SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs726443 | snp | C/T | 0.496746 | 0.040204 | intron-variant | CBLB | GRCh38.p7 | 3:105719476 | ATCATGGTGATCCTA[C/T]AAGATTATAATGAAG | 868 |
rs726444 | snp | C/T | 0.319376 | 0.240181 | intron-variant | CBLB | GRCh38.p7 | 3:105719694 | tggtttatgtactta[C/T]tatactatacttttt | 868 |
rs769315 | snp | A/G | 0.491051 | 0.0662916 | intron-variant | CBLB | GRCh38.p7 | 3:105802181 | CAGATTCTTTTCTTC[A/G]TTACTCGGCCCCTGC | 868 |
rs769316 | snp | C/T | 0.247621 | 0.249989 | intron-variant | CBLB | GRCh38.p7 | 3:105802190 | TTCTTCATTACTCGG[C/T]CCCTGCCCCTAGCCT | 868 |
rs769317 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | CBLB | GRCh38.p7 | 3:105802210 | GCCCCTAGCCTCTTT[C/T]CTTACTGTAGCTTTC | 868 |
rs894541 | snp | C/G | 0.334412 | 0.235318 | intron-variant | CBLB | GRCh38.p7 | 3:105789807 | CCTGGATATTGGCTT[C/G]TCTAGTTCTATTCAA | 868 |
rs894937 | snp | A/G | 0.339656 | 0.233371 | intron-variant, utr-variant-5-prime | CBLB | GRCh38.p7 | 3:105724109 | ATTCTCAGTGCATTT[A/G]TATACATATAATTTT | 868 |
rs920711 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CBLB | GRCh38.p7 | 3:105857558 | CTTGTATTGGATTAA[C/T]GATATTTTAATGGTC | 868 |
rs964173 | snp | A/G | 0.197703 | 0.244469 | intron-variant | CBLB | GRCh38.p7 | 3:105770690 | TGGGAAGACGAAGAG[A/G]GGCATGGCTTTTTGA | 868 |
rs971109 | snp | C/T | 0.236434 | 0.249632 | intron-variant | CBLB | GRCh38.p7 | 3:105828517 | AAATATTAAGATAGA[C/T]GCCAAAATACTTGAA | 868 |
rs971110 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | CBLB | GRCh38.p7 | 3:105828620 | CACATTTTTTTAGCA[C/T]AAAATAGAAAAGAAA | 868 |
rs976961 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CBLB | GRCh38.p7 | 3:105783987 | ATTTTAACTTTGCAT[C/T]AATGCTAAAGCAGGA | 868 |
rs976962 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CBLB | GRCh38.p7 | 3:105784042 | CAAATGGTTTTAATC[C/T]GGAAAATCTATTATG | 868 |
rs981479 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | CBLB | GRCh38.p7 | 3:105787200 | ATTTTTTAAAGGTCT[A/C]AGACTTTCACAAATG | 868 |
rs999046 | snp | A/G | 0.341685 | 0.232581 | intron-variant | CBLB | GRCh38.p7 | 3:105701421 | ACAAGTTGTGTTACT[A/G]TACATGTCATAAATC | 868 |
rs1020327 | snp | A/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105715322 | AAAGTATTTTGTGAT[A/T]CTAACTAGAATATGT | 868 |
rs1025885 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | CBLB | GRCh38.p7 | 3:105789386 | ATTATAAATTTTACA[A/T]GTTCTGTATTTTCTC | 868 |
rs1025886 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | CBLB | GRCh38.p7 | 3:105789436 | GGAACGTTTTTAGAA[A/G]AAATTTGTACTATCC | 868 |
rs1036877 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CBLB | GRCh38.p7 | 3:105716741 | TATCTAACTCCCATA[A/G]GAAAGTATAACAAGA | 868 |
rs1036982 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CBLB | GRCh38.p7 | 3:105687534 | TAAAATCTGTGTAAG[C/T]TGACAATTTATACTA | 868 |
rs1036983 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CBLB | GRCh38.p7 | 3:105687354 | CAAATTAGCCACAAC[A/G]TATGTGATTTAAAAA | 868 |
rs1042852 | snp | A/G | 0.3512 | 0.228601 | utr-variant-3-prime, nc-transcript-variant | CBLB | GRCh38.p7 | 3:105658671 | TTTACCTTGTTTACA[A/G]TTTGGCAAAGTTGCA | 868 |
rs1075739 | snp | C/T | 0.294576 | 0.245994 | intron-variant | CBLB | GRCh38.p7 | 3:105722289 | TTAACACATGAAGAA[C/T]GGAAAGCAGTACTTT | 868 |
rs1155058 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CBLB | GRCh38.p7 | 3:105747815 | ATTAGTGGAAGAGTG[G/T]TTGAAAAAAAATGCT | 868 |
rs1292862 | snp | A/T | 0 | 0 | intron-variant | CBLB | GRCh38.p7 | 3:105679336 | TTTTTTTTTTTTTTT[A/T]AAGACTCAAGGTAAT | 868 |
rs1348348 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CBLB | GRCh38.p7 | 3:105754315 | GTATATGAGAGGAAG[G/T]GAACCCAGAAAGCAT | 868 |
rs1372982 | snp | A/T | 0.494855 | 0.0504572 | intron-variant | CBLB | GRCh38.p7 | 3:105730158 | GGTGTAAAACAGCGA[A/T]AAAAATGCAGTCTTA | 868 |
rs1443098 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CBLB | GRCh38.p7 | 3:105749486 | AAATATGTCCACATA[C/T]TAAATAGCAGTTTAG | 868 |
rs1443099 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105769403 | AGATGCAGTCTCTGC[C/T]TCCAAATAAACTTTC | 868 |
rs1443100 | snp | A/T | 0.227664 | 0.249 | intron-variant | CBLB | GRCh38.p7 | 3:105849532 | GACATTTAAGTTTTG[A/T]TTGATAATGTATAGA | 868 |
rs1443101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CBLB | GRCh38.p7 | 3:105844581 | TGAGGATATATGTAT[A/G]CATCAATGGTTCATA | 868 |
rs1443102 | snp | G/T | 0.491263 | 0.0655142 | intron-variant | CBLB | GRCh38.p7 | 3:105806447 | AGAAGTGGTAACTAT[G/T]TATATGGGTTTGTGA | 868 |
rs1443103 | snp | A/G | 0.437824 | 0.164991 | intron-variant | CBLB | GRCh38.p7 | 3:105829108 | ATCCCCTGTCCTCCC[A/G]TGTAATGAATGCTGA | 868 |
rs1443104 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CBLB | GRCh38.p7 | 3:105697765 | TTAGGACAATGTCAC[C/T]GTAAGTTACATGACC | 868 |
rs1443105 | snp | C/T | 0.339656 | 0.233371 | intron-variant | CBLB | GRCh38.p7 | 3:105703180 | TAATCTGATGATTGA[C/T]TTGTAATTTTAATGT | 868 |
rs1443106 | snp | A/C | 0.351635 | 0.228408 | intron-variant | CBLB | GRCh38.p7 | 3:105703302 | GTAATACAGGAAAAT[A/C]AAACACTACTAAATA | 868 |
rs1443107 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CBLB | GRCh38.p7 | 3:105703451 | TTAACTGTAGAGTAA[A/G]AATTATGTCTTTAAT | 868 |
rs1443108 | snp | C/T | 0.349452 | 0.229367 | intron-variant | CBLB | GRCh38.p7 | 3:105703561 | TTCCCTCTTCTGAGT[C/T]GCCTTGAAACAAGGG | 868 |
rs1470283 | snp | C/G | 0.492435 | 0.0610346 | intron-variant | CBLB | GRCh38.p7 | 3:105838857 | GTTGGCCAGGATGGT[C/G]TTGATCTCCTGACCT | 868 |
rs1522287 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | CBLB | GRCh38.p7 | 3:105677712 | AAGACTTAATAAACT[A/G]TCTGTTGCATTAGTT | 868 |
rs1530420 | snp | A/G | 0.352287 | 0.228117 | intron-variant | CBLB | GRCh38.p7 | 3:105673548 | TTAGTTTCTGCTTTG[A/G]TATACTCTATTAAAA | 868 |
rs1530421 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CBLB | GRCh38.p7 | 3:105673492 | CAGGTGGTTTATGGA[C/T]GGCCAGGGAGGAAAT | 868 |
rs1545304 | snp | C/T | 0.32955 | 0.237006 | intron-variant | CBLB | GRCh38.p7 | 3:105702979 | TATTCTGGTAATAAC[C/T]GATAAAGAAGCAGAG | 868 |
rs1546733 | snp | A/G | 0.496874 | 0.0394129 | intron-variant | CBLB | GRCh38.p7 | 3:105690477 | TAGAAGAGAGGATCA[A/G]TTTAACTTAAATTAT | 868 |
rs1548056 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CBLB | GRCh38.p7 | 3:105704244 | TGTTCTTAAAGAATA[C/T]ATTTGGTTGGAAGAA | 868 |
rs1550711 | snp | G/T | 0.492966 | 0.0588865 | intron-variant | CBLB | GRCh38.p7 | 3:105746345 | AATTATTTCATTTGT[G/T]TTTTACAATGGTCAC | 868 |
rs1550712 | snp | A/G | 0.403334 | 0.197456 | intron-variant | CBLB | GRCh38.p7 | 3:105679203 | TAAGTAGTGCTTGGA[A/G]CCAGAGAAGGTTCTA | 868 |
rs1550713 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | CBLB | GRCh38.p7 | 3:105701142 | AGAAATCATTTACTT[G/T]AGAATTCTTGGTAGT | 868 |
rs1561919 | snp | C/T | 0.493432 | 0.0569306 | intron-variant, utr-variant-5-prime | CBLB | GRCh38.p7 | 3:105724099 | TATAACTGGAAAAAT[C/T]ATATGTATATAAATG | 868 |
rs1561920 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | CBLB | GRCh38.p7 | 3:105805000 | CCATACCCACCACCA[C/T]AGTAGTTGCTGTTTG | 868 |
rs1561921 | snp | A/C | 0.030665 | 0.119967 | intron-variant | CBLB | GRCh38.p7 | 3:105807568 | TTAATGGAAAAACAT[A/C]ATTTCATCATAGTTG | 868 |
rs1561922 | snp | C/T | 0.290718 | 0.246662 | intron-variant | CBLB | GRCh38.p7 | 3:105807880 | AGAGGACTTGCATGA[C/T]ACAACTAGTTGGAAA | 868 |
rs1568575 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CBLB | GRCh38.p7 | 3:105679877 | AGCAAAACTCTGTCT[C/T]GTGCATCTTCAGATG | 868 |
rs1584028 | snp | C/T | 0.492775 | 0.059668 | intron-variant | CBLB | GRCh38.p7 | 3:105772079 | caaagcaatactaag[C/T]gaaaagaacaaatct | 868 |
rs1814078 | snp | G/T | 0.194902 | 0.243853 | intron-variant | CBLB | GRCh38.p7 | 3:105853781 | ATTGGAGATAGTAAG[G/T]TAAGATCATTATTTA | 868 |
rs1822348 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CBLB | GRCh38.p7 | 3:105772241 | agctaactgatcttc[A/G]acaaagcatacaaaa | 868 |
rs1838045 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CBLB | GRCh38.p7 | 3:105762103 | tctaagcagcaaagc[A/G]ttcaagaggtgactt | 868 |
rs1838046 | snp | C/T | 0.457504 | 0.139435 | intron-variant | CBLB | GRCh38.p7 | 3:105766711 | ACAGTATAGTATAAA[C/T]ACAACTTCTATATTC | 868 |
rs1867189 | snp | A/G | 0.339882 | 0.233284 | intron-variant | CBLB | GRCh38.p7 | 3:105728902 | TGACACAGCTACTGC[A/G]CATTTCTTAAGTTTT | 868 |
rs1867190 | snp | C/T | 0.319136 | 0.24025 | intron-variant | CBLB | GRCh38.p7 | 3:105755691 | tgagaatttacacag[C/T]acttctagaaggcaa | 868 |
rs1867191 | snp | A/C | 0.493013 | 0.058691 | intron-variant | CBLB | GRCh38.p7 | 3:105760008 | TATCTTTCACATATT[A/C]ATATTCTGCAGCCTA | 868 |
rs1867192 | snp | A/G | 0.407845 | 0.193868 | intron-variant | CBLB | GRCh38.p7 | 3:105849402 | TGTTCACTGTCCTAA[A/G]TGCAACCCTAAGACA | 868 |
rs1867193 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CBLB | GRCh38.p7 | 3:105849327 | TATTACTGTTATCCT[C/T]GTTCTGTTTACTGAC | 868 |
rs1867194 | snp | C/T | 0.235854 | 0.249599 | intron-variant | CBLB | GRCh38.p7 | 3:105823591 | TATTCCAAATCCTCC[C/T]GACTGAGTCACCAGC | 868 |
rs1867195 | snp | A/G | 0.49263 | 0.0602539 | intron-variant | CBLB | GRCh38.p7 | 3:105829332 | AGATGTTTTGTCACA[A/G]TAAAGGCAAGAAGAT | 868 |
rs1867428 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105729286 | GACACAATCCTTAGC[C/T]CCAAGAAGTTAAAGT | 868 |
rs1867429 | snp | A/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105724637 | ACGAGTTTTTTCAAA[A/T]GTTAAGATATGTTTC | 868 |
rs1947000 | snp | G/T | 0.296873 | 0.245566 | intron-variant | CBLB | GRCh38.p7 | 3:105751290 | CTCACTCTAAACTTT[G/T]AACAATGACCAAACA | 868 |
rs1972938 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CBLB | GRCh38.p7 | 3:105679660 | GCCTCCCGAGTAGCC[A/G]GGATTACAGTCACGT | 868 |
rs1972939 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CBLB | GRCh38.p7 | 3:105679626 | ACCATGCCCGGCTAA[C/T]TTTTTGTATTTTAGC | 868 |
rs1992520 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105733907 | CACAATCATTTCAAA[C/T]AAAGCACTTACCAGC | 868 |
rs1992521 | snp | C/T | 0.239614 | 0.249784 | intron-variant | CBLB | GRCh38.p7 | 3:105792352 | TCAGTCCCTCCCAAG[C/T]GGGGAGGCTGCTAAC | 868 |
rs1992522 | snp | C/T | 0.490673 | 0.0676508 | intron-variant | CBLB | GRCh38.p7 | 3:105826019 | AGCTTCAACTAAGCT[C/T]CTTAACAACAATTTC | 868 |
rs2028597 | snp | A/G | 0.208779 | 0.246578 | intron-variant | CBLB | GRCh38.p7 | 3:105839993 | AAATGAGACCCAGCT[A/G]ACCAGGATGGAAATC | 868 |
rs2028598 | snp | G/T | 0.186421 | 0.24178 | intron-variant | CBLB | GRCh38.p7 | 3:105756032 | TTTAATAACTGGCTT[G/T]TGGAAGGGATTATAA | 868 |
rs2028599 | snp | A/G | 0.187369 | 0.242028 | intron-variant | CBLB | GRCh38.p7 | 3:105757493 | AAGATGCAGGCAGCA[A/G]GGTATTACTACTTTA | 868 |
rs2034157 | snp | C/T | 0.49917 | 0.0203505 | intron-variant | CBLB | GRCh38.p7 | 3:105682002 | GTGTTACTTGAGATA[C/T]TTACTTCTACATTTT | 868 |
rs2044164 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | CBLB | GRCh38.p7 | 3:105795171 | CCCAACTCGGCCTCC[C/G]AAAGTGCTGGGATTA | 868 |
rs2053626 | snp | A/G | 0.40157 | 0.198813 | intron-variant | CBLB | GRCh38.p7 | 3:105665583 | ttgttatacaaatat[A/G]tggttatataatatg | 868 |
rs2055557 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | CBLB | GRCh38.p7 | 3:105843394 | ATTTTCTATGTGCAA[C/T]AGGGAAAAGTTTATA | 868 |
rs2055558 | snp | C/G | 0.227664 | 0.249 | intron-variant | CBLB | GRCh38.p7 | 3:105843403 | GTGCAATAGGGAAAA[C/G]TTTATAAACAGATTT | 868 |
rs2055559 | snp | C/T | 0.227664 | 0.249 | intron-variant | CBLB | GRCh38.p7 | 3:105843663 | TATTATTGGGAAATG[C/T]AGAATATGCCATGTT | 868 |
rs2055560 | snp | C/G | 0 | 0 | intron-variant | CBLB | GRCh38.p7 | 3:105843699 | ATATATTTATAAAAA[C/G]TAATGCATAAATTAA | 868 |
rs2083757 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CBLB | GRCh38.p7 | 3:105722536 | aaatattttagtatc[A/G]taactaaaaaccaag | 868 |
rs2083758 | snp | A/G | 0.354665 | 0.227036 | intron-variant | CBLB | GRCh38.p7 | 3:105759318 | cccagaaaaagctcc[A/G]taagttttcactccc | 868 |
rs2083759 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | CBLB | GRCh38.p7 | 3:105796089 | agaattagaaaaaaa[A/T]ctattttaaaattca | 868 |
rs2083760 | snp | A/T | | | intron-variant | CBLB | GRCh38.p7 | 3:105838250 | caacacacctggcta[A/T]ttttttttttttttt | 868 |
rs2083761 | snp | A/G | 0.319136 | 0.24025 | intron-variant | CBLB | GRCh38.p7 | 3:105715912 | ggcgtggtggcaggc[A/G]tctgcaatcccagct | 868 |
rs2089091 | snp | A/G | 0.391024 | 0.206427 | intron-variant | CBLB | GRCh38.p7 | 3:105849758 | CCTTGTCAATGTACT[A/G]ATACCCTAAAGAGTA | 868 |
rs2099892 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | CBLB | GRCh38.p7 | 3:105838496 | TAATAAGAAAGAATA[C/T]CTGCATAAACTGGAA | 868 |
rs2120102 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | CBLB | GRCh38.p7 | 3:105800351 | AGTAGGAGGATGCTT[C/T]CTAGTTCCTTCTAAC | 868 |
rs2120103 | snp | A/G | 0.276534 | 0.248588 | intron-variant | CBLB | GRCh38.p7 | 3:105800472 | AATCACAGCCTTAGC[A/G]GTACCAAAGCACTGG | 868 |
rs2120104 | snp | C/T | 0.318896 | 0.240319 | intron-variant | CBLB | GRCh38.p7 | 3:105804066 | TCAACATTTTTAATA[C/T]ACACATAAAAATCAT | 868 |
rs2120105 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | CBLB | GRCh38.p7 | 3:105809091 | ACAGCAGTGAATGTA[C/T]AGAAAGATATCTGGA | 868 |
rs2120584 | snp | A/C | | | intron-variant | CBLB | GRCh38.p7 | 3:105688019 | AAATCTAATTATTTT[A/C]CCTGTTATTTAGTAG | 868 |
rs2120585 | snp | C/T | 0.335788 | 0.23482 | intron-variant | CBLB | GRCh38.p7 | 3:105683900 | TTAGAATTATCAACA[C/T]TCTGCTGAATTATTA | 868 |
rs2197208 | snp | C/T | 0.287606 | 0.247155 | intron-variant | CBLB | GRCh38.p7 | 3:105746560 | AGACTTTGTATTTGC[C/T]GATGCCTTTACTTGA | 868 |
rs2197209 | snp | G/T | 0.392325 | 0.205532 | intron-variant | CBLB | GRCh38.p7 | 3:105849321 | TGTTATCCTTGTTCT[G/T]TTTACTGACAATGTT | 868 |
rs2197351 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CBLB | GRCh38.p7 | 3:105735321 | TTAGTTTTATTTCTT[C/T]TCCATTTTTATGCAT | 868 |
rs2221379 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | CBLB, LOC107986109 | GRCh38.p7 | 3:105867694 | GCATCTTCCTCCATC[A/G]ATTAGAGCAAAACCA | 868 |