SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4187 | in-del | -/ATAAAG/TAAAGA | 0.499308 | 0.0185838 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532197 | TGTATTTAAAAAAAA[-/ATAAAG/TAAAGA]TAATCAAATGCTTTT | 55213 |
rs16659 | in-del | -/ACTTTATCATCTTTC | 0 | 0 | utr-variant-3-prime, cds-indel, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533076 | ATTGGCTTATGTGAA[-/ACTTTATCATCTTTC]ACTTTTGGTTTTCCT | 55213 |
rs729051 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546073 | CAACCTGGATCACTG[A/G]TGGGTAAAAGAATAC | 55213 |
rs874398 | snp | C/T | 0.431473 | 0.171952 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551155 | CTCCTTCTCCCTCCC[C/T]GCTTCCCCCTTCCCC | 55213 |
rs882970 | snp | A/C | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570859 | GACAGATGAGGACTG[A/C]GGCTCAAAGGTGAAA | 55213 |
rs942871 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550485 | GGACATAGGAGGTAA[A/G]ACCTTACAATTAGGC | 55213 |
rs1046027 | snp | A/G | 0.487558 | 0.0778863 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533187 | CTACTATATATGACT[A/G]GAAGAAGTGGTTCTT | 55213 |
rs1046028 | snp | A/G | 0.487368 | 0.0784625 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533153 | GTCAACCCTCTTACA[A/G]GACTTAGTGGAATTT | 55213 |
rs1046034 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532675 | AATTTGTGTCTATTG[G/T]GGTGGGAAGGGGAGT | 55213 |
rs1062975 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533780 | GGAAGTTGGCAGCAC[A/T]CTCCTGGGCCATGTA | 55213 |
rs1062979 | snp | C/G | 0.487113 | 0.0792303 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533239 | CATGTATAGTATACT[C/G]TTGCCTTCCTAAATT | 55213 |
rs1128767 | snp | G/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533095 | CACACATTGGCTTAT[G/T]TGAAACTTTATCATC | 55213 |
rs1198421 | snp | C/T | 0.162909 | 0.23434 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575719 | taaagacaggaacaa[C/T]agacactggagacta | 55213 |
rs1198422 | snp | A/G | 0.165853 | 0.235413 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581606 | ggaaaaaagcaagtg[A/G]aataaggagagcaga | 55213 |
rs1325658 | snp | G/T | 0.311614 | 0.242289 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586896 | TTTTCTTCAACAGCC[G/T]CCAAAGTACACATCA | 55213 |
rs1325659 | snp | A/G | 0.444267 | 0.157354 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586906 | CAGCCTCCAAAGTAC[A/G]CATCAGTTTCCTACT | 55213 |
rs1359541 | snp | A/G | 0.47709 | 0.104548 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584803 | TACATGCAAATAAAT[A/G]AAAACAAAAGGCCAC | 55213 |
rs1359542 | snp | A/G | 0.261608 | 0.24973 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584937 | GCACGCCTGGATAAA[A/G]GTCCTCACTAACAAA | 55213 |
rs1359543 | snp | A/G | 0.477004 | 0.104734 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585029 | GCACTACTCTCAGGA[A/G]ACGAAGGAGAGATGC | 55213 |
rs1409013 | snp | A/T | 0.146314 | 0.227484 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543254 | GGGTGACAGAATGAG[A/T]CTCTGTCTCAAAAAA | 55213 |
rs1536192 | snp | A/G | 0.2462 | 0.249971 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546849 | CACCTCCTGCCGTGC[A/G]ACCCAGTTAATAACA | 55213 |
rs1536195 | snp | C/T | 0.279991 | 0.248195 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541533 | AACTACACAATACTA[C/T]TTTTAAAGATACTTA | 55213 |
rs1570883 | snp | A/G | 0.279991 | 0.248195 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547075 | TACAAATCTGAAGAT[A/G]TGTACAGAAGTGCTT | 55213 |
rs1570884 | snp | A/G | 0.498673 | 0.0257246 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547375 | GAAAATTAACCTTCA[A/G]TATCAATTGCTGAAC | 55213 |
rs1853829 | snp | C/T | 0.495213 | 0.048687 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583691 | AGCTGGGACTACAGG[C/T]GCACACCACCACGCC | 55213 |
rs1886793 | snp | C/T | 0.261332 | 0.249743 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571313 | ATTGCACCACTGCAC[C/T]CCAGCCTGGGGAAGA | 55213 |
rs1925742 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535448 | AGCTTGACTTTATTA[C/T]AACTTGGTTAGCTGG | 55213 |
rs1925743 | snp | A/G | 0.440746 | 0.161604 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585117 | AAAACGGCACCCACA[A/G]CAGTCAGACTTCAGC | 55213 |
rs1969881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542230 | aaaaaaaaaaaaaaG[G/T]AAGTATATTAACTAC | 55213 |
rs1977352 | snp | G/T | 0.499942 | 0.00539106 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535793 | ACTTTGGGAGGCTGA[G/T]GCGGGCAGATCACGA | 55213 |
rs1977353 | snp | A/G | 0.270892 | 0.249126 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542002 | ggtagatcacctgag[A/G]tcaggagttcgagac | 55213 |
rs1998780 | snp | A/G | 0.245061 | 0.249951 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554708 | GCATCTAGGCTGTGC[A/G]CTCCATATGAGAATC | 55213 |
rs1998781 | snp | C/G | 0.245061 | 0.249951 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555037 | GGGTAACTAAAGGGA[C/G]AGTTGTTAAAAGTAG | 55213 |
rs2002407 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551058 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 55213 |
rs2038881 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561041 | ATTCTGATGAAGACA[A/G]CTTTTCTTGTGTTAT | 55213 |
rs2093472 | snp | A/T | 0.499759 | 0.0109798 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571258 | GGCTGAGGCAGGAGA[A/T]TCGCTTGAACCTGGG | 55213 |
rs2104183 | snp | C/T | 0.261884 | 0.249717 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575809 | tcactacctgggtga[C/T]ggaattattcgtact | 55213 |
rs2274278 | snp | A/G | 0.24909 | 0.249998 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552246 | TGCCATTGTTTCCCA[A/G]GCCCAGCTGACCGTT | 55213 |
rs2274279 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552354 | AAGAGACAAAAAAAC[C/T]AGCCCATCTAAACAA | 55213 |
rs2274280 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552369 | CAGCCCATCTAAACA[A/G]ATCAGATACTTCCAA | 55213 |
rs2274281 | snp | C/T | 0.442926 | 0.158996 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552531 | TTCCTGTTTAATACA[C/T]GAGGAAGTTGAGCCT | 55213 |
rs2274282 | snp | G/T | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555181 | TGTACAGTTGACATT[G/T]TTTCATTGGAAGAGA | 55213 |
rs2274283 | snp | C/T | 0.429087 | 0.174436 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555463 | TTGTGAAGAAACTGA[C/T]GTGTAATTGAAAAAG | 55213 |
rs2274284 | snp | A/G | 0.263012 | 0.249661 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555479 | GTGTAATTGAAAAAG[A/G]AGGTAGAAAGGGAAA | 55213 |
rs2296502 | snp | A/T | 0.135838 | 0.222412 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540845 | AAAGGGAGTTAAAGG[A/T]GGTCTGGTTTCTGTT | 55213 |
rs2407696 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538389 | ACATTAGTCAATTAC[A/G]TAACTTGTATTGTAA | 55213 |
rs2407697 | snp | G/T | 0.279991 | 0.248195 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546299 | ACCATGTGACTTTCC[G/T]TCTAACACTCAGATG | 55213 |
rs2897741 | snp | C/T | 0.32627 | 0.238082 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538416 | GTAACCTAAGAAATA[C/T]ACCCTAGAAAGAggc | 55213 |
rs3039280 | in-del | -/A | 0.67801 | 0.108985 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547175 | GCAAAAAAAAAAAAA[-/A]TACTGTATTATACCT | 55213 |
rs3186012 | snp | C/G | 0.487621 | 0.0776941 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533837 | GTCGTTTTTGGTCTT[C/G]TTTTCATTTTTGATT | 55213 |
rs3186013 | snp | C/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533768 | AACTCTCCTGGGCCA[C/T]GTATCAACAATCTTC | 55213 |
rs3186024 | snp | C/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532448 | GTAACAATCACTGTT[C/T]TATAGGCTTATGATC | 55213 |
rs3215806 | in-del | -/A | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552346 | TAAGAAGGAAGAGAC[-/A]AAAAAACCAGCCCAT | 55213 |
rs3751381 | snp | C/G | 0.341668 | 0.232587 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549696 | GTGTGGTGTGCTGTG[C/G]GCTTCTGTGATCATG | 55213 |
rs3751382 | snp | A/C/G/T | 0.35518 | 0.234281 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549552 | GTGCCGGGGTCAGTC[A/C/G/T]GTGATCCTCCCGCAC | 55213 |
rs3751383 | snp | C/T | 0.34065 | 0.232986 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549513 | CTTCTCCTGCACCGA[C/T]GACGTGTTTGCCTGC | 55213 |
rs3751384 | snp | C/G | 0.485509 | 0.0840565 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549486 | CTGCTTTGCCACTCC[C/G]GCCGTCTCGTGGCGC | 55213 |
rs3764082 | snp | C/G | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551029 | TGCAACCTTCACTTC[C/G]TGGGTTCAAGTGATT | 55213 |
rs3794376 | snp | A/G | 0.279991 | 0.248195 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540355 | TGAGTTCTTAATCTG[A/G]GATTCACAGATCTGT | 55213 |
rs3794377 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536999 | ATATTAAGACCATCA[A/G]TGCTCTGTGTTTTGT | 55213 |
rs3990354 | in-del | -/CAGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535569 | GGTGGGAATGTTAGA[-/CAGA]GTGGAAGGGGCCCAC | 55213 |
rs4085853 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535979 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55213 |
rs4941644 | snp | A/G | 0.411578 | 0.190768 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531569 | aactcaggcagtaat[A/G]ctcactcatccgcca | 55213 |
rs4941645 | snp | C/T | 0.28052 | 0.24813 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559457 | gtcaggagatcgaga[C/T]catcctggctaacac | 55213 |
rs4941646 | snp | A/T | 0.444666 | 0.15686 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571662 | GGTTTTGTGGGGCTA[A/T]GTGCCAGGCAGAACA | 55213 |
rs4941647 | snp | C/G | 0.0562535 | 0.1581 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581654 | CTAAGAAACTCCAAC[C/G]GGAAAGGGACAGGGA | 55213 |
rs4941648 | snp | A/G | 0.26326 | 0.249648 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582029 | atcacagaatgtgat[A/G]gagttgcaggacgtt | 55213 |
rs4942838 | snp | A/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531771 | attctactatgtctc[A/T]atgaatttgactaag | 55213 |
rs4942839 | snp | G/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531818 | catcacatagtattt[G/T]tctgtgagtggctta | 55213 |
rs4942840 | snp | C/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531942 | AAAAAAACAACTCTA[C/T]GTGCCTGTTTTAATG | 55213 |
rs4942841 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532196 | AGTGTATTTAAAAAA[A/G]ATAATCAAATGCTTT | 55213 |
rs4942842 | snp | A/C | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535149 | CACTAATATCTCAGA[A/C]CATCACCCCCACAGA | 55213 |
rs4942843 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535151 | CTAATATCTCAGAAC[A/G]TCACCCCCACAGAAG | 55213 |
rs4942844 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542516 | TAAAGTGAAAGAAAT[G/T]CAGAAACAAGAGTTC | 55213 |
rs4942845 | snp | G/T | 0.303938 | 0.244112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548792 | ggttgctaggggttg[G/T]ggggagaggagaatg | 55213 |
rs4942847 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559415 | taatcccagcacttt[G/T]ggaggccaaggcggg | 55213 |
rs4942848 | snp | A/G | 0.472875 | 0.113254 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567209 | GTGCCGAAGACACAC[A/G]CCTTCCGAATAGACG | 55213 |
rs4942849 | snp | A/C | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571644 | AGACAAGGTTCCCTG[A/C]GAGGTTTTGTGGGGC | 55213 |
rs5803469 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541438 | ACTTAAAAATAAATT[-/A]AAAAAAAAAAAGTCC | 55213 |
rs5803471 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551917 | AAAAAAAAAAAAAAA[-/A]GCATTAGAAAAGCCT | 55213 |
rs5803472 | in-del | -/T | 0.314544 | 0.241524 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551959 | TACTGAATTTTTCCA[-/T]TTTTTTTTTTTTTTT | 55213 |
rs6145049 | in-del | -/TGTG | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583387 | GTGTGCTTTTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 55213 |
rs6420300 | snp | A/C | 0.270621 | 0.249148 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551799 | CAGCTACTCGGGAGG[A/C]TGAGGCAGGAGAATG | 55213 |
rs6561539 | snp | C/G | 0.228547 | 0.249078 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537993 | ACTTTCGTAGAAAGA[C/G]AAGAAACATTGGAAG | 55213 |
rs6561540 | snp | C/G | 0.245346 | 0.249957 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543982 | ATGAGCCACCATGCT[C/G]AGCCTAGAACATTCT | 55213 |
rs6561541 | snp | C/T | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553144 | CCAAGATCGTGCTAC[C/T]GTACTCCAGCCTGGC | 55213 |
rs6561542 | snp | C/T | 0.270892 | 0.249126 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553384 | TCCCTCGTTAGCAAA[C/T]AGGTGAGCTCTGATG | 55213 |
rs6561544 | snp | G/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572787 | GAGTGATAAGAGTGA[G/T]ACTCTGTCTCAAAAT | 55213 |
rs7140107 | snp | C/T | 0.429388 | 0.174127 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561909 | CCAGACTGGCCAACA[C/T]AGTGAAACCCCACAT | 55213 |
rs7317140 | snp | A/T | 0.279726 | 0.248226 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542900 | ATTTTCTTATGTATA[A/T]CACAGTTGTATCTTT | 55213 |
rs7317982 | snp | C/T | 0.499585 | 0.0143996 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534116 | AGAACCCAGCAGCCT[C/T]GCGCTTCAGTTCTTA | 55213 |
rs7320475 | snp | A/T | 0.432504 | 0.170857 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566304 | aataaataaataaat[A/T]aaAAAGTTGCATTGC | 55213 |
rs7322077 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534721 | GAAGAGATATGGTCA[A/G]CCTAAAGTGGCACAT | 55213 |
rs7322971 | snp | C/T | 0.381503 | 0.21262 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553583 | GGTTCCAAATAGCCA[C/T]AGGAAAAAGTACTGA | 55213 |
rs7324024 | snp | C/T | 0.258288 | 0.249863 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587376 | GGCATGGGGTGTGAG[C/T]AATCAAATATGTCCT | 55213 |
rs7325207 | snp | C/G | 0.400147 | 0.19989 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538707 | ggcaacagaacaaga[C/G]cctgtatcaccagga | 55213 |
rs7325667 | snp | A/G | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566393 | CCACAGCTTTATGGA[A/G]GCAGTCGAAAACCTC | 55213 |
rs7325851 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539079 | ttcaccatgttggcc[A/G]ggctggtctcaaact | 55213 |
rs7326825 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539314 | TGGAGTCTTTCTAAA[A/G]GAAGTTTTTATCATG | 55213 |
rs7327411 | snp | C/T | 0.140919 | 0.224948 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539086 | tgttggccaggctgg[C/T]ctcaaactcctgatc | 55213 |