SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs538327774 | snp | A/G | | | | | GRCh38.p7 | 17:18738350 | TCAAGACAAATTGGG[A/G]TCAGCTTGGACTGCC | 10517 |
rs538432795 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750198 | TTTTCGTGTTGAGGC[A/T]GATATGACTGTGGAC | 10517 |
rs538451037 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741035 | CAAAGTACTGGGATT[A/G]CAAGCGTGAACCACC | 10517 |
rs538458415 | in-del | -/AAT | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745289 | ATAGCTTAAGGGCCA[-/AAT]AAGTCTAGGGTGGTA | 10517 |
rs538509587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757860 | TGGTATCTACTAGCA[C/T]AGGACTTTGAACCTA | 10517 |
rs538660813 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743109 | TTTGTCTGGCCTTCC[C/T]GATTAATTAAATATT | 10517 |
rs538664713 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767402 | GGAAAATTGCTTGAA[C/T]CAGGGAGGCAGACGT | 10517 |
rs538667327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771027 | CTTTTAGTGAAACTT[C/T]ATTAGTATTATTTAC | 10517 |
rs538699140 | snp | C/T | 2.04861e-05 | 0.00320041 | stop-gained, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778975 | CCCCTGACCAGTATG[C/T]AGGTCATTAAACCAA | 10517 |
rs538704043 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770554 | TGATCCACCCGTCAC[A/G]GCCTTCCAAAGCGCT | 10517 |
rs538705234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778390 | AATGTGCTTCGAAGT[C/T]TGAATGCCCAAGTAC | 10517 |
rs538740318 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777839 | TGAGCCACCGCGCCC[C/G]GCCTCAACTTCACAT | 10517 |
rs538846675 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759488 | GAACTGTTTTTGAGA[G/T]TCACCTATATGATGC | 10517 |
rs538849483 | snp | A/C/G | 3.33029e-05 | 0.00408051 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758485 | CTTTCTCCTAAGCGG[A/C/G]AGCTATGACCTAAGT | 10517 |
rs538876633 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766336 | TTAATTTTACCTGCC[A/C]CTACTCAAGCTGTAT | 10517 |
rs538884850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765208 | TGGGGAATATAATAA[G/T]TCCATGAACAACAAT | 10517 |
rs538911970 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742332 | CGCACTCACTTGCTC[C/T]AGAGCACCCCTTGTC | 10517 |
rs538914810 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772598 | AAGAGAGTCTGTATC[C/T]AGTAAACAAACTGTG | 10517 |
rs538950615 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770849 | AGCTGGTGAGCTTAC[A/G]AAACCAGTACCATGA | 10517 |
rs539113997 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18764507 | GCCTGACCAACGACT[C/T]TTATTATTATTTCCA | 10517 |
rs539416490 | snp | A/G | 0.000178945 | 0.00945731 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744245 | GGTTATCTTAGGATC[A/G]TGGAAAACCTGGAAT | 10517 |
rs539418429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756638 | GGTGTTATATTACAC[A/G]TATTTCTGTAACCCA | 10517 |
rs539621794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746857 | CTTCATCCCATTCAC[A/C]ATAGGAATGGGCTAT | 10517 |
rs539658978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745835 | TTTGGCCAGATAGTT[C/G]AGGGAAGCAGAAGAA | 10517 |
rs539659207 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754779 | GAAGGCAGGCAGGCA[A/G]GAAGGAAATAAAGAA | 10517 |
rs539681050 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765750 | TTTTTTTTTTGAGAT[-/G]GGAGTCTTGCTCTGT | 10517 |
rs539696689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761598 | TAACAGCTATAGTAT[A/G]TAAGTTTTGAGTTTT | 10517 |
rs539809521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761378 | TCATGCCATTCTCCT[A/G]CCTCAGCCTCCCGAG | 10517 |
rs539903903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767641 | ACCCCTAGCCTTAGC[A/G]GGTGGTGTTGATATA | 10517 |
rs539909246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775013 | TGTACCCATAAAAAA[C/T]AAGATAGTGATATTT | 10517 |
rs539940892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774142 | GAGTTGCTTAACATT[C/T]TGCTGTAAAGAGGTG | 10517 |
rs540103684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762087 | CCTTCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10517 |
rs540289146 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18762224 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACTG | 10517 |
rs540322279 | in-del | -/CTTC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768051 | TTCCTTCCTTCCTTC[-/CTTC]TTTCTTTCTTTCTTT | 10517 |
rs540336572 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774712 | AGGCAGGAGAATCAC[G/T]TGAACCCAGGAGGTG | 10517 |
rs540581492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777312 | CAGGTGATCTACCCA[C/T]CTAGGCCTCCCAAAG | 10517 |
rs540676777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747739 | AATTTTACAATGGGG[G/T]CGTGCTGAAAAGCTA | 10517 |
rs540685766 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740196 | TCCTTGAGTGACCTA[C/G]TCCCTGGTTTCCCCC | 10517 |
rs540735715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757105 | ATATACACATATGTA[C/T]ATGTATATATATACA | 10517 |
rs540863284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763377 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 10517 |
rs540883005 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741706 | GAGGTCGCAGATGTC[C/T]TTCGCATCCTATAGC | 10517 |
rs540898458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777921 | CTCACTTAGAGGCTA[A/G]TATACTCTTTACTCA | 10517 |
rs540915504 | snp | C/G/T | 0.000165389 | 0.00909225 | missense, synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778611 | TAGCGCCCTGCAGCA[C/G/T]GCCCATAATTCCGGG | 10517 |
rs541014989 | snp | G/T | 0.00120239 | 0.0244898 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749838 | TTGGTTGACCTGGAT[G/T]ACATCAGAGACCTGT | 10517 |
rs541022363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759031 | AGAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT | 10517 |
rs541178993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771482 | CGGAGCTCTTTGTCT[A/G]TGGAGCATTAAAGTG | 10517 |
rs541234792 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18760427 | CAGATGAAGCCCAAA[A/G]GCCATCTGCCAGAGA | 10517 |
rs541286001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759576 | TCGTAACTCATTTAT[C/T]TGTTTTTCTGTTGGT | 10517 |
rs541321686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750513 | ATGTTTATAAGGCTG[A/C]AAAGTTTTTTTTTAA | 10517 |
rs541486961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772167 | AGAAGTGAAACAATC[A/G]GAACATATGTGCCCC | 10517 |
rs541595172 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743662 | TTGACTACAGTGAGA[C/T]TTCTGGTTAGTATTG | 10517 |
rs541632392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751202 | GAGTTCTGTGTTGCT[A/G]CTGACTTACAAGACA | 10517 |
rs541796940 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774422 | GACAATAAACAATAT[G/T]GTGTTTGGTAGAAAA | 10517 |
rs541840360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746054 | GAAATCAATGTATCA[C/T]GAGGCAAGAGAAGTA | 10517 |
rs541840819 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774518 | ATAATGTATAGCCGG[A/G]CGCAGTGACTCATGC | 10517 |
rs542077035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760083 | ATTAATTTACATTCC[C/T]ATTAGCAGCATATGA | 10517 |
rs542202815 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739134 | AGGCCAAGGCAGGTG[C/G]ATCATCAGGTCAGGA | 10517 |
rs542210234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762743 | TGGGCATCTTCATCT[A/T]GTTCCCCTTCTGGAA | 10517 |
rs542214482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755092 | ACGTGGTGAAACTCC[A/G]TCGCTGCTAAAAATA | 10517 |
rs542228857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745437 | TCTTTTTTTTTTGAG[A/G]TGGAGTCTCGCTCTG | 10517 |
rs542238369 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18763120 | TATTAATCGTTTTTA[A/T]GTGCCAAGCCTCACA | 10517 |
rs542264617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753467 | GTCTGTAAGAGAGTG[C/T]GGCTTCTAATGTAAC | 10517 |
rs542327361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769341 | AAACATGATCATCTA[C/T]ATGTTAGATAAAAAA | 10517 |
rs542366042 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776254 | TGAACCAGAGAGGGG[G/T]GGGGGTTGCAGTGAG | 10517 |
rs542441842 | snp | A/G | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 17:18740862 | ACCTCCCGGGTTCTC[A/G]CCATTCTCCTGCCTC | 10517 |
rs542471358 | snp | A/G | 3.66885e-05 | 0.00428286 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18756155 | CATTCTCTCTGACAC[A/G]TAGGTACTGGGGTCA | 10517 |
rs542478469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747813 | CAAATAAAAACAGAC[A/G]TAACTGCTCTGGTCC | 10517 |
rs542644262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769842 | CCAGTGCTGCTCAAT[C/G]ACACACAAAATGCTC | 10517 |
rs542659751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778059 | ATCGAGGCCATCCTG[A/G]CTAACACGGTGAAAC | 10517 |
rs542715440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768790 | ACATCGTGTTCTCTG[A/C]ACCTCACCCTCTCTG | 10517 |
rs542791296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748685 | GTGCCCACAAGACAC[A/G]TCTGAAGATAGAGAT | 10517 |
rs542923479 | snp | A/G | 1.74054e-05 | 0.00294998 | synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778509 | ACAAAAACAAGGACA[A/G]TTGGAAACTCCTGGA | 10517 |
rs542924824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764276 | GCACAATCTCAGCTC[A/G]CTGCAACCTCTGCCT | 10517 |
rs543074072 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741795 | ATTTGCCCACCTGCC[C/T]GTTTGAGTACCACTG | 10517 |
rs543149019 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770308 | TGTTCATTTTGACTT[-/T]TTTTTTTTTTTTTGA | 10517 |
rs543181459 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18757975 | TGACGTTTTCCAAGA[A/G]AAAAGGTTTCCGTGA | 10517 |
rs543230024 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765109 | GGAGAAAAAAAATAA[A/T]AGGATATGGCCCTTT | 10517 |
rs543267116 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762595 | CCAAAGTGCTGGAAT[C/T]ACAGGCATGAGCCAC | 10517 |
rs543294496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772241 | CTCCTGCTGCATCTC[C/T]TGGTAACTTTCACCA | 10517 |
rs543392050 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742601 | CCTGGGGTGGTGGCT[A/C]ACGCTGTAATCCCAG | 10517 |
rs543446348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759641 | TTTTTGAGATGGAGT[C/T]TCACTGTGTCACCCA | 10517 |
rs543450107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759950 | ATTTCAAAGAATGCT[C/G]CCAGAGACGGGTCTT | 10517 |
rs543484433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767006 | TCTAAAGGGGAAGGC[C/T]CCAAAGTGAGGCATT | 10517 |
rs543505125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758655 | CTTTTTTTTGGCAAG[A/G]AAAAAGTCAGGAATG | 10517 |
rs543668594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751808 | CGAATTCGGCTCCCT[C/T]ATCCCTCACTTCCAG | 10517 |
rs543845842 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774541 | ACTCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 10517 |
rs543942409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772774 | CGGGGAGGACTGGTT[C/T]GTTTGTGGAATATTT | 10517 |
rs544105481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775341 | AACTCTTTCTCTCAC[G/T]CTAGTTTCGTATTGT | 10517 |
rs544144960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768471 | TTCATCTGAAGAAGC[C/T]TCAGCTTTGGTTCTT | 10517 |
rs544234426 | snp | A/G | | | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743110 | TTGTCTGGCCTTCCC[A/G]ATTAATTAAATATTA | 10517 |
rs544267199 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18740074 | AGGAATCTGCTCTTC[A/C]AGACAATAATAGACA | 10517 |
rs544357344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769058 | CTCCTGTCTCAGCTT[C/T]CTAAGTAGCTGGGAC | 10517 |
rs544460327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760815 | AATATGAATGTAATA[A/G]AATATCAGTTTATCA | 10517 |
rs544498950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767990 | CATTGGCCTTCTTTT[C/T]TTCTTTTATTTTTTC | 10517 |
rs544592101 | snp | C/T | 1.671e-05 | 0.00289045 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747987 | TTCCCCTGAGAAAGA[C/T]CACAGCTCCAAGTCT | 10517 |
rs544619439 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739232 | GCATGGTGGTGCGTG[C/T]CTGTAATCCCAGCTA | 10517 |
rs544706827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756252 | TACATGGAAAGGCAA[A/G]CTCTCCTCACCTCAA | 10517 |
rs544742007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762989 | CTGTGCCATCATTCA[A/G]TGCACTGTGGCTGCA | 10517 |
rs544781033 | snp | A/G | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 17:18741659 | GGGGACTGGCATGAA[A/G]CCTCCAGGCTGCTCG | 10517 |
rs544816805 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741101 | CAAGTGTAATACCAC[A/G]TGATGGGAAGGCGAG | 10517 |
rs544853836 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748763 | GGGCCACAATCCATT[G/T]TCTAGTCCCTGGGCT | 10517 |
rs544862758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769449 | GGGAAGAGGTATGTC[C/T]TGAGAGAAGCTCACG | 10517 |
rs544863050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777246 | TTTTTGTATTTTTAG[C/T]ACAGACGGGTTTTCT | 10517 |
rs544902517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776363 | ATGACTCATGACTGG[C/G]ATGTCCCTTTGTTAT | 10517 |
rs544940180 | in-del | -/A | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18760779 | GCGAAACTCGGTCTC[-/A]AAAAAAAAAAAAAAA | 10517 |
rs544979522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757000 | ACTAGTTGAATTCTA[A/G]GTATGACCAACGGAA | 10517 |
rs545016225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763998 | TCTTTACTGTGGGGC[C/T]TGCCCTGTGCAATGT | 10517 |
rs545078528 | snp | C/G | 1.66247e-05 | 0.00288307 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778590 | TGACCAATTCCTCCT[C/G]ACTGTTAGCGCCCTG | 10517 |
rs545130621 | snp | C/T | 0.000214127 | 0.0103449 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769958 | TCCCTTCTCTTCCTC[C/T]GGGTCATCAGCGCCT | 10517 |
rs545198601 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18762442 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10517 |
rs545340192 | snp | A/G | 0.000149443 | 0.00864288 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758305 | TCCCCTGGCACTCAG[A/G]TGGGATCAAAACCGA | 10517 |
rs545382552 | in-del | -/TTCA | 0.000758463 | 0.0194591 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749861 | GACCTGTCTTCTGGG[-/TTCA]TTCAGCAAATACCGA | 10517 |
rs545383638 | snp | C/T | 3.30682e-05 | 0.00406608 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764900 | TTTTCTAAGAAGTTT[C/T]CCCCGACCCACGGGT | 10517 |
rs545645738 | snp | C/G/T | 3.29561e-05 | 0.00405921 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772537 | AAAAAGAAGAAAATA[C/G/T]TCTCATGGAAATTCT | 10517 |
rs545784792 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744399 | GGATCAATGACATAT[C/T]ACAGAGGAGGTTTCT | 10517 |
rs545827590 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743575 | CCGAGTCTTACCTGC[A/G]GTAGGAGAATTATCT | 10517 |
rs545866125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752825 | CTGAGGCTCAGAGAG[G/T]TCAAGCTCTCCCAGC | 10517 |
rs545866747 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742757 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10517 |
rs545897359 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776700 | TTGCAATATATGAGA[A/G]ACCCCACTGCATTTG | 10517 |
rs545965387 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18738993 | CTTTCAAGTTCAAGA[C/T]CTTTCTTCTTGATAT | 10517 |
rs546043363 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774420 | ACGACAATAAACAAT[A/G]TGGTGTTTGGTAGAA | 10517 |
rs546058863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766581 | GCTAGGCCACGGGAA[C/G]TCCTTCTAGAATCTG | 10517 |
rs546071981 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760249 | GTTGAACACCTTTTC[-/AT]ATGTGTATTAGTCAG | 10517 |
rs546095101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772901 | GAACATTCTGGTTTG[C/T]AAAAGCTAGATTTTC | 10517 |
rs546205050 | snp | C/G/T | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18775145 | ATTTAGCAGTGTTAA[C/G/T]AGAGGAACTTCAAAG | 10517 |
rs546210164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751995 | CCCCCCACTCTGCTT[A/G]AAGTCTATTTTAAAG | 10517 |
rs546298465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767384 | ACTTGGGAGGCTGAA[A/G]CAGGAAAATTGCTTG | 10517 |
rs546319501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767043 | CTGTGGAGGGTAGGG[A/G]CTCCACCACCCACAT | 10517 |
rs546518495 | in-del | -/CTCA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771522 | GAAGTTAGAAATCAT[-/CTCA]CTTTATAAAGTATAG | 10517 |
rs546581623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753185 | GGCACAGAGGGAAGT[G/T]GGGGGACAGTCTCTT | 10517 |
rs546647103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760407 | ACCCAGGAGAGCCAA[C/T]GGTGCAGATGAAGCC | 10517 |
rs546765450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775930 | CTCAGGAAGCTGAGG[C/T]GGGAGGATCCTTTGA | 10517 |
rs546803909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746539 | AATTAGATCACAATA[C/T]ATGTCACTTGATTTA | 10517 |
rs546809458 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18739352 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 10517 |
rs546848020 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18738385 | TTTATTGAATCCCTG[C/T]GGGTTGTTGGTGCTT | 10517 |
rs546873625 | snp | C/G/T | 0.0166325 | 0.0896639 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747510 | GCAGTGAGCCAAGAC[C/G/T]GAGCCATTGCACTCC | 10517 |
rs546912477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755429 | GCATGGTGGTGCACG[C/T]TTGTAGTCCCAGTTA | 10517 |
rs546965539 | in-del | -/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 17:18740973 | TCACCGTGTTAGCCA[-/G]GATGGTCTCGATCTC | 10517 |
rs547008970 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 17:18740918 | GGCACCCACCACCAC[A/G]CCCAGCTAATGTTTT | 10517 |
rs547019797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776617 | AGCCAAAGGATAAGT[A/G]CATTCAAAAACTAGA | 10517 |
rs547046379 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740664 | AAAAACCTTTCCCCC[A/G]CATTAATAACTTAAG | 10517 |
rs547166740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756346 | TTGGCAGTGGGTAAA[A/G]GACACTTTCCCTTTC | 10517 |
rs547225174 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769499 | AAATGACAGCAGGCC[A/G]GGCATGGTGGCGCAC | 10517 |
rs547248070 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765097 | CTAAGTGCTGAGGAG[-/A]AAAAAAAATAATAGG | 10517 |
rs547285516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762461 | TAGCTGGGACTACAG[A/G]CATGTGCCACCACGC | 10517 |
rs547361764 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770449 | CTGGGATTACAGGCG[A/C]CCACCAGTATGCCCG | 10517 |
rs547507052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749476 | GGCGTGAACCCGGGA[A/G]GCGGAGCTTGCAGTG | 10517 |
rs547523064 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745115 | AGCTCGAGAGGGTTG[C/T]AAAGGGGAAGCTTTT | 10517 |
rs547619830 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770899 | TACTGTGCTTTATAT[A/G]TGCGTAGACTCAGGG | 10517 |
rs547692781 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742981 | AAATAAACAAGTTAA[C/T]TACGAAAAAAAAAAA | 10517 |
rs547763481 | snp | A/C/T | 0.000277599 | 0.0117783 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750065 | GAGCCAGCACTGGGC[A/C/T]GCCATGGCTCAACAG | 10517 |
rs547871316 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755622 | TTGGCTTAAAATCCC[-/CT]GAGTGTGCTTTGTAC | 10517 |
rs548250743 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772474 | ACATAAAGTGGCAGT[A/G]TGCCGTGGAAAAAAC | 10517 |
rs548251875 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766136 | GTGTTGAAGCAGCAG[C/T]AAACCCACCCCTAGC | 10517 |
rs548286781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW10, TVP23B | GRCh38.p7 | 17:18779688 | ATTTTTGCACAGAAG[C/T]CTGATAAAACCCATT | 10517 |
rs548325264 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770054 | AATGGCAGAGGTGAT[C/G]CTGTGCTGTCCTTCT | 10517 |
rs548397937 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751442 | TCACCGTGTTAGCCC[A/G]GATGGTCTTGATCTC | 10517 |
rs548430067 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18756238 | CCCTGACCTTTGTGT[A/G]CATGGAAAGGCAAGC | 10517 |
rs548466922 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18752560 | TCTACTAAAAATACA[A/C]AAAATTAGCCAGGCA | 10517 |
rs548550978 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18777786 | CTGACCTCGTGATCC[A/G]CCCTCCTGGGTCTCC | 10517 |
rs548604656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754335 | TAATTCAGGCTGGGA[A/T]ATGGAAAACTCCCTG | 10517 |
rs548628284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761543 | GTGCTGGGATTACAG[A/G]CATGAGCCACCGCGC | 10517 |
rs548642847 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753206 | ACAGTCTCTTGGGTA[A/G]CTACCAAACTTCACC | 10517 |
rs548679688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761092 | GGTGCTATCTTTATC[A/G]CATTGAAATTTCCCA | 10517 |
rs548699221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746604 | TAGAATGAAGACACA[C/G]TGAATCCTAGGGTGT | 10517 |
rs548846857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767484 | ATGGGGTGAGGGGAT[G/T]AACAAAGCATTTTTT | 10517 |
rs548885371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774086 | CAATTACAAGGGGAG[C/T]TGCTTAACATTCTGC | 10517 |
rs549048724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777442 | TAAAGATCAAATTTT[G/T]CAACATAATTACTGT | 10517 |
rs549182287 | snp | C/T | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 17:18740385 | CTGGGGAGGAGGCCC[C/T]TGCAGGGCAACCTGC | 10517 |
rs549221104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747381 | GCCTGGCCAACATGG[C/T]GAAACCCCATCTCTA | 10517 |
rs549385441 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759428 | TTGAACTCAACATAA[A/G]AAGAATCATATTTTA | 10517 |
rs549403226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770148 | TTTTTGATTTTTTTC[C/T]TCCCCTGGGATACCA | 10517 |
rs549660866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763434 | GTGCTGGGATTACAG[A/G]TGTGAGCCACCGTGC | 10517 |
rs549670370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756397 | CAACAACCTTTTGCA[C/T]AAGTCACACATAAAA | 10517 |
rs549709184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755640 | AGTGTGCTTTGTACT[A/G]TCACGTAGATGTAAT | 10517 |
rs549751503 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778276 | AAACAAACAAACAAA[A/C]AAATTTGTTTTATTA | 10517 |
rs549798710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750612 | TCTCACCCTAAACCA[C/T]GGATTTTGGTAACTT | 10517 |
rs549807967 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741252 | CATGGTCTCTACTTC[A/G]TGGAAGAGGAGCAGG | 10517 |
rs549823780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771004 | TGTCCCTAAACCATA[C/T]TGCCTTCCTTTTAGT | 10517 |
rs549990200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765157 | TCTTCAAAGGGCTCA[C/T]TGTCTCCTAATGGAA | 10517 |
rs550053513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW10, TVP23B | GRCh38.p7 | 17:18779703 | CCTGATAAAACCCAT[G/T]AAGAATTTAAAAGGG | 10517 |
rs550093364 | in-del | -/A | 0.409041 | 0.192888 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767444 | GAGATCATGCGTCTC[-/A]AAAAAAAAAAAAAAA | 10517 |
rs550117830 | snp | A/G | 1.70702e-05 | 0.00292144 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778698 | AATTTCATACCCAAG[A/G]AAGGTCTTGAATTTC | 10517 |
rs550280331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773015 | CTCACCGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 10517 |
rs550589167 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759850 | TCGATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 10517 |
rs550602662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760145 | CTTACTATTGACAGT[C/G]TAACAGTTTTGTCAA | 10517 |
rs550631486 | snp | C/T | 0.000934651 | 0.0215975 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766787 | GGCCACCAGGATCAA[C/T]GATACCTACATTGTG | 10517 |
rs550748670 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18738282 | GAAAAAAAAAAAAAA[A/T]AAAAAGATATGCTAT | 10517 |
rs550784729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745528 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 10517 |
rs550819237 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744467 | TTACACTATTTCCAA[A/T]ATATCCTTCAGACCA | 10517 |
rs550821268 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753077 | CCACTTTAAGTTCCA[C/G]GTCCCTTTCTAGTCT | 10517 |
rs550859873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752254 | GGGCCAGCTGCTCAT[C/G]AGTTCTGGCTAATTA | 10517 |
rs550930753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761560 | ATGAGCCACCGCGCC[C/T]GGCCTCACTTTTCTT | 10517 |
rs550951587 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740518 | CTCTATTTCTGGCTT[A/G]CTCTGTAGTCTTGTT | 10517 |
rs551063670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754479 | AGGCATGGAGCAGAA[A/G]GCTAAGGTTTGGAAG | 10517 |
rs551111079 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777725 | ATTTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT | 10517 |
rs551216108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766418 | GAATTAGCTGATTAG[A/G]GATGAGCTGTCTAGC | 10517 |
rs551270192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768288 | GGCCAGGATGGTCTC[A/C]ATCTCCTGACCTTGT | 10517 |
rs551275661 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768890 | ACTCTCCCTTGTTTT[C/T]TTGTGAAGTAACTAT | 10517 |
rs551419389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755282 | AAAATTGCGGCCGGG[A/C]CTGGTGGCTCACGCC | 10517 |
rs551436544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770832 | ACAGTGGGGGAAAGC[C/T]GAGCTGGTGAGCTTA | 10517 |
rs551456563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762280 | AATTGGTTTTTCTAC[A/G]TAGACAATCCTATCA | 10517 |
rs551527597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756524 | AGAAAGGCAAAGTTT[C/T]CCTGTAGTCTATCAC | 10517 |
rs551565010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763451 | GTGAGCCACCGTGCC[C/T]GGCTGTTAAGTACAA | 10517 |
rs551795311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764381 | TAACTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 10517 |
rs551930724 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761918 | TTGCCAAACTCTCTT[A/G]TTAGTTGTAAAAGCA | 10517 |
rs552070478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749408 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCTCCT | 10517 |
rs552107969 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18748799 | ATGGTGGCCAGCTCT[A/G]GAATTAAACCCACCA | 10517 |
rs552181911 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744047 | AAGGAGGTCTGTACA[A/G]AAAGCCAGACTTCTG | 10517 |
rs552220921 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743160 | CCAGATTCCTCTTCA[A/G]ACAGAAGAGGTTGAG | 10517 |
rs552378785 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776926 | GGAAAGAGATCCACA[A/G]TACATTATCATTTGA | 10517 |
rs552396019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759684 | GTGGCGCCATGTTGG[C/T]TCACTGCAAGCTCCA | 10517 |
rs552400908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774022 | GACTAGATCGGCTAC[A/T]ATTGATTACACTCTA | 10517 |
rs552459509 | snp | C/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775350 | TCTCACTCTAGTTTC[C/G]TATTGTTTTCCAGCA | 10517 |
rs552477680 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766018 | AAGCATGAGCCACTG[A/G]GCCCGGCATTAACTT | 10517 |
rs552514703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772352 | GGGATGGTAACTGCA[A/G]TGCATCTTTCGGTGG | 10517 |
rs552606435 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767577 | GAGAGAACATGGATG[A/G]TCTTGAAAGTGATTG | 10517 |
rs552644224 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750733 | CCTGTGGCATTTGGT[C/G]TTTATTTTTCTCCTC | 10517 |
rs552726618 | snp | A/G | | | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742118 | CGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 10517 |
rs552764013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751600 | TTTGGTTGTCCTCTC[A/G]GGGTTCTTCCTTACT | 10517 |
rs552816076 | snp | C/T | | | | | GRCh38.p7 | 17:18739318 | GCCGATATTGCACCA[C/T]TGCACTCCAGCCTGG | 10517 |
rs553036479 | snp | A/T | 3.57175e-05 | 0.00422581 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744252 | TTAGGATCATGGAAA[A/T]CCTGGAATCAAGGCT | 10517 |
rs553145739 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739851 | GATTGGCCCAATCAC[A/G]GAGCTCTTATCCCCT | 10517 |
rs553184304 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739015 | TCTTGATATGGAAGA[A/G]CAAAGCAGAATTAAG | 10517 |
rs553308443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744818 | GCTTCAGAAATCTGT[A/G]AGGAACTGCAGTTGT | 10517 |
rs553309377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769331 | TGCAAGAGACAAACA[G/T]GATCATCTATATGTT | 10517 |
rs553448656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761390 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10517 |
rs553456119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775066 | TCAGCCCCATTATTA[C/T]TGATTATATTATTTT | 10517 |
rs553485508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760505 | ATGAATTTTGTTGAA[C/T]AAAAATTCTCAATAT | 10517 |
rs553489763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768317 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10517 |
rs553595143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763671 | AGTTGAGAGACCTTG[A/G]GCAAGTGTTCTTGTT | 10517 |
rs553686294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776965 | AAATTAATAAACAAT[A/G]AGCTCATCACAATTC | 10517 |
rs553798905 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750394 | CAGAGCCTTTCCAAC[A/G]CCTCACAAAGCAGAG | 10517 |
rs553835798 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18775872 | TGTCTCTACCAAAAA[A/T]TCAAAAAATTGGCCA | 10517 |
rs553875483 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18741520 | ATCTGGCCCAGCAGC[A/G]GCCGCACCTTCCAAG | 10517 |
rs553942895 | in-del | -/TTTAT | 0.000858553 | 0.0207012 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756433 | ATTTTTTGAAATATC[-/TTTAT]TTTGTTTTATTAATT | 10517 |
rs553984918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747741 | TTTTACAATGGGGGC[A/G]TGCTGAAAAGCTAAC | 10517 |
rs554209229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748368 | GTGAGCCGAGATCAT[G/T]CCACTGCACTCCAGC | 10517 |
rs554387711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18771783 | CCTAGGTACGTGGCA[C/T]TCACTCCAGGAACAG | 10517 |
rs554441890 | snp | C/G | 1.75293e-05 | 0.00296046 | missense, intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18778492 | GATGATGTGGAGAAA[C/G]CACAAAAACAAGGAC | 10517 |
rs554504257 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743387 | TAACAGTAACAATAG[C/T]AGCAACAACTGATCT | 10517 |
rs554625201 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773229 | TGGGCCACCGTGCCC[A/G]GCCTGCAAGAGCTAG | 10517 |
rs554653829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758608 | TATTTAACAGTTTTC[C/T]TAGAAGATACTGACT | 10517 |
rs554688200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765440 | CCAAATCCCGGCTCT[A/G]CCACTCACCACCTGC | 10517 |
rs554763780 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759521 | GTGGCAGTAATTAAC[-/TT]ATTTTCACTGAGATA | 10517 |
rs554791092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760431 | TGAAGCCCAAAGGCC[A/G]TCTGCCAGAGAATAC | 10517 |
rs554860994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750342 | CAGTGCATCTCACAA[A/G]GACAATAGGGATAGA | 10517 |
rs554985610 | snp | A/G | 0.000212772 | 0.0103122 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766889 | GTGGGCTACCTTGGC[A/G]GAAAGGGCACTGGGG | 10517 |
rs555168495 | in-del | -/A | 0.00557542 | 0.0525036 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743776 | TTTAGCATCATTGGG[-/A]TAGCCAGTTTGTAAC | 10517 |
rs555225559 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768382 | CCATCGGCCTTCTTA[A/C/G]AGCAAAAGCAGGATT | 10517 |
rs555606530 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18754869 | CTGAGTCCCAGATAC[C/G]TTATCTGTAAAATAA | 10517 |
rs555747570 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739931 | TAAATATACGTGGCA[C/T]TTATAATGCGCAAGC | 10517 |
rs555837138 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762745 | GGCATCTTCATCTTG[A/T]TCCCCTTCTGGAAGG | 10517 |
rs555875555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753537 | GACTGTCAAGCCACC[C/T]TTCGCCTTTCTCTCC | 10517 |
rs555875588 | snp | A/G | 0 | 0 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761935 | TAGTTGTAAAAGCAT[A/G]TATGTTTCATAATTG | 10517 |
rs555999349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747536 | ACTCCACCCTGGGCA[A/G]TAAGAGCAAAACTCA | 10517 |
rs556079526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770502 | AGAGACGGGGTTTCA[C/T]CATCTTGGCCAGGCT | 10517 |
rs556103426 | snp | C/T | 1.7403e-05 | 0.00294978 | synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778510 | CAAAAACAAGGACAA[C/T]TGGAAACTCCTGGAA | 10517 |
rs556240140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749609 | TCTAGTGGCCTAAGG[G/T]TAGAGTCTGAGGAGG | 10517 |
rs556293584 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772540 | AAGAAGAAAATAGTC[A/T]CATGGAAATTCTCTC | 10517 |
rs556309266 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742229 | CCAAATGGCTTCAAC[A/T]TCCCCCCAAAGTCAG | 10517 |
rs556324591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777229 | ACCACGCCCGGCTAA[C/T]TTTTTTGTATTTTTA | 10517 |
rs556383013 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741079 | CTTTTTAAAATTCAA[A/C]TTCCAACAAGTGTAA | 10517 |
rs556584759 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741613 | AGGTTTTATCGGGAT[C/T]GTGAATAAAACAGGG | 10517 |
rs556668461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765712 | TCATTCCTGAATTCA[C/T]AGAGATCACTTTCAA | 10517 |
rs556798274 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766267 | GGGTCAGGAAGACAA[A/C]ATCTGGGAAAAATGA | 10517 |
rs557032735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758741 | TTCTAATTGATGACT[A/G]CAAATCAGAAAAATT | 10517 |
rs557174791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745276 | TCCAAGGCTGGAGAT[A/G]GCTTAAGGGCCAAAT | 10517 |
rs557211805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752735 | AAAAAAAAGAAAACA[C/T]ATTTCTGGATTTCCT | 10517 |
rs557257349 | snp | A/G | 3.60731e-05 | 0.00424679 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744212 | TGCCGTTGCAAGTGC[A/G]CAGGGCTAAAATGGA | 10517 |
rs557415792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767029 | GAGGCATTCAGAGTC[C/T]GTGGAGGGTAGGGGC | 10517 |
rs557435227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745733 | ATTCTGTATTTCTAA[C/T]AAGTTTCCAGCTAGT | 10517 |
rs557516185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773397 | AGACAGAAGTTGTTA[A/T]AAGCAGAAAAATGAT | 10517 |
rs557613559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761185 | AAATCCCCCTCCTTG[A/G]AAACTGTTTGTTTTG | 10517 |
rs557620413 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769242 | GCCCAGCCAATAATA[A/C]TATTTTAGAAAGAAT | 10517 |
rs557657364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776040 | AAAAAAAAAAGTGGC[C/T]GGGCGCGGTGGCTCA | 10517 |
rs557986433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755000 | GGGCGTGGTGGCTCA[C/T]ACGTGTAATCCCAGC | 10517 |
rs558249402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762610 | TACAGGCATGAGCCA[C/T]CACGCCCGGCCGACA | 10517 |
rs558343615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777904 | GTTGCATTCAAAATA[C/T]GCTCACTTAGAGGCT | 10517 |
rs558353319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764063 | TAGATGCCAGTGGCA[A/C]CTCCTTCCCGGCTTG | 10517 |
rs558373849 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18741696 | AAATACTTGAGAGGT[C/G]GCAGATGTCCTTCGC | 10517 |
rs558393426 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778416 | AGTACTTAATGCATA[C/T]GTACTTAATATTTTT | 10517 |
rs558410570 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749784 | CTGTTTTCTGGAAAA[C/G]GAGACATAACCAAGC | 10517 |
rs558485286 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772125 | ATAAAAAAATAAAAA[A/T]AAAAAATAAAAAAGC | 10517 |
rs558493668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748247 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10517 |
rs558512330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750202 | CGTGTTGAGGCTGAT[A/G]TGACTGTGGACCTTT | 10517 |
rs558541751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764586 | AGTTACACCAAATAG[A/G]TGCTGCAGCTGGGAT | 10517 |
rs558549771 | snp | A/C | 1.66153e-05 | 0.00288225 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758488 | TCTCCTAAGCGGGAG[A/C]TATGACCTAAGTATC | 10517 |
rs558570102 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770902 | TGTGCTTTATATATG[C/T]GTAGACTCAGGGTGC | 10517 |
rs558632727 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742370 | TCTCAGGAGGCAGCC[C/T]GTTGTCATCTTCTCA | 10517 |
rs558810541 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766338 | AATTTTACCTGCCCC[C/T]ACTCAAGCTGTATGC | 10517 |
rs558938003 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773335 | CAACCAATACCCCCA[C/T]CCCCCAAATTCAAAA | 10517 |
rs559007236 | snp | A/G | 2.0304e-05 | 0.00318615 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779053 | AAAGAACGGCCTCGC[A/G]TCTATACAGCCCTTG | 10517 |
rs559008663 | in-del | -/T | 0.000253398 | 0.0112532 | intron-variant, frameshift-variant | FBXW10 | GRCh38.p7 | 17:18749996 | GTTTCTGGGTCCATC[-/T]TTTTTTTTTCCAGGA | 10517 |
rs559151054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759535 | CTTATTTTCACTGAG[A/G]TACTGTATTAAATTG | 10517 |
rs559294952 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765924 | AGTAGAGACGGGGTT[C/T]CACCATGTTGGCTAG | 10517 |
rs559368390 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744406 | TGACATATCACAGAG[A/G]AGGTTTCTAGTTGGC | 10517 |
rs559376021 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773206 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGGGCCAC | 10517 |
rs559499483 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742813 | GAGGTTGCAGTGAGC[C/T]GAGATGCCACCACTG | 10517 |
rs559545909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767108 | GGCTGCATTCTGACT[C/T]AGCATGAGATATGGG | 10517 |
rs559579640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752128 | CAGAGAGAGCATCTA[A/G]CTCATATGACCTGTA | 10517 |
rs559661927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774720 | GAATCACGTGAACCC[A/C]GGAGGTGGAGGTTGC | 10517 |
rs559680478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766590 | CGGGAAGTCCTTCTA[C/G]AATCTGACTTGATGG | 10517 |
rs559742325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752870 | AGGCATTCATTTGAA[C/T]GTGGACCTGTTTTTG | 10517 |
rs559849336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768109 | CTCACTCTGTCACCA[C/G]GCTGGAGCACAGCAG | 10517 |
rs560003293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745378 | CTCCCCCAGAACTTC[A/G]GACTCAGCAGGTCTG | 10517 |
rs560040047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762097 | CCTCCCGAGTAGCTG[C/G]GACTACAGGCGCCCA | 10517 |
rs560226885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775630 | GGCTGGTTTCAGAGA[G/T]AATTTTAAGAGACTT | 10517 |
rs560290820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776640 | AAACTAGAAAGATAT[C/T]GCCAAGGTTGTCCTG | 10517 |
rs560545599 | in-del | -/TTTTTC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761952 | ATGTTTCATAATTGG[-/TTTTTC]TTTTTCTTTTTCTTT | 10517 |
rs560579997 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740246 | TCCATTCCAGGGGCC[A/G]CCACTCCAGCCCCAG | 10517 |
rs560619643 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770631 | ATTCATCCTAGGTGT[C/T]TGTGGGAATTGCAGT | 10517 |
rs560629578 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764237 | AGACAGAGTCTCGCT[C/G]TATTGGCAGGCTGGA | 10517 |
rs560629629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756354 | GGGTAAAGGACACTT[G/T]CCCTTTCTAAATTTT | 10517 |
rs560637686 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769511 | GCCGGGCATGGTGGC[A/G]CACGCCTGTAATCCC | 10517 |
rs560771896 | snp | A/G | 0.00120239 | 0.0244898 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749839 | TGGTTGACCTGGATG[A/G]CATCAGAGACCTGTC | 10517 |
rs560873788 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770119 | GGTCAGAACTGTGAG[C/T]GATTCTGTTGGATTT | 10517 |
rs560900878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759039 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 10517 |
rs560989409 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757134 | CATAAAAATATATGT[A/G]TATACACACACACAT | 10517 |
rs561024916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749019 | CAAATTTCAAAAGTA[C/T]GTAGAACAGTATGAT | 10517 |
rs561032149 | snp | A/G | 4.15412e-05 | 0.00455729 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779107 | TTCGTGCTGTTGACC[A/G]TGAAGGAGGAGAAGG | 10517 |
rs561038138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765857 | TCAGCCTCCCGAGTA[A/G]CTGGGACTACAGTCG | 10517 |
rs561038454 | snp | C/G | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 17:18741725 | GCATCCTATAGCCTT[C/G]CTCGGAGAAGTGCTC | 10517 |
rs561072436 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774830 | AACAAAAAACCAATA[A/G]TGTATTGTATATTTC | 10517 |
rs561075774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764945 | GTTTTGCTCATTTCT[A/G]TAGGCAGGCAGTCAT | 10517 |
rs561103604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771489 | CTTTGTCTATGGAGC[A/G]TTAAAGTGGGGATCA | 10517 |
rs561143642 | snp | C/T | 0.000231696 | 0.0107608 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778623 | GCACGCCCATAATTC[C/T]GGGGAATTTGCCTAT | 10517 |
rs561372191 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743691 | TGTGAAGCAGTTAAA[A/T]AACTTAAATTTACAT | 10517 |
rs561399042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751205 | TTCTGTGTTGCTACT[A/G]ACTTACAAGACACTT | 10517 |
rs561495245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773697 | CTACAAATAGTCAGC[C/T]ATCTCTTGAGAGGAG | 10517 |
rs561602850 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742991 | GTTAATTACGAAAAA[A/T]AAAAAAGAGCTACTT | 10517 |
rs561816690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752194 | CGTGTGGGCAGTAGC[A/G]GACGGTGTGGCTGTC | 10517 |
rs561817076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760675 | GGGCATGGTGGCACA[C/T]GCCTGTAATCTCAGC | 10517 |
rs561923805 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776514 | TTTTATGAGGGCTGC[A/G]CTAACAATGGGCATC | 10517 |
rs562009288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767884 | TCCAAGAAGGTAGTG[C/T]CTGTCCCAAACACAG | 10517 |
rs562016390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745438 | CTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 10517 |
rs562045732 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751386 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 10517 |
rs562094513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755094 | GTGGTGAAACTCCGT[C/T]GCTGCTAAAAATACA | 10517 |
rs562104161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768863 | TTCTCTGTCTGACTG[C/T]TAACCTCTTCTACTC | 10517 |
rs562139212 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774520 | AATGTATAGCCGGGC[A/G]CAGTGACTCATGCCT | 10517 |
rs562179110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752976 | CCAACAGAAGGACTA[C/G]CCAGCCAGTGTTTGA | 10517 |
rs562230495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18776276 | TGCAGTGAGCTGAGA[C/T]CGTGCCACTGCAACT | 10517 |
rs562268406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775797 | CTTTGGGAGACCAAG[G/T]TGGGAGGATTCCTTA | 10517 |
rs562419546 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747822 | ACAGACATAACTGCT[C/T]TGGTCCATTCTGTAC | 10517 |
rs562455960 | snp | A/T | 0.000128927 | 0.00802787 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756157 | TTCTCTCTGACACGT[A/T]GGTACTGGGGTCAGA | 10517 |
rs562456338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747387 | CCAACATGGCGAAAC[C/T]CCATCTCTACTAAAA | 10517 |
rs562474239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761548 | GGGATTACAGGCATG[A/G]GCCACCGCGCCCGGC | 10517 |
rs562542706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778066 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 10517 |
rs562592386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762208 | ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 10517 |
rs562619424 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740480 | GCCATCCCTGCCTTG[C/T]TGGAATGTGCCTAGT | 10517 |
rs562633121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769410 | GGCCCTGTGACCTAA[C/T]TGCGGGGAAAGTAGC | 10517 |
rs562661643 | snp | C/G | | | intron-variant, missense, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775433 | TTCTCCCAAGAGTGA[C/G]TGGTTTTCCTTAATT | 10517 |
rs562682608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777658 | ATGCCATTCTCCTGC[A/C]TCAGCCTCCCGAGTA | 10517 |
rs562707968 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776951 | ATTTGAAAAAAGACA[A/C]ATTAATAAACAATGA | 10517 |
rs562741438 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740873 | TCTCACCATTCTCCT[G/T]CCTCAGCCTCCCGAG | 10517 |
rs562742170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770161 | TCCTCCCCTGGGATA[C/T]CAGCCCTGGATTTGC | 10517 |
rs562864917 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770799 | ATAGGAGAGTGGAGG[C/G]TGGCAGCAGCAGGGG | 10517 |
rs563028491 | snp | A/C/T | 0.00112507 | 0.0236914 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764771 | AAAGTGGGGTTTGCA[A/C/T]ACGAATCTTCGGTGG | 10517 |
rs563168954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757442 | CTATACATCCCTGTT[A/T]ATTGGAACAATCCCT | 10517 |
rs563176232 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742636 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 10517 |
rs563226722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764281 | ATCTCAGCTCGCTGC[A/G]ACCTCTGCCTGCCGG | 10517 |
rs563247337 | snp | C/T | 0.000170692 | 0.00923672 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778704 | ATACCCAAGGAAGGT[C/T]TTGAATTTCAAAGGA | 10517 |
rs563294580 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18775798 | TTTGGGAGACCAAGT[G/T]GGGAGGATTCCTTAA | 10517 |
rs563349636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750365 | GGGATAGAGACCGCT[C/G]AGGAGCAGAGAGACA | 10517 |
rs563375741 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741822 | ACTGGCGCCATGTCC[C/T]CGCATTGGCCTATCC | 10517 |
rs563388788 | snp | A/G | 0.0011603 | 0.0240584 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749912 | CATCCACCTCTCCAA[A/G]TACATTCTAAGTATG | 10517 |
rs563438377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772824 | GATATAAATCCTAAC[C/G]CTCCAGGAAGGTAGG | 10517 |
rs563475584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772244 | CTGCTGCATCTCCTG[A/G]TAACTTTCACCACTC | 10517 |
rs563613935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW10, TVP23B | GRCh38.p7 | 17:18779481 | CAGAAGGAGGTTGGG[C/T]GAGATTAGCATCTGT | 10517 |
rs563622713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759647 | AGATGGAGTCTCACT[A/G]TGTCACCCAGGCTGG | 10517 |
rs563655471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759980 | TGGATGTGTCCCCTG[A/G]TGCCCATGTGCACGA | 10517 |
rs563658871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766560 | GTGAGCCTGCTCTGC[A/G]GAGGTGCTAGGCCAC | 10517 |
rs563833346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759102 | GTGAACCTGGGAGGT[A/G]GAGCTTGCAGTGAGC | 10517 |
rs563837621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774639 | TCTCTACTAAAAATA[C/G]AAAAAAATTAGCCGG | 10517 |
rs564016743 | snp | C/T | 6.59131e-05 | 0.0057404 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772577 | TAATATTCAGGTTCA[C/T]AGCCCAAGAGAGTCT | 10517 |
rs564207111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767344 | AATTAGCCGGGCATG[A/G]TGGTGGGCGCTTGTA | 10517 |
rs564207913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753144 | GCCAGAAAGAACAGA[C/G]AGTAAAACACAGATA | 10517 |
rs564244983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760867 | CTGTGATTCTTCCCT[C/T]TTCTAGGTCATAGAG | 10517 |
rs564260933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753608 | CCAGGCGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 10517 |
rs564396088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761481 | TGTGCTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 10517 |
rs564515224 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740139 | CCTAGGGTGCTGCTG[C/T]GTTTTCGCAGGCCAT | 10517 |
rs564553540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747117 | ATTTCTAATAGAGAC[A/G]GGGTTTCACCGTGTT | 10517 |
rs564583174 | snp | A/G | 3.34437e-05 | 0.0040891 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748005 | CAGCTCCAAGTCTGC[A/G]ACCTCACAAGTCTAT | 10517 |
rs564806816 | snp | A/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 17:18741126 | GGCGAGAGATGAGAT[A/G]TCACACTTTTTCCAC | 10517 |
rs564843445 | snp | C/T | 0.0581099 | 0.160244 | | | GRCh38.p7 | 17:18740909 | GGGACTACAGGCACC[C/T]ACCACCACGCCCAGC | 10517 |
rs564843453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748825 | CACCAATGGCTATTT[C/T]TGCAGTATTGGATTC | 10517 |
rs564963221 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768796 | GTTCTCTGCACCTCA[-/C]CCCTCTCTGCTTCCC | 10517 |
rs564977321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756297 | CTTGCACATGATCCC[A/G]TGTAGACAATACCTG | 10517 |
rs565011836 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763096 | CATATCCAAAAAACT[A/T]CAAAGACATATTAAT | 10517 |
rs565069560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770836 | TGGGGGAAAGCTGAG[A/C]TGGTGAGCTTACAAA | 10517 |
rs565261803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765777 | CTGTGGCCAGGTTAG[A/G]GTGCAGTGGCACAAT | 10517 |
rs565382287 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750422 | GAGAACCCCCAGCCC[C/G]CAGGGAGTTATATTG | 10517 |
rs565557139 | snp | A/G | 0.000399281 | 0.0141238 | splice-acceptor-variant, missense | FBXW10 | GRCh38.p7 | 17:18750009 | ATCTTTTTTTTTCCA[A/G]GAATGCTGGATAGAC | 10517 |
rs565648885 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772353 | GGATGGTAACTGCAG[G/T]GCATCTTTCGGTGGC | 10517 |
rs565650775 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765308 | CCCATTGGTAATTTT[A/G]TAAATGGGCCAAGAT | 10517 |
rs565784384 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761545 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 10517 |
rs565821598 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744063 | AAAGCCAGACTTCTG[C/T]TGGCAGTTACTGAGA | 10517 |
rs565835035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759238 | CATTACTCAGGCCAA[A/G]AAATAAGATACCACC | 10517 |
rs565858823 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743256 | CCATTGCCAACAAAA[C/T]CCCAGCGATGGACTC | 10517 |
rs566000799 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758540 | CATGATCCCTGTCCC[A/G]CCTAGGGCCTAGAGG | 10517 |
rs566188926 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751432 | AGGCGGGGTTTCACC[A/G]TGTTAGCCCAGATGG | 10517 |
rs566266027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760408 | CCCAGGAGAGCCAAC[A/G]GTGCAGATGAAGCCC | 10517 |
rs566306292 | snp | A/G | 0.000114325 | 0.00755972 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744858 | AGGTAGACAGAGATT[A/G]CACAGAACTCAGCAT | 10517 |
rs566422723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753195 | GAAGTGGGGGGACAG[C/T]CTCTTGGGTAACTAC | 10517 |
rs566653935 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745121 | AGAGGGTTGTAAAGG[A/G]GAAGCTTTTGTTTTT | 10517 |
rs566718611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769522 | TGGCGCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 10517 |
rs566720105 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:18739359 | AAGACTCCGTCTCAA[A/G]AAAAAAAAAAAGAGT | 10517 |
rs566758958 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18738386 | TTATTGAATCCCTGC[A/G]GGTTGTTGGTGCTTG | 10517 |
rs566783729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745657 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 10517 |
rs566875496 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769080 | AGCTGGGACTACAGG[C/T]GCCCACCACCACACC | 10517 |
rs567006874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747522 | GACCGAGCCATTGCA[C/T]TCCACCCTGGGCAAT | 10517 |
rs567034852 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740692 | AAGTAGTGACCCTGA[A/T]GATCACCTGAAAGAA | 10517 |
rs567079709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754838 | GTCACGACTTGATAA[A/G]ATTGATTTCCTTTCC | 10517 |
rs567087323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764502 | ACTGTGCCTGACCAA[C/T]GACTCTTATTATTAT | 10517 |
rs567099034 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740984 | GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCATG | 10517 |
rs567124615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763719 | TCTTTGCTCCCATCT[A/G]TCTCTTAGATATGCT | 10517 |
rs567161168 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755533 | TACACTCCAGCCTGG[C/T]GACAGAGCGAGACTC | 10517 |
rs567196476 | in-del | -/C | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 17:18741251 | CCATGGTCTCTACTT[-/C]ATGGAAGAGGAGCAG | 10517 |
rs567198390 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762462 | AGCTGGGACTACAGG[A/C]ATGTGCCACCACGCC | 10517 |
rs567236221 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740974 | CACCGTGTTAGCCAG[G/T]ATGGTCTCGATCTCC | 10517 |
rs567273021 | snp | A/T | 1.69605e-05 | 0.00291204 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748156 | TAGGTGCGGTGGCTC[A/T]TGCCTGTAATCCCAG | 10517 |
rs567354095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770918 | GTAGACTCAGGGTGC[A/T]ATTATATGAAAATAA | 10517 |
rs567410950 | snp | A/G | 5.27565e-05 | 0.00513571 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758421 | TACCCGTTGAATTCC[A/G]AGGCCATGCTGGGAG | 10517 |
rs567492186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778167 | CTGAGGCAGGAGAAC[A/G]GCGTGAACCCGGAAG | 10517 |
rs567595049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770464 | CCCACCAGTATGCCC[A/G]GCTAATTTTTAGTAT | 10517 |
rs567614733 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18762063 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTTCCT | 10517 |
rs567739741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749510 | CGAGATCGCGCCACT[A/G]CACTCCAACCTGGGC | 10517 |
rs567878675 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742124 | CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 10517 |
rs567973545 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18763807 | GTTTGCAGATCCACT[C/G]TACCGTGGAATCAGT | 10517 |
rs568090172 | in-del | -/AGAA | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775705 | ATAAAGAGATAAGGG[-/AGAA]AGAGAGATGGGGATG | 10517 |
rs568114049 | snp | C/T | 3.58339e-05 | 0.00423269 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744194 | TCTAGTGTTTGGTGG[C/T]GTTGCCGTTGCAAGT | 10517 |
rs568142347 | snp | A/G | | | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744965 | TCTTGAAAATGATCA[A/G]TGCAGGAGGAAGTAC | 10517 |
rs568146214 | in-del | -/C | 0.0043611 | 0.0464922 | intron-variant, nc-transcript-variant, frameshift-variant | FBXW10 | GRCh38.p7 | 17:18744781 | GCAGAGACTAGAGGG[-/C]CCCCGAAGACCAGAA | 10517 |
rs568192302 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755820 | GGCACATGGAAAATC[-/AA]AGAGATGAAAGAAGA | 10517 |
rs568227517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772056 | AGGTTGCAGTGAGCT[A/G]AGATCATGCCACTGC | 10517 |
rs568320340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760450 | GCCAGAGAATACCCT[C/T]TTGCCAGGACTATCT | 10517 |
rs568394726 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750961 | GGAATTGATCCTAAT[C/T]ATGCCAATAAGGTTT | 10517 |
rs568555990 | snp | C/G/T | 8.26145e-05 | 0.0064266 | missense, synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744457 | CTTATATTTGTTACA[C/G/T]TATTTCCAAAATATC | 10517 |
rs568575965 | in-del | -/TACT | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743365 | TATCTAGGGTAATAA[-/TACT]TAGTAACAGTAACAA | 10517 |
rs568604183 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754426 | AGATTAAGAAGGAGA[G/T]GGAGCAGAGGAAAGA | 10517 |
rs568641099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768217 | GGATTACAGGTGTGT[C/G]CCACCATGCCCAGCT | 10517 |
rs568642666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753273 | ATGAGCACATTCCTT[G/T]CCATTCAAGTGCACT | 10517 |
rs568699018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767490 | TGAGGGGATGAACAA[A/T]GCATTTTTTCCTAAG | 10517 |
rs568713530 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18738532 | TTTATTTTTAAAAAA[A/G]TCGAGATGCCTGTCT | 10517 |
rs568773331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774824 | CAAATAAACAAAAAA[A/C]CAATAATGTATTGTA | 10517 |
rs568823594 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773461 | ATAATGTTTGTAGCT[A/G]GAAAATCTTACGTAT | 10517 |
rs568936552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769138 | GATGGGGTTTCACGG[C/T]GTTAGCCAGGATGGT | 10517 |
rs568954590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18752188 | ACGGGTCGTGTGGGC[A/G]GTAGCGGACGGTGTG | 10517 |
rs569124218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763444 | TACAGGTGTGAGCCA[C/T]CGTGCCCGGCTGTTA | 10517 |
rs569150011 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739444 | TTTCTTGGTCTAAAA[A/G]CTGAAAAATGACTAA | 10517 |
rs569196810 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775455 | TCCTTAATTGTCCCT[C/T]TTCTGACTTGAGGCC | 10517 |
rs569237832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762573 | ATGATCTGCCCACCT[C/T]GGCCTACCAAAGTGC | 10517 |
rs569428045 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18756752 | TGCTGAGAGACGAAG[G/T]TCCTTTAATAAGCAA | 10517 |
rs569565112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748230 | CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 10517 |
rs569601943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747615 | TTTTGACTCGAGGGT[A/G]GTTATTTCTATCATT | 10517 |
rs569643010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771007 | CCCTAAACCATATTG[C/T]CTTCCTTTTAGTGAA | 10517 |
rs569667556 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741298 | GAATTATTCAGGCAT[A/G]TGAAGCTGCTCCGTG | 10517 |
rs569678702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778361 | TGGCATACCTGTTGG[A/G]CAACAAAGACCTCAA | 10517 |
rs569814844 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777822 | TGTGGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 10517 |
rs569844204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750187 | GACCAGCTTCATTTT[C/T]GTGTTGAGGCTGATA | 10517 |
rs569849615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765195 | CATAAATATATAGTG[A/G]GGAATATAATAAGTC | 10517 |
rs569928091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757797 | TTTTATGGGACAATA[A/C]GCTCATTGTAAGTAA | 10517 |
rs570001125 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18771643 | GAAGAGGCCTCCCCA[G/T]TAGAGAGCTTTCCTC | 10517 |
rs570385440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760306 | CAATGTGTATATACA[C/T]AGGAGATTTACTATA | 10517 |
rs570422359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751524 | CGTGAGCCACCGCGC[C/T]CAGCCCGACACTTCC | 10517 |
rs570449348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759861 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCTAA | 10517 |
rs570460208 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18753041 | TTGACAGAATTGTAC[G/T]GTCATCTTGGACAAA | 10517 |
rs570622688 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18757680 | GTCCCCTTTCACAAT[-/A]AAAAACTCTCAGTTT | 10517 |
rs570833192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768293 | GGATGGTCTCAATCT[C/T]CTGACCTTGTGATCC | 10517 |
rs570869439 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774938 | TTATCTTGATCTGAT[A/C]ATTACACATTTTATG | 10517 |
rs570955421 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740583 | CCAAGTACTGGAAAA[C/G]GAGGGAGAACAGATC | 10517 |
rs570981251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754718 | GGAATGCCAGAAGGT[C/G]TGTGATAGAGGAAGC | 10517 |
rs570992488 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739732 | TTATTCTTGTCTCAA[C/T]TTTTTGAAATCTGAG | 10517 |
rs571031178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746847 | TCTTCCAAAACTTCA[C/T]CCCATTCACCATAGG | 10517 |
rs571051772 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753325 | ACTCGGGGGTATGCC[A/T]GCAGCTGCAGAAAGA | 10517 |
rs571078217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770364 | GCTGGAGTGCAGTGA[G/T]GTGATCTCGGCTCAC | 10517 |
rs571089556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761297 | TTAAGACGGAGTCTC[A/G]CTCTCTCGCCCAGGC | 10517 |
rs571116933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769717 | GGTAGGTGGGGGTTG[C/T]AGTGAGCCAAGATCG | 10517 |
rs571119522 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761561 | TGAGCCACCGCGCCC[A/G]GCCTCACTTTTCTTT | 10517 |
rs571273985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755323 | GCACTTTGGGAAGCC[A/G]AGGCAGGCAGATCAC | 10517 |
rs571360474 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777726 | TTTTTTGTATTTTTA[A/G/T]TAGAGACGGGGTTTC | 10517 |
rs571444422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763475 | AGTACAATTATTATT[C/T]TCAGTTTACAGATGA | 10517 |
rs571577913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748277 | ACAAAAAAATTAGCC[A/G]GGCGCAGTGGCAGGC | 10517 |
rs571795031 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778417 | GTACTTAATGCATAC[A/G]TACTTAATATTTTTC | 10517 |
rs571868490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749416 | GCCGGGCGTGGTGGC[A/G]GGCTCCTGTAGTCCC | 10517 |
rs571871313 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742392 | ATCTTCTCAAAGAAG[C/T]TGTTTAGAAAAGGAG | 10517 |
rs572008814 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18741701 | CTTGAGAGGTCGCAG[A/T]TGTCCTTCGCATCCT | 10517 |
rs572080408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764655 | ATCTGCTGCCTCCCA[A/G]CTAACTACTTATCTA | 10517 |
rs572087913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765814 | TCACTGCAACCTCTG[A/C]CTCCCGGGTTCAAGT | 10517 |
rs572210815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764107 | TATCTCCAGATATTT[C/T]CAAATGGCCTATGGG | 10517 |
rs572216942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771067 | GAGGGCAGCCTGGTA[A/G]TAAGGCTCAATTAAT | 10517 |
rs572270058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759901 | ATTACAGGTGTGAGC[C/T]ACCGCGCCGGGCCCT | 10517 |
rs572287138 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749795 | AAAAGGAGACATAAC[C/T]AAGCCAGGGTACGAT | 10517 |
rs572301799 | in-del | -/CTTC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768031 | TTCCTTCCTTTCTTC[-/CTTC]CTTCCTTCCTTCCTT | 10517 |
rs572302093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750203 | GTGTTGAGGCTGATA[C/T]GACTGTGGACCTTTC | 10517 |
rs572309511 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779264 | AGCAAGGGAAAACAG[C/T]GGCCCCTGAACTTGG | 10517 |
rs572403066 | snp | A/C/T | 6.21077e-05 | 0.00557231 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779094 | AGTGAACACTGAGTT[A/C/T]GTGCTGTTGACCGTG | 10517 |
rs572448055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766378 | TATGAAATCTACTCG[A/C]TAGCAAGCATTTTTC | 10517 |
rs572513399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751164 | AGAGGATCACGGCAG[G/T]TGACACTCCTTAAGG | 10517 |
rs572878431 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743627 | TCTGTGAGCTGCCCA[A/G]TATGTTTTGCCTGGG | 10517 |
rs572883925 | snp | C/T | 0.000527174 | 0.0162268 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744304 | TTGTGAGAAGGGAAC[C/T]GATTCCATCCCTCTA | 10517 |
rs572921307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751669 | GTCATTTAGTGGCAA[A/G]TTCAGAGGCCAGGAG | 10517 |
rs573010066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773630 | TTGGCATGTGAAATT[A/G]GATCCACAGATCTAT | 10517 |
rs573154445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753447 | TGAATCCTTAAAGAC[C/T]CTTAGTCTGTAAGAG | 10517 |
rs573282645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762107 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 10517 |
rs573413481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18760531 | AATATGGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 10517 |
rs573417583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768355 | ACAGGCATGAGCCAC[C/T]GCACCCGGCCTCCAT | 10517 |
rs573466042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756747 | CAATATGCTGAGAGA[C/T]GAAGTTCCTTTAATA | 10517 |
rs573507761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18745945 | AAAGAGTTTTATTTG[G/T]CTCACAGTTCTGAAG | 10517 |
rs573539157 | in-del | -/AG | 0.00593379 | 0.054145 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744535 | CAACCTCAGCAAGAA[-/AG]AGGGGAAAGTTGTGA | 10517 |
rs573577739 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765684 | AGCACCTTTGAAGGA[A/G]ACTTTAATGTTTTCA | 10517 |
rs573594899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769335 | AGAGACAAACATGAT[C/T]ATCTATATGTTAGAT | 10517 |
rs573945690 | snp | A/G | 0.000122471 | 0.00782435 | synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778494 | TGATGTGGAGAAAGC[A/G]CAAAAACAAGGACAA | 10517 |
rs573967966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777993 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 10517 |
rs574078152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748648 | ATGGCCCCCAAACCC[A/G]TATTTGCACCTCTCC | 10517 |
rs574107244 | snp | A/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 17:18740860 | CCACCTCCCGGGTTC[A/T]CACCATTCTCCTGCC | 10517 |
rs574165270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771190 | TCGGCTTGAGTGAAC[A/G]TAAGTCTAAAAGGGA | 10517 |
rs574226976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770720 | GCTCTTTGATCATGC[C/T]TTTGGCTGCCTGAGA | 10517 |
rs574377467 | snp | C/T | 3.29815e-05 | 0.00406075 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749858 | CAGAGACCTGTCTTC[C/T]GGGTTCAGCAAATAC | 10517 |
rs574427490 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773993 | TCCATACAAAGGCTA[A/C]CATACAGATGTAAGA | 10517 |
rs574453122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750347 | CATCTCACAAGGACA[A/G]TAGGGATAGAGACCG | 10517 |
rs574470468 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759634 | GTTTTTTTTTTTGAG[A/G]TGGAGTCTCACTGTG | 10517 |
rs574491263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758611 | TTAACAGTTTTCCTA[A/G]AAGATACTGACTTCT | 10517 |
rs574628183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758018 | GGGCAATGCCACATA[C/T]TCCATTCTCTCTCTT | 10517 |
rs574667905 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743430 | GCAATCCTAGAAGGT[A/G]GTTATCATTTTTATT | 10517 |
rs574673503 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742532 | GACTCCCAAGTTTGT[A/G]GCCCTGAAATGTGAA | 10517 |
rs574696922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751791 | AATGCCTAGGGCCTA[G/T]ACGAATTCGGCTCCC | 10517 |
rs574708526 | snp | C/T | 0.00010552 | 0.00726283 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779141 | ACCAGGAAGCCAAGA[C/T]GAAGGAATATCAGGC | 10517 |
rs574755111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766486 | AGGTCTTCTGGATTG[C/T]GGGCTCCCTCAACCA | 10517 |
rs574790785 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18773944 | AAGATCCTTTAAATA[C/G]ACAAAAACAGAGGTG | 10517 |
rs574791808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772739 | AGAGCAGGTCGGGGT[C/T]TGGTGGGGGTGGTGG | 10517 |
rs574835569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759909 | TGTGAGCCACCGCGC[C/T]GGGCCCTTGTTTCTA | 10517 |
rs574878645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18774481 | AGCGTTTGGTTGCAC[A/G]GTAGGATGACTACAA | 10517 |
rs574904473 | snp | A/G/T | 4.94184e-05 | 0.00497063 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744337 | CCGGAAGTGTGAGAC[A/G/T]TGTGTCTTAGCCTGG | 10517 |
rs574942001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771244 | CATTCCATTCCAGCA[C/G]TTCCAGCCAAAACAA | 10517 |
rs575326988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744984 | AGGAGGAAGTACACA[A/T]CTTTTAACTCACAAG | 10517 |
rs575351091 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771072 | CAGCCTGGTAATAAG[G/T]CTCAATTAATGAACA | 10517 |
rs575367155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761414 | GGGACTACAGGCACC[C/T]GCCACCACGCCTGGC | 10517 |
rs575712739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754946 | AAGGACAAATGAAAG[C/T]TGCAGATGTATGAAA | 10517 |
rs575788868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749612 | AGTGGCCTAAGGTTA[C/G]AGTCTGAGGAGGTTT | 10517 |
rs575803573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18746267 | ACATGAGATTTGGAG[A/G]GGACAAATATCCAAA | 10517 |
rs575840469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18753572 | TCTTTAATTCTTACA[C/T]GTGTAATTTAAGAAA | 10517 |
rs575893123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777244 | TTTTTTTGTATTTTT[A/G]GTACAGACGGGTTTT | 10517 |
rs575919208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18763983 | CTGGGGCTGGGAAAT[C/T]CTTTACTGTGGGGCC | 10517 |
rs575924038 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18739959 | AGCTGCTGTGCTAGA[C/T]GCTAAGAAAGAGTAA | 10517 |
rs575925142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748717 | AGAAAGGAAACTATC[A/C]ATGATTTCCTTTGGA | 10517 |
rs575958345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770537 | TTGAACTCCCGACCT[C/T]GTGATCCACCCGTCA | 10517 |
rs575996487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762891 | AAATACCTTTTCTTG[A/C]ATAAATTTAAAAAAC | 10517 |
rs576010543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18771329 | TTGAAGCAGAAAGAA[A/G]CCTGTGCAGAGTATT | 10517 |
rs576048793 | snp | C/T | 8.37472e-05 | 0.00647044 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778575 | AATCCCTATGTCACC[C/T]GACCAATTCCTCCTG | 10517 |
rs576180375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18754277 | GATGAGCAAGGGCCA[A/G]TGAATTCTCACCTGG | 10517 |
rs576268339 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751244 | TTTTTTTTTTTTAAT[A/G]AGATGGAGTCTCGCT | 10517 |
rs576378190 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18771967 | ACAAAATGAGCTGGG[C/T]GTGGTGGTGCGTACC | 10517 |
rs576529715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758853 | TTTGAGACAGACTAT[A/G]GAGGCAAAATAGTGC | 10517 |
rs576572715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18765725 | CATAGAGATCACTTT[C/T]AACTTCTTCCTTTTT | 10517 |
rs576717539 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764861 | GAGATTGCCAGGTAA[A/G]AGGTGAGAAAGAAGT | 10517 |
rs576950207 | snp | A/G | 0.00678292 | 0.0578399 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772586 | GGTTCACAGCCCAAG[A/G]GAGTCTGTATCCAGT | 10517 |
rs577007298 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751044 | TCCGAAGTGGAAGCT[A/G]AGAACGAAGGTGGGT | 10517 |
rs577007612 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742694 | ACGTGGCAAAACCTC[A/G]TCTCTACTAAAAATA | 10517 |
rs577044735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750368 | ATAGAGACCGCTCAG[A/G]AGCAGAGAGACAGAG | 10517 |
rs577118252 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745371 | CAAGCTCCTCCCCCA[G/T]AACTTCGGACTCAGC | 10517 |
rs577133444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772836 | AACCCTCCAGGAAGG[C/T]AGGAGCCATTCTCTC | 10517 |
rs577143653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751920 | GACCGGAAGACTCTT[C/T]GAGCTCTTTGCTTTG | 10517 |
rs577179836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18759982 | GATGTGTCCCCTGGT[A/G]CCCATGTGCACGAGT | 10517 |
rs577202082 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768557 | TGGCCATGAGGGAGC[C/T]GTGAAATGCCTGTTC | 10517 |
rs577239851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775517 | TCCAGTTTTTGGCTG[A/C]CTGCCTGCCTCTGTT | 10517 |
rs577316735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767617 | GAAACATATTCTTGC[C/T]GGATCTGAACCCCTA | 10517 |
rs577329970 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747116 | TATTTCTAATAGAGA[C/T]GGGGTTTCACCGTGT | 10517 |
rs577340315 | snp | C/T | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 17:18738672 | CCTCATGAATGGCCA[C/T]GAAGACACCATGCTT | 10517 |
rs577378221 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765048 | ATCCATTCAACAGCT[A/G]TCTGTAGAATACCTA | 10517 |
rs577458569 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW10 | GRCh38.p7 | 17:18767036 | TCAGAGTCTGTGGAG[G/T]GTAGGGGCTCCACCA | 10517 |
rs577561014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769301 | TATTGTATAAGTAAA[C/T]GCTAGGAATCAAATT | 10517 |
rs577736643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18762622 | CCACCACGCCCGGCC[A/G]ACAATATATTATCTT | 10517 |
rs577740020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18755018 | GTGTAATCCCAGCAC[C/T]TTGGGAGGCTGAGGC | 10517 |
rs577907105 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW10 | GRCh38.p7 | 17:18761501 | CGATCTCCTGACCTC[A/G]TGATTCGCCCGCCTC | 10517 |
rs578122287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18777913 | AAAATATGCTCACTT[A/C]GAGGCTAATATACTC | 10517 |
rs578143029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747687 | GCAATTCCTGACCTC[C/G]ACTCTCTCTCTCTCT | 10517 |
rs578144393 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:18740187 | TGTCTTGTGTCCTTG[A/G]GTGACCTAGTCCCTG | 10517 |
rs578202191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770566 | CACGGCCTTCCAAAG[C/T]GCTGGGATTACAGGT | 10517 |
rs745380596 | in-del | -/AAAAGAAGAATAAGGAGAAAGAGGAGGA | 1.64754e-05 | 0.00287009 | frameshift-variant, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772495 | TGGAAAAAACGAAAC[-/AAAAGAAGAATAAGGAGAAAGAGGAGGA]AAAAGAAGAAAATAG | 10517 |
rs745390011 | in-del | -/A | 4.55187e-05 | 0.00477046 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779238 | GGCCTGCCTATTGAT[-/A]AATTTCACGAAGCAA | 10517 |
rs745522658 | snp | C/G | 6.76979e-05 | 0.00581759 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750038 | ACACACCCTGAACAA[C/G]TGCGCCTCTGTGAGC | 10517 |
rs745535174 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744341 | AAGTGTGAGACGTGT[A/G]TCTTAGCCTGGAAGA | 10517 |
rs745650756 | snp | A/G | 3.38742e-05 | 0.00411533 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778669 | ACAGAAATTACTGAT[A/G]TCTGGGGACCTTCAA | 10517 |
rs745713216 | snp | G/T | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744560 | GTTGTGAAGTCCTCC[G/T]TGAACCAAATGTTGG | 10517 |
rs745763424 | in-del | -/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770255 | TGGTGGGGACTAACA[-/G]GGCTTTGCACAAAAC | 10517 |
rs745827822 | snp | A/G | 1.80843e-05 | 0.00300696 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756151 | TTCGCATTCTCTCTG[A/G]CACGTAGGTACTGGG | 10517 |
rs745852663 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766483 | CCAAGGTCTTCTGGA[C/T]TGTGGGCTCCCTCAA | 10517 |
rs745856269 | snp | A/G | 4.57247e-05 | 0.00478124 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779239 | GGCCTGCCTATTGAT[A/G]ATTTCACGAAGCAAG | 10517 |
rs745906947 | snp | C/T | 0.000125494 | 0.00792031 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758330 | AACCGAGTCATCCAC[C/T]ATTCCGGGGGAGATC | 10517 |
rs745917852 | snp | C/G | 4.96767e-05 | 0.00498356 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749672 | TGTTCTTGGCCTGGA[C/G]TTTCTACAGAGCCAA | 10517 |
rs745979010 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18758130 | GTCATCGTGTGAGAG[C/T]GGGGATCCCTCAAGG | 10517 |
rs746021756 | snp | C/T | 1.68493e-05 | 0.00290248 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775086 | TATATTATTTTATGC[C/T]CTAATCGAAGTATAT | 10517 |
rs746109912 | snp | A/C | 1.66125e-05 | 0.00288201 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775201 | AGAGATGGTAAGAAG[A/C]GAGTTTATTCTGTTC | 10517 |
rs746209573 | snp | A/G | 9.14838e-05 | 0.00676266 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750136 | AGATTACCTTCTTGC[A/G]GGTACTTCCTGCAAG | 10517 |
rs746212338 | snp | C/G | 1.745e-05 | 0.00295376 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766819 | GCAGCTGTGAGCGAG[C/G]GCTGGTGAAAGTGTG | 10517 |
rs746212661 | snp | C/T | | | | | GRCh38.p7 | 17:18741946 | GCAGTGGCACATCTC[C/T]GCTCACTGCAAGCTC | 10517 |
rs746288637 | snp | A/G | 4.94507e-05 | 0.00497221 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750946 | GGGTCCTACACAAGA[A/G]GAATTGATCCTAATT | 10517 |
rs746315631 | snp | C/T | 3.35655e-05 | 0.00409654 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778816 | ATCCAGAAACTGCAG[C/T]CCAACTTGAAGATCT | 10517 |
rs746362158 | snp | A/G | 2.04255e-05 | 0.00319567 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744736 | GTTTCTGAGAGAGGA[A/G]AACAATATCTCAGGT | 10517 |
rs746485337 | snp | C/T | 3.37878e-05 | 0.00411008 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766667 | AACCTTTCCTTTTCC[C/T]CCTTTTTCCCCACTC | 10517 |
rs746487298 | snp | C/T | 1.69456e-05 | 0.00291075 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750044 | CCTGAACAAGTGCGC[C/T]TCTGTGAGCCAGCAC | 10517 |
rs746488842 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770267 | ACAGGGCTTTGCACA[A/G]AACTTAGTAATCAGG | 10517 |
rs746575161 | snp | C/T | 1.77599e-05 | 0.00297987 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750104 | GGACTTGTCAGCGCA[C/T]GGCTTCATTCAGAAC | 10517 |
rs746610802 | snp | C/T | 3.41606e-05 | 0.00413269 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778692 | ACCTTCAATTTCATA[C/T]CCAAGGAAGGTCTTG | 10517 |
rs746699036 | snp | A/G | 1.69298e-05 | 0.0029094 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778786 | GATGTGAAACGAACC[A/G]GTATTCCCCTTGAAA | 10517 |
rs746782375 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746262 | TTTCAACATGAGATT[G/T]GGAGGGGACAAATAT | 10517 |
rs746786440 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769963 | TCTCTTCCTCCGGGT[A/C]ATCAGCGCCTGTGCA | 10517 |
rs746890436 | snp | A/G | 5.01995e-05 | 0.00500972 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758339 | ATCCACTATTCCGGG[A/G]GAGATCTGATAGCTG | 10517 |
rs746970458 | snp | C/G/T | 4.94224e-05 | 0.00497083 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749756 | ACTCCGGTGTATATC[C/G/T]GAAATGAATAGGCTG | 10517 |
rs747046811 | snp | A/T | 1.66147e-05 | 0.0028822 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775208 | GTAAGAAGAGAGTTT[A/T]TTCTGTTCATAAGGG | 10517 |
rs747087169 | in-del | -/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767443 | CGAGATCATGCGTCT[-/C]AAAAAAAAAAAAAAA | 10517 |
rs747124829 | snp | C/T | 1.79364e-05 | 0.00299464 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744237 | AATGGACTGGTTATC[C/T]TAGGATCATGGAAAA | 10517 |
rs747150776 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773864 | GTGCAAAGTTTGAGG[A/G]CAGCATCCAGGGACA | 10517 |
rs747162478 | in-del | -/CCAGAACGAGGAAACGCAGCAGGTCCTGT | 1.67567e-05 | 0.00289449 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756070 | CCTGTGGACTGCATA[lengthTooLong]CCAGAACGAGGAAAC | 10517 |
rs747191444 | snp | A/C/G | 7.14699e-05 | 0.0059775 | missense, intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18778480 | TTTGAAAAAGCAGAT[A/C/G]ATGTGGAGAAAGCAC | 10517 |
rs747256397 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750955 | ACAAGAGGAATTGAT[C/T]CTAATTATGCCAATA | 10517 |
rs747327285 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18764682 | TCTACATGGGTTCTA[C/T]GCAGTATGATCCTCT | 10517 |
rs747346107 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751036 | GTGAAACATCCGAAG[C/T]GGAAGCTGAGAACGA | 10517 |
rs747464074 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770079 | CCTTCTTTATTCAGG[A/G]CAACAGGTGGGTGGT | 10517 |
rs747526788 | snp | C/T | 1.66172e-05 | 0.00288242 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748020 | GACCTCACAAGTCTA[C/T]TGGACAGCCAAAACT | 10517 |
rs747551952 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18772454 | TCTCATGTTCCAGTT[G/T]GAGCACATAAAGTGG | 10517 |
rs747613611 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744609 | AGATGAAAGAGATCT[C/T]GTACTGGTTTGCGAA | 10517 |
rs747650857 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750927 | ATTTTTTGTCTTTTT[C/T]CAGGGGTCCTACACA | 10517 |
rs747684182 | snp | G/T | 7.24205e-05 | 0.00601706 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778928 | GAGACCAAGTGACCA[G/T]TTCAATTGAAAGGGC | 10517 |
rs747690582 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765438 | GTCCAAATCCCGGCT[C/T]TGCCACTCACCACCT | 10517 |
rs747702974 | snp | A/G/T | 3.46268e-05 | 0.00416082 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744710 | ACTGCTGCCAATGTG[A/G/T]TCAGAGTCCTGTTTC | 10517 |
rs747820522 | snp | C/T | 3.77708e-05 | 0.00434557 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758360 | CTGATAGCTGTGTCA[C/T]CTAATCGAAAGATCC | 10517 |
rs747900542 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18755709 | AAGGGCACCTGTGAC[-/T]TTTATGTTGTGAGGA | 10517 |
rs747945937 | in-del | -/C | 1.69029e-05 | 0.00290709 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766665 | GTAACCTTTCCTTTT[-/C]CCCCTTTTTCCCCAC | 10517 |
rs747969403 | in-del | -/CT | 0.000308499 | 0.0124159 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758266 | CAGGAGGGACACTGA[-/CT]CTTCTTTCATGGATA | 10517 |
rs748093008 | snp | C/T | 0.000198702 | 0.00996551 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749900 | CCGTTACCTGCCCAT[C/T]CACCTCTCCAAGTAC | 10517 |
rs748130978 | snp | A/C | 1.78784e-05 | 0.00298979 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744249 | ATCTTAGGATCATGG[A/C]AAACCTGGAATCAAG | 10517 |
rs748140429 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744330 | CTCTATGCCGGAAGT[A/G]TGAGACGTGTGTCTT | 10517 |
rs748236715 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747137 | TTCACCGTGTTAGCC[C/G]GGATGGTCTCCATCT | 10517 |
rs748242541 | snp | C/G/T | 0.000576552 | 0.0169696 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751049 | AGTGGAAGCTGAGAA[C/G/T]GAAGGTGGGTTCCAA | 10517 |
rs748325326 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768629 | GGTCATGGCCTGGAG[C/T]ATGGTGGGGAAGTAC | 10517 |
rs748374907 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747901 | TTTCCTCAACACACC[C/T]GCTTCAAGAGCAACC | 10517 |
rs748415263 | snp | A/C | 3.65838e-05 | 0.00427675 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756009 | TGGGTATTTGAAGTT[A/C]CCACTGAGCTTTAAC | 10517 |
rs748445796 | snp | C/T | 2.0354e-05 | 0.00319007 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779058 | ACGGCCTCGCATCTA[C/T]ACAGCCCTTGATCCT | 10517 |
rs748452812 | snp | A/G | 2.09879e-05 | 0.00323937 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779176 | GAGTCCACTGGAGTG[A/G]TTGATCCAGGAAAAG | 10517 |
rs748464601 | snp | A/G | 3.30104e-05 | 0.00406252 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748044 | CAAAACTCAGCACAC[A/G]TCCCTTCCTTTGTCC | 10517 |
rs748507705 | in-del | -/GA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767946 | ATTCCTCCTTAACCC[-/GA]GAGAGAGAGCTCTAT | 10517 |
rs748544745 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774407 | TACTTGGTTTCATAC[A/G]ACAATAAACAATATG | 10517 |
rs748597514 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773581 | TATGTGTGGGTTAGA[A/G]TAGCAAGACTCCTTC | 10517 |
rs748688767 | snp | C/G | 4.96907e-05 | 0.00498426 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764829 | CTTGTGTAAGAACAG[C/G]CTCGTATCTGGAGGA | 10517 |
rs748702838 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751184 | ACTCCTTAAGGAAGA[C/T]GAGAGTTCTGTGTTG | 10517 |
rs748805688 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant, splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18770049 | AAGCCAATGGCAGAG[A/G]TGATCCTGTGCTGTC | 10517 |
rs748833737 | in-del | -/CGATAC | 2.95129e-05 | 0.0038413 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758402 | TCATACAAGTGAAAG[-/CGATAC]CGATACCCGTTGAAT | 10517 |
rs748893485 | snp | A/C/G | 3.61508e-05 | 0.00425139 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758462 | CTCTTCCTGTGTGAG[A/C/G]AGGAAAACTTTCTCC | 10517 |
rs748902728 | snp | A/G | 3.30945e-05 | 0.0040677 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758554 | CACCTAGGGCCTAGA[A/G]GCAGCTCATGGAAGA | 10517 |
rs748947198 | snp | A/T | 1.64827e-05 | 0.00287073 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749844 | GACCTGGATGACATC[A/T]GAGACCTGTCTTCTG | 10517 |
rs748992311 | snp | A/G | | | | | GRCh38.p7 | 17:18739941 | TGGCATTTATAATGC[A/G]CAAGCTGCTGTGCTA | 10517 |
rs749037300 | snp | A/G | 1.6585e-05 | 0.00287962 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749914 | TCCACCTCTCCAAGT[A/G]CATTCTAAGTATGCT | 10517 |
rs749171353 | in-del | -/T | 8.24382e-05 | 0.00641968 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770131 | AGTGATTCTGTTGGA[-/T]TTTTTTGATTTTTTT | 10517 |
rs749229888 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759671 | AGGCTGGAGAGCAGT[A/G]GCGCCATGTTGGCTC | 10517 |
rs749232563 | snp | A/G | 3.30355e-05 | 0.00406407 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744427 | TCTAGTTGGCATTCT[A/G]AAGCAGTTAAATAGC | 10517 |
rs749257121 | snp | A/G | 6.59381e-05 | 0.00574149 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768635 | GGCCTGGAGCATGGT[A/G]GGGAAGTACGAGCGC | 10517 |
rs749345541 | snp | C/T | 9.71086e-05 | 0.00696741 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756036 | TAACTTCAAATATTC[C/T]CTTGTTAGAATGAGT | 10517 |
rs749345594 | snp | C/T | 0.000959374 | 0.0218807 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768724 | TGGTGTCCTTCCCTT[C/T]CCCGTCATAGCCTAG | 10517 |
rs749377506 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18754072 | GCTCTGCATACAGCA[C/T]TTACTTGATTTCACC | 10517 |
rs749398167 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748065 | TCCTTTGTCCAAAGC[C/T]CCAGAAAATGAACAC | 10517 |
rs749433523 | snp | G/T | 3.43909e-05 | 0.00414659 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756139 | GGACCTACAATGTTC[G/T]CATTCTCTCTGACAC | 10517 |
rs749540424 | snp | A/G | 6.97764e-05 | 0.00590621 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779347 | AACAGAAAGCCAAGC[A/G]GATGTTGCTATTTGG | 10517 |
rs749639755 | snp | A/G | 1.6554e-05 | 0.00287693 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764852 | CTGGAGGAAGAGATT[A/G]CCAGGTAAAAGGTGA | 10517 |
rs749770488 | snp | C/G | 0.000231154 | 0.0107482 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750107 | CTTGTCAGCGCACGG[C/G]TTCATTCAGAACCAG | 10517 |
rs749832838 | snp | C/G | | | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18771662 | AGAGCTTTCCTCATT[C/G]CCAGCAGCAATAGTA | 10517 |
rs749881859 | snp | A/G | 2.59272e-05 | 0.00360041 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779316 | CAGCCTTGGGAAATT[A/G]CAATGTTTTACAATA | 10517 |
rs749895678 | snp | C/T | 1.66665e-05 | 0.00288669 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748134 | CAGCAAGAAAGCCAA[C/T]ATGGGCTAGGTGCGG | 10517 |
rs749931345 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772571 | TAAGTGTAATATTCA[C/G]GTTCACAGCCCAAGA | 10517 |
rs749932685 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18748781 | TAGTCCCTGGGCTCT[A/G]GCATGGTGGCCAGCT | 10517 |
rs749958789 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775462 | TTGTCCCTTTTCTGA[C/G]TTGAGGCCACAGAGG | 10517 |
rs749985513 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749700 | CAACTCAACCACGTA[C/T]CTTTCTCTGGCTTCA | 10517 |
rs750014374 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774165 | AAGAGGTGACAATCA[C/G]AAGGGTGTCTATCTC | 10517 |
rs750025167 | snp | C/T | 1.67234e-05 | 0.00289161 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772677 | AAGCCGGCCAAGTTC[C/T]CTTCAGGTAAAAAAC | 10517 |
rs750117309 | snp | C/T | 3.34119e-05 | 0.00408715 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775113 | ATATAATGACTACAG[C/T]TTCTTCCTCAATCTC | 10517 |
rs750186899 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18771989 | GTGCGTACCTGTAAT[C/T]CCAGCTACTCAAGAG | 10517 |
rs750193700 | snp | G/T | 5.296e-05 | 0.0051456 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750095 | GGTCAAGATGGACTT[G/T]TCAGCGCACGGCTTC | 10517 |
rs750234857 | snp | A/T | 5.78341e-05 | 0.00537715 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750905 | TCTGTTTTTATTTTT[A/T]TTTTTTATTTTTTGT | 10517 |
rs750276989 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769733 | AGTGAGCCAAGATCG[C/T]ACCGTTGCACTCCAG | 10517 |
rs750294589 | snp | A/G | 1.69398e-05 | 0.00291026 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778768 | TTGAGCAATCCTCCT[A/G]TAGATGTGAAACGAA | 10517 |
rs750314402 | snp | C/T | 4.94996e-05 | 0.00497467 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744645 | CCCAGTGGACCAAGG[C/T]GAATTATACTCTCTT | 10517 |
rs750451171 | snp | C/G | 0.000437626 | 0.0147859 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744789 | TAGAGGGCCCCCGAA[C/G]ACCAGAAGGCAAGGC | 10517 |
rs750484981 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770010 | TTTACAATTTCCTCA[A/G]CGGGAACTGTATGAA | 10517 |
rs750549670 | in-del | -/G | 1.65353e-05 | 0.00287531 | splice-acceptor-variant | FBXW10 | GRCh38.p7 | 17:18750930 | TTTTGTCTTTTTCCA[-/G]GGGTCCTACACAAGA | 10517 |
rs750574960 | snp | A/T | 2.72989e-05 | 0.00369442 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758413 | GAAAGCGATACCCGT[A/T]GAATTCCGAGGCCAT | 10517 |
rs750685668 | snp | C/T | 0.000230593 | 0.0107351 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749811 | AAGCCAGGGTACGAT[C/T]CCTGCAATCTATTGG | 10517 |
rs750765822 | snp | G/T | 5.42461e-05 | 0.0052077 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778456 | CCGATTTTTTAAAAT[G/T]TTCTTTTTTTTGAAA | 10517 |
rs750777371 | snp | C/G | 1.8037e-05 | 0.00300303 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744218 | TGCAAGTGCGCAGGG[C/G]TAAAATGGACTGGTT | 10517 |
rs750855958 | snp | C/G | 5.82213e-05 | 0.00539512 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766902 | GCGGAAAGGGCACTG[C/G]GGAGGAGATGGGTGG | 10517 |
rs750868323 | snp | A/G | 1.75576e-05 | 0.00296285 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778534 | CCTGGAAAACTGCCC[A/G]GTCACCCAAAGAAAA | 10517 |
rs750888583 | in-del | -/TTG | 1.65614e-05 | 0.00287757 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764814 | ATCACTTGCATGGAC[-/TTG]TTGTGTAAGAACAGG | 10517 |
rs750999763 | snp | A/G | 1.66493e-05 | 0.0028852 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775124 | ACAGCTTCTTCCTCA[A/G]TCTCAATTTAGCAGT | 10517 |
rs751018013 | in-del | -/CAT | 0.00130963 | 0.0255558 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758386 | GATCCATCTTCTGGA[-/CAT]CATACAAGTGAAAGC | 10517 |
rs751095242 | snp | A/G | 5.40916e-05 | 0.00520028 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744208 | GCGTTGCCGTTGCAA[A/G]TGCGCAGGGCTAAAA | 10517 |
rs751099965 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18772820 | TGAGGATATAAATCC[C/T]AACCCTCCAGGAAGG | 10517 |
rs751234040 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765894 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTTTTA | 10517 |
rs751256085 | snp | A/G | | | | | GRCh38.p7 | 17:18740969 | GGTTTCACCGTGTTA[A/G]CCAGGATGGTCTCGA | 10517 |
rs751260413 | snp | A/G/T | 5.02975e-05 | 0.00501464 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750919 | TATTTTTTATTTTTT[A/G/T]TCTTTTTCCAGGGGT | 10517 |
rs751331527 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775584 | ATCAATCTGAGAAAT[A/G]GGCACAATAAAAGAG | 10517 |
rs751420281 | snp | C/G | 2.05476e-05 | 0.00320521 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779008 | CGCATGCTAGCTCCA[C/G]AAGTGGGCACAGCCA | 10517 |
rs751450587 | snp | C/T | 1.68946e-05 | 0.00290638 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744813 | GCAAGGCTTCAGAAA[C/T]CTGTAAGGAACTGCA | 10517 |
rs751617669 | snp | A/G | 1.65425e-05 | 0.00287593 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758497 | CGGGAGCTATGACCT[A/G]AGTATCAGGTGAGGA | 10517 |
rs751621514 | in-del | -/A | 1.65466e-05 | 0.00287628 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764869 | CAGGTAAAAGGTGAG[-/A]AAGAAGTGCCTTAAA | 10517 |
rs751638860 | snp | A/G | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764744 | CTGATTCCTGCAGAT[A/G]CTGGGATCTGAAAAG | 10517 |
rs751676368 | in-del | -/A | 1.67288e-05 | 0.00289208 | frameshift-variant, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778577 | TCCCTATGTCACCTG[-/A]CCAATTCCTCCTGAC | 10517 |
rs751724596 | snp | G/T | 1.66313e-05 | 0.00288364 | intron-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18749981 | TTGGCCCAGTTCTGG[G/T]GTTTCTGGGTCCATC | 10517 |
rs751755092 | snp | A/G | 1.74254e-05 | 0.00295168 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778547 | CCAGTCACCCAAAGA[A/G]AAAGTCTTGGAAAAT | 10517 |
rs751769200 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761664 | TAGACTTTATTTGGG[C/T]TGCATTGAATTTATA | 10517 |
rs751820849 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744313 | GGGAACCGATTCCAT[C/T]CCTCTATGCCGGAAG | 10517 |
rs751842019 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18755223 | AGCCAAGATCATGAC[A/G]TTGCACTCCAGCCTG | 10517 |
rs751888365 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776799 | TTCTAGGTTGACCAT[C/T]AACAAACTAAATGTC | 10517 |
rs751906564 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18750691 | TATGGTGAGGCTGGC[A/G]ACAGTCTGACCGTCT | 10517 |
rs751908282 | snp | C/T | 3.29979e-05 | 0.00406175 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744398 | AGGATCAATGACATA[C/T]CACAGAGGAGGTTTC | 10517 |
rs751924298 | snp | A/C/G | 4.96564e-05 | 0.00498258 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778624 | CACGCCCATAATTCC[A/C/G]GGGAATTTGCCTATC | 10517 |
rs751979001 | snp | C/T | 1.6531e-05 | 0.00287493 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751105 | GCGTCTCATTCTAAT[C/T]GTCATTGAAGGCTGA | 10517 |
rs751996609 | in-del | -/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768010 | TTTATTTTTTCTTTT[-/C]CTTCCTTCCTTCCTT | 10517 |
rs752021686 | snp | C/G/T | 0.000173274 | 0.00930655 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768695 | GGTGCCTGTGAAGCC[C/G/T]GGAGCGATGAACCTG | 10517 |
rs752065276 | snp | A/G | 6.63383e-05 | 0.00575888 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756086 | CCAGAACGAGGAAAC[A/G]CAGCAGGTCCTGATA | 10517 |
rs752076802 | snp | A/C | 1.68408e-05 | 0.00290175 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744279 | GGCTCAAGAATGCCC[A/C]CTATTTTCGTTGTGA | 10517 |
rs752144572 | in-del | -/A | 0.000184978 | 0.00961534 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775092 | TTTTATGCCCTAATC[-/A]GAAGTATATAATGAC | 10517 |
rs752159519 | in-del | -/AA/AAA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776016 | CCTTGCCTCTTAAAG[-/AA/AAA]AAAAGAAAAAAAAAA | 10517 |
rs752194941 | snp | A/C/T | 0.00013178 | 0.0081164 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751018 | GACGGGAAGAGCATG[A/C/T]GTGTGAAACATCCGA | 10517 |
rs752311721 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744190 | TTCCTCTAGTGTTTG[G/T]TGGCGTTGCCGTTGC | 10517 |
rs752402292 | snp | C/G | 3.29886e-05 | 0.00406118 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751075 | TCCAACAGCATCTGG[C/G]GCAAGTAGCTGTGAG | 10517 |
rs752414135 | snp | C/T | 2.02661e-05 | 0.00318318 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779027 | TGGGCACAGCCACCC[C/T]GTCTCTTAAGAAAGA | 10517 |
rs752488928 | in-del | -/A | | | | | GRCh38.p7 | 17:18739356 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 10517 |
rs752491652 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772505 | GAAACAAAAGAAGAA[C/T]AAGGAGAAAGAGGAG | 10517 |
rs752506165 | snp | C/T | 1.7072e-05 | 0.00292159 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772403 | ACAACCCTGTTGTTT[C/T]GGTTCCAGGATGGTG | 10517 |
rs752543524 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758505 | ATGACCTAAGTATCA[A/G]GTGAGGAGTCCAAAG | 10517 |
rs752721490 | snp | G/T | 1.65715e-05 | 0.00287845 | intron-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18749990 | TTCTGGGGTTTCTGG[G/T]TCCATCTTTTTTTTT | 10517 |
rs752799794 | snp | C/T | 1.70203e-05 | 0.00291716 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778564 | AAGTCTTGGAAAATC[C/T]CTATGTCACCTGACC | 10517 |
rs752811151 | snp | A/G | 1.74382e-05 | 0.00295276 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750077 | GGCCGCCATGGCTCA[A/G]CAGGTCAAGATGGAC | 10517 |
rs752855099 | in-del | -/TGAA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746699 | AAAGTCCAGGGCATC[-/TGAA]TGACTTTGCTTAGGT | 10517 |
rs752861486 | snp | A/C | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744520 | TAACAGGTCCCGGAT[A/C]AACCTCAGCAAGAAA | 10517 |
rs752873990 | snp | A/C/T | 3.30291e-05 | 0.0040637 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744417 | AGAGGAGGTTTCTAG[A/C/T]TGGCATTCTGAAGCA | 10517 |
rs752927524 | in-del | -/T | 0.000116185 | 0.00762097 | frameshift-variant, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778855 | AGTCCTAGAGTCCAG[-/T]CCACCATACCCCAGC | 10517 |
rs752963501 | snp | A/C | 1.67405e-05 | 0.00289309 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756119 | GGAGAGAAATGTTTT[A/C]TGTGGGACCTACAAT | 10517 |
rs752981304 | snp | A/G | 1.73531e-05 | 0.00294555 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768699 | CCTGTGAAGCCCGGA[A/G]CGATGAACCTGGTGT | 10517 |
rs753012031 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769413 | CCTGTGACCTAATTG[C/T]GGGGAAAGTAGCTGC | 10517 |
rs753040628 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18757052 | TTGCTCCTTATATAT[A/G]TGTGTGTACATATAC | 10517 |
rs753045368 | snp | C/T | 0.00021723 | 0.0104196 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748140 | GAAAGCCAATATGGG[C/T]TAGGTGCGGTGGCTC | 10517 |
rs753130860 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18753074 | CCGCCACTTTAAGTT[C/T]CAGGTCCCTTTCTAG | 10517 |
rs753152013 | snp | C/T | 0.000176196 | 0.0093844 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758300 | CCTTTTCCCCTGGCA[C/T]TCAGGTGGGATCAAA | 10517 |
rs753178575 | snp | A/G | 2.84669e-05 | 0.00377262 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779335 | TGTTTTACAATAAAC[A/G]GAAAGCCAAGCGGAT | 10517 |
rs753236251 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749717 | TTTCTCTGGCTTCAC[C/T]CTAGAGGAACCATGG | 10517 |
rs753266896 | snp | A/C | 5.08522e-05 | 0.00504217 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772696 | CAGGTAAAAAACTGA[A/C]ATACCAGCAAGTTCA | 10517 |
rs753275379 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746198 | AGGAATCTGCCCCCA[A/T]GACCCAAAAACCTCC | 10517 |
rs753325528 | snp | C/G | 1.66907e-05 | 0.00288879 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748010 | CCAAGTCTGCGACCT[C/G]ACAAGTCTATTGGAC | 10517 |
rs753375635 | snp | C/G | 2.02579e-05 | 0.00318254 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779045 | CTCTTAAGAAAGAAC[C/G]GCCTCGCATCTATAC | 10517 |
rs753475598 | snp | C/G/T | 0.000126256 | 0.00794449 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779127 | GGAGGAGAAGGAGCA[C/G/T]CAGGAAGCCAAGATG | 10517 |
rs753482544 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747364 | TCAGGAGTTCGAGAC[A/G]AGCCTGGCCAACATG | 10517 |
rs753514138 | snp | A/G | 1.6596e-05 | 0.00288058 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748120 | GGTAAGTGAACTTTC[A/G]GCAAGAAAGCCAATA | 10517 |
rs753546278 | snp | A/G | 0.000447038 | 0.0149439 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772661 | GTCCCGAGTACTCCT[A/G]AAGCCGGCCAAGTTC | 10517 |
rs753552819 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772551 | AGTCTCATGGAAATT[C/G]TCTCTAAGTGTAATA | 10517 |
rs753639945 | snp | C/T | 6.62383e-05 | 0.00575454 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764781 | TTGCACACGAATCTT[C/T]GGTGGTCACCAGGGG | 10517 |
rs753676821 | in-del | -/AAGA | 2.02116e-05 | 0.0031789 | frameshift-variant, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779035 | GCCACCCTGTCTCTT[-/AAGA]AAGAACGGCCTCGCA | 10517 |
rs753694558 | snp | A/G | 1.65501e-05 | 0.00287659 | splice-acceptor-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18750008 | CATCTTTTTTTTTCC[A/G]GGAATGCTGGATAGA | 10517 |
rs753741780 | snp | C/T | 1.66446e-05 | 0.00288479 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778642 | GAATTTGCCTATCCC[C/T]GTAGGCCCCAAACAG | 10517 |
rs753781961 | snp | A/T | 1.75274e-05 | 0.0029603 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750087 | GCTCAACAGGTCAAG[A/T]TGGACTTGTCAGCGC | 10517 |
rs753966727 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744628 | CTGGTTTGCGAACAG[C/T]ACCCAGTGGACCAAG | 10517 |
rs754103635 | in-del | -/A | 1.65795e-05 | 0.00287914 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756100 | GCAGCAGGTCCTGAT[-/A]AGAGGAGAGAAATGT | 10517 |
rs754115646 | snp | C/G/T | 4.94363e-05 | 0.00497153 | synonymous-codon, missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749738 | GGAACCATGGAGGAA[C/G/T]TCACTCCGGTGTATA | 10517 |
rs754128458 | snp | C/T | 0.000230593 | 0.0107351 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769997 | GGCAAGATCCGAATT[C/T]ACAATTTCCTCAACG | 10517 |
rs754266034 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749794 | GAAAAGGAGACATAA[A/C]CAAGCCAGGGTACGA | 10517 |
rs754355428 | snp | A/T | 0.000164266 | 0.00906123 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778450 | AGAACGCCGATTTTT[A/T]AAAATTTTCTTTTTT | 10517 |
rs754378643 | snp | A/G | 3.44234e-05 | 0.00414856 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766804 | ATACCTACATTGTGA[A/G]CAGCTGTGAGCGAGG | 10517 |
rs754384552 | in-del | -/TG | 1.69548e-05 | 0.00291154 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750047 | GAACAAGTGCGCCTC[-/TG]TGAGCCAGCACTGGG | 10517 |
rs754430640 | in-del | -/AG | | | | | GRCh38.p7 | 17:18741901 | TTTTTTTTTTGAGAC[-/AG]AGTCTTGCTCTCTCG | 10517 |
rs754505561 | snp | A/G | 1.72062e-05 | 0.00293306 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766800 | AATGATACCTACATT[A/G]TGAGCAGCTGTGAGC | 10517 |
rs754580294 | in-del | -/CTTCCTTCCTTG/CTTT | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768054 | TTCCTTCCTTCCTTC[-/CTTCCTTCCTTG/CTTT]TTTCTTTCTTTCTTT | 10517 |
rs754631393 | snp | C/G | 1.69261e-05 | 0.00290908 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778787 | ATGTGAAACGAACCA[C/G]TATTCCCCTTGAAAT | 10517 |
rs754642552 | snp | A/C/G | 0.000250104 | 0.01118 | synonymous-codon, missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778890 | GATTATCCGCTCCAG[A/C/G]TTCTCTGGCAGCTTA | 10517 |
rs754700744 | snp | A/T | 1.66535e-05 | 0.00288556 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744674 | TTACTGCTGCAGATG[A/T]GCAACCCCAAATTAC | 10517 |
rs754706695 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751013 | TAGATGACGGGAAGA[A/G]CATGCGTGTGAAACA | 10517 |
rs754945951 | snp | A/C | 1.65384e-05 | 0.00287557 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758498 | GGGAGCTATGACCTA[A/C]GTATCAGGTGAGGAG | 10517 |
rs754979656 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18764686 | CATGGGTTCTACGCA[A/G]TATGATCCTCTGGGC | 10517 |
rs755009683 | snp | A/G | 4.95708e-05 | 0.00497825 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749887 | ACCGAGACTTCATCC[A/G]TTACCTGCCCATCCA | 10517 |
rs755097685 | snp | C/T | 9.88354e-05 | 0.00702908 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744323 | TCCATCCCTCTATGC[C/T]GGAAGTGTGAGACGT | 10517 |
rs755214578 | snp | C/G | 3.47222e-05 | 0.00416652 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778551 | TCACCCAAAGAAAAA[C/G]TCTTGGAAAATCCCT | 10517 |
rs755278655 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768618 | ACTGATGGCCTGGTC[A/G]TGGCCTGGAGCATGG | 10517 |
rs755332256 | snp | A/G | 1.65422e-05 | 0.0028759 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756003 | GGACTGTGGGTATTT[A/G]AAGTTACCACTGAGC | 10517 |
rs755381863 | snp | C/T | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756096 | GAAACGCAGCAGGTC[C/T]TGATAGAGGAGAGAA | 10517 |
rs755411623 | snp | A/C | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748037 | GGACAGCCAAAACTC[A/C]GCACACATCCCTTCC | 10517 |
rs755412292 | snp | C/T | 4.21585e-05 | 0.00459102 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779157 | GAAGGAATATCAGGC[C/T]AGGGAGTCCACTGGA | 10517 |
rs755503206 | snp | A/G | 1.67055e-05 | 0.00289006 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748138 | AAGAAAGCCAATATG[A/G]GCTAGGTGCGGTGGC | 10517 |
rs755603242 | snp | C/T | | | | | GRCh38.p7 | 17:18741209 | CTACTCATTTGACCC[C/T]GACAGCCACCTATGA | 10517 |
rs755659255 | snp | C/T | 0.000310668 | 0.0124594 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778934 | AAGTGACCAGTTCAA[C/T]TGAAAGGGCTGTGTG | 10517 |
rs755680334 | snp | C/T | 2.02116e-05 | 0.0031789 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779031 | CACAGCCACCCTGTC[C/T]CTTAAGAAAGAACGG | 10517 |
rs755693485 | in-del | -/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773529 | TGGGGGTGCAGGCAT[-/G]GGCCAATGCCATTTA | 10517 |
rs755725915 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775559 | TCCTCACTTCTTGGA[C/T]TGTTATGTCATCAAT | 10517 |
rs755739662 | snp | A/G | 5.0114e-05 | 0.00500545 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747991 | CCTGAGAAAGACCAC[A/G]GCTCCAAGTCTGCGA | 10517 |
rs755751288 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770040 | AGGTGTTAAAAGCCA[A/G]TGGCAGAGGTGATCC | 10517 |
rs755767902 | snp | A/G | 6.80249e-05 | 0.00583162 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772404 | CAACCCTGTTGTTTC[A/G]GTTCCAGGATGGTGG | 10517 |
rs755774489 | snp | C/T | 3.35971e-05 | 0.00409846 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744861 | TAGACAGAGATTGCA[C/T]AGAACTCAGCATAGG | 10517 |
rs755777437 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774261 | AAAGGTCTGGAAGGA[A/G]TGGTCACGCACCAGA | 10517 |
rs755870273 | in-del | -/T | 0.000101238 | 0.007114 | frameshift-variant, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778903 | AGGTTCTCTGGCAGC[-/T]TAAAGGGTGGAGACC | 10517 |
rs755893116 | in-del | -/GT | 9.18552e-05 | 0.00677637 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766852 | CATTGCCATGGCCCA[-/GT]GTTGGTAAAGGTAAG | 10517 |
rs755896307 | snp | A/G | 1.6501e-05 | 0.00287232 | intron-variant | FBXW10 | GRCh38.p7 | 17:18758526 | GAGTCCAAAGGCATC[A/G]TGATCCCTGTCCCAC | 10517 |
rs755913280 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761674 | TTGGGTTGCATTGAA[C/T]TTATAGATTAGTTTG | 10517 |
rs755982110 | snp | A/G | 1.658e-05 | 0.00287919 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749910 | CCCATCCACCTCTCC[A/G]AGTACATTCTAAGTA | 10517 |
rs756073865 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18750005 | GTCCATCTTTTTTTT[C/T]CCAGGAATGCTGGAT | 10517 |
rs756298001 | snp | A/G | 3.29804e-05 | 0.00406068 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744530 | CGGATCAACCTCAGC[A/G]AGAAAGAGGGGAAAG | 10517 |
rs756396074 | snp | C/T | 1.67391e-05 | 0.00289297 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756120 | GAGAGAAATGTTTTC[C/T]GTGGGACCTACAATG | 10517 |
rs756480720 | snp | A/G | 4.01204e-05 | 0.00447868 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779337 | TTTTACAATAAACAG[A/G]AAGCCAAGCGGATGT | 10517 |
rs756500053 | snp | A/G | 1.67323e-05 | 0.00289239 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748144 | GCCAATATGGGCTAG[A/G]TGCGGTGGCTCATGC | 10517 |
rs756523383 | snp | A/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749722 | CTGGCTTCACTCTAG[A/T]GGAACCATGGAGGAA | 10517 |
rs756535576 | snp | A/G | 1.69743e-05 | 0.00291322 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772699 | GTAAAAAACTGAAAT[A/G]CCAGCAAGTTCAGTG | 10517 |
rs756600340 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18753867 | GGGCAAGAGAGCGAG[A/T]CTCCATCTCAAAAAA | 10517 |
rs756627325 | snp | C/T | 1.68527e-05 | 0.00290277 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766674 | CCTTTTCCCCCTTTT[C/T]CCCCACTCCCATGTC | 10517 |
rs756785563 | snp | A/C | 1.66776e-05 | 0.00288765 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748012 | AAGTCTGCGACCTCA[A/C]AAGTCTATTGGACAG | 10517 |
rs756800959 | snp | C/G | 1.66582e-05 | 0.00288597 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748130 | CTTTCAGCAAGAAAG[C/G]CAATATGGGCTAGGT | 10517 |
rs756824000 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746309 | GGCAAGAGAATTGAG[C/T]TTTGGAGGGGTCCAG | 10517 |
rs756831537 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773148 | ATGTTGATCAGGCTG[G/T]TCTCAAACTCCCGAC | 10517 |
rs756843209 | snp | C/T | 1.64974e-05 | 0.00287201 | synonymous-codon, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18772442 | AGAGAGCAATGTTCT[C/T]ATGTTCCAGTTTGAG | 10517 |
rs756911244 | snp | C/G | 1.65594e-05 | 0.0028774 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764782 | TGCACACGAATCTTC[C/G]GTGGTCACCAGGGGA | 10517 |
rs756931177 | snp | G/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772560 | GAAATTCTCTCTAAG[G/T]GTAATATTCAGGTTC | 10517 |
rs757001235 | snp | A/C | 4.98732e-05 | 0.00499341 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750026 | AATGCTGGATAGACA[A/C]ACCCTGAACAAGTGC | 10517 |
rs757074249 | snp | C/G | 1.65332e-05 | 0.00287512 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764907 | AGAAGTTTCCCCCGA[C/G]CCACGGGTTACCAAA | 10517 |
rs757117927 | snp | A/G | 1.65236e-05 | 0.00287429 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744445 | GCAGTTAAATAGCTT[A/G]TATTTGTTACACTAT | 10517 |
rs757205842 | snp | C/T | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744556 | GAAAGTTGTGAAGTC[C/T]TCCTTGAACCAAATG | 10517 |
rs757266140 | snp | A/G | 1.90022e-05 | 0.00308233 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768728 | GTCCTTCCCTTCCCC[A/G]TCATAGCCTAGACTG | 10517 |
rs757339926 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18757670 | AATAAATAGTGTCCC[C/G]TTTCACAATAAAAAA | 10517 |
rs757404382 | snp | G/T | 1.76608e-05 | 0.00297155 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756147 | AATGTTCGCATTCTC[G/T]CTGACACGTAGGTAC | 10517 |
rs757434421 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761652 | ATAAAACCTAACTAG[A/C]CTTTATTTGGGTTGC | 10517 |
rs757438421 | snp | C/T | 4.94254e-05 | 0.00497094 | splice-donor-variant, upstream-variant-2KB | FBXW10, TVP23B | GRCh38.p7 | 17:18779350 | AGAAAGCCAAGCGGA[C/T]GTTGCTATTTGGCCT | 10517 |
rs757644169 | snp | A/G/T | 3.60549e-05 | 0.00424572 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744216 | GTTGCAAGTGCGCAG[A/G/T]GCTAAAATGGACTGG | 10517 |
rs757710777 | snp | A/T | 8.55786e-05 | 0.00654079 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778454 | CGCCGATTTTTTAAA[A/T]TTTTCTTTTTTTTGA | 10517 |
rs757740595 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750932 | TTGTCTTTTTCCAGG[A/G]GTCCTACACAAGAGG | 10517 |
rs757764850 | in-del | -/C | 1.85713e-05 | 0.00304718 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750147 | TGCAGGTACTTCCTG[-/C]CAAGTCTGAAAGGGG | 10517 |
rs757798707 | snp | A/G | 9.66772e-05 | 0.00695192 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766893 | GCTACCTTGGCGGAA[A/G]GGGCACTGGGGAGGA | 10517 |
rs757856483 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744675 | ACTGCTGCAGATGTG[-/C]CAACCCCAAATTACT | 10517 |
rs757987309 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764798 | GTGGTCACCAGGGGA[C/T]TATCACTTGCATGGA | 10517 |
rs757989491 | snp | C/T | 1.67514e-05 | 0.00289403 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772680 | CCGGCCAAGTTCTCT[C/T]CAGGTAAAAAACTGA | 10517 |
rs758019233 | in-del | -/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749098 | TTATTCCATTCATTT[-/C]CCCCCCCTTTCTTAA | 10517 |
rs758028438 | snp | C/T | 1.76739e-05 | 0.00297265 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750097 | TCAAGATGGACTTGT[C/T]AGCGCACGGCTTCAT | 10517 |
rs758077250 | snp | A/G | 0.000182256 | 0.00954437 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764912 | TTTCCCCCGACCCAC[A/G]GGTTACCAAAATGCT | 10517 |
rs758122859 | snp | A/T | 1.65941e-05 | 0.00288041 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744561 | TTGTGAAGTCCTCCT[A/T]GAACCAAATGTTGGA | 10517 |
rs758295600 | snp | A/G | 4.98931e-05 | 0.00499441 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778883 | AGCCCATGATTATCC[A/G]CTCCAGGTTCTCTGG | 10517 |
rs758298921 | snp | A/G | 9.9023e-05 | 0.00703574 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744646 | CCAGTGGACCAAGGC[A/G]AATTATACTCTCTTA | 10517 |
rs758317019 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770011 | TTACAATTTCCTCAA[C/T]GGGAACTGTATGAAG | 10517 |
rs758319701 | snp | A/C/G | 0.000296476 | 0.012172 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769959 | CCCTTCTCTTCCTCC[A/C/G]GGTCATCAGCGCCTG | 10517 |
rs758413794 | snp | G/T | 5.96214e-05 | 0.00545959 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758333 | CGAGTCATCCACTAT[G/T]CCGGGGGAGATCTGA | 10517 |
rs758422728 | in-del | -/CTGAGAACGAAGGTGGGTTCCAACAGCAT | 1.64749e-05 | 0.00287005 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751042 | CATCCGAAGTGGAAG[lengthTooLong]CTGGGGCAAGTAGCT | 10517 |
rs758477768 | in-del | -/T | 1.65616e-05 | 0.00287759 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764819 | TTGCATGGACTTGTG[-/T]TAAGAACAGGCTCGT | 10517 |
rs758531135 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761470 | CAAGGTTTCTCTGTG[C/T]TAGCCAGGATGGTCT | 10517 |
rs758626362 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749815 | CAGGGTACGATCCCT[A/G]CAATCTATTGGTTGA | 10517 |
rs758706531 | snp | C/T | 0.000546978 | 0.0165285 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778460 | TTTTTTAAAATTTTC[C/T]TTTTTTTGAAAAAGC | 10517 |
rs758716390 | snp | C/T | 8.25825e-05 | 0.0064253 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749882 | CAAATACCGAGACTT[C/T]ATCCGTTACCTGCCC | 10517 |
rs758716432 | snp | A/G | 1.80218e-05 | 0.00300176 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744220 | CAAGTGCGCAGGGCT[A/G]AAATGGACTGGTTAT | 10517 |
rs758748915 | in-del | -/A | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776323 | AGCAAGATTCCGTTT[-/A]AAAAAAAAAAAGTTT | 10517 |
rs758801435 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774416 | TCATACGACAATAAA[C/T]AATATGGTGTTTGGT | 10517 |
rs758802594 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744305 | TGTGAGAAGGGAACC[C/G]ATTCCATCCCTCTAT | 10517 |
rs758853846 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18775734 | GGATGCACCTTTTAA[A/G]AAGTGTTGCTAGGAT | 10517 |
rs758854805 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768604 | TCCTCTCAGGAAGTA[C/T]TGATGGCCTGGTCAT | 10517 |
rs758874897 | snp | A/C/T | 0.000184432 | 0.00960144 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744871 | TTGCACAGAACTCAG[A/C/T]ATAGGTTTTTTGAAC | 10517 |
rs758945103 | snp | G/T | 1.65119e-05 | 0.00287327 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751095 | GTAGCTGTGAGCGTC[G/T]CATTCTAATTGTCAT | 10517 |
rs758964354 | snp | A/G | 8.85857e-05 | 0.0066547 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778443 | TTTTCATAGAACGCC[A/G]ATTTTTTAAAATTTT | 10517 |
rs759030475 | snp | C/T | 2.03229e-05 | 0.00318764 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779050 | AAGAAAGAACGGCCT[C/T]GCATCTATACAGCCC | 10517 |
rs759049953 | snp | C/G | 7.73664e-05 | 0.0062191 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766883 | TGGGCAGTGGGCTAC[C/G]TTGGCGGAAAGGGCA | 10517 |
rs759102264 | snp | A/T | 1.77609e-05 | 0.00297995 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744262 | GGAAAACCTGGAATC[A/T]AGGCTCAAGAATGCC | 10517 |
rs759117935 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759774 | CCCGCCACCACACCA[C/G]GCTATTTTTTTTTGT | 10517 |
rs759170145 | snp | G/T | 1.64749e-05 | 0.00287005 | stop-gained, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778513 | AAACAAGGACAATTG[G/T]AAACTCCTGGAAAAC | 10517 |
rs759207227 | in-del | -/C | 1.64977e-05 | 0.00287203 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764721 | AGGAACTCTCACATT[-/C]TTTTGGCCTGATTCC | 10517 |
rs759240876 | snp | C/T | | | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18745026 | GATTTCTGCATCTCA[C/T]AGGCCCAGAAATGGC | 10517 |
rs759260883 | snp | A/G | 6.59131e-05 | 0.0057404 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768558 | GGCCATGAGGGAGCC[A/G]TGAAATGCCTGTTCT | 10517 |
rs759260979 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXW10, TVP23B | GRCh38.p7 | 17:18779766 | GACAACATTGAGCTT[C/T]TCCTTCTCAGGGCTA | 10517 |
rs759377290 | snp | A/G | 2.05038e-05 | 0.00320179 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779011 | ATGCTAGCTCCACAA[A/G]TGGGCACAGCCACCC | 10517 |
rs759378911 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751063 | ACGAAGGTGGGTTCC[A/G]ACAGCATCTGGGGCA | 10517 |
rs759399336 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773982 | GAATTCAGTTTTCCA[G/T]ACAAAGGCTAACATA | 10517 |
rs759450526 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772229 | CAAAGCTAACGACTC[C/T]TGCTGCATCTCCTGG | 10517 |
rs759466599 | snp | A/C | 1.66197e-05 | 0.00288263 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747960 | CAATCAAGACATCAC[A/C]GATGTGTGTTTTTCC | 10517 |
rs759466840 | snp | C/G | 1.76126e-05 | 0.00296749 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756053 | TTGTTAGAATGAGTA[C/G]AACCTGTGGACTGCA | 10517 |
rs759505188 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772490 | TGCCGTGGAAAAAAC[A/G]AAACAAAAGAAGAAT | 10517 |
rs759554633 | snp | A/C | 8.24178e-05 | 0.00641889 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748079 | CCCCAGAAAATGAAC[A/C]CTTGCTTGGGGCAGC | 10517 |
rs759598751 | snp | C/G | | | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764759 | ACTGGGATCTGAAAA[C/G]TGGGGTTTGCACACG | 10517 |
rs759641114 | in-del | -/CTGA | 4.99156e-05 | 0.00499553 | frameshift-variant, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778588 | CCTGACCAATTCCTC[-/CTGA]CTGTTAGCGCCCTGC | 10517 |
rs759684647 | snp | A/G | 1.65405e-05 | 0.00287576 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764884 | AAAGAAGTGCCTTAA[A/G]TTTTCTAAGAAGTTT | 10517 |
rs759696705 | snp | A/G | 1.73634e-05 | 0.00294642 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750066 | AGCCAGCACTGGGCC[A/G]CCATGGCTCAACAGG | 10517 |
rs759734557 | snp | C/T | 3.32154e-05 | 0.00407512 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18749986 | CCAGTTCTGGGGTTT[C/T]TGGGTCCATCTTTTT | 10517 |
rs759800252 | snp | C/T | 0.000131911 | 0.00812022 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744513 | TCATCTATAACAGGT[C/T]CCGGATCAACCTCAG | 10517 |
rs759970209 | snp | C/T | 3.3983e-05 | 0.00412193 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778739 | CAATCCAACGTGCAG[C/T]TGATCGGTTGAGATT | 10517 |
rs759992785 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769981 | CAGCGCCTGTGCAGA[A/T]GGCAAGATCCGAATT | 10517 |
rs760016525 | snp | G/T | 0.000131893 | 0.00811969 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744620 | ATCTTGTACTGGTTT[G/T]CGAACAGCACCCAGT | 10517 |
rs760081035 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744359 | TTAGCCTGGAAGATC[G/T]TCTCTACCAAAGAGT | 10517 |
rs760118486 | snp | A/G | 2.14959e-05 | 0.00327834 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756204 | ATGCTTGAGTTACCC[A/G]CACTGACATTTGGGA | 10517 |
rs760177378 | snp | C/G | 1.64757e-05 | 0.00287012 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768595 | AGTGGCATCTCCTCT[C/G]AGGAAGTACTGATGG | 10517 |
rs760199170 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18762241 | TGCTGGGATTACTGG[C/T]GTGAGCTACTGCACC | 10517 |
rs760267143 | snp | A/G | 1.68108e-05 | 0.00289916 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768668 | CCTGATGGCCTTCAA[A/G]CATCCCAAGTAGGTG | 10517 |
rs760408977 | snp | A/C | 1.67913e-05 | 0.00289748 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756068 | CAACCTGTGGACTGC[A/C]TACCAGAACGAGGAA | 10517 |
rs760425075 | snp | C/G | 4.15119e-05 | 0.00455568 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779105 | AGTTCGTGCTGTTGA[C/G]CGTGAAGGAGGAGAA | 10517 |
rs760484732 | snp | C/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748102 | GGGGCAGCATCTAAC[C/T]CTGGTAAGTGAACTT | 10517 |
rs760542102 | snp | A/G/T | 0.000163576 | 0.00904246 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779247 | TATTGATAATTTCAC[A/G/T]AAGCAAGGGAAAACA | 10517 |
rs760708112 | snp | C/T | 1.67736e-05 | 0.00289595 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775101 | CCTAATCGAAGTATA[C/T]AATGACTACAGCTTC | 10517 |
rs760735331 | snp | A/G | 0.000855798 | 0.020668 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750080 | CGCCATGGCTCAACA[A/G]GTCAAGATGGACTTG | 10517 |
rs760762304 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772133 | ATAAAAATAAAAAAT[A/G]AAAAAGCATTTTGAC | 10517 |
rs760798310 | snp | C/T | 3.3173e-05 | 0.00407252 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766727 | AGTATGGGATGTAGA[C/T]ACAGGGAAGTGCCTG | 10517 |
rs760869979 | in-del | -/CA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767443 | CGAGATCATGCGTCT[-/CA]AAAAAAAAAAAAAAA | 10517 |
rs760915440 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744625 | GTACTGGTTTGCGAA[A/C]AGCACCCAGTGGACC | 10517 |
rs760930640 | snp | A/G | 3.39599e-05 | 0.00412053 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778745 | AACGTGCAGTTGATC[A/G]GTTGAGATTGAGCAA | 10517 |
rs760942911 | snp | A/G | | | intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18771692 | AATATTGGGTTTGGA[A/G]GCTGTGCTTAAAACA | 10517 |
rs760978206 | snp | G/T | | | | | GRCh38.p7 | 17:18741599 | GTTGTGTGCTGAGGA[G/T]GTTTTATCGGGATCG | 10517 |
rs761003044 | snp | A/T | 3.41875e-05 | 0.00413431 | intron-variant, nc-transcript-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18744775 | CCACAGGCAGAGACT[A/T]GAGGGCCCCCGAAGA | 10517 |
rs761104995 | snp | C/T | 0.000181185 | 0.00951628 | stop-gained, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769991 | GCAGATGGCAAGATC[C/T]GAATTTACAATTTCC | 10517 |
rs761120885 | snp | A/G | 1.67483e-05 | 0.00289377 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758481 | AAAACTTTCTCCTAA[A/G]CGGGAGCTATGACCT | 10517 |
rs761173469 | snp | A/C/T | 0.000147423 | 0.00858452 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758403 | TCATACAAGTGAAAG[A/C/T]GATACCCGTTGAATT | 10517 |
rs761243720 | in-del | -/CAG | | | | | GRCh38.p7 | 17:18738265 | CCGGGGCAACAGAGC[-/CAG]AAAAAAAAAAAAAAA | 10517 |
rs761279662 | snp | A/C | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749782 | GGCTGTTTTCTGGAA[A/C]AGGAGACATAACCAA | 10517 |
rs761289184 | snp | G/T | | | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748104 | GGCAGCATCTAACCC[G/T]GGTAAGTGAACTTTC | 10517 |
rs761301655 | snp | C/T | 4.95242e-05 | 0.0049759 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769919 | CCTGCTACTCTGTTC[C/T]CTTCCAGGGAGGTGC | 10517 |
rs761389563 | snp | A/T | 1.92506e-05 | 0.0031024 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756174 | GTACTGGGGTCAGAA[A/T]CTGGGTCTCTAGGGA | 10517 |
rs761490921 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749763 | TGTATATCCGAAATG[A/C]ATAGGCTGTTTTCTG | 10517 |
rs761519774 | snp | A/G | 2.40295e-05 | 0.00346615 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779263 | AAGCAAGGGAAAACA[A/G]CGGCCCCTGAACTTG | 10517 |
rs761557714 | snp | A/C/G | 0.00178342 | 0.0298086 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749697 | AGCCAACTCAACCAC[A/C/G]TACCTTTCTCTGGCT | 10517 |
rs761594979 | in-del | -/G | 5.93771e-05 | 0.0054484 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744819 | TTCAGAAATCTGTAA[-/G]GGAACTGCAGTTGTA | 10517 |
rs761599044 | snp | A/C | 1.66302e-05 | 0.00288355 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766743 | ACAGGGAAGTGCCTG[A/C]AGACGTTTAGACACA | 10517 |
rs761607617 | snp | C/T | 1.65965e-05 | 0.00288062 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772666 | GAGTACTCCTGAAGC[C/T]GGCCAAGTTCTCTTC | 10517 |
rs761689141 | snp | C/T | 5.91092e-05 | 0.00543609 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750178 | AATGTCTGAGACCAG[C/T]TTCATTTTCGTGTTG | 10517 |
rs761690193 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751698 | AGCAACCCCATCAGC[C/G]CATGCCTCTGGAGGC | 10517 |
rs761762042 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776318 | GACAGAGCAAGATTC[C/T]GTTTAAAAAAAAAAA | 10517 |
rs761849181 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744630 | GGTTTGCGAACAGCA[C/G]CCAGTGGACCAAGGC | 10517 |
rs761880174 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772094 | CCCGGGTGACAGAGC[A/G]AGACTCCTTCTCAAA | 10517 |
rs761931712 | snp | A/G/T | 6.58962e-05 | 0.00573974 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750973 | AATTATGCCAATAAG[A/G/T]TTTCTATCCCAGTTC | 10517 |
rs761939225 | snp | C/T | 4.14774e-05 | 0.00455379 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744782 | CAGAGACTAGAGGGC[C/T]CCCGAAGACCAGAAG | 10517 |
rs761958523 | snp | C/T | 1.65932e-05 | 0.00288034 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778865 | TCCAGTCCACCATAC[C/T]CCAGCCCATGATTAT | 10517 |
rs762050160 | snp | A/G | 6.58892e-05 | 0.00573936 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770001 | AGATCCGAATTTACA[A/G]TTTCCTCAACGGGAA | 10517 |
rs762063548 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18754311 | GGGAGAATCCAGGGC[A/G]GCATTATTTAATTCA | 10517 |
rs762114335 | in-del | -/CA | 1.73438e-05 | 0.00294476 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772721 | AGTTCAGTGATAACC[-/CA]CAGAGCAGGTCGGGG | 10517 |
rs762213451 | in-del | -/A | 1.65375e-05 | 0.0028755 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764755 | AGATACTGGGATCTG[-/A]AAAGTGGGGTTTGCA | 10517 |
rs762288070 | in-del | -/CCGAGTAGCTGGGACTACAGTCG | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18765850 | TCCTGCCTCAGCCTC[-/CCGAGTAGCTGGGACTACAGTCG]CACGCCACCACGCCC | 10517 |
rs762343730 | snp | A/C | 9.89625e-05 | 0.0070336 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764709 | CTCTGGGCCCTCAGG[A/C]ACTCTCACATTCTTT | 10517 |
rs762357073 | snp | A/C/G | 8.7301e-05 | 0.00660635 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778522 | CAATTGGAAACTCCT[A/C/G]GAAAACTGCCCAGTC | 10517 |
rs762412690 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751225 | ACAAGACACTTCCTC[C/T]TTTTTTTTTTTTTTT | 10517 |
rs762413363 | snp | C/T | 3.31257e-05 | 0.00406962 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744289 | TGCCCCCTATTTTCG[C/T]TGTGAGAAGGGAACC | 10517 |
rs762420229 | snp | A/C | 1.6516e-05 | 0.00287362 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749701 | AACTCAACCACGTAC[A/C]TTTCTCTGGCTTCAC | 10517 |
rs762433594 | snp | A/G/T | 0.000100116 | 0.00707453 | intron-variant, stop-gained, missense | FBXW10 | GRCh38.p7 | 17:18749968 | GACACCTCCCCTCTT[A/G/T]GCCCAGTTCTGGGGT | 10517 |
rs762467517 | snp | G/T | 3.33962e-05 | 0.0040862 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775114 | TATAATGACTACAGC[G/T]TCTTCCTCAATCTCA | 10517 |
rs762483019 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744192 | CCTCTAGTGTTTGGT[A/G]GCGTTGCCGTTGCAA | 10517 |
rs762523622 | in-del | -/AA | 3.2962e-05 | 0.00405954 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749843 | GACCTGGATGACATC[-/AA]AGAGACCTGTCTTCT | 10517 |
rs762601352 | snp | C/T | 1.798e-05 | 0.00299827 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744202 | TTGGTGGCGTTGCCG[C/T]TGCAAGTGCGCAGGG | 10517 |
rs762689214 | snp | C/T | 1.77811e-05 | 0.00298165 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744260 | ATGGAAAACCTGGAA[C/T]CAAGGCTCAAGAATG | 10517 |
rs762703769 | snp | C/T | 0.00105664 | 0.0229609 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778439 | ATATTTTTCATAGAA[C/T]GCCGATTTTTTAAAA | 10517 |
rs762735663 | snp | C/G | 1.68425e-05 | 0.00290189 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766769 | ACACAAAGACCCCAT[C/G]TTGGCCACCAGGATC | 10517 |
rs762817428 | in-del | -/CT | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18764616 | TTCAAATCCAGGCCC[-/CT]GACTCTAAGCTGAAC | 10517 |
rs762826427 | snp | A/G | 1.90656e-05 | 0.00308746 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766869 | TTGGTAAAGGTAAGT[A/G]GGCAGTGGGCTACCT | 10517 |
rs762829645 | snp | A/C | 5.06214e-05 | 0.00503072 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744791 | GAGGGCCCCCGAAGA[A/C]CAGAAGGCAAGGCTT | 10517 |
rs762907012 | snp | G/T | | | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756109 | TCCTGATAGAGGAGA[G/T]AAATGTTTTCTGTGG | 10517 |
rs762916065 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750982 | AATAAGGTTTCTATC[A/C]CAGTTCCTAAAATGG | 10517 |
rs762917745 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768548 | GACTCTCAGTGGCCA[C/T]GAGGGAGCCGTGAAA | 10517 |
rs762928879 | snp | A/G/T | 6.14651e-05 | 0.00554341 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778994 | TCATTAAACCAAACC[A/G/T]CATGCTAGCTCCACA | 10517 |
rs762987907 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18764436 | CAATCTCTTGATCTC[A/G]TGATCTGCCCGCCTC | 10517 |
rs763012583 | snp | A/G | 5.24132e-05 | 0.00511897 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779080 | CTTGATCCTTTTAGA[A/G]TGAACACTGAGTTCG | 10517 |
rs763068044 | snp | C/T | 1.65367e-05 | 0.00287543 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747943 | TTCTGTGTTTCAGGG[C/T]TCAATCAAGACATCA | 10517 |
rs763084743 | snp | C/T | 3.49656e-05 | 0.0041811 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772368 | TGCATCTTTCGGTGG[C/T]CTCCACAGTCCTTTT | 10517 |
rs763100987 | snp | C/T | 6.58913e-05 | 0.00573945 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772478 | AAAGTGGCAGTATGC[C/T]GTGGAAAAAACGAAA | 10517 |
rs763114150 | snp | C/T | 1.65121e-05 | 0.00287329 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764733 | ATTCTTTTGGCCTGA[C/T]TCCTGCAGATACTGG | 10517 |
rs763236104 | snp | C/T | 0.000545722 | 0.0165095 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778541 | AACTGCCCAGTCACC[C/T]AAAGAAAAAGTCTTG | 10517 |
rs763278932 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747165 | TCTCCTGACCTTGTG[A/T]TCCGCCTGCCTCAGC | 10517 |
rs763387114 | snp | G/T | 6.66678e-05 | 0.00577317 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18749975 | CCCCTCTTGGCCCAG[G/T]TCTGGGGTTTCTGGG | 10517 |
rs763413140 | snp | C/T | 1.70223e-05 | 0.00291734 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778727 | TCAAAGGAAAATCAA[C/T]CCAACGTGCAGTTGA | 10517 |
rs763441089 | snp | A/G | 1.73489e-05 | 0.00294519 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750062 | TGTGAGCCAGCACTG[A/G]GCCGCCATGGCTCAA | 10517 |
rs763469446 | snp | C/T | 8.23716e-05 | 0.00641709 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744364 | CTGGAAGATCTTCTC[C/T]ACCAAAGAGTGGTTC | 10517 |
rs763471972 | snp | C/T | 3.30846e-05 | 0.00406709 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778617 | CCTGCAGCACGCCCA[C/T]AATTCCGGGGAATTT | 10517 |
rs763491396 | snp | C/T | 1.71097e-05 | 0.00292481 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768685 | ATCCCAAGTAGGTGC[C/T]TGTGAAGCCCGGAGC | 10517 |
rs763532039 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768599 | GCATCTCCTCTCAGG[A/G]AGTACTGATGGCCTG | 10517 |
rs763621391 | snp | C/G | 1.69568e-05 | 0.00291172 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18768677 | CTTCAAGCATCCCAA[C/G]TAGGTGCCTGTGAAG | 10517 |
rs763626510 | snp | A/G | 0.000300752 | 0.0122591 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756073 | TGTGGACTGCATACC[A/G]GAACGAGGAAACGCA | 10517 |
rs763643420 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766925 | ATGGGTGGGCTCCCC[A/C]TACCTAGCTCCTCAG | 10517 |
rs763718808 | snp | G/T | 3.30535e-05 | 0.00406518 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18748106 | CAGCATCTAACCCTG[G/T]TAAGTGAACTTTCAG | 10517 |
rs763815117 | snp | C/T | 3.31076e-05 | 0.0040685 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764773 | AGTGGGGTTTGCACA[C/T]GAATCTTCGGTGGTC | 10517 |
rs764073637 | snp | C/T | 3.30682e-05 | 0.00406608 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764904 | CTAAGAAGTTTCCCC[C/T]GACCCACGGGTTACC | 10517 |
rs764109786 | snp | A/G | 1.69746e-05 | 0.00291325 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778746 | ACGTGCAGTTGATCG[A/G]TTGAGATTGAGCAAT | 10517 |
rs764119996 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774067 | TTCTGCTGTAAAGAG[A/G]TGACAATTACAAGGG | 10517 |
rs764159611 | snp | A/T | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744547 | GAAAGAGGGGAAAGT[A/T]GTGAAGTCCTCCTTG | 10517 |
rs764249402 | snp | A/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744626 | TACTGGTTTGCGAAC[A/T]GCACCCAGTGGACCA | 10517 |
rs764300127 | in-del | -/ACAC | 1.65968e-05 | 0.00288065 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750023 | AGGAATGCTGGATAG[-/ACAC]ACCCTGAACAAGTGC | 10517 |
rs764324133 | in-del | -/A | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18755936 | AGCCTCAGCCTTCAG[-/A]GGAAGAATCCGTGAG | 10517 |
rs764386817 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769942 | GGAGGTGCTCGACGT[A/G]TCCCTTCTCTTCCTC | 10517 |
rs764417683 | snp | C/T | | | intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18771803 | TCCAGGAACAGAAAT[C/T]CATTTAAAAGCATTT | 10517 |
rs764461169 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776789 | CCGCATTTTCTTCTA[G/T]GTTGACCATTAACAA | 10517 |
rs764561068 | snp | A/G | | | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742790 | GAATCACTTTAACCC[A/G]GGAAGCAGAGGTTGC | 10517 |
rs764573852 | snp | C/T | 5.41257e-05 | 0.00520192 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744211 | TTGCCGTTGCAAGTG[C/T]GCAGGGCTAAAATGG | 10517 |
rs764661560 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18757212 | TTTTTCAGAGTGAAC[C/T]TCATTCTGTCGTCCA | 10517 |
rs764725786 | snp | A/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749865 | CTGTCTTCTGGGTTC[A/G]GCAAATACCGAGACT | 10517 |
rs764731483 | snp | A/G | 1.66624e-05 | 0.00288633 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748133 | TCAGCAAGAAAGCCA[A/G]TATGGGCTAGGTGCG | 10517 |
rs764739612 | snp | C/T | 3.91573e-05 | 0.00442461 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756184 | CAGAATCTGGGTCTC[C/T]AGGGATGCTTGAGTT | 10517 |
rs764875887 | snp | C/G | 4.96011e-05 | 0.00497977 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764908 | GAAGTTTCCCCCGAC[C/G]CACGGGTTACCAAAA | 10517 |
rs764881647 | snp | A/G | 2.4131e-05 | 0.00347346 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779265 | GCAAGGGAAAACAGC[A/G]GCCCCTGAACTTGGA | 10517 |
rs764972880 | snp | A/G | 3.31978e-05 | 0.00407404 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772667 | AGTACTCCTGAAGCC[A/G]GCCAAGTTCTCTTCA | 10517 |
rs765061605 | snp | C/T | 1.67393e-05 | 0.00289299 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775108 | GAAGTATATAATGAC[C/T]ACAGCTTCTTCCTCA | 10517 |
rs765077954 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769696 | ACAGGAGAATCGCTT[C/G]TATCTGGTAGGTGGG | 10517 |
rs765092613 | in-del | -/AAGAG | | | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18742996 | TTACGAAAAAAAAAA[-/AAGAG]CTACTTTTAGCTTGC | 10517 |
rs765119598 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18752197 | GTGGGCAGTAGCGGA[C/T]GGTGTGGCTGTCATG | 10517 |
rs765147247 | snp | A/G | 4.99738e-05 | 0.00499844 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766748 | GAAGTGCCTGAAGAC[A/G]TTTAGACACAAAGAC | 10517 |
rs765173017 | snp | C/T | 1.65941e-05 | 0.00288041 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778866 | CCAGTCCACCATACC[C/T]CAGCCCATGATTATC | 10517 |
rs765191686 | snp | A/G | 2.36549e-05 | 0.00343903 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750886 | GAGCCAAGAGAAGCC[A/G]TTTTCTGTTTTTATT | 10517 |
rs765225589 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744635 | GCGAACAGCACCCAG[C/T]GGACCAAGGCGAATT | 10517 |
rs765244687 | snp | C/T | 0.00013149 | 0.00810725 | intron-variant, nc-transcript-variant, stop-gained | FBXW10 | GRCh38.p7 | 17:18744785 | AGACTAGAGGGCCCC[C/T]GAAGACCAGAAGGCA | 10517 |
rs765251864 | snp | G/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772267 | CACCACTCTCCACCC[G/T]CCAGCTGCCTACACT | 10517 |
rs765268839 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770003 | ATCCGAATTTACAAT[C/T]TCCTCAACGGGAACT | 10517 |
rs765491085 | in-del | -/GAG | 1.95923e-05 | 0.00312982 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744731 | GTCCTGTTTCTGAGA[-/GAG]GAGAACAATATCTCA | 10517 |
rs765536462 | snp | C/T | 2.84629e-05 | 0.00377235 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758406 | TACAAGTGAAAGCGA[C/T]ACCCGTTGAATTCCG | 10517 |
rs765579388 | snp | A/G | | | | | GRCh38.p7 | 17:18740952 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 10517 |
rs765610933 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749807 | AACCAAGCCAGGGTA[C/T]GATCCCTGCAATCTA | 10517 |
rs765612082 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744297 | ATTTTCGTTGTGAGA[A/G]GGGAACCGATTCCAT | 10517 |
rs765632725 | snp | A/T | 2.77789e-05 | 0.00372675 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778455 | GCCGATTTTTTAAAA[A/T]TTTCTTTTTTTTGAA | 10517 |
rs765683588 | in-del | -/T | 3.30904e-05 | 0.00406744 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764760 | CTGGGATCTGAAAAG[-/T]GGGGTTTGCACACGA | 10517 |
rs765693813 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18752996 | CCAGTGTTTGACATT[C/G]TAGGAATGTTTTGAC | 10517 |
rs765718863 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18763627 | TCCTGTCTCAAAAGC[A/G]GCCTACCTGAAGCGG | 10517 |
rs765721109 | in-del | -/CC/TCCC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768007 | CTTTTATTTTTTCTT[-/CC/TCCC]TTCCTTCCTTCCTTC | 10517 |
rs765739140 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18761077 | CCTGCATTGATTTGA[A/G]GTGCTATCTTTATCA | 10517 |
rs765742103 | in-del | -/TTTTTAT | 0.000127451 | 0.0079818 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750900 | CATTTTCTGTTTTTA[-/TTTTTAT]TTTTTATTTTTTGTC | 10517 |
rs765811738 | snp | G/T | 6.58968e-05 | 0.00573969 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744360 | TAGCCTGGAAGATCT[G/T]CTCTACCAAAGAGTG | 10517 |
rs765943002 | snp | C/T | 8.33743e-05 | 0.00645602 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775119 | TGACTACAGCTTCTT[C/T]CTCAATCTCAATTTA | 10517 |
rs765980822 | snp | A/G | 1.80364e-05 | 0.00300298 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744204 | GGTGGCGTTGCCGTT[A/G]CAAGTGCGCAGGGCT | 10517 |
rs766060802 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775573 | ACTGTTATGTCATCA[A/G]TCTGAGAAATGGGCA | 10517 |
rs766106119 | snp | C/T | 3.3873e-05 | 0.00411526 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766775 | AGACCCCATCTTGGC[C/T]ACCAGGATCAATGAT | 10517 |
rs766200951 | snp | A/T | 7.02691e-05 | 0.00592703 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750912 | TTATTTTTATTTTTT[A/T]TTTTTTGTCTTTTTC | 10517 |
rs766201075 | snp | A/G | 0.000292886 | 0.0120978 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766878 | GTAAGTGGGCAGTGG[A/G]CTACCTTGGCGGAAA | 10517 |
rs766244795 | snp | A/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775578 | TATGTCATCAATCTG[A/T]GAAATGGGCACAATA | 10517 |
rs766293489 | snp | C/G | 1.68975e-05 | 0.00290662 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744792 | AGGGCCCCCGAAGAC[C/G]AGAAGGCAAGGCTTC | 10517 |
rs766381921 | snp | C/T | 3.47729e-05 | 0.00416956 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772379 | GTGGCCTCCACAGTC[C/T]TTTTGTGGACAACCC | 10517 |
rs766384103 | in-del | -/GT | 1.6549e-05 | 0.0028765 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18764864 | ATTGCCAGGTAAAAG[-/GT]GAGAAAGAAGTGCCT | 10517 |
rs766487517 | snp | A/G | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749883 | AAATACCGAGACTTC[A/G]TCCGTTACCTGCCCA | 10517 |
rs766590138 | snp | C/T | 4.95413e-05 | 0.00497677 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764735 | TCTTTTGGCCTGATT[C/T]CTGCAGATACTGGGA | 10517 |
rs766657219 | snp | C/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772158 | TTTGACTTGAGAAGT[C/G]AAACAATCGGAACAT | 10517 |
rs766680128 | snp | C/G | 1.66427e-05 | 0.00288462 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18749980 | CTTGGCCCAGTTCTG[C/G]GGTTTCTGGGTCCAT | 10517 |
rs766712663 | snp | A/G | 1.76412e-05 | 0.0029699 | synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778545 | GCCCAGTCACCCAAA[A/G]AAAAAGTCTTGGAAA | 10517 |
rs766775413 | snp | A/G | 1.71475e-05 | 0.00292805 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768687 | CCCAAGTAGGTGCCT[A/G]TGAAGCCCGGAGCGA | 10517 |
rs766798493 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768605 | CCTCTCAGGAAGTAC[C/T]GATGGCCTGGTCATG | 10517 |
rs766956821 | snp | A/G | | | intron-variant, missense, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775426 | GCCTGGCTTCTCCCA[A/G]GAGTGACTGGTTTTC | 10517 |
rs766966483 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766310 | TATGCCATGATTTTC[-/T]TTTTTTTTTTTTAAT | 10517 |
rs767042398 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768569 | AGCCGTGAAATGCCT[A/G]TTCTTTGACCAGTGG | 10517 |
rs767063943 | snp | A/G | 1.75277e-05 | 0.00296033 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744269 | CTGGAATCAAGGCTC[A/G]AGAATGCCCCCTATT | 10517 |
rs767072423 | snp | C/T | 5.80647e-05 | 0.00538785 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766888 | AGTGGGCTACCTTGG[C/T]GGAAAGGGCACTGGG | 10517 |
rs767128309 | snp | C/G | 1.64895e-05 | 0.00287132 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751067 | AGGTGGGTTCCAACA[C/G]CATCTGGGGCAAGTA | 10517 |
rs767154850 | snp | C/G | 2.05042e-05 | 0.00320182 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779013 | GCTAGCTCCACAAGT[C/G]GGCACAGCCACCCTG | 10517 |
rs767164305 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751015 | GATGACGGGAAGAGC[A/G]TGCGTGTGAAACATC | 10517 |
rs767186893 | in-del | -/T | 1.6517e-05 | 0.00287372 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764737 | TTTTGGCCTGATTCC[-/T]GCAGATACTGGGATC | 10517 |
rs767330910 | snp | C/T | 1.72065e-05 | 0.00293308 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772394 | CTTTTGTGGACAACC[C/T]TGTTGTTTCGGTTCC | 10517 |
rs767437618 | snp | A/G | 1.66236e-05 | 0.00288297 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747961 | AATCAAGACATCACA[A/G]ATGTGTGTTTTTCCC | 10517 |
rs767505981 | snp | C/G | 1.65858e-05 | 0.00287969 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18749989 | GTTCTGGGGTTTCTG[C/G]GTCCATCTTTTTTTT | 10517 |
rs767506616 | snp | G/T | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764760 | CTGGGATCTGAAAAG[G/T]GGGGTTTGCACACGA | 10517 |
rs767509205 | snp | A/G | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748088 | ATGAACACTTGCTTG[A/G]GGCAGCATCTAACCC | 10517 |
rs767594821 | snp | A/G | 4.96167e-05 | 0.00498055 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764891 | TGCCTTAAATTTTCT[A/G]AGAAGTTTCCCCCGA | 10517 |
rs767659270 | in-del | -/CA | 1.66333e-05 | 0.00288381 | frameshift-variant, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778837 | TTGAAGATCTCTTTG[-/CA]CAGTCCTAGAGTCCA | 10517 |
rs767736420 | snp | C/T | 3.48724e-05 | 0.00417552 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750075 | TGGGCCGCCATGGCT[C/T]AACAGGTCAAGATGG | 10517 |
rs767794604 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769937 | TCCAGGGAGGTGCTC[A/G]ACGTGTCCCTTCTCT | 10517 |
rs767824789 | snp | C/T | 4.94662e-05 | 0.00497299 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744515 | ATCTATAACAGGTCC[C/T]GGATCAACCTCAGCA | 10517 |
rs767836752 | snp | A/G | 1.65531e-05 | 0.00287686 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778625 | ACGCCCATAATTCCG[A/G]GGAATTTGCCTATCC | 10517 |
rs767853916 | snp | A/G | 5.20386e-05 | 0.00510065 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768696 | GTGCCTGTGAAGCCC[A/G]GAGCGATGAACCTGG | 10517 |
rs767878650 | snp | A/T | 2.1852e-05 | 0.00330537 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756206 | GCTTGAGTTACCCAC[A/T]CTGACATTTGGGATT | 10517 |
rs767909348 | snp | A/G | 4.01381e-05 | 0.00447967 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779328 | ATTACAATGTTTTAC[A/G]ATAAACAGAAAGCCA | 10517 |
rs767922842 | snp | A/T | 1.69853e-05 | 0.00291416 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778742 | TCCAACGTGCAGTTG[A/T]TCGGTTGAGATTGAG | 10517 |
rs768040976 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18753060 | ATCTTGGACAAACAC[C/T]GCCACTTTAAGTTCC | 10517 |
rs768125463 | snp | C/T | 3.08295e-05 | 0.00392604 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758393 | CTTCTGGACATCATA[C/T]AAGTGAAAGCGATAC | 10517 |
rs768136371 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18767334 | AAATACAAAAAATTA[G/T]CCGGGCATGGTGGTG | 10517 |
rs768267575 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769905 | GAGGATGGGTACTGC[C/T]TGCTACTCTGTTCCC | 10517 |
rs768340726 | snp | A/G | 0.000196502 | 0.00991022 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758340 | TCCACTATTCCGGGG[A/G]AGATCTGATAGCTGT | 10517 |
rs768357383 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769964 | CTCTTCCTCCGGGTC[A/G]TCAGCGCCTGTGCAG | 10517 |
rs768357844 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744590 | GATAAAACAGTAGAA[C/G]AGAAGATGAAAGAGA | 10517 |
rs768457127 | snp | A/G | 1.67691e-05 | 0.00289556 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775102 | CTAATCGAAGTATAT[A/G]ATGACTACAGCTTCT | 10517 |
rs768482194 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751591 | GTGGATTGATTTGGT[C/T]GTCCTCTCAGGGTTC | 10517 |
rs768710089 | snp | C/T | 4.98691e-05 | 0.0049932 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775211 | AGAAGAGAGTTTATT[C/T]TGTTCATAAGGGAAC | 10517 |
rs768750926 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751170 | TCACGGCAGGTGACA[A/C]TCCTTAAGGAAGACG | 10517 |
rs768795815 | snp | C/T | 1.79512e-05 | 0.00299588 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766838 | GGTGAAAGTGTGGCA[C/T]ATTGCCATGGCCCAG | 10517 |
rs768828168 | snp | A/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750957 | AAGAGGAATTGATCC[A/T]AATTATGCCAATAAG | 10517 |
rs768905724 | snp | G/T | 0.000155123 | 0.00880553 | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744779 | AGGCAGAGACTAGAG[G/T]GCCCCCGAAGACCAG | 10517 |
rs768995518 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747892 | CCACCTCATTTTCCT[C/T]AACACACCCGCTTCA | 10517 |
rs769088495 | snp | C/G/T | 4.07102e-05 | 0.00451151 | missense, synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779055 | AGAACGGCCTCGCAT[C/G/T]TATACAGCCCTTGAT | 10517 |
rs769168829 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770093 | GGCAACAGGTGGGTG[G/T]TAGGTGTGGAGGTCA | 10517 |
rs769199343 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769974 | GGGTCATCAGCGCCT[A/G]TGCAGATGGCAAGAT | 10517 |
rs769255040 | snp | C/T | 4.94254e-05 | 0.00497094 | missense, nc-transcript-variant, stop-lost | FBXW10 | GRCh38.p7 | 17:18772462 | TCCAGTTTGAGCACA[C/T]AAAGTGGCAGTATGC | 10517 |
rs769394464 | snp | C/T | 7.31823e-05 | 0.00604862 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758365 | AGCTGTGTCATCTAA[C/T]CGAAAGATCCATCTT | 10517 |
rs769409249 | snp | A/G | | | | | GRCh38.p7 | 17:18740800 | GAGTCTCACTCTGTC[A/G]CCTAGGCTGGAGTGC | 10517 |
rs769478058 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749767 | TATCCGAAATGAATA[C/G]GCTGTTTTCTGGAAA | 10517 |
rs769484259 | snp | A/G | 4.93364e-05 | 0.00496647 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758442 | ATGCTGGGAGTGTCC[A/G]GGCCCTCTTCCTGTG | 10517 |
rs769542638 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759450 | CATATTTTAAAAATT[C/T]GTTGGTACCTCATTC | 10517 |
rs769553087 | snp | A/C | 1.78707e-05 | 0.00298915 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744250 | TCTTAGGATCATGGA[A/C]AACCTGGAATCAAGG | 10517 |
rs769617817 | snp | C/T | 3.58886e-05 | 0.00423592 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744200 | GTTTGGTGGCGTTGC[C/T]GTTGCAAGTGCGCAG | 10517 |
rs769661808 | in-del | -/C | 9.98153e-05 | 0.00706383 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758317 | CAGGTGGGATCAAAA[-/C]CGAGTCATCCACTAT | 10517 |
rs769736616 | snp | A/G | 1.67091e-05 | 0.00289038 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775236 | GGGAACAAGTGGCAC[A/G]GATGGTGGGCAGGAG | 10517 |
rs769755483 | in-del | -/AG | 5.80872e-05 | 0.0053889 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744851 | ACAACATAGGTAGAC[-/AG]AGATTGCACAGAACT | 10517 |
rs769796646 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744336 | GCCGGAAGTGTGAGA[C/T]GTGTGTCTTAGCCTG | 10517 |
rs769858176 | snp | A/G | 3.59357e-05 | 0.0042387 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756015 | TTTGAAGTTACCACT[A/G]AGCTTTAACTTCAAA | 10517 |
rs769908640 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768541 | TCTTGCAGACTCTCA[A/G]TGGCCATGAGGGAGC | 10517 |
rs769951813 | snp | C/T | 2.03593e-05 | 0.00319049 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778987 | ATGCAGGTCATTAAA[C/T]CAAACCGCATGCTAG | 10517 |
rs769960878 | snp | C/T | 4.94972e-05 | 0.00497455 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748048 | ACTCAGCACACATCC[C/T]TTCCTTTGTCCAAAG | 10517 |
rs769976547 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747148 | AGCCCGGATGGTCTC[C/T]ATCTCCTGACCTTGT | 10517 |
rs769981277 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772473 | CACATAAAGTGGCAG[C/T]ATGCCGTGGAAAAAA | 10517 |
rs769985306 | snp | A/G | 8.15228e-05 | 0.00638395 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779059 | CGGCCTCGCATCTAT[A/G]CAGCCCTTGATCCTT | 10517 |
rs770017471 | snp | C/G | 3.29946e-05 | 0.00406155 | intron-variant | FBXW10 | GRCh38.p7 | 17:18747930 | CCTTGTCTTGGTCTT[C/G]TGTGTTTCAGGGCTC | 10517 |
rs770069929 | snp | C/G | 1.64953e-05 | 0.00287182 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764713 | GGGCCCTCAGGAACT[C/G]TCACATTCTTTTGGC | 10517 |
rs770119093 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766453 | GGGCCTCAAGGCTAA[C/G]TTCCAGGGCCATAGC | 10517 |
rs770158814 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774831 | ACAAAAAACCAATAA[C/T]GTATTGTATATTTCA | 10517 |
rs770209628 | snp | G/T | 3.29587e-05 | 0.00405934 | stop-gained, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772587 | GTTCACAGCCCAAGA[G/T]AGTCTGTATCCAGTA | 10517 |
rs770297146 | snp | C/T | 4.96989e-05 | 0.00498467 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764832 | GTGTAAGAACAGGCT[C/T]GTATCTGGAGGAAGA | 10517 |
rs770473344 | snp | A/C | 1.72567e-05 | 0.00293735 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750058 | CCTCTGTGAGCCAGC[A/C]CTGGGCCGCCATGGC | 10517 |
rs770529003 | in-del | -/T | 1.65315e-05 | 0.00287498 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758499 | GAGCTATGACCTAAG[-/T]TATCAGGTGAGGAGT | 10517 |
rs770535291 | snp | C/G | 0.000115406 | 0.00759537 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749850 | GATGACATCAGAGAC[C/G]TGTCTTCTGGGTTCA | 10517 |
rs770579718 | in-del | -/GAT | 1.68182e-05 | 0.00289979 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18772412 | TTGTTTCGGTTCCAG[-/GAT]GGTGGTCAACACAGA | 10517 |
rs770621487 | snp | A/C/G | 3.5557e-05 | 0.00421633 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744261 | TGGAAAACCTGGAAT[A/C/G]AAGGCTCAAGAATGC | 10517 |
rs770623649 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18769694 | AGACAGGAGAATCGC[-/T]TGTATCTGGTAGGTG | 10517 |
rs770652948 | snp | G/T | 1.65938e-05 | 0.00288039 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749918 | CCTCTCCAAGTACAT[G/T]CTAAGTATGCTGGGG | 10517 |
rs770821544 | snp | A/G | | | | | GRCh38.p7 | 17:18739708 | AATTTTAACCACCAC[A/G]TCCATAATTTATTCT | 10517 |
rs770862147 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768552 | CTCAGTGGCCATGAG[C/G]GAGCCGTGAAATGCC | 10517 |
rs770947926 | snp | C/T | 3.30044e-05 | 0.00406216 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768644 | CATGGTGGGGAAGTA[C/T]GAGCGCTGCCTGATG | 10517 |
rs770949713 | snp | G/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751053 | GAAGCTGAGAACGAA[G/T]GTGGGTTCCAACAGC | 10517 |
rs771017904 | snp | A/G | 3.7372e-05 | 0.00432257 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779218 | GCATGGATCAGGAAG[A/G]TCAAAGGCCTGCCTA | 10517 |
rs771033031 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748072 | TCCAAAGCCCCAGAA[A/C]ATGAACACTTGCTTG | 10517 |
rs771034619 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773873 | TTGAGGGCAGCATCC[A/C]GGGACACAGGGGCAC | 10517 |
rs771037943 | snp | A/G | 3.74188e-05 | 0.00432528 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756046 | TATTCCCTTGTTAGA[A/G]TGAGTACAACCTGTG | 10517 |
rs771093921 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747296 | TTGGGCGCAGTGGCT[C/T]ACGCTTGTAATCCCA | 10517 |
rs771107608 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772599 | AGAGAGTCTGTATCC[A/G]GTAAACAAACTGTGA | 10517 |
rs771108861 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774516 | CAATAATGTATAGCC[A/G]GGCGCAGTGACTCAT | 10517 |
rs771116274 | snp | A/T | 0.000115839 | 0.00760962 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764858 | GAAGAGATTGCCAGG[A/T]AAAAGGTGAGAAAGA | 10517 |
rs771199945 | snp | C/T | 3.50656e-05 | 0.00418707 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772723 | TTCAGTGATAACCCA[C/T]AGAGCAGGTCGGGGT | 10517 |
rs771406499 | snp | C/T | 8.46489e-05 | 0.00650517 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778796 | GAACCAGTATTCCCC[C/T]TGAAATCCAGAAACT | 10517 |
rs771417449 | snp | A/T | 1.78318e-05 | 0.0029859 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750111 | TCAGCGCACGGCTTC[A/T]TTCAGAACCAGATTA | 10517 |
rs771494320 | snp | A/G | 1.66407e-05 | 0.00288446 | intron-variant, synonymous-codon | FBXW10 | GRCh38.p7 | 17:18749933 | TCTAAGTATGCTGGG[A/G]TGTATGAGGGGATTT | 10517 |
rs771525026 | in-del | -/CT | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18747688 | AATTCCTGACCTCGA[-/CT]CTCTCTCTCTCTCTG | 10517 |
rs771568445 | in-del | -/T | 2.45161e-05 | 0.00350106 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779290 | CTTGGACAAAATGTA[-/T]TTATCTAAACCAGCC | 10517 |
rs771599192 | in-del | -/AA | | | | | GRCh38.p7 | 17:18739580 | CCATTATGTAGACTT[-/AA]ACAAAAAAAAAAAAA | 10517 |
rs771707792 | snp | C/T | 0.00010154 | 0.00712458 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750041 | CACCCTGAACAAGTG[C/T]GCCTCTGTGAGCCAG | 10517 |
rs771780376 | snp | C/T | 1.7029e-05 | 0.00291791 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778678 | ACTGATGTCTGGGGA[C/T]CTTCAATTTCATACC | 10517 |
rs771780713 | snp | C/T | 0.000100252 | 0.00707927 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769880 | ACAAACAAACCCAGG[C/T]ATTTTACGAGAGGAT | 10517 |
rs771803969 | snp | A/C | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744455 | AGCTTATATTTGTTA[A/C]ACTATTTCCAAAATA | 10517 |
rs771826360 | snp | C/G | 1.65803e-05 | 0.00287922 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768656 | GTACGAGCGCTGCCT[C/G]ATGGCCTTCAAGCAT | 10517 |
rs771879072 | snp | C/G/T | 6.96959e-05 | 0.00590287 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779246 | CTATTGATAATTTCA[C/G/T]GAAGCAAGGGAAAAC | 10517 |
rs771918107 | snp | C/G | 6.8451e-05 | 0.00584985 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756059 | GAATGAGTACAACCT[C/G]TGGACTGCATACCAG | 10517 |
rs771968862 | snp | A/G | 3.29766e-05 | 0.00406045 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772633 | AAGAGCTCCTACCAG[A/G]CAAACCTCCCAAGTC | 10517 |
rs771979100 | snp | G/T | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772099 | GTGACAGAGCGAGAC[G/T]CCTTCTCAAAATAAA | 10517 |
rs772029466 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776401 | GGACATTGGTAAAAA[C/T]TTAAAATGTCTTTCA | 10517 |
rs772172387 | snp | A/G | 1.65534e-05 | 0.00287688 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749681 | CCTGGAGTTTCTACA[A/G]AGCCAACTCAACCAC | 10517 |
rs772178881 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770597 | GTGAGCCACCACGCC[C/T]GGCCTGTTTTGACTC | 10517 |
rs772238272 | snp | A/T | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766720 | CCTGTTCAGTATGGG[A/T]TGTAGACACAGGGAA | 10517 |
rs772264031 | snp | A/G | 8.23757e-05 | 0.00641725 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749746 | GGAGGAATTCACTCC[A/G]GTGTATATCCGAAAT | 10517 |
rs772287091 | in-del | -/A | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18753876 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAGAA | 10517 |
rs772319592 | in-del | -/T | 8.39835e-05 | 0.00647956 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744281 | CTCAAGAATGCCCCC[-/T]ATTTTCGTTGTGAGA | 10517 |
rs772325828 | snp | A/G | 5.5829e-05 | 0.00528312 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750149 | GCAGGTACTTCCTGC[A/G]AGTCTGAAAGGGGAA | 10517 |
rs772332798 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744621 | TCTTGTACTGGTTTG[C/T]GAACAGCACCCAGTG | 10517 |
rs772340479 | snp | A/C/G | 3.49774e-05 | 0.00418183 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766820 | CAGCTGTGAGCGAGG[A/C/G]CTGGTGAAAGTGTGG | 10517 |
rs772433848 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750952 | TACACAAGAGGAATT[C/G]ATCCTAATTATGCCA | 10517 |
rs772489152 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774487 | TGGTTGCACGGTAGG[A/G]TGACTACAATTAACA | 10517 |
rs772543220 | snp | C/G | | | upstream-variant-2KB | FBXW10 | GRCh38.p7 | 17:18743040 | TAGGGTAACGTGCTC[C/G]CCTTACAGATCCAAA | 10517 |
rs772587385 | snp | C/G | 1.67399e-05 | 0.00289304 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778821 | GAAACTGCAGCCCAA[C/G]TTGAAGATCTCTTTG | 10517 |
rs772587885 | snp | A/G | 2.22427e-05 | 0.0033348 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744743 | AGAGAGGAGAACAAT[A/G]TCTCAGGTAAACAAG | 10517 |
rs772588045 | in-del | -/AT | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18757077 | TATACACACACACAT[-/AT]ATATATATACACATA | 10517 |
rs772596321 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769982 | AGCGCCTGTGCAGAT[A/G]GCAAGATCCGAATTT | 10517 |
rs772660060 | snp | A/T | 6.23746e-05 | 0.00558421 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756199 | TAGGGATGCTTGAGT[A/T]ACCCACACTGACATT | 10517 |
rs772666896 | in-del | -/CT | 5.01274e-05 | 0.00500612 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747977 | ATGTGTGTTTTTCCC[-/CT]GAGAAAGACCACAGC | 10517 |
rs772729001 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769977 | TCATCAGCGCCTGTG[C/G]AGATGGCAAGATCCG | 10517 |
rs772747993 | snp | C/T | 0.000145767 | 0.00853595 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758366 | GCTGTGTCATCTAAT[C/T]GAAAGATCCATCTTC | 10517 |
rs772761166 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770064 | GTGATCCTGTGCTGT[A/C]CTTCTTTATTCAGGG | 10517 |
rs772826093 | snp | A/G | 3.59538e-05 | 0.00423976 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744201 | TTTGGTGGCGTTGCC[A/G]TTGCAAGTGCGCAGG | 10517 |
rs772848370 | snp | A/C/G/T | 6.58898e-05 | 0.00573948 | synonymous-codon, missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749768 | ATCCGAAATGAATAG[A/C/G/T]CTGTTTTCTGGAAAA | 10517 |
rs772936873 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749840 | GGTTGACCTGGATGA[C/T]ATCAGAGACCTGTCT | 10517 |
rs772967550 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18763025 | GCTCTGAGAAACTGG[-/T]TAAGGCATTGGTAAG | 10517 |
rs773099096 | snp | G/T | 5.76984e-05 | 0.00537084 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778430 | ACGTACTTAATATTT[G/T]TCATAGAACGCCGAT | 10517 |
rs773105903 | snp | A/C/G | 6.5908e-05 | 0.00574023 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751050 | GTGGAAGCTGAGAAC[A/C/G]AAGGTGGGTTCCAAC | 10517 |
rs773127975 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773846 | CTAAAAGAGTTTACC[C/G]GAGTGCAAAGTTTGA | 10517 |
rs773167803 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759651 | GGAGTCTCACTGTGT[C/T]ACCCAGGCTGGAGAG | 10517 |
rs773188970 | snp | A/G | 1.87644e-05 | 0.00306298 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18766863 | GCCCAGTTGGTAAAG[A/G]TAAGTGGGCAGTGGG | 10517 |
rs773189502 | snp | A/G | 1.65201e-05 | 0.00287398 | splice-acceptor-variant | FBXW10 | GRCh38.p7 | 17:18747939 | GGTCTTCTGTGTTTC[A/G]GGGCTCAATCAAGAC | 10517 |
rs773196325 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750979 | GCCAATAAGGTTTCT[A/G]TCCCAGTTCCTAAAA | 10517 |
rs773224164 | snp | C/T | 3.50091e-05 | 0.0041837 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772362 | CTGCAGTGCATCTTT[C/T]GGTGGCCTCCACAGT | 10517 |
rs773249720 | snp | C/G | 1.65203e-05 | 0.002874 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778992 | GGTCATTAAACCAAA[C/G]CGCATGCTAGCTCCA | 10517 |
rs773277201 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768547 | AGACTCTCAGTGGCC[A/G]TGAGGGAGCCGTGAA | 10517 |
rs773342278 | snp | A/T | 2.03776e-05 | 0.00319192 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779061 | GCCTCGCATCTATAC[A/T]GCCCTTGATCCTTTT | 10517 |
rs773355954 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772126 | TAAAAAAATAAAAAT[A/G]AAAAATAAAAAAGCA | 10517 |
rs773488351 | snp | A/G | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764833 | TGTAAGAACAGGCTC[A/G]TATCTGGAGGAAGAG | 10517 |
rs773609087 | snp | A/G | 1.65405e-05 | 0.00287576 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778612 | AGCGCCCTGCAGCAC[A/G]CCCATAATTCCGGGG | 10517 |
rs773630301 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18758521 | GTGAGGAGTCCAAAG[A/G]CATCATGATCCCTGT | 10517 |
rs773672287 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749777 | GAATAGGCTGTTTTC[C/T]GGAAAAGGAGACATA | 10517 |
rs773718297 | in-del | -/TTTG | 1.65976e-05 | 0.00288072 | frameshift-variant, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18775159 | TAGAGGAACTTCAAA[-/TTTG]GTCAAGGAAAGTCAA | 10517 |
rs773751826 | snp | C/T | 1.66771e-05 | 0.00288761 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18749971 | ACCTCCCCTCTTGGC[C/T]CAGTTCTGGGGTTTC | 10517 |
rs773803327 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766937 | CCCCTACCTAGCTCC[C/T]CAGGTCATCCTAGAG | 10517 |
rs773841637 | snp | C/T | 6.98422e-05 | 0.00590899 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750060 | TCTGTGAGCCAGCAC[C/T]GGGCCGCCATGGCTC | 10517 |
rs773849873 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744363 | CCTGGAAGATCTTCT[C/T]TACCAAAGAGTGGTT | 10517 |
rs773850660 | snp | C/G | 1.76983e-05 | 0.0029747 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758465 | TTCCTGTGTGAGGAG[C/G]AAAACTTTCTCCTAA | 10517 |
rs773866777 | snp | G/T | 8.3053e-05 | 0.00644357 | splice-donor-variant, missense | FBXW10 | GRCh38.p7 | 17:18749924 | CAAGTACATTCTAAG[G/T]ATGCTGGGGTGTATG | 10517 |
rs773879085 | snp | G/T | 1.74239e-05 | 0.00295155 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778511 | AAAAACAAGGACAAT[G/T]GGAAACTCCTGGAAA | 10517 |
rs773938679 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749854 | ACATCAGAGACCTGT[C/T]TTCTGGGTTCAGCAA | 10517 |
rs773965324 | snp | C/T | 0.000327999 | 0.012802 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778442 | TTTTTCATAGAACGC[C/T]GATTTTTTAAAATTT | 10517 |
rs774063948 | in-del | -/G | 3.35464e-05 | 0.00409537 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18772415 | TTTCGGTTCCAGGAT[-/G]GTGGTCAACACAGAG | 10517 |
rs774102601 | in-del | -/T | 0.000253398 | 0.0112532 | intron-variant, frameshift-variant | FBXW10 | GRCh38.p7 | 17:18749997 | GTTTCTGGGTCCATC[-/T]TTTTTTTTCCAGGAA | 10517 |
rs774122950 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18756856 | TTTTGGCCATGAATC[C/T]TATTAACAAATTGCA | 10517 |
rs774127786 | in-del | -/AA | 0.00301037 | 0.0386797 | frameshift-variant, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779038 | ACCCTGTCTCTTAAG[-/AA]AGAACGGCCTCGCAT | 10517 |
rs774151800 | in-del | -/G | 3.29881e-05 | 0.00406115 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764707 | TCCTCTGGGCCCTCA[-/G]GAACTCTCACATTCT | 10517 |
rs774252765 | snp | C/T | 4.49964e-05 | 0.00474301 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779234 | TCAAAGGCCTGCCTA[C/T]TGATAATTTCACGAA | 10517 |
rs774324143 | snp | A/C | 1.64836e-05 | 0.0028708 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751062 | AACGAAGGTGGGTTC[A/C]AACAGCATCTGGGGC | 10517 |
rs774356318 | snp | G/T | 4.13882e-05 | 0.00454889 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779092 | AGAGTGAACACTGAG[G/T]TCGTGCTGTTGACCG | 10517 |
rs774413740 | snp | C/T | 1.78379e-05 | 0.00298641 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756051 | CCTTGTTAGAATGAG[C/T]ACAACCTGTGGACTG | 10517 |
rs774428326 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18747948 | TGTTTCAGGGCTCAA[C/T]CAAGACATCACAGAT | 10517 |
rs774459802 | snp | A/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772601 | AGAGTCTGTATCCAG[A/T]AAACAAACTGTGATC | 10517 |
rs774518194 | snp | C/T | 0.000115362 | 0.00759393 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748074 | CAAAGCCCCAGAAAA[C/T]GAACACTTGCTTGGG | 10517 |
rs774549138 | snp | A/G | 1.65485e-05 | 0.00287645 | splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18764864 | ATTGCCAGGTAAAAG[A/G]TGAGAAAGAAGTGCC | 10517 |
rs774562596 | in-del | -/TA | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759476 | ATTCTTACATGGAAC[-/TA]TGTTTTTGAGATTCA | 10517 |
rs774634144 | snp | C/T | 1.70113e-05 | 0.00291639 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778732 | GGAAAATCAATCCAA[C/T]GTGCAGTTGATCGGT | 10517 |
rs774635369 | snp | C/T | 3.32077e-05 | 0.00407465 | intron-variant | FBXW10 | GRCh38.p7 | 17:18766701 | TGTCTTCCTCTCTCT[C/T]CCTCCTGTTCAGTAT | 10517 |
rs774691557 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744614 | AAAGAGATCTTGTAC[C/T]GGTTTGCGAACAGCA | 10517 |
rs774900818 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18772015 | AAGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 10517 |
rs774939642 | snp | C/G | 8.73019e-05 | 0.00660631 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778520 | GACAATTGGAAACTC[C/G]TGGAAAACTGCCCAG | 10517 |
rs774975314 | snp | A/G | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744456 | GCTTATATTTGTTAC[A/G]CTATTTCCAAAATAT | 10517 |
rs775014083 | snp | G/T | 1.66189e-05 | 0.00288256 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768659 | CGAGCGCTGCCTGAT[G/T]GCCTTCAAGCATCCC | 10517 |
rs775041774 | snp | C/T | 6.61759e-05 | 0.00575183 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778604 | TGACTGTTAGCGCCC[C/T]GCAGCACGCCCATAA | 10517 |
rs775075540 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759958 | GAATGCTGCCAGAGA[C/T]GGGTCTTGGATGTGT | 10517 |
rs775087357 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744355 | TGTCTTAGCCTGGAA[A/G]ATCTTCTCTACCAAA | 10517 |
rs775126333 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768587 | CTTTGACCAGTGGCA[C/T]CTCCTCTCAGGAAGT | 10517 |
rs775158775 | in-del | -/TAAGTG | 1.64781e-05 | 0.00287033 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18772556 | CATGGAAATTCTCTC[-/TAAGTG]TAATATTCAGGTTCA | 10517 |
rs775189504 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18762228 | CGGCCTCCCAAAGTG[C/T]TGGGATTACTGGCGT | 10517 |
rs775310713 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769886 | AAACCCAGGCATTTT[A/G]CGAGAGGATGGGTAC | 10517 |
rs775381414 | snp | A/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774840 | CAATAATGTATTGTA[A/T]ATTTCAAAATAGCTA | 10517 |
rs775450140 | in-del | -/A | 3.30775e-05 | 0.00406665 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764890 | TGCCTTAAATTTTCT[-/A]AAGAAGTTTCCCCCG | 10517 |
rs775496250 | snp | A/G | 4.96093e-05 | 0.00498018 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764894 | CTTAAATTTTCTAAG[A/G]AGTTTCCCCCGACCC | 10517 |
rs775561183 | snp | C/T | 1.65501e-05 | 0.00287659 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749685 | GAGTTTCTACAGAGC[C/T]AACTCAACCACGTAC | 10517 |
rs775598490 | snp | A/G | 1.65847e-05 | 0.0028796 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766724 | TTCAGTATGGGATGT[A/G]GACACAGGGAAGTGC | 10517 |
rs775647144 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774583 | TGGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA | 10517 |
rs775688571 | snp | A/G | 1.86118e-05 | 0.0030505 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750150 | CAGGTACTTCCTGCA[A/G]GTCTGAAAGGGGAAT | 10517 |
rs775778020 | snp | A/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750953 | ACACAAGAGGAATTG[A/T]TCCTAATTATGCCAA | 10517 |
rs775852531 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744622 | CTTGTACTGGTTTGC[A/G]AACAGCACCCAGTGG | 10517 |
rs775852762 | snp | G/T | 3.03219e-05 | 0.00389359 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758396 | CTGGACATCATACAA[G/T]TGAAAGCGATACCCG | 10517 |
rs775957475 | snp | C/T | 1.66197e-05 | 0.00288263 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778839 | GAAGATCTCTTTGCA[C/T]AGTCCTAGAGTCCAG | 10517 |
rs776043297 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769990 | TGCAGATGGCAAGAT[C/T]CGAATTTACAATTTC | 10517 |
rs776045350 | snp | A/C/G/T | 0.000142611 | 0.00844332 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778967 | GTACGGGTCCCCTGA[A/C/G/T]CAGTATGCAGGTCAT | 10517 |
rs776078947 | snp | G/T | 1.70699e-05 | 0.00292142 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768683 | GCATCCCAAGTAGGT[G/T]CCTGTGAAGCCCGGA | 10517 |
rs776133597 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770067 | ATCCTGTGCTGTCCT[C/T]CTTTATTCAGGGCAA | 10517 |
rs776168798 | snp | C/G | 1.6513e-05 | 0.00287336 | intron-variant | FBXW10 | GRCh38.p7 | 17:18769918 | GCCTGCTACTCTGTT[C/G]CCTTCCAGGGAGGTG | 10517 |
rs776183385 | in-del | -/T | | | | | GRCh38.p7 | 17:18740769 | TTAAATTTTTTTTTC[-/T]TTTTTTTTTGAGACG | 10517 |
rs776221289 | snp | C/T | 0.000828349 | 0.0203344 | intron-variant | FBXW10 | GRCh38.p7 | 17:18749696 | GAGCCAACTCAACCA[C/T]GTACCTTTCTCTGGC | 10517 |
rs776223797 | snp | C/T | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744461 | TATTTGTTACACTAT[C/T]TCCAAAATATCCTTC | 10517 |
rs776261775 | snp | A/G | 0.000152923 | 0.00874288 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756167 | CACGTAGGTACTGGG[A/G]TCAGAATCTGGGTCT | 10517 |
rs776353995 | snp | A/G | 4.13232e-05 | 0.00454531 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758351 | GGGGGAGATCTGATA[A/G]CTGTGTCATCTAATC | 10517 |
rs776445674 | snp | C/G | 2.33828e-05 | 0.00341919 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779250 | TGATAATTTCACGAA[C/G]CAAGGGAAAACAGCG | 10517 |
rs776524391 | snp | C/T | 3.59544e-05 | 0.0042398 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766840 | TGAAAGTGTGGCACA[C/T]TGCCATGGCCCAGTT | 10517 |
rs776527900 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771147 | GGCCATTTTTTACTC[A/G]CAGCATCCAAAGAAA | 10517 |
rs776529830 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751685 | TTCAGAGGCCAGGAG[C/T]AACCCCATCAGCCCA | 10517 |
rs776627302 | snp | A/G | 1.67646e-05 | 0.00289517 | intron-variant | FBXW10 | GRCh38.p7 | 17:18775103 | TAATCGAAGTATATA[A/G]TGACTACAGCTTCTT | 10517 |
rs776639243 | snp | C/T | 1.66258e-05 | 0.00288316 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766741 | ACACAGGGAAGTGCC[C/T]GAAGACGTTTAGACA | 10517 |
rs776718779 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775232 | ATAAGGGAACAAGTG[A/G]CACGGATGGTGGGCA | 10517 |
rs776725881 | snp | G/T | 0.00021311 | 0.0103204 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750172 | AAGGGGAATGTCTGA[G/T]ACCAGCTTCATTTTC | 10517 |
rs776828221 | snp | A/G | | | intron-variant, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18744780 | GGCAGAGACTAGAGG[A/G]CCCCCGAAGACCAGA | 10517 |
rs776854482 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774652 | TACAAAAAAATTAGC[C/T]GGTGTGGTGGCGCAT | 10517 |
rs776926279 | snp | C/T | 2.03863e-05 | 0.00319261 | synonymous-codon, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778968 | TACGGGTCCCCTGAC[C/T]AGTATGCAGGTCATT | 10517 |
rs776929448 | in-del | -/ACTGGGATCTG | 3.30398e-05 | 0.00406434 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764744 | CTGATTCCTGCAGAT[-/ACTGGGATCTG]AAAAGTGGGGTTTGC | 10517 |
rs776987029 | snp | C/T | 3.30077e-05 | 0.00406236 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749874 | GGGTTCAGCAAATAC[C/T]GAGACTTCATCCGTT | 10517 |
rs776987447 | in-del | -/CTCC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768010 | TTATTTTTTCTTTTC[-/CTCC]CTTCCTTCCTTCCTT | 10517 |
rs777050740 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773882 | GCATCCAGGGACACA[A/G]GGGCACCAAAGACTA | 10517 |
rs777084970 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751029 | CATGCGTGTGAAACA[C/T]CCGAAGTGGAAGCTG | 10517 |
rs777087025 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18772748 | CGGGGTTTGGTGGGG[A/G]TGGTGGGAGACGGGG | 10517 |
rs777099746 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | FBXW10 | GRCh38.p7 | 17:18770109 | TAGGTGTGGAGGTCA[A/G]AACTGTGAGTGATTC | 10517 |
rs777149022 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18752844 | AGCTCTCCCAGCCAG[C/T]TGAGTGAAAGAGGCA | 10517 |
rs777174863 | snp | A/G | 1.67953e-05 | 0.00289782 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744863 | GACAGAGATTGCACA[A/G]AACTCAGCATAGGTT | 10517 |
rs777274994 | snp | A/G | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758444 | GCTGGGAGTGTCCGG[A/G]CCCTCTTCCTGTGTG | 10517 |
rs777368102 | snp | C/T | 2.02669e-05 | 0.00318324 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778955 | GGGCTGTGTGCAGTA[C/T]GGGTCCCCTGACCAG | 10517 |
rs777394339 | snp | C/T | | | | | GRCh38.p7 | 17:18739940 | GTGGCATTTATAATG[C/T]GCAAGCTGCTGTGCT | 10517 |
rs777463549 | snp | C/T | 4.06488e-05 | 0.00450807 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779044 | TCTCTTAAGAAAGAA[C/T]GGCCTCGCATCTATA | 10517 |
rs777465150 | snp | A/G | 4.9722e-05 | 0.00498583 | synonymous-codon, nc-transcript-variant, missense | FBXW10 | GRCh38.p7 | 17:18772427 | GATGGTGGTCAACAC[A/G]GAGAGCAATGTTCTC | 10517 |
rs777473501 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771468 | GGGAGGGCAAGTTCC[A/G]GAGCTCTTTGTCTAT | 10517 |
rs777652149 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant, missense | FBXW10 | GRCh38.p7 | 17:18750007 | CCATCTTTTTTTTTC[C/T]AGGAATGCTGGATAG | 10517 |
rs777653714 | in-del | -/CCA | 4.0935e-05 | 0.00452391 | cds-indel, upstream-variant-2KB, intron-variant, downstream-variant-500B | FBXW10, TVP23B | GRCh38.p7 | 17:18779005 | AACCGCATGCTAGCT[-/CCA]CAAGTGGGCACAGCC | 10517 |
rs777742132 | snp | C/T | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744424 | GTTTCTAGTTGGCAT[C/T]CTGAAGCAGTTAAAT | 10517 |
rs777857310 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751284 | AGGCTGGAGTGCAGT[A/G]GCACAATCTTGGCTC | 10517 |
rs777892730 | in-del | -/CTT | 3.29454e-05 | 0.00405852 | cds-indel, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770065 | TGATCCTGTGCTGTC[-/CTT]CTTTATTCAGGGCAA | 10517 |
rs777918770 | snp | C/T | 1.67942e-05 | 0.00289772 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748147 | AATATGGGCTAGGTG[C/T]GGTGGCTCATGCCTG | 10517 |
rs777938309 | snp | A/G | 3.55259e-05 | 0.00421446 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756017 | TGAAGTTACCACTGA[A/G]CTTTAACTTCAAATA | 10517 |
rs777941855 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768634 | TGGCCTGGAGCATGG[C/T]GGGGAAGTACGAGCG | 10517 |
rs777947709 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772591 | ACAGCCCAAGAGAGT[C/T]TGTATCCAGTAAACA | 10517 |
rs777971670 | snp | A/G | 4.19639e-05 | 0.00458041 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779179 | TCCACTGGAGTGGTT[A/G]ATCCAGGAAAAGTCA | 10517 |
rs778009785 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18745803 | CAGGCCTAGGGTGTT[A/G]GAGAATCTTGGAAGT | 10517 |
rs778026610 | snp | C/T | 1.74418e-05 | 0.00295307 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768703 | TGAAGCCCGGAGCGA[C/T]GAACCTGGTGTCCTT | 10517 |
rs778033611 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744654 | CCAAGGCGAATTATA[-/CT]CTCTTACTGCTGCAG | 10517 |
rs778060036 | snp | C/T | 0.000235789 | 0.0108554 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779346 | AAACAGAAAGCCAAG[C/T]GGATGTTGCTATTTG | 10517 |
rs778116642 | snp | A/G | 5.11409e-05 | 0.00505646 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756135 | TGTGGGACCTACAAT[A/G]TTCGCATTCTCTCTG | 10517 |
rs778138114 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18775763 | ATGGGCATAGTGGCT[A/C]ATGCCTGTAATTCCA | 10517 |
rs778208032 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749726 | CTTCACTCTAGAGGA[A/G]CCATGGAGGAATTCA | 10517 |
rs778236718 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772711 | AATACCAGCAAGTTC[A/G]GTGATAACCCACAGA | 10517 |
rs778414216 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746570 | TTTGGTGTGTCAGGG[G/T]TATAGAAGAATGATA | 10517 |
rs778519253 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18772444 | AGAGCAATGTTCTCA[C/T]GTTCCAGTTTGAGCA | 10517 |
rs778519342 | snp | A/G | 2.10657e-05 | 0.00324537 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779133 | GAAGGAGCACCAGGA[A/G]GCCAAGATGAAGGAA | 10517 |
rs778552789 | in-del | -/TCTC | 3.29571e-05 | 0.00405924 | frameshift-variant, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772550 | TAGTCTCATGGAAAT[-/TCTC]TCTAAGTGTAATATT | 10517 |
rs778597832 | snp | C/T | 3.52125e-05 | 0.00419583 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750093 | CAGGTCAAGATGGAC[C/T]TGTCAGCGCACGGCT | 10517 |
rs778607269 | snp | C/T | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772565 | TCTCTCTAAGTGTAA[C/T]ATTCAGGTTCACAGC | 10517 |
rs778612144 | snp | A/T | 1.68405e-05 | 0.00290172 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778654 | CCCTGTAGGCCCCAA[A/T]CAGAAATTACTGATG | 10517 |
rs778618821 | snp | C/T | 1.656e-05 | 0.00287745 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764791 | ATCTTCGGTGGTCAC[C/T]AGGGGACTATCACTT | 10517 |
rs778707969 | snp | C/T | 1.65239e-05 | 0.00287431 | | | GRCh38.p7 | 17:18744446 | CAGTTAAATAGCTTA[C/T]ATTTGTTACACTATT | 10517 |
rs778714457 | snp | A/C | 1.6708e-05 | 0.00289028 | | | GRCh38.p7 | 17:18769876 | ACCTACAAACAAACC[A/C]AGGCATTTTACGAGA | 10517 |
rs778797983 | snp | C/T | 1.6513e-05 | 0.00287336 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744558 | AAGTTGTGAAGTCCT[C/T]CTTGAACCAAATGTT | 10517 |
rs778965004 | in-del | -/GAAT | 2.11017e-05 | 0.00324814 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779145 | GAAGCCAAGATGAAG[-/GAAT]GAATATCAGGCCAGG | 10517 |
rs779077981 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18754816 | GGAAGCAAATGAAAG[C/T]GCCCTTGTCACGACT | 10517 |
rs779081541 | snp | C/T | 1.7822e-05 | 0.00298507 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756149 | TGTTCGCATTCTCTC[C/T]GACACGTAGGTACTG | 10517 |
rs779169292 | snp | C/T | 7.81036e-05 | 0.00624866 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758323 | GGATCAAAACCGAGT[C/T]ATCCACTATTCCGGG | 10517 |
rs779200766 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18774334 | CACTTTTCCCTGTCA[C/G]ATACGTCAGTTTAGA | 10517 |
rs779242805 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749740 | AACCATGGAGGAATT[C/T]ACTCCGGTGTATATC | 10517 |
rs779254315 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773521 | GTATGTAGGTGGGGG[C/T]GCAGGCATGGCCAAT | 10517 |
rs779337212 | snp | C/G | 1.80299e-05 | 0.00300243 | utr-variant-5-prime, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744217 | TTGCAAGTGCGCAGG[C/G]CTAAAATGGACTGGT | 10517 |
rs779377047 | snp | G/T | 1.69086e-05 | 0.00290758 | intron-variant | FBXW10 | GRCh38.p7 | 17:18772693 | CTTCAGGTAAAAAAC[G/T]GAAATACCAGCAAGT | 10517 |
rs779448821 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750940 | TTCCAGGGGTCCTAC[A/G]CAAGAGGAATTGATC | 10517 |
rs779534818 | snp | A/G | 5.31872e-05 | 0.00515663 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744716 | GCCAATGTGATCAGA[A/G]TCCTGTTTCTGAGAG | 10517 |
rs779595825 | in-del | -/CTC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749197 | TGATACTCTAGACTT[-/CTC]CTTGGGCTGAAAAAG | 10517 |
rs779653217 | snp | A/T | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18764806 | CAGGGGACTATCACT[A/T]GCATGGACTTGTGTA | 10517 |
rs779685590 | snp | C/T | 1.70705e-05 | 0.00292147 | missense, intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778688 | GGGGACCTTCAATTT[C/T]ATACCCAAGGAAGGT | 10517 |
rs779717723 | snp | A/G | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744651 | GGACCAAGGCGAATT[A/G]TACTCTCTTACTGCT | 10517 |
rs779743177 | snp | A/G | 8.47221e-05 | 0.00650798 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750042 | ACCCTGAACAAGTGC[A/G]CCTCTGTGAGCCAGC | 10517 |
rs779743327 | snp | A/G | 3.30617e-05 | 0.00406568 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764914 | TCCCCCGACCCACGG[A/G]TTACCAAAATGCTTT | 10517 |
rs779813238 | snp | C/T | 4.95569e-05 | 0.00497755 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744566 | AAGTCCTCCTTGAAC[C/T]AAATGTTGGATAAAA | 10517 |
rs779830992 | snp | C/T | 1.77146e-05 | 0.00297607 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750100 | AGATGGACTTGTCAG[C/T]GCACGGCTTCATTCA | 10517 |
rs779844273 | snp | C/T | 5.72721e-05 | 0.00535096 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758335 | AGTCATCCACTATTC[C/T]GGGGGAGATCTGATA | 10517 |
rs779955136 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770017 | TTTCCTCAACGGGAA[C/T]TGTATGAAGGTGTTA | 10517 |
rs780054431 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770107 | GGTAGGTGTGGAGGT[C/T]AGAACTGTGAGTGAT | 10517 |
rs780114730 | snp | A/G | 2.60971e-05 | 0.00361218 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758423 | CCCGTTGAATTCCGA[A/G]GCCATGCTGGGAGTG | 10517 |
rs780135543 | snp | G/T | 2.05708e-05 | 0.00320702 | intron-variant | FBXW10 | GRCh38.p7 | 17:18778467 | AAATTTTCTTTTTTT[G/T]GAAAAAGCAGATGAT | 10517 |
rs780212893 | snp | A/C | 1.64727e-05 | 0.00286986 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749816 | AGGGTACGATCCCTG[A/C]AATCTATTGGTTGAC | 10517 |
rs780225956 | in-del | -/GAG | 1.65059e-05 | 0.00287275 | cds-indel, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744403 | CAATGACATATCACA[-/GAG]GAGGTTTCTAGTTGG | 10517 |
rs780231488 | snp | C/T | 3.32303e-05 | 0.00407603 | intron-variant, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18775205 | ATGGTAAGAAGAGAG[C/T]TTATTCTGTTCATAA | 10517 |
rs780284992 | in-del | -/T | 1.65109e-05 | 0.00287318 | intron-variant | FBXW10 | GRCh38.p7 | 17:18751092 | AAGTAGCTGTGAGCG[-/T]TCTCATTCTAATTGT | 10517 |
rs780342106 | snp | A/T | 1.66095e-05 | 0.00288175 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768506 | GAGTCACAGTCTGAG[A/T]TGAAGACAGTGGTAT | 10517 |
rs780425394 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18746717 | ACTTTGCTTAGGTCA[C/G]CCACCACGTGGGCTG | 10517 |
rs780430044 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18751034 | GTGTGAAACATCCGA[A/G]GTGGAAGCTGAGAAC | 10517 |
rs780481998 | snp | A/G | 1.66228e-05 | 0.0028829 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748019 | CGACCTCACAAGTCT[A/G]TTGGACAGCCAAAAC | 10517 |
rs780498326 | snp | A/G | 3.44045e-05 | 0.00414741 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18766803 | GATACCTACATTGTG[A/G]GCAGCTGTGAGCGAG | 10517 |
rs780630095 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18773269 | CTTATAAGAACCTTT[C/G]CACAGTAGATAAGAC | 10517 |
rs780678096 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770746 | TGAGAGCTCTATCAG[C/T]TATCTTTGATGCCTC | 10517 |
rs780780178 | snp | G/T | 1.77817e-05 | 0.0029817 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18750106 | ACTTGTCAGCGCACG[G/T]CTTCATTCAGAACCA | 10517 |
rs780820275 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18769969 | CCTCCGGGTCATCAG[C/T]GCCTGTGCAGATGGC | 10517 |
rs780869672 | snp | C/G | 0.0001168 | 0.0076411 | intron-variant | FBXW10 | GRCh38.p7 | 17:18750921 | TTTTTTATTTTTTGT[C/G]TTTTTCCAGGGGTCC | 10517 |
rs780882213 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744595 | AACAGTAGAACAGAA[A/G]ATGAAAGAGATCTTG | 10517 |
rs780904982 | in-del | -/G | 1.67612e-05 | 0.00289488 | frameshift-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756123 | AGAAATGTTTTCTGT[-/G]GGACCTACAATGTTC | 10517 |
rs780906120 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18770022 | TCAACGGGAACTGTA[G/T]GAAGGTGTTAAAAGC | 10517 |
rs780962211 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749834 | TCTATTGGTTGACCT[A/G]GATGACATCAGAGAC | 10517 |
rs780972225 | snp | C/T | 1.67298e-05 | 0.00289217 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744681 | TGCAGATGTGCAACC[C/T]CAAATTACTGCTCAC | 10517 |
rs780996071 | snp | A/G | 2.48629e-05 | 0.00352574 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758438 | GGCCATGCTGGGAGT[A/G]TCCGGGCCCTCTTCC | 10517 |
rs781052077 | snp | C/T | 1.78979e-05 | 0.00299143 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744246 | GTTATCTTAGGATCA[C/T]GGAAAACCTGGAATC | 10517 |
rs781060223 | snp | A/G | 0.000830663 | 0.0203627 | intron-variant, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18744836 | GAACTGCAGTTGTAG[A/G]CAACATAGGTAGACA | 10517 |
rs781083979 | snp | A/G | 9.91326e-05 | 0.00703964 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18758501 | AGCTATGACCTAAGT[A/G]TCAGGTGAGGAGTCC | 10517 |
rs781249754 | snp | C/T | 3.30961e-05 | 0.0040678 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18749896 | TCATCCGTTACCTGC[C/T]CATCCACCTCTCCAA | 10517 |
rs781252290 | in-del | -/T/TT/TTT | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768934 | TTGAGAAGTTATTGA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10517 |
rs781255360 | snp | A/G | 3.29603e-05 | 0.00405944 | stop-gained, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18768625 | GCCTGGTCATGGCCT[A/G]GAGCATGGTGGGGAA | 10517 |
rs781343720 | snp | A/G | 3.30781e-05 | 0.00406669 | intron-variant | FBXW10 | GRCh38.p7 | 17:18756005 | ACTGTGGGTATTTGA[A/G]GTTACCACTGAGCTT | 10517 |
rs781368408 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18775901 | CAGATATGGTAGCAC[A/G]CACCTCCTAGCTACT | 10517 |
rs781374954 | snp | C/G | 1.75668e-05 | 0.00296363 | missense, intron-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18778488 | AGCAGATGATGTGGA[C/G]AAAGCACAAAAACAA | 10517 |
rs781375191 | snp | G/T | 1.65083e-05 | 0.00287296 | intron-variant | FBXW10 | GRCh38.p7 | 17:18768529 | AGTGGTATCTTTTCT[G/T]GCAGACTCTCAGTGG | 10517 |
rs781446955 | in-del | -/A | 0.000148802 | 0.00862432 | intron-variant | FBXW10 | GRCh38.p7 | 17:18764905 | AAGAAGTTTCCCCCG[-/A]ACCCACGGGTTACCA | 10517 |
rs781458691 | snp | A/C | 5.13281e-05 | 0.00506571 | missense, intron-variant, utr-variant-3-prime, downstream-variant-500B | FBXW10 | GRCh38.p7 | 17:18778561 | AAAAAGTCTTGGAAA[A/C]TCCCTATGTCACCTG | 10517 |
rs781567982 | snp | C/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18748041 | AGCCAAAACTCAGCA[C/G]ACATCCCTTCCTTTG | 10517 |
rs781635518 | snp | C/G | 3.3232e-05 | 0.00407614 | missense, nc-transcript-variant | FBXW10 | GRCh38.p7 | 17:18756107 | GGTCCTGATAGAGGA[C/G]AGAAATGTTTTCTGT | 10517 |
rs781649698 | snp | A/G | 1.67066e-05 | 0.00289016 | intron-variant | FBXW10 | GRCh38.p7 | 17:18748139 | AGAAAGCCAATATGG[A/G]CTAGGTGCGGTGGCT | 10517 |
rs781659075 | snp | A/G | 4.2131e-05 | 0.00458952 | missense, upstream-variant-2KB, nc-transcript-variant | FBXW10, TVP23B | GRCh38.p7 | 17:18779158 | AAGGAATATCAGGCC[A/G]GGGAGTCCACTGGAG | 10517 |
rs781721897 | snp | G/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant, utr-variant-3-prime | FBXW10 | GRCh38.p7 | 17:18772585 | AGGTTCACAGCCCAA[G/T]AGAGTCTGTATCCAG | 10517 |
rs781761766 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18751077 | CAACAGCATCTGGGG[A/C]AAGTAGCTGTGAGCG | 10517 |
rs796250548 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18776045 | AAAAAGTGGCCGGGC[A/G]CGGTGGCTCACACCT | 10517 |
rs796253828 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768177 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCACCC | 10517 |
rs796272729 | snp | A/C | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18770354 | TGTCGCACAGGCTGG[A/C]GTGCAGTGATGTGAT | 10517 |
rs796312716 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749525 | ACACTCCAACCTGGG[C/T]GACAGAGCGAGACTC | 10517 |
rs796336491 | in-del | -/CAG | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18768122 | CAGGCTGGAGCACAG[-/CAG]TGGTGAGATCTTGGC | 10517 |
rs796366686 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant, splice-donor-variant | FBXW10 | GRCh38.p7 | 17:18770050 | AGCCAATGGCAGAGG[C/T]GATCCTGTGCTGTCC | 10517 |
rs796388539 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18760845 | AGGGTTTTTTTTTTC[C/T]TCATTTCTGTGATTC | 10517 |
rs796496273 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749271 | CGGCCGAGTGCGGTG[C/G]CTCACGCCTGTAATC | 10517 |
rs796640824 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759610 | CATTTGCATTGTTTC[C/T]AGTTTTTTGTTTTTT | 10517 |
rs796679780 | in-del | -/AC | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771117 | TGCTAAAAAAAAAAA[-/AC]AAAACAAAACTCTGG | 10517 |
rs796831953 | snp | C/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749299 | ATCCCAGCACTCTGG[C/G]AGGCCGAGGCGGGCG | 10517 |
rs796832576 | snp | C/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18766379 | ATGAAATCTACTCGA[C/T]AGCAAGCATTTTTCA | 10517 |
rs796857677 | in-del | -/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18759619 | TGTTTCTAGTTTTTT[-/G]TTTTTTTTTTTGAGA | 10517 |
rs796865771 | snp | A/G | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18749262 | TTCTATTCTCGGCCG[A/G]GTGCGGTGGCTCACG | 10517 |
rs796970573 | snp | G/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18771191 | CGGCTTGAGTGAACG[G/T]AAGTCTAAAAGGGAT | 10517 |
rs796981569 | in-del | -/T | | | intron-variant | FBXW10 | GRCh38.p7 | 17:18777063 | CTTGATTTCACTCAG[-/T]TTTTTTTTTTTTTTT | 10517 |