ACTTTTCTTTGATTT[G/T]AGTAGCCTGTTTATC | 5896 |
rs4151025 | snp | A/G | 0.0221141 | 0.102801 | RAG1 | 11 | allele_origin=G(germline)/A(germline) | 11:36573607 | AGCAAGAGGCAAAGC[A/G]ATCCATCAAGCCAAC | 5896 |
rs4151026 | in-del | -/C | 0.0110494 | 0.0735024 | frameshift-variant | RAG1 | GRCh38.p7 | 11:36573640 | CGACATCTCTGCCGC[-/C]ATCTGTGGGAATTCT | 5896 |
rs4151027 | snp | C/G/T | 0.000263706 | 0.0114798 | missense | RAG1 | GRCh38.p7 | 11:36573810 | AGGCAGATGTTGACT[C/G/T]GATCCACCCCACTGA | 5896 |
rs4151028 | snp | A/C/T | 0.0329012 | 0.124701 | synonymous-codon | RAG1 | GRCh38.p7 | 11:36573934 | CCCCCACACACCATC[A/C/T]TGTGACATCTGCAAC | 5896 |
rs4151029 | snp | A/G/T | 0.000428456 | 0.0146303 | missense | RAG1 | GRCh38.p7 | 11:36574044 | AAGCAAGACAAGCCC[A/G/T]TCAGCGCAAGAGAAG | 5896 |
rs4151030 | snp | A/C | 0.0147491 | 0.0845991 | RAG1 | 11 | allele_origin=A(germline)/C(germline) | 11:36574210 | ACACATTCTGGCTGA[A/C]CCTGTGGAGACCAAC | 5896 |
rs4151031 | snp | A/G | 0.0206614 | 0.0995179 | missense | RAG1 | GRCh38.p7 | 11:36574650 | CGAGGAATGAGCACA[A/G]GCAAGCTGATGAGCT | 5896 |
rs4151032 | snp | C/T | 0.00543836 | 0.0518614 | missense | RAG1 | GRCh38.p7 | 11:36574877 | TTTGAGTGGCAGCCA[C/T]CTCTGAAGAATGTGT | 5896 |
rs4151033 | snp | A/G | 0.00888638 | 0.0660622 | RAG1 | 11 | allele_origin=G(germline)/A(germline) | 11:36575942 | TCCGAGGAGAGGCAC[A/G]AGGCTCTGAGGGAGC | 5896 |
rs4151034 | snp | A/G | 0.00701122 | 0.0587916 | missense | RAG1 | GRCh38.p7 | 11:36575963 | CTGAGGGAGCTGATG[A/G]ATCTTTACCTGAAGA | 5896 |
rs4151035 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36576674 | TTATCTGAAAGCTCA[A/G]TAACTCAGAACAGGA | 5896 |
rs4151036 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36576834 | TTTTCCCCCTTGATT[A/G]ATTATATTTTGTATT | 5896 |
rs4151037 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36576856 | TTTTGTATTGAGATA[C/T]GATAAGTGCCTTCTA | 5896 |
rs4151038 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36577025 | TGCATTTACCCATTC[A/G]TTATATAAATATGTT | 5896 |
rs4151039 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36577175 | TACACCTGTTAGCTA[C/T]AGTTAGTTATTAAAT | 5896 |
rs4151040 | snp | C/T | 0.117188 | 0.211804 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36577519 | TGTGTAGCAGGATAA[C/T]CTTGTATTTTTCCAT | 5896 |
rs4151041 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36577540 | ATTTTTCCATCCGCT[A/G]AGTTTAGATGGAGTC | 5896 |
rs4151042 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36577930 | TCTGGCTCTTTTGAT[A/C]GAAGAAAGCAACACA | 5896 |
rs4151043 | snp | C/G | 0.00344233 | 0.0413439 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36578369 | TAGTTTTTTTGAAAA[C/G]TCTTGGTTTTGTTTT | 5896 |
rs4151044 | snp | C/T | 0.029116 | 0.117091 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36578414 | GGCCACTAAGCCACA[C/T]TTTCCCTTCATCCTG | 5896 |
rs4151045 | snp | C/T | 0.118584 | 0.212673 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36578682 | CTTAATCAGATCACA[C/T]TTTGATAAACCCTGG | 5896 |
rs4151046 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36578765 | TGCCCTTACTGTTGA[G/T]ACTGCAATATCCTAG | 5896 |
rs4151047 | snp | G/T | 0.0448719 | 0.142907 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36578966 | AAGTTTTCCTGCCAA[G/T]CCACTCAGGTGCATT | 5896 |
rs4151048 | in-del | -/T | 0.118235 | 0.212457 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36579134 | TAGTTTTGCCTCAGA[-/T]TTTTTTTCCCACAAG | 5896 |
rs4151049 | in-del | -/A | 0.0137924 | 0.0818901 | utr-variant-3-prime | RAG1 | GRCh38.p7 | 11:36579743 | TTGAATATTTGAAAT[-/A]AAAGTTTAAGATTTG | 5896 |
rs4151050 | snp | A/G | 0.0134861 | 0.0810011 | downstream-variant-500B | RAG1 | GRCh38.p7 | 11:36580161 | CTCATTGCAAACTCC[A/G]CCTCCTGGGTTCAGG | 5896 |