SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7089 | snp | C/T | 0.485731 | 0.0832509 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191649 | GGACTGGGTATGGAT[C/T]GCTGGGCCCTAGGCT | 79089 |
rs12421 | snp | A/G | 0.00338409 | 0.040995 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191384 | TATGGGCACCTAGCC[A/G]CCTTCACCTTCTTCC | 79089 |
rs757430 | snp | A/G | 0.202217 | 0.245391 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190906 | AAAAGTGGGGAGGCC[A/G]TAAAGGAGAAAGACC | 79089 |
rs2240226 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | TMUB2 | GRCh38.p7 | 17:44188850 | CAACCTAAACCTAAA[A/G]ACCTACCCTACCCTT | 79089 |
rs2285952 | snp | C/T | 0.0785177 | 0.181917 | utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44191227 | CCCTTGCAGGCAGCC[C/T]TGGGTGCTGGGGGCA | 79089 |
rs2285953 | snp | C/G | 0.0790111 | 0.182384 | utr-variant-3-prime, splice-donor-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190887 | AGGAGAAAGACCATG[C/G]CTTTCATTTTCTTCC | 79089 |
rs4793082 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187594 | TAAATCATGGTTAAT[A/G]ACATTAACCTTCTTA | 79089 |
rs5820525 | in-del | -/G | 0.0588605 | 0.161139 | upstream-variant-2KB, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186611 | CGAATCCAATCAGCC[-/G]GGGAGGCAGACAGCA | 79089 |
rs7224350 | snp | A/G | 0.030278 | 0.119257 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185196 | ggactacaggtgcat[A/G]ccactgtgcctagcT | 79089 |
rs8073555 | snp | C/G | 0.149149 | 0.23222 | intron-variant | TMUB2 | GRCh38.p7 | 17:44188856 | AGGGTAGGTCTTTAG[C/G]TTTAGGTTGGGGTGC | 79089 |
rs9895154 | snp | A/C/G | 0.0374636 | 0.131642 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190581 | CAGCCCGCACACTGC[A/C/G]TTCTCTGAACATTAC | 79089 |
rs9898613 | snp | A/G | 0.496279 | 0.0429702 | intron-variant | TMUB2 | GRCh38.p7 | 17:44189922 | AGGCTGAGGCAGGAG[A/G]ATCGCTTGAACCCAG | 79089 |
rs11080007 | snp | C/T | 0.495782 | 0.0457324 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44188074 | ATGGTAATCACCAGA[C/T]TGGATTTGCCCAGGG | 79089 |
rs11656871 | snp | C/G | 0.485528 | 0.0838238 | downstream-variant-500B, utr-variant-3-prime | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191773 | TTGCGCTGCCCCCAG[C/G]AAAATGGTAATGAGA | 79089 |
rs28609241 | snp | A/T | | | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186336 | TCAAAAAAGAAAAAA[A/T]TTTAACTGCAAAAAT | 79089 |
rs34097625 | in-del | -/A | | | intron-variant | TMUB2 | GRCh38.p7 | 17:44190371 | AAAAAAAAAAAAAAA[-/A]GGATAAAGATGAGGG | 79089 |
rs34260880 | in-del | -/A | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB, frameshift-variant, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187355 | CCAGTCCAACGCCGA[-/A]GGGAATAGGACCATC | 79089 |
rs35026282 | in-del | -/A | | | intron-variant | TMUB2 | GRCh38.p7 | 17:44190183 | TACTAAAAAAAAAAA[-/A]TACAAAAATTAGCTG | 79089 |
rs35179907 | in-del | -/C | | | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185721 | CTAATTATCTATTTC[-/C]TTGATCTAAGTGCTA | 79089 |
rs35187489 | in-del | -/T | 0 | 0 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185864 | TTTTTTTTTTTTTTT[-/T]GGAGACAAGGCCTCC | 79089 |
rs35231320 | snp | G/T | 0.01739 | 0.091611 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192111 | GGTGGACGACACCTA[G/T]CCGGGGTGGGAAGGA | 79089 |
rs35357997 | in-del | -/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187415 | GTGCGGGACCCCTCC[-/C]TCACCGTGCGGTCAC | 79089 |
rs35675776 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192130 | GGTGGGAAGGATGGG[-/G]AATTGAAACCCACAC | 79089 |
rs56049912 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186627 | GGGAGGCAGACAGCA[A/G]GGCCGGAAGAACAAA | 79089 |
rs56521244 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191967 | CCCTCCCCCAATGAC[C/T]CCAGCATGCGGTAAT | 79089 |
rs58236343 | snp | A/T | 0.0126866 | 0.078628 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190639 | CTCACCCCCAGGGTC[A/T]GCTGTTCCAGGCCCC | 79089 |
rs58885394 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185423 | TTCTTTTTTTTTTTT[-/TT]CCTGAGACAGAGTCT | 79089 |
rs59377393 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | TMUB2 | GRCh38.p7 | 17:44188794 | GAGTTTGAGAGAGGA[A/G]GGTCACAGAACGTGA | 79089 |
rs61416700 | in-del | -/G | 0.14232 | 0.226801 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192204 | ACATGGTAGGGGGGG[-/G]CACTCTCTCCCCAGA | 79089 |
rs62078937 | snp | C/T | 0.5 | 0 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190121 | GGAGGCCAAGGCGGG[C/T]AGATCACAAGGTCAA | 79089 |
rs71371974 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185926 | AGCTCACTGCAGCCT[C/G]GAACTCCTGAGCTCA | 79089 |
rs72822681 | snp | A/G | 0.00154743 | 0.0277726 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190684 | CCCCTCGGCCACTGA[A/G]CCACCCAGCCTTGGT | 79089 |
rs74350299 | snp | A/C | 0.5 | 0 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190349 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 79089 |
rs74490235 | snp | A/G | 0.0456336 | 0.143994 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187518 | CGGGCCCCTCCCCAC[A/G]AGAGTTCCCTGTGTC | 79089 |
rs74644652 | snp | A/T | 0.5 | 0 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190194 | TACTAAAAAAAAAAA[A/T]ACAAAAATTAGCTGG | 79089 |
rs75441414 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192204 | GTTCAACTACATGGT[A/G]GGGGGGGCACTCTCT | 79089 |
rs76812311 | snp | A/G | 0.0197687 | 0.0974348 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191675 | AGGCTCTTGCTTCTG[A/G]GGCTATTGGAGGGTC | 79089 |
rs76913347 | snp | C/T | 0.079617 | 0.182947 | intron-variant | TMUB2 | GRCh38.p7 | 17:44189680 | ACATGGGAGCTGCAG[C/T]AAAGTGTAAGATCCA | 79089 |
rs77014340 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185022 | ATGTACTTAATGCCA[A/C]TGAATTGCAAACTTA | 79089 |
rs77167612 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186432 | GCCTTCTTTGAAATG[A/C]TTTCCCGCCTTCTTT | 79089 |
rs77360759 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186568 | ATCCCCGCTAACCTG[C/G]AGTTAGGTGCGCGTT | 79089 |
rs78072309 | snp | A/T | 0.5 | 0 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190193 | CTACTAAAAAAAAAA[A/T]TACAAAAATTAGCTG | 79089 |
rs78472647 | snp | G/T | 0.00478085 | 0.0486577 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192099 | CACAGGATACAGGGT[G/T]GACGACACCTAGCCG | 79089 |
rs78867692 | snp | C/G | 0.121022 | 0.21416 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186505 | GGATGCTGACTAACT[C/G]GTCTCCTTATCTGTC | 79089 |
rs79273076 | snp | C/T | | | upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186784 | TCACCCTGGATTGCC[C/T]AAGGCCCCGCCCACC | 79089 |
rs79991893 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185851 | CAAACTCCAGCGCTT[C/T]TTTTTTTTTTTTTGG | 79089 |
rs111520430 | in-del | -/CCTC | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185961 | ATCCTCCCACCTCTG[-/CCTC]CCAAAGCGGTGGGAT | 79089 |
rs112348960 | in-del | -/GG | 0.0622301 | 0.165053 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190117 | TTGGGAGGCCAAGGC[-/GG]GGGCAGATCACAAGG | 79089 |
rs112973874 | in-del | -/G | 0.0456336 | 0.143994 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, frameshift-variant, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187308 | CGGAGGCTGGGGCCA[-/G]GCAGCCCTTCGGTTC | 79089 |
rs113028675 | snp | A/G/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192016 | GGGCATGCGGGGGGG[A/G/T]GTGATGCATGGAAGG | 79089 |
rs113163847 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185414 | GGTAATTCTTTCTTT[C/T]TTTTTTTTTTCCTGA | 79089 |
rs113669068 | snp | C/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192212 | ACATGGTAGGGGGGG[C/G]ACTCTCTCCCCAGAA | 79089 |
rs114359465 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187877 | CTCCAGGGCCGGTAT[A/T]TTAAATAAGGATGTT | 79089 |
rs115478072 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191341 | TGAAATCACACTGGC[A/G]GGAATGAAGATTGTG | 79089 |
rs137911830 | snp | C/T | 0.000873312 | 0.0208781 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190586 | CGCACACTGCGTTCT[C/T]TGAACATTACCGACA | 79089 |
rs138269684 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187382 | CATCCAAAAGCGGAA[A/C]CTTCGCCTCAGAAAA | 79089 |
rs139203660 | snp | A/G | 6.64121e-05 | 0.00576209 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190823 | CTGGTGGGAGTCACC[A/G]TCTTCTTCAGCTTCC | 79089 |
rs139562104 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189459 | GCAGTCCAGAGGCCC[C/T]CCTGAGATCTGAGGA | 79089 |
rs139943526 | snp | C/T | 0.079617 | 0.182947 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185440 | CCTGAGACAGAGTCT[C/T]GCTCTGTCACCCCAG | 79089 |
rs139943695 | snp | A/G | 0.00020573 | 0.0101401 | utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190865 | ATGTATGGACGATAA[A/G]GACATAGGAAGAAAA | 79089 |
rs140245554 | snp | A/C | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185810 | TCTGGATTATTTATC[A/C]TTTAATCAGTAGTTC | 79089 |
rs140370315 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190050 | CCCTCATTAGTTAAG[A/G]ATAAAGATGAGGGGG | 79089 |
rs140699235 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185071 | TTAAGTTTTATGTTA[C/T]GTATATGTATATATT | 79089 |
rs141290597 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190674 | CCTCCTTGGCCCCCT[C/T]GGCCACTGAGCCACC | 79089 |
rs141546343 | in-del | -/AA | 0.0134861 | 0.0810011 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191473 | TTATTTTATTTTTTT[-/AA]GAGTCCTTCATAGAG | 79089 |
rs141661121 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186665 | AGGGAAACGTCGCAC[A/C/T]GGCTCTGCCCAGCGG | 79089 |
rs142473401 | snp | A/G | 0.00018125 | 0.009518 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190598 | TCTCTGAACATTACC[A/G]ACAACTGTGTGATTC | 79089 |
rs142571127 | snp | A/C | 0.000118974 | 0.00771186 | missense, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189263 | GTGGCAGGCCAAGGC[A/C]ACCCCGAGCCAACTG | 79089 |
rs142871071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMUB2 | GRCh38.p7 | 17:44188812 | TCACAGAACGTGAAA[A/G]CAAGAGTTTCACAAT | 79089 |
rs143020566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44188053 | TGCTGTGAGAATAGT[C/T]TGATAATGGTAATCA | 79089 |
rs143067102 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44192114 | GGACGACACCTAGCC[A/G]GGGTGGGAAGGATGG | 79089 |
rs143176592 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185571 | TGCGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 79089 |
rs143341364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMUB2 | GRCh38.p7 | 17:44189783 | TTTGGGAGGCCGAGG[A/C]GGGTGCATCACGAGG | 79089 |
rs143994586 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | TMUB2 | GRCh38.p7 | 17:44190344 | AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 79089 |
rs144005882 | in-del | -/CTC | 0.0225045 | 0.103662 | cds-indel, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190982 | GGATGTGATGGAAAT[-/CTC]CTCCATAGGACACAG | 79089 |
rs144708577 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190634 | CACCGCTCACCCCCA[A/G]GGTCAGCTGTTCCAG | 79089 |
rs144752033 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185291 | GTTGGATTCCATTTA[C/T]AGCAAGTACAAAAAC | 79089 |
rs144997451 | snp | C/G | 0.079617 | 0.182947 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185501 | TGCAACCTCCGCCTC[C/G]CAGGTTCAAGCCATT | 79089 |
rs145522005 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189164 | TCTACCTACGTAGCA[A/G]ACAGCGGTAGCAACC | 79089 |
rs145889254 | snp | A/G | 0.000168523 | 0.00917787 | missense, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189531 | GGCTCAAATTCCTCA[A/G]TGATACCGAGGAGCT | 79089 |
rs147444461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44188114 | AAAGCAGCAGATTCT[C/T]CAAGGGAAATAGTAG | 79089 |
rs147462268 | snp | C/T | 0.000149824 | 0.00865387 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190828 | GGGAGTCACCGTCTT[C/T]TTCAGCTTCCTAGTA | 79089 |
rs147544296 | in-del | -/TT/TTC | 0.49621 | 0.0433651 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185411 | TGGGGTAATTCTTTC[-/TT/TTC]TTTTTTTTTTTTCCT | 79089 |
rs147722819 | snp | C/T | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189190 | CAACCAGCTCCTGGG[C/T]GCTATTGTGTCAGCA | 79089 |
rs147909757 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185391 | AGACATGAAGGGGGA[A/G]ATTCTGGGGTAATTC | 79089 |
rs148535813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44188326 | TGGTGCTTCTGGTGT[C/T]TGTCCCAAGTTGCTC | 79089 |
rs148821684 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190562 | GGCCGCCTGCTACAA[A/G]ACCCAGCCCGCACAC | 79089 |
rs149071671 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44190933 | TTTTCCTGGCCAGAG[C/G]TGGGCCCAAGGGCCG | 79089 |
rs149121939 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185558 | AGGATTACAGGCGTG[C/T]GCCACCACGCCCGGC | 79089 |
rs149647542 | snp | C/T | 0.00285166 | 0.0376523 | intron-variant, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187771 | TTTAACCCCATTTTA[C/T]TGATGAGAAAGCTGA | 79089 |
rs149934257 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185470 | GCTGGCGTGCAGTGG[C/T]TCCATCTCAGCTCAC | 79089 |
rs150466963 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44186734 | CCCCTTTCCCAAGTA[C/T]CTCCGCGCTAACTCC | 79089 |
rs150570603 | snp | C/T | 0.000362516 | 0.0134583 | synonymous-codon, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189157 | TTGGCTCTCTACCTA[C/T]GTAGCAGACAGCGGT | 79089 |
rs181352974 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187913 | GTTCCACAGATAATT[A/C]TTTGAGCAACTACTG | 79089 |
rs181575979 | snp | A/G | 0.00019985 | 0.00999425 | missense, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44189512 | CCTGGCCTCATCACT[A/G]TGCGGCTCAAATTCC | 79089 |
rs182197199 | snp | G/T | | | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44187184 | TCCTCGCGTCCTGAA[G/T]CCCCGCCCCCAGTTC | 79089 |
rs182649754 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TMUB2, ATXN7L3 | GRCh38.p7 | 17:44191844 | TACACCAGCAGCCAT[C/G]GGGGCAGAGGGAATA | 79089 |
rs183875470 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TMUB2, ASB16-AS1 | GRCh38.p7 | 17:44185932 | CTGCAGCCTCGAACT[C/T]CTGAGCTCAAGCGAT | 79089 |
rs183912955 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMUB2 | GRCh38.p7 | 17:44191053 | TACAGATGTCCCTCC[C/T]GTGCGAGCACAACTC | 79089 |
rs185626119 | snp | G/T | | | intron-variant | TMUB2 | GRCh38.p7 | 17:44188775 | CACACTCATTGGGAA[G/T]TTGGAGTTTGAGAGA | 79089 |