SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs748913 | snp | C/G | 0.128632 | 0.218563 | intron-variant, utr-variant-3-prime | CBLC | GRCh38.p7 | 19:44800321 | AATCTTTCCCTCTGC[C/G]CCTCTTCCCTGTCCC | 23624 |
rs899087 | snp | A/G | 0.368119 | 0.220336 | intron-variant | CBLC | GRCh38.p7 | 19:44791300 | ttttttttgcgggac[A/G]gagccccactccgtt | 23624 |
rs1079419 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | CBLC | GRCh38.p7 | 19:44778981 | CTGAGGGCATGGGTG[C/T]CCAAGGAAGGAGAAA | 23624 |
rs1382090 | snp | C/G/T | 0.0315095 | 0.1215 | intron-variant, missense, nc-transcript-variant | CBLC | GRCh38.p7 | 19:44784417 | ACACCCTCCTCCTAC[C/G/T]AGAATGGAGACTCAC | 23624 |
rs1809335 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CBLC | GRCh38.p7 | 19:44780734 | tgtaatcccagcact[C/T]tgggaggctgaggtg | 23624 |
rs1809336 | snp | A/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44778760 | gggcctggacccctg[A/G]gtctgagggaggagg | 23624 |
rs1903830 | snp | A/G | 0.386884 | 0.209196 | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44794621 | AAAAATTAGCGGGGC[A/G]TGGTGGTGGGTGCCT | 23624 |
rs1903831 | snp | C/G/T | 0.135463 | 0.222223 | | | GRCh38.p7 | 19:44794197 | AAGGGGCACCTGGGG[C/G/T]GGGACAGAGGAAGGA | 23624 |
rs1903832 | snp | C/T | 0.0539704 | 0.155153 | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44792923 | CTGACCTCAAGTGAT[C/T]CACCCACCCCGGCCT | 23624 |
rs1903833 | snp | C/T | 0.0539704 | 0.155153 | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44792828 | CACTATTCTCAGCCC[C/T]GTTCTCCAGGGGACG | 23624 |
rs1973164 | snp | C/G/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44781746 | gagtccaggccccag[C/G/T]ccctcctccctcaga | 23624 |
rs2014155 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | CBLC | GRCh38.p7 | 19:44778852 | ctgagggaggagggg[A/C]tgggggctggatccc | 23624 |
rs2014163 | snp | A/C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44778705 | ctgagggaggagggg[A/C/G]tggggcctggacccc | 23624 |
rs2376550 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CBLC | GRCh38.p7 | 19:44799951 | CACCCTTCTGCTCAC[C/T]TGTGTGCCCCACAGA | 23624 |
rs2376551 | snp | A/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44799672 | CTTTTCTTTCTTTTT[A/T]AAAaacaacaacaac | 23624 |
rs2376552 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | CBLC | GRCh38.p7 | 19:44795688 | CTTTGAACATACAGC[A/C]GAGCAGGGCCCCGAG | 23624 |
rs2889414 | snp | C/T | 0.495963 | 0.0447464 | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44794671 | TCTAGACCAGCCTGA[C/T]CAACATGGTGAAATT | 23624 |
rs2927441 | snp | C/G | 0 | 0 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800966 | agggaggaggggctg[C/G]agtatggactcctgg | 23624 |
rs2927442 | snp | A/G | 0.5 | 0 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800942 | CTCCTGGGTCTGAGG[A/G]AGGAGGGGCTGCAGT | 23624 |
rs2927443 | snp | A/G/T | 0.046775 | 0.145601 | intron-variant | CBLC | GRCh38.p7 | 19:44797322 | cggaggttgcaatgg[A/G/T]ctgagatcgtgccac | 23624 |
rs2927444 | snp | C/T | 0.046775 | 0.145601 | intron-variant | CBLC | GRCh38.p7 | 19:44796799 | AAGCCTGTGTGTACT[C/T]AGCCGGAGATACTAA | 23624 |
rs2927445 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | CBLC | GRCh38.p7 | 19:44795124 | ctaaaaatccaaaaa[G/T]tagtcgggcatggtg | 23624 |
rs2927447 | snp | A/G | 0.455263 | 0.142713 | intron-variant | CBLC | GRCh38.p7 | 19:44787220 | attttcagtagagac[A/G]gggtttcaccgtgtt | 23624 |
rs2927448 | snp | A/C | 0.361474 | 0.223771 | intron-variant | CBLC | GRCh38.p7 | 19:44784592 | GGCCACTTTGTGCGA[A/C]CCTCAGAGGCGCCCC | 23624 |
rs2927450 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | CBLC | GRCh38.p7 | 19:44780582 | AGGAGGCTGAGGCAG[C/G]AGAATCGCTGGAGCC | 23624 |
rs2927485 | snp | C/G | 0.255224 | 0.249945 | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44776717 | CCACACCATTAGGGG[C/G]ACCCAGAAATCTTGT | 23624 |
rs2965112 | snp | C/T | 0.368529 | 0.220116 | intron-variant | CBLC | GRCh38.p7 | 19:44799256 | ttgacctcctgggct[C/T]aaaccatcctcctgc | 23624 |
rs2965113 | snp | A/G | 0.37955 | 0.213815 | intron-variant | CBLC | GRCh38.p7 | 19:44798667 | CTCACTGCAACTTCC[A/G]CCTCCTGGCGGAAGC | 23624 |
rs2965114 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | CBLC | GRCh38.p7 | 19:44796762 | TGCTTCTCCCCAGCA[A/G]TCCAGGGTCCCAAAA | 23624 |
rs2965115 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CBLC | GRCh38.p7 | 19:44796270 | tgtcacctctctgaa[C/T]ttttttcctctggaa | 23624 |
rs2965117 | snp | C/T | 0.215144 | 0.247558 | intron-variant | CBLC | GRCh38.p7 | 19:44790462 | GGCGACAGAAGAGAT[C/T]CTGTCTCTAAAAATA | 23624 |
rs2965118 | snp | C/G | 0.384976 | 0.210431 | intron-variant | CBLC | GRCh38.p7 | 19:44789032 | ATTCCGACATGTATA[C/G]CACATGAAATATTGG | 23624 |
rs2965119 | snp | C/G | 0.188316 | 0.242271 | intron-variant | CBLC | GRCh38.p7 | 19:44788262 | CATGGTGGCATGTGC[C/G]TGTGGTCTCAGCTAC | 23624 |
rs2965120 | snp | A/T | 0.00319169 | 0.0398203 | intron-variant | CBLC | GRCh38.p7 | 19:44787483 | taaattagaaaaaaa[A/T]tttaaatGCAGCGTC | 23624 |
rs2965121 | snp | C/T | 0.360842 | 0.224085 | intron-variant | CBLC | GRCh38.p7 | 19:44787428 | AAGAAGGGACTTCTA[C/T]GATTGACTTTATTTT | 23624 |
rs2965122 | snp | C/T | 0.140581 | 0.224783 | intron-variant | CBLC | GRCh38.p7 | 19:44787120 | AGGCGTGAGCCACTG[C/T]GCCCAGCTTATGATT | 23624 |
rs2965123 | snp | C/T | 0.195214 | 0.243923 | intron-variant | CBLC | GRCh38.p7 | 19:44785117 | GGGTGTGGTGGTGGG[C/T]GCCTGTAATCCCACC | 23624 |
rs2965124 | snp | C/T | 0.164219 | 0.234823 | intron-variant | CBLC | GRCh38.p7 | 19:44783006 | CTGGAAGAATGCTAA[C/T]GCACTCACCGTCCTA | 23624 |
rs2965125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CBLC | GRCh38.p7 | 19:44782154 | agagtccaggccccc[A/C]gccctcccctccctc | 23624 |
rs2965126 | snp | A/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44782124 | caaaccctggagtcc[A/G]ggccctcaccccctc | 23624 |
rs2965127 | snp | C/G | | | missense, nc-transcript-variant | CBLC | GRCh38.p7 | 19:44780912 | TGGCCAGCTTGGCCA[C/G]CTGTCGCCTGTGGGG | 23624 |
rs2965143 | snp | A/G | 0.45198 | 0.147323 | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44776083 | gaccacttgagcccc[A/G]gaggtcaaggctgca | 23624 |
rs2965144 | snp | C/G | 0.0517044 | 0.152246 | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44777228 | AGCCTGGGAGACAGA[C/G]GTTGCAGTGAGCTAA | 23624 |
rs2967668 | snp | C/T | 0.272511 | 0.248984 | intron-variant | CBLC | GRCh38.p7 | 19:44799694 | tctttctctctctct[C/T]tctttACTTTTCTTT | 23624 |
rs2967669 | snp | A/G | 0.384593 | 0.210677 | intron-variant | CBLC | GRCh38.p7 | 19:44798685 | AAGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 23624 |
rs3208856 | snp | C/T | 0.0577857 | 0.159855 | missense, nc-transcript-variant | CBLC | GRCh38.p7 | 19:44793549 | AGTATCTACCAGTTC[C/T]ACGGTCAGGCTACTG | 23624 |
rs3894294 | snp | A/C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44778742 | ctgagggaggagggg[A/C/G]tgggggcctgagttt | 23624 |
rs4803756 | snp | A/G | 0.386884 | 0.209196 | intron-variant | CBLC | GRCh38.p7 | 19:44783382 | agcgtggtggcgtgc[A/G]cctgtaatcccagct | 23624 |
rs6509171 | snp | A/G | 0.158302 | 0.232576 | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44775900 | gcctgtaatcccagc[A/G]ttgtgggaggcccag | 23624 |
rs7256808 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CBLC | GRCh38.p7 | 19:44795344 | aacatcacaagaccc[A/C]aacactacaaaaaaa | 23624 |
rs7259180 | snp | C/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800843 | cctcctccctcagac[C/T]caggagtccatactc | 23624 |
rs7259193 | snp | C/G | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800894 | ccaggagtccatact[C/G]cagcccctcctccct | 23624 |
rs7508548 | snp | A/T | | | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44777630 | attttatttttaaaa[A/T]ttttttagagatagg | 23624 |
rs9630872 | snp | C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44786524 | ggcgtgaaccctgga[C/G]gcggaggttgcagtg | 23624 |
rs10401942 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CBLC | GRCh38.p7 | 19:44789178 | TACAaccctggttct[C/T]ggtctctctggtcct | 23624 |
rs10405573 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CBLC | GRCh38.p7 | 19:44793077 | gaatcacttgaacct[C/G]ggaggcagaggttgc | 23624 |
rs10416628 | snp | A/G | 0.0170109 | 0.0906425 | synonymous-codon, intron-variant, nc-transcript-variant | CBLC | GRCh38.p7 | 19:44782477 | TCTGCAGGCCTGCAG[A/G]GACAAGCCAGGCAGG | 23624 |
rs10418198 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | CBLC | GRCh38.p7 | 19:44800054 | GCAGCATGGACTAGG[A/G]ACAAGGCCAAAGGTC | 23624 |
rs10419669 | snp | A/G | 0.247621 | 0.249989 | intron-variant | CBLC | GRCh38.p7 | 19:44794812 | gatgtgtcctacctc[A/G]gggcctttgcataag | 23624 |
rs10420519 | snp | G/T | 0.0948562 | 0.196037 | intron-variant | CBLC | GRCh38.p7 | 19:44795204 | ctcagctgatccacc[G/T]ccttggcctcccaaa | 23624 |
rs10423426 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | CBLC | GRCh38.p7 | 19:44791687 | cagtgagccaagatc[A/G]cgccactgcactcca | 23624 |
rs10423646 | snp | A/G | 0.081446 | 0.184634 | intron-variant | CBLC | GRCh38.p7 | 19:44791771 | GTAGACATGTAGGAG[A/G]CCATTGGACATGCCA | 23624 |
rs10424785 | snp | C/T | 0.182933 | 0.240836 | intron-variant | CBLC | GRCh38.p7 | 19:44791775 | ACATGTAGGAGGCCA[C/T]TGGACATGCCAGCCT | 23624 |
rs10426226 | snp | A/G | 0.211516 | 0.24702 | intron-variant | CBLC | GRCh38.p7 | 19:44787010 | gaattgcttgaaccc[A/G]ggaggttgaggctgc | 23624 |
rs10675488 | in-del | -/AAAAT | | | upstream-variant-2KB | CBLC | GRCh38.p7 | 19:44776162 | AGACCCTGTCTCAAA[-/AAAAT]AAAATAAAATAAAAT | 23624 |
rs11667464 | snp | G/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44785104 | agccgcctgagtagg[G/T]gggattacaggcacc | 23624 |
rs11671247 | snp | C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44785135 | caccaccacacccgg[C/G]taattttttgtgtgt | 23624 |
rs12327715 | snp | A/G | 0.306431 | 0.243548 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800804 | GCCCCTCCTCCCTCA[A/G]ACCCAGGAGTCCATA | 23624 |
rs12327718 | snp | C/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800978 | actccagcccctcct[C/T]cctcagacccaggag | 23624 |
rs12327719 | snp | C/T | 0 | 0 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44801011 | catactgcagcccct[C/T]ctccctcagacccag | 23624 |
rs12327720 | snp | A/G | 0.110872 | 0.20771 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44801065 | tcctcagacccagga[A/G]tccatactgcagccc | 23624 |
rs12327723 | snp | G/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800991 | ctccctcagacccag[G/T]agtccatactgcagc | 23624 |
rs12327896 | snp | C/T | 0 | 0 | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44801050 | actgcagcccctcct[C/T]cctcagacccaggaa | 23624 |
rs12610209 | snp | G/T | | | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44792890 | ggtggctcacgcctg[G/T]aatctcagcactttg | 23624 |
rs12971367 | snp | C/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44778463 | ccagcccctcctccc[C/T]cagacccaggggtcc | 23624 |
rs12972139 | snp | C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44797569 | TTGCTATGTGCCTGG[C/G]ATTGCTTTTTTTTTT | 23624 |
rs12973841 | snp | G/T | 0 | 0 | intron-variant | CBLC | GRCh38.p7 | 19:44797594 | TTTTTTTTTTTAAGA[G/T]GGGGTCTCTGTCtag | 23624 |
rs12975775 | snp | A/C | | | intron-variant | CBLC | GRCh38.p7 | 19:44778526 | actcaggcccccacc[A/C]cctcctccctcagac | 23624 |
rs12976028 | snp | C/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44778633 | gaactcaggccccca[C/T]cccctcctccctcag | 23624 |
rs12976053 | snp | C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44778657 | ccctcagactcaggG[C/G]tccagcccccagccc | 23624 |
rs12976054 | snp | C/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44778663 | gactcaggGCtccag[C/G]ccccagcccctcctc | 23624 |
rs12978314 | snp | A/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44795287 | ttgggaggccaaggc[A/G]ggaggacggcttgag | 23624 |
rs12980982 | snp | C/T | | | intron-variant | CBLC | GRCh38.p7 | 19:44797505 | atctgcctgcctcgg[C/T]cttcttaagtgctgg | 23624 |
rs12983234 | snp | C/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800798 | actccagcccctcct[C/T]cctcagacccaggag | 23624 |
rs12983468 | snp | C/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800880 | ctcctccctcagacc[C/T]aggagtccatactcc | 23624 |
rs12983676 | snp | G/T | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44800811 | ctccctcagacccag[G/T]agtccatactgcagc | 23624 |
rs17852620 | snp | C/T | | | missense, nc-transcript-variant | CBLC | GRCh38.p7 | 19:44793573 | GCTACTGCTGAGGAC[C/T]CAGGGAACAGCAGTG | 23624 |
rs28427198 | snp | G/T | 0.375 | 0.216506 | intron-variant | CBLC | GRCh38.p7 | 19:44784954 | GCTAGACAGGTGTTT[G/T]TTTTTTTTTTTTTTT | 23624 |
rs28431193 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | CBLC | GRCh38.p7 | 19:44787199 | GAGATCGAGACCATC[C/T]TGGCTAACACGGTGA | 23624 |
rs28465377 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | CBLC | GRCh38.p7 | 19:44787373 | TACTTCAGCCTGGGT[A/G]ACAGAACCAGACTCT | 23624 |
rs28465492 | snp | A/C | | | intron-variant | CBLC | GRCh38.p7 | 19:44791025 | TTGGGAGGCTGAGGC[A/C]CGAGAATCACTTGAA | 23624 |
rs28528835 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CBLC | GRCh38.p7 | 19:44798512 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCCGGCCA | 23624 |
rs28534944 | snp | C/T | 0.213937 | 0.247385 | intron-variant | CBLC | GRCh38.p7 | 19:44797831 | CTATAGCCTCAATCT[C/T]CTGGGCTCAAGTGAT | 23624 |
rs28756246 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | CBLC | GRCh38.p7 | 19:44785841 | TACTCCAGAGGCAGA[A/G]GCAGAATTGCTTGAA | 23624 |
rs34114727 | snp | G/T | 0.5 | 0 | intron-variant | CBLC | GRCh38.p7 | 19:44788656 | GGCTAATTATTATTG[G/T]ATTTATTTATTTATT | 23624 |
rs34252312 | snp | C/G | | | downstream-variant-500B | CBLC | GRCh38.p7 | 19:44801038 | CCAGGAGTCCATACT[C/G]CAGCCCCTCCTTCCT | 23624 |
rs34259391 | in-del | -/C/CC/G | 0.033314 | 0.125471 | intron-variant, utr-variant-3-prime | CBLC | GRCh38.p7 | 19:44794193 | TTCTCCTTCCTCTGT[-/C/CC/G]CCCACCCCAGGTGCC | 23624 |
rs34266599 | in-del | -/G | | | intron-variant | CBLC | GRCh38.p7 | 19:44794882 | TCCCATCCCTTTTCA[-/G]GGGAGGCCTTCCCTG | 23624 |
rs34511517 | in-del | -/C | | | intron-variant | CBLC | GRCh38.p7 | 19:44781109 | CTGGCCCAGGGACCC[-/C]AGGGGTCCAGGCCCA | 23624 |
rs34556417 | snp | G/T | | | intron-variant, downstream-variant-500B | CBLC | GRCh38.p7 | 19:44792809 | CGTCTCTGAGCCTTA[G/T]CCTCGTCCCCTGGAG | 23624 |