SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12007 | snp | C/T | 0.482234 | 0.0925596 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676926 | GCTTACTTCTAAAAA[C/T]TGAGGTTAAGATATA | 140545 |
rs1014831 | snp | A/G | 0.472522 | 0.113946 | intron-variant, downstream-variant-500B | RNF32, LOC101927858 | GRCh38.p7 | 7:156654377 | ACTCCACCATCTTCT[A/G]TCAGGGACTTGAGCA | 140545 |
rs1024605 | snp | C/T | 0.380529 | 0.213219 | intron-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156673002 | gagcttttcaggctt[C/T]gccccgggcctgccg | 140545 |
rs1045032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF32 | GRCh38.p7 | 7:156665707 | ATTCTCCACTCCCAC[C/T]CACCAGCCATCTCGA | 140545 |
rs2108794 | snp | C/T | 0.179105 | 0.239737 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655014 | TGGGACACAGCTGCT[C/T]CTGGGAAGCCCCCCA | 140545 |
rs2159195 | snp | A/G | 1.65403e-05 | 0.00287574 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RNF32, LOC101927858 | GRCh38.p7 | 7:156654729 | CTAGCTCACCCTCGT[A/G]TGCTAAACACCTGAG | 140545 |
rs2240646 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156677750 | TTATTCATAAATGAT[A/G]CATACATATGTAGCT | 140545 |
rs2302145 | snp | C/T | 0.489602 | 0.0713489 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676496 | TCTGGAACGCCTGCC[C/T]GCACCCACGCGCTGA | 140545 |
rs2302146 | snp | A/G | 0.466727 | 0.124616 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676485 | TGCCTGCACCCACGC[A/G]CTGACCGCCAGCAGC | 140545 |
rs2302147 | snp | C/G | 0.465247 | 0.127225 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676439 | GCAGATGGAGCACTC[C/G]TGGGTCTCCCGGCGC | 140545 |
rs2302148 | snp | C/T | 0.075637 | 0.179158 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676429 | CACTCGTGGGTCTCC[C/T]GGCGCAGAGCCTGCG | 140545 |
rs2302149 | snp | A/G | 0.491904 | 0.063107 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156676402 | TGCGGCACACAGGAC[A/G]GGAAGAGGCCACGCG | 140545 |
rs2302150 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | RNF32 | GRCh38.p7 | 7:156662169 | GCTGTTGAGTTCTAC[C/T]CATACAGGCATACAA | 140545 |
rs2365509 | snp | C/T | 0.437401 | 0.165472 | intron-variant | RNF32 | GRCh38.p7 | 7:156671286 | CAGCACCAATCAGAT[C/T]ATGTATGTGTTACTC | 140545 |
rs2365510 | snp | A/G | 0.442655 | 0.159323 | intron-variant | RNF32 | GRCh38.p7 | 7:156671395 | CTCTTTACAGAAGAA[A/G]GCTGATGTGCTGATA | 140545 |
rs2365511 | snp | A/G | 0.37955 | 0.213815 | intron-variant | RNF32 | GRCh38.p7 | 7:156671417 | GTGCTGATACCTGAC[A/G]AAAGAGATTCTAAAG | 140545 |
rs2365513 | snp | A/G | 0.487305 | 0.0786545 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675962 | AGGACTCACTTTGGG[A/G]AGCCTAGGAGTGTCA | 140545 |
rs2365514 | snp | C/T | 0.480539 | 0.0967035 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156676065 | TAGGAGTGTCAGTCC[C/T]GGGGTAACCGCTGCC | 140545 |
rs2886380 | snp | C/G | 0.473948 | 0.111829 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675683 | AGCTTACCCGCCCCC[C/G]CCTCCTCCTCAGTTC | 140545 |
rs2886381 | snp | A/C | 0.447966 | 0.161595 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675684 | GCTTACCCGCCCCCG[A/C]CTCCTCCTCAGTTCA | 140545 |
rs3030984 | in-del | -/AA/AG/GA | | | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156673920 | taaaaaaaaaaaaaa[-/AA/AG/GA]aaGAAAAAGTGAACG | 140545 |
rs3217035 | in-del | -/GTTT | | | intron-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156657386 | TACTATTTATTGTTT[-/GTTT]AGCACAGCACAAGTA | 140545 |
rs3735189 | snp | A/G | 0.21695 | 0.247806 | upstream-variant-2KB, nc-transcript-variant | RNF32, C7orf13 | GRCh38.p7 | 7:156638860 | GAAACAGCAACAGAC[A/G]TGAAATGGCAGTTGT | 140545 |
rs3823615 | snp | A/C | 0.444533 | 0.157025 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156676062 | AGCGGTTACCCCGGG[A/C]CTGACACTCCTAGGC | 140545 |
rs3823617 | snp | A/G | 0.0752019 | 0.178733 | splice-donor-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675865 | CTGCCAGCCAAACCT[A/G]CCTGCACTTGGATTT | 140545 |
rs4716437 | snp | C/T | 0.453575 | 0.145111 | intron-variant | RNF32 | GRCh38.p7 | 7:156649341 | GGTTTTCTGAGTAAG[C/T]TGATCTCTGCAGTGA | 140545 |
rs4716438 | snp | C/T | 0.464203 | 0.128908 | intron-variant | RNF32 | GRCh38.p7 | 7:156649509 | acacgtttcatttac[C/T]tacttatgtgatgtt | 140545 |
rs4716439 | snp | A/G | 0.4776 | 0.103433 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156677564 | AACTACAAGGGGCAA[A/G]GAAAGGGCAGGGTGT | 140545 |
rs4716647 | snp | C/T | 0.475437 | 0.108066 | intron-variant | RNF32 | GRCh38.p7 | 7:156648167 | AAGTTAGAAATATGA[C/T]TTTTTATTGATAGGC | 140545 |
rs4716648 | snp | A/C | 0.46865 | 0.121211 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156656762 | AAAACCCTTCGCCTG[A/C]CCCCACCGCTTTGCT | 140545 |
rs4716649 | snp | A/T | 0.470034 | 0.11868 | intron-variant | RNF32 | GRCh38.p7 | 7:156671534 | ATAAAAACTGACCAT[A/T]CGCTTGTCCATGATG | 140545 |
rs6945589 | snp | C/T | 0.497881 | 0.0324789 | intron-variant | RNF32 | GRCh38.p7 | 7:156663585 | GCTGTGCATTTAGGA[C/T]TTTACAGGTTAACTC | 140545 |
rs6947383 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | RNF32 | GRCh38.p7 | 7:156642703 | agaggacggcatccc[A/G]tggcagggcacactc | 140545 |
rs6948790 | snp | A/G | 0.222928 | 0.24853 | intron-variant | RNF32 | GRCh38.p7 | 7:156647132 | gttgggattaaaggc[A/G]tgagtcaccatgcct | 140545 |
rs6954377 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RNF32 | GRCh38.p7 | 7:156668684 | AGCAGCACGCTTTCC[A/G]TCGTCAGCGGGGCTT | 140545 |
rs6965850 | snp | A/G | 0.475259 | 0.108435 | intron-variant | RNF32 | GRCh38.p7 | 7:156664043 | CAGACAAAACACCAC[A/G]ATCCTAGCAGAACGT | 140545 |
rs6973359 | snp | A/T | 0.459233 | 0.136827 | intron-variant | RNF32 | GRCh38.p7 | 7:156647163 | ggccTGttttttttt[A/T]attttttgtttgttt | 140545 |
rs6977459 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | RNF32 | GRCh38.p7 | 7:156653351 | accagctaagcatgt[A/G]tacatatgctgtgat | 140545 |
rs6978799 | snp | A/G | 0.476401 | 0.106032 | intron-variant | RNF32 | GRCh38.p7 | 7:156654142 | TCCTATATACAGTCC[A/G]CCATTTGTATCCGTG | 140545 |
rs6980337 | snp | A/G | 0.472335 | 0.114312 | intron-variant, upstream-variant-2KB | RNF32, C7orf13 | GRCh38.p7 | 7:156641852 | GTCTTGATGAGATAC[A/G]GGGTGGAACTTATTT | 140545 |
rs7776665 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | RNF32 | GRCh38.p7 | 7:156669670 | CTCAGAGCCCCGGGG[A/G]TGCGAGGTCAGCAGC | 140545 |
rs7780080 | snp | C/T | 0.00822766 | 0.0636093 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676707 | AAAAGTTTACCATCA[C/T]TTTGGATGAACTGCA | 140545 |
rs7786612 | snp | A/G | 0.378174 | 0.214642 | intron-variant | RNF32 | GRCh38.p7 | 7:156671645 | TGGGTGTACTGCAGG[A/G]CGCCGATGTTTGCGG | 140545 |
rs7787888 | snp | C/T | 0.0217676 | 0.102029 | upstream-variant-2KB, nc-transcript-variant, intron-variant | RNF32, C7orf13 | GRCh38.p7 | 7:156640354 | CGGGCGGCTGAGGAG[C/T]GTGGCTGCGCCCACA | 140545 |
rs7788200 | snp | C/G | 0.474427 | 0.110148 | upstream-variant-2KB, nc-transcript-variant, intron-variant | RNF32, C7orf13 | GRCh38.p7 | 7:156640549 | ACCTGCGTCTAGACG[C/G]TGACGCCGTGCGCGG | 140545 |
rs7790357 | snp | C/T | 0.362104 | 0.223456 | intron-variant | RNF32 | GRCh38.p7 | 7:156671520 | ACAAATATATCATTA[C/T]AAAAACTGACCATAC | 140545 |
rs7792326 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | RNF32 | GRCh38.p7 | 7:156669248 | GTGGAGGCCGCTCGG[G/T]TGGTTCGCGCCTGCT | 140545 |
rs7797221 | snp | A/G | 0.357024 | 0.225933 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156673918 | TAATAAAAAAAAAAA[A/G]AAAAGAAAAAGTGAA | 140545 |
rs7797375 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156674010 | CATTTTCCCCATCAC[A/G]TATCTAAATGTGTGA | 140545 |
rs7800925 | snp | C/T | 0.448963 | 0.151372 | intron-variant | RNF32 | GRCh38.p7 | 7:156646103 | gtttgtgcctgtaaa[C/T]aaaggcatgcaaatc | 140545 |
rs7803221 | snp | A/G | 0.499902 | 0.00698814 | intron-variant | RNF32 | GRCh38.p7 | 7:156671817 | ATGTTCCCTGACCAC[A/G]GTGCAGCTGAGGCTA | 140545 |
rs7803361 | snp | A/G | 0.435263 | 0.167862 | intron-variant | RNF32 | GRCh38.p7 | 7:156671884 | CGTTTGAAAATAAAC[A/G]GTTCTAAATAACGTA | 140545 |
rs7804211 | snp | C/T | 0.380138 | 0.213458 | intron-variant | RNF32 | GRCh38.p7 | 7:156644075 | AAAAACAATCTCTGG[C/T]GATATTTACTGCAAG | 140545 |
rs7804623 | snp | A/C | 0.46875 | 0.121031 | intron-variant | RNF32 | GRCh38.p7 | 7:156668488 | GCGGGTGGAGCCGGG[A/C]TCCAGTGACTTGCAC | 140545 |
rs7805523 | snp | C/T | 0.439502 | 0.163061 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156674547 | TGCCTCAGATGACAC[C/T]GGTGGCCACTCTGTA | 140545 |
rs7805578 | snp | C/T | 0.346147 | 0.230772 | upstream-variant-2KB, nc-transcript-variant | RNF32, C7orf13 | GRCh38.p7 | 7:156639037 | CGTCCCATCCCAGGA[C/T]TGAAGAAGTACCAGG | 140545 |
rs7806832 | snp | A/G | 0.469049 | 0.120489 | intron-variant | RNF32 | GRCh38.p7 | 7:156644171 | TAAGCTGAAATGGCA[A/G]GAGTCTCCTTAGTAG | 140545 |
rs7806861 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RNF32 | GRCh38.p7 | 7:156644252 | CATGCACAGGTTTAT[A/G]GGTCATAATGAATTT | 140545 |
rs7811858 | snp | A/G | 0.128288 | 0.218372 | intron-variant | RNF32 | GRCh38.p7 | 7:156669266 | GTTCGCGCCTGCTGC[A/G]GGGCACGCTTCCTGC | 140545 |
rs7812229 | snp | C/T | 0.153 | 0.230415 | intron-variant | RNF32 | GRCh38.p7 | 7:156665768 | GACTCTGCTGAACTA[C/T]GAGAGAAATCTGGGG | 140545 |
rs9632531 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675628 | ATAGATGGTCAGGCT[C/T]GAGAGCGCTTCCCTG | 140545 |
rs9638048 | snp | A/C | 0.469544 | 0.119585 | intron-variant, upstream-variant-2KB | C7orf13, RNF32 | GRCh38.p7 | 7:156638358 | AAAATAAAAAATTCA[A/C]AATATTCTTCGTGGC | 140545 |
rs10227910 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156677741 | ACATTATATAGCTAC[A/G]TATGTATGTATCATT | 140545 |
rs10228019 | snp | A/G | 0.480697 | 0.0963277 | downstream-variant-500B, intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156677816 | ATGTATACTATCAAA[A/G]AATTTGCAGACTAAT | 140545 |
rs10235562 | snp | A/C | 0.471578 | 0.115772 | intron-variant | RNF32 | GRCh38.p7 | 7:156644300 | GGCTTTCATAATTAA[A/C]TGAAAAGATATTCCT | 140545 |
rs10236219 | snp | C/T | 0.472616 | 0.113763 | intron-variant | RNF32 | GRCh38.p7 | 7:156653624 | TTTTATGCATTGACC[C/T]GTCTTTGGGGTGCGG | 140545 |
rs10238744 | snp | C/T | 0.469148 | 0.120308 | intron-variant | RNF32 | GRCh38.p7 | 7:156670096 | TTATAAATTTTATGA[C/T]TTTCACAGTGCATCT | 140545 |
rs10242736 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | RNF32 | GRCh38.p7 | 7:156670932 | AGACATTGATTCCAC[C/T]GAACAAGAAAACTCA | 140545 |
rs10243532 | snp | C/T | 0.472616 | 0.113763 | intron-variant | RNF32 | GRCh38.p7 | 7:156645768 | gtgtgaatatgtatt[C/T]agagtaagaccaaaa | 140545 |
rs10244351 | snp | C/T | 0.496999 | 0.0386216 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655449 | TGTAACAATTTCCCA[C/T]GTGGTGTGGCATTAC | 140545 |
rs10245086 | snp | C/T | 0.499137 | 0.0207489 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655998 | ATTCCATTATTTTTA[C/T]TTGGTTTTGATATAA | 140545 |
rs10251049 | snp | G/T | 0.475437 | 0.108066 | intron-variant | RNF32 | GRCh38.p7 | 7:156647208 | ttcttttttatttAt[G/T]tttatttcaatagct | 140545 |
rs10251511 | snp | A/G | 0.472522 | 0.113946 | intron-variant | RNF32 | GRCh38.p7 | 7:156653706 | CAGTTGCTTTTTCAA[A/G]GTGAGTGTTTCCCAC | 140545 |
rs10253748 | snp | A/G | 0.471483 | 0.115954 | intron-variant | RNF32 | GRCh38.p7 | 7:156645821 | aaaacaacatgaaat[A/G]tatcccaaacaaaaa | 140545 |
rs10259532 | snp | C/G | 0.473451 | 0.112115 | intron-variant | RNF32 | GRCh38.p7 | 7:156664321 | ACAATATTAGCCGGG[C/G]GTGGTGGCGCACGCC | 140545 |
rs10262406 | snp | G/T | 0.434109 | 0.169127 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655293 | ATGCATATATATATA[G/T]AGAGAGAGAGAGAGA | 140545 |
rs10644735 | in-del | -/CT | 0.464416 | 0.128553 | intron-variant | RNF32 | GRCh38.p7 | 7:156650025 | CATCTGGGCCTGAGG[-/CT]CTTTTTTTCCTTTAA | 140545 |
rs11289679 | in-del | -/A | 0.18134 | 0.240387 | intron-variant | RNF32 | GRCh38.p7 | 7:156672046 | GGTTTTCTTCTGTGG[-/A]ATCAAACACCTGAGT | 140545 |
rs11375940 | in-del | -/T | 0.46865 | 0.121211 | intron-variant | RNF32 | GRCh38.p7 | 7:156671840 | GAGGCTAGAAATAAA[-/T]TTTTTTTTAAAAAAA | 140545 |
rs11450384 | in-del | -/T | 0.465208 | 0.127223 | intron-variant | RNF32 | GRCh38.p7 | 7:156648029 | TTGTTTTTTTTTTTT[-/T]CTTGCTGATTTGTTT | 140545 |
rs11771028 | snp | A/C | 0.499942 | 0.00539106 | intron-variant | RNF32 | GRCh38.p7 | 7:156663157 | CATTCTTAATAATGA[A/C]AGACACTAGAACTAG | 140545 |
rs11974552 | snp | C/T | 0.030665 | 0.119967 | intron-variant, utr-variant-3-prime, upstream-variant-2KB | RNF32, LOC101927858 | GRCh38.p7 | 7:156660102 | CTGCTGCCTCCTCGT[C/T]CTGAGCCCTCATCGC | 140545 |
rs11975186 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF32 | GRCh38.p7 | 7:156670676 | ATTTCCCAGTGGGAG[C/T]GGCAGAAGGTGAGAT | 140545 |
rs11981703 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RNF32 | GRCh38.p7 | 7:156670660 | ACCCTGGGACCTGCA[C/G]ATTTCCCAGTGGGAG | 140545 |
rs12697992 | snp | A/C | 0.46137 | 0.133501 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156675134 | CCGAAGAGGCAGCGG[A/C]GACCCGAAGGGGCAG | 140545 |
rs13231848 | snp | C/T | 0.343477 | 0.231866 | intron-variant, upstream-variant-2KB | C7orf13, RNF32 | GRCh38.p7 | 7:156638289 | GAATTTATCGAATTA[C/T]CACGTTATCCAAAAA | 140545 |
rs13239577 | snp | C/G | 0.477345 | 0.103991 | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655262 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 140545 |
rs13244139 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNF32, C7orf13 | GRCh38.p7 | 7:156640877 | GGGCGGGGTCCATGG[A/T]TTCGGGGTGAGGGCC | 140545 |
rs17563187 | snp | A/C | 0.367091 | 0.220884 | intron-variant | RNF32 | GRCh38.p7 | 7:156667820 | TAAGAATATTCATCC[A/C]AGTTCACTGTTTAAA | 140545 |
rs34197477 | in-del | -/C | | | intron-variant, nc-transcript-variant | RNF32, LOC101927858 | GRCh38.p7 | 7:156655395 | ACTTAGATTTATCAG[-/C]AAGTGTGTGTGTGCG | 140545 |
rs34281476 | snp | C/T | 0.24932 | 0.249999 | intron-variant | RNF32 | GRCh38.p7 | 7:156651651 | ACTAATAACATTCAG[C/T]GTTTACTCTGTTACA | 140545 |
rs34334634 | in-del | -/CACT | 0.472335 | 0.114312 | intron-variant | RNF32 | GRCh38.p7 | 7:156653092 | TTCACACTCACTCAG[-/CACT]CACTCACTGACTCAC | 140545 |
rs34350577 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RNF32, LOC101927858 | GRCh38.p7 | 7:156660888 | CATCAGTCAGTACAT[-/G]GGAAGTTATACATTG | 140545 |
rs34374516 | in-del | -/A | 0.472429 | 0.114129 | intron-variant | RNF32 | GRCh38.p7 | 7:156652930 | GCTAAATGTTATTGT[-/A]AAAAATTTAAAAGTT | 140545 |
rs34432951 | snp | A/G | 0.223522 | 0.248594 | intron-variant | RNF32 | GRCh38.p7 | 7:156664330 | GCCGGGCGTGGTGGC[A/G]CACGCCTGTAATCCC | 140545 |
rs34490738 | in-del | -/ATA | 0.499801 | 0.00998203 | intron-variant, upstream-variant-2KB | RNF32, LOC101927858 | GRCh38.p7 | 7:156661210 | CAGCAAGGAGTGGGC[-/ATA]ATAAGGGGCATCTCA | 140545 |
rs34583699 | in-del | -/A | 0 | 0 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156673907 | TTGCTCCACATTAAT[-/A]AAAAAAAAAAAAAAA | 140545 |
rs34754466 | in-del | -/C | | | intron-variant, upstream-variant-2KB | RNF32 | GRCh38.p7 | 7:156642832 | GAGGACGTGCAAACT[-/C]CCAAACAGACAGTGG | 140545 |
rs34768691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | RNF32, LMBR1 | GRCh38.p7 | 7:156674072 | CTTTGTGCTTCAAGC[C/T]GGATTCCATGAAGCA | 140545 |
rs34819142 | snp | A/G | 0.00165136 | 0.0286872 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF32, LMBR1 | GRCh38.p7 | 7:156676479 | CTCTCCGCTGCTGGC[A/G]GTCAGCGCGTGGGTG | 140545 |