SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3370 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405071 | GACGCACAGAGAGGT[C/T]TCTTCCTGACCCAGA | 5192 |
rs1129171 | snp | A/G | 0.425123 | 0.178415 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405593 | GCTGTCCCTGGCTGC[A/G]CTTTCTCAGCCCTGG | 5192 |
rs1129332 | snp | A/G | 0.367913 | 0.220446 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404771 | GAGATTTCCTGAAGC[A/G]CAGTGTTAAAATGCC | 5192 |
rs1143016 | snp | C/T | 0.10084 | 0.200627 | PEX10 | 1 | allele_origin=T(germline)/C(germline) | 1:2408773 | CTCGCTGCGCCGTGG[C/T]GTGCTGGTGACGCTG | 5192 |
rs1143017 | snp | A/C/G | 5.31307e-05 | 0.00515389 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405718 | CCTCTACGGGAGTCT[A/C/G]AACGCCAAGATTTAG | 5192 |
rs2494426 | snp | C/G | 0.354235 | 0.227234 | intron-variant | PEX10 | GRCh38.p7 | 1:2406098 | AGCTGACACAGCCCA[C/G]GAAGCCCAGCTCCTG | 5192 |
rs2494427 | snp | C/T | 0.353371 | 0.227628 | intron-variant | PEX10 | GRCh38.p7 | 1:2407130 | GACCAGCCTTGGCAT[C/T]ACCAGTGCAGAAAGA | 5192 |
rs2494428 | snp | C/T | 0.373196 | 0.217538 | intron-variant | PEX10 | GRCh38.p7 | 1:2407635 | AAACCACATCAAATA[C/T]GCAAGTGAGGCTGGG | 5192 |
rs2494429 | snp | A/G | 0.370162 | 0.219229 | intron-variant | PEX10 | GRCh38.p7 | 1:2407956 | ATAGGCAGAGGTGCC[A/G]ACGGCTGTGGAGGGG | 5192 |
rs2494430 | snp | C/T | 0.031825 | 0.122064 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414064 | ACCCGGCATCGCCCA[C/T]GTGGAGCCGCTGAGG | 5192 |
rs2494593 | snp | A/G | 0.0763149 | 0.179815 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414732 | CCGCCCCACCTCCCT[A/G]AGACCCCCTCCAGGC | 5192 |
rs2494595 | snp | C/T | 0.21695 | 0.247806 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413252 | GAACCACGCGGCGGC[C/T]TCCCGGCTGCCCCCC | 5192 |
rs2494597 | snp | A/G | 0.208779 | 0.246578 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411755 | AGCCCAGGAGTTTGA[A/G]ACCAGCCTGGGCAAC | 5192 |
rs2494598 | snp | A/G | 0.352672 | 0.227954 | PEX10 | 1 | allele_origin=G(germline)/A(germline) | 1:2408761 | TGGCGTGCTGGTGAC[A/G]CTGCATGCCGTCCTG | 5192 |
rs2494599 | snp | A/G | 0.286825 | 0.247273 | intron-variant | PEX10 | GRCh38.p7 | 1:2407676 | CTCGTCGCAGAGCCA[A/G]TGGTCAGGTCTTCGT | 5192 |
rs3795269 | snp | G/T | 0.486432 | 0.0812835 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406687 | ACATGGGGGCTGGGG[G/T]TGTCCTGGGCACTTC | 5192 |
rs3795270 | snp | A/G | 0.103038 | 0.202251 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405755 | GCTGAGCCGGCGCCC[A/G]GGTGGGCCTGGACAC | 5192 |
rs3820009 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405893 | GAAAAGAAATGCCGA[C/T]GGGGATGGGCATGGC | 5192 |
rs4648634 | snp | C/T | 0.436123 | 0.166908 | intron-variant | PEX10 | GRCh38.p7 | 1:2407988 | GAAGGTGGGAACGGC[C/T]GTCTGATGGGGCAGA | 5192 |
rs4648839 | snp | C/T | 0.181978 | 0.240568 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415043 | GCAGTGGCGGGATCT[C/T]GGCTCACTGCAAGCT | 5192 |
rs6671420 | snp | A/G | 0.448963 | 0.151372 | intron-variant | PEX10 | GRCh38.p7 | 1:2407440 | CAGCCAGACAGCCTC[A/G]GCCCAGGGCCGGGAA | 5192 |
rs6671730 | snp | A/G | 0.449726 | 0.150364 | intron-variant | PEX10 | GRCh38.p7 | 1:2407700 | CGACGAGGTCACGGT[A/G]GCCTCCTGTTTAGGG | 5192 |
rs7556447 | snp | C/G | 0.260227 | 0.249791 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414660 | GAATCGAATCTAGAT[C/G]AGAACCACTGGCGAA | 5192 |
rs9424320 | snp | C/T | 0.217851 | 0.247924 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413486 | GCCCTGAGCTGGGGG[C/T]GGGAAGGGCTGGGGC | 5192 |
rs10910064 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410513 | CTGAGGATGAGGGAC[C/G]ACAGTCCTCCCCCAG | 5192 |
rs10910065 | snp | C/G | 0.368529 | 0.220116 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415084 | ggttcgcaccattct[C/G]ttgcctcagcctcct | 5192 |
rs10910066 | snp | C/T | 0.367708 | 0.220556 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415085 | gttcgcaccattctg[C/T]tgcctcagcctcctg | 5192 |
rs11544146 | snp | G/T | | | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408801 | TGGACCCATCGCGGA[G/T]ACATGTGCCCTCCTC | 5192 |
rs11544147 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405337 | GCCAGCCTCCGTGCC[C/G]CACCCCACCCAGCAC | 5192 |
rs11586985 | snp | C/T | 0.259134 | 0.249833 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405838 | GGGACACTCCGCCTG[C/T]GGAGAGGAGAAAGGG | 5192 |
rs11808033 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PEX10 | GRCh38.p7 | 1:2407226 | AAGGAGGCGGGGAGC[A/G]GAAATGTGGGGCTGC | 5192 |
rs11811122 | snp | G/T | 0.117886 | 0.21224 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414527 | CTTCCTGAGGGCGAC[G/T]TGAATACGGCGGTCC | 5192 |
rs11811535 | snp | C/T | 0.0452528 | 0.143452 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415135 | gcccgccaccacgcc[C/T]ggctaattttttgta | 5192 |
rs12083799 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PEX10 | GRCh38.p7 | 1:2406115 | AAGCCCAGCTCCTGG[C/G]AAAGCGTGCGCTCTC | 5192 |
rs12085089 | snp | C/G | 0.436123 | 0.166908 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404530 | CTGCCCACCCGGCCG[C/G]AGCCCCCAGTGCCTC | 5192 |
rs12089619 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411894 | CCTGGCTGAGCCTAC[A/G]CTGGGGTCAGCAGGG | 5192 |
rs12092052 | snp | C/T | 0.41441 | 0.188333 | intron-variant | PEX10 | GRCh38.p7 | 1:2409065 | AGCACATGACAGGCC[C/T]GGCCAATGGCTGCCC | 5192 |
rs34134106 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414992 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 5192 |
rs34154371 | snp | A/G | 0.0374363 | 0.131593 | PEX10 | 1 | allele_origin=G(germline)/A(germline) | 1:2406576 | AGAAACCCCCTGTGC[A/G]CCCTGTGCCTGGAGG | 5192 |
rs34301537 | in-del | -/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408095 | CTATGTCACTGCTGT[-/G]GGGGAACAAACAGCT | 5192 |
rs34997431 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407713 | GCCTCCACACACACC[C/T]TAAACAGGAGGCCAC | 5192 |
rs35082957 | snp | A/G | 0.00472588 | 0.0483798 | PEX10 | 1 | allele_origin=G(germline)/A(unknown) | 1:2406553 | CCTGGAGGAGCGCAG[A/G]CACCCAACAGCCACG | 5192 |
rs35190685 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414426 | AAGGCCCAGCCAAGG[-/C]CTAGAGCCAAGGCTT | 5192 |
rs35373002 | in-del | -/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408385 | CACTGGACTTGGGTG[-/C]CATGCACAGAGCTGG | 5192 |
rs35426403 | snp | C/T | 0.00318256 | 0.0397637 | PEX10 | 1 | allele_origin=T(germline)/C(unknown) | 1:2408720 | TGGACAAGGCCCTGC[C/T]CCCCCTGGAGCAGGA | 5192 |
rs35832275 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405583 | GCTGCGCTTTCTCAG[-/C]CCTGGGAGGGGCGCC | 5192 |
rs35859093 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405009 | GGGCTGCCAGGGGCG[-/C]CCCGAGCCCTCTCCT | 5192 |
rs36083229 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414397 | TTGAACCGTGGGGGA[-/C]CCCCCAAGCCCCACC | 5192 |
rs41300094 | snp | C/T | 0.000195981 | 0.00989707 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405714 | GAGACTAAATCTTGG[C/T]GTTCAGACTCCCGTA | 5192 |
rs41310349 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405080 | GGAAGAGACCTCTCT[C/G]TGCGTCTCAGGCTGA | 5192 |
rs41315652 | snp | A/G | 0.0128859 | 0.0792269 | intron-variant | PEX10 | GRCh38.p7 | 1:2410477 | AAACAGTATTAGTCC[A/G]GGGGAGCTGGTGGGC | 5192 |
rs55746053 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PEX10 | GRCh38.p7 | 1:2406121 | AGCTCCTGGGAAAGC[A/G]TGCGCTCTCACCCTG | 5192 |
rs55868349 | snp | C/G | 0.0970103 | 0.197722 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415176 | AGACGGGGTTTCACC[C/G]TGTTAGCCAGGATGG | 5192 |
rs57464405 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407888 | TGGTGGTGGGACCAC[A/G]GGGGAGGCTTCGTTG | 5192 |
rs58178170 | snp | A/C/G | 0.5 | 0 | intron-variant | PEX10 | GRCh38.p7 | 1:2407847 | GGCTCTGGTGGGCCA[A/C/G]GGACTAACGCTGTGG | 5192 |
rs58827215 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | PEX10 | GRCh38.p7 | 1:2407219 | CTCAGAAAAGGAGGC[A/G]GGGAGCGGAAATGTG | 5192 |
rs58886116 | snp | C/T | 0.0770498 | 0.180522 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404434 | CGCTCAGGCCTAAGG[C/T]GTGACAGGAAGTCGC | 5192 |
rs61373429 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PEX10 | GRCh38.p7 | 1:2407776 | CAGTGCAGCTCTAGG[G/T]ACAAAAGGAAGGGGG | 5192 |
rs61736380 | snp | C/G/T | 0.00296127 | 0.0383667 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406784 | GCCGCTGCCTGAAAC[C/G/T]GTACAGCTGCAGCCC | 5192 |
rs61750432 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412451 | CGCGCGGCGCAGAAG[A/G]ACGAGTACTACCGCG | 5192 |
rs61750434 | snp | C/T | 0.000153988 | 0.00877328 | PEX10 | 1 | allele_origin=T(germline)/C(germline) | 1:2408679 | GACCCCGACAGTGGG[C/T]GACCCTTGCAGGGGA | 5192 |
rs61750435 | in-del | -/A | 4.27954e-05 | 0.00462557 | PEX10 | 1 | allele_origin=A(germline)/+.-----(germline) | 1:2406791 | GTCCATGGGGCTGCA[-/A]GCTGTACGGTTTCAG | 5192 |
rs61752092 | snp | C/G/T | 4.44148e-05 | 0.00471227 | PEX10 | 1 | allele_origin=T(germline)/C(germline) | 1:2406766 | TTCAGGCAGCGGCAG[C/G/T]GAGCCAGGAAGGAGT | 5192 |
rs61752093 | in-del | -/CT | 0.000101198 | 0.00711259 | PEX10 | 1 | allele_origin=C(unknown)/+.-----(germline) | 1:2406581 | GTTTCCAGAAACCCC[-/CT]GTGCACCCTGTGCCT | 5192 |
rs61752094 | snp | C/G | | | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406528 | GCCACGCCCTGCGGC[C/G]ACCTGTTCTGCTGGG | 5192 |
rs61752095 | snp | C/G | | | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406526 | CACGCCCTGCGGCCA[C/G]CTGTTCTGCTGGGAG | 5192 |
rs61752096 | snp | A/G | 5.06359e-05 | 0.00503144 | PEX10 | 1 | allele_origin=G(germline)/A(unknown) | 1:2406515 | GCCACCTGTTCTGCT[A/G]GGAGTGCATCACCGC | 5192 |
rs61760854 | snp | C/T | 0.29175 | 0.246489 | intron-variant | PEX10 | GRCh38.p7 | 1:2409621 | CCTCTCCCCTGCCCA[C/T]GTCCCTGGAATGCCC | 5192 |
rs62636524 | in-del | -/G | 8.83561e-05 | 0.00664607 | PEX10, PLCH2 | 1 | allele_origin=G(unknown)/+.-----(germline) | 1:2412499 | GAACCCGCGGCCATG[-/G]CCCCGGCCGCCGCCA | 5192 |
rs62641225 | snp | A/G/T | 1.68547e-05 | 0.00290294 | PEX10 | 1 | allele_origin=G(germline)/T(unknown) | 1:2406561 | ACCCTGTGCCTGGAG[A/G/T]AGCGCAGGCACCCAA | 5192 |
rs66876402 | multinucleotide-polymorphism | CC/GT | 0.5 | 0 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415084 | GGTTCGCACCATTCT[CC/GT]TGCCTCAGCCTCCTG | 5192 |
rs72642194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405920 | TTTCCTGTCCACATT[C/G]TCTGCACATGACACA | 5192 |
rs72642195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2405949 | CACAACATAAATGTT[G/T]TATTTCCTTCAACTA | 5192 |
rs72642198 | snp | C/T | 0.15698 | 0.23205 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411128 | TTGGCCACGACACCC[C/T]CACCACTGGGCTCTA | 5192 |
rs72642199 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415313 | AACCACAGGCATTGG[A/G]CAGAAGTGGCCAACA | 5192 |
rs72924936 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404303 | CTTGTGTGTCCCTGA[C/T]CCAAGATAGCCAGTG | 5192 |
rs72924937 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405171 | GCCAAATGCTTCCGA[C/T]GGAGGTGCTGGCCTT | 5192 |
rs74049248 | snp | A/G | 0.0792508 | 0.182605 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404432 | AGCGCTCAGGCCTAA[A/G]GTGTGACAGGAAGTC | 5192 |
rs75124172 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PEX10 | GRCh38.p7 | 1:2407703 | CGAGGTCACGGTGGC[C/T]TCCTGTTTAGGGTGT | 5192 |
rs75377471 | snp | A/G | 0.000322015 | 0.0126848 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408497 | GTGGTAGAAGACACC[A/G]TGGATGTAAAACCAG | 5192 |
rs75437503 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PEX10 | GRCh38.p7 | 1:2405964 | GTATTTCCTTCAACT[A/G]ATGACCAAGAAAGCC | 5192 |
rs75668279 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PEX10 | GRCh38.p7 | 1:2410046 | CAGGGCACTGTCACA[C/T]GGGCACTGCACCCTA | 5192 |
rs76232811 | snp | A/G | 0.117188 | 0.211804 | intron-variant | PEX10 | GRCh38.p7 | 1:2408170 | CGGGGCCCCCCGGTC[A/G]GTAAAGAGCTAAGCG | 5192 |
rs76530653 | snp | C/G | 0.000671488 | 0.018311 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408634 | TCCAGCGCCGCGCCC[C/G]TGAGCAGCCACGCCC | 5192 |
rs77098501 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411535 | ACCACACCCGGCATC[-/T]TTTTTTTTTCGTTTT | 5192 |
rs77398469 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410994 | AATTCTCATCATGTC[A/C]CTCTCCTGTTCAGAA | 5192 |
rs77530733 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412054 | GAAGCACTTGCCAAG[A/G]CCTCACACCTGGAGG | 5192 |
rs77818102 | snp | A/G | 0.0168055 | 0.0901129 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405084 | GAGACCTCTCTGTGC[A/G]TCTCAGGCTGAGATG | 5192 |
rs77863194 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405090 | TCTCTGTGCGTCTCA[A/G]GCTGAGATGCAGATT | 5192 |
rs78277543 | snp | A/C/G | 0.004783 | 0.0487016 | intron-variant | PEX10 | GRCh38.p7 | 1:2409754 | GCTGCTTGCTCTGCC[A/C/G]GTCTGGAAAATGCTC | 5192 |
rs78620392 | snp | A/G | 0.000542106 | 0.0164548 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406500 | TTGCTGCTGCACCAC[A/G]CGGTGATGCACTCCC | 5192 |
rs79073409 | snp | A/G | 0.0174175 | 0.0916809 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404674 | CAAACAGCAAGACAT[A/G]GTTTGCGCGGGTCTT | 5192 |
rs79338697 | snp | G/T | 0.126909 | 0.217598 | intron-variant | PEX10 | GRCh38.p7 | 1:2408134 | GGGCCCAGGTTCAGG[G/T]ATCTGTGGTGAGGCG | 5192 |
rs111376812 | snp | A/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406966 | GCCTGCTGGGAGGGT[A/C]ACACGTTCAGTTGGC | 5192 |
rs111413105 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412603 | TCTGCGTGCGGCGCA[C/G]ACCTCTGCGTCAAGG | 5192 |
rs111500533 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404453 | ACAGGAAGTCGCACG[C/T]GCTTGGCCAGAGCAC | 5192 |
rs111515011 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PEX10 | GRCh38.p7 | 1:2409838 | TGTGACGCAGCCACA[A/T]CTGTCTCCCGCCCAC | 5192 |
rs112094671 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407482 | GGTGGCAGGTCACAC[C/T]GCCAGCATGGGCCCT | 5192 |
rs112163061 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410442 | CTCCACTCCAGCCAC[C/T]TCCTCGCACCTGAGA | 5192 |
rs112471479 | snp | C/G | 0.0337757 | 0.125487 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412497 | GCTGGCGGCGGCCGG[C/G]GCCATGGCCGCGGGT | 5192 |
rs112472583 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412732 | GAAGGTAGTCGGAGG[C/G]GCAGGGCGGAGCGGA | 5192 |
rs112628678 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411804 | CTGCCTCCCAAACTG[C/T]TGGGATGACAGGTGC | 5192 |
rs113220539 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415164 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCCTGT | 5192 |
rs113386569 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414787 | GGCTGACCAGGCAAC[C/G]TGGGAGCTCTGGTTG | 5192 |
rs113396547 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411727 | ATTTTTTGTAGAGAC[C/G]GGGTCTTGCCATGTT | 5192 |
rs113755914 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415505 | CTTGCCACTCAGCCT[A/G]TGTGCCGCCCGGCTT | 5192 |
rs114177386 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PEX10 | GRCh38.p7 | 1:2407276 | CCCTGCTACAGGGAC[C/T]GAAGCCCCAGTGTAA | 5192 |
rs114238434 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404449 | TGTGACAGGAAGTCG[C/T]ACGCGCTTGGCCAGA | 5192 |
rs115010992 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414624 | TTATAGGGGATTAGG[C/T]GGTGAGTTTTGCCCC | 5192 |
rs115207852 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415620 | GCCATTTACAGGGGG[C/T]TCTCACACCCATTCC | 5192 |
rs115495903 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414318 | CGACAAATCCCAGCC[C/T]CACAGTGGGAGGGGC | 5192 |
rs115513809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PEX10 | GRCh38.p7 | 1:2409420 | CTCTGTGGATGGCAA[C/T]GCCAGGCCTCCGGTT | 5192 |
rs115735911 | snp | C/G/T | 0.0182089 | 0.0937193 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405414 | TTCTCACAATATAAA[C/G/T]GAATAAAGTGTCTTC | 5192 |
rs115843065 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413745 | CCTCAGTGGGGAGGG[C/T]CTCCAGTTCCTTGCC | 5192 |
rs115904429 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413010 | CGAGCTCCCAGCGCC[G/T]GCCGCGGCGGTCCCG | 5192 |
rs116081827 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PEX10 | GRCh38.p7 | 1:2407959 | GGCAGAGGTGCCAAC[A/G]GCTGTGGAGGGGAGA | 5192 |
rs116195638 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414578 | GTGGCAGCGTCAGCC[C/T]GTCTGCTCTCCACCG | 5192 |
rs116304725 | snp | C/T | 0.00183855 | 0.0302637 | intron-variant | PEX10 | GRCh38.p7 | 1:2408414 | TGGGGGTGACAAGGA[C/T]GGCCTAAGCAGCTGT | 5192 |
rs116354317 | snp | A/G | 8.48284e-05 | 0.00651207 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408469 | ACGTGATCCCCGTGA[A/G]CCTCTTGGCCAGGTG | 5192 |
rs116441921 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412302 | CGGGCCCAGGCGACC[A/G]TGACCACACACGGCA | 5192 |
rs116579215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406990 | AGTTGGCACAGAGCA[C/T]GTTAGAACCAGGCCT | 5192 |
rs117732581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410679 | TCCCACCTGTGCTCA[C/T]CTCTTGCTCCGGGAT | 5192 |
rs137939573 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PEX10 | GRCh38.p7 | 1:2406117 | GCCCAGCTCCTGGGA[A/C]AGCGTGCGCTCTCAC | 5192 |
rs138171306 | snp | C/T | 0.000163305 | 0.00903471 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408629 | ACGCATCCAGCGCCG[C/T]GCCCCTGAGCAGCCA | 5192 |
rs138326779 | snp | C/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414455 | TTGTAATGGCACCCG[C/G]GACCCTCAGTTGCCT | 5192 |
rs138406081 | snp | A/G | 0.000135373 | 0.00822606 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406502 | GCTGCTGCACCACGC[A/G]GTGATGCACTCCCAG | 5192 |
rs138489241 | snp | C/T | 0.000917586 | 0.0213998 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406874 | CCCTCAGGTCCTCTC[C/T]GGGCAGGCTGCGGAC | 5192 |
rs138843050 | snp | C/T | 0.00018112 | 0.00951458 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408627 | TGACGCATCCAGCGC[C/T]GCGCCCCTGAGCAGC | 5192 |
rs139004865 | snp | C/T | 0.0098832 | 0.0695983 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406436 | CCAGGTGCATCTTGC[C/T]GGCACAGCCGCTGAC | 5192 |
rs139119874 | snp | A/G | 0.00774325 | 0.0617387 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410721 | ACTGTTCTAGGGCCT[A/G]TGAGGGCCACATGGA | 5192 |
rs139190493 | snp | C/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415195 | TAGCCAGGATGGTCT[C/G]GACCTCCTGACCTTG | 5192 |
rs139215764 | snp | C/T | 0.0618563 | 0.164627 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415035 | GCTGGAGTGCAGTGG[C/T]GGGATCTTGGCTCAC | 5192 |
rs139345520 | snp | C/G | 0.00411574 | 0.0451767 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406811 | GCCCCATGGACAGCA[C/G]CAGGTGCAGCAGTGA | 5192 |
rs139821134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411029 | CCAATGGCTGCCCAC[A/C]TGACACCCATGGGCC | 5192 |
rs139887525 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407636 | AACCACATCAAATAC[A/C/G]CAAGTGAGGCTGGGT | 5192 |
rs140051834 | snp | A/C | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413968 | TGACCCCGCGGGTGC[A/C]CCCGTGTCTCCTGGA | 5192 |
rs140107510 | snp | C/G | 0.00311883 | 0.0393661 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406875 | CCTCAGGTCCTCTCC[C/G]GGCAGGCTGCGGACA | 5192 |
rs140133667 | snp | C/T | 0.000218446 | 0.0104487 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406731 | GCACCTGCGGTGAGA[C/T]AGGCCGCGGTGCAGC | 5192 |
rs140253593 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PEX10 | GRCh38.p7 | 1:2408185 | AGTAAAGAGCTAAGC[A/G]CAGGGCCCGGTGTCC | 5192 |
rs140273455 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411231 | CTTGATGGCTTTGCC[-/T]TTTTTTTTTTTTTTT | 5192 |
rs140340426 | snp | A/G | 0.000673253 | 0.018335 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408736 | GCAGGGCCTTGTCCA[A/G]CAGGTAGGGCAGGAC | 5192 |
rs140666446 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404673 | TCAAACAGCAAGACA[C/T]GGTTTGCGCGGGTCT | 5192 |
rs140861161 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PEX10 | GRCh38.p7 | 1:2407096 | CGTAGCCTAGCATGA[C/T]GGAGAGGCCTGAGCT | 5192 |
rs140890506 | snp | C/T | 3.77537e-05 | 0.00434458 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405770 | CGGGCGCCGGCTCAG[C/T]GGTAGTGCCGAAGGT | 5192 |
rs140931939 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PEX10 | GRCh38.p7 | 1:2409004 | CACCCCGTGCTGGCT[C/G]AGGCCAACATGACCT | 5192 |
rs141263967 | snp | C/T | 4.99106e-05 | 0.00499528 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410420 | TGAGAGCAGCTCAAC[C/T]TCCTTCCTCCACTCC | 5192 |
rs141430704 | snp | A/C/T | 0.00290424 | 0.0379965 | synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406869 | ACGGGCCCTCAGGTC[A/C/T]TCTCCGGGCAGGCTG | 5192 |
rs141839636 | in-del | -/TCA | 0.00755907 | 0.0610114 | utr-variant-3-prime, cds-indel, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405213 | CTCTGCCCCGTGTGG[-/TCA]TCAAGTCCTGGGGGA | 5192 |
rs142006474 | in-del | -/GA | 0.00795532 | 0.062565 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405661 | ACATGACAAAAAACT[-/GA]GAGTGTTCTAACTTC | 5192 |
rs142088776 | snp | A/G | 0.000151762 | 0.00870964 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406584 | CACAGGGTGCACAGG[A/G]GGTTTCTGGAAACGG | 5192 |
rs142205326 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PEX10 | GRCh38.p7 | 1:2407689 | CATTGGCTCTGCGAC[A/G]AGGTCACGGTGGCCT | 5192 |
rs142257121 | snp | C/T | 0.000152142 | 0.00872056 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406771 | TTCCTGGCTCGCTGC[C/T]GCTGCCTGAAACCGT | 5192 |
rs142302722 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405121 | TCTGTTTTCTAAAAC[C/T]GGAAGCGACCTTGAC | 5192 |
rs142572177 | in-del | -/T | 0.0821764 | 0.185298 | intron-variant | PEX10 | GRCh38.p7 | 1:2409101 | TCCCAGGGCCTTGGC[-/T]GGCCAGTGTCCCTCC | 5192 |
rs142626035 | snp | C/T | 0.000232307 | 0.010775 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408772 | GCAGTGTCACCAGCA[C/T]GCCACGGCGCAGCGA | 5192 |
rs142854762 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404345 | TGGTACTTCTGGTAC[C/T]GTGTTGAGACACTTG | 5192 |
rs143073325 | snp | A/G | 0.00129834 | 0.0254457 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410743 | CCACATGGAAAGATG[A/G]TCTGGGGTATTAAGA | 5192 |
rs143213680 | snp | C/G/T | 0.0813909 | 0.187196 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415037 | TGGAGTGCAGTGGCG[C/G/T]GATCTTGGCTCACTG | 5192 |
rs143303491 | in-del | -/A | 0.15698 | 0.23205 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411219 | CCCCCCAAAGACTTG[-/A]ATGGCTTTGCCTTTT | 5192 |
rs143387999 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415658 | CTCCCCTGGGCTTCC[A/G]TCTTCTGGTCTGTGG | 5192 |
rs143472520 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PEX10 | GRCh38.p7 | 1:2406012 | CCGAGTCCCAGTGGG[G/T]GCTGGGGCGGGGCTG | 5192 |
rs143794576 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409677 | GGCTTACAAAACTCA[C/T]GAGCCCCCCGGGGTC | 5192 |
rs144132608 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415264 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCAAGGCT | 5192 |
rs144264865 | snp | C/T | 0.000752516 | 0.0193828 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406922 | ATGGCGCCACACTCA[C/T]CAGGACCCTGAGGGG | 5192 |
rs144440263 | snp | A/C | 0.000798403 | 0.0199641 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406580 | CAGGCACAGGGTGCA[A/C]AGGGGGTTTCTGGAA | 5192 |
rs144627253 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404753 | TGTGGCACACGCCCT[C/T]GAGGCATTTTAACAC | 5192 |
rs144628899 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PEX10 | GRCh38.p7 | 1:2406291 | AAAGCCTCAATACAC[A/G]TGAATTTGGAACTTT | 5192 |
rs145668796 | snp | A/G | 3.3216e-05 | 0.00407515 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410384 | ACCTGCAAGTGTGGT[A/G]AGGCCAAAGTAGGCC | 5192 |
rs146037818 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415409 | GCCTTTAAACCGAGC[A/G]TTATTCTTGTTGGCA | 5192 |
rs146452560 | snp | C/T | 0.0137548 | 0.0817815 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408734 | GAGCAGGGCCTTGTC[C/T]AGCAGGTAGGGCAGG | 5192 |
rs146696957 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413933 | AAACCTCCCAGCGCC[C/T]CCGCGCCCCTTTGGA | 5192 |
rs146908276 | snp | C/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414721 | GGGAAGGAAGCGCCT[C/G]GAGGGGGTCTCAGGG | 5192 |
rs147311828 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410654 | AGCTGCAGACAGTCT[G/T]CGAAGAATCTCCCAC | 5192 |
rs147472677 | snp | G/T | 0.0205511 | 0.0992634 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415042 | TGCAGTGGCGGGATC[G/T]TGGCTCACTGCAAGC | 5192 |
rs147489074 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410996 | TTCTCATCATGTCAC[A/T]CTCCTGTTCAGAATC | 5192 |
rs147848221 | snp | C/T | 6.7807e-05 | 0.00582227 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408496 | GGTGGTAGAAGACAC[C/T]GTGGATGTAAAACCA | 5192 |
rs147885700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407611 | CCTCACCAACATGGA[C/T]GGGGCAAGAAACCAC | 5192 |
rs148057567 | snp | A/G | 3.65985e-05 | 0.00427761 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405807 | GCTTCTGGGGAGGGA[A/G]CTTCTCCCGGCAGAG | 5192 |
rs148830444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409432 | CAACGCCAGGCCTCC[A/G]GTTCCTGAGGTCAAG | 5192 |
rs148903253 | snp | A/C/G | 0.000361356 | 0.0134371 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405780 | CTCAGCGGTAGTGCC[A/C/G]AAGGTAGATGAGCTT | 5192 |
rs149226357 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414601 | CTCCACCGGGCTCCC[C/T]GGTAGAGTTATAGGG | 5192 |
rs149421567 | snp | A/G | 0.000135561 | 0.00823178 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410448 | TCCAGCCACTTCCTC[A/G]CACCTGAGAGGAGAA | 5192 |
rs149615608 | snp | A/G/T | 0.000307633 | 0.0123987 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406892 | GCAGGCTGCGGACAC[A/G/T]GAGCTGTAAGGCAGA | 5192 |
rs149822209 | snp | C/G/T | 8.73172e-05 | 0.00660689 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406913 | GTAAGGCAGATGGCG[C/G/T]CACACTCATCAGGAC | 5192 |
rs149877113 | snp | C/G/T | 4.40997e-05 | 0.00469556 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406765 | CACTCCTTCCTGGCT[C/G/T]GCTGCCGCTGCCTGA | 5192 |
rs149985150 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411363 | TCAGCCTCCCAAGTA[A/C/G]CTGGGATTACACGCA | 5192 |
rs150136015 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405123 | TGTTTTCTAAAACTG[A/G]AAGCGACCTTGACGT | 5192 |
rs150308008 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414095 | TGATCATGTGTTCTG[A/G]TCAATGCTTAGATAA | 5192 |
rs150344828 | snp | A/G | 0.000990792 | 0.0222354 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408557 | GCCCTGTCTGAGGAC[A/G]AAGACCGCCCGCAGC | 5192 |
rs151222738 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PEX10 | GRCh38.p7 | 1:2408166 | GACCCGGGGCCCCCC[A/G]GTCAGTAAAGAGCTA | 5192 |
rs180799991 | snp | A/C | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412015 | TGACCCCTCTGCTCA[A/C]AGGGGAGGATCGGAG | 5192 |
rs180943456 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405010 | AGGAGAGGGCTCGGG[C/T]GCCCCTGGCAGCCCC | 5192 |
rs181397097 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413964 | GTTCTGACCCCGCGG[G/T]TGCACCCGTGTCTCC | 5192 |
rs181424630 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411062 | CCGGCACGGAGCCTG[A/G]CTGTCCTCTGATATT | 5192 |
rs181981813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411421 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 5192 |
rs182102623 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415599 | GCTGTGCCCTCCGCC[A/G]GCCCTGCCATTTACA | 5192 |
rs182425795 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404380 | TCTCAGACTGTGGAC[A/G]GGAGTGTTTGTCATT | 5192 |
rs183587100 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415165 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCCTGTT | 5192 |
rs183944818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409306 | AGGTCCGCCACCTAC[C/G]TGACATCGCCATGTA | 5192 |
rs184150138 | snp | C/T | 0.000169776 | 0.00921191 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408525 | CAGGCAACATGTAGC[C/T]GCTGGAGGCAGGCGA | 5192 |
rs185014726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410718 | GCAACTGTTCTAGGG[C/T]CTATGAGGGCCACAT | 5192 |
rs185244266 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412248 | CCCTGAATGGCCGCA[A/G]GGCAGGCGAAGGAGA | 5192 |
rs185395915 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405492 | GGGAAACCTAAAATC[C/T]CGTCCAAATAAGTGA | 5192 |
rs185598733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411646 | CGGGCTCAGGCGATT[A/C]TCTTGCCTCAGCCTC | 5192 |
rs185811960 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404653 | CATCCTCATTCCTAA[G/T]TAAGTCAAACAGCAA | 5192 |
rs186645234 | snp | G/T | 0.0248432 | 0.108648 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415019 | TCGCTTTGTCGCCCA[G/T]GCTGGAGTGCAGTGG | 5192 |
rs187143794 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PEX10 | GRCh38.p7 | 1:2409518 | CCCTGCTCTGTACCA[A/C]CACCATCCTGTGGGG | 5192 |
rs188664283 | snp | C/T | 0 | 0 | intron-variant | PEX10 | GRCh38.p7 | 1:2407450 | GCCTCGGCCCAGGGC[C/T]GGGAACCACATACAG | 5192 |
rs188900370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408911 | GCTGCCGCGGGGACA[A/G]GCTCCCGGCGCCCCT | 5192 |
rs189455993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411981 | ACCGAGGTATGAGGC[G/T]TTCGCGCCGCGGGCG | 5192 |
rs189798947 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404693 | TGCGCGGGTCTTTGC[C/T]GGAAGCCGGTCCTGC | 5192 |
rs189915753 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413797 | GGAGCTCAGCTGTGG[C/G]ATCATCCCCAGACTG | 5192 |
rs190254261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405928 | CCACATTCTCTGCAC[A/G]TGACACACAACATAA | 5192 |
rs190297056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411076 | GGCTGTCCTCTGATA[C/T]TTACCCATGCTCTTC | 5192 |
rs191375480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2409287 | TTGTGAGTGCCAGCC[A/G]TGCAGGTCCGCCACC | 5192 |
rs191757772 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415120 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCT | 5192 |
rs191854937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408156 | GGTGAGGCGTGACCC[A/G]GGGCCCCCCGGTCAG | 5192 |
rs199667764 | snp | A/G/T | 5.42219e-05 | 0.00520658 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408625 | GGTGACGCATCCAGC[A/G/T]CCGCGCCCCTGAGCA | 5192 |
rs199683357 | snp | A/G | 0.000235956 | 0.0108592 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406575 | TCCTCCAGGCACAGG[A/G]TGCACAGGGGGTTTC | 5192 |
rs199777923 | snp | A/G | 8.65808e-05 | 0.00657898 | intron-variant | PEX10 | GRCh38.p7 | 1:2408877 | CGAGGAAGAGGATGG[A/G]TATGTGGACCCTGAG | 5192 |
rs199877853 | snp | A/G | 0.00299555 | 0.038585 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408573 | AAGACCGCCCGCAGC[A/G]GCGCCCTCCTCTGCT | 5192 |
rs199934621 | snp | C/T | 0.000677413 | 0.0183915 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406885 | TCTCCGGGCAGGCTG[C/T]GGACACGGAGCTGTA | 5192 |
rs200050809 | snp | G/T | 0.000256612 | 0.0113243 | intron-variant | PEX10 | GRCh38.p7 | 1:2410480 | CAGTATTAGTCCGGG[G/T]GAGCTGGTGGGCATC | 5192 |
rs200139330 | snp | A/G | 4.17999e-05 | 0.00457146 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405833 | CAGAGGGGACACTCC[A/G]CCTGCGGAGAGGAGA | 5192 |
rs200610722 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405246 | TGTGCTCTGCCCAGC[A/C]GCCCTCGGGGAGAGC | 5192 |
rs201328179 | snp | C/T | 0.000104361 | 0.00722284 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406640 | GAAGGTGGGGCAGAG[C/T]GTCAAGGTGGGTGCA | 5192 |
rs201488304 | snp | A/G | 0.00199797 | 0.0315435 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408465 | ACGTACGTGATCCCC[A/G]TGAGCCTCTTGGCCA | 5192 |
rs201639783 | snp | C/T | 0.000118308 | 0.00769026 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406597 | GGGGGTTTCTGGAAA[C/T]GGCTCTCTCCTCCAA | 5192 |
rs201828636 | snp | G/T | 3.40443e-05 | 0.00412565 | intron-variant | PEX10 | GRCh38.p7 | 1:2408429 | CGGCCTAAGCAGCTG[G/T]GCCCTCAGCGCCTGC | 5192 |
rs201932122 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414429 | TCACTAGAATGGAAG[A/G]CTGTTCCTCCTAAAA | 5192 |
rs202035960 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410379 | CTTCTACCTGCAAGT[A/G]TGGTGAGGCCAAAGT | 5192 |
rs267608183 | snp | A/G | 1.69911e-05 | 0.00291466 | PEX10 | 1 | allele_origin=G(germline)/A(germline) | 1:2408451 | ACGGGGATCACGTAC[A/G]TAAGTAGCAGGCGCT | 5192 |
rs367561091 | snp | C/T | 8.072e-05 | 0.00635244 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406688 | AAGTGCCCAGGACAC[C/T]CCCAGCCCCCATGTG | 5192 |
rs367644095 | snp | A/G | 5.02399e-05 | 0.00501173 | intron-variant | PEX10 | GRCh38.p7 | 1:2410325 | CCGTCCCCAGACTTG[A/G]TGTGTGTGGCTGCCC | 5192 |
rs367762165 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411298 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTTACTG | 5192 |
rs367845280 | snp | A/G | 0.00157069 | 0.02798 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405756 | TGTCCAGGCCCACCC[A/G]GGCGCCGGCTCAGCG | 5192 |
rs367879169 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414571 | CCGGCAGGTGGCAGC[A/G]TCAGCCCGTCTGCTC | 5192 |
rs368064077 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415321 | GCATTGGGCAGAAGT[A/G]GCCAACAGGGCCCAG | 5192 |
rs368143757 | snp | A/C/T | 0.000161846 | 0.00899439 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406855 | AGCCTGTAGCTAACA[A/C/T]GGGCCCTCAGGTCCT | 5192 |
rs368273118 | snp | A/C/T | 0.00588984 | 0.0539473 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408617 | GGCCGTGTGGTGACG[A/C/T]ATCCAGCGCCGCGCC | 5192 |
rs368331719 | snp | G/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407940 | TCAGCTGGGGGTCAG[G/T]ATAGGCAGAGGTGCC | 5192 |
rs368439785 | snp | A/C | 0.000153988 | 0.00877327 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406728 | CACGCACCTGCGGTG[A/C]GACAGGCCGCGGTGC | 5192 |
rs368443682 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414251 | GGAGGCATCCCCCAC[-/C]GCTGTCCTGGCTCAG | 5192 |
rs368453129 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415428 | TTCTTGTTGGCAGCG[C/T]CTTACATCCTTCTGG | 5192 |
rs368549140 | snp | A/C/G | 4.29353e-05 | 0.00463316 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406780 | CGCTGCCGCTGCCTG[A/C/G]AACCGTACAGCTGCA | 5192 |
rs368695131 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406080 | GTTCCCTCCTGCTCC[C/T]GCAGCTGACACAGCC | 5192 |
rs368710052 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404363 | GTTGAGACACTTGGG[A/G]TTCTCAGACTGTGGA | 5192 |
rs368827705 | snp | C/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413740 | GCTGACCTCAGTGGG[C/G]AGGGCCTCCAGTTCC | 5192 |
rs368864383 | snp | C/T | 5.12781e-05 | 0.00506324 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408556 | GGCCCTGTCTGAGGA[C/T]GAAGACCGCCCGCAG | 5192 |
rs369211467 | snp | A/C/G | 0.000153988 | 0.00877327 | intron-variant | PEX10 | GRCh38.p7 | 1:2406970 | GCTGGGAGGGTCACA[A/C/G]GTTCAGTTGGCACAG | 5192 |
rs369508440 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415027 | TCGCCCAGGCTGGAG[C/G/T]GCAGTGGCGGGATCT | 5192 |
rs369643163 | snp | C/G | 2.61462e-05 | 0.00361558 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406898 | TGCGGACACGGAGCT[C/G]TAAGGCAGATGGCGC | 5192 |
rs369771250 | snp | C/T | 5.12667e-05 | 0.00506268 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406456 | CAGCCGCTGACCACC[C/T]CAGGACGGCAGCAGG | 5192 |
rs369786539 | snp | A/C/G | 0.000676373 | 0.0183779 | intron-variant | PEX10 | GRCh38.p7 | 1:2408909 | CTGCTGCCGCGGGGA[A/C/G]AGGCTCCCGGCGCCC | 5192 |
rs369965266 | snp | A/G | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408700 | TGTCGGGGTCAGCCT[A/G]CAGCTCCTGCTCCAG | 5192 |
rs370077726 | snp | A/G | 0.00018615 | 0.00964575 | intron-variant | PEX10 | GRCh38.p7 | 1:2406986 | GTTCAGTTGGCACAG[A/G]GCACGTTAGAACCAG | 5192 |
rs370167317 | snp | G/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410365 | AGGTCCCGTGGGAGC[G/T]TCTACCTGCAAGTGT | 5192 |
rs370404012 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415220 | ACCTTGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 5192 |
rs370417276 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410262 | TGAAGCAACCTCACC[C/T]GGGCCAGCTCCAGGA | 5192 |
rs370555040 | snp | C/T | 1.65974e-05 | 0.0028807 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408782 | CAGCACGCCACGGCG[C/T]AGCGAGGAGGGCACA | 5192 |
rs370594705 | snp | A/G | 0.000514712 | 0.0160341 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406712 | CCATGTGTGGCCCCC[A/G]CACGCACCTGCGGTG | 5192 |
rs370684081 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415408 | AGCCTTTAAACCGAG[C/T]GTTATTCTTGTTGGC | 5192 |
rs370810788 | snp | C/T | 1.66012e-05 | 0.00288103 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408806 | GGGCACATGTATCCG[C/T]GATGGGTCCACCTGG | 5192 |
rs370826120 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405143 | GACCTTGACGTGTAT[C/T]GAAGGTGTGTGTGCC | 5192 |
rs371030713 | snp | C/T | 0.000203255 | 0.010079 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406501 | TGCTGCTGCACCACG[C/T]GGTGATGCACTCCCA | 5192 |
rs371200386 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411528 | GTGAGCCACCACACC[C/T]GGCATCTTTTTTTTT | 5192 |
rs371260973 | snp | C/G | 3.53638e-05 | 0.00420484 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405787 | GTAGTGCCGAAGGTA[C/G]ATGAGCTTCTGGGGA | 5192 |
rs371502268 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405895 | CATGCCCATCCCCAT[C/T]GGCATTTCTTTTCCT | 5192 |
rs371502874 | snp | A/G | 1.6649e-05 | 0.00288518 | intron-variant | PEX10 | GRCh38.p7 | 1:2410363 | TGAGGTCCCGTGGGA[A/G]CTTCTACCTGCAAGT | 5192 |
rs371680815 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406604 | TCTGGAAACGGCTCT[C/T]TCCTCCAAGGAGGCC | 5192 |
rs371979619 | snp | C/T | 0.000304739 | 0.01234 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406891 | GGCAGGCTGCGGACA[C/T]GGAGCTGTAAGGCAG | 5192 |
rs372022952 | snp | A/G/T | 0.000157067 | 0.00886074 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405727 | GGCGTTCAGACTCCC[A/G/T]TAGAGGTCATCTGTG | 5192 |
rs372024936 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411485 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 5192 |
rs372429166 | snp | C/T | 0.000170879 | 0.00924176 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406462 | CTGACCACCCCAGGA[C/T]GGCAGCAGGCTCCCA | 5192 |
rs372509245 | snp | C/T | 6.54757e-05 | 0.00572133 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406747 | AGGCCGCGGTGCAGC[C/T]TCCACTCCTTCCTGG | 5192 |
rs372574195 | snp | C/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406798 | CCGTACAGCTGCAGC[C/T]CCATGGACAGCACCA | 5192 |
rs372638745 | snp | C/T | 3.36621e-05 | 0.00410243 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408737 | CAGGGCCTTGTCCAG[C/T]AGGTAGGGCAGGACG | 5192 |
rs372779905 | snp | C/T | 1.69527e-05 | 0.00291137 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406499 | CTTGCTGCTGCACCA[C/T]GCGGTGATGCACTCC | 5192 |
rs372894429 | snp | C/T | 3.32016e-05 | 0.00407427 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408804 | GAGGGCACATGTATC[C/T]GCGATGGGTCCACCT | 5192 |
rs372911923 | in-del | -/CGTGGGGCCTTTCAG | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406231 | GATGCGTGGTGCAAG[-/CGTGGGGCCTTTCAG]GGCTGGCCACTACCC | 5192 |
rs372914003 | snp | A/G | 0.000127325 | 0.00797786 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408628 | GACGCATCCAGCGCC[A/G]CGCCCCTGAGCAGCC | 5192 |
rs372987455 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413764 | CAGTTCCTTGCCTCA[C/T]CTCTGGTTCCATCTA | 5192 |
rs373091552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2410311 | CAGCCCCCTGGCCAC[C/T]GTCCCCAGACTTGGT | 5192 |
rs373182598 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414976 | AGGCTGTGGATTTTT[-/C]TTTTTTTTTTTTTTT | 5192 |
rs373559391 | snp | A/G | 3.3961e-05 | 0.0041206 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408456 | CTGCTACTTACGTAC[A/G]TGATCCCCGTGAGCC | 5192 |
rs373676994 | snp | A/C/G | 0.000321579 | 0.0126768 | intron-variant | PEX10 | GRCh38.p7 | 1:2406971 | CTGGGAGGGTCACAC[A/C/G]TTCAGTTGGCACAGA | 5192 |
rs373901113 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415226 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 5192 |
rs374203579 | snp | A/G | 0.000416623 | 0.014427 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405850 | CTGCGGAGAGGAGAA[A/G]GGGGGTCACAGCAGC | 5192 |
rs374371284 | snp | C/T | 1.69928e-05 | 0.00291481 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406485 | GGCTCCCACCTCACC[C/T]TGCTGCTGCACCACG | 5192 |
rs374678390 | snp | C/T | 1.68545e-05 | 0.00290292 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406538 | CAGGTGGCCGCAGGG[C/T]GTGGCTGTTGGGTGC | 5192 |
rs374719922 | snp | A/G | 2.14941e-05 | 0.0032782 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406716 | GTGTGGCCCCCGCAC[A/G]CACCTGCGGTGAGAC | 5192 |
rs374732672 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414522 | GGGTCCTTCCTGAGG[A/G]CGACTTGAATACGGC | 5192 |
rs374808879 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414539 | GACTTGAATACGGCG[A/G]TCCTATCCTGGGATG | 5192 |
rs374891812 | snp | C/T | 0.000372972 | 0.0136509 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405832 | GCAGAGGGGACACTC[C/T]GCCTGCGGAGAGGAG | 5192 |
rs375032738 | snp | A/G | 8.47882e-05 | 0.00651052 | intron-variant | PEX10 | GRCh38.p7 | 1:2408863 | GGTCTGGTAGCCTGC[A/G]AGGAAGAGGATGGGT | 5192 |
rs375152882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410831 | GTGAGGTCTTTCTGG[A/G]ATCTCAATTTGCTCA | 5192 |
rs375171673 | snp | A/G | 1.74148e-05 | 0.00295078 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408600 | TGCTGCTCAGTCAGG[A/G]TGGCCGTGTGGTGAC | 5192 |
rs375173883 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415598 | TGCTGTGCCCTCCGC[C/T]GGCCCTGCCATTTAC | 5192 |
rs375325159 | snp | C/G | 1.66112e-05 | 0.00288189 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410411 | GGCCACATCTGAGAG[C/G]AGCTCAACCTCCTTC | 5192 |
rs375445295 | snp | G/T | 2.21693e-05 | 0.00332929 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406762 | CTCCACTCCTTCCTG[G/T]CTCGCTGCCGCTGCC | 5192 |
rs375649043 | snp | C/T | 0.000132791 | 0.00814726 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408777 | GTCACCAGCACGCCA[C/T]GGCGCAGCGAGGAGG | 5192 |
rs375764873 | snp | A/C | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413167 | TCCCCAGTAATCCTG[A/C]GCGAAAAGCACACGG | 5192 |
rs375803322 | snp | A/G | 5.10217e-05 | 0.00505057 | intron-variant | PEX10 | GRCh38.p7 | 1:2408439 | AGCTGTGCCCTCAGC[A/G]CCTGCTACTTACGTA | 5192 |
rs375846571 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PEX10 | GRCh38.p7 | 1:2408919 | GGGGACAGGCTCCCG[C/G]CGCCCCTGCCAGCCG | 5192 |
rs375855913 | snp | A/C/T | 5.32173e-05 | 0.00515813 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408688 | AGGGTCGCCCACTGT[A/C/T]GGGGTCAGCCTGCAG | 5192 |
rs375859860 | snp | A/C/T | 0.000591734 | 0.0171925 | intron-variant | PEX10 | GRCh38.p7 | 1:2406977 | GGGTCACACGTTCAG[A/C/T]TGGCACAGAGCACGT | 5192 |
rs376017092 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | PEX10 | GRCh38.p7 | 1:2410312 | AGCCCCCTGGCCACC[A/G]TCCCCAGACTTGGTG | 5192 |
rs376036793 | snp | C/T | 0.000121027 | 0.00777809 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406635 | CTGGGGAAGGTGGGG[C/T]AGAGCGTCAAGGTGG | 5192 |
rs376143098 | snp | A/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2405984 | CCAAGAAAGCCAGCC[A/T]TTTTTCAGAAGGCCG | 5192 |
rs376475423 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PEX10 | GRCh38.p7 | 1:2408886 | GGATGGGTATGTGGA[C/T]CCTGAGACTGCTGCC | 5192 |
rs376548146 | snp | A/G | 0.000387317 | 0.0139107 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406650 | CAGAGCGTCAAGGTG[A/G]GTGCACCTTACAGGT | 5192 |
rs376629096 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409460 | AAGCCCAAGGGGCAC[C/T]CTGCATGCACCTTCC | 5192 |
rs376720233 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409487 | TTCCCTGTGTGTTCC[A/G]CCCCCTCGCTGCCGC | 5192 |
rs376805362 | snp | C/G | 0.000152619 | 0.00873419 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408476 | CCCCGTGAGCCTCTT[C/G]GCCAGGTGGTAGAAG | 5192 |
rs376926204 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409947 | CTACATGCTGAGCTG[A/G]GGTTGGGAGCCTGAG | 5192 |
rs377135853 | snp | A/G | 4.97987e-05 | 0.00498968 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408805 | AGGGCACATGTATCC[A/G]CGATGGGTCCACCTG | 5192 |
rs377376099 | snp | C/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414518 | CCGAGGGTCCTTCCT[C/G]AGGGCGACTTGAATA | 5192 |
rs377421777 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408917 | GCGGGGACAGGCTCC[C/T]GGCGCCCCTGCCAGC | 5192 |
rs377439419 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405137 | GGAAGCGACCTTGAC[G/T]TGTATTGAAGGTGTG | 5192 |
rs377530881 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409920 | AACCAGGCTGGCACT[C/T]GGTGGTCCTTGCTAC | 5192 |
rs377762521 | snp | G/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414053 | TGGACCAGGCAACCC[G/T]GCATCGCCCACGTGG | 5192 |
rs386627610 | multinucleotide-polymorphism | AGC/GGT | | | downstream-variant-500B, utr-variant-3-prime, cds-indel | PEX10, RER1 | GRCh38.p7 | 1:2404432 | AGCGCTCAGGCCTAA[AGC/GGT]GTGACAGGAAGTCGC | 5192 |
rs386627611 | multinucleotide-polymorphism | AG/CC | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412809 | GGGCGCTGGCGAGGC[AG/CC]CGGGATGGGCTCGCG | 5192 |
rs386627612 | multinucleotide-polymorphism | CGG/TGT | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415035 | GCTGGAGTGCAGTGG[CGG/TGT]GATCTTGGCTCACTG | 5192 |
rs386627613 | multinucleotide-polymorphism | CC/GT | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415084 | GGTTCGCACCATTCT[CC/GT]TGCCTCAGCCTCCTG | 5192 |
rs527458591 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415265 | AGGTGTGAGCCACCG[C/T]GCCTGGCCAAGGCTG | 5192 |
rs527733234 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414654 | CAAAGGGAATCGAAT[C/T]TAGATCAGAACCACT | 5192 |
rs527846920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409221 | AGTCCCATGGCTCTC[C/T]ACCAACCACACAGCT | 5192 |
rs528381804 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412495 | GGGCTGGCGGCGGCC[G/T]GGGCCATGGCCGCGG | 5192 |
rs528387404 | snp | C/T | 0.000275801 | 0.0117399 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406711 | CCCATGTGTGGCCCC[C/T]GCACGCACCTGCGGT | 5192 |
rs528451537 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411013 | TCCTGTTCAGAATCC[A/C]CCAATGGCTGCCCAC | 5192 |
rs529051574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411653 | AGGCGATTCTCTTGC[C/T]TCAGCCTCCTGAAGA | 5192 |
rs529178636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411264 | TTTTTGAGATGGAGT[C/T]TCACTCTGTTGCCCA | 5192 |
rs529217596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409902 | GGCGAGCCCCTCGTA[A/G]GGAACCAGGCTGGCA | 5192 |
rs529257401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415577 | GGCTGGCCTCTGACC[A/G]CAGCCTGCTGTGCCC | 5192 |
rs529280054 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405282 | CGCCTCCCATGGGGC[C/T]GTGGGGCTGCTGTTC | 5192 |
rs529280069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410608 | CTCTGCTTCTGTCTC[C/T]GGAGGCACCACCTTG | 5192 |
rs529536785 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405798 | GGTAGATGAGCTTCT[A/G]GGGAGGGAACTTCTC | 5192 |
rs529685341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408307 | TTTCCAAGCAGAGGA[C/T]TTGGGTTCCTGCCTT | 5192 |
rs529798731 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413211 | GACGCCCCCCTGGTG[C/T]CCACGGGAGGCAGGG | 5192 |
rs529835967 | snp | A/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406068 | CTCGGCCGGGAGGTT[A/C]CCTCCTGCTCCCGCA | 5192 |
rs530360131 | in-del | -/CTC | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410983 | CACACACAAAAAATT[-/CTC]ATCATGTCACTCTCC | 5192 |
rs530407697 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412608 | GTGCGGCGCAGACCT[C/T]TGCGTCAAGGTGCTG | 5192 |
rs530469357 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413084 | CCAGTTCCGGGGAGC[C/G]GGTCGGTTTGGGGGC | 5192 |
rs530721381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407659 | GGCTGGGTACGCTGA[A/G]GACGAAGACCTGACC | 5192 |
rs530996597 | snp | A/C | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415552 | GGGACGCTGCACAGC[A/C]GTGCTTCCTGGCTGG | 5192 |
rs531013743 | in-del | -/A | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412615 | GCAGACCTCTGCGTC[-/A]AGGTGCTGGGGCGGG | 5192 |
rs531036211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411579 | GGGTCTGGCCCCGTC[A/G]CCCAGGCTGGAGTGC | 5192 |
rs531302531 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404581 | TAGAGGGTCACGGCC[C/G]CCCCGCCCTCCTCCG | 5192 |
rs531441290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PEX10 | GRCh38.p7 | 1:2409119 | CCAGTGTCCCTCCCT[C/T]TCTTGGCTTCTCCCC | 5192 |
rs531987102 | snp | A/G | 9.9827e-05 | 0.00706424 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408833 | CTGGATGATGCTGAC[A/G]TACTCCTCCCCCAGG | 5192 |
rs532098059 | in-del | -/CGTA | 0.000684409 | 0.0184861 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405726 | TGGCGTTCAGACTCC[-/CGTA]GAGGTCATCTGTGTC | 5192 |
rs532149116 | snp | A/G/T | 2.17953e-05 | 0.00330109 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406730 | CGCACCTGCGGTGAG[A/G/T]CAGGCCGCGGTGCAG | 5192 |
rs532243871 | snp | A/G | 1.70365e-05 | 0.00291855 | intron-variant | PEX10 | GRCh38.p7 | 1:2408415 | GGGGGTGACAAGGAC[A/G]GCCTAAGCAGCTGTG | 5192 |
rs532737531 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413312 | TCCACCCTCCACCCT[C/G]CCTGGCCTGAGCCCC | 5192 |
rs532802755 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414036 | GCTGAACCCCTCATC[C/T]GTGGACCAGGCAACC | 5192 |
rs533135716 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415076 | GCCTCTGGGGTTCGC[A/G]CCATTCTGTTGCCTC | 5192 |
rs533193430 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415196 | AGCCAGGATGGTCTC[A/G]ACCTCCTGACCTTGT | 5192 |
rs533282954 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415624 | TTTACAGGGGGCTCT[C/T]ACACCCATTCCATCT | 5192 |
rs533402607 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413782 | CTGGTTCCATCTACA[A/G]GAGCTCAGCTGTGGG | 5192 |
rs533688981 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404682 | AAGACATGGTTTGCG[C/T]GGGTCTTTGCCGGAA | 5192 |
rs533734995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409544 | TGGGGGACTGTCACA[C/G]CCTCTGTAGTCTCCC | 5192 |
rs533795387 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2404809 | ATCTTGTGTTAGTAA[C/T]GTACCCACATTTTGC | 5192 |
rs533916771 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414244 | TGCTCTAGGAGGCAT[A/C]CCCCACCGCTGTCCT | 5192 |
rs533977936 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408538 | GCCGCTGGAGGCAGG[C/T]GAGGCCCTGTCTGAG | 5192 |
rs534043338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409981 | TTCTGTCAACAACTC[C/T]CTCTAAAGGGTGGTG | 5192 |
rs534045332 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414830 | TGGGGTGGGGCATGG[A/G]GGTCCTGCCAGGGGA | 5192 |
rs534173317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408047 | AGGGGCTGGGGCCGG[A/G]GCTGCAGTCCATGCT | 5192 |
rs534308992 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2406018 | CCCAGTGGGGGCTGG[G/T]GCGGGGCTGGGGGCG | 5192 |
rs534312526 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413529 | CCCACGCAGGTCGCC[C/T]GCGGTGTCTGCGGCC | 5192 |
rs534368883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415679 | TGGTCTGTGGAATGG[A/G]ACTGGGTAATAATCA | 5192 |
rs534597063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411321 | GCTTACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 5192 |
rs534664201 | snp | C/T | 0.000119764 | 0.0077374 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406441 | TGCATCTTGCCGGCA[C/T]AGCCGCTGACCACCC | 5192 |
rs534972616 | in-del | -/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414250 | AGGAGGCATCCCCCA[-/C]CGCTGTCCTGGCTCA | 5192 |
rs535130776 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405304 | CTGCTGTTCTCACTG[C/T]ACTGGCTGAAGCAAC | 5192 |
rs535220804 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415468 | CTCTTGAATCAATAA[A/G]CCCCGATATGCCTCA | 5192 |
rs535415147 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415649 | CCATCTGAACTCCCC[C/T]GGGCTTCCGTCTTCT | 5192 |
rs535424233 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404708 | CGGAAGCCGGTCCTG[C/T]TGGCCAGGTGTTTTA | 5192 |
rs535474070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410723 | TGTTCTAGGGCCTAT[A/G]AGGGCCACATGGAAA | 5192 |
rs535610933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406404 | GCTCAGAGCCAGACT[C/T]CCCACTTCTGCTGCA | 5192 |
rs535945054 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PEX10 | GRCh38.p7 | 1:2407282 | TACAGGGACCGAAGC[A/C]CCAGTGTAACAAGGC | 5192 |
rs536485197 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412716 | CGGGGCGGGGCAGCG[A/G]GAAGGTAGTCGGAGG | 5192 |
rs536486149 | snp | A/G | 0.000162967 | 0.00902535 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406856 | GCCTGTAGCTAACAC[A/G]GGCCCTCAGGTCCTC | 5192 |
rs536532078 | snp | G/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410634 | CCTTGACTTGCCTTA[G/T]CGTGAGCTGCAGACA | 5192 |
rs536767890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411847 | TACACTGGCTTCTGT[A/G]CTCAGCTCCCGGCCT | 5192 |
rs537290614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411381 | GGGATTACACGCACG[C/T]GCCACCACGCCCTGC | 5192 |
rs537690829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408985 | TCGCCCTTGAGCCCA[C/T]TGTCACCCCGTGCTG | 5192 |
rs538089648 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415103 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGG | 5192 |
rs538221980 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412809 | GGGCGCTGGCGAGGC[A/C]GCGGGATGGGCTCGC | 5192 |
rs538285288 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413451 | AGAACCTTCCCCAGC[C/T]GCTGGCCACAGCTGG | 5192 |
rs538909327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2407873 | TGTGGCAGGTGGACA[C/T]GGTGGTGGGACCACG | 5192 |
rs539190559 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415515 | AGCCTATGTGCCGCC[C/G/T]GGCTTCAAAACCAGG | 5192 |
rs539208584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2407337 | CACCCTCCTGCTGGT[A/G]ACACAGGTAGCTTCT | 5192 |
rs539298450 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412019 | CCCTCTGCTCACAGG[A/G]GAGGATCGGAGGGAG | 5192 |
rs539363003 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412773 | GCCCGCGAGCCGAGG[C/T]GGGGGCGGGGCACGC | 5192 |
rs539432060 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408920 | GGGACAGGCTCCCGG[C/G/T]GCCCCTGCCAGCCGA | 5192 |
rs539433248 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415132 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT | 5192 |
rs539561833 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414682 | ACTGGCGAAGTGGAG[C/T]GACCATCTGCCCGAA | 5192 |
rs539645701 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411461 | TGGTCTCGAACTCCT[A/G]ACCTCAAGTGATCCA | 5192 |
rs539701257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2409624 | CTCCCCTGCCCACGT[C/T]CCTGGAATGCCCCAA | 5192 |
rs539709509 | snp | C/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415026 | GTCGCCCAGGCTGGA[C/G]TGCAGTGGCGGGATC | 5192 |
rs539764213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2410135 | GTCTCAGTGGCACCC[A/G]GGGTAAAGTCTTAAA | 5192 |
rs539850807 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405456 | TGAATTACTTCTCAA[C/T]TGTATGGTTTGGGGA | 5192 |
rs540025435 | snp | A/C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404451 | TGACAGGAAGTCGCA[A/C/T]GCGCTTGGCCAGAGC | 5192 |
rs540114200 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PEX10 | GRCh38.p7 | 1:2409884 | TGGCGGCAGGATGCC[C/T]GGGGCGAGCCCCTCG | 5192 |
rs540331171 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412867 | TCCTACGCTGCCAGG[G/T]GCCCCTGCTCTGCTC | 5192 |
rs541080552 | snp | C/T | 3.35593e-05 | 0.00409616 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410441 | CCTCCACTCCAGCCA[C/T]TTCCTCGCACCTGAG | 5192 |
rs541143756 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405494 | GAAACCTAAAATCCC[A/G]TCCAAATAAGTGAAA | 5192 |
rs541353467 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415184 | TTTCACCCTGTTAGC[C/T]AGGATGGTCTCGACC | 5192 |
rs541381011 | in-del | -/CTG | 0.00159617 | 0.0282053 | intron-variant | PEX10 | GRCh38.p7 | 1:2406412 | CCAGACTCCCCACTT[-/CTG]CTGCAGCCAGGTGCA | 5192 |
rs541886810 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405463 | CTTCTCAACTGTATG[A/G]TTTGGGGAAGGGAGG | 5192 |
rs541897300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409136 | CTTGGCTTCTCCCCA[A/G]GAGTCTCTGCTCTTT | 5192 |
rs542076490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409246 | ACAGCTGGCACCACC[C/T]GATTTATGCCCAGCC | 5192 |
rs542371595 | snp | A/C | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412052 | TTGAAGCACTTGCCA[A/C]GGCCTCACACCTGGA | 5192 |
rs542779592 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415585 | TCTGACCGCAGCCTG[C/T]TGTGCCCTCCGCCGG | 5192 |
rs542788558 | snp | C/T | 3.37018e-05 | 0.00410485 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406562 | TGGGTGCCTGCGCTC[C/T]TCCAGGCACAGGGTG | 5192 |
rs542805840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412307 | CCAGGCGACCGTGAC[A/C]ACACACGGCAGACAC | 5192 |
rs542965472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411396 | CGCCACCACGCCCTG[C/T]TGATTTTTGTATTTT | 5192 |
rs543256365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411005 | TGTCACTCTCCTGTT[C/T]AGAATCCACCAATGG | 5192 |
rs543407738 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415198 | CCAGGATGGTCTCGA[C/T]CTCCTGACCTTGTGA | 5192 |
rs543589588 | snp | G/T | 0.00446177 | 0.0470211 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410890 | GGAGGGATGTTTGAA[G/T]ATTCAATATTTGTAA | 5192 |
rs543635075 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405653 | AGTATCTTACATGAC[A/T]AAAAACTGAGAGTGT | 5192 |
rs543652305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2406056 | CAGGGTGTGGGGCTC[A/G]GCCGGGAGGTTCCCT | 5192 |
rs543666634 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415545 | GCTGCTGGGGACGCT[C/G]CACAGCAGTGCTTCC | 5192 |
rs543847534 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409968 | GGAGCCTGAGAGCTT[C/T]TGTCAACAACTCCCT | 5192 |
rs543908187 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411864 | TCAGCTCCCGGCCTG[A/G]TGAGGCAGGCAGGGC | 5192 |
rs543982780 | snp | A/G | 7.07114e-05 | 0.00594564 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408689 | GGGTCGCCCACTGTC[A/G]GGGTCAGCCTGCAGC | 5192 |
rs544185202 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413137 | CGGGACCTTCCAGGC[C/T]CCGAGCAGCCGCCTT | 5192 |
rs544671218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411641 | TCCCTCGGGCTCAGG[A/C]GATTCTCTTGCCTCA | 5192 |
rs544734638 | snp | C/T | 1.69821e-05 | 0.00291389 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406610 | AACGGCTCTCTCCTC[C/T]AAGGAGGCCCTGGGG | 5192 |
rs545634167 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411061 | CCCGGCACGGAGCCT[A/G]GCTGTCCTCTGATAT | 5192 |
rs545870848 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414568 | TGGCCGGCAGGTGGC[A/C]GCGTCAGCCCGTCTG | 5192 |
rs545933839 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415015 | AGTCTCGCTTTGTCG[C/T]CCAGGCTGGAGTGCA | 5192 |
rs546098123 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404960 | AACACAGCAGTGACC[A/G]TGGGTCAGCAGGTCG | 5192 |
rs546296536 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407984 | GGGAGAAGGTGGGAA[C/T]GGCCGTCTGATGGGG | 5192 |
rs546350388 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413242 | CCTGGCGGGTGGGGG[G/T]CAGCCGGGAAGCCGC | 5192 |
rs546573745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2408315 | CAGAGGATTTGGGTT[C/T]CTGCCTTGACACAGA | 5192 |
rs546620685 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414991 | CTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC | 5192 |
rs546887000 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405136 | TGGAAGCGACCTTGA[C/T]GTGTATTGAAGGTGT | 5192 |
rs547030861 | in-del | -/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414846 | GGTCCTGCCAGGGGA[-/G]GGGGCGTTTGCCGCT | 5192 |
rs547282250 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PEX10 | GRCh38.p7 | 1:2410014 | CAGCCTGGGCCACAG[A/G]CCCACCACTGCTCCA | 5192 |
rs547690547 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408216 | ATGAGGGGCTGCAGC[A/G]GGAGTTCATTCTACA | 5192 |
rs547758104 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415269 | GTGAGCCACCGTGCC[C/T]GGCCAAGGCTGTGGA | 5192 |
rs547988419 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404509 | TGGATGGAGCCACGG[C/T]GGCATCTGCCCACCC | 5192 |
rs548318428 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404598 | CCCGCCCTCCTCCGT[C/T]TCTGGCAAGCTGACC | 5192 |
rs548372048 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404419 | TGTTTTCTTAATAAG[C/T]GCTCAGGCCTAAGGT | 5192 |
rs548575410 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414152 | GGGTTCATGGCTCCA[C/T]GTCTGATTCTGAGGA | 5192 |
rs548964694 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405283 | GCCTCCCATGGGGCC[A/G]TGGGGCTGCTGTTCT | 5192 |
rs549043477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411681 | AGAGCTGGGATTACA[A/G]ACGCCGCCACCACGT | 5192 |
rs549108289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410612 | GCTTCTGTCTCCGGA[A/G]GCACCACCTTGACTT | 5192 |
rs549197030 | snp | A/G | 0.000314048 | 0.012527 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406641 | AAGGTGGGGCAGAGC[A/G]TCAAGGTGGGTGCAC | 5192 |
rs549233351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411266 | TTTGAGATGGAGTCT[C/T]ACTCTGTTGCCCAGA | 5192 |
rs549271413 | snp | A/G/T | 1.69861e-05 | 0.00291424 | synonymous-codon, missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408526 | AGGCAACATGTAGCC[A/G/T]CTGGAGGCAGGCGAG | 5192 |
rs549332290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2406427 | CTGCTGCAGCCAGGT[C/G]CATCTTGCCGGCACA | 5192 |
rs549421342 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415253 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 5192 |
rs549491284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409946 | GCTACATGCTGAGCT[G/T]GGGTTGGGAGCCTGA | 5192 |
rs549991648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405935 | CTCTGCACATGACAC[A/G]CAACATAAATGTTGT | 5192 |
rs549991770 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411163 | CACTGCTCCCTGAAA[C/G]GTTCTGCTGGGAGTT | 5192 |
rs550016644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409889 | GCAGGATGCCCGGGG[C/T]GAGCCCCTCGTAGGG | 5192 |
rs550021617 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415636 | TCTCACACCCATTCC[A/C]TCTGAACTCCCCTGG | 5192 |
rs550149577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407240 | CGGAAATGTGGGGCT[A/G]CAGACGCTGCCCACC | 5192 |
rs550225118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411857 | TCTGTACTCAGCTCC[C/T]GGCCTGGTGAGGCAG | 5192 |
rs550288451 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412613 | GCGCAGACCTCTGCG[C/T]CAAGGTGCTGGGGCG | 5192 |
rs550539856 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408148 | GGATCTGTGGTGAGG[C/T]GTGACCCGGGGCCCC | 5192 |
rs551046093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406330 | CAACGAACCCACATC[C/T]GACCTACCTGGGAGC | 5192 |
rs551571597 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414491 | ATTGGGGCTTCGAAG[A/G/T]CCTCTGGTGCCCCGA | 5192 |
rs551883360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405902 | ATCCCCATCGGCATT[G/T]CTTTTCCTGTCCACA | 5192 |
rs551902431 | snp | C/G | 0.00665919 | 0.0573171 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410809 | GCAGCTCTCCAACTT[C/G]CTGGCTGTGAGGTCT | 5192 |
rs552608686 | in-del | -/A | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412694 | GGAGTCCGAACCAGC[-/A]GCAGCGCGGGGCGGG | 5192 |
rs552883480 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404524 | CGGCATCTGCCCACC[C/T]GGCCGCAGCCCCCAG | 5192 |
rs552933945 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413336 | GAGCCCCGCAGGTGC[G/T]CTGGGGAACCACATC | 5192 |
rs553002321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407298 | CCAGTGTAACAAGGC[A/G]CGTGGCCCCAGGGAC | 5192 |
rs553718951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2409027 | CATGACCTTCTGTCG[C/T]TAAGCCCACTGTGAG | 5192 |
rs553744857 | snp | A/C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409854 | CTGTCTCCCGCCCAC[A/C/T]GAGCACACTCTCCAT | 5192 |
rs553809676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414939 | TCCCTCTCTTCTTTG[A/G]GGATCGAGGTCAGGA | 5192 |
rs553925067 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404911 | AAACATCAAATGGAG[A/G]CGGGAAATAGGCTGG | 5192 |
rs553956330 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413693 | GGATTGCAGGAGGAA[A/G]GCAGGGCACGACAAG | 5192 |
rs554019258 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PEX10 | GRCh38.p7 | 1:2408058 | CCGGGGCTGCAGTCC[A/G]TGCTCCCACACTGTC | 5192 |
rs554023029 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411290 | GCCCAGACTGGAGTG[C/T]AGTGGCACGATCTTG | 5192 |
rs554076987 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415128 | TACAGGCGCCCGCCA[C/T]CACGCCTGGCTAATT | 5192 |
rs554286706 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414255 | GCATCCCCCACCGCT[C/G]TCCTGGCTCAGGACT | 5192 |
rs554294948 | snp | C/T | 0.000171223 | 0.00925107 | intron-variant, synonymous-codon, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406911 | CTGTAAGGCAGATGG[C/T]GCCACACTCATCAGG | 5192 |
rs554353794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408994 | AGCCCACTGTCACCC[C/T]GTGCTGGCTGAGGCC | 5192 |
rs554357307 | in-del | -/TC | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405106 | GCTGAGATGCAGATT[-/TC]TGTTTTCTAAAACTG | 5192 |
rs554490737 | snp | C/T | 0.000189151 | 0.00972316 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408711 | GCCTGCAGCTCCTGC[C/T]CCAGGGGGAGCAGGG | 5192 |
rs554812809 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412810 | GGCGCTGGCGAGGCA[C/G]CGGGATGGGCTCGCG | 5192 |
rs554887865 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414821 | CCAGGGTTCTGGGGT[A/G]GGGCATGGGGGTCCT | 5192 |
rs555015713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2407451 | CCTCGGCCCAGGGCC[A/G]GGAACCACATACAGA | 5192 |
rs555275465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408023 | TGGGCCAGGCAGGGG[C/T]GAGGGGTGAGGGGCT | 5192 |
rs555410374 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405491 | AGGGAAACCTAAAAT[C/G]CCGTCCAAATAAGTG | 5192 |
rs555420029 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415469 | TCTTGAATCAATAAG[C/T]CCCGATATGCCTCAC | 5192 |
rs555673697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2405990 | AAGCCAGCCTTTTTT[C/T]AGAAGGCCGAGTCCC | 5192 |
rs555696882 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409025 | AACATGACCTTCTGT[C/T]GCTAAGCCCACTGTG | 5192 |
rs555698841 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415174 | AGAGACGGGGTTTCA[C/T]CCTGTTAGCCAGGAT | 5192 |
rs555898270 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415427 | ATTCTTGTTGGCAGC[A/G]CCTTACATCCTTCTG | 5192 |
rs556147666 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404976 | TGGGTCAGCAGGTCG[C/T]CTGCCCAGCAGGCCC | 5192 |
rs556196440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409640 | CCTGGAATGCCCCAA[A/G]CCTCGCACAGGGAAA | 5192 |
rs556266822 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PEX10 | GRCh38.p7 | 1:2408921 | GGACAGGCTCCCGGC[A/G]CCCCTGCCAGCCGAC | 5192 |
rs556461016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2410222 | ATGCCTCGCCTCCCT[C/T]GGAGCAGTACCTCCT | 5192 |
rs556510984 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404358 | ACCGTGTTGAGACAC[C/T]TGGGATTCTCAGACT | 5192 |
rs556526252 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405415 | TCTCACAATATAAAC[A/G]AATAAAGTGTCTTCT | 5192 |
rs556603981 | snp | C/T | 1.68607e-05 | 0.00290346 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406531 | AGCAGAACAGGTGGC[C/T]GCAGGGCGTGGCTGT | 5192 |
rs556816263 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404912 | AACATCAAATGGAGG[C/T]GGGAAATAGGCTGGG | 5192 |
rs556865194 | snp | C/T | | | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410447 | CTCCAGCCACTTCCT[C/T]GCACCTGAGAGGAGA | 5192 |
rs557133818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411393 | ACGCGCCACCACGCC[C/T]TGCTGATTTTTGTAT | 5192 |
rs557862367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406021 | AGTGGGGGCTGGGGC[A/G]GGGCTGGGGGCGTAG | 5192 |
rs557937818 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415712 | TGGTATTTATTAAGA[C/G]CCTGCTTTGCTCCTG | 5192 |
rs557941413 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405321 | CTGGCTGAAGCAACC[C/T]GCCAGCCTCCGTGCC | 5192 |
rs558076748 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415512 | CTCAGCCTATGTGCC[A/G]CCCGGCTTCAAAACC | 5192 |
rs558332508 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414352 | GGCAGGACCTGAAAC[A/C]AAGTGTCCCAGTGTC | 5192 |
rs558462057 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413748 | CAGTGGGGAGGGCCT[C/T]CAGTTCCTTGCCTCA | 5192 |
rs559016271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407356 | CAGGTAGCTTCTGAC[C/T]GTGCCACTGAAGGAC | 5192 |
rs559261648 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412788 | TGGGGGCGGGGCACG[C/T]GCGAGGGGCGCTGGC | 5192 |
rs559287645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407045 | CAGAAACGATCAAGC[C/T]AGGGGGCAGGTTCAG | 5192 |
rs559342009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405886 | CCACTGGGCCATGCC[C/T]ATCCCCATCGGCATT | 5192 |
rs559431523 | snp | C/T | 0.00545947 | 0.0519608 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412476 | CGCGCGGATCACCTC[C/T]GGGGGGCTGGCGGCG | 5192 |
rs559505991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412946 | GGAGACGCTGCAGGC[C/T]CATTTACGGCTGGGG | 5192 |
rs559507146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411006 | GTCACTCTCCTGTTC[A/G]GAATCCACCAATGGC | 5192 |
rs559578551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411694 | CAGACGCCGCCACCA[C/T]GTCCGGCTAATTTTC | 5192 |
rs559655579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410636 | TTGACTTGCCTTAGC[A/G]TGAGCTGCAGACAGT | 5192 |
rs559791241 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415592 | GCAGCCTGCTGTGCC[C/T]TCCGCCGGCCCTGCC | 5192 |
rs560099788 | snp | C/T | 5.02441e-05 | 0.00501194 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408751 | GCAGGTAGGGCAGGA[C/T]GGCATGCAGTGTCAC | 5192 |
rs560268157 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414022 | GTTGAGCACCTTGGG[C/T]TGAACCCCTCATCCG | 5192 |
rs560331403 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414534 | AGGGCGACTTGAATA[C/T]GGCGGTCCTATCCTG | 5192 |
rs560602310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407626 | CGGGGCAAGAAACCA[C/T]ATCAAATACGCAAGT | 5192 |
rs560823479 | snp | C/T | 9.84931e-05 | 0.0070169 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405741 | CGTAGAGGTCATCTG[C/T]GTCCAGGCCCACCCG | 5192 |
rs560833081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408240 | TTCTACACTTAGGGT[C/G]TGGACTTCCTTGGAT | 5192 |
rs560961305 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413960 | TGGAGTTCTGACCCC[A/G]CGGGTGCACCCGTGT | 5192 |
rs561354291 | snp | A/G | 1.71185e-05 | 0.00292557 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406624 | CCAAGGAGGCCCTGG[A/G]GAAGGTGGGGCAGAG | 5192 |
rs561415178 | snp | C/G | 3.55714e-05 | 0.00421716 | intron-variant, synonymous-codon, utr-variant-3-prime | PEX10 | GRCh38.p7 | 1:2406932 | ACTCATCAGGACCCT[C/G]AGGGGATCTGGCCTC | 5192 |
rs561420179 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412295 | TGTGGGACGGGCCCA[A/G]GCGACCGTGACCACA | 5192 |
rs561751738 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404641 | GGAATACAGGGTCAT[C/T]CTCATTCCTAAGTAA | 5192 |
rs561812569 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405011 | GGAGAGGGCTCGGGC[A/G]CCCCTGGCAGCCCCC | 5192 |
rs561822721 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415743 | CCCAGTGCACACATC[A/G]TCTGGGGTCTGGTCA | 5192 |
rs561968508 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412926 | TGGGGACAGCGCTGC[A/G]GAGTGGAGACGCTGC | 5192 |
rs562047724 | snp | C/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413086 | AGTTCCGGGGAGCCG[C/G]TCGGTTTGGGGGCCA | 5192 |
rs562078651 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410042 | CCACCAGGGCACTGT[C/T]ACACGGGCACTGCAC | 5192 |
rs562327614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409152 | GAGTCTCTGCTCTTT[A/C]CCCTTTCTCCCTAGC | 5192 |
rs562505753 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404557 | CCTCTCCTGGTGGTC[C/T]TCCCAGTCTAGAGGG | 5192 |
rs562610179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409066 | GCACATGACAGGCCC[A/G]GCCAATGGCTGCCCT | 5192 |
rs562815786 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414086 | CCGCTGAGGTGATCA[C/T]GTGTTCTGGTCAATG | 5192 |
rs563364677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409899 | CGGGGCGAGCCCCTC[A/G]TAGGGAACCAGGCTG | 5192 |
rs563545807 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415567 | AGTGCTTCCTGGCTG[G/T]CCTCTGACCGCAGCC | 5192 |
rs563552129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406070 | CGGCCGGGAGGTTCC[C/T]TCCTGCTCCCGCAGC | 5192 |
rs563570780 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415473 | GAATCAATAAGCCCC[A/G]ATATGCCTCACCATC | 5192 |
rs563991373 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405534 | AAGTGGCTGAGTCCT[A/G]CCAGGTTGGGGTTAG | 5192 |
rs564161873 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415074 | CTGCCTCTGGGGTTC[A/G]CACCATTCTGTTGCC | 5192 |
rs564814652 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413025 | GGCCGCGGCGGTCCC[A/G]CCCTCGCGCCCTTTG | 5192 |
rs564840396 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PEX10 | GRCh38.p7 | 1:2409880 | TCCATGGCGGCAGGA[G/T]GCCCGGGGCGAGCCC | 5192 |
rs564874037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407640 | ACATCAAATACGCAA[A/G]TGAGGCTGGGTACGC | 5192 |
rs565417487 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406147 | CCCTGCCGGCATCTT[A/C/T]GGTGGGTGTGAGTCA | 5192 |
rs565418478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411509 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCAC | 5192 |
rs565434060 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415666 | GGCTTCCGTCTTCTG[C/G]TCTGTGGAATGGGAC | 5192 |
rs565556676 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411270 | AGATGGAGTCTCACT[C/T]TGTTGCCCAGACTGG | 5192 |
rs565878700 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405288 | CCATGGGGCCGTGGG[G/T]CTGCTGTTCTCACTG | 5192 |
rs565988216 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415005 | TTTGAGACAGAGTCT[C/T]GCTTTGTCGCCCAGG | 5192 |
rs566022295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409970 | AGCCTGAGAGCTTCT[A/G]TCAACAACTCCCTCT | 5192 |
rs566178191 | snp | C/T | 0.000184997 | 0.00961583 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410722 | CTGTTCTAGGGCCTA[C/T]GAGGGCCACATGGAA | 5192 |
rs566905295 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412764 | CGGGGCGGGGCCCGC[A/G]AGCCGAGGTGGGGGC | 5192 |
rs566941490 | snp | A/G | 0.000149443 | 0.00864288 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405771 | GGGCGCCGGCTCAGC[A/G]GTAGTGCCGAAGGTA | 5192 |
rs566965897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PEX10 | GRCh38.p7 | 1:2407299 | CAGTGTAACAAGGCA[C/T]GTGGCCCCAGGGACA | 5192 |
rs567350507 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412686 | AGCGGGGCTGGAGTC[C/G]GAACCAGCGCAGCGC | 5192 |
rs567795875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411876 | CTGGTGAGGCAGGCA[A/G]GGCCTGGCTGAGCCT | 5192 |
rs568024041 | snp | C/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411199 | CTTTAACGACTGCCT[C/G]CCCCACCCCCCAAAG | 5192 |
rs568100676 | snp | A/G | | | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405896 | ATGCCCATCCCCATC[A/G]GCATTTCTTTTCCTG | 5192 |
rs568204577 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415121 | CTGGGACTACAGGCG[A/C]CCGCCACCACGCCTG | 5192 |
rs568319775 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413526 | AGGCCCACGCAGGTC[C/G]CCTGCGGTGTCTGCG | 5192 |
rs568472874 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414210 | CTGGGTTCTATGATG[A/G]GCCCCTGACGGGAGG | 5192 |
rs568518336 | snp | C/T | 3.68209e-05 | 0.00429058 | intron-variant | PEX10 | GRCh38.p7 | 1:2408901 | CCCTGAGACTGCTGC[C/T]GCGGGGACAGGCTCC | 5192 |
rs568936483 | snp | C/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408352 | ATGTAGAACCCTGTT[C/G]GCTGAGAGGCCTGGA | 5192 |
rs569435477 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414085 | GCCGCTGAGGTGATC[A/G]TGTGTTCTGGTCAAT | 5192 |
rs569569436 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413363 | CATCGCAGGCGCTCC[C/G]ATCCCTCTGCTCCCA | 5192 |
rs569578897 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415640 | ACACCCATTCCATCT[A/G]AACTCCCCTGGGCTT | 5192 |
rs569675194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409359 | CCACCCCTGCCGAGA[C/T]AGCTTTCAGCGCCCC | 5192 |
rs569738189 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404694 | GCGCGGGTCTTTGCC[A/G]GAAGCCGGTCCTGCT | 5192 |
rs569812075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408981 | CTTGTCGCCCTTGAG[C/T]CCACTGTCACCCCGT | 5192 |
rs569825475 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411209 | TGCCTGCCCCACCCC[C/G/T]CAAAGACTTGATGGC | 5192 |
rs569889116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406360 | CCTTTAAAAAGATGC[C/T]CACCTCTGTACCCTC | 5192 |
rs570192538 | in-del | -/CA | 0.00914312 | 0.0669923 | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412553 | GGCCACGCCCACGCC[-/CA]GACGGGCGAGAACTG | 5192 |
rs570218479 | in-del | -/CCA | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411011 | TCTCCTGTTCAGAAT[-/CCA]CCAATGGCTGCCCAC | 5192 |
rs570339278 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415511 | ACTCAGCCTATGTGC[C/T]GCCCGGCTTCAAAAC | 5192 |
rs570474024 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414672 | GATCAGAACCACTGG[C/T]GAAGTGGAGCGACCA | 5192 |
rs570600956 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414279 | CAGGACTGCTTTCCC[C/T]ACTCTTCTCATCTGC | 5192 |
rs570673853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410689 | GCTCATCTCTTGCTC[C/T]GGGATTCCCCTGAGC | 5192 |
rs570706924 | snp | A/G | 0.000102992 | 0.00717533 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408568 | GGACGAAGACCGCCC[A/G]CAGCAGCGCCCTCCT | 5192 |
rs570780407 | in-del | -/TCCACCC | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413290 | GGCGGAAGGTGGCCT[-/TCCACCC]TCCACCCTCCACCCT | 5192 |
rs571008930 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411375 | GTAGCTGGGATTACA[A/C/T]GCACGCGCCACCACG | 5192 |
rs571035626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409247 | CAGCTGGCACCACCC[A/G]ATTTATGCCCAGCCT | 5192 |
rs571178917 | snp | C/T | 2.17996e-05 | 0.00330141 | stop-gained, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406750 | CCGCGGTGCAGCCTC[C/T]ACTCCTTCCTGGCTC | 5192 |
rs571414682 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409501 | CACCCCCTCGCTGCC[A/G]CCCCTGCTCTGTACC | 5192 |
rs572188523 | snp | C/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409375 | AGCTTTCAGCGCCCC[C/G]ACCCAGAAAAGCCTG | 5192 |
rs572193108 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411374 | AGTAGCTGGGATTAC[A/G]CGCACGCGCCACCAC | 5192 |
rs572500055 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415124 | GGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT | 5192 |
rs572629073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PEX10 | GRCh38.p7 | 1:2409780 | TGCTCTTCCCTAAGA[C/T]GTGGTCTTTATCTCT | 5192 |
rs572664807 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412966 | TACGGCTGGGGAGAC[A/G]GAGGCTTTCGCTTGG | 5192 |
rs572727550 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413704 | GGAAGGCAGGGCACG[A/G]CAAGGGGGCGTCTGC | 5192 |
rs573184334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411479 | CTCAAGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 5192 |
rs573471417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412005 | GCGGGCGCTCTGACC[A/C]CTCTGCTCACAGGGG | 5192 |
rs573851032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406086 | TCCTGCTCCCGCAGC[C/T]GACACAGCCCACGAA | 5192 |
rs574147256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411395 | GCGCCACCACGCCCT[A/G]CTGATTTTTGTATTT | 5192 |
rs574502240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409000 | CTGTCACCCCGTGCT[A/G]GCTGAGGCCAACATG | 5192 |
rs574639596 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414822 | CAGGGTTCTGGGGTG[A/G]GGCATGGGGGTCCTG | 5192 |
rs574840898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2407494 | CACCGCCAGCATGGG[C/T]CCTGGGTGTCCAGCC | 5192 |
rs574868842 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412846 | GTGGTTGCTGCGACC[C/T]CGGGGTCCTACGCTG | 5192 |
rs574904063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2408040 | AGGGGTGAGGGGCTG[C/G]GGCCGGGGCTGCAGT | 5192 |
rs575067189 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414398 | GGTGGGGCTTGGGGG[A/T]CCCCCACGGTTCAAG | 5192 |
rs575681775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412082 | AGGGGACAGAGTCTT[C/T]CCCAGCCGCTGGCGT | 5192 |
rs575744602 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412807 | AGGGGCGCTGGCGAG[A/G]CAGCGGGATGGGCTC | 5192 |
rs575744709 | snp | A/G | 2.79857e-05 | 0.0037406 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406909 | AGCTGTAAGGCAGAT[A/G]GCGCCACACTCATCA | 5192 |
rs576061423 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415137 | CCGCCACCACGCCTG[A/G]CTAATTTTTTGTATT | 5192 |
rs576076985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409653 | AAGCCTCGCACAGGG[A/C]AAGCTATGGGCTTAC | 5192 |
rs576138110 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405007 | CCCAGGAGAGGGCTC[A/G]GGCGCCCCTGGCAGC | 5192 |
rs576140178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2410223 | TGCCTCGCCTCCCTC[A/G]GAGCAGTACCTCCTG | 5192 |
rs576401163 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405458 | AATTACTTCTCAACT[A/G]TATGGTTTGGGGAAG | 5192 |
rs576625546 | snp | A/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411854 | GCTTCTGTACTCAGC[A/T]CCCGGCCTGGTGAGG | 5192 |
rs576723258 | snp | C/T | 0.0189827 | 0.0955563 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410873 | AGTAATAAGTCCTAC[C/T]TGGAGGGATGTTTGA | 5192 |
rs576809614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409055 | GAGCTCAGGCAGCAC[A/G]TGACAGGCCCGGCCA | 5192 |
rs576870974 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415014 | GAGTCTCGCTTTGTC[A/G]CCCAGGCTGGAGTGC | 5192 |
rs576950761 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415131 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 5192 |
rs577024790 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414558 | TATCCTGGGATGGCC[A/G]GCAGGTGGCAGCGTC | 5192 |
rs577197641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2409622 | CTCTCCCCTGCCCAC[A/G]TCCCTGGAATGCCCC | 5192 |
rs577644074 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409753 | GGCTGCTTGCTCTGC[C/T]GGTCTGGAAAATGCT | 5192 |
rs577664932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PEX10 | GRCh38.p7 | 1:2406030 | TGGGGCGGGGCTGGG[A/G]GCGTAGGGCTCAGGG | 5192 |
rs577780277 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415730 | TGCTTTGCTCCTGCC[A/C]AGTGCACACATCGTC | 5192 |
rs577852739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410885 | TACTTGGAGGGATGT[C/T]TGAAGATTCAATATT | 5192 |
rs577918637 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415514 | CAGCCTATGTGCCGC[C/T]CGGCTTCAAAACCAG | 5192 |
rs724159999 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408715 | AAGGCCCTGCTCCCC[-/C]TGGAGCAGGAGCTGC | 5192 |
rs724160000 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406566 | TGTGCACCCTGTGCC[C/T]GGAGGAGCGCAGGCA | 5192 |
rs724160001 | snp | A/G/T | 7.53977e-05 | 0.00613948 | PEX10, RER1 | 1 | allele_origin=G(germline)/A(germline) | 1:2405815 | AGTGTCCCCTCTGCC[A/G/T]GGAGAAGTTCCCTCC | 5192 |
rs724160002 | snp | C/T | | | missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412501 | CCGAACCCGCGGCCA[C/T]GGCCCCGGCCGCCGC | 5192 |
rs745469808 | snp | C/T | 5.47111e-05 | 0.00522997 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408645 | GCCCCTGAGCAGCCA[C/T]GCCCACCTGGCCCCA | 5192 |
rs745524830 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410857 | GCTCATCTATCAGAA[A/G]AGTAATAAGTCCTAC | 5192 |
rs745550991 | snp | A/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410019 | TGGGCCACAGACCCA[A/C]CACTGCTCCACCAGG | 5192 |
rs745552298 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415066 | TGCAAGCTCTGCCTC[-/TG]GGGTTCGCACCATTC | 5192 |
rs745758097 | snp | A/C | 2.21036e-05 | 0.00332435 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406832 | GCAGCAGTGAGATGA[A/C]CCCCAGCAGCCTGTA | 5192 |
rs745818681 | snp | A/G | 6.53161e-05 | 0.00571435 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406772 | TCCTGGCTCGCTGCC[A/G]CTGCCTGAAACCGTA | 5192 |
rs745845751 | snp | C/T | 3.33578e-05 | 0.00408384 | intron-variant | PEX10 | GRCh38.p7 | 1:2410356 | TCAGTCCTGAGGTCC[C/T]GTGGGAGCTTCTACC | 5192 |
rs746145292 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407394 | TGCCCTCGGCTTCCC[A/G]TGTCACTTTCCACTG | 5192 |
rs746394182 | snp | G/T | 1.6904e-05 | 0.00290719 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406598 | GGGGTTTCTGGAAAC[G/T]GCTCTCTCCTCCAAG | 5192 |
rs746497851 | snp | A/T | 1.73661e-05 | 0.00294665 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408597 | CTCTGCTGCTCAGTC[A/T]GGGTGGCCGTGTGGT | 5192 |
rs746556714 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414977 | GGCTGTGGATTTTTC[-/TTT]TTTTTTTTTTTTTGA | 5192 |
rs746710198 | snp | A/G | 6.46879e-05 | 0.00568681 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406819 | GACAGCACCAGGTGC[A/G]GCAGTGAGATGACCC | 5192 |
rs746807325 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409922 | CCAGGCTGGCACTCG[A/G]TGGTCCTTGCTACAT | 5192 |
rs746952615 | snp | C/T | 4.97896e-05 | 0.00498922 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408785 | CACGCCACGGCGCAG[C/T]GAGGAGGGCACATGT | 5192 |
rs746997905 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414246 | CTCTAGGAGGCATCC[C/T]CCACCGCTGTCCTGG | 5192 |
rs747149152 | snp | A/G | 0.000664452 | 0.0182149 | missense, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412462 | TCGTCCTTCTGCGCC[A/G]CGCGGATCACCTCCG | 5192 |
rs747171383 | snp | G/T | 5.10738e-05 | 0.00505315 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406617 | CTCTCCTCCAAGGAG[G/T]CCCTGGGGAAGGTGG | 5192 |
rs747287376 | snp | A/G | 1.89737e-05 | 0.00308002 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410491 | CGGGGGAGCTGGTGG[A/G]CATCCTCTGAGGATG | 5192 |
rs747316054 | snp | C/G | | | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405890 | TGGGCCATGCCCATC[C/G]CCATCGGCATTTCTT | 5192 |
rs747389749 | snp | A/G | 1.68607e-05 | 0.00290346 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406579 | CCAGGCACAGGGTGC[A/G]CAGGGGGTTTCTGGA | 5192 |
rs747538698 | snp | C/G | 1.81214e-05 | 0.00301004 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408631 | GCATCCAGCGCCGCG[C/G]CCCTGAGCAGCCACG | 5192 |
rs747613107 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414615 | CCGGTAGAGTTATAG[A/G]GGATTAGGCGGTGAG | 5192 |
rs747771124 | snp | C/T | 4.41384e-05 | 0.00469758 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406763 | TCCACTCCTTCCTGG[C/T]TCGCTGCCGCTGCCT | 5192 |
rs747776170 | snp | C/T | 8.54756e-05 | 0.00653686 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406715 | TGTGTGGCCCCCGCA[C/T]GCACCTGCGGTGAGA | 5192 |
rs747921371 | snp | A/G | 3.31928e-05 | 0.00407373 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408781 | CCAGCACGCCACGGC[A/G]CAGCGAGGAGGGCAC | 5192 |
rs747996191 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408442 | TGTGCCCTCAGCGCC[C/T]GCTACTTACGTACGT | 5192 |
rs748282979 | snp | C/G | 3.32458e-05 | 0.00407698 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410373 | TGGGAGCTTCTACCT[C/G]CAAGTGTGGTGAGGC | 5192 |
rs748299996 | in-del | -/G | 3.55562e-05 | 0.00421626 | intron-variant, frameshift-variant, utr-variant-3-prime | PEX10 | GRCh38.p7 | 1:2406934 | TCATCAGGACCCTGA[-/G]GGGATCTGGCCTCAG | 5192 |
rs748350205 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415542 | CAGGCTGCTGGGGAC[A/G]CTGCACAGCAGTGCT | 5192 |
rs748431314 | snp | C/T | 3.39541e-05 | 0.00412018 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406491 | CACCTCACCTTGCTG[C/T]TGCACCACGCGGTGA | 5192 |
rs748517055 | snp | A/G | 7.13598e-05 | 0.00597284 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405881 | TGGGGCCACTGGGCC[A/G]TGCCCATCCCCATCG | 5192 |
rs748545159 | snp | C/G | 1.72261e-05 | 0.00293475 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408581 | CCGCAGCAGCGCCCT[C/G]CTCTGCTGCTCAGTC | 5192 |
rs748760810 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404827 | ACCCACATTTTGCTG[G/T]AGTTAGTTTATTAAA | 5192 |
rs748829349 | snp | A/G | 1.69795e-05 | 0.00291367 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406611 | ACGGCTCTCTCCTCC[A/G]AGGAGGCCCTGGGGA | 5192 |
rs748839957 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411120 | CTGTTCCTTTGGCCA[C/G/T]GACACCCCCACCACT | 5192 |
rs748921131 | snp | A/C | 1.69115e-05 | 0.00290782 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408728 | CAGGGGGAGCAGGGC[A/C]TTGTCCAGCAGGTAG | 5192 |
rs749170555 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407653 | AAGTGAGGCTGGGTA[C/T]GCTGAGGACGAAGAC | 5192 |
rs749301360 | snp | C/T | 1.74525e-05 | 0.00295397 | intron-variant | PEX10 | GRCh38.p7 | 1:2408882 | AAGAGGATGGGTATG[C/T]GGACCCTGAGACTGC | 5192 |
rs749540064 | snp | C/T | 1.71947e-05 | 0.00293207 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408572 | GAAGACCGCCCGCAG[C/T]AGCGCCCTCCTCTGC | 5192 |
rs749637005 | snp | C/T | 1.69605e-05 | 0.00291204 | stop-gained, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408510 | CCGTGGATGTAAAAC[C/T]AGGCAACATGTAGCC | 5192 |
rs749847706 | snp | C/G | 3.13357e-05 | 0.00395814 | utr-variant-5-prime, missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412505 | CGGCCGGGGCCATGG[C/G]CGCGGGTTCGGGTGG | 5192 |
rs749957135 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406277 | AACCTGCATTCGGCA[A/G]AGCCTCAATACACGT | 5192 |
rs750002192 | snp | C/T | 0.000152862 | 0.00874116 | synonymous-codon, splice-donor-variant | PEX10 | GRCh38.p7 | 1:2408455 | CCTGCTACTTACGTA[C/T]GTGATCCCCGTGAGC | 5192 |
rs750185424 | snp | A/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414192 | GGCTCCTTTGGATTC[A/T]CACTGGGTTCTATGA | 5192 |
rs750267481 | snp | A/G | 1.71917e-05 | 0.00293182 | intron-variant | PEX10 | GRCh38.p7 | 1:2410458 | TCCTCGCACCTGAGA[A/G]GAGAAACAGTATTAG | 5192 |
rs750424221 | snp | A/G | 1.68564e-05 | 0.00290309 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406558 | CTGTTGGGTGCCTGC[A/G]CTCCTCCAGGCACAG | 5192 |
rs750507518 | snp | A/G | 3.43277e-05 | 0.00414278 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408564 | CTGAGGACGAAGACC[A/G]CCCGCAGCAGCGCCC | 5192 |
rs750516730 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404567 | TGGTCCTCCCAGTCT[A/G]GAGGGTCACGGCCCC | 5192 |
rs750769868 | snp | C/T | 0.000154319 | 0.0087827 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406738 | CGGTGAGACAGGCCG[C/T]GGTGCAGCCTCCACT | 5192 |
rs750832855 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409397 | AAAAGCCTGCTCCCC[A/G]TTTCCATCTCTGTGG | 5192 |
rs750844789 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414978 | GCTGTGGATTTTTCT[-/TT]TTTTTTTTTTTTTGA | 5192 |
rs750860014 | snp | A/G | 1.66023e-05 | 0.00288113 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408810 | ACATGTATCCGCGAT[A/G]GGTCCACCTGGATGA | 5192 |
rs750947589 | snp | A/G | 1.65957e-05 | 0.00288055 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408762 | AGGACGGCATGCAGT[A/G]TCACCAGCACGCCAC | 5192 |
rs750991912 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413061 | CGCGGGCTCTCAGCG[C/T]GGGTTGGCCAGTTCC | 5192 |
rs751010435 | in-del | -/C | 3.51352e-05 | 0.00419122 | intron-variant | PEX10 | GRCh38.p7 | 1:2408885 | GGATGGGTATGTGGA[-/C]CCCTGAGACTGCTGC | 5192 |
rs751098874 | snp | C/T | 5.4745e-05 | 0.00523159 | intron-variant, synonymous-codon, missense | PEX10 | GRCh38.p7 | 1:2406950 | GGGATCTGGCCTCAG[C/T]GCCTGCTGGGAGGGT | 5192 |
rs751219789 | snp | C/G | 2.46588e-05 | 0.00351124 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406882 | TCCTCTCCGGGCAGG[C/G]TGCGGACACGGAGCT | 5192 |
rs751311027 | snp | C/G | 8.43149e-05 | 0.00649233 | intron-variant | PEX10 | GRCh38.p7 | 1:2410338 | TGGTGTGTGTGGCTG[C/G]CCTCAGTCCTGAGGT | 5192 |
rs751497313 | snp | C/T | 1.78726e-05 | 0.00298931 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408619 | CCGTGTGGTGACGCA[C/T]CCAGCGCCGCGCCCC | 5192 |
rs751497956 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412010 | CGCTCTGACCCCTCT[A/G]CTCACAGGGGAGGAT | 5192 |
rs751654066 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413897 | CCTGGGTGGCCCCGC[C/T]CCGCAGGCCCTCTGG | 5192 |
rs751762735 | snp | C/T | 2.19754e-05 | 0.00331469 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406735 | CTGCGGTGAGACAGG[C/T]CGCGGTGCAGCCTCC | 5192 |
rs751771614 | snp | C/T | 1.80299e-05 | 0.00300243 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406667 | TGCACCTTACAGGTC[C/T]TTGTGAAGTGCCCAG | 5192 |
rs751911581 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408759 | GGCAGGACGGCATGC[A/G]GTGTCACCAGCACGC | 5192 |
rs751979606 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407314 | CGTGGCCCCAGGGAC[A/G]CTGCTGCCACCCTCC | 5192 |
rs752078998 | snp | A/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409245 | CACAGCTGGCACCAC[A/C]CGATTTATGCCCAGC | 5192 |
rs752135780 | snp | C/T | 2.14691e-05 | 0.00327629 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406809 | CAGCCCCATGGACAG[C/T]ACCAGGTGCAGCAGT | 5192 |
rs752180749 | in-del | -/TAAG | 1.69861e-05 | 0.00291424 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406488 | CCCACCTCACCTTGC[-/TAAG]TGCTGCACCACGCGG | 5192 |
rs752243854 | snp | C/T | 1.66649e-05 | 0.00288655 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410426 | CAGCTCAACCTCCTT[C/T]CTCCACTCCAGCCAC | 5192 |
rs752331746 | snp | A/G | 1.67435e-05 | 0.00289335 | intron-variant | PEX10 | GRCh38.p7 | 1:2410331 | CCAGACTTGGTGTGT[A/G]TGGCTGCCCTCAGTC | 5192 |
rs752396864 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404767 | TCGAGGCATTTTAAC[A/G]CTGCGCTTCAGGAAA | 5192 |
rs752452960 | in-del | -/TG | 1.74701e-05 | 0.00295546 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408699 | CTGTCGGGGTCAGCC[-/TG]CAGCTCCTGCTCCAG | 5192 |
rs752506584 | snp | C/T | 1.66488e-05 | 0.00288515 | splice-acceptor-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405835 | GAGGGGACACTCCGC[C/T]TGCGGAGAGGAGAAA | 5192 |
rs752729702 | snp | A/C | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411947 | AGGCCTAGGAAAGGC[A/C]GGGGTCAGTGTGAAC | 5192 |
rs752730970 | snp | C/T | 5.08625e-05 | 0.00504269 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408478 | CCGTGAGCCTCTTGG[C/T]CAGGTGGTAGAAGAC | 5192 |
rs752928632 | snp | A/G | 1.68621e-05 | 0.00290358 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406573 | GCTCCTCCAGGCACA[A/G]GGTGCACAGGGGGTT | 5192 |
rs753071243 | snp | A/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2405983 | ACCAAGAAAGCCAGC[A/C]TTTTTTCAGAAGGCC | 5192 |
rs753282581 | snp | A/T | 3.32314e-05 | 0.0040761 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408822 | GATGGGTCCACCTGG[A/T]TGATGCTGACGTACT | 5192 |
rs753300436 | snp | C/G | 2.40024e-05 | 0.00346419 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406873 | GCCCTCAGGTCCTCT[C/G]CGGGCAGGCTGCGGA | 5192 |
rs753384584 | snp | A/G | 3.79615e-05 | 0.00435652 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405819 | GGAACTTCTCCCGGC[A/G]GAGGGGACACTCCGC | 5192 |
rs753569980 | snp | C/T | 4.04785e-05 | 0.00449862 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405761 | AGGCCCACCCGGGCG[C/T]CGGCTCAGCGGTAGT | 5192 |
rs753603145 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404665 | TAAGTAAGTCAAACA[C/G]CAAGACATGGTTTGC | 5192 |
rs753617772 | snp | A/G | 1.69689e-05 | 0.00291275 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408467 | GTACGTGATCCCCGT[A/G]AGCCTCTTGGCCAGG | 5192 |
rs753621056 | in-del | -/C | 0.000579359 | 0.0170101 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405724 | CTTGGCGTTCAGACT[-/C]CCGTAGAGGTCATCT | 5192 |
rs753648556 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415036 | CTGGAGTGCAGTGGC[A/G]GGATCTTGGCTCACT | 5192 |
rs753697426 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415503 | CTCTTGCCACTCAGC[C/T]TATGTGCCGCCCGGC | 5192 |
rs753709035 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405193 | GCTGGCCTTGGTTGG[C/T]TTCTCTCTGCCCCGT | 5192 |
rs753786568 | snp | C/T | 2.35253e-05 | 0.00342959 | missense, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412435 | GCGCTCCGCAGCCCA[C/T]CGCGGTAGTACTCGT | 5192 |
rs753802197 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413366 | CGCAGGCGCTCCGAT[A/C/T]CCTCTGCTCCCAGGG | 5192 |
rs753953758 | snp | C/G | 0.000153438 | 0.0087576 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406471 | CCAGGACGGCAGCAG[C/G]CTCCCACCTCACCTT | 5192 |
rs754059734 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410635 | CTTGACTTGCCTTAG[C/T]GTGAGCTGCAGACAG | 5192 |
rs754308567 | in-del | -/T | 1.77333e-05 | 0.00297764 | intron-variant | PEX10 | GRCh38.p7 | 1:2410470 | AGAGGAGAAACAGTA[-/T]TAGTCCGGGGGAGCT | 5192 |
rs754329521 | snp | C/T | 2.13276e-05 | 0.00326548 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406802 | ACAGCTGCAGCCCCA[C/T]GGACAGCACCAGGTG | 5192 |
rs754536602 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410188 | AAGGCTGGAAAAGTC[A/G]GCTCCCTGCTGGGAG | 5192 |
rs754556033 | snp | C/G | 3.32535e-05 | 0.00407746 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408828 | TCCACCTGGATGATG[C/G]TGACGTACTCCTCCC | 5192 |
rs754733400 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414567 | ATGGCCGGCAGGTGG[C/T]AGCGTCAGCCCGTCT | 5192 |
rs754746510 | snp | C/T | 8.04764e-05 | 0.00634285 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405762 | GGCCCACCCGGGCGC[C/T]GGCTCAGCGGTAGTG | 5192 |
rs755173802 | snp | C/G | 1.70324e-05 | 0.00291821 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406474 | GGACGGCAGCAGGCT[C/G]CCACCTCACCTTGCT | 5192 |
rs755353408 | snp | C/T | 5.1616e-05 | 0.0050799 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408575 | GACCGCCCGCAGCAG[C/T]GCCCTCCTCTGCTGC | 5192 |
rs755438382 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406288 | GGCAAAGCCTCAATA[C/T]ACGTGAATTTGGAAC | 5192 |
rs755446919 | snp | C/T | 4.28119e-05 | 0.00462646 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406806 | CTGCAGCCCCATGGA[C/T]AGCACCAGGTGCAGC | 5192 |
rs755607874 | snp | A/G | 1.65952e-05 | 0.00288051 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408771 | TGCAGTGTCACCAGC[A/G]CGCCACGGCGCAGCG | 5192 |
rs755636065 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407036 | AGTGCCCGGCAGAAA[C/T]GATCAAGCCAGGGGG | 5192 |
rs755842530 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414288 | TTTCCCCACTCTTCT[C/T]ATCTGCACCCTGGGC | 5192 |
rs755971878 | snp | A/C | 5.04681e-05 | 0.0050231 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412375 | GCGAGGACGTCCGGC[A/C]GCGCCCGGCCCTCAC | 5192 |
rs755981829 | snp | C/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410582 | GCCAACACTCACTCC[C/G]TGGCCTCCCTCTCTG | 5192 |
rs756029304 | snp | A/G | 1.77015e-05 | 0.00297497 | intron-variant | PEX10 | GRCh38.p7 | 1:2410467 | CTGAGAGGAGAAACA[A/G]TATTAGTCCGGGGGA | 5192 |
rs756094275 | snp | A/G | 9.27687e-05 | 0.00680997 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405839 | GGACACTCCGCCTGC[A/G]GAGAGGAGAAAGGGG | 5192 |
rs756149538 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414110 | GTCAATGCTTAGATA[-/AC]AGTTTGAGATGCCGC | 5192 |
rs756297578 | snp | C/T | 0.000206023 | 0.0101474 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408567 | AGGACGAAGACCGCC[C/T]GCAGCAGCGCCCTCC | 5192 |
rs756342887 | snp | G/T | 3.38937e-05 | 0.00411652 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408502 | AGAAGACACCGTGGA[G/T]GTAAAACCAGGCAAC | 5192 |
rs756537855 | snp | A/G | 2.20262e-05 | 0.00331853 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406739 | GGTGAGACAGGCCGC[A/G]GTGCAGCCTCCACTC | 5192 |
rs756544191 | in-del | -/A | 1.78439e-05 | 0.00298691 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406659 | AGGTGGGTGCACCTT[-/A]ACAGGTCCTTGTGAA | 5192 |
rs756590714 | snp | G/T | 6.64165e-05 | 0.00576228 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408812 | ATGTATCCGCGATGG[G/T]TCCACCTGGATGATG | 5192 |
rs756634017 | in-del | -/G | 1.86336e-05 | 0.00305229 | intron-variant | PEX10 | GRCh38.p7 | 1:2408904 | TGAGACTGCTGCCGC[-/G]GGGACAGGCTCCCGG | 5192 |
rs756706668 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405617 | GGACAGCTTTCTGTT[C/T]TCTCCCAGGGTGGCT | 5192 |
rs756958133 | snp | G/T | 1.68097e-05 | 0.00289906 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410443 | TCCACTCCAGCCACT[G/T]CCTCGCACCTGAGAG | 5192 |
rs757071778 | snp | A/G | 4.32788e-05 | 0.00465162 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406820 | ACAGCACCAGGTGCA[A/G]CAGTGAGATGACCCC | 5192 |
rs757119183 | snp | A/C | 1.67326e-05 | 0.00289241 | intron-variant | PEX10 | GRCh38.p7 | 1:2410339 | GGTGTGTGTGGCTGC[A/C]CTCAGTCCTGAGGTC | 5192 |
rs757203243 | snp | C/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412127 | CTGAGCTGGGGACGG[C/G]AAGGGCTTGGGCGGG | 5192 |
rs757219158 | snp | A/G | 0.000392481 | 0.0140031 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406467 | CACCCCAGGACGGCA[A/G]CAGGCTCCCACCTCA | 5192 |
rs757238209 | snp | A/T | 1.69499e-05 | 0.00291112 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408492 | GCCAGGTGGTAGAAG[A/T]CACCGTGGATGTAAA | 5192 |
rs757622465 | snp | C/G | 3.68854e-05 | 0.00429434 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406677 | AGGTCCTTGTGAAGT[C/G]CCCAGGACACCCCCA | 5192 |
rs757778155 | snp | A/G | 3.43289e-05 | 0.00414286 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408714 | TGCAGCTCCTGCTCC[A/G]GGGGGAGCAGGGCCT | 5192 |
rs757820207 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415516 | GCCTATGTGCCGCCC[A/G]GCTTCAAAACCAGGC | 5192 |
rs757868505 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413288 | GGGCGGAAGGTGGCC[-/TG]TTCCACCCTCCACCC | 5192 |
rs757934099 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404920 | ATGGAGGCGGGAAAT[A/G]GGCTGGGGCCGAGCT | 5192 |
rs757974161 | in-del | -/GCACAGGGT | 1.68599e-05 | 0.00290338 | cds-indel, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406568 | CCTGCGCTCCTCCAG[-/GCACAGGGT]GCACAGGGGGTTTCT | 5192 |
rs758081067 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405462 | ACTTCTCAACTGTAT[A/G]GTTTGGGGAAGGGAG | 5192 |
rs758140351 | snp | A/G/T | 3.34696e-05 | 0.00409071 | intron-variant | PEX10 | GRCh38.p7 | 1:2410337 | TTGGTGTGTGTGGCT[A/G/T]CCCTCAGTCCTGAGG | 5192 |
rs758228587 | snp | C/G | 1.67136e-05 | 0.00289076 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408848 | GTACTCCTCCCCCAG[C/G]GTCTGGTAGCCTGCG | 5192 |
rs758250423 | snp | G/T | 1.66551e-05 | 0.00288571 | splice-acceptor-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405836 | AGGGGACACTCCGCC[G/T]GCGGAGAGGAGAAAG | 5192 |
rs758262648 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410690 | CTCATCTCTTGCTCC[A/G]GGATTCCCCTGAGCA | 5192 |
rs758364619 | snp | A/G | 1.70991e-05 | 0.00292391 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408558 | CCCTGTCTGAGGACG[A/G]AGACCGCCCGCAGCA | 5192 |
rs758406273 | snp | C/G | 0.000345602 | 0.0131408 | missense, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412439 | TCCGCAGCCCACCGC[C/G]GTAGTACTCGTCCTT | 5192 |
rs758678654 | snp | C/T | 0.000168603 | 0.00918003 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406557 | GCTGTTGGGTGCCTG[C/T]GCTCCTCCAGGCACA | 5192 |
rs758743429 | snp | C/T | 1.7396e-05 | 0.00294919 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408701 | GTCGGGGTCAGCCTG[C/T]AGCTCCTGCTCCAGG | 5192 |
rs758986479 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407224 | AAAAGGAGGCGGGGA[A/G]CGGAAATGTGGGGCT | 5192 |
rs759013217 | in-del | -/TG | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405739 | CCCGTAGAGGTCATC[-/TG]TGTCCAGGCCCACCC | 5192 |
rs759220912 | snp | C/T | 1.75148e-05 | 0.00295924 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408605 | CTCAGTCAGGGTGGC[C/T]GTGTGGTGACGCATC | 5192 |
rs759306542 | snp | A/G | 0.000102463 | 0.00715687 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408554 | GAGGCCCTGTCTGAG[A/G]ACGAAGACCGCCCGC | 5192 |
rs759366394 | in-del | -/CA | 1.77396e-05 | 0.00297817 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408688 | GGGTCGCCCACTGTC[-/CA]GGGGTCAGCCTGCAG | 5192 |
rs759617739 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405206 | GGTTTCTCTCTGCCC[A/C]GTGTGGTCATCAAGT | 5192 |
rs759667036 | snp | A/G | 3.34812e-05 | 0.00409139 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408752 | CAGGTAGGGCAGGAC[A/G]GCATGCAGTGTCACC | 5192 |
rs759742774 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411581 | GTCTGGCCCCGTCGC[C/T]CAGGCTGGAGTGCAG | 5192 |
rs759790014 | snp | G/T | 3.03651e-05 | 0.00389636 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406919 | CAGATGGCGCCACAC[G/T]CATCAGGACCCTGAG | 5192 |
rs760162500 | snp | C/G | 1.70298e-05 | 0.00291798 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408541 | GCTGGAGGCAGGCGA[C/G]GCCCTGTCTGAGGAC | 5192 |
rs760288494 | snp | A/C | 4.14791e-05 | 0.00455388 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405759 | CCAGGCCCACCCGGG[A/C]GCCGGCTCAGCGGTA | 5192 |
rs760304310 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408986 | CGCCCTTGAGCCCAC[C/T]GTCACCCCGTGCTGG | 5192 |
rs760359176 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408099 | TGTTTGTTCCCCACA[A/G]CAGTGACATAGGCAG | 5192 |
rs760413807 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405350 | CCCCACCCCACCCAG[C/T]ACGCACTCATTCAGT | 5192 |
rs760613101 | snp | A/G/T | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404596 | CCCCCGCCCTCCTCC[A/G/T]TCTCTGGCAAGCTGA | 5192 |
rs760632208 | snp | A/C/G | 0.000151297 | 0.00869654 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406724 | CCCGCACGCACCTGC[A/C/G]GTGAGACAGGCCGCG | 5192 |
rs760677467 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405172 | CCAAATGCTTCCGAC[A/G]GAGGTGCTGGCCTTG | 5192 |
rs760694123 | in-del | -/GAGGCCCTGTCTGAGGACGAA | 1.70285e-05 | 0.00291787 | cds-indel, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408539 | CCGCTGGAGGCAGGC[-/GAGGCCCTGTCTGAGGACGAA]GACCGCCCGCAGCAG | 5192 |
rs760785367 | snp | C/G | 5.40049e-05 | 0.00519611 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408621 | GTGTGGTGACGCATC[C/G]AGCGCCGCGCCCCTG | 5192 |
rs760844335 | snp | C/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408924 | CAGGCTCCCGGCGCC[C/G]CTGCCAGCCGACCCT | 5192 |
rs760917162 | snp | G/T | 2.32951e-05 | 0.00341277 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406858 | CTGTAGCTAACACGG[G/T]CCCTCAGGTCCTCTC | 5192 |
rs760925882 | snp | G/T | 1.66018e-05 | 0.00288108 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410394 | GTGGTGAGGCCAAAG[G/T]AGGCCACATCTGAGA | 5192 |
rs761005209 | snp | A/G | 8.61122e-05 | 0.00656115 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406785 | CCGCTGCCTGAAACC[A/G]TACAGCTGCAGCCCC | 5192 |
rs761143756 | snp | A/C | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410595 | CCCTGGCCTCCCTCT[A/C]TGCTTCTGTCTCCGG | 5192 |
rs761202759 | snp | G/T | 1.70017e-05 | 0.00291558 | intron-variant | PEX10 | GRCh38.p7 | 1:2408443 | GTGCCCTCAGCGCCT[G/T]CTACTTACGTACGTG | 5192 |
rs761303238 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411328 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 5192 |
rs761449217 | snp | A/G | 5.65595e-05 | 0.00531757 | intron-variant, missense | PEX10 | GRCh38.p7 | 1:2406951 | GGATCTGGCCTCAGC[A/G]CCTGCTGGGAGGGTC | 5192 |
rs761537188 | snp | A/C | 0.000129862 | 0.00805692 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410864 | TATCAGAAGAGTAAT[A/C]AGTCCTACTTGGAGG | 5192 |
rs761745874 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413994 | CTGGACACAGAGGCT[A/G]CCCTCTGATTGGGTT | 5192 |
rs761845010 | snp | C/T | 3.59984e-05 | 0.00424239 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408678 | CTCCCCTGCAAGGGT[C/T]GCCCACTGTCGGGGT | 5192 |
rs761935062 | snp | A/T | 2.14475e-05 | 0.00327464 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406781 | GCTGCCGCTGCCTGA[A/T]ACCGTACAGCTGCAG | 5192 |
rs761942658 | snp | C/T | 6.60131e-05 | 0.00574476 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406736 | TGCGGTGAGACAGGC[C/T]GCGGTGCAGCCTCCA | 5192 |
rs762000671 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405153 | TGTATTGAAGGTGTG[C/T]GTGCCAAATGCTTCC | 5192 |
rs762111818 | snp | A/C/G | 3.32023e-05 | 0.00407434 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408807 | GGCACATGTATCCGC[A/C/G]ATGGGTCCACCTGGA | 5192 |
rs762351770 | snp | G/T | 3.5598e-05 | 0.00421873 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405795 | GAAGGTAGATGAGCT[G/T]CTGGGGAGGGAACTT | 5192 |
rs762506636 | in-del | -/GCTC | 1.73598e-05 | 0.00294611 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408703 | CGGGGTCAGCCTGCA[-/GCTC]CTGCTCCAGGGGGAG | 5192 |
rs762621275 | snp | A/C | 5.08522e-05 | 0.00504217 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410431 | CAACCTCCTTCCTCC[A/C]CTCCAGCCACTTCCT | 5192 |
rs762621687 | snp | A/G | 0.000337194 | 0.0129801 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406532 | GCAGAACAGGTGGCC[A/G]CAGGGCGTGGCTGTT | 5192 |
rs762783424 | snp | A/C/G | 3.61456e-05 | 0.00425109 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408674 | CAGGCTCCCCTGCAA[A/C/G]GGTCGCCCACTGTCG | 5192 |
rs763003956 | snp | A/G | 1.76955e-05 | 0.00297447 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406653 | AGCGTCAAGGTGGGT[A/G]CACCTTACAGGTCCT | 5192 |
rs763039001 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411968 | CAGTGTGAACCGGAC[C/T]GAGGTATGAGGCGTT | 5192 |
rs763092580 | snp | A/C | 3.34375e-05 | 0.00408872 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408755 | GTAGGGCAGGACGGC[A/C]TGCAGTGTCACCAGC | 5192 |
rs763230837 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413775 | CTCACCTCTGGTTCC[A/G]TCTACAGGAGCTCAG | 5192 |
rs763336688 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414635 | TAGGCGGTGAGTTTT[A/G]CCCCAAAGGGAATCG | 5192 |
rs763465246 | snp | A/C/T | 8.50527e-05 | 0.00652073 | intron-variant | PEX10 | GRCh38.p7 | 1:2408438 | CAGCTGTGCCCTCAG[A/C/T]GCCTGCTACTTACGT | 5192 |
rs763493320 | snp | A/G/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412921 | CCCACTGGGGACAGC[A/G/T]CTGCGGAGTGGAGAC | 5192 |
rs763626682 | snp | C/T | 0.00104015 | 0.0227814 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410433 | ACCTCCTTCCTCCAC[C/T]CCAGCCACTTCCTCG | 5192 |
rs763636557 | snp | C/T | 4.93547e-05 | 0.00496738 | intron-variant, synonymous-codon | PEX10 | GRCh38.p7 | 1:2406947 | GAGGGGATCTGGCCT[C/T]AGCGCCTGCTGGGAG | 5192 |
rs763663936 | in-del | -/ATGGGT | 1.71669e-05 | 0.00292971 | intron-variant | PEX10 | GRCh38.p7 | 1:2408873 | CCTGCGAGGAAGAGG[-/ATGGGT]ATGTGGACCCTGAGA | 5192 |
rs763969391 | snp | A/G | 1.7079e-05 | 0.00292219 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406463 | TGACCACCCCAGGAC[A/G]GCAGCAGGCTCCCAC | 5192 |
rs764202710 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411990 | TGAGGCGTTCGCGCC[A/G]CGGGCGCTCTGACCC | 5192 |
rs764377290 | snp | A/C | 1.8002e-05 | 0.00300011 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406666 | GTGCACCTTACAGGT[A/C]CTTGTGAAGTGCCCA | 5192 |
rs764465144 | snp | C/T | 3.34292e-05 | 0.00408821 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408756 | TAGGGCAGGACGGCA[C/T]GCAGTGTCACCAGCA | 5192 |
rs764599567 | snp | C/G | 9.61723e-05 | 0.00693375 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405745 | GAGGTCATCTGTGTC[C/G]AGGCCCACCCGGGCG | 5192 |
rs764706602 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409218 | TCCAGTCCCATGGCT[C/T]TCCACCAACCACACA | 5192 |
rs764748388 | snp | A/G | 2.13856e-05 | 0.00326991 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406807 | TGCAGCCCCATGGAC[A/G]GCACCAGGTGCAGCA | 5192 |
rs764783812 | snp | C/T | 1.66538e-05 | 0.00288559 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410424 | AGCAGCTCAACCTCC[C/T]TCCTCCACTCCAGCC | 5192 |
rs764858963 | snp | A/G | 3.4212e-05 | 0.0041358 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406446 | CTTGCCGGCACAGCC[A/G]CTGACCACCCCAGGA | 5192 |
rs764894972 | in-del | -/AG | | | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405850 | CTGCGGAGAGGAGAA[-/AG]GGGGTCACAGCAGCT | 5192 |
rs764918823 | in-del | -/GTCA | 1.76069e-05 | 0.00296701 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408692 | TCGCCCACTGTCGGG[-/GTCA]GCCTGCAGCTCCTGC | 5192 |
rs764948458 | snp | A/G | 3.50385e-05 | 0.00418546 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408606 | TCAGTCAGGGTGGCC[A/G]TGTGGTGACGCATCC | 5192 |
rs765098120 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405279 | CGCCGCCTCCCATGG[A/G]GCCGTGGGGCTGCTG | 5192 |
rs765256675 | snp | G/T | 1.67365e-05 | 0.00289275 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408753 | AGGTAGGGCAGGACG[G/T]CATGCAGTGTCACCA | 5192 |
rs765345003 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410655 | GCTGCAGACAGTCTG[C/T]GAAGAATCTCCCACC | 5192 |
rs765641188 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410699 | TGCTCCGGGATTCCC[-/CT]GAGCAACTGTTCTAG | 5192 |
rs765658863 | snp | G/T | 2.39489e-05 | 0.00346033 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406872 | GGCCCTCAGGTCCTC[G/T]CCGGGCAGGCTGCGG | 5192 |
rs765774546 | in-del | -/TC | | | intron-variant | PEX10 | GRCh38.p7 | 1:2406067 | GCTCGGCCGGGAGGT[-/TC]CCTCCTGCTCCCGCA | 5192 |
rs765940676 | snp | A/G | 4.11024e-05 | 0.00453315 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405760 | CAGGCCCACCCGGGC[A/G]CCGGCTCAGCGGTAG | 5192 |
rs765965290 | snp | A/G | 7.55601e-05 | 0.00614608 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405816 | GAGGGAACTTCTCCC[A/G]GCAGAGGGGACACTC | 5192 |
rs766015781 | snp | C/T | 1.70324e-05 | 0.00291821 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408544 | GGAGGCAGGCGAGGC[C/T]CTGTCTGAGGACGAA | 5192 |
rs766103610 | snp | C/T | 8.48543e-05 | 0.00651306 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408464 | TACGTACGTGATCCC[C/T]GTGAGCCTCTTGGCC | 5192 |
rs766262651 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415484 | CCCCGATATGCCTCA[C/T]CATCTCTTGCCACTC | 5192 |
rs766283608 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405187 | GGAGGTGCTGGCCTT[A/G]GTTGGTTTCTCTCTG | 5192 |
rs766291975 | snp | C/G | 0.00012518 | 0.00791039 | missense, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412401 | CTCACCCGCCAGGCT[C/G]TGCAGGGCGCCGCCC | 5192 |
rs766311098 | snp | C/G | 1.7072e-05 | 0.00292159 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406468 | ACCCCAGGACGGCAG[C/G]AGGCTCCCACCTCAC | 5192 |
rs766506813 | snp | C/G/T | 3.57943e-05 | 0.00423038 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408680 | CCCCTGCAAGGGTCG[C/G/T]CCACTGTCGGGGTCA | 5192 |
rs766596553 | snp | C/T | 0.000235092 | 0.0108393 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408624 | TGGTGACGCATCCAG[C/T]GCCGCGCCCCTGAGC | 5192 |
rs766700445 | snp | C/G | 2.35441e-05 | 0.00343096 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406861 | TAGCTAACACGGGCC[C/G]TCAGGTCCTCTCCGG | 5192 |
rs766739631 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409469 | GGGCACCCTGCATGC[A/G]CCTTCCCTGTGTGTT | 5192 |
rs766750402 | snp | A/G | 6.3987e-05 | 0.00565592 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406801 | TACAGCTGCAGCCCC[A/G]TGGACAGCACCAGGT | 5192 |
rs766765054 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | PEX10 | GRCh38.p7 | 1:2408906 | AGACTGCTGCCGCGG[A/G]GACAGGCTCCCGGCG | 5192 |
rs766966222 | snp | C/T | 1.66142e-05 | 0.00288216 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408819 | CGCGATGGGTCCACC[C/T]GGATGATGCTGACGT | 5192 |
rs767000685 | snp | A/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410488 | GTCCGGGGGAGCTGG[A/T]GGGCATCCTCTGAGG | 5192 |
rs767019718 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413153 | CCGAGCAGCCGCCTT[C/T]CCCAGTAATCCTGCG | 5192 |
rs767042266 | snp | C/T | 6.02355e-05 | 0.00548763 | intron-variant, missense, splice-acceptor-variant | PEX10 | GRCh38.p7 | 1:2406954 | TCTGGCCTCAGCGCC[C/T]GCTGGGAGGGTCACA | 5192 |
rs767442631 | snp | C/T | 1.7124e-05 | 0.00292604 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408563 | TCTGAGGACGAAGAC[C/T]GCCCGCAGCAGCGCC | 5192 |
rs767777126 | in-del | -/C | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407565 | GTTTGAGCCCCACTT[-/C]CATGCCCCTGTCACA | 5192 |
rs767807384 | snp | A/G | 2.19845e-05 | 0.00331539 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406737 | GCGGTGAGACAGGCC[A/G]CGGTGCAGCCTCCAC | 5192 |
rs768005610 | snp | A/C | 0.000194624 | 0.00986278 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412524 | GGGTTCGGGTGGTCC[A/C]GAGCAGCCACGCCGG | 5192 |
rs768340395 | snp | A/C | 1.6987e-05 | 0.00291431 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406612 | CGGCTCTCTCCTCCA[A/C]GGAGGCCCTGGGGAA | 5192 |
rs768438726 | snp | C/T | 4.99139e-05 | 0.00499544 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408832 | CCTGGATGATGCTGA[C/T]GTACTCCTCCCCCAG | 5192 |
rs768652461 | snp | G/T | 8.33507e-05 | 0.00645511 | intron-variant | PEX10 | GRCh38.p7 | 1:2410357 | CAGTCCTGAGGTCCC[G/T]TGGGAGCTTCTACCT | 5192 |
rs768742151 | snp | C/T | 0.000248104 | 0.0111351 | intron-variant | PEX10 | GRCh38.p7 | 1:2408888 | ATGGGTATGTGGACC[C/T]TGAGACTGCTGCCGC | 5192 |
rs768794174 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414453 | CCTTGTAATGGCACC[C/T]GCGACCCTCAGTTGC | 5192 |
rs768805802 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | PEX10, RER1 | GRCh38.p7 | 1:2404437 | TCAGGCCTAAGGTGT[C/G]ACAGGAAGTCGCACG | 5192 |
rs768893724 | in-del | -/GCAGCCCCATGG | 2.14135e-05 | 0.00327205 | cds-indel, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406793 | TGAAACCGTACAGCT[-/GCAGCCCCATGG]ACAGCACCAGGTGCA | 5192 |
rs769013489 | snp | C/T | 0.000114071 | 0.00755131 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405859 | GGAGAAAGGGGGTCA[C/T]AGCAGCTGGGGCCAC | 5192 |
rs769097644 | snp | A/G | 0.000282177 | 0.0118747 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405788 | TAGTGCCGAAGGTAG[A/G]TGAGCTTCTGGGGAG | 5192 |
rs769189410 | snp | A/C | 1.69694e-05 | 0.0029128 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408514 | GGATGTAAAACCAGG[A/C]AACATGTAGCCGCTG | 5192 |
rs769251149 | snp | C/T | 1.69479e-05 | 0.00291095 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406606 | TGGAAACGGCTCTCT[C/T]CTCCAAGGAGGCCCT | 5192 |
rs769337013 | snp | A/G | 1.68692e-05 | 0.00290419 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406525 | ACTCCCAGCAGAACA[A/G]GTGGCCGCAGGGCGT | 5192 |
rs769348142 | snp | G/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410946 | GGGGTAAGTGCCAAG[G/T]GTACTGTAAAACAAG | 5192 |
rs769426993 | snp | C/T | 1.8256e-05 | 0.0030212 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408652 | AGCAGCCACGCCCAC[C/T]TGGCCCCAGGCTCCC | 5192 |
rs769600472 | snp | C/T | 2.23531e-05 | 0.00334306 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406842 | GATGACCCCCAGCAG[C/T]CTGTAGCTAACACGG | 5192 |
rs769734201 | in-del | -/AAAC | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410148 | CCGGGGTAAAGTCTT[-/AAAC]AAAGAACCCCAGGGA | 5192 |
rs769793734 | snp | C/T | 6.17583e-05 | 0.00555656 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406700 | CACCCCCAGCCCCCA[C/T]GTGTGGCCCCCGCAC | 5192 |
rs769847524 | snp | A/G | 1.65941e-05 | 0.00288041 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408786 | ACGCCACGGCGCAGC[A/G]AGGAGGGCACATGTA | 5192 |
rs770053457 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414899 | CAGCCTCCTCTTGAG[C/T]CCTTGGGACTTTTCA | 5192 |
rs770307040 | snp | A/G | 1.71193e-05 | 0.00292564 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406437 | CAGGTGCATCTTGCC[A/G]GCACAGCCGCTGACC | 5192 |
rs770336711 | snp | A/C | 0.000601504 | 0.0173318 | missense, utr-variant-5-prime, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412499 | TGGCGGCGGCCGGGG[A/C]CATGGCCGCGGGTTC | 5192 |
rs770358289 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404858 | GATGCCTACGGTGAA[-/CT]CTCTGGCGCAGGTTA | 5192 |
rs770527158 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409965 | TTGGGAGCCTGAGAG[C/T]TTCTGTCAACAACTC | 5192 |
rs770580431 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409020 | AGGCCAACATGACCT[C/T]CTGTCGCTAAGCCCA | 5192 |
rs770597274 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2414990 | TCTTTTTTTTTTTTT[C/T]TTGAGACAGAGTCTC | 5192 |
rs770764603 | snp | A/G | 1.70461e-05 | 0.00291938 | intron-variant | PEX10 | GRCh38.p7 | 1:2408868 | GGTAGCCTGCGAGGA[A/G]GAGGATGGGTATGTG | 5192 |
rs770937339 | in-del | -/C | 1.70772e-05 | 0.00292204 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408556 | GGCCCTGTCTGAGGA[-/C]GAAGACCGCCCGCAG | 5192 |
rs770950166 | snp | C/T | 1.66557e-05 | 0.00288575 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405722 | ATCTTGGCGTTCAGA[C/T]TCCCGTAGAGGTCAT | 5192 |
rs771084314 | snp | C/G | 3.71195e-05 | 0.00430794 | intron-variant | PEX10 | GRCh38.p7 | 1:2407002 | GCACGTTAGAACCAG[C/G]CCTCTCACTGGCATG | 5192 |
rs771134921 | snp | A/G | 5.99622e-05 | 0.00547517 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410503 | TGGGCATCCTCTGAG[A/G]ATGAGGGACCACAGT | 5192 |
rs771349796 | snp | C/T | 3.3211e-05 | 0.00407485 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410405 | AAAGTAGGCCACATC[C/T]GAGAGCAGCTCAACC | 5192 |
rs771353520 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413317 | CCTCCACCCTGCCTG[A/G]CCTGAGCCCCGCAGG | 5192 |
rs771384712 | snp | A/G | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415740 | CTGCCCAGTGCACAC[A/G]TCGTCTGGGGTCTGG | 5192 |
rs771809433 | snp | A/G | 1.72552e-05 | 0.00293723 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406633 | CCCTGGGGAAGGTGG[A/G]GCAGAGCGTCAAGGT | 5192 |
rs771821210 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408971 | ACAGCCCCATCTTGT[C/T]GCCCTTGAGCCCACT | 5192 |
rs772097260 | snp | A/G | 5.3859e-05 | 0.00518908 | intron-variant, synonymous-codon, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406902 | GACACGGAGCTGTAA[A/G]GCAGATGGCGCCACA | 5192 |
rs772131234 | snp | C/G | 1.67835e-05 | 0.0028968 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408743 | CTTGTCCAGCAGGTA[C/G]GGCAGGACGGCATGC | 5192 |
rs772255287 | in-del | -/TAAG | 1.70307e-05 | 0.00291806 | intron-variant | PEX10 | GRCh38.p7 | 1:2408418 | GTGACAAGGACGGCC[-/TAAG]TAAGCAGCTGTGCCC | 5192 |
rs772275107 | snp | A/G | 3.32314e-05 | 0.0040761 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2410377 | AGCTTCTACCTGCAA[A/G]TGTGGTGAGGCCAAA | 5192 |
rs772303662 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405162 | GGTGTGTGTGCCAAA[C/T]GCTTCCGACGGAGGT | 5192 |
rs772362644 | snp | A/G | 3.72689e-05 | 0.0043166 | intron-variant | PEX10 | GRCh38.p7 | 1:2408902 | CCTGAGACTGCTGCC[A/G]CGGGGACAGGCTCCC | 5192 |
rs772618705 | snp | C/T | 8.62076e-05 | 0.00656478 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408582 | CGCAGCAGCGCCCTC[C/T]TCTGCTGCTCAGTCA | 5192 |
rs772790675 | snp | A/G | 0.000119176 | 0.00771842 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408539 | CCGCTGGAGGCAGGC[A/G]AGGCCCTGTCTGAGG | 5192 |
rs773055716 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2408975 | CCCCATCTTGTCGCC[C/T]TTGAGCCCACTGTCA | 5192 |
rs773147980 | snp | C/T | 0.000129604 | 0.00804891 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406723 | CCCCGCACGCACCTG[C/T]GGTGAGACAGGCCGC | 5192 |
rs773164888 | in-del | -/T | 1.69706e-05 | 0.0029129 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408460 | TACTTACGTACGTGA[-/T]CCCCGTGAGCCTCTT | 5192 |
rs773303566 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405168 | TGTGCCAAATGCTTC[C/T]GACGGAGGTGCTGGC | 5192 |
rs773433357 | snp | A/C/G | 9.33012e-05 | 0.0068296 | intron-variant | PEX10 | GRCh38.p7 | 1:2408904 | TGAGACTGCTGCCGC[A/C/G]GGGACAGGCTCCCGG | 5192 |
rs773572267 | snp | C/G | 1.71214e-05 | 0.00292582 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406434 | AGCCAGGTGCATCTT[C/G]CCGGCACAGCCGCTG | 5192 |
rs773660202 | snp | C/T | 1.72627e-05 | 0.00293786 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408587 | CAGCGCCCTCCTCTG[C/T]TGCTCAGTCAGGGTG | 5192 |
rs773673732 | snp | C/G | 7.26546e-05 | 0.00602678 | intron-variant | PEX10 | GRCh38.p7 | 1:2410478 | AACAGTATTAGTCCG[C/G]GGGAGCTGGTGGGCA | 5192 |
rs773805218 | snp | A/G | 0.000185684 | 0.00963366 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410816 | TCCAACTTGCTGGCT[A/G]TGAGGTCTTTCTGGA | 5192 |
rs773893558 | snp | A/G | 4.18559e-05 | 0.00457452 | utr-variant-5-prime, missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412535 | GTCCCGAGCAGCCAC[A/G]CCGGCCACGCCCACG | 5192 |
rs774205482 | snp | A/G | 1.68505e-05 | 0.00290258 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406539 | AGGTGGCCGCAGGGC[A/G]TGGCTGTTGGGTGCC | 5192 |
rs774301205 | snp | G/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408676 | GGCTCCCCTGCAAGG[G/T]TCGCCCACTGTCGGG | 5192 |
rs774512733 | snp | C/T | 1.77451e-05 | 0.00297863 | intron-variant | PEX10 | GRCh38.p7 | 1:2408889 | TGGGTATGTGGACCC[C/T]GAGACTGCTGCCGCG | 5192 |
rs774522472 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407405 | TCCCGTGTCACTTTC[C/T]ACTGGCTGGGAAATG | 5192 |
rs774861304 | snp | C/T | 1.65509e-05 | 0.00287666 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405793 | CCGAAGGTAGATGAG[C/T]TTCTGGGGAGGGAAC | 5192 |
rs774922599 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410187 | AAAGGCTGGAAAAGT[C/T]GGCTCCCTGCTGGGA | 5192 |
rs774947164 | snp | A/C | 1.65822e-05 | 0.00287938 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405749 | TCATCTGTGTCCAGG[A/C]CCACCCGGGCGCCGG | 5192 |
rs774949268 | snp | A/G | 1.69838e-05 | 0.00291404 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408520 | AAAACCAGGCAACAT[A/G]TAGCCGCTGGAGGCA | 5192 |
rs774999714 | snp | A/G | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410956 | CCAAGTGTACTGTAA[A/G]ACAAGTAAGTACACA | 5192 |
rs775041092 | snp | A/G | 1.80919e-05 | 0.00300759 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408672 | CCCAGGCTCCCCTGC[A/G]AGGGTCGCCCACTGT | 5192 |
rs775373821 | snp | C/T | 1.75004e-05 | 0.00295802 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408607 | CAGTCAGGGTGGCCG[C/T]GTGGTGACGCATCCA | 5192 |
rs775448187 | snp | C/T | 3.31967e-05 | 0.00407397 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408798 | AGCGAGGAGGGCACA[C/T]GTATCCGCGATGGGT | 5192 |
rs775560308 | snp | A/G | 4.56007e-05 | 0.00477475 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406848 | CCCCAGCAGCCTGTA[A/G]CTAACACGGGCCCTC | 5192 |
rs775663727 | snp | A/C | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413576 | CCTGGCCAGGGAGGG[A/C]AGGAGATGCCTGGTA | 5192 |
rs775743858 | snp | C/G | 1.67265e-05 | 0.00289188 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408754 | GGTAGGGCAGGACGG[C/G]ATGCAGTGTCACCAG | 5192 |
rs775772867 | snp | A/G | 0.000315272 | 0.0125514 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408784 | GCACGCCACGGCGCA[A/G]CGAGGAGGGCACATG | 5192 |
rs775842120 | snp | C/T | 1.66399e-05 | 0.00288438 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405728 | GCGTTCAGACTCCCG[C/T]AGAGGTCATCTGTGT | 5192 |
rs776004824 | snp | C/T | 1.70153e-05 | 0.00291674 | intron-variant | PEX10 | GRCh38.p7 | 1:2408433 | CTAAGCAGCTGTGCC[C/T]TCAGCGCCTGCTACT | 5192 |
rs776078242 | snp | A/G | 3.09919e-05 | 0.00393637 | utr-variant-5-prime, missense, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412504 | GCGGCCGGGGCCATG[A/G]CCGCGGGTTCGGGTG | 5192 |
rs776096476 | snp | A/G | 6.59609e-05 | 0.00574248 | intron-variant, synonymous-codon, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406925 | GCGCCACACTCATCA[A/G]GACCCTGAGGGGATC | 5192 |
rs776183397 | snp | C/G | 0.000370508 | 0.0136058 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410725 | TTCTAGGGCCTATGA[C/G]GGCCACATGGAAAGA | 5192 |
rs776214063 | snp | C/T | 3.42208e-05 | 0.00413633 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406439 | GGTGCATCTTGCCGG[C/T]ACAGCCGCTGACCAC | 5192 |
rs776218721 | snp | A/G | 1.74561e-05 | 0.00295428 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408603 | TGCTCAGTCAGGGTG[A/G]CCGTGTGGTGACGCA | 5192 |
rs776308498 | snp | C/T | 1.70414e-05 | 0.00291898 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408546 | AGGCAGGCGAGGCCC[C/T]GTCTGAGGACGAAGA | 5192 |
rs776437168 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405690 | TTCTGTGCAAGCAAG[A/G]TTAATCCTGAGACTA | 5192 |
rs776503441 | snp | A/G | 0.000237138 | 0.0108864 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406725 | CCGCACGCACCTGCG[A/G]TGAGACAGGCCGCGG | 5192 |
rs776590711 | in-del | -/CT | 1.81516e-05 | 0.00301255 | frameshift-variant, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408634 | TCCAGCGCCGCGCCC[-/CT]GAGCAGCCACGCCCA | 5192 |
rs776619119 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407288 | GACCGAAGCCCCAGT[A/G]TAACAAGGCACGTGG | 5192 |
rs776727990 | snp | C/T | 0.000105219 | 0.00725247 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405726 | TGGCGTTCAGACTCC[C/T]GTAGAGGTCATCTGT | 5192 |
rs776807122 | snp | C/T | | | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406685 | GTGAAGTGCCCAGGA[C/T]ACCCCCAGCCCCCAT | 5192 |
rs776816396 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409085 | AATGGCTGCCCTTGG[C/T]TCCCAGGGCCTTGGC | 5192 |
rs776893505 | snp | C/T | | | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405922 | TCCTGTCCACATTCT[C/T]TGCACATGACACACA | 5192 |
rs776985569 | snp | C/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413327 | GCCTGGCCTGAGCCC[C/G]GCAGGTGCTCTGGGG | 5192 |
rs777066508 | snp | C/T | 1.68806e-05 | 0.00290517 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406511 | CCACGCGGTGATGCA[C/T]TCCCAGCAGAACAGG | 5192 |
rs777133959 | in-del | -/AG | 1.6863e-05 | 0.00290365 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406572 | CGCTCCTCCAGGCAC[-/AG]GGTGCACAGGGGGTT | 5192 |
rs777156669 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411663 | CTTGCCTCAGCCTCC[C/T]GAAGAGCTGGGATTA | 5192 |
rs777177898 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410962 | TACTGTAAAACAAGT[-/A]AAGTACACACACAAA | 5192 |
rs777291538 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405473 | GTATGGTTTGGGGAA[A/G]GGAGGGAAACCTAAA | 5192 |
rs777319062 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2404881 | CGCAGGTTAAATGCA[A/G]TTTTGAAAACCTGGA | 5192 |
rs777484312 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409921 | ACCAGGCTGGCACTC[A/G]GTGGTCCTTGCTACA | 5192 |
rs777541029 | snp | C/G | 2.15766e-05 | 0.00328448 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406817 | TGGACAGCACCAGGT[C/G]CAGCAGTGAGATGAC | 5192 |
rs777570617 | snp | A/G | 4.30802e-05 | 0.00464093 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405837 | GGGGACACTCCGCCT[A/G]CGGAGAGGAGAAAGG | 5192 |
rs777747777 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413291 | GCGGAAGGTGGCCTT[C/T]CACCCTCCACCCTCC | 5192 |
rs777809806 | snp | A/G | 1.83374e-05 | 0.00302793 | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2410481 | AGTATTAGTCCGGGG[A/G]AGCTGGTGGGCATCC | 5192 |
rs777833967 | snp | C/T | 2.74337e-05 | 0.00370353 | intron-variant, missense, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406904 | CACGGAGCTGTAAGG[C/T]AGATGGCGCCACACT | 5192 |
rs777938524 | snp | C/T | 0.000975134 | 0.0220594 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412452 | GCGGTAGTACTCGTC[C/T]TTCTGCGCCGCGCGG | 5192 |
rs777975362 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415576 | TGGCTGGCCTCTGAC[C/T]GCAGCCTGCTGTGCC | 5192 |
rs778031802 | snp | C/T | 1.72609e-05 | 0.00293771 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408708 | TCAGCCTGCAGCTCC[C/T]GCTCCAGGGGGAGCA | 5192 |
rs778322648 | snp | A/G | 1.81628e-05 | 0.00301348 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408630 | CGCATCCAGCGCCGC[A/G]CCCCTGAGCAGCCAC | 5192 |
rs778438020 | snp | A/G | 6.82652e-05 | 0.00584191 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406466 | CCACCCCAGGACGGC[A/G]GCAGGCTCCCACCTC | 5192 |
rs778512940 | snp | A/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414304 | ATCTGCACCCTGGGC[A/G]ACAAATCCCAGCCTC | 5192 |
rs778521596 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405046 | CCCCAGGACCTGGCT[C/T]GTGAGTGCGTCTGGG | 5192 |
rs778631805 | snp | C/G | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2413180 | TGCGCGAAAAGCACA[C/G]GGCCGGCTTGGTGTG | 5192 |
rs778701948 | snp | A/G | 3.95593e-05 | 0.00444726 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405763 | GCCCACCCGGGCGCC[A/G]GCTCAGCGGTAGTGC | 5192 |
rs778774616 | snp | C/T | 4.97913e-05 | 0.00498931 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408780 | ACCAGCACGCCACGG[C/T]GCAGCGAGGAGGGCA | 5192 |
rs778793845 | snp | A/G | 5.34117e-05 | 0.00516749 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405715 | AGACTAAATCTTGGC[A/G]TTCAGACTCCCGTAG | 5192 |
rs778879720 | snp | A/G | 9.30103e-05 | 0.00681883 | intron-variant | PEX10 | GRCh38.p7 | 1:2406984 | ACGTTCAGTTGGCAC[A/G]GAGCACGTTAGAACC | 5192 |
rs778898442 | snp | C/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2409712 | TCCCAAACCGCCAAG[C/G]ACGTGTTCTTCTCAG | 5192 |
rs778931694 | snp | C/T | 1.69243e-05 | 0.00290893 | intron-variant | PEX10 | GRCh38.p7 | 1:2408862 | GGGTCTGGTAGCCTG[C/T]GAGGAAGAGGATGGG | 5192 |
rs779199089 | snp | A/G | | | stop-lost, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405768 | CCCGGGCGCCGGCTC[A/G]GCGGTAGTGCCGAAG | 5192 |
rs779239377 | in-del | -/G | 2.1365e-05 | 0.00326834 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406796 | AACCGTACAGCTGCA[-/G]CCCCATGGACAGCAC | 5192 |
rs779334862 | snp | A/G | 0.000229978 | 0.0107208 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405860 | GAGAAAGGGGGTCAC[A/G]GCAGCTGGGGCCACT | 5192 |
rs779337517 | snp | A/G | 3.44513e-05 | 0.00415024 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408576 | ACCGCCCGCAGCAGC[A/G]CCCTCCTCTGCTGCT | 5192 |
rs779704977 | snp | C/G | 1.70168e-05 | 0.00291687 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408722 | CTGCTCCAGGGGGAG[C/G]AGGGCCTTGTCCAGC | 5192 |
rs779713764 | snp | C/T | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406788 | CTGCCTGAAACCGTA[C/T]AGCTGCAGCCCCATG | 5192 |
rs779726539 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405047 | CCCAGGACCTGGCTC[A/G]TGAGTGCGTCTGGGT | 5192 |
rs779833827 | snp | C/G | 5.15119e-05 | 0.00507477 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406895 | GGCTGCGGACACGGA[C/G]CTGTAAGGCAGATGG | 5192 |
rs780035162 | snp | C/T | | | upstream-variant-2KB, intron-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2414415 | CCCCACGGTTCAAGC[C/T]TTGGCTCTAGGCCTT | 5192 |
rs780114946 | snp | A/G | 3.55828e-05 | 0.00421783 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405784 | GCGGTAGTGCCGAAG[A/G]TAGATGAGCTTCTGG | 5192 |
rs780210608 | snp | A/C | 1.66921e-05 | 0.00288891 | intron-variant, downstream-variant-500B | PEX10, RER1 | GRCh38.p7 | 1:2405846 | CCGCCTGCGGAGAGG[A/C]GAAAGGGGGTCACAG | 5192 |
rs780407557 | in-del | -/A | 1.78731e-05 | 0.00298935 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406662 | GTGGGTGCACCTTAC[-/A]GGTCCTTGTGAAGTG | 5192 |
rs780436903 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405055 | CTGGCTCGTGAGTGC[A/G]TCTGGGTCAGGAAGA | 5192 |
rs780485807 | snp | A/C | 0.000101731 | 0.00713128 | missense, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408505 | AGACACCGTGGATGT[A/C]AAACCAGGCAACATG | 5192 |
rs780495120 | in-del | -/A | 1.75875e-05 | 0.00296538 | intron-variant | PEX10 | GRCh38.p7 | 1:2410465 | CCTGAGAGGAGAAAC[-/A]AGTATTAGTCCGGGG | 5192 |
rs780507609 | snp | A/G | 0.000415987 | 0.014416 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406744 | GACAGGCCGCGGTGC[A/G]GCCTCCACTCCTTCC | 5192 |
rs780593226 | snp | C/G | 2.04417e-05 | 0.00319694 | intron-variant, downstream-variant-500B | PEX10 | GRCh38.p7 | 1:2406696 | AGGACACCCCCAGCC[C/G]CCATGTGTGGCCCCC | 5192 |
rs780687424 | snp | C/T | 1.81919e-05 | 0.00301589 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408635 | CCAGCGCCGCGCCCC[C/T]GAGCAGCCACGCCCA | 5192 |
rs780850148 | snp | A/G | 2.18233e-05 | 0.00330321 | missense, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406828 | AGGTGCAGCAGTGAG[A/G]TGACCCCCAGCAGCC | 5192 |
rs780928201 | snp | A/G | | | intron-variant | PEX10 | GRCh38.p7 | 1:2410263 | GAAGCAACCTCACCC[A/G]GGCCAGCTCCAGGAG | 5192 |
rs780974415 | snp | A/G | 8.35652e-05 | 0.00646341 | intron-variant | PEX10 | GRCh38.p7 | 1:2410344 | GTGTGGCTGCCCTCA[A/G]TCCTGAGGTCCCGTG | 5192 |
rs780985318 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2412267 | AGGCGAAGGAGACTG[C/T]CGGGTCCCAGGTTGT | 5192 |
rs781194710 | snp | C/T | 3.60263e-05 | 0.00424404 | missense, downstream-variant-500B, nc-transcript-variant | PEX10, RER1 | GRCh38.p7 | 1:2405779 | GCTCAGCGGTAGTGC[C/T]GAAGGTAGATGAGCT | 5192 |
rs781306925 | snp | A/G | 0.000404613 | 0.0142177 | missense, utr-variant-5-prime, nc-transcript-variant | PEX10, PLCH2 | GRCh38.p7 | 1:2412481 | GGATCACCTCCGGGG[A/G]GCTGGCGGCGGCCGG | 5192 |
rs781574886 | snp | C/T | | | intron-variant | PEX10 | GRCh38.p7 | 1:2407385 | ACAGCTGGCTGCCCT[C/T]GGCTTCCCGTGTCAC | 5192 |
rs781710848 | snp | A/G/T | 3.41135e-05 | 0.00412987 | synonymous-codon, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2408719 | CTCCTGCTCCAGGGG[A/G/T]AGCAGGGCCTTGTCC | 5192 |
rs796431871 | snp | C/T | | | upstream-variant-2KB, intron-variant | PLCH2 | GRCh38.p7 | 1:2415426 | TATTCTTGTTGGCAG[C/T]GCCTTACATCCTTCT | 5192 |
rs796971884 | snp | C/T | | | intron-variant, upstream-variant-2KB | PEX10, PLCH2 | GRCh38.p7 | 1:2411512 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 5192 |
rs797044762 | in-del | -/G | | | frameshift-variant, downstream-variant-500B, nc-transcript-variant | PEX10 | GRCh38.p7 | 1:2406528 | GCCACGCCCTGCGGC[-/G]CACCTGTTCTGCTGG | 5192 |