SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs112542272 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424414 | GCACTCCAGCCTGGA[C/T]GACAGAGCAAGACTC | 55779 |
rs112558867 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367127 | GACTCCACCTCTGTG[C/G]GCAGGGCATAGCTGA | 55779 |
rs112559446 | snp | C/T | 0.184838 | 0.241358 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385012 | CTGGTGGAAGGTAAT[C/T]GGATCATTGGGGCAG | 55779 |
rs112577257 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426736 | AGGAGGAATGTACAC[A/G]GCCTGCAATACTCTA | 55779 |
rs112623705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299457 | GAAACCCTCATACAC[A/G]GTTGGTGGGAATGTA | 55779 |
rs112627982 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422268 | CTTGAGCCCTTGTTT[A/G]AAAACAAATTCTGAT | 55779 |
rs112628290 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287126 | GCTGGCGCGGGACAG[A/T]CTCCTAACCTGGGGC | 55779 |
rs112630644 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377947 | TGAGCCACTGCACCC[A/G]GCCAAAAATAATTTT | 55779 |
rs112673238 | snp | C/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339834 | AAACAGAGCTAGGGG[C/G]AGCCCTCTCACTTAG | 55779 |
rs112685944 | snp | C/T | 0.420733 | 0.18262 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415168 | GGTATCTATGGTATT[C/T]TCTGATGGTAGTCTG | 55779 |
rs112713396 | snp | A/G | 0.231189 | 0.249291 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325496 | GTCGCCCAGACTGGA[A/G]TGCAGTGGCATGATC | 55779 |
rs112731478 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381125 | CATAGTTTAAAGAGA[C/T]TATAAATAAAAATAT | 55779 |
rs112731668 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367318 | GTAGGGGCCAACAGA[C/T]ACCTCATACAGGCGG | 55779 |
rs112733969 | snp | C/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386947 | TCACAACAGAAAGCA[C/G]CTTTGGGCACAACTC | 55779 |
rs112734753 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396645 | CCCGCAAAAATCGTG[A/G]GCCCTTTTGGATCAT | 55779 |
rs112772152 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318342 | ATGAGGAAAGAATCT[C/T]AGTTCGAGGAATGCT | 55779 |
rs112773870 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353114 | CCAGAGCTGTGGGCA[C/T]TTGATCCCTGCATCT | 55779 |
rs112777073 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325257 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55779 |
rs112782784 | snp | C/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348135 | AGAGGGGTTTCTGCT[C/G]CTGCATTGGTGAGTG | 55779 |
rs112784771 | snp | A/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441878 | ACATCAACAACAAAG[A/T]TACATCGTGGGATTT | 55779 |
rs112792360 | snp | C/T | 0.180702 | 0.240204 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383954 | CCCTCCCTGTGTCCA[C/T]GTGTTCTCATTGTTC | 55779 |
rs112797646 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439850 | CAATCCCAGCAGTGT[A/G]CCAGAGGTGGTTATT | 55779 |
rs112798526 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407306 | GCTACCTAATGCAGT[A/G]CCCTCCAGCTATGTG | 55779 |
rs112799197 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425513 | CTTTATATTTTGTGC[C/T]CTGTTTCCTAAGAAT | 55779 |
rs112805696 | snp | A/C | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304561 | TGATATGTATTCCTG[A/C]AATTTAATATAAGTT | 55779 |
rs112825239 | snp | A/C | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368270 | CCTTGAAAAGAGCAA[A/C]CCCAAGACACATAAT | 55779 |
rs112843658 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396950 | ACTGAATGAACAAAC[A/T]GCAGAGTGTCTGCCT | 55779 |
rs112853390 | snp | A/C | 0.5 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428813 | CTGTAGATATCAAAA[A/C]TAACCTGCTGGGATT | 55779 |
rs112863305 | snp | C/T | 0.199873 | 0.244923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320699 | AAAAGCCAGTCCAAG[C/T]CCCAAAACTGAAGAA | 55779 |
rs112873023 | in-del | -/T | 0.0683004 | 0.171713 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373392 | TGGTTTTTTTAAAGC[-/T]TTTTGAAATACTGCT | 55779 |
rs112893585 | snp | A/C | 0.48 | 0.0979796 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379092 | ATCTGCACAAGAAGA[A/C]ATATAAAAGAGATGT | 55779 |
rs112919148 | snp | A/G | 0.0272206 | 0.113443 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291755 | GGCATTGCCCTGTTG[A/G]AAGAAAACAGCTCCC | 55779 |
rs112930879 | snp | G/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317740 | GAGGGGTGAGATGCA[G/T]GAGTTCCTGGGCTGG | 55779 |
rs112956403 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403136 | TAACATTTCTTAAAG[A/C]ATGTCAATAGAACAC | 55779 |
rs112981338 | snp | G/T | 0.121022 | 0.21416 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348232 | TCAAAACCGCGGGCG[G/T]TTTTTCCTTTCACAT | 55779 |
rs112982126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332556 | AACCACATTAGGTTA[C/T]GATGTATCGAGTTCT | 55779 |
rs112989292 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440891 | TTAGCAACTCATGAT[A/T]GACTGGACACACTGA | 55779 |
rs112998943 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419075 | TTTTATAACAAAATA[C/T]TAAAATAGAAATTTT | 55779 |
rs113010274 | snp | A/G | 0.00694303 | 0.0585091 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446583 | CAATTACATTTTAAC[A/G]TGTACCTTTGCTCTT | 55779 |
rs113011286 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422511 | GGTACTGGATCTGTT[C/T]AAGAAAAAGAAATTT | 55779 |
rs113020195 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445114 | ATTCACAGGGAGCTG[C/T]AGGTCAGTTGGTTGT | 55779 |
rs113046091 | snp | A/G | 0.0106147 | 0.0720743 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358725 | CAAACATCTTAGCTT[A/G]TAGAGAATATGGATC | 55779 |
rs113058153 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417224 | TTCCAGACCAGGTTA[C/T]ATCACAATTTTTAAA | 55779 |
rs113059793 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393363 | TTGGAATTTGATCTC[C/T]AATGTTAGACATGGG | 55779 |
rs113060529 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351032 | ATGGGTATTCAGTAA[A/G]TTATAAGGAAACTCT | 55779 |
rs113080283 | snp | C/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319461 | CCTGGCCTACAAAAA[C/G]ACTTAGACAACCACA | 55779 |
rs113092104 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408603 | GGCACAGTGGCTTAC[G/T]CCTGCAATCCCAGCA | 55779 |
rs113093882 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393201 | CAGGTCAGTTACATA[C/G/T]AGTAATTTACTTTTT | 55779 |
rs113101974 | snp | A/G | 4.95323e-05 | 0.00497631 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396628 | CCAAAATTTTCTTCC[A/G]TCCCGCAAAAATCGT | 55779 |
rs113104064 | snp | C/T | 0.165853 | 0.235413 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410627 | gtgcatgtgtcttta[C/T]agtagcatgatttat | 55779 |
rs113106469 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325619 | TTGGAAAACTCAATG[C/T]AGTAAAGATACCAGT | 55779 |
rs113118917 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337739 | GAGTAATTGGACATC[C/T]GTAAGAAAAAAACAA | 55779 |
rs113163403 | in-del | -/ATT | 0.0887219 | 0.191022 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381259 | TATTGTTATATCATT[-/ATT]AAGTGATTAAAGATT | 55779 |
rs113164275 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305793 | AAAATCATCTATTGG[A/G]GTATAAATTGAAAAT | 55779 |
rs113186880 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445251 | ACTTAAAAGTCAGAG[C/T]AGGGAAAGGGAAGTA | 55779 |
rs113188674 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296042 | GGTAATTTTTCAACC[C/G]TCACCCCCACCATCC | 55779 |
rs113215702 | snp | A/C | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368864 | TCACTTACAGAGATA[A/C]ACATAGGCTCAAAAT | 55779 |
rs113237911 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390013 | CAAGGCCAGTACTAC[C/G]CTAATACCAAAGCCA | 55779 |
rs113293038 | snp | A/T | 0.5 | 0 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113308268 | CTCTCCTCATCTTCA[A/T]CTATGGAAAGAGGAG | 55779 |
rs113301319 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355292 | TTGGGAGGCCTAGGC[A/G]GGTGGATCACGAGGT | 55779 |
rs113306247 | snp | C/T | 0.0437281 | 0.141251 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441621 | AACCCGGTACCTATC[C/T]GCCCTTTGGTCGGGC | 55779 |
rs113316270 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327317 | TTGTTTTTTAGGGAA[C/T]CCAACTCACCAGACT | 55779 |
rs113333879 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355853 | ACAATCAAAATTTAC[C/T]AGGCAGATAGGCAAA | 55779 |
rs113402880 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338767 | GACCTTGGCCTTACT[A/G]GGCCCAAATTCACTG | 55779 |
rs113403333 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316606 | GGCTGTAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 55779 |
rs113404249 | snp | C/G | 0.199873 | 0.244923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312404 | AATTCAGTTTTAAAA[C/G]GGAAACAGAGCATAA | 55779 |
rs113421560 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357964 | AACAGTAGAAGGGAT[A/G]AACTGTGGTATAATC | 55779 |
rs113423863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342021 | AACACAGAGAATATA[C/T]TGAATTTGTAAATCA | 55779 |
rs113428799 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387894 | CTTGAGTGAGAATCA[G/T]CAATAGCCAGGGAGT | 55779 |
rs113495704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327883 | CATTTTTAAACTATC[G/T]AACAGTACTAATTTG | 55779 |
rs113495736 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374861 | GGCTGGTCTGGAACT[C/G]CTGGCCTCAAGTGAT | 55779 |
rs113508425 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303111 | GACAATATGGAGCCT[A/G]GGCAATTCTCACACA | 55779 |
rs113521857 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346608 | ATTGTAAATGCACCA[A/G]TCAACACTCTGTAAA | 55779 |
rs113526593 | in-del | -/AGAGTG | 0.484561 | 0.0864924 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375154 | CATAAGAAAGAAAGT[-/AGAGTG]ATGGTTGCCAGGGGC | 55779 |
rs113598923 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419190 | GCTCCTGAAACCTCA[C/T]AGGCTCCGACTGACT | 55779 |
rs113655085 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435581 | AAAAAAAATTTTAAA[C/T]GGCCAGGCATAGTGA | 55779 |
rs113674532 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437512 | ATATATTCCCCAAAT[A/G]GCTAATACTACCATG | 55779 |
rs113691094 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442866 | TTATTAAATGGTATA[C/T]CTAGGTGCCAGAAAA | 55779 |
rs113704467 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296616 | GCCAAAGGGGGCTCG[C/T]GGACCAGCTCCAGCT | 55779 |
rs113708497 | snp | C/G | 0.183929 | 0.242117 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368411 | CAGAAACCCTACAAG[C/G]CAGAAGAGAGTGTGG | 55779 |
rs113725311 | snp | A/G | 0.16976 | 0.236773 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389446 | CTCAAATAACTAATG[A/G]CATATCTTAAAGAAC | 55779 |
rs113738948 | in-del | -/T/TT | 0.199564 | 0.24486 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338549 | CCAGATTTTTTTTTT[-/T/TT]AATCCCCAAATCTCT | 55779 |
rs113748141 | snp | A/T | 0.029116 | 0.117091 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412380 | GGGACCCCTTTTCCA[A/T]GACAATTCCATTAAA | 55779 |
rs113757183 | snp | A/C | 0.103438 | 0.202533 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372488 | ACAAGGACAGAAAAC[A/C]AAGCACCACATATTC | 55779 |
rs113791617 | snp | G/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312075 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTTTTTTTT | 55779 |
rs113798711 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424164 | AGTAGAGGGCTAGGC[A/G]CGGTGGCTCACACCT | 55779 |
rs113814652 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435377 | GGAGAAGTGCAGAGC[A/G]AAGGGGAAGAAAACC | 55779 |
rs113814729 | snp | C/G/T | 0.0221587 | 0.10322 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376693 | GAGATATCCCAACTG[C/G/T]AATGGGTTGAAGATC | 55779 |
rs113815064 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359634 | AACATGATTAAATCA[C/T]GATTTCACCAAAGCA | 55779 |
rs113819192 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426597 | CCAGCCATGCAGAAC[C/T]GTGAGTCAAGTAAAC | 55779 |
rs113839387 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432125 | CCAGGTCTCTTTCCA[C/G]TACATTGTATCAGAA | 55779 |
rs113847023 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385569 | TATTCTACAGCTGTC[A/G]GTGGACTGCTCTGAA | 55779 |
rs113849642 | snp | A/C | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400512 | TAAAACAAAACAAGG[A/C]CAGACATATTTTTAT | 55779 |
rs113916845 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308553 | AATTCCTAACTCATA[A/C]GATGCTCTAAAATCA | 55779 |
rs113919430 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366424 | ATGGACTGAATTGTA[C/T]ACCCCTAAAATTCCT | 55779 |
rs113938890 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388203 | CATAGGCAGTAGCCA[C/G]GGAGTGGTTACCACA | 55779 |
rs113949508 | in-del | -/A | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331028 | CAGGGAGGAAGGGAA[-/A]GGCAATTAATTCATT | 55779 |
rs113955304 | snp | A/G | 0.5 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406747 | GTAAGTATGGATTAT[A/G]ACAATTTCAGGGAAA | 55779 |
rs113956665 | snp | A/G | 0.00592071 | 0.0540861 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409356 | GCCTAATAAATAAGG[A/G]CACATTTATTTCATT | 55779 |
rs113970665 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289338 | GGGAATAATTATCCC[A/G]ATTAGCTTTCCTCTC | 55779 |
rs113986901 | snp | C/T | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319139 | TTAAAAGCTAGAGTG[C/T]CAAACTGGATAAAAA | 55779 |
rs114002906 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337970 | CTGTGACAAAACTCT[C/G]TAATAAGGGAGGCCA | 55779 |
rs114003689 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319081 | GATCAAAAATCACAC[A/G]TATCAATACTAACCT | 55779 |
rs114040402 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442788 | CATTTATTTGCAATA[C/T]TGAAATGTCCTCTTT | 55779 |
rs114092660 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382336 | GGTCAAGAAAGATAA[A/G]AACTAAATGTTAAAT | 55779 |
rs114100688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438747 | CTTATTTTTTCTTCC[G/T]AGAACACACAGAACA | 55779 |
rs114122454 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403419 | AGAAGAATGTAGCAT[C/T]CATAGGCAAACTCCA | 55779 |
rs114124315 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413853 | TATGGGGTCTTCTTT[A/G]ATTCCACGTGAAACT | 55779 |
rs114126208 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393466 | AGGGGGTGGGTTCTT[C/G]TTCTATTCATTCCCA | 55779 |
rs114147485 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379083 | TGTACAATTATCTGC[A/G]CAAGAAGACATATAA | 55779 |
rs114162388 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288214 | TAAACAGGGTCCTAG[A/G]GAAGAGTCACTCTGA | 55779 |
rs114177282 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347365 | AACTCTCAAAGTCAC[A/G]TCGCCCAAGCAAGGC | 55779 |
rs114178193 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321109 | TCTGATGAGCATAGA[C/T]GCAAAAATATTCAAA | 55779 |
rs114215826 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318724 | TCAGGCTAGCAGCAG[A/G]CCTCTGAGCAGAAAT | 55779 |
rs114236241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432189 | GAACTCTAGACCAGA[C/T]GTGTGGATAGGTTAT | 55779 |
rs114260508 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313103 | GGAAAAGCCGCAGAC[A/G]CTCAATGCCAGCCCG | 55779 |
rs114261108 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386801 | GAAAGAGGCACTGCA[G/T]AGGGTAGGAAAGACA | 55779 |
rs114265530 | snp | C/T | 0.0879971 | 0.190408 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421655 | GAAATACTATACAGC[C/T]GTGAAAAGAATGAAA | 55779 |
rs114272880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445878 | TTACTGAACTCAGTA[A/G]TAAGAAATGCAAAGA | 55779 |
rs114273168 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427393 | AAACATTTTCTTATT[G/T]CTAAAGTAGCTAAAA | 55779 |
rs114344317 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444978 | GATCAACTAAGATAT[A/C]CTAAACCTCAAAAAA | 55779 |
rs114361491 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308754 | CACCATTATGCCCAG[A/C]TAATTTTTGGTTTTT | 55779 |
rs114372427 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319453 | AAGTTCTTCCTGGCC[C/T]ACAAAAAGACTTAGA | 55779 |
rs114378814 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291878 | CTGTTCCTTAATCTC[A/G]GGAGCCTTCAATTCC | 55779 |
rs114379050 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446331 | ATATGGGAAGCTCTA[C/G]CTGAAACCAGTAATT | 55779 |
rs114431253 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325438 | TAGAGATATATTGTG[C/T]CTTTTTTATTTTTTA | 55779 |
rs114436661 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375880 | GAATAGTAAAAGAAT[A/G]TATAACTAATAATCT | 55779 |
rs114437663 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339765 | CTCAAATGTGCCCTG[A/C]CAAATTTGCAGTTCT | 55779 |
rs114440843 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394775 | AAGAAAGTTTATGAA[C/T]TTGTGTTGCGCCTCA | 55779 |
rs114468573 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347157 | AGTGACTAGCGTGGC[C/T]GCCGGACTAAAGACA | 55779 |
rs114470599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425137 | CATGAAGAGAGAAAA[C/T]TCCAGGTTACAAGAT | 55779 |
rs114488147 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431461 | ACACTGCCGAGGACT[A/G]GAAACCAACACACAG | 55779 |
rs114499101 | snp | C/T | 0.084364 | 0.187256 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435819 | AGGCATTCTTCTGGG[C/T]TACAAAAATAATGTT | 55779 |
rs114502694 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290293 | TTAAATAGGAATATG[A/C]AGGAATCTTAGGAAG | 55779 |
rs114540242 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319080 | GGATCAAAAATCACA[C/T]GTATCAATACTAACC | 55779 |
rs114587314 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319594 | AATTGGACCTAATAC[A/G/T]CATCTACAGAACACT | 55779 |
rs114610519 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355046 | GTACCAACCTGGAGC[A/C]CGGTAGCTCTGCTGG | 55779 |
rs114625238 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405659 | TTGCCCTCTAAAAAT[A/T]TGATATTTATTTCTA | 55779 |
rs114672211 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319955 | CTTCTGAGACTATTA[A/T]GAACACTTCTATGCA | 55779 |
rs114676938 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376654 | GAATTGACCTCTGAG[C/T]TTATCATCATTAGTG | 55779 |
rs114697653 | snp | C/T | 0.0520825 | 0.152737 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287437 | TTCTAAATAAATGTT[C/T]AGTCTTCCCTGTAAC | 55779 |
rs114699562 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340693 | GCAGCTGAAGCCCCA[A/G]TGGGCGTGTCTTACA | 55779 |
rs114716554 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362785 | AACGAAGCCAGCCAC[C/T]GGACGCTTCAGGCCA | 55779 |
rs114747999 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347477 | TCTGAGGCTAATCCC[A/G]CTTCTAAAAACTACC | 55779 |
rs114748205 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374943 | GCCTGGCCCCAAATG[G/T]CTATTTATGACTGAG | 55779 |
rs114792336 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292942 | TGTGAAACATGGGAG[C/T]TGAAGCAGCTGTCAT | 55779 |
rs114817148 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350920 | GATCTAGGTCTTGAT[C/T]GGTTGCCATACAGGG | 55779 |
rs114834190 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392550 | CATGTCAAAATAACT[A/C]AAAGAGTATGAGTGG | 55779 |
rs114851819 | snp | A/C | 0.0869089 | 0.189476 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446243 | ACCCCACCCAAGCAC[A/C]AGGACTGGGGGAACC | 55779 |
rs114861284 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412835 | GTTGTAATAAACATA[C/T]GTGTGCATGTCTCTT | 55779 |
rs114890078 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307082 | TCTACTGAACCGTTC[A/G]TCTATTGAGACTGCA | 55779 |
rs114933575 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313548 | GAGGGGCAAGGGGGC[A/G]GAATGATATGGTTTG | 55779 |
rs114936422 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302725 | AAGATCACGCCACCA[C/T]GATAGAGGTGAGACT | 55779 |
rs114954577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291928 | TAGAAATGTGTGCCT[C/T]TGGGCTAATAAACAA | 55779 |
rs114966549 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331056 | ATTTTCCTCCTGGAA[A/C]TTTGAATCCCTTTGA | 55779 |
rs114972285 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381453 | GCGTGTGTGGATGGC[A/G]TAGTCAGTCCCATCC | 55779 |
rs114999582 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396012 | TTATTTCTAAAACTT[A/G]CTCAATTTTCCCCAT | 55779 |
rs115046855 | snp | C/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286966 | TTTTTCTATTATAGC[C/T]ATATTTATATATTTA | 55779 |
rs115052367 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426663 | TGTTTATTAGCAGCA[C/T]GAGAACGGACTAATA | 55779 |
rs115090627 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438131 | TGGTTAGGAATCATG[A/C]GTTTATATAAAACAC | 55779 |
rs115099030 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359322 | TTTTTGTTGAATCTC[C/T]TTCACAAAGGGCTCC | 55779 |
rs115102436 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400449 | TCCCCTTTTGGGAAA[A/T]TCCCCAAATGCTCTT | 55779 |
rs115140031 | snp | A/C | 0.422787 | 0.180679 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415210 | GTTCAGTGGTGATTT[A/C]CCCTTTATTACTTTT | 55779 |
rs115141397 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393294 | GACTTTTAAATTATG[A/C]TGAGTGTTTTGGTCT | 55779 |
rs115143832 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438247 | ATGGAATCTTCAGAG[C/T]TGAAAGAGGACTTTA | 55779 |
rs115149191 | snp | C/G | 0.180702 | 0.240204 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374605 | GCATTATTCACAATA[C/G]CCAAAAGGTGGGAAC | 55779 |
rs115168806 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328237 | TGAAAATTTTCAAAA[C/T]CACAGAATGGTAAAT | 55779 |
rs115170508 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299533 | ACTAAAAACAGAGCT[A/G]TCATATGATCCAGCA | 55779 |
rs115184130 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396367 | GTTATTCACAGACTA[C/T]GCTGAAAGAATATGA | 55779 |
rs115184231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377428 | CCAGATTGCTTGAGT[C/T]CAGATTCTAGTTTCA | 55779 |
rs115197350 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375327 | AAAATGGTTAAGATG[A/G]TCAATTTTATGTTAT | 55779 |
rs115197503 | snp | C/T | 0.00538539 | 0.051611 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406876 | ATGTGTGCTTTCATA[C/T]ATGTACTTGAAAACA | 55779 |
rs115202998 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416841 | TTTACTTTAAGACAG[C/T]CATTTCTAACTCTAC | 55779 |
rs115219798 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393148 | TTCAGCTGGTAAGGG[C/T]TAAGACCTATTGCAA | 55779 |
rs115233927 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384812 | TAAGTATCCAGTGGG[G/T]AGCTGTGAAAGTGTG | 55779 |
rs115240204 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409908 | CTCCCACCAGCACCA[C/T]GACAGTTTATAAATA | 55779 |
rs115243117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386999 | TATTTAGACCAGCCC[A/G]AGTCAGAGGGGAATG | 55779 |
rs115243877 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432221 | ATCAACTTGTGTGCC[A/G]GGAGCTGTGATAAAT | 55779 |
rs115257050 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389442 | AAACCTCAAATAACT[A/G]ATGGCATATCTTAAA | 55779 |
rs115262098 | snp | A/G | 0.000906476 | 0.0212701 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427176 | ACTGACAGAAAACTA[A/G]TAATACCTACCTGTA | 55779 |
rs115277470 | snp | C/T | 0.0190085 | 0.0957962 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289221 | ATATTTTGTCCAATT[C/T]AAAATAAAGTAATTC | 55779 |
rs115284660 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330732 | AACTGTATGGAATAT[A/G]ATCTGCTCTTTTCTG | 55779 |
rs115299299 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440752 | GAGCTCAGATTCCTC[A/G]GTCTGGTGTAAAGGT | 55779 |
rs115304628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353005 | CCCCAGATCAGGGAC[A/G]GAAAGCAGGAGTTAA | 55779 |
rs115352248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428579 | GAATAAATCAGTATT[C/T]GCCTTTCTATTCTTG | 55779 |
rs115365310 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313896 | CAGCAGTGTGAGAAC[A/G]GACTAATACACCAAG | 55779 |
rs115385009 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364901 | CAGACCAGTGCTGAG[C/T]TTAGTTGTTTTCTGT | 55779 |
rs115403962 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393293 | TGACTTTTAAATTAT[A/G]CTGAGTGTTTTGGTC | 55779 |
rs115405123 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348941 | TTTAGCTACAACCTG[A/T]GAGTTGGAGATACCT | 55779 |
rs115421979 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357304 | TTATTTGAAAATAGG[G/T]TCTTGATAGAGGTAA | 55779 |
rs115425545 | snp | A/C | 0.0854556 | 0.188216 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317689 | TATGGCCAGCACTTG[A/C]GCTGGGGAGGAGCCC | 55779 |
rs115445838 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372841 | TAAGTTAAGGAGACA[A/G]GCCTCAGGAGAAACC | 55779 |
rs115468630 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437611 | ACCAAGGAATTTGCC[C/G/T]GGTGTTCTGATGTAG | 55779 |
rs115528521 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394887 | CCTTTGTGAAACCTT[A/G]TTATTCAATGATAAG | 55779 |
rs115548548 | snp | A/T | 0.0876345 | 0.190099 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398805 | AAATATTTCCCCAAA[A/T]ACTTCCATGGCATTT | 55779 |
rs115548730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430839 | GAACAAAATACCTCC[C/T]AAAATTATTAAATAA | 55779 |
rs115558470 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397779 | CTGTGACAGAAAACA[C/G]TGGAAGGGAGCCAGG | 55779 |
rs115560694 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389819 | TGAAGAAATTCAAAA[C/T]GTGAACAGACCAATT | 55779 |
rs115583420 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361231 | GAGAGAGATAAACCG[C/G]GTATGTAATTTCATC | 55779 |
rs115601200 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427778 | TTGGCTTTAGGACAA[A/G]CTGGGAATGAGAACT | 55779 |
rs115610953 | snp | A/G | 0.000988321 | 0.0222077 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366180 | ACTTTTAATACATCC[A/G]TAATTATTGTCATGC | 55779 |
rs115613171 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317559 | AGTTTCCTGGCAACC[A/G]CGAAGCAAATTGGAT | 55779 |
rs115716337 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428935 | TCTCCTCTCCAGCTA[G/T]CTGAGAGATACTGCT | 55779 |
rs115721054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362814 | CAATTTTTGTTTATA[C/T]TTCAGTGTATCTGTT | 55779 |
rs115740965 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336315 | TAACATGGGTAAATC[A/G]CTAGCTGGAATGATC | 55779 |
rs115744413 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385936 | GGCATGAGGCACTGC[A/G]CCCTGCCTCTGTTTC | 55779 |
rs115746070 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340864 | GGGCTTGGAGAATGA[A/G]TACAAATTTTTATAG | 55779 |
rs115750112 | snp | A/T | 0.00319116 | 0.0398171 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426271 | GGAGCAGGGGTTTGC[A/T]GAGGTACTAAAAAAA | 55779 |
rs115758280 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382987 | TGGATTATGTCCAGG[A/C]CATTTTAATCACTAA | 55779 |
rs115762803 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432925 | TATTATTTAACATTT[C/T]TAACTTTCTTGGAGG | 55779 |
rs115773781 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328168 | CTCCATAGTATCTCT[A/T]CAATCCCTTTTATAT | 55779 |
rs115822656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315573 | CAACAGCATCAACAA[C/T]CAACAGGATTTAAAT | 55779 |
rs115824144 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348944 | AGCTACAACCTGAGA[G/T]TTGGAGATACCTGGT | 55779 |
rs115825912 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394574 | ATTTTAACTTCTTCC[C/T]TTCTTGATAGTTCCC | 55779 |
rs115857396 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342778 | AGGCAGATTGCCTGA[A/G]CTCAGGAGTTCAAGA | 55779 |
rs115896038 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301722 | GAATGGCTAGATTGA[C/T]AGATTGAGCTAATTA | 55779 |
rs115897524 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379022 | TGCCTGGAACATGTA[A/T]GATTGACAAGCAGAT | 55779 |
rs115901000 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322992 | GCAGAGTGAAGTTGG[C/T]GGCGGGGAAGCCCCT | 55779 |
rs115928492 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393543 | TTTGTTTGTTTGTTT[C/G]TGATAGGGTCTCACT | 55779 |
rs115960952 | snp | A/C | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380143 | CTGCACCCACTAACT[A/C]GTCATCTAGCATTAG | 55779 |
rs115963143 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385786 | CTGGGACTATAGGCA[C/T]GCCACCACAAAGCTA | 55779 |
rs115964089 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319273 | AAAACAAAAAAAGAG[C/T]AGGAGTTGCTATTCT | 55779 |
rs115967798 | snp | C/T | 0.00051549 | 0.0160462 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291588 | TGTATCTCTTTCTCT[C/T]GTGGAGACTGAATGG | 55779 |
rs115985382 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386259 | CATGGAATGTCTTTT[C/T]TCATCTCTTCACTTT | 55779 |
rs116001330 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391791 | GAGAATGGCAAACAG[A/G]TATATGAAAAGGTGC | 55779 |
rs116005061 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340389 | GACCTCCCAGTTAGG[G/T]TGGAGTTTTTAAAAC | 55779 |
rs116005274 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381202 | CTGCAGTTATTGGTA[A/G]AAAGTCAAGTTTATT | 55779 |
rs116037863 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357269 | TGAGGCCCTAACCCC[C/T]AGCACCTCAGAGTGT | 55779 |
rs116105460 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314372 | CGAAAGGAAATGACA[C/T]AATGATTTTTCAAGT | 55779 |
rs116111943 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297323 | ATGGTCAGCCTGCCT[A/G]CCCTGCTTTCTCTCC | 55779 |
rs116158229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416773 | GGCATCAGATAAATA[G/T]TTAATGATGGATACA | 55779 |
rs116159308 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322190 | ATAGACCGCAAGATC[A/C]GAATAGAAAACTCAG | 55779 |
rs116172873 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422497 | ATAAAGCATTTCAGG[A/G]TACTGGATCTGTTCA | 55779 |
rs116214931 | snp | A/C | 0.039522 | 0.134904 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295330 | CTAAGCCTCTCAAGT[A/C]GCTGGGACTACTGGT | 55779 |
rs116231275 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306695 | CATAACAGAATGGGA[A/T]TCAAGTGCATTATCT | 55779 |
rs116237698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439594 | CATATTCCATTGCAA[C/T]GCCTTACTCCCGAAT | 55779 |
rs116238200 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315090 | CTAAAATACCAACAA[C/T]TGTATTAAATGTAAA | 55779 |
rs116238612 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393566 | GTCTCACTCTTGACA[A/C]CCAAGCTGGATGGAG | 55779 |
rs116246678 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383627 | ATTAAGTTAGGAAAA[A/G]CAAATGGTAAATGAA | 55779 |
rs116253916 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372826 | GAAGGCAAATATCTA[C/T]AAGTTAAGGAGACAG | 55779 |
rs116265957 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338054 | GATCACTTGAGGTCA[A/G]GGGTTCCAAACCAGC | 55779 |
rs116266837 | snp | C/T | 0.00595416 | 0.0542368 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344602 | TCTGATTGACTAGCT[C/T]GTTTGAATTTGGAGT | 55779 |
rs116272072 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424540 | ACTTAGGGAATACCT[C/G]ATGGCTGACTTGTTC | 55779 |
rs116336859 | snp | C/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290442 | CTGAGTTCCCTTCTA[C/T]ATTTATGCAATGTTC | 55779 |
rs116343292 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331443 | TTAAGAGTTACTTTG[C/T]ATAAACATACAGTTT | 55779 |
rs116357241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336230 | AATAATAGTAAATCA[A/G]TGACAGAGAAAGCAG | 55779 |
rs116361478 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399518 | CATGAGGGGCAAGTA[C/T]TTTTTGTCTTTTTAT | 55779 |
rs116361526 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392205 | CATATACACAATGTG[C/T]ACTCTTCAGCCATAA | 55779 |
rs116378040 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442250 | AATCAGATATATGTA[G/T]GGCCAATAAGCACAT | 55779 |
rs116378146 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400084 | TACATGTTGAATATT[A/G]TAACAAGAAATTTCT | 55779 |
rs116389539 | snp | A/G | 0.0923359 | 0.194016 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426359 | TGAATTGTAGTTCCC[A/G]TAATCTCCACATGTC | 55779 |
rs116430861 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336799 | CCCAATTTTATGTTG[C/T]CTAGTGAAGTTAGTA | 55779 |
rs116438669 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383635 | AGGAAAAGCAAATGG[C/T]AAATGAAATACAGGT | 55779 |
rs116447061 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348043 | TCTAAGAGGAAAACT[A/G]GTGTTTTTGCTGCTG | 55779 |
rs116447840 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351552 | ACTCTCCAAAACCGC[C/T]AAGACCTAGATCTCC | 55779 |
rs116455142 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393520 | CCTGGCACCTCCCCA[C/G]TCCCTCTTTTGTTTG | 55779 |
rs116542883 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355793 | AAAGTTACAAAAAAA[A/C]TTTAAGTATATACAG | 55779 |
rs116655314 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414710 | TACCAGGGATGAAGG[C/G/T]GGCGTGATCATGGTG | 55779 |
rs116664374 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347614 | TTTTTGCCCAAAGCC[C/T]CATTGGGTGGGGAGA | 55779 |
rs116667489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301030 | TTTTAGAAACTCTTG[C/T]AAACATATACCATGT | 55779 |
rs116703810 | snp | C/T | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421636 | TGTGGCATATATACA[C/T]CATGAAATACTATAC | 55779 |
rs116742421 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416957 | ATATAGATTGCAAGC[C/T]CTAACACCCAGAGTT | 55779 |
rs116759691 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394889 | TTTGTGAAACCTTAT[C/T]ATTCAATGATAAGGT | 55779 |
rs116761287 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345194 | ATGTGTTTTGATGCA[C/T]AGATATACAAATAAA | 55779 |
rs116774265 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398356 | GCTATGCAGAGATGA[C/T]GTCTGACCTGAGCTG | 55779 |
rs116776709 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440786 | TTGTCAGAGGGTCTG[C/T]AGCTTATTGCAGCCC | 55779 |
rs116778701 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361476 | ATATAATTATACATA[C/T]TGTAGAATAAAGACC | 55779 |
rs116817864 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387149 | CAAGTCCTGGTGCTG[C/T]ACTGGGCTCAGAGCC | 55779 |
rs116864580 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333962 | CAATTAAACTTTTTT[A/T]TTTTTTTTTGAGACG | 55779 |
rs116875746 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374564 | GGTCTCAAAGAGATA[C/T]TTGAACACCCACCTC | 55779 |
rs116961541 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392556 | AAAATAACTAAAAGA[G/T]TATGAGTGGATTGTT | 55779 |
rs117100814 | snp | C/T | 0.000978665 | 0.0220992 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330216 | TTTAATCTCGTCTCT[C/T]TTCATAATTTCCAGC | 55779 |
rs117105529 | snp | G/T | 0.193194 | 0.243461 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400389 | TGGCTGCTGTGTTTT[G/T]TGGCCTCTCCTCTCC | 55779 |
rs117113971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322182 | ACAGACACATAGACC[A/G]CAAGATCAGAATAGA | 55779 |
rs117128195 | snp | C/T | 0.0517044 | 0.152246 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288305 | CTTCTGCATCCTTTT[C/T]CCATCAAGCTCAACG | 55779 |
rs117186346 | snp | A/G | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433095 | CTCCATCATTTTTAT[A/G]GAGCCCACCTTCCTA | 55779 |
rs117211710 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347257 | CCTGGAAACAGCTTC[C/T]GCTTTTGGGCTGAGC | 55779 |
rs117239166 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352410 | CACCACCTTTAAGAG[C/G]TGTAAACACTTGCTG | 55779 |
rs117283094 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375301 | TTTACTACTACTGAG[C/T]TGTACACTTAAAAAT | 55779 |
rs117390274 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288260 | GCATCCTCTGCTGGC[C/T]AAAATAAGTATAGCA | 55779 |
rs117483743 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391938 | AGTAAATTATACTGT[G/T]GGTAGGAATGTAAAT | 55779 |
rs117654664 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373136 | CCTTCATTTCTGACT[A/C]TGTAAGTAGCATCCT | 55779 |
rs117795653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383168 | GGGCATTGGAAGAAT[A/G]TTATTGATCCTTGTT | 55779 |
rs117801399 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300022 | GAAGACAGAGTGAGA[A/C]CCTGTCTCAAAGAGA | 55779 |
rs117845620 | snp | A/G | 0.0379877 | 0.132479 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444433 | TGAACCCAGGAGACT[A/G]AGGTGGCAGTGAACC | 55779 |
rs117900602 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441359 | ATAACACTGGTCCAG[C/T]CTGAGAGAAGCCCAA | 55779 |
rs117926314 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414984 | CTGCTGTGAATCTAT[C/G]TGGTCCTGGAGTTTT | 55779 |
rs117960120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347853 | GGTAAAGTCCCGATA[C/T]TAACAGGAGAATGCC | 55779 |
rs117998903 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336488 | AAATTTCTTCAAAGA[A/C]ACAAATTATAAAAAC | 55779 |
rs118078754 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347611 | TAATTTTTGCCCAAA[A/G]CCCCATTGGGTGGGG | 55779 |
rs118127000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388695 | GAAAGTAAAGGAACA[G/T]AAAGATGTTCCATGC | 55779 |
rs118134360 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292910 | AATAAAAGGGACAGA[A/G]GAGGCTGGTGCATGG | 55779 |
rs118168339 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396059 | CCATGTGTTTCAGTA[A/T]GTGGTTCTGAAAATA | 55779 |
rs137867766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343217 | CAGGAATGTGCCACC[A/G]TGCTTAGCTAATTAT | 55779 |
rs137868746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431064 | GAATACAAGGACTTT[C/T]ATTCATTCTACATGA | 55779 |
rs137871732 | snp | A/G | 3.38558e-05 | 0.00411422 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401224 | TAGGAGAAAATAAGA[A/G]TAATAGGCAACTTAC | 55779 |
rs137913414 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396971 | GTGTCTGCCTACCAC[A/G]TGCTAAGCACCTATC | 55779 |
rs137913500 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446494 | CATACCAGCTTTAGG[A/G]TAACAGGAATGATAA | 55779 |
rs137979754 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395278 | TACCGAATTACCAAT[C/T]GCTAAGAAAGAAGAA | 55779 |
rs137984476 | in-del | -/T/TTTAT/TTTATTTC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374399 | TTATTTATTTATTTA[-/T/TTTAT/TTTATTTC]TTATTATACTTTAAG | 55779 |
rs137990729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300998 | CTGTTCTACTTTTAG[G/T]TATGAAACCCTTATA | 55779 |
rs137996514 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369165 | ACCCCACTGTCATTA[G/T]TAGATCAACGAGACA | 55779 |
rs138006295 | snp | G/T | 0.000545513 | 0.0165063 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420116 | CCCAGCTATGTATAT[G/T]GCGATACTGTCGTCC | 55779 |
rs138021847 | in-del | -/AAGA | 0.113685 | 0.209567 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439254 | GGAGTCACCAGTGTT[-/AAGA]AAGAACCCTGACAAA | 55779 |
rs138091336 | snp | C/T | 0.000165096 | 0.00908408 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373449 | ATTGTCCTCTGTATC[C/T]GCAAGATAACGGACA | 55779 |
rs138105090 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434653 | TCAACATTCTTCTAC[A/G]ATATGCCTGGCAAGC | 55779 |
rs138132142 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340944 | TCCCTGGAGTTGGGC[A/C]ACTCGGCAGCCCCAG | 55779 |
rs138169971 | snp | A/C/T | 0.000232664 | 0.0107834 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400000 | TAGATTCGAACAGAG[A/C/T]CTATAGAAAGACAGT | 55779 |
rs138181902 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299395 | TTAAAATGGCTTTTA[A/T]CCAAAAGACAGACAG | 55779 |
rs138207355 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355374 | AAATACAAAAAAATT[C/T]GCCGGGCATGGTGGC | 55779 |
rs138219518 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346164 | AACACTCTGTAAAAA[C/T]GCACCAATCAGCGCT | 55779 |
rs138233936 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391123 | GGAACCAAAACAGCA[C/T]GGTACTGACATAAAA | 55779 |
rs138249029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313996 | ACTGAACAATAGACA[C/T]CATCCAATTTGAAAA | 55779 |
rs138255690 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319390 | AGGAAGACTTAACTA[G/T]CCGAAATATATATGC | 55779 |
rs138263784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382326 | GATGCTAAGAGGTCA[A/C]GAAAGATAAGAACTA | 55779 |
rs138299853 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423546 | CTTTGTCTTATCTCA[C/T]CCTCTCTTCTGGCTT | 55779 |
rs138305977 | in-del | -/TTTG | 0.106278 | 0.204558 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437793 | TTGGTTTTTTGGGGT[-/TTTG]TTTGTTTGTTTGTTT | 55779 |
rs138323865 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351931 | GACCCACTGGCCCTT[C/T]GGCTGACCTAGAGAG | 55779 |
rs138343070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113330005 | TGATTTCCAGAAGGC[C/T]AAGGATGGGGAGGAA | 55779 |
rs138366746 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441417 | GATTTAAGGGGGAGG[C/G]TGTGGAAACTGCCGG | 55779 |
rs138380482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376464 | AGAGGGGGCCCAAGG[C/T]CGCACTCTGGAGTAT | 55779 |
rs138432166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419223 | CCTCCACAAAATCCA[C/T]GACCCTTACATTGGG | 55779 |
rs138540115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343719 | AGCTGAACAGTATGA[C/G]AAAGCACTACTGGAA | 55779 |
rs138567356 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323915 | TGGGCATGGTGGCAC[A/G]TGCCTATAGTCCCAG | 55779 |
rs138579167 | snp | C/T | 3.29598e-05 | 0.00405941 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366173 | TAGCAATACTTTTAA[C/T]ACATCCATAATTATT | 55779 |
rs138608282 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311912 | TTTAGCAAAGAGACT[A/G]GGGGCATTTTGCCCC | 55779 |
rs138612294 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299988 | GTAAGCCATGATTGC[A/G]CTACTGCACTCCAGC | 55779 |
rs138633846 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289601 | GGCAGCTGCTTCTTG[G/T]GGCTGCCAGCTCCCA | 55779 |
rs138639506 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364232 | AACCCAGTGAACAAA[A/G]TAGTCTTAGTTTGCT | 55779 |
rs138640334 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325227 | GAGTGGTGTGAACCC[A/G]AGGGCGGAGCTTGCA | 55779 |
rs138640777 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434443 | GGTGGGTACCATATC[A/T]TAAAGTTGTCTCTAA | 55779 |
rs138656627 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335747 | TCTTGTCCTAATTGA[A/C]ATTTATAGAACACTA | 55779 |
rs138667245 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395958 | AACGCTATCTCTATC[A/T]ACAATGGTCATATAT | 55779 |
rs138671839 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429723 | CTACCTGTCCTTTTT[C/T]CCTCTTTTTCTCTTT | 55779 |
rs138720026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406334 | ATGGGGAAAAGTAAG[C/T]AACATAAATACTGCA | 55779 |
rs138722231 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415065 | GGTCTATTCAGGGAT[C/T]CAACTTCTTTCTGGT | 55779 |
rs138725993 | snp | C/T | 0.000415389 | 0.0144056 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416559 | TCTCAGAGAAGGATA[C/T]TCATAGATGATAATA | 55779 |
rs138757399 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402230 | CTCCATTAGAAAATG[C/T]TTCTCTTCCTGAATA | 55779 |
rs138758917 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360836 | AGGATGGGAAAAATC[G/T]ACTTTTATAAAGTAG | 55779 |
rs138797280 | in-del | -/T | 0.00292908 | 0.038157 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399894 | GTAGTTCATTATAAC[-/T]AACAAACTTACCATT | 55779 |
rs138842815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428933 | CCTCTCCTCTCCAGC[A/T]ATCTGAGAGATACTG | 55779 |
rs138860348 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446809 | TAGGTCCAACGAGGT[-/A]AAATTATTTGTAACT | 55779 |
rs138874152 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371180 | TCATAGATTCAATGC[C/T]ATCCCCATCAAGCTA | 55779 |
rs138876191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446997 | TCCCATGCTATTCTC[A/G]TGATAGTAAATAAGT | 55779 |
rs138884397 | snp | C/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288569 | CAGAGGCCCCCCAAT[C/G]TGAGCTGTAACTCAC | 55779 |
rs138892747 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359979 | AGAAATAGAAGCACA[G/T]ACAATCAAATTATAC | 55779 |
rs138916073 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349963 | GCTTATCTAATCCTA[C/T]ATGCCCATTCTGCAA | 55779 |
rs138928190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307707 | AGGCACGATGGCTCA[C/T]GCCTGTAATCCTAGC | 55779 |
rs138934568 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414293 | CTAAATATAAAGTCA[C/T]GTCATCTGCAAACAG | 55779 |
rs138938038 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381503 | CTATCTGTCTCAGTT[G/T]AACAAACGTGGATGT | 55779 |
rs138951295 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305647 | AGAAATAATACATCA[A/G]AAATATTTCTGAACA | 55779 |
rs139009209 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348183 | AGGGTCCAGGGACCA[C/T]TGCAGGTTCTTGGGT | 55779 |
rs139062856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321970 | GATTCAATGCTACTC[C/T]TATCAAATTACCAAC | 55779 |
rs139064694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384997 | TGTCATGGGAGGGAC[C/T]TGGTGGAAGGTAATC | 55779 |
rs139101047 | snp | A/G | 0.000148267 | 0.00860879 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426170 | AATCCAGAGTCACAA[A/G]AGGCATCGAAGCAAG | 55779 |
rs139115343 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393106 | GCAGAAGCTTAATAC[A/G]TTATGCTCAGATATG | 55779 |
rs139123336 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316702 | TGTGAAACCCCATCT[C/T]TACTAAAAATATAAA | 55779 |
rs139139657 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386977 | CAGCCAGTGCCCACA[G/T]ACAGAGTATTTAGAC | 55779 |
rs139139768 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350540 | CTATAATTGATAATT[C/G]ACAGTCTTCTCCATG | 55779 |
rs139177621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383605 | GAAATGAAGAAAAGA[A/G]TGAACTATTAAGTTA | 55779 |
rs139197419 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352376 | AATAAATCTTGCTGC[C/T]GCTCACTCTTTGGGT | 55779 |
rs139222287 | in-del | -/TTTTCAGTCTT | 0.0463947 | 0.145069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437268 | GAGATCACTTTCTAC[-/TTTTCAGTCTT]TTTTCTGAATAAATT | 55779 |
rs139241604 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443690 | GCAGCACAGCATAGG[C/T]TTTGGAGAAAGACTG | 55779 |
rs139247364 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421615 | TGGTGCACTGGATAA[C/T]GAAAATGTGGCATAT | 55779 |
rs139273415 | in-del | -/TAT | 0.0248432 | 0.108648 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440361 | CCACCGCGCACAGCC[-/TAT]TATTATTATTTTTGA | 55779 |
rs139304129 | in-del | -/ATTT/ATTTATTT/ATTTATTTATTT | 0.29175 | 0.246489 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418057 | ATTTATTGAGACACA[-/ATTT/ATTTATTT/ATTTATTTATTT]ATTTATTTATTTATT | 55779 |
rs139326759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318756 | TTACAAGCAAGAAGA[A/G]ACTGGGGGCCTATTT | 55779 |
rs139370954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354990 | TGGCTTCAAGACCTG[A/G]AGACGGATCACATCA | 55779 |
rs139405247 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292248 | ACATATACATCACTA[G/T]AATTTACAGAATATT | 55779 |
rs139413931 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290177 | TTAGGATATACAACA[C/T]AGAAAGTGATTTAAA | 55779 |
rs139426984 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309116 | GTCCTTTTTCTGACT[A/C]GTTCCTGACCTTGAG | 55779 |
rs139429031 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339542 | GAAAACTGAGTACCT[A/T]GGGCCTGTTTATGCC | 55779 |
rs139431890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398327 | AACTCTACTTGAAGG[C/T]AGATTCATGGAGGGC | 55779 |
rs139440699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326148 | TCACCAAATAAGATA[C/T]ACATATGGCAAATAA | 55779 |
rs139442941 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388290 | AGTTGTGGGAACTTG[A/C]TTATTAGTTTGTTTA | 55779 |
rs139463730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388917 | AGATCAACCCCAATA[C/T]AACAATAGCTGGAGA | 55779 |
rs139513797 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326940 | ATTGAATATGTGGAT[A/G]TCAGCTAATATTTTT | 55779 |
rs139537550 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432517 | AGCTTTTAATCTTTT[C/T]TCTTCTGATATTTAC | 55779 |
rs139545239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335988 | GTCAAGGAAGAAATC[A/G]CAAGGGATATTAGAA | 55779 |
rs139552927 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363693 | TCACAAAAATCCAAG[-/G]GAAAAAAATGCAGTT | 55779 |
rs139570235 | snp | C/G/T | 0.00398691 | 0.0444912 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384036 | TTAGTTTGCTGAGAA[C/G/T]GATGATTTCCAAATA | 55779 |
rs139585891 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332135 | ATATCATACCTGCCC[A/C]TCTCCTCTAGCTAGA | 55779 |
rs139611288 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433431 | CAAAACTCCATCTCA[A/G]AAAAAAAAAAAAAAA | 55779 |
rs139646573 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400716 | ATCAAGTTTAAAAAA[-/A]TGCAAAGATAAAAAT | 55779 |
rs139650591 | snp | A/G | 0.0043256 | 0.0463043 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404067 | AACAGGTAAGTGTAC[A/G]TATTTATGCCTCAAA | 55779 |
rs139658190 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311995 | TGGCGGGAGAAAATT[C/T]TAAGCAACAAAACAT | 55779 |
rs139658810 | in-del | -/T/TT | 0.107341 | 0.205301 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410152 | TTTTCTTTTTTTTTT[-/T/TT]ATTATACTTTAAGTT | 55779 |
rs139667227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312594 | ATCTCCAGGGCATGT[C/T]GGAGGCCTTCACACA | 55779 |
rs139674175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374039 | TATTGCTCCAACTCT[A/G]ATTTCCTTATTACTG | 55779 |
rs139677672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375231 | TTTCAGTGTTACAGG[A/G]TGAGGAGGACGGTAG | 55779 |
rs139756640 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344569 | TTTTCAAACCTGTCC[A/G]ATTTGCTTGGTTTTC | 55779 |
rs139778143 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371403 | ACCAATGGAACAGAA[C/T]AGAAGCCTCAGAAAT | 55779 |
rs139799216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352774 | ATATGAAAGGAAATG[A/C]TGAACCCCACCAATA | 55779 |
rs139802265 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421301 | TGAGATACCATCTCA[C/T]ACCAGTCAGAATGGC | 55779 |
rs139819718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369853 | GACTAATAAAGAAGA[A/G]AAGAGAGGAATCAAA | 55779 |
rs139880676 | snp | A/G | 1.71734e-05 | 0.00293026 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373529 | GGGGGAACTCACAGT[A/G]ATATAGAAAACCAGA | 55779 |
rs139904178 | snp | G/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380940 | AATGGAAACATTTTA[G/T]GCACATGTCTTTGAT | 55779 |
rs139975019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315650 | GTTTCTGACTTAAAA[C/T]GTTTTGACTTATGAT | 55779 |
rs139984949 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317071 | GCTGGGAACCCTGAA[C/T]GGGGTAACCAAACAC | 55779 |
rs139991242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356189 | GATATATGGTTGTAA[A/C]CACTGTAAAAATATT | 55779 |
rs139992058 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424844 | GTTTAGAATTTAGGC[A/G]TATTTGTCTAATACA | 55779 |
rs140006074 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345590 | CTATTTGCCTCTGTA[A/G]AAAACATTAAGCTCA | 55779 |
rs140013993 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403426 | TGTAGCATCCATAGG[C/T]AAACTCCATCAGTTC | 55779 |
rs140014871 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313118 | GCTCAATGCCAGCCC[A/G]TGAAAGCAGCTGGGA | 55779 |
rs140031940 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367477 | AAACTCCAACAGACC[G/T]GCAGCTGAGGGCCCT | 55779 |
rs140039825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437634 | TGATGTAGCAATACC[A/G]GACAATAAATACTAT | 55779 |
rs140040978 | in-del | -/ATTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407158 | TTCATTCATTCATTC[-/ATTT]ATCTGATTAAGATTT | 55779 |
rs140045020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367331 | GACACCTCATACAGG[C/T]GGGTGCCCTTCTGGG | 55779 |
rs140046846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328374 | GTATCCCAAGTCCTG[A/G]TCCAGACTTTAATCC | 55779 |
rs140063644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436614 | GTGACTATGATTGAT[C/T]GATAATGATTTCTTT | 55779 |
rs140064707 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349598 | CTGCTCCCTTGCCCA[C/T]GTCCACTATCCCGAG | 55779 |
rs140078186 | snp | G/T | 0.021333 | 0.101051 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413345 | TCTAATGATAGTTTA[G/T]TTTGCTGTGCAGAAG | 55779 |
rs140083309 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362124 | TTCTTTTTAGAAGAT[A/C]TTGGTTGAGGGAGAA | 55779 |
rs140099087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432912 | CTATCAGATAATCTA[C/T]TATTTAACATTTTTA | 55779 |
rs140101713 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444247 | GCTCACACCTGTAAT[C/G]CCGGCACTTTGGGAA | 55779 |
rs140194770 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346785 | GGAAATGGGCAGGGA[C/T]AAATAAGGGAATAAA | 55779 |
rs140202687 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407320 | TACCCTCCAGCTATG[A/T]GTGACTATTTAAATT | 55779 |
rs140218323 | snp | A/C/T | 6.65857e-05 | 0.00576961 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401739 | TCTCAAAATCCCATA[A/C/T]CTTGTAAAATGAAAA | 55779 |
rs140239272 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379203 | AAAAAAAAATAAATA[G/T]ATAAATGAAATCTTA | 55779 |
rs140307657 | snp | C/T | 0.000792707 | 0.0198928 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399951 | TCCTTGTTTGAATTT[C/T]ATCTGGGCCAAAGGA | 55779 |
rs140312239 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313796 | GCCTTTTGCCTCCCA[A/C]CATGATTCTGAGGCA | 55779 |
rs140313099 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375782 | GCTGAGACGGCACCA[C/T]TGCACTCCAGCCTGG | 55779 |
rs140315044 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364312 | ACAGAAGATAGGTCT[C/T]TGTTTTGCTGTCATT | 55779 |
rs140332097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439721 | ACACATTGATGCAGA[A/G]GAGTGTGTTGCTAGA | 55779 |
rs140352403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434479 | GCTAAGAAGTTTATA[C/T]CTTATTTCCTTGACA | 55779 |
rs140356033 | snp | C/T | 0.00641896 | 0.0562875 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400593 | GAGGAGAAACAGCCA[C/T]GGCTTCAATAGCTCC | 55779 |
rs140397848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296457 | AAATGAGATCTCTCC[A/G]TAATCTTTCATCCAT | 55779 |
rs140435028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291816 | TCCATGCCCTTATAC[C/T]GTGTATCTGTGATGA | 55779 |
rs140435169 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361503 | GACCTGTTTTGTTTT[G/T]TTTTTTTTTGAGATG | 55779 |
rs140452068 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329928 | CTTCCCCTTCATTCT[G/T]TGTCAGCTTTCCAAA | 55779 |
rs140453389 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390494 | ACTGGAAGTTCTAGA[C/T]AGAGTAATCAGATAA | 55779 |
rs140472129 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372171 | TGGAAGACAGTGTGG[C/T]GATTCCTCAAGGATC | 55779 |
rs140472725 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434303 | GAGACATGGATGATG[A/G]TCAGGAGTTGGCCAG | 55779 |
rs140474057 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415734 | TCTGAGAGACTGTTA[C/T]GATTTCAACTCTTAT | 55779 |
rs140486511 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295556 | ATGGAGCCATTGGAC[-/A]ACACAGCACTAGGAA | 55779 |
rs140515266 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412912 | TATTGCTGGGTCAAA[C/T]GGCATTTCTGGTTGT | 55779 |
rs140515790 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345926 | TTTCTTTCATACATA[C/T]TATCTTTCTCATCTC | 55779 |
rs140520666 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367933 | ACAGGACGAGAACTT[C/T]GTGACGCATGCACAA | 55779 |
rs140541330 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351734 | CTGGAGTTGGGCGAC[A/G]TGGCTTCTCCCCTTT | 55779 |
rs140559990 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386505 | GTTCAAAAGCATATT[A/G]CATGAAACAGTGAAG | 55779 |
rs140606553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298430 | CAACAAGCTAACTGC[A/G]GTGTTATTCACCACT | 55779 |
rs140627216 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293500 | TATACTGTGTAAAGA[A/G]ACAGATAACTAGTAA | 55779 |
rs140637542 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363925 | ACATGAATCATTTGT[C/T]CAAATACCTCAGTGT | 55779 |
rs140654929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417497 | AAATAAGCTGTTATA[A/G]GGATAAGCTATTTAA | 55779 |
rs140684107 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375407 | AAAGTTACGAAGCTG[C/G]AACAGAGATCAGAAA | 55779 |
rs140719234 | snp | C/T | 0.000790436 | 0.0198644 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403934 | CCATTGTGACATGAC[C/T]TGCTTGTCCCTCGAC | 55779 |
rs140800675 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351652 | GGATAGTACGAGATG[A/C]CAACCGGCATTTACA | 55779 |
rs140820257 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417427 | CTGTTATTTTTGTCT[A/G/T]TTGGTAAGCCAAATG | 55779 |
rs140861873 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440751 | AGAGCTCAGATTCCT[C/T]GGTCTGGTGTAAAGG | 55779 |
rs140889873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397834 | TTGTTGATTTAGAGA[A/G]AGGGATGATTGGGGA | 55779 |
rs140907742 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368552 | TGCTGAGAGATTTTG[C/T]CACCACCAGGCCTGC | 55779 |
rs140918936 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323999 | CAGTGAGCACAGATC[A/G]CGCCACCGCACTCCA | 55779 |
rs140939394 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359297 | CTGGTGTCTTCTTGA[C/T]ATCACCAAGTTTTTG | 55779 |
rs140949736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428159 | CCAAGAGGGGGCCCT[A/G]GAGAACTACTCTCTA | 55779 |
rs140973883 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409249 | CAGTGTGTAGTCAGG[G/T]TTACTACCAACAGAG | 55779 |
rs140993489 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399700 | CAAATCTACAGGTGG[C/T]AAAAAATTTCACTAA | 55779 |
rs141004555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304471 | ATAAGGCTGATCTTG[C/T]TGTTGTTGTTTTCCT | 55779 |
rs141013353 | snp | A/G | 1.66164e-05 | 0.00288235 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445316 | CTTCACTTATGATAC[A/G]TGGGTAGAAAGAGCA | 55779 |
rs141025018 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318461 | TATGACTCATTGGTA[C/T]TCCTGAGAAAGAAGG | 55779 |
rs141033656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395620 | CTGAGCTTTCTGTTG[C/T]CGCATCCCTGACCCT | 55779 |
rs141039341 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410571 | ATTTGGGTTGGTTCC[A/T]GGTCTTTGCTATTGT | 55779 |
rs141051699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422295 | TGATTTTAGAGAATT[C/T]CACTTATTCATAAGT | 55779 |
rs141093042 | in-del | -/T/TT | 0.39811 | 0.248073 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414995 | TATCTGGTCCTGGAG[-/T/TT]TTTTTTTTGGTTGGT | 55779 |
rs141117734 | snp | A/G | 0.000920355 | 0.021432 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445393 | GGAAAAAATTTAGAT[A/G]GTAATTAGAAACATG | 55779 |
rs141151774 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300024 | AGACAGAGTGAGACC[A/C]TGTCTCAAAGAGAGA | 55779 |
rs141154769 | snp | A/G | 0.000413568 | 0.014374 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420026 | GCATACCCCAATGAC[A/G]CCAATTCCTTCACCA | 55779 |
rs141157891 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331506 | CTTACAAAAGCTACA[C/T]ATATATTTACTATCT | 55779 |
rs141166873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392749 | AACTCTCAAGATTCT[A/G]GCTTTAGTGACAGGG | 55779 |
rs141191312 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292777 | CCCAACACCCTCTGC[C/G]TCTTCTCCCTTGCTC | 55779 |
rs141220795 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340570 | AGGGTGTGCGATGGG[G/T]GTGTGGCTCGCTTCT | 55779 |
rs141226712 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399215 | TTATTCCAGGCCCAG[A/C]CATTCATGTCTTCCC | 55779 |
rs141226859 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288351 | TGTGGAAGTGCAGCA[C/T]GGTTTTCAGGAAAGC | 55779 |
rs141264789 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294202 | TAGGTATATCCACCA[A/C]ATACAATGTATTAAG | 55779 |
rs141269867 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387850 | GGACTGCCAGCATTC[A/G]CCACAAGCTGACTGA | 55779 |
rs141319155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333748 | ATTTTTTAAAAGTCA[A/G]TTACTATTTTTAAAG | 55779 |
rs141321505 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394525 | CCTACCAATTTCTCA[A/C]AATCAAGGTACAATA | 55779 |
rs141353606 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320949 | CACCCAGGATCAATA[A/C]TTTGCATCCTTCAAT | 55779 |
rs141358352 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377699 | TGCTCTGTCACCAGG[C/T]TGGAGTGTAGTGGCA | 55779 |
rs141478548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342700 | ATAATTTAAAAATTA[C/T]TGGCTTTATGGCCAG | 55779 |
rs141491751 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372324 | GCAAAGACTTGGAAC[C/T]AACCCAAATGTCCAT | 55779 |
rs141521842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357112 | ATGATTGGTACATAT[A/G]TGAAAAGGGACTGAA | 55779 |
rs141525635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424974 | AGCACAGTAGGTCCC[A/G]GAAGGCATCAGAGCA | 55779 |
rs141528536 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423166 | GTCACCCAGCCTGGA[A/G]TGCAGTGGCATGAAC | 55779 |
rs141547615 | snp | A/G | 0.000214318 | 0.0103495 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363240 | TTTGCTCTCTCTTCC[A/G]TGCCTTTATTTCTCC | 55779 |
rs141556461 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443375 | ATTAGGAGAAATCCA[G/T]TAACTGCAAGAAAGA | 55779 |
rs141599408 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348468 | AAGAGGGAAGGCAAA[C/T]AGAGTGAAATACCTT | 55779 |
rs141610268 | snp | A/C | 0.000632444 | 0.0177714 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446641 | CCTGAGGTGGCATTT[A/C]GTGGAGAACAAGAAT | 55779 |
rs141641699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361267 | GTCCTACTTTTGGCA[C/T]GCCTGAAGAAGTGCT | 55779 |
rs141644653 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432235 | CAGGAGCTGTGATAA[A/G]TAAGTAAAACACAGA | 55779 |
rs141707963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307551 | TGACTTCTTATATTT[A/G]TTGTCTTTCTCCACT | 55779 |
rs141721546 | snp | A/C | 0.00265252 | 0.0363211 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330125 | AATTTTTTCCCTTCT[A/C]TTCTCTCTTTCAGCT | 55779 |
rs141725293 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391537 | CAGCAAAGGAAGACA[C/T]CAATAAAGTGAAGAG | 55779 |
rs141728435 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320435 | TATATGATATATATT[G/T]ATATATATGATATAT | 55779 |
rs141739578 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334935 | GCGTGTACACATAGC[G/T]CTCACAGGAAACCCA | 55779 |
rs141750648 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424369 | TGAACCCGGCAGGCG[A/G]AGGTTGCAGTAAGCA | 55779 |
rs141762230 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323161 | GATTTCGGTAGGGAC[A/G]CAGCCAAACCATAAC | 55779 |
rs141777925 | in-del | -/AAATT | 0.354665 | 0.227036 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422073 | AGTATGTTTAAGTCA[-/AAATT]AATATGCCCAAAATA | 55779 |
rs141804798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429777 | ACTCTTTAGAATTCT[A/G]TTTAAATTTCTGTTG | 55779 |
rs141809703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427416 | AGCTAAAACTTCCAA[C/T]TTCCTTGTGCTATAG | 55779 |
rs141834606 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414647 | CTTTGGTTCTGTTTA[C/T]GTGATGGATTACGTT | 55779 |
rs141847284 | snp | A/C/G | 0.00372105 | 0.042985 | missense, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396529 | TTACCCCTGTGGCTA[A/C/G]AATTTCCCCATCACG | 55779 |
rs141899714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358617 | TGACAAGAGGATTCC[C/T]TGAGATTTCAAGTCA | 55779 |
rs141941073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346272 | TAAAGGATTGTAAAT[G/T]CACTAATCAGCACTC | 55779 |
rs141943096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405913 | CAAGGCTTTTTACTT[C/G]CTCCTATATACCATG | 55779 |
rs141968810 | in-del | -/T/TG | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430428 | GCTGGAAAAATAAAT[-/T/TG]GAAAAAAAAAAAAAA | 55779 |
rs141969684 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369610 | TTATAGCACTAAATG[A/C]CCGCAAGAGAAAGCA | 55779 |
rs141977215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402818 | TTAACTTCTTTTCTC[C/T]TGAGGTTTTCTCCCA | 55779 |
rs142052922 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423132 | TTTTTTTTTTTTTTG[G/T]GAGATGGGGTCTCAC | 55779 |
rs142060163 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378575 | TAATGATCTTCCACA[C/T]ACACTTTTATGAAAT | 55779 |
rs142124252 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311914 | TAGCAAAGAGACTGG[A/G]GGCATTTTGCCCCTG | 55779 |
rs142128398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372825 | AGAAGGCAAATATCT[A/G]TAAGTTAAGGAGACA | 55779 |
rs142137005 | in-del | -/TC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320225 | GAGGAGGTATATTAG[-/TC]TCTCTCTCTCTCTCT | 55779 |
rs142141209 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310192 | CACCAAGATGCCTGT[A/G]GAGGCCATGTGATAG | 55779 |
rs142148775 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307730 | ATCCTAGCACTTTGG[G/T]AGGCTGAGGCAGGTG | 55779 |
rs142166823 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371212 | CAATGACTTTCTTCA[A/C]AGAATTGGAAAAAAC | 55779 |
rs142176353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305233 | ATGAAGGCATCTTGG[A/G]AGGAAGTAAAGCATG | 55779 |
rs142198130 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349337 | AAAAGCTAGCCCTGG[G/T]CCCTGAACAAAATCT | 55779 |
rs142208833 | snp | C/G | 0.0879971 | 0.190408 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411301 | AATTAAGTCTTTAAT[C/G]CATCTTGAATTAATT | 55779 |
rs142283493 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345750 | GGCATTGGTTCATAA[C/T]TATCACACACACACA | 55779 |
rs142292288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363617 | AAGTAAATTAAAAAC[C/T]CAAATTGGTTCGGTT | 55779 |
rs142295460 | snp | C/T | 0.0002188 | 0.0104572 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433552 | TAAAAGTATACATAT[C/T]ATCTTTACTTACATC | 55779 |
rs142299289 | snp | A/G | 0.000199983 | 0.00999758 | stop-gained, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426272 | GAGCAGGGGTTTGCT[A/G]AGGTACTAAAAAAAT | 55779 |
rs142304373 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371682 | TGGGCAAAGACTTCA[C/T]GTCTAAAACACCAAA | 55779 |
rs142306471 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288614 | GGTTTTTACATTTTT[-/T]CCTTTTTCTCCTTGA | 55779 |
rs142311264 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347631 | ATTGGGTGGGGAGAC[C/G]AACTATCCTTTTAGG | 55779 |
rs142334202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386755 | AAATCAGGTGAGTGA[C/T]GACAATACTTGGTTT | 55779 |
rs142339650 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388442 | ACCAGAGAAAATCAC[C/T]GTCACTAAAACGTAG | 55779 |
rs142401442 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386094 | CTGAGGTGGGATGTA[C/T]ATATATTCATAATTG | 55779 |
rs142402576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322995 | GAGTGAAGTTGGCGG[C/T]GGGGAAGCCCCTTAT | 55779 |
rs142416772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338652 | ACATCTCTCCAGGAA[C/T]GTTCAAACATTTGGG | 55779 |
rs142421848 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426992 | TCAGAGTACTCTATG[C/T]GATCCTCAGAAATAA | 55779 |
rs142425145 | snp | C/T | 0.000248067 | 0.0111343 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401647 | GAAGAGATTCACATT[C/T]TTGTCTACTTGAAGT | 55779 |
rs142426658 | snp | C/T | 0.00122425 | 0.0247109 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366080 | TGTCTTTCCTTAGCA[C/T]AAATTCAGAAAAAAT | 55779 |
rs142439441 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418193 | CCAGGCTCAAGCAAT[-/T]TCTCGTGCCTCAGCC | 55779 |
rs142502427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326358 | GTTATAGTGAAAAAA[A/T]TAAGGTATCTAATAG | 55779 |
rs142526654 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288856 | AAGTTGTGACAGAGG[A/G]GCTGGACTCTGTGGT | 55779 |
rs142538233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317725 | CTCAGAGAGTATTGA[A/G]AGGGGTGAGATGCAT | 55779 |
rs142546092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360216 | TACTGACTGGCCAGA[A/T]AAAAAGAAGCTTAAA | 55779 |
rs142547260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354409 | CAGTTCTCAGCCCTG[C/T]TCAGCAGCTGCCTGG | 55779 |
rs142563282 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421616 | GGTGCACTGGATAAC[A/G]AAAATGTGGCATATA | 55779 |
rs142658669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375284 | ACAACATTGTGAATA[C/T]GTTTACTACTACTGA | 55779 |
rs142684951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335828 | TACGTAGATAGACTG[C/T]ATATGCGTGGCCATA | 55779 |
rs142694868 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416790 | TAATGATGGATACAA[C/T]TGAAACTGAAAACTA | 55779 |
rs142705009 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368819 | TAAAAAGTCATGACC[C/T]ATCAGTGTGCTGTAT | 55779 |
rs142713897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441448 | CTGCTGAGGTCCAAA[C/T]TCACCGAAGGTACTG | 55779 |
rs142752826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371449 | CAAACATCTGATCTT[C/T]GACAAACCTGACAAA | 55779 |
rs142804587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419271 | ACAGTTATTGCCACA[A/T]TATCATGTACTTGTG | 55779 |
rs142809515 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303644 | ACCTGGGTAGTCTTG[C/T]ACTTGGGTTATTATT | 55779 |
rs142851572 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346957 | CCGCGAAGGCCCGTG[G/T]CTTCATTCTTGAAGT | 55779 |
rs142922522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354155 | TCAAGAATAGTTAAA[A/G]GTATACAGAGATTAA | 55779 |
rs142932637 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348005 | GGGCCACTAAATCCA[A/G]CCTTCCTCTGTCCTC | 55779 |
rs142933837 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367366 | AGCTTCTAGAGGAAG[C/G]ATCAGGCAGCAATAT | 55779 |
rs142935053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297002 | ATGAAAGATTTTATG[C/T]CATCAGTGATTTTTC | 55779 |
rs142984350 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314847 | GATGACATTGCTAGA[C/T]TGGGATAAATGATGA | 55779 |
rs143011495 | snp | C/T | 0.000577496 | 0.0169828 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373459 | GTATCCGCAAGATAA[C/T]GGACATCAATAGGTT | 55779 |
rs143018643 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352180 | TGTGTCTAGCTAAAA[G/T]ATTGTAAATGCACAA | 55779 |
rs143022464 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312866 | GAACCTCCGCCTAGA[C/T]TTCAGAGGATGTATG | 55779 |
rs143064768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372678 | GCATATGTATACCTA[C/T]GTAACAAATGTGCAC | 55779 |
rs143067161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415163 | ATAGAGGTATCTATG[C/G]TATTCTCTGATGGTA | 55779 |
rs143131044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293561 | TCTAAGCTGTTTCCT[C/T]TCCAATGTATCTGGA | 55779 |
rs143153988 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399827 | TTTGAGTCAGCAAAT[A/C]TCTATATTTCCAGAA | 55779 |
rs143156033 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429520 | TCATTATGCTTAACA[C/T]GTGTTTTCTATGAGC | 55779 |
rs143158884 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317218 | ATGTGTGACCTGGCA[A/G]GGGGATCTCCCCAGG | 55779 |
rs143172736 | in-del | -/G | | | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441457 | TCCAAACTCACCGAA[-/G]GTACTGACCGCCGCG | 55779 |
rs143174852 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445141 | TTGTTGAAAACTTAT[A/T]TGAGAAAGTCAAAAA | 55779 |
rs143199235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353004 | TCCCCAGATCAGGGA[C/T]GGAAAGCAGGAGTTA | 55779 |
rs143205209 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421370 | GCTACAGACAAAAGC[G/T]AATGCTTATATACTA | 55779 |
rs143224864 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351657 | GTACGAGATGCCAAC[C/T]GGCATTTACAGGAAA | 55779 |
rs143237574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329351 | TGGTGGAAGGAAGTC[A/G]TTACTGGTAGAAGGA | 55779 |
rs143242353 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417458 | TGTAGGAAGGGTAAA[C/T]GGCCAGCCAAAAAAT | 55779 |
rs143290581 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355624 | TCACAAGGACAGAAA[A/G]CCAAACACCACATGT | 55779 |
rs143296841 | snp | C/T | 1.67279e-05 | 0.002892 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396703 | CTTCAAATCCTACAA[C/T]AATTTGTGCTCCAGT | 55779 |
rs143297997 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424165 | GTAGAGGGCTAGGCG[C/T]GGTGGCTCACACCTG | 55779 |
rs143379035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314262 | ACTAAAGACAAAGAA[A/G]AAGTCTTGAAAGCAT | 55779 |
rs143438399 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290698 | AAGGTGATTGTTAAA[C/G]ATGATCTCTAGTAAA | 55779 |
rs143438550 | snp | A/G | 0.000959121 | 0.0218779 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401635 | TTTTATCATAGAGAA[A/G]AGATTCACATTCTTG | 55779 |
rs143464254 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305942 | CATTTATTGTATGGG[G/T]AGGGGCTCCATTTTC | 55779 |
rs143476632 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336915 | TAAGATAAGGAACAA[A/G]GTGTGGATGCTAGTT | 55779 |
rs143476887 | snp | A/C/G | 0.00289383 | 0.0379286 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446670 | ATTACCAGTAGCCCC[A/C/G]GAAGATCTATTCATG | 55779 |
rs143482430 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410426 | TCCTTGCAATAGTTT[G/T]CTCAGAATGATGGTT | 55779 |
rs143545175 | in-del | -/T | 0.0581099 | 0.160244 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290085 | TAAGTTTGGGGGTAA[-/T]TTTTTTACCGCAATA | 55779 |
rs143565247 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297981 | ATTCTATGTAAGTAA[C/T]GCCCCACGGACATGT | 55779 |
rs143566374 | snp | C/T | 0.000741003 | 0.0192341 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409201 | AGCTTTTGTCCTTAG[C/T]ATGGGTTGTTCTTCT | 55779 |
rs143567721 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299330 | CTCAACATTGCTGAT[A/C]GTCAGAAAAGTGCAA | 55779 |
rs143568739 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368395 | ACAGCAGATCTCTCG[A/G]CAGAAACCCTACAAG | 55779 |
rs143576436 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436272 | ATTATGCAGCCAATT[C/T]AGTTATTACAGAGTT | 55779 |
rs143587726 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404712 | CTCATTCTCCTAGAA[C/G]AAACAGCTTTTTCTG | 55779 |
rs143627453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403711 | TTACCACAAGAGAAG[C/T]ATTATTTAAAGTGAG | 55779 |
rs143653499 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287249 | ACAGCAAGGGGCACG[A/G]TATCACAGCCTGGAG | 55779 |
rs143667410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399278 | AATCCATCTCTGCTG[C/T]CACCCGAATCCCAAC | 55779 |
rs143727609 | in-del | -/T | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331455 | AACATACAGTTTTTT[-/T]AAAGATCAAAAGTCA | 55779 |
rs143824679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382101 | GCTTTTATAAGAAAA[C/T]TGTGGCTTGGATGGC | 55779 |
rs143847345 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435131 | GACAGGCTGAGGCAG[A/G]AGGACTGCTTGAGAC | 55779 |
rs143860248 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382514 | ATATGGTAGTAGCTA[C/G]AGGAGAATATAAGAT | 55779 |
rs143863007 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369257 | ATCTATAGAACTCTC[C/T]ATCTCAAATCAACAG | 55779 |
rs143892533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423722 | TAAATGGCACATTTC[A/T]TGCTATTAAAAGAAA | 55779 |
rs143893557 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377922 | TCCCAAAGTGCTGAG[A/G]TTACAGGTGTGAGCC | 55779 |
rs143895284 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307269 | ATATATATGTAAATT[A/C]CAGTCTGGCATTTCT | 55779 |
rs143935892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316441 | TCATAAAGATAAGAG[C/T]AGAAATCAATGAAAT | 55779 |
rs143958816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337475 | AAATTTATATGGAAA[A/G]ACAAAGTAATTATAA | 55779 |
rs143982723 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351379 | CTAATACCCCTAATT[A/G]TAGGGTTAGGAATGG | 55779 |
rs143992203 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442394 | ATGGAGCAACTGGAA[C/T]TCGCATACACTGCTG | 55779 |
rs144002231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385264 | ATGTCTTTATCAGTA[A/G]TGTGAAAACAGACTA | 55779 |
rs144023559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379663 | CAGCTCTGTAACAAA[C/T]AATATTTAAAAATAC | 55779 |
rs144128052 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378440 | TTAGTAATACAAAAG[A/T]TACATTTCTAGGAAA | 55779 |
rs144146436 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330808 | CATACCTTTTTACCA[C/G]CAAGTTTCCCTTTTC | 55779 |
rs144169285 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420770 | ACACCATTTGATAAC[A/G]TGATTATAATAAATT | 55779 |
rs144198096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339625 | TCCTGCTTTACATTG[C/T]GCCTGTTGCCTGGCT | 55779 |
rs144221955 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443827 | TCCCATAAGGTGTCA[C/T]GAAGCACATAAAGTG | 55779 |
rs144223597 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295911 | GCATTTATACTTTTT[-/A]AAAAAATGTAGGTTC | 55779 |
rs144257440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309589 | GGTTTTGGATAAGGG[A/G]TTGTAGACCTTTCCA | 55779 |
rs144257674 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371605 | TAAAGACTTAAATGT[A/G]AGACCTAAAGCCATA | 55779 |
rs144257757 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368062 | GTAAAAAGAAATGAA[C/G]AAAGTCTCCAAGAAA | 55779 |
rs144260282 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439486 | AGCCAAGGATAATTA[C/T]CTCAAAATAATTATG | 55779 |
rs144272792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319630 | CAACAACTTAGAATA[C/T]ACATTCTTCTCATCT | 55779 |
rs144276951 | snp | C/T | 0.331411 | 0.236373 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411743 | TGGGCAGTATGGCCA[C/T]GTTCATGATATTGAT | 55779 |
rs144315055 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442729 | AAAATTGCTATAATA[C/T]AATTTGTGTTTATTA | 55779 |
rs144363351 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369193 | ACAGAAGGTTAACAA[C/T]GATATCCAGGATTTC | 55779 |
rs144387613 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313128 | AGCCCGTGAAAGCAG[A/C]TGGGAGGGAGGCTGT | 55779 |
rs144397872 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374974 | TATATAAGCAAAATA[C/T]GGTACATACTTAAAG | 55779 |
rs144427615 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310409 | AAGAGGCCCCCTATC[C/T]CTTGGGTGACAATGA | 55779 |
rs144438768 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290091 | TTGGGGGTAATTTTT[C/T]ACCGCAATAAATAAG | 55779 |
rs144439529 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372256 | AGGATTATAAATCAT[C/G]CTACTATAAGGACAC | 55779 |
rs144441265 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415930 | CTTGTTAATTTTCTG[A/T]CTCATTGATTTAATA | 55779 |
rs144479732 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413112 | TTTTGATTTGCATTT[A/C]TCTGATGATCAGTGA | 55779 |
rs144496814 | snp | C/T | 0.000169067 | 0.00919267 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401280 | TTCCATATGGCTCCA[C/T]TGGCATCCTAAAAAA | 55779 |
rs144500668 | snp | A/G | 0.0012509 | 0.0249777 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296701 | CCAGATTCAACCAAA[A/G]ATCAACCCCCTTCTC | 55779 |
rs144560404 | in-del | -/AG | 0.339882 | 0.233284 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350176 | GAGAGAGAGAGAGAG[-/AG]GAAGAGACAGAGAGA | 55779 |
rs144588810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351076 | TTAGGAAAATTGCCT[A/C]ATAATGGGTCCGCTC | 55779 |
rs144600353 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416364 | TTAGCCCATTTACAT[G/T]TAAGGTTAGTATTGT | 55779 |
rs144618966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360921 | GAAGCTTGATGCTAC[C/T]AATATAAAAAAAAAA | 55779 |
rs144634987 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311828 | TGGACAATAAGGTCC[A/G]GGCTGAGGTGGTCTC | 55779 |
rs144686610 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414115 | TATTTTATTCTCTTT[G/T]TAGTGATTGTGAATG | 55779 |
rs144719856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374513 | AGTCTCATAGACTTA[C/T]GGAGAAAGAAATAAT | 55779 |
rs144732759 | snp | C/T | 1.6615e-05 | 0.00288223 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445317 | TTCACTTATGATACA[C/T]GGGTAGAAAGAGCAA | 55779 |
rs144801166 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292157 | ATGTTTCACACATCA[C/T]TTTCAGGGAGGCCTT | 55779 |
rs144808013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344304 | AAGTGGACATGGAGC[A/G]TTTCTTGGGAAAATG | 55779 |
rs144811021 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402400 | GGGAGAGGAGTCTAG[A/G]ATACTATAGGAAGAG | 55779 |
rs144813319 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361720 | AGCCAGGATGCTCTC[A/G]AACTCCTGACCTCAT | 55779 |
rs144824721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360390 | TATTTGAGAATGAGT[A/G]GTGTCTATTGGGGTT | 55779 |
rs144850021 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397975 | CATGTAAACCTACCA[A/G]TGTTGGAATGTACCA | 55779 |
rs144850503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357898 | CGTACACAATGTTCA[C/T]AGTAGCATTATTTAT | 55779 |
rs144873260 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372521 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 55779 |
rs144890206 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393583 | CAAGCTGGATGGAGC[A/G]CAGTGGCACGATCTT | 55779 |
rs144907390 | snp | A/G | 0.00245188 | 0.0349275 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409279 | GGCCAGCAAGTTACC[A/G]CTGTAGTTAAAGTCC | 55779 |
rs144938961 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322090 | AAGATAATCCACAAA[C/G]CTGGAGGCATCACAC | 55779 |
rs144946100 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414020 | TCCGTTTGTTTGTGT[C/T]CTCTCTTACTTCCTT | 55779 |
rs144955566 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357767 | TGTAAATTTTCAAAC[C/T]GTTTTGAAAAACTGA | 55779 |
rs144958590 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426858 | ATGCTGAGTTCTGGT[C/T]GGTCATGGCGCAACA | 55779 |
rs144976010 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369928 | ACAGAAATACAAACT[A/G]CCATCAGAGAATACT | 55779 |
rs144983005 | snp | A/G | 0.0345262 | 0.126772 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444329 | ACATGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 55779 |
rs145005916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292943 | GTGAAACATGGGAGC[C/T]GAAGCAGCTGTCATG | 55779 |
rs145030038 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288524 | TCTGGGGTGGGTAGG[C/G]CTGACGCTCTCAGTC | 55779 |
rs145055714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394838 | ATGGGATGGACAAGC[C/T]TGGTCTACACCATTG | 55779 |
rs145060128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317031 | TTGAGAGGCAACAGC[A/G]AAGGTGAGGCTGAAG | 55779 |
rs145105791 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349786 | CCAGGAAATTGACTT[C/T]CTCCTGGACACTGGT | 55779 |
rs145126236 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348109 | CAGGGACCATTGCAG[A/G]TTCTTGGGCAAGAGG | 55779 |
rs145143666 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332533 | CCTTGAAATGTGCAA[-/C]CCTCCACAACCACAT | 55779 |
rs145147051 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398745 | CAAATTTACTTTTAG[C/T]CTGGAATATTTTCTC | 55779 |
rs145226875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349028 | ACCAGTCAGCAAGCC[A/G]TCACCAGTATGGATC | 55779 |
rs145229009 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412561 | CTGGTGTGTGTTGTT[A/C]CCCTCTCTGTGTCCA | 55779 |
rs145250809 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298892 | GGAAGATGAAAAGTG[C/T]TCTGGAGATGGATGG | 55779 |
rs145261273 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347369 | CTCAAAGTCACGTCG[C/T]CCAAGCAAGGCTCAC | 55779 |
rs145326895 | snp | C/T | 3.32165e-05 | 0.00407519 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286827 | CCGGGGCCACTGGTG[C/T]GTGTGTCTTTTGAAA | 55779 |
rs145348656 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376003 | AATAGAAATAATTAG[G/T]AAGATAGTAGATTTA | 55779 |
rs145391746 | snp | A/G | 0.000544793 | 0.0164954 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396633 | ATTTTCTTCCGTCCC[A/G]CAAAAATCGTGAGCC | 55779 |
rs145409635 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292515 | CTGTGAAAGGAAAGA[C/T]ATAATACTTGCGTGG | 55779 |
rs145414908 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362979 | TAAAAGGGATAAACC[C/T]CACATACAAATTAAA | 55779 |
rs145436802 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347665 | CTTCCTCAGACAAGC[A/G]GGCCTAACAAAAGCT | 55779 |
rs145449188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334677 | ATTGAAAAAAAAATG[C/T]TTAAACCAGTTGGGC | 55779 |
rs145492370 | snp | C/T | 0.0010103 | 0.0224529 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330369 | AGAGAGTTTGAGGAA[C/T]CCTCCAACTGGGCCT | 55779 |
rs145494780 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391935 | TGGAGTAAATTATAC[C/T]GTTGGTAGGAATGTA | 55779 |
rs145496901 | snp | C/G | 0.135484 | 0.22223 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440198 | CCTCCCGAGTAGCTG[C/G]GATTACAGGCGCACA | 55779 |
rs145505315 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353089 | TCAAAGGAGGATGGG[C/T]AAGTGGGTCCCAGAG | 55779 |
rs145508439 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375775 | GTAGTGAGCTGAGAC[A/G]GCACCATTGCACTCC | 55779 |
rs145525630 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389705 | AGAAATTCAAAGGAT[A/C]AGTAGAGGCTACTAT | 55779 |
rs145534563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332278 | TCCAAATGGTCATTA[C/G]TAAAATGTCCAAATT | 55779 |
rs145537296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434496 | TTATTTCCTTGACAA[C/T]TGAAAACCATTAAAG | 55779 |
rs145545301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404298 | TATACAATAGACTTC[C/T]TGGTACATCTCTTAG | 55779 |
rs145552671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393236 | TAGTAATTTGCAAAT[A/G]ACATTAGAAATACAA | 55779 |
rs145575983 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328528 | TCTCCTGAGGAAACT[A/G]GAACAATAGGAAGAG | 55779 |
rs145588415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345994 | ACTTTTAAATTTTAG[C/T]CTTTCCATGAGACCC | 55779 |
rs145590512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313162 | CTGCAAAGCCACAGG[G/T]GTAGAGCTGCCCAAG | 55779 |
rs145643304 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403876 | TCCATCTGACCCAAC[A/G]GTGATAACTTCACCC | 55779 |
rs145654409 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333581 | CCAGGTTTACTCTTG[A/T]ATCTATTAGAAAAAC | 55779 |
rs145669094 | in-del | -/GAAA | 0.0228947 | 0.104514 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406142 | ATAAGAGAAAGAAAG[-/GAAA]GAAACTAACAATATT | 55779 |
rs145671475 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427663 | TTACTAACTTTTATA[A/G]GGAACCTGTTACGTT | 55779 |
rs145674035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329962 | AAAAAAAAAGTTTAA[A/G]AGCTCTGTAGTTCTG | 55779 |
rs145684729 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438487 | GCACCTACTGGATAA[A/G]GTTGTTCTGAGTCAA | 55779 |
rs145698781 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364068 | CTTGAAAGAGAAAGA[C/T]ATGAAATCAGAAATA | 55779 |
rs145698947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434317 | GGTCAGGAGTTGGCC[A/T]GGCAAAGAATGTGAA | 55779 |
rs145757058 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299471 | CGGTTGGTGGGAATG[C/T]AAATTAGTGCAACCA | 55779 |
rs145768933 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340788 | CTTATCACAAGGACA[C/G]AGGGATTTCTGTATC | 55779 |
rs145769724 | in-del | -/C | 0.0839998 | 0.186933 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437192 | TAATGGGTCAAGTTC[-/C]ACCTAGTGATTTGAA | 55779 |
rs145807146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406069 | GAAGCTATGTAAAAT[A/G]TTGATAGAGAACTAA | 55779 |
rs145836568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417685 | GGATACCATTATTAT[C/T]TCCATCTTATTGATG | 55779 |
rs145838773 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372949 | GTCTGTGGTGTTTTA[C/T]TGTGGCAGCCCTAGC | 55779 |
rs145845832 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401895 | AACACCAGCCAAAAC[C/G]TGACCCCTGAAATTT | 55779 |
rs145870771 | snp | A/T | 1.65556e-05 | 0.00287707 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395841 | TCCACTTCAAAGAAG[A/T]AAACAGTTTGATCTT | 55779 |
rs145874948 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332925 | CAAAATATAAGCTTA[C/T]CCATGAAACTGGTAC | 55779 |
rs145876815 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393751 | AACTGCTGCACTCAA[A/G]TGATCTACTTGCCTT | 55779 |
rs145880392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414350 | TTTGAATACGCTTCA[C/T]TTCTTTCTCTTGCCT | 55779 |
rs145892348 | snp | C/T | 0.000398146 | 0.0141037 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446669 | AATTACCAGTAGCCC[C/T]GGAAGATCTATTCAT | 55779 |
rs145938465 | in-del | -/AAGA | 0.342582 | 0.232225 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336629 | TCCTTAGTAAAGCAG[-/AAGA]AAGAAAACAGAAATC | 55779 |
rs146017167 | in-del | -/CT | 0.0869089 | 0.189476 | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441481 | CGCCGCGGCTCCTCT[-/CT]TCACAGCGTCTGCCG | 55779 |
rs146024970 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355905 | AATGAAGAGAAATAT[A/G]TCAGTCAATAGAAAC | 55779 |
rs146032295 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352546 | TAAAAATTAAAAATT[A/C]TGCACAGTTAGAAAA | 55779 |
rs146035558 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392695 | TATATCTACCATGTA[G/T]CCACAAAAATTACAA | 55779 |
rs146067340 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305576 | ATTTCTAAAGCACAT[C/T]CTCCATGTCCTAGAA | 55779 |
rs146076803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370182 | ACCACTCCTTCTGAA[A/G]CTATTCCAATCAATA | 55779 |
rs146120998 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307556 | TCTTATATTTATTGT[C/G]TTTCTCCACTAGACT | 55779 |
rs146131909 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302426 | ATATTAAGATTTAAA[A/G]CATCTGTATCCAAAG | 55779 |
rs146134433 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328514 | CCCCAAGGGCTGATT[C/T]TCCTGAGGAAACTGG | 55779 |
rs146144072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346737 | CTCTGTAAAATGGAC[C/T]AATCAGCACTCTGTA | 55779 |
rs146155884 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345299 | AAAAATAATTTTTAA[C/T]TCTCATTCCCCAGAG | 55779 |
rs146163928 | snp | A/C | 0.0383868 | 0.133201 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368699 | AACAGGCAAAATAAC[A/C]AGCTAACATCCTAAT | 55779 |
rs146164033 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410162 | GTTTTCTTTTTTTTT[A/T]ATTATACTTTAAGTT | 55779 |
rs146168043 | snp | A/G | 0.0027978 | 0.0372971 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426150 | AAGATCCAGTGGTAT[A/G]TTTGAATCCAGAGTC | 55779 |
rs146246191 | in-del | -/GAT | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433457 | AAAAAAAAAAAAAAA[-/GAT]CTATTTTATAACATC | 55779 |
rs146264670 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325545 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGTCT | 55779 |
rs146277401 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384198 | CAAGTAGGTGGGACT[G/T]CAGGTGCCCGCCACC | 55779 |
rs146289673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408003 | AGAAAATATAAGAAA[C/T]TGGAAAATTTTCACA | 55779 |
rs146335051 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325179 | TGGTGGTGGGAGCCT[A/G]TAATCCCAGCTACTT | 55779 |
rs146362879 | in-del | -/TAAAAAAA | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328696 | GAAATTTAGAGAGCT[-/TAAAAAAA]AAAAAAAAAAAAAAA | 55779 |
rs146387973 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371303 | AAGAACAAAGCTGGA[C/G]GCATCACATTACCTG | 55779 |
rs146397370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303023 | AAAATGTGAATAAAA[A/G]CCACAATGAAATGTA | 55779 |
rs146398409 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369477 | CTGCTCCTGAATGAC[C/T]ACTGGGTAAATAACA | 55779 |
rs146398752 | snp | A/G | 0.097727 | 0.198275 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411313 | AATCCATCTTGAATT[A/G]ATTTTTGTATAAGGT | 55779 |
rs146428408 | in-del | -/C | 0.0513262 | 0.151752 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414038 | TCTTACTTCCTTGAG[-/C]CAGTGGTTTGTAGTT | 55779 |
rs146437864 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351394 | ATAGGGTTAGGAATG[A/G]CTACTGCTACAGGAA | 55779 |
rs146447153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386773 | CAATACTTGGTTTTA[A/C]CTTTACATCACTGAA | 55779 |
rs146448726 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349717 | GCTCCCGGGGCAAGT[A/G]CCAGCTCATGTCATC | 55779 |
rs146459508 | in-del | -/TT | 0.312925 | 0.244695 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286896 | TATTGTTTTTTTTTT[-/TT]AAAAAAAAAAAGAAG | 55779 |
rs146460031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379968 | GACACTGGTATTTCC[A/G]CCTCCCATCTTTTAC | 55779 |
rs146560979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340511 | TCACACTCACCTTCC[A/G]CAATCCCCAGTTTAA | 55779 |
rs146569166 | snp | C/T | 0.00140235 | 0.0264426 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433599 | AGACCTCAGAGACTT[C/T]TTCCCATCACTCTTT | 55779 |
rs146573028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369836 | AGAGAGAGCACTGGC[A/C]AGACTAATAAAGAAG | 55779 |
rs146574347 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444078 | ATATGAGTCTAAACA[C/T]AAGTAATCTCAGTTT | 55779 |
rs146584274 | snp | A/C | 0.040671 | 0.13668 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368271 | CTTGAAAAGAGCAAC[A/C]CCAAGACACATAATT | 55779 |
rs146585320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439678 | GGTCAACTCTAAGGA[A/C]GTATAAAGAAAAAGG | 55779 |
rs146650849 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378843 | TATCTTCCTAGACTT[A/G]CATATGACCCCACAG | 55779 |
rs146691746 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421542 | ACATGCACTCATATG[C/T]TTATCACAGCACTAT | 55779 |
rs146703836 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417491 | AAATAAAAATAAGCT[A/G]TTATAAGGATAAGCT | 55779 |
rs146706608 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308576 | AAAATCAGACAAAAA[-/T]TTTTTTTTTCTTTTT | 55779 |
rs146768252 | snp | C/G | 0.000265759 | 0.0115243 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445323 | TATGATACATGGGTA[C/G]AAAGAGCAAACCAGC | 55779 |
rs146801974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297983 | TCTATGTAAGTAATG[A/C]CCCACGGACATGTAT | 55779 |
rs146813075 | snp | A/G | 0.000203004 | 0.0100728 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403817 | CTACAAGTCTTAAAC[A/G]TGGGTGCTACCATCC | 55779 |
rs146813385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363843 | TGTTCATATGCTATT[A/C]ACACAGAATTCACAA | 55779 |
rs146825265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399307 | ACACAAAGACTACAT[G/T]AGCAAAATAAAATGA | 55779 |
rs146894944 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354975 | AGGTTCTGGTATCCA[C/T]GGCTTCAAGACCTGA | 55779 |
rs146905592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390160 | ATCATGGCCAAGTGG[C/G]AATTATCCCAGGGAT | 55779 |
rs146905659 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352075 | GAGGGGGGATTGAGA[A/G]GTGAAGCCAGCTGGA | 55779 |
rs146944073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445437 | TTTACAGATCATTTA[A/G]ACCAAGTGCATAAAA | 55779 |
rs146953721 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441749 | ATACCGTCGAAGATA[A/C]CTGCCTGATATTCCA | 55779 |
rs146999886 | in-del | -/GGGG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350703 | CATTCAATCTGTGGC[-/GGGG]GGTGGCTGCTTTGCT | 55779 |
rs147001739 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346157 | ACCAATCAACACTCT[A/G]TAAAAACGCACCAAT | 55779 |
rs147011679 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342857 | AAAAAAAAATTAGCC[A/G]GGTGTAATCCCAGTT | 55779 |
rs147025470 | snp | C/T | 8.29236e-05 | 0.00643855 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366071 | TGGCCTTCATGTCTT[C/T]CCTTAGCATAAATTC | 55779 |
rs147034055 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318992 | ACAATACCCTTTAGC[A/C]CACAGCTGGCAGGCA | 55779 |
rs147048701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423334 | TGCCCAGGCTGGTCT[C/T]GCACTCCTGAGCTCA | 55779 |
rs147056360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419197 | AAACCTCATAGGCTC[C/T]GACTGACTTCCCTCC | 55779 |
rs147102499 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323781 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55779 |
rs147107696 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386639 | AGGGAGGAGGCAGAG[A/C]AAGATGGCTGATTAG | 55779 |
rs147146958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296066 | ACCATCCTCCCCGCT[A/G]CTGGAGTCCCCAGTG | 55779 |
rs147150470 | snp | A/G | 8.44773e-05 | 0.00649858 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366314 | CTTTGTTAATGCTAC[A/G]AAACAAAAAATGTAA | 55779 |
rs147156621 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291290 | GCTGCAATCATGAAA[C/T]ACAGCCTTCCGAGAC | 55779 |
rs147180334 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412799 | TTGGGTTGGTTCCAC[A/G]TCTTTGCTATTGTAA | 55779 |
rs147256606 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350410 | GAAGAGACAGACAAA[C/G]AGGGAGTCAGAAAGA | 55779 |
rs147266799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383376 | GGACAGAGAGAAGAA[A/G]CTCTGGTCTCTTCAT | 55779 |
rs147267187 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348657 | AAGGAAATAAGCAAA[C/G]AAATCTCCAAGGGAC | 55779 |
rs147277344 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378288 | TTATCCCTTTATCCT[C/T]TGAACTCCATACAAT | 55779 |
rs147323810 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437498 | TGCTATCTTAAACAA[C/T]ATATTCCCCAAATGG | 55779 |
rs147329022 | snp | C/T | 0.000307953 | 0.0124049 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426216 | GAAGAAGCTCTCTGA[C/T]ATTTTCTTCTTAACT | 55779 |
rs147360661 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335894 | ATACAGACTATTTTC[G/T]ATTACCACAAACAAC | 55779 |
rs147370655 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331893 | TTTGACCATTAAATT[A/C]ACCCTATGAGGTATA | 55779 |
rs147370784 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368906 | GGAAGATCTACCAAG[C/G]AAATGGAAAGCAAAA | 55779 |
rs147380370 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367226 | TTCTCCCAGCACAGC[A/G]TTCAAGCTCTGAAAA | 55779 |
rs147384408 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436606 | TGACTGAAGTGACTA[C/T]GATTGATCGATAATG | 55779 |
rs147393078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375222 | GTATGGGAGTTTCAG[C/T]GTTACAGGATGAGGA | 55779 |
rs147474342 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312923 | TTTGCTGCAGGGGTG[A/G]GGCACTCATGGAGAA | 55779 |
rs147475903 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352225 | AATGGACCAATCAGC[A/G]CTCTGTAAAATGGAC | 55779 |
rs147486043 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351023 | AAAGACTCAATGGGT[A/G]TTCAGTAAGTTATAA | 55779 |
rs147487436 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415248 | TCTATTTGATTCTTC[G/T]CTTCCTTCTTCCTTA | 55779 |
rs147499241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432873 | GTTCTATAAATTCCA[C/T]TCAGTTCAATTTTCT | 55779 |
rs147508833 | snp | A/G | 3.30775e-05 | 0.00406665 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401716 | TATTACATCAGCAGT[A/G]TCTATTGTCTCAAAA | 55779 |
rs147625487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305181 | CGTGTTGTGAAATGG[A/T]GACAAGACTCAATAA | 55779 |
rs147627723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349154 | ATGAATTATTCAATG[A/T]TGTCCACCATAACTC | 55779 |
rs147638253 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409744 | GGTGGTTGGCACAAG[A/T]TACAGGTCAAAAGAC | 55779 |
rs147648213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405822 | ATCTTAGCTTAATTC[C/T]TACAGTATTGAGAAT | 55779 |
rs147658672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427972 | ACCAGAGCTACATAG[C/T]AGATCTGAGATGAGG | 55779 |
rs147661037 | snp | A/C | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396648 | GCAAAAATCGTGAGC[A/C]CTTTTGGATCATAAA | 55779 |
rs147698315 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347338 | GTTGGTTGACCCTGT[A/T]GCCATGAGTGGAACT | 55779 |
rs147732360 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332659 | TAAGGAATTAATATA[C/G]CAGGAAGAGGAACTT | 55779 |
rs147735822 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403891 | AGTGATAACTTCACC[C/T]TCATACAGCATTATC | 55779 |
rs147738985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328817 | CTTGTTTAACAAACT[G/T]GAATTATTCCTGCAT | 55779 |
rs147743063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389913 | ATGGCTTCACTGTTG[A/T]ATTCTACCAAACATT | 55779 |
rs147753322 | snp | A/C | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433181 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCAGA | 55779 |
rs147753437 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386649 | CAGAGCAAGATGGCT[C/G]ATTAGAAGCCTCCAC | 55779 |
rs147760700 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410298 | ATGCTATCCCTACCC[C/T]CTCTCCCACCCCACG | 55779 |
rs147795940 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430811 | TACACAAAATATTTT[-/T]GAAAATAGAAAAGAA | 55779 |
rs147845586 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372280 | AGGACACATGCATAC[A/G]TATGTTTATTGCAGC | 55779 |
rs147904085 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310112 | GATGGTGTTAGAGAA[A/G]GGCAAGCAGGGAGCC | 55779 |
rs147942441 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361996 | TCTGATAGCTTCCCA[C/T]CACACACTGAAGGTT | 55779 |
rs147952692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358530 | AATTTTTAAAATGTA[A/G]GTGTTAAACAAATTT | 55779 |
rs147964021 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422866 | TAATTTTAGCAGGAA[A/G]ACTCCCTTTTACATG | 55779 |
rs147976745 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446634 | CCCACTTCCTGAGGT[A/G]GCATTTAGTGGAGAA | 55779 |
rs147992303 | in-del | -/T | 0.0869089 | 0.189476 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393682 | ACCTGGCTAATTTTT[-/T]GTATTTTTTGTAGAG | 55779 |
rs148002022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306544 | TGATGTTGTGAGCAG[C/T]ACTCTGAAGCAGGCT | 55779 |
rs148017168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410559 | TCATTGATGGACATT[C/T]GGGTTGGTTCCAGGT | 55779 |
rs148021531 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334767 | AAAATTGAAGAATTA[C/T]TCTCTACAGAAACTG | 55779 |
rs148022625 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355758 | CACCTGTACCCTAGA[A/G]TTTAAAGTATTAAAA | 55779 |
rs148027382 | snp | C/G | 0.0865458 | 0.189163 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424334 | CCAGCTACTCGGGAG[C/G]CTGAGGCAGGAGAAT | 55779 |
rs148097687 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113287994 | TAATTGAAATTTTAA[A/T]ATCTTTATATGTGGA | 55779 |
rs148121030 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352310 | GCCAGCAGCAGCAAC[C/T]TGCTCAGGTCCCCTT | 55779 |
rs148165600 | snp | A/G | 0.199873 | 0.244923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312197 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55779 |
rs148175703 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414366 | TTCTTTCTCTTGCCT[A/G]ATTTCCCTGTCCAGA | 55779 |
rs148186633 | in-del | -/TTTATTTA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374364 | CAACTGTCAATTTCT[-/TTTATTTA]TTTATTTATTTATTT | 55779 |
rs148186793 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392745 | GAATAACTCTCAAGA[C/T]TCTGGCTTTAGTGAC | 55779 |
rs148196485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435310 | CTCAGGACACTTACA[A/G]TCATAGCAGAAGGGG | 55779 |
rs148208340 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347290 | CGGTCAAGAGAGAGG[-/A]AAAATCATTCAGTTC | 55779 |
rs148218053 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346346 | TGTAAGTGCACCAAT[C/T]AGCACTCTGTAAAAA | 55779 |
rs148227684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372819 | CATGCAAGAAGGCAA[A/T]TATCTATAAGTTAAG | 55779 |
rs148237267 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387789 | TTGGACACCATTTCT[A/C/G]GTCCTGGGCCAGAGG | 55779 |
rs148258112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293592 | CTGATCAAAGCACAT[C/T]GACTCAACAAATGTT | 55779 |
rs148268161 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342602 | GAGTAAGTCCAATTC[A/G]ATACATACAATTTGA | 55779 |
rs148290111 | snp | C/T | 0.078151 | 0.181571 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418845 | GAGTAGCCGGGATTA[C/T]AGGCGCGTGCCACCA | 55779 |
rs148313437 | snp | C/G | 1.68329e-05 | 0.00290106 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396711 | CCTACAATAATTTGT[C/G]CTCCAGTGAAGTTTA | 55779 |
rs148383364 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377745 | GCAACCTTCACCTCC[C/T]GGGTTCAAGCAATTC | 55779 |
rs148394161 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360963 | ATTTGTTTTATCTGT[A/G]TATGAATTTTGATGG | 55779 |
rs148479680 | snp | C/G/T | 0.0260105 | 0.111035 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313281 | AGACTTGCATGGGCC[C/G/T]TGTAATCTCTTTGTT | 55779 |
rs148490630 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351361 | CAGCACAGAGCCATA[C/T]AACTAATACCCCTAA | 55779 |
rs148494467 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416741 | TAGGCTTTACTCTAA[C/T]AGAAAACTCAAAAAT | 55779 |
rs148496465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303616 | CGATTGTATCTCAAC[A/G]TTTTCTTTCTTAACC | 55779 |
rs148499027 | in-del | -/TA | 0.0577344 | 0.159793 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385969 | TATTGATTTTCGATC[-/TA]TATGTTTTATCCATT | 55779 |
rs148511672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439322 | ACGCTTGTATGCTGG[A/G]TAACTATCCCAAAAG | 55779 |
rs148547745 | snp | A/G/T | 0.000674276 | 0.0183489 | missense, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296800 | TTCTTCAAGTGTTGT[A/G/T]TTAACAGAAAGCGTT | 55779 |
rs148555075 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389720 | CAGTAGAGGCTACTA[C/T]GAGCAACTTTATGCA | 55779 |
rs148600803 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331330 | CCAGCTGTCTCCCTG[A/G]TCTGTGTTTTCTAAA | 55779 |
rs148648151 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385789 | GGACTATAGGCATGC[A/C]ACCACAAAGCTAATT | 55779 |
rs148665243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349238 | AGAAAATATACTCCC[C/T]TGTCAGCCGACTCCC | 55779 |
rs148701698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378471 | AGTTGAGGAGGGAAA[A/G]AGTCAACACTCATCA | 55779 |
rs148753842 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412115 | GCACAAGACAGGGAT[A/G]CCCTCTCTCACCACT | 55779 |
rs148761833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338189 | TTGAACCCAGGAGGC[A/G]GAGTTTGCAGTGAGC | 55779 |
rs148764231 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426859 | TGCTGAGTTCTGGTC[A/G]GTCATGGCGCAACAG | 55779 |
rs148772141 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369200 | GTTAACAACGATATC[C/T]AGGATTTCAACTCAG | 55779 |
rs148772261 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443041 | TCTGAGAAAGATACA[A/G]TAAATTCACTATACA | 55779 |
rs148790805 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328651 | AGGAGAGAAAGAGAT[C/T]TGTGGGTTTGGAGCA | 55779 |
rs148814842 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305746 | AAATTGGTGGTCTCC[A/T]ACATGGGATGCATGC | 55779 |
rs148826245 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347718 | GAGCTTCAGAAATGA[C/T]ATCCTTCCTATTCAA | 55779 |
rs148827847 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410395 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG | 55779 |
rs148861553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353255 | ACAAAAACCACAGAA[G/T]GAAAGGACTAAAAGA | 55779 |
rs148866914 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299173 | ATTCATCTGACAAGG[A/G]GTTAATAACCAGAAT | 55779 |
rs148871158 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368348 | CCAGAGAGAAAGGTC[A/G]GGTTACCCACAAAGG | 55779 |
rs148881356 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404404 | ACTTGTAAGGCCAGT[A/C]CTGAATTAAGTAGAT | 55779 |
rs148922119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333004 | AGAAATGCTAACTCA[A/G]CAAAGATGTATTAAT | 55779 |
rs148923207 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393782 | GGCCTCCCAAAGTGC[G/T]GGGATTACAGGCGTG | 55779 |
rs148954914 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409192 | CTGAGAAAAAGCTTT[C/T]GTCCTTAGTATGGGT | 55779 |
rs148985133 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333609 | ACAGACAACCCCCCC[-/C]ACACACAAATATGAC | 55779 |
rs149018684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381661 | TTGACTTCAAAACCA[C/T]GCATTTAATCATGAA | 55779 |
rs149036131 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311817 | TGATAGTGATATGGA[C/T]AATAAGGTCCAGGCT | 55779 |
rs149037901 | snp | A/G | 0.103438 | 0.202533 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372532 | GGAATTGAACAATGA[A/G]AACACATGGACACAG | 55779 |
rs149066781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322172 | ACAAAAACAGACAGA[C/T]ACATAGACCGCAAGA | 55779 |
rs149077800 | snp | C/T | 0.00133504 | 0.0258019 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341898 | CTATTATTGATTCTT[C/T]TTGTATGGTAACACT | 55779 |
rs149083836 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429463 | TGCTTACTGTTTGCA[A/T]GATGTATCTTTTTCT | 55779 |
rs149088102 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369959 | ATAAACACCTCTATG[C/T]AAATAAACTAGAAAA | 55779 |
rs149091837 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444708 | ACATTTAAAAACTAC[A/G]TAAGATTTTATAATA | 55779 |
rs149130341 | snp | A/G/T | 0.0010561 | 0.0229553 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363196 | ATTCATTTCTAATAG[A/G/T]TTACAAAATTCACTC | 55779 |
rs149135090 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433221 | ATCACCTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 55779 |
rs149205210 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418377 | CAGGCAGGAGCCACC[A/G]CGCCAAGCCAGGAGT | 55779 |
rs149227964 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286843 | GTGTGTCTTTTGAAA[C/T]ACCACCTCTCACAAT | 55779 |
rs149231234 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352013 | AGCAGGAAGTAGCTG[A/G]AGCAGTCATTGCCCA | 55779 |
rs149237909 | snp | C/G | 6.89988e-05 | 0.00587321 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400615 | AATAGCTCCAGAATG[C/G]AAGGAGAAGAGGCAT | 55779 |
rs149266055 | in-del | -/AATGAAA | 0.19646 | 0.2442 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338303 | AAACTCTGTTAAGGG[-/AATGAAA]AATGAAAAGACAAGC | 55779 |
rs149281764 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296655 | GCTTCATGGGTACCA[C/T]TTCCTGCTCCCTGGG | 55779 |
rs149305126 | in-del | -/T/TT/TTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385810 | GTATTTTTTTTTTTT[-/T/TT/TTT]TGGTAGAGACAGGGT | 55779 |
rs149336889 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289667 | CCTGTTCAGTCCCCT[C/T]CCACATCACACAGGG | 55779 |
rs149345765 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346810 | AATAAAAGCTGGCCA[C/G]CCCAGCCAGCAGCGG | 55779 |
rs149355729 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374442 | TGTGCACACGTGCAG[C/G]TTTGTTACATATATG | 55779 |
rs149365044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387426 | CCAGATGATATCTCC[A/G]GACACACCCTGGGAC | 55779 |
rs149387293 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325133 | ACAGTGAAACCCTGT[C/G]TCTACTAAAAATAGA | 55779 |
rs149399915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343736 | AAGCACTACTGGAAA[C/T]GTAGAACAGGGATAG | 55779 |
rs149400517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402308 | CCAAGTGCATACCAC[A/C]AAACATGTCTCAGTA | 55779 |
rs149405770 | snp | A/T | 0.176219 | 0.238865 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367807 | AGCTAAAGGAGCATG[A/T]TCTAACCCATTGCAA | 55779 |
rs149408867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350026 | GGCACCCCCATTAAA[C/T]ATCACAAGGAAACCA | 55779 |
rs149410989 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447156 | ACTGTAAGTCCAATT[A/C]AACCTCTTTTTCTTC | 55779 |
rs149453265 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365804 | ACTACATAGAAAAAC[G/T]GACACATTCTTTTTT | 55779 |
rs149454871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435080 | AGAAAGATATAGACC[A/G]AGCTCAGTGGCTCAT | 55779 |
rs149477584 | snp | C/T | 0.000266276 | 0.0115355 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420157 | GGTTGGCTCGCTTTC[C/T]ACAGTCATAACCAAA | 55779 |
rs149600253 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355469 | AGGTTGCAGTGAGCC[A/G]TGATCACGCCACTAC | 55779 |
rs149610951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302359 | AGCAAGACACACACA[A/C]ATACACATAGTGCAC | 55779 |
rs149612822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369174 | TCATTATTAGATCAA[C/T]GAGACAGAAGGTTAA | 55779 |
rs149615145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314062 | ACCCCAGAGCCTCAG[G/T]GACCTTTTGGATTAT | 55779 |
rs149622278 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407244 | ATGATCAAAACAGGC[A/G]AAAAATAAAATTTCC | 55779 |
rs149675798 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375764 | AAGTAGAGGCTGTAG[C/T]GAGCTGAGACGGCAC | 55779 |
rs149680126 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327552 | TTGAGTTAAGAAGAA[A/G]AAGAAATCAAGTTTC | 55779 |
rs149684089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389063 | TTTTATCCAATGGCT[A/G]CAGAATACACATTAT | 55779 |
rs149716115 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345943 | ATCTTTCTCATCTCT[C/T]TAAGACTTATTTCCT | 55779 |
rs149724986 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351055 | GAAACTCTTGTAGAG[A/G]CAGGGTTAGGAAAAT | 55779 |
rs149761596 | snp | A/G | 0.000164734 | 0.00907413 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403952 | CTTGTCCCTCGACAG[A/G]GCTCCACTTTGATCA | 55779 |
rs149771918 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367746 | ATTTTGATGAGTTAG[C/T]TGACAGAAGTAGGCT | 55779 |
rs149812284 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381046 | TTCACAGATAATTAG[C/T]AAAGTACTTTCAGGC | 55779 |
rs149841499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332867 | GGCAACGAAAAACTA[C/T]ATCCAATGAGGATTT | 55779 |
rs149852060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437664 | TTCCTACCTTTCCTG[A/G]GTCATAAAAGGTAAC | 55779 |
rs149882274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322074 | AGCCAATGCAATCCT[A/C]AAGATAATCCACAAA | 55779 |
rs149895620 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426778 | TACTACTGGCTGGAA[G/T]ATAGGAAGCAGTCAT | 55779 |
rs149929891 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369927 | CACAGAAATACAAAC[C/T]ACCATCAGAGAATAC | 55779 |
rs149938527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378332 | AATTGTTTTATAAAA[C/G]ACAGACGACAGGCAG | 55779 |
rs149939657 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409553 | TGAGAAAAACACTTT[A/G]AGAACATATTCCATT | 55779 |
rs149950883 | in-del | -/A | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326084 | CTCTCCAAACTCAAC[-/A]GTAAAAAAAGCAAAT | 55779 |
rs149982482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398616 | CTGCCAATCTAAATG[C/T]TCTGTCATTTCTACT | 55779 |
rs150050439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362650 | ATCAGAGTGCAGGGA[C/T]GCACATAGGAATCAC | 55779 |
rs150050997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292502 | TGCATGAATACATCT[G/T]TGAAAGGAAAGACAT | 55779 |
rs150087045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347664 | CCTTCCTCAGACAAG[C/T]GGGCCTAACAAAAGC | 55779 |
rs150117339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371146 | ATATCATGAACATGG[C/T]CATATTGTCCAAGGT | 55779 |
rs150147481 | snp | C/T | 6.59239e-05 | 0.00574087 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366142 | GCAGTCACCAAGAAA[C/T]GATCATCAAAGCTAT | 55779 |
rs150156132 | in-del | -/T | 0.0752113 | 0.178743 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292197 | TGGACTAGGTTAGGA[-/T]TTTCCTGCTTTCTGT | 55779 |
rs150161457 | snp | A/G | 0.000812788 | 0.0201428 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395710 | GTTTCACTATGTAGT[A/G]ATTGAGATTCAAACA | 55779 |
rs150171115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440773 | GTGTAAAGGTCCCTT[C/G]TCAGAGGGTCTGTAG | 55779 |
rs150202826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324743 | GGCCAGAAAATGAAA[C/T]AGGCATCCTGATCAG | 55779 |
rs150209514 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359678 | ATTGGCAAAGTGCTT[C/T]TAGAATTACAGGACT | 55779 |
rs150214250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428226 | AAAGACTATTTCCTC[A/G]TTTCAAGATTAGGGC | 55779 |
rs150253449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381182 | AAAACACACTTAATT[C/T]CTCACTGCAGTTATT | 55779 |
rs150254098 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318690 | GAGAAGGGTCAAGTC[A/C]CATACAGAGAGAAAC | 55779 |
rs150263680 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422698 | CCCCTTCTTCCCTTT[C/G]TTTCTTTCCCTCTTC | 55779 |
rs150272289 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308008 | AATATCCTTACACTT[-/A]AAAAAAGGTATTCAT | 55779 |
rs150296773 | snp | A/T | 0.0861826 | 0.188849 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311528 | CATGTTTCTGAGGCA[A/T]CCCCAGCCATGTGGA | 55779 |
rs150325790 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406609 | AGCCTGGGCAACAGA[A/G]CGAGACCCTGTCTCA | 55779 |
rs150348327 | snp | C/T | 0.00130813 | 0.0255412 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399991 | GCAAAATCATAGATT[C/T]GAACAGAGCCTATAG | 55779 |
rs150368128 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295436 | AATTATTTTAGATTG[C/G]ATATATTATCGCCAA | 55779 |
rs150379366 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400859 | GCTGTGTGATTTTGC[A/G]CAAGTCACCTCAAAT | 55779 |
rs150419220 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298510 | AAAGAAATGGAAGCA[A/G]AGACATAAAGAGATA | 55779 |
rs150421509 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391046 | ACAAAGCTATGCTGA[A/G]CAGAAAGAACAAAGC | 55779 |
rs150455314 | in-del | -/AA | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316377 | ACAACAAAACCTAAA[-/AA]CATGGAAGTATAAAA | 55779 |
rs150465824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351835 | TGTTTCCTCCAGAAT[C/T]GATGCCATCAAGCTA | 55779 |
rs150520448 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326380 | ATCTAATAGGTCCCT[C/T]AGTTACCTCTCTATT | 55779 |
rs150529149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343637 | AGGTCACTCTGGCAG[G/T]AGCCTGGGTGAGGAA | 55779 |
rs150530123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361287 | GAAGAAGTGCTTCAG[A/G]GGGTGAATATTCAGC | 55779 |
rs150531720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432250 | ATAAGTAAAACACAG[A/T]CAGCTCTTAAGGAAC | 55779 |
rs150574179 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320788 | GGAGGCTAGGCCAGT[C/G]TAGTTTTTTCACATT | 55779 |
rs150626627 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414940 | CAGAAGGAATGGTAC[C/T]AGCTCCTCTTTGTAT | 55779 |
rs150689399 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367397 | TTGCTGTTCTGCAAT[A/G]TTTGCCATTCTGCAG | 55779 |
rs150695011 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312466 | ATAGAAAAGAAAAAC[A/G]CATTTTCTGAGGAGA | 55779 |
rs150695313 | snp | G/T | 0.0011772 | 0.0242325 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373518 | TTCATCACAAGGGGG[G/T]AACTCACAGTGATAT | 55779 |
rs150696585 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402861 | ACATTTTGGGGTAAC[A/G]TATATCTTGGAAAGA | 55779 |
rs150736204 | snp | C/T | 0.000164766 | 0.00907502 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379450 | CTGAAATTCTTTTTC[C/T]CCATCTTCTCCCATC | 55779 |
rs150737765 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300715 | AGACATTTTATAGAA[C/T]AGGAAACATTAAAGG | 55779 |
rs150741757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392787 | AGTCCAAGAATAATA[C/T]GGGAGGAAGAACATG | 55779 |
rs150746112 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346597 | CTAGCTACAGGATTG[C/T]AAATGCACCAATCAA | 55779 |
rs150759371 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419568 | TCTTTCACTCCATAT[A/G]TCTCAACATATCCTG | 55779 |
rs150782091 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352355 | CTTTGTTCTTTCGCT[C/T]TTCACAATAAATCTT | 55779 |
rs150834943 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377795 | GTAGCTGGGACTACA[A/G]GCACCTGCTACCATG | 55779 |
rs150899265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339332 | GGGAATAGAGGCAGC[C/T]CTCATTCCTTTCCTT | 55779 |
rs150899816 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398148 | TGTACCAGTAACTAT[A/G]GAGGCACTGGAGATG | 55779 |
rs150910154 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443562 | AATGGTGATACCACA[A/G]CTTATAGTACGGTGT | 55779 |
rs150920790 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417003 | CAGGCTGGGACTCAA[G/T]AATTTGCATTTACAT | 55779 |
rs151009123 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440236 | GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGACG | 55779 |
rs151015917 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375342 | GTCAATTTTATGTTA[C/T]ATGTCTTTTACTTCA | 55779 |
rs151023574 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359072 | CTTCGCAATTAACAA[C/T]AATACAAATAAAGCT | 55779 |
rs151058234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304428 | CCATTTAGCTCATCC[A/G]GTTTGGGTCAGGTTA | 55779 |
rs151059898 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394188 | AGTATAGAATGTGTG[A/T]ACAGCTCTACAGCAT | 55779 |
rs151069523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408609 | GTGGCTTACGCCTGC[A/C]ATCCCAGCACTTTGG | 55779 |
rs151077666 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354338 | ATGCAGGTTCCCTGA[C/G]ATGCCAAAAAACTGA | 55779 |
rs151175783 | snp | A/G/T | 0.0883596 | 0.190715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351731 | CCTCTGGAGTTGGGC[A/G/T]ACATGGCTTCTCCCC | 55779 |
rs151218147 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310520 | GAGAAATTTGAGTAA[A/C]ACAGAAAATTTAAAT | 55779 |
rs151225935 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349457 | CCGCAGGCTTAGTCA[A/T]GGCCCTCAGACAAAC | 55779 |
rs151231648 | snp | A/G | 0.0225045 | 0.103662 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445233 | TGAAAGAAGGATATA[A/G]AAACTTAAAAGTCAG | 55779 |
rs151236498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329675 | GAAATAAGAATAGTC[A/G]CCATTCCAGCTCCAG | 55779 |
rs151237099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390281 | TGCTGAAAATGCACT[A/T]GATAAAATTCAACAT | 55779 |
rs151243104 | snp | C/T | 9.89103e-05 | 0.00703174 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427258 | TCCTCATCTGAGTCT[C/T]CTTCTAAATATGATC | 55779 |
rs151268169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345924 | CTTTTCTTTCATACA[C/T]ACTATCTTTCTCATC | 55779 |
rs151274053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434252 | ATGTATAGCAAGAAG[C/G]CTAAAACATGATGGG | 55779 |
rs151277714 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371953 | AATAGAAGACATTTA[C/T]GCAGCCAACAGACAC | 55779 |
rs151290171 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386463 | CTGTCTTCTTTTGTG[C/T]TTGTCATTTAAGGCA | 55779 |
rs151312099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292183 | GCCTTCTTTGCCCCA[C/T]GGACTAGGTTAGGAT | 55779 |
rs151318445 | snp | C/T | 0.000494519 | 0.0157167 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363239 | ATTTGCTCTCTCTTC[C/T]GTGCCTTTATTTCTC | 55779 |
rs180815972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446295 | CCCATTCAAGGCACA[C/T]CTGTGTGTCCTGCCG | 55779 |
rs180822873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334009 | CCTGGCTGGAGTGAA[C/T]TGTGTGATCTTGGCT | 55779 |
rs180838428 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381213 | GGTAAAAAGTCAAGT[A/T]TATTAATAATTATTA | 55779 |
rs180839602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418822 | GTGGTTCTCTGCCTC[A/G]GGCTCCTGAGTAGCC | 55779 |
rs180844830 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351829 | CAAATTTGTTTCCTC[C/T]AGAATCGATGCCATC | 55779 |
rs180856647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361247 | GTATGTAATTTCATC[C/T]GTCAGTCCTACTTTT | 55779 |
rs180857227 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371141 | AATCAATATCATGAA[C/T]ATGGCCATATTGTCC | 55779 |
rs180862575 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312701 | CAGCCTAGGGACTTG[G/T]TGCCCTGAATCCCAG | 55779 |
rs180875616 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397257 | CACAAGCACTCCTAA[C/G]AGAGAATTTAACTTG | 55779 |
rs180876808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431944 | TAAAATTCCTCCTTT[A/T]TTCTTCCATTGCAGC | 55779 |
rs180890919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415978 | AATTCTCCCACTACT[A/C]TTGTGTGGGAGTCTA | 55779 |
rs180896906 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440059 | TAGGTACCATTATTA[C/T]TTTATTTATGTATTT | 55779 |
rs180916033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391932 | ATGTGGAGTAAATTA[C/T]ACTGTTGGTAGGAAT | 55779 |
rs180963955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367882 | AGAATGAACAGTGTA[C/G]AGAAGATCTTAAATG | 55779 |
rs180965078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347145 | CAGCCAGTTAAAAGT[A/G]ACTAGCGTGGCCGCC | 55779 |
rs180973192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424163 | AAGTAGAGGGCTAGG[C/T]GCGGTGGCTCACACC | 55779 |
rs180976175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355375 | AATACAAAAAAATTC[A/G]CCGGGCATGGTGGCA | 55779 |
rs180979053 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317602 | CTGGAACCTGACCCT[A/G]ACCCTGAATCTCAAG | 55779 |
rs181001642 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308573 | CTCTAAAATCAGACA[A/G]AAATTTTTTTTTCTT | 55779 |
rs181003229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336979 | TCTAGCCAGTGCAAT[A/C]AGAAAAGGAAATAAG | 55779 |
rs181003887 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402823 | TTCTTTTCTCCTGAG[G/T]TTTTCTCCCACTTGG | 55779 |
rs181023262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329306 | AGCCATGCTTTGAAT[C/G]ATAACTCAACTCTGG | 55779 |
rs181027864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418317 | GTCTTGAACTCCTGG[A/C]CTCAAGTGATCCACC | 55779 |
rs181038134 | snp | A/G | 0.00335757 | 0.0408352 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361856 | GCTATTCTGACCACA[A/G]TTTTTTTTTACCAGA | 55779 |
rs181038602 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375167 | AGTATGGTTGCCAGG[C/G]GCTGAGAGAAGGGAA | 55779 |
rs181040940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342901 | AAGTACCAGAATTGC[C/T]TGAACCTGAGAGGTG | 55779 |
rs181043288 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370846 | CCACTGTCTCAGCCC[A/C]AAATCTCCTTAAGCT | 55779 |
rs181057224 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445030 | AAAATGTATTAATAA[A/C]AAAAACCCTTAAAAT | 55779 |
rs181057895 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297061 | ATTTAAAAATGCCCA[C/T]TCGGTATTGTCTTTT | 55779 |
rs181087032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322935 | CACAGTAGAAAGGGA[A/T]GCAAACATGTCCTCC | 55779 |
rs181090879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383148 | CAGAGGGATAAAGGA[A/C]ATCAGGGCATTGGAA | 55779 |
rs181092220 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303613 | CTTCGATTGTATCTC[A/G]ACGTTTTCTTTCTTA | 55779 |
rs181121271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433831 | AGGGTGCAACTACCA[C/T]CAGAGACCTCTGACC | 55779 |
rs181136739 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410473 | TCCCTGCAAAGGACA[C/T]GAACTCATCCTTTTT | 55779 |
rs181140499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312474 | GAAAAACGCATTTTC[G/T]GAGGAGAAATTCAAG | 55779 |
rs181145748 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291329 | CAATCTAGTAGGTTC[A/G]AAACATCTAAAATGA | 55779 |
rs181178081 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351177 | AAATTCTAAGTTAAT[A/G]TGGACTGAACGAGAT | 55779 |
rs181181451 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333115 | CTTGATGACCCTGCC[A/G]TACCTGTCAGGCAAT | 55779 |
rs181230363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308120 | TTGCCAATCAATATT[C/G]ACACTTCACAGAGAA | 55779 |
rs181514775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367051 | CTAAGTAAACAAAGC[A/G]GTTGGGAAGCTCTAA | 55779 |
rs181515041 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346362 | AGCACTCTGTAAAAA[C/T]GCACCAATCAGCGCT | 55779 |
rs181534417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405803 | AAGGATTCTATTGAT[A/C]TTTATCTTAGCTTAA | 55779 |
rs181534633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425492 | TATTCTCCAAACCAA[C/T]TAAAACTTTATATTT | 55779 |
rs181538710 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327402 | TACAGAATATCAGAC[C/T]AAATTTACTAAAAAA | 55779 |
rs181658485 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432645 | ACTTGCTATCTCTCC[A/G]CCCTTGCAATATAAT | 55779 |
rs181689208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311681 | CAAAAATATGGAAGC[A/G]ACTTTGGAACTGGGT | 55779 |
rs181705186 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377434 | TGCTTGAGTCCAGAT[C/T]CTAGTTTCACTTCTC | 55779 |
rs181711211 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290252 | ATTAATGGTGACAAG[C/T]GCAAACAATAAGGTA | 55779 |
rs181718778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415747 | TATGATTTCAACTCT[C/T]ATGCATTTGCTGAGG | 55779 |
rs181770191 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405058 | TTTATGGAGCTTCTG[C/T]ACAGACTGATGTTCC | 55779 |
rs181778451 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376528 | GCCAGCAAAAGAGGC[A/T]GAAATGGAATGGTCA | 55779 |
rs181780427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356503 | TGGATAGACAGATAG[G/T]CCAATGAGATAGAAT | 55779 |
rs181788615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410119 | TGGAGTAGCCATTCT[C/T]TTATTCCTTTACTTT | 55779 |
rs181801458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424947 | TTCCCAAGTCCCTCT[A/C]CACAAAGAACTAGCA | 55779 |
rs181816287 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446393 | TGAATTTTACCTTAT[A/T]CCTTAGTTACCCTAG | 55779 |
rs181828132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337722 | TTTCAACAAAAATGC[C/T]AGAGTAATTGGACAT | 55779 |
rs181835371 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317960 | TCTCCCACTCCCTCA[A/C]CCCTACTTCAGAACA | 55779 |
rs181838673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297135 | GGATTATGGACTGAT[A/C]TGCCCCTCCTCAGAC | 55779 |
rs181839063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322560 | TCACACCAGTCAGAA[A/T]AACTATTATTAAAAA | 55779 |
rs181862379 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361717 | GTTAGCCAGGATGCT[C/T]TCGAACTCCTGACCT | 55779 |
rs181874509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391453 | ATTTCTTGAATAACA[C/T]CCCACAAGCACAGGC | 55779 |
rs181944961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291932 | AATGTGTGCCTTTGG[A/G]CTAATAAACAACTCT | 55779 |
rs181946272 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341576 | ACCAAAGTATCACCA[C/T]CCTAAAAGATCCAGC | 55779 |
rs181948942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321973 | TCAATGCTACTCCTA[C/T]CAAATTACCAACATC | 55779 |
rs181954203 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301006 | CTTTTAGGTATGAAA[A/C]CCTTATATTTTTAGA | 55779 |
rs181968681 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307725 | CTGTAATCCTAGCAC[A/T]TTGGGAGGCTGAGGC | 55779 |
rs181995969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346155 | GCACCAATCAACACT[C/T]TGTAAAAACGCACCA | 55779 |
rs182093442 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301887 | GTTCTTTGGATCTCA[C/T]TGAAATTTTGTATCC | 55779 |
rs182118232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381939 | TGTCATAAGAACAAG[G/T]AGGTTGTATAAAGCT | 55779 |
rs182120141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411498 | CTGTTCTGCTCCATT[A/G]GTCTATATATCTGTT | 55779 |
rs182122312 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434529 | TTTTAAAGAGGGGAG[C/T]GACACAACAGGTTTT | 55779 |
rs182126584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342394 | CTACTATGAATTCAA[C/T]CCCATAATAAGTACT | 55779 |
rs182128817 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384391 | AAGCTTGAGCTCTTA[C/T]AGTTGTTATGTGCTG | 55779 |
rs182135202 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335523 | GTGAACCACCATGAA[C/G]CTGGGCAAAGAACAA | 55779 |
rs182186266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362319 | CAGTACACTAGAAGG[C/T]ACTCCTCGTGATGCT | 55779 |
rs182189116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316093 | TTGAAATAATACAGA[A/G]TATGTTCTCCGACCA | 55779 |
rs182197972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294534 | GTAATGTGGCTAACA[C/G]CAACTCAGTGTCCTC | 55779 |
rs182199561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343283 | GGCCAGGCTGGCCTC[A/G]GACTCCTGACCTCAA | 55779 |
rs182242538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327194 | TGATATTCAATCATA[C/T]ATTACACTGAAGCTG | 55779 |
rs182263031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339073 | AAAGCCTGCACATAT[A/G]GGGCTTCAGACCATC | 55779 |
rs182269027 | snp | A/C/T | 1.76104e-05 | 0.00296731 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366001 | CACTATTTTTAAATA[A/C/T]AGTTTGTTATTAATT | 55779 |
rs182298399 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442279 | ATGGATAGATGCTTA[A/G]AAGTAGTCATAAGGG | 55779 |
rs182306263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319170 | GACAAGAACCAACCA[C/T]CTGTTGTCTTCAAGA | 55779 |
rs182310210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417925 | GTCAAAGAAATCTGG[A/G]TGAAGATTCATGCAA | 55779 |
rs182311539 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297839 | AATATGCAGCAAGAT[G/T]ATTCAATTCTTTTAT | 55779 |
rs182370379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394107 | GGTATCACATACCCT[A/T]CACTCAGTTTCTACC | 55779 |
rs182376296 | snp | A/C | 0.0883596 | 0.190715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369761 | GATAGAGACAAAAAA[A/C]CCCTTCAAAAAATCA | 55779 |
rs182469021 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373068 | CCTAGTTCTCAATTA[C/T]TAAAGGGCTAATGAT | 55779 |
rs182522960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399339 | TATTTTATGCCACTA[A/C]ATTTTGAGATAGTTT | 55779 |
rs182523236 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421959 | TATCCTTAAAACAAA[A/C]CTGCATGTGTACCCT | 55779 |
rs182530888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304690 | ATTTTAGCATGATTA[A/G]TCCATGTATAGATAA | 55779 |
rs182627618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357744 | TGGTAAGTGTGTAAA[C/T]TGAAGAGTGTAAATT | 55779 |
rs182659239 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406268 | AATGCCACATGGTTG[C/T]ATATAACCTTTGACC | 55779 |
rs182748665 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353666 | GAATTCAACTATTCA[A/G]GGATTTAATACCTGG | 55779 |
rs182772365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399768 | ATTTCTATTACATTC[C/T]GACTAAAATAAACTA | 55779 |
rs182783939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315627 | CAAAACAGCAGAATA[C/T]ACAGACAGTTTCTGA | 55779 |
rs182811607 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342162 | ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55779 |
rs182817937 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352676 | TTAAAAATAATGTGG[A/G]AAATAAACAGAACCC | 55779 |
rs182824946 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420899 | TCTGAGCTTATTAGT[A/G]TATGTATTGGTGTGT | 55779 |
rs182852629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322993 | CAGAGTGAAGTTGGC[A/G]GCGGGGAAGCCCCTT | 55779 |
rs182931350 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426385 | ATGTCATGGGAGAGA[C/T]CTGGTAGGAGGTAAT | 55779 |
rs182946938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393630 | AAGCGATCCTCCCAC[C/T]TCAACCTCCCGAGTA | 55779 |
rs182949265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348725 | AGCTGTAGGGGGAGG[A/G]GAATTTGGCCCAACC | 55779 |
rs182958015 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369392 | GTCTCTCAGACCACA[C/G]TGCAATCAAACTAGA | 55779 |
rs182993705 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287907 | AACATTGCCAGAGTA[G/T]TTGACTCACTAGTTT | 55779 |
rs183022277 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347889 | CTCTAACAGGTTTTT[G/T]AGTATGCATCAGTAA | 55779 |
rs183028814 | snp | C/T | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330325 | CTAGATATTGAATCA[C/T]GGGTTGTCAAATCCC | 55779 |
rs183033242 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309349 | AATTTTCTGTCCACT[G/T]ACGCCCACTCTGTTC | 55779 |
rs183066007 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335291 | TATCTCCTGGCTGCC[A/G/T]CAGAGAGGAAATTAC | 55779 |
rs183077884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398458 | TTAAAATCCATATGA[A/T]CATTACTCGAATATA | 55779 |
rs183083173 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293092 | TCCTATTTGTTTAAG[A/G]TACTCTCAATAGGGC | 55779 |
rs183090671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372595 | GGAGTGGGGGGCAGA[A/G]GGAGGGATAGCATTA | 55779 |
rs183093898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358738 | TTGTAGAGAATATGG[A/T]TCCTACCGATTCTTT | 55779 |
rs183095032 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352377 | ATAAATCTTGCTGCT[C/G]CTCACTCTTTGGGTC | 55779 |
rs183098632 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339546 | ACTGAGTACCTTGGG[C/T]CTGTTTATGCCATGA | 55779 |
rs183101994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320425 | ACATGATATATATAT[C/G]ATATATATTGATATA | 55779 |
rs183102971 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372885 | CTTGATCTTGGAACT[C/G]TAGCCTCCAGAACTG | 55779 |
rs183114171 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419609 | CAATCTATGTCTACA[A/T]CCTATGTGTGTGTCT | 55779 |
rs183152666 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334400 | ACAAAACATTGTAAA[C/T]TATCAGAAAAGCTAA | 55779 |
rs183159466 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314645 | CTTTTCTCCTCTCTT[C/T]GAGTGTTTAAATTAT | 55779 |
rs183165775 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292363 | CCAAAGTGCTTGTTT[C/G]ATACCTATCTTTCCT | 55779 |
rs183224276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436281 | CCAATTCAGTTATTA[A/C]AGAGTTTGGTTATAA | 55779 |
rs183279280 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287474 | ACTGAGTCATGTGTG[A/G]GTCAGCATTTTCTTT | 55779 |
rs183368295 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416783 | AAATATTTAATGATG[G/T]ATACAATTGAAACTG | 55779 |
rs183381188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338243 | GCCTGGACAACACAC[A/G]AGACAATGTCTCAAA | 55779 |
rs183401709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297431 | CAGGCTCACCCCAGC[C/T]TCATTTCCTCCTATC | 55779 |
rs183424324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413072 | ATTGCCATTCTGACT[A/G]GCATGAGATGGTATC | 55779 |
rs183424503 | snp | C/T | 0.000164829 | 0.00907674 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427182 | AGAAAACTAATAATA[C/T]CTACCTGTAGTGCTT | 55779 |
rs183429293 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379930 | CTTCATCATCTATCA[A/G]TTGTCCTTTGCAAAA | 55779 |
rs183430835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408033 | ATATAGCTAGCAGAA[A/G]GTTATTTGACAATTC | 55779 |
rs183503117 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324006 | CACAGATCGCGCCAC[C/T]GCACTCCAGCCTGGT | 55779 |
rs183533385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362789 | AAGCCAGCCACCGGA[C/T]GCTTCAGGCCAATTT | 55779 |
rs183606005 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441793 | GAGCCCTGATCGCGG[A/C]GTTCCTATGTTGAGG | 55779 |
rs183617341 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318645 | TCACCAAGGACAATG[A/C]AAAAGAAAAAAATCT | 55779 |
rs183642117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347785 | ATCCCTTCCCTCCCT[C/T]AGGGTATGGTCCTCT | 55779 |
rs183660420 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308802 | GTAGAGACAGGGTTT[C/T]GCCATGTTGCCCAGG | 55779 |
rs183662849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357022 | CATATCCAGAAGATA[C/T]ACATAATTCCTGCAA | 55779 |
rs183670237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414130 | GTAGTGATTGTGAAT[A/G]GAAGTTCATTCATGA | 55779 |
rs183673206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438209 | ATTCTCTTTGACACA[C/T]GTAGGGTTCAATAAA | 55779 |
rs183679991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392883 | CACCAAGTTCTGTCA[A/G]TTCTCTCTTCTAAAT | 55779 |
rs183695260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435775 | TAACATGATACTCAT[A/G]TTATTAAATTTTGTA | 55779 |
rs183724203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389707 | AAATTCAAAGGATCA[A/G]TAGAGGCTACTATGA | 55779 |
rs183727719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365201 | ATACTTTCCCTCCTG[A/C]AATTCCTTTTTCTGA | 55779 |
rs183766507 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385475 | ATTTTCTTTCTTTTT[A/T]AAAAAACTTCATTGT | 55779 |
rs183791211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304838 | CTAATGGGCCACAGG[A/G]AAATATCCATGTTTT | 55779 |
rs183792481 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360884 | ATTCTCTTTTTGTGT[A/G]GTGGAAACTGGCTCT | 55779 |
rs183865165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341029 | TGCTGGCATCTGTTG[A/C]TGCCTGTCAGCGTGC | 55779 |
rs183865493 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298761 | ATACTGTATTATTCT[C/T]CTCATTATGAAGTAC | 55779 |
rs183868719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329680 | AAGAATAGTCGCCAT[C/T]CCAGCTCCAGAACAA | 55779 |
rs183874771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321865 | CTGAGAGAAATCAGA[A/G]ATGACAAAAATAAAT | 55779 |
rs183882292 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300332 | TGAATAATAACTTAA[C/T]TGTACATTTTAAAAT | 55779 |
rs183893431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416213 | CCTTTCCATTTACTT[A/G]GTAAATTTTCCTCCA | 55779 |
rs183902340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368483 | GAATTTCATATCCAG[C/T]CAAACTAAGCTTCAT | 55779 |
rs184005450 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324568 | TTCACCCCCATTCAC[A/G]AAAAAAATTCATGAA | 55779 |
rs184012346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305186 | TGTGAAATGGTGACA[A/G]GACTCAATAAACATA | 55779 |
rs184071075 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441122 | GCTGAGCGCAGGGCA[A/G]GTGTCTCACTGGAGC | 55779 |
rs184151422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423183 | GCAGTGGCATGAACA[C/T]GGCTCCCTGCAGGCT | 55779 |
rs184174498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375239 | TTACAGGATGAGGAG[G/T]ACGGTAGAACAGATG | 55779 |
rs184204578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424219 | AAGGCGGGCAGATCA[C/T]GAGGTCAGGAGTTCG | 55779 |
rs184213667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418195 | CAGGCTCAAGCAATT[C/T]TCGTGCCTCAGCCTC | 55779 |
rs184220501 | snp | A/T | 0.000801488 | 0.0200025 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396770 | TGAAACTAGTTAAAT[A/T]GAGAAAGTTGTACTA | 55779 |
rs184233473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306424 | TTCAGAATCAATAAT[G/T]TCTATTTATGGATCC | 55779 |
rs184254816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311826 | TATGGACAATAAGGT[A/C]CAGGCTGAGGTGGTC | 55779 |
rs184261084 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290398 | GGCACATTAGCAGGC[C/T]AATCACAGGTGAGGA | 55779 |
rs184273627 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370540 | CAACAGCCCTTCATG[C/T]TAAAAACTCTCAATA | 55779 |
rs184278023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429018 | AGATTGAGAACACTA[C/T]AAGAAAGCCTACAAA | 55779 |
rs184278099 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350175 | AGACCAGCAGAGAGG[A/G]AAGAGAGAGAGAGAG | 55779 |
rs184286585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332488 | CTATTAATATAACCA[C/T]GATGTGATTGGCACC | 55779 |
rs184292806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403702 | TGCAAATATTTACCA[C/T]AAGAGAAGCATTATT | 55779 |
rs184293519 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345805 | TTATTTTTGTATAGA[A/T]TGATTATTCCTAGCT | 55779 |
rs184312294 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387543 | AATCAACAGTGATGG[A/C]CAGGTAGTACACACT | 55779 |
rs184325751 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364219 | GAAGGAGAATTATAA[C/T]CCAGTGAACAAAATA | 55779 |
rs184356176 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401402 | TATCAAAAGCTCACA[A/T]ATATTTTAAAGTATA | 55779 |
rs184364899 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325589 | AGCTCGGACTACGGC[A/G]TATTGTGCTTTCCAT | 55779 |
rs184379414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316423 | AAGCAGGAAAAAATG[G/T]AATCATAAAGATAAG | 55779 |
rs184388098 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295268 | TCTTATTGCTCCATC[A/G]GTTGCTCACTGCAAC | 55779 |
rs184407325 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374196 | GACAACAGCAGACTA[A/G]ATTGTTTCAGCCAAA | 55779 |
rs184411656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354405 | GGGGCAGTTCTCAGC[C/T]CTGCTCAGCAGCTGC | 55779 |
rs184411917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307751 | GAGGCAGGTGGATCA[A/T]GAGGTCAGGAGATCA | 55779 |
rs184414762 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336007 | GGGATATTAGAAATA[C/G]TTTGGACTAAGTGAT | 55779 |
rs184419247 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288105 | GCCTGTATTTTCTAG[A/T]TTTCTGTAAAATTGA | 55779 |
rs184496609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380476 | CACTCTGTCACCTGA[A/G]CTGGAGTGCATTGGT | 55779 |
rs184518108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430036 | CACATTCAAGCATAC[A/G]TGGGTCATTTACCAA | 55779 |
rs184538361 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310074 | TCACAGGGCTGTAAC[A/G]AGGTGTCCCAACACT | 55779 |
rs184547807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311130 | ATAAAGTATTTAAAA[C/T]AGCCATGATAAAAAT | 55779 |
rs184557052 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289993 | TGAGCCAGAACACCC[A/G]GCCAAGCTGTCCCCA | 55779 |
rs184713877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295888 | ACTCCATTTCTAAAA[C/T]TGTCAGAGCATTTAT | 55779 |
rs184894381 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440224 | GCACACCACCTCGCC[C/G]GGCTAATTTTTGTAT | 55779 |
rs184928575 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354859 | TGAAAGCACCACCTC[C/T]TGGCTGGAGGCCAAC | 55779 |
rs184948085 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316996 | AAAAATGTCTCCAGA[G/T]AGAAAATGCCAAGAG | 55779 |
rs184954217 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402454 | CGGTGGCAGGGAGGC[A/T]CAGCAGGACCTCCCC | 55779 |
rs184956704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416007 | TAAGTCTCTTAGTAG[A/G]TCTCTAAGAACTTGT | 55779 |
rs184979428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392678 | TGTACCCCATAAATA[C/T]ATATATCTACCATGT | 55779 |
rs185028096 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409420 | TCAGCCCATGGTGAT[A/G]TAAGAATGCCAAGAA | 55779 |
rs185030216 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432073 | TTTCCAAGATCAAGC[A/G]TCTCTAAATGGTAGA | 55779 |
rs185049962 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336450 | CTTATGCCAATAAAA[C/T]TGACAACTTAGATGA | 55779 |
rs185066981 | snp | G/T | 0.000798403 | 0.0199641 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341901 | TTATTGATTCTTCTT[G/T]TATGGTAACACTCCC | 55779 |
rs185078655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340043 | ATGTCCATTGGCCCT[G/T]TGGGGTTGCGGCTAC | 55779 |
rs185081844 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374632 | GAACAATCCAAGTGT[C/T]TATTTTTGTGTGTTT | 55779 |
rs185082084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322984 | GGAGAAGTGCAGAGT[A/G]AAGTTGGCGGCGGGG | 55779 |
rs185086524 | snp | A/G | 0.00321801 | 0.0399831 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304042 | TTCGTTCTTGCAGCC[A/G]TCTCAAGGCATGGTT | 55779 |
rs185091139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381296 | ATAATTATTAAAATT[A/G]GATTTACATTTGGTT | 55779 |
rs185101875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361340 | CTGAGGCAAAAGTTG[C/T]GTACTATAGTATAAT | 55779 |
rs185112791 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418485 | GGTAGGGTGCCCAAA[C/G]ACTTTTCTCATAGGT | 55779 |
rs185114918 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361956 | CAGCACAAGTGTTAT[A/G]AGATTAAATGCCTAC | 55779 |
rs185116999 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343005 | AAATAAATAAATAAA[A/T]AATTAAAAAAAAATG | 55779 |
rs185123431 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396952 | TGAATGAACAAACAG[A/C]AGAGTGTCTGCCTAC | 55779 |
rs185144458 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444141 | TAGAGCCAGGGAGCA[A/G]AGATCATTCAAAAAA | 55779 |
rs185149017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299151 | TGAGAGAAAATATTT[A/G]CAAATTATTCATCTG | 55779 |
rs185179923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366728 | ACAGTGGGTGCAGCC[A/G]ATGGAGGGCAAGCCG | 55779 |
rs185184371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355392 | CGGGCATGGTGGCAG[G/T]TGCCTGCAATCCCAG | 55779 |
rs185187118 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360100 | AAAAAAAAAGTGTGG[C/T]AGGTAAATCCAATAG | 55779 |
rs185204546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321337 | ATCTTCATAATAAAA[A/G]TCCTTGACAGACTAG | 55779 |
rs185215043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408494 | TTTGGAAATACCATC[C/T]CAATGTTAGTTATTA | 55779 |
rs185216206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297089 | TTTCACCTTCTGAAT[C/T]CTGTGTAAAACTGAC | 55779 |
rs185217845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415604 | CTTCTTGATTTCTGC[C/T]TTAATTTCATTATTT | 55779 |
rs185244700 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327235 | GAAACTCACCAGCTT[A/C]TTTTTCAGTTGTTTT | 55779 |
rs185251410 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337061 | TCTACACTTAAAATA[C/T]CAAGAAACCTACCAA | 55779 |
rs185257635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317616 | TGACCCTGAATCTCA[A/G]GATATCCCAGTGTCT | 55779 |
rs185291874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390361 | TCAACACAATAAAAC[C/T]CATATATGACAGACC | 55779 |
rs185308499 | snp | A/C/G | 0.00358923 | 0.042236 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346177 | AACGCACCAATCAGC[A/C/G]CTCTGTGTCTAGCTA | 55779 |
rs185316151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438805 | AATAATTGTAGTTGG[C/T]TCTCATTTCTCTCCA | 55779 |
rs185438944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383818 | AGGTTTGTTACATAG[A/G]TATACACGTGCCATG | 55779 |
rs185439083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445577 | TCTTACTGATTTAGG[A/G]GTCATAATTTTTTTA | 55779 |
rs185517461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331355 | TCTAAATGCCATTCT[A/G]AGAGCCTGAGAGCAC | 55779 |
rs185586265 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391521 | TTAAAAACCTTCTGC[A/G]CAGCAAAGGAAGACA | 55779 |
rs185592278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415837 | GAATGTATATTCTGT[A/T]GATTTGGAGTAGGGG | 55779 |
rs185627434 | snp | A/C | | | splice-donor-variant | CFAP44 | GRCh38.p7 | 3:113308156 | GGTTTTATCTAACTT[A/C]CTTGTTGGGCAAATA | 55779 |
rs185645925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367346 | CGGGTGCCCTTCTGG[A/G]ATGAAGCTTCTAGAG | 55779 |
rs185660779 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346745 | AATGGACCAATCAGC[A/G]CTCTGTAAAATGGAC | 55779 |
rs185668843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327490 | AGGAAAAAGGAGGAG[A/G]GGGAAAGAAGACAAG | 55779 |
rs185715806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322269 | AAAACATGCAATGGA[A/G]AAAGAAGTTCCTATT | 55779 |
rs185716015 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349633 | TTACTGGAAGGTGCA[A/C]TGCCGCAGAGGACAA | 55779 |
rs185732646 | snp | G/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443602 | TAATGGCTCAATAAG[G/T]AACAGCTATTCTTAT | 55779 |
rs185747115 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394785 | ATGAATTTGTGTTGC[A/G]CCTCATTCAAAGCCC | 55779 |
rs185816989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347258 | CTGGAAACAGCTTCC[A/G]CTTTTGGGCTGAGCC | 55779 |
rs185848564 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370376 | ACATCAAAAAGCTTA[A/T]CCACCACAATCCAGT | 55779 |
rs185880665 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418097 | ATTTATTGAGACACA[A/T]TTTATTTATTGAGAC | 55779 |
rs185882487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308601 | CTTTTTTTTTTCTTT[C/T]TTCTTTTGAGACAGG | 55779 |
rs185940424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368035 | CAAGAAGACAAGATT[A/G]GAGAAAAAAGAGTAA | 55779 |
rs185950034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335237 | ATAAGCAGCATAAAA[C/T]TGTAATTCTTGAGAA | 55779 |
rs185950712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329512 | GAAGCTACTGAGGGC[A/G]TCACCACAGGGTGAA | 55779 |
rs185959832 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315168 | AAAACATTATCCAAT[C/G]ATACGCTGACTACCA | 55779 |
rs185968248 | snp | A/G | 0.000617729 | 0.0175637 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333370 | TTAAGAACCCAGGGT[A/G]CCTTCTCCATTGTCA | 55779 |
rs185980281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398598 | ATAGTGAGTGAGCTA[C/G]GTCTGCCAATCTAAA | 55779 |
rs185988424 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372694 | GTAACAAATGTGCAC[A/G]TTGTGCACATGTACC | 55779 |
rs185990569 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352557 | AATTCTGCACAGTTA[G/T]AAAAATATGAACAAA | 55779 |
rs186000405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370901 | AGGATACAAAATCAA[C/T]GTACAAAAATCACAA | 55779 |
rs186037743 | snp | C/T | 0.00051549 | 0.0160462 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291587 | CTGTATCTCTTTCTC[C/T]CGTGGAGACTGAATG | 55779 |
rs186093603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338093 | CATGATGAAACCCTG[C/T]CTCTACTAAAAAAAA | 55779 |
rs186096535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351549 | GTGACTCTCCAAAAC[C/T]GCCAAGACCTAGATC | 55779 |
rs186107707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312539 | ATGTTAATTCCCCAT[G/T]GTTGTAGGGAATGTT | 55779 |
rs186122233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377085 | AAGAAAAGGAAATTC[C/T]ATCTGCTTTTATTTT | 55779 |
rs186126256 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405118 | TAATTTTTACCTGCA[A/T]GCTCTAGAGGTCTAC | 55779 |
rs186142941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356571 | CTGACTTATGACAAA[A/G]GCATCACTACAATCT | 55779 |
rs186322055 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410517 | TATTCCATGGTTATA[G/T]GTGCCACATTTTCTT | 55779 |
rs186406175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435076 | ATCAAGAAAGATATA[G/T]ACCGAGCTCAGTGGC | 55779 |
rs186418420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425111 | TGTCCAAAGATAAGG[A/G]AAAAAAAAGCCATGA | 55779 |
rs186467721 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433926 | CTTTGGTTTTCCAGA[C/G]GTCCACTACCAAAGT | 55779 |
rs186476147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439560 | CTCCCTAAATACACA[C/T]ATAGTTTACCATGGC | 55779 |
rs186481979 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357249 | GTCCCCCCAAAAAGC[A/T]ATGTTGAGGCCCTAA | 55779 |
rs186498857 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405863 | GATGATTTAAGATCA[C/T]CTCATGGATTTAGAC | 55779 |
rs186520302 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319211 | AGATATAATTATACC[C/G]ATTGGCTCAAAGTGA | 55779 |
rs186525257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318692 | GAAGGGTCAAGTCAC[A/G]TACAGAGAGAAACCC | 55779 |
rs186540265 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298234 | CAGTGTCCTTCTCCT[A/G]TGCTGAAGAGGCCAG | 55779 |
rs186556698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292182 | GGCCTTCTTTGCCCC[A/G]TGGACTAGGTTAGGA | 55779 |
rs186557716 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379220 | TAAATGAAATCTTAA[C/T]ATAAGAGTAAGAAAG | 55779 |
rs186558915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357768 | GTAAATTTTCAAACC[A/G]TTTTGAAAAACTGAC | 55779 |
rs186569037 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339207 | AACCCTTGTGCAGAG[G/T]GCTATGAGAGGTTTT | 55779 |
rs186584327 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334100 | GGGACTACAGGCATG[C/T]GCCACCACACCCAGC | 55779 |
rs186595320 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313083 | ACAGCTTGCACCGTG[C/T]ACCTGGAAAAGCCGC | 55779 |
rs186597488 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113382034 | TAAGGGAGGGTTTGA[A/G]GGAGCAAGTCCTCAA | 55779 |
rs186619145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342663 | GCCAACTAAAAAACT[C/T]ATCAGAAACACAATC | 55779 |
rs186619599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433488 | TCCTGCTCTTTCCAT[C/T]CTACTATAAAAATTA | 55779 |
rs186625633 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442453 | TGGAAAACTATTTGA[C/G]AGGTTTCTTCAAAAG | 55779 |
rs186641705 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418024 | TGGGGTTGAGTTTGG[G/T]AGTTTTATTTATTTA | 55779 |
rs186687861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302494 | AAGATAGCCAGGCAC[C/T]GTGGCTCTCGCCTGT | 55779 |
rs186694530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338920 | GGAGAGAGCTGACTC[C/T]TCTGCTGGGGGTGCC | 55779 |
rs186712356 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425882 | ATAAAGGGAAGGTAG[C/T]AAATAGTTTTTGCCT | 55779 |
rs186756243 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297733 | CTTTCCCCAATGTGA[C/G/T]AACACTAGAACACCT | 55779 |
rs186776609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297220 | TTTACAGCATCTAGT[A/G]TTAAGAATAGAGCAG | 55779 |
rs186840655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361750 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 55779 |
rs186846582 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292576 | GCTCTCTCATCTAAT[A/C]CCCAAAATGACTCTG | 55779 |
rs186859045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410254 | TGCTTCACCCATTAA[C/G]TCAACATTTACATTA | 55779 |
rs186894118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322563 | CACCAGTCAGAATAA[A/C]TATTATTAAAAAGTC | 55779 |
rs186980530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318220 | AAACCAAATTTTTAA[A/G]GTTTTTAAACATTTT | 55779 |
rs187089636 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436825 | TCTTCTGTAAGTAGG[A/T]ACTGTTTAGTTTTCC | 55779 |
rs187119838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345129 | TACATATATAATAGA[C/T]TATTATATAAAATGT | 55779 |
rs187124390 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324617 | ACTTCCTTAACTTAA[C/T]AGAGTATCTATAAAA | 55779 |
rs187129443 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306222 | TGACAATGTATCATA[C/T]TCCTTTTTGAGGTTA | 55779 |
rs187135733 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388879 | CAGATATATAAGCCA[A/T]ATATTATTAGAGCTA | 55779 |
rs187140418 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413299 | GGTAGATTGCAAAAA[C/T]TTTCTCCCTCTCTGT | 55779 |
rs187143836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364779 | TACAATACTGAAGAC[G/T]GGGCATCACCTTCAG | 55779 |
rs187153186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416465 | TGAAATAATGTCACA[A/C]CTTCTTCAGAATGTT | 55779 |
rs187160037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368487 | TTCATATCCAGTCAA[A/G]CTAAGCTTCATCAGT | 55779 |
rs187176746 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420922 | TGGTGTGTAGGTAAC[C/T]AGTGTGTGTGTATAT | 55779 |
rs187225734 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422707 | CCCTTTCTTTCTTTC[C/G]CTCTTCCCAGGTGGC | 55779 |
rs187238003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416858 | ATTTCTAACTCTACA[A/G]TTTCTTTCATTGCCA | 55779 |
rs187241438 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113442146 | GTGACAAAGGACTTT[C/G]TATACAGAATGTATA | 55779 |
rs187243413 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401419 | TATTTTAAAGTATAA[A/T]TGAAATTTAATAAAA | 55779 |
rs187266046 | snp | A/T | 0.00282828 | 0.0374985 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330342 | GGTTGTCAAATCCCC[A/T]TCCTTTCTAGAAGAG | 55779 |
rs187282969 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309544 | ATCTTCAGAAATATT[A/T]CTGAACACAAAAATA | 55779 |
rs187288883 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393869 | CTCTATACAGGCTAA[A/C]TCCTTTTCACCTTCT | 55779 |
rs187304331 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369712 | AAGCTAGCAGAAGGC[A/C]AGAAATAACTAAGAT | 55779 |
rs187308329 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348226 | AACAAATCAAAACCG[C/T]GGGCGGTTTTTCCTT | 55779 |
rs187316110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397481 | AGTTGGGTTCCAGGG[A/G]GAAGTGGTAGTGACA | 55779 |
rs187341603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393174 | TGCAATTTGGACAAT[C/T]AAAGTCTGTAGCAGG | 55779 |
rs187360798 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446309 | ACCTGTGTGTCCTGC[C/T]GTAAATATATGGGAA | 55779 |
rs187378113 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441124 | TGAGCGCAGGGCAGG[C/T]GTCTCACTGGAGCGG | 55779 |
rs187405587 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352148 | CTAGAGGATTGTAAA[C/T]GCACCAATCAGCGCT | 55779 |
rs187424734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426809 | CGGTGAGCATGGAAG[A/G]AAGAGCCATTATGCC | 55779 |
rs187430295 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304901 | ATAAGACAAGTGTAG[A/G]TGTCATTCTACAGGT | 55779 |
rs187439123 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394549 | TACAATAATACAAAA[A/T]AATAACTTAATTTTA | 55779 |
rs187448479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349455 | GGCCGCAGGCTTAGT[C/T]ATGGCCCTCAGACAA | 55779 |
rs187508230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310101 | CACTCCCACTGGATG[A/G]TGTTAGAGAAGGGCA | 55779 |
rs187520552 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287529 | TATTTGAAGAAAATA[C/T]CCACTTACAATATTT | 55779 |
rs187545367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329858 | ATCTAAAAGCTGCTC[C/T]TCCACTTCCCCTTTA | 55779 |
rs187549739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309062 | ATCATGTTGACAAAG[A/C]CTCTCTCCTTTGACC | 55779 |
rs187582136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419455 | ATTGCTGAACTTATT[A/G]ATTAGTCTTATAACA | 55779 |
rs187588765 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371243 | TACTTTAAACTTCAT[A/T]TGGAGCCAAAAAAGA | 55779 |
rs187619093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335344 | ATCCCAAATACAGCC[C/T]AGTGAACTCACTGAC | 55779 |
rs187631208 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293868 | TGCTTCAGAATCCCC[A/G]GGAAGGCTGGTTAAT | 55779 |
rs187649755 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301191 | TATATGCTATATTAC[A/G]TCTACTCTTATGAAT | 55779 |
rs187688640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369777 | CCCTTCAAAAAATCA[A/G]TGAATCCAGGAGCTG | 55779 |
rs187697362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407087 | CAAAGATATTTTATT[G/T]ATTTTTATTTTAATA | 55779 |
rs187714175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358892 | TGCAGATAAGAAGAT[C/G]TGTTCATCAAAATGG | 55779 |
rs187747128 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, splice-acceptor-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427555 | TTTCACTTCATTTTC[A/C]GTCTATTTCCTATCA | 55779 |
rs187750106 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379971 | ACTGGTATTTCCGCC[C/T]CCCATCTTTTACTAC | 55779 |
rs187753420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408121 | ACAAAAAGACCAGAT[A/T]TAAATTGAGACAAGA | 55779 |
rs187753788 | snp | A/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330556 | GATATGTGAAGAGTC[A/G]ACTGAATGTTCTTCA | 55779 |
rs187764646 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288721 | GCACTGGAATCATAG[C/T]ACTCAATGGATTTAG | 55779 |
rs187859440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362492 | TTAGAGTTACCCAAA[A/C]TGACAATCTTTGGGC | 55779 |
rs187884332 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412084 | CAAAAACTGGAAGCA[C/T]TCCCTTTGAAAACTG | 55779 |
rs187886383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353707 | TATAACTTTCAGAGT[A/G]AAGTACCAGAGAGGA | 55779 |
rs187892823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384895 | TGATGCTGTTTGATC[A/G]ATTATCCACATGGTT | 55779 |
rs187903225 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335539 | CTGGGCAAAGAACAA[C/T]TCCTAGGAAAAGTAC | 55779 |
rs187940490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372975 | CTAGCAAACTAATAC[A/G]AAAGAATAGAGAAAA | 55779 |
rs188030587 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408781 | GGCAGGAGAATCGCT[G/T]GAACCCAGGAGGCGG | 55779 |
rs188103404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321893 | AATGGAAAAACATCC[C/T]ATGCTCATAGATTAG | 55779 |
rs188108506 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360377 | CTATATGTCTGAGTA[C/T]TTGAGAATGAGTGGT | 55779 |
rs188111296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300470 | GAATATCCCATATAT[C/T]TTATAAATATATATA | 55779 |
rs188119393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380735 | ATTTCAGTATCTATT[C/T]ACTACTGCCTTCTAA | 55779 |
rs188121463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408978 | AAAATAACATATTTT[G/T]AAATAATTCTAATGT | 55779 |
rs188136859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361028 | GCTGGGCACATTTAT[C/T]GTTGCACAGGATTCC | 55779 |
rs188150549 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287927 | CTCACTAGTTTAAAA[C/T]CAACATTTACTTACT | 55779 |
rs188195906 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385739 | CTGCCTCCCGGGTTC[A/C]AGCGATTCTCCCACC | 55779 |
rs188218886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435990 | CCTTCCACCTAATTG[C/T]AGAATATATACCTTT | 55779 |
rs188229069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353437 | TTGCGAGTTAGGATT[A/C]ATATATATGTATGAA | 55779 |
rs188256168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399600 | TCTGTAAATATTAAT[A/G]GAATGAATGAAATCA | 55779 |
rs188334735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113380032 | CCTAACTTATTTTTT[A/T]AAATTTTATTTATTA | 55779 |
rs188342330 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445812 | CCCTATCATTTAATA[A/T]CTTTCCCCTATCATT | 55779 |
rs188353127 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, splice-donor-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429062 | CATACAGAAAAATCC[A/G]TAAGAGCTACTTTAT | 55779 |
rs188400583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340640 | GCGGGCAGGCTGTGG[A/G]GCTCCGACCCCATGG | 55779 |
rs188408465 | snp | A/G | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298864 | AGTTACTGTTTAGTG[A/G]ATATGGAGTTTGGGA | 55779 |
rs188473402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412857 | ATGTCTCTTTACAGC[A/T]GAATGATTTATATTC | 55779 |
rs188475758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415871 | GCTCTGTAGAGGTCT[A/G]TCAGGTCCACTTGAT | 55779 |
rs188483267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363055 | AAAAAAGAAAGATGA[C/T]TTTAAGTGTTTCTAC | 55779 |
rs188484003 | snp | A/G | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440016 | TCTACACATATTATC[A/G]TACAATTCTCAAAAC | 55779 |
rs188485886 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391816 | AGGTGCTCAACATCA[C/G]GAATCATCAGAGAAA | 55779 |
rs188599500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370550 | TCATGCTAAAAACTC[C/T]CAATAAACTAGGTAT | 55779 |
rs188601632 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350735 | GCAGAAGAAAGTGGG[A/G]AAATAACTTTTAGAG | 55779 |
rs188619845 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418267 | AATTTTTGTATTTTT[A/C]GTAGATACGGGGTTT | 55779 |
rs188628384 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444272 | TGGGAAACCAAGGCA[C/G]GTGGATCATTTGAGG | 55779 |
rs188642071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396900 | GTTCCTTATAACCAA[C/T]GACCACAGGAAGGAT | 55779 |
rs188684504 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347818 | TTCATTTTGGGGGCA[C/T]AACATCTTTATAGGA | 55779 |
rs188742378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339565 | TTTATGCCATGAAGC[A/G]TGGTCTCCTTCCATG | 55779 |
rs188744957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327319 | GTTTTTTAGGGAACC[C/T]AACTCACCAGACTGG | 55779 |
rs188752729 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308092 | AGAGAAACCAAAAAG[A/C/G]GTCTTCCCAGTATTG | 55779 |
rs188755141 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354630 | CACAGCAGCCACAGC[A/C]AGTCCCGCCCAAGGA | 55779 |
rs188755326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336137 | AGAATCAAAGCTTAT[A/G]CACAAGTTTACACAT | 55779 |
rs188777186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299856 | AACATAGCAAGATCC[C/T]GTCTCTACAAAAACA | 55779 |
rs188788498 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374392 | TTATTTATTTATTTA[C/T]TTATTTATTATTATA | 55779 |
rs188896169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323348 | GGTGATAATCCTAAG[C/T]GAATTCACACAGGAA | 55779 |
rs189001631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351773 | GTGACAGCCATCTTG[C/T]TATTACTCACCTTCG | 55779 |
rs189023219 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312564 | AATGTTAATCCCCAA[A/G]ACAATGGGGAATATA | 55779 |
rs189031228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320665 | CCTAAAATAGACTGT[C/G]TGCAAGCTGAGGAGC | 55779 |
rs189108509 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421986 | CCCTCTGTATCTAAA[A/T]TAAATATATTTTTTT | 55779 |
rs189165633 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343318 | TTCACCTGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 55779 |
rs189184472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373154 | TAAGTAGCATCCTCC[A/T]AGGTAGCAGAATGTA | 55779 |
rs189235851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304695 | AGCATGATTAGTCCA[A/T]GTATAGATAAAGATG | 55779 |
rs189283398 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311372 | AAATAATTTGAATCA[C/T]GGGGGCAGTTTCCCC | 55779 |
rs189291309 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290158 | CTTGAAAGGCACACA[G/T]GGCTTAGGATATACA | 55779 |
rs189297861 | snp | C/T | 0.00092645 | 0.0215027 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333510 | GATTGAAATCTCCCA[C/T]ATACACCTGGGCTTC | 55779 |
rs189317298 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349634 | TACTGGAAGGTGCAC[A/T]GCCGCAGAGGACAAA | 55779 |
rs189321743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331359 | AATGCCATTCTGAGA[G/T]CCTGAGAGCACATGC | 55779 |
rs189338961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431147 | AAGGTTTTCAGGGGT[C/G]GGGGGAATGCAGCTA | 55779 |
rs189342919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397208 | AGCTGATAACAAAAG[A/G]ATGTTCAGGAATTAG | 55779 |
rs189368690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381649 | CAGACCTGTCTCTTG[A/G]CTTCAAAACCATGCA | 55779 |
rs189410522 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409988 | CCTAAGTTCCAGGAA[C/T]TGCCCACCCGTTTCC | 55779 |
rs189416958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432350 | AAAATTATTTTGCCC[A/G]TTTTTTTGACTTTTA | 55779 |
rs189477605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423668 | TTAAGTTCTGTATAA[C/T]CTCTTTTAAAATTAT | 55779 |
rs189495699 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374751 | GCAATTCTCCTGCCT[C/T]GGCCTCCCGGGTAGC | 55779 |
rs189524611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337104 | ACTGAGACAGTTCAG[A/T]AAGGTCACAGGATAC | 55779 |
rs189524647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390056 | TCATAAAAAGAAAAC[C/T]ATAGGCCACTATCAC | 55779 |
rs189524927 | snp | C/T | 0.00159617 | 0.0282053 | missense, nc-transcript-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296765 | TTTGCTAGCTCCTTT[C/T]GAAGTTTTCTGATCT | 55779 |
rs189528530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317907 | TGATTGGAGGGGGCT[C/T]CCCCAAGGCCCAGGA | 55779 |
rs189538150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297133 | CTGGATTATGGACTG[A/C]TCTGCCCCTCCTCAG | 55779 |
rs189542323 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438557 | GTAAAATGGTTGCAG[G/T]AATGAATTTATTGAT | 55779 |
rs189550045 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404511 | ATTTTCCCAAGTGCA[G/T]GCCACCAAACATTAG | 55779 |
rs189550936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304552 | TTCTCTTAATGATAT[A/G]TATTCCTGCAATTTA | 55779 |
rs189551821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414389 | TGTCCAGAACTTCCA[A/G]TACTATGTTGAATAG | 55779 |
rs189554618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336657 | GAAATCCAAAAAATA[A/G]AACAAACAGAAAACA | 55779 |
rs189558327 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375340 | TGGTCAATTTTATGT[C/T]ATATGTCTTTTACTT | 55779 |
rs189617853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418782 | ATGATCTCAGTTCAC[C/T]GCAACCTCCACTTCC | 55779 |
rs189629378 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370964 | AAGCCAAATCATGAG[G/T]GAACTCCCATTCACA | 55779 |
rs189728249 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290780 | AAACCTGAAAGAAAA[C/T]GGCAGGGGACATGAG | 55779 |
rs189732472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321386 | TCAAAATAATAAGAG[C/T]GCTATGTCAAATCCA | 55779 |
rs189750775 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402704 | GGGTAAGAGGTAAAG[A/T]TTTACTGTGTGAAGG | 55779 |
rs189824117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354986 | TCCATGGCTTCAAGA[C/T]CTGAAGACGGATCAC | 55779 |
rs189831110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346308 | AAATGCACCAATCAG[C/T]GCTCTGTGTCTAGCT | 55779 |
rs189841634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317198 | GGACCCCATGACTCC[A/C]ATGGATGTGTGACCT | 55779 |
rs189863599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362108 | AAGACTAAAATATTA[C/T]TTCTTTTTAGAAGAT | 55779 |
rs189867330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316620 | ACGCCTGTAATCCTA[C/G]CACTTTGAGAGACCG | 55779 |
rs189879917 | snp | A/T | 0.00334587 | 0.0407645 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343009 | AAATAAATAAAAAAT[A/T]AAAAAAAAATGGCTG | 55779 |
rs189883837 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322989 | AGTGCAGAGTGAAGT[C/T]GGCGGCGGGGAAGCC | 55779 |
rs189893980 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434441 | AAGGTGGGTACCATA[C/T]CATAAAGTTGTCTCT | 55779 |
rs189902555 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384168 | GGTTTACACCATTCT[C/G]CTGCCTCAGCCTCCC | 55779 |
rs189907997 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410562 | TTGATGGACATTTGG[A/G]TTGGTTCCAGGTCTT | 55779 |
rs189969697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311984 | TTTAAGGTGTCTGGC[A/G]GGAGAAAATTCTAAG | 55779 |
rs190012012 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367669 | CAAAAACCAGAGCAC[C/G]TCTTCTCCTCCAAAG | 55779 |
rs190018046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346877 | TTGTTTTTTTGCTCT[G/T]CACAATAAATCTTGC | 55779 |
rs190024141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297760 | ACCTCTCCAAGAAAA[C/T]ATAATCTTGTAACAG | 55779 |
rs190028363 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327512 | GAAGACAAGAAAGAG[A/G]TAAGGGCTAGAACAA | 55779 |
rs190078067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366936 | CTCAGCGGGTCCCAC[A/G]CCCATGGAGCTTTGC | 55779 |
rs190087556 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308443 | CCTGCAGAGGGTTGT[A/G]CAGTTACTATCAATG | 55779 |
rs190127410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295584 | GAAGCTCTCCTCCTA[C/T]CCCATCTGCTAATGA | 55779 |
rs190141758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438992 | CACTTTCCAGAAGAG[C/T]GGAACTACCAATTCA | 55779 |
rs190156480 | snp | A/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391401 | CAATTAAAAGAAAAC[A/G/T]TTGGGGAAACTCTCC | 55779 |
rs190159137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322741 | TAGTGGGTATATACA[A/C]AAAGGAAAATAGATC | 55779 |
rs190165167 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303066 | ACAGGCTGGCAAAAA[G/T]ATTAAAGTCTGATAA | 55779 |
rs190251570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372728 | GAACTTAAAGTATAA[C/T]AATAAAAAAAAAGAA | 55779 |
rs190253430 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399103 | AGCCACATGGAGAGG[G/T]TGTTAGGTATAAACA | 55779 |
rs190269755 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352579 | ATGAACAAAGTTTAA[A/G]GCAAATGGCAGAGCA | 55779 |
rs190284399 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420287 | AGATGAAGATGTGAG[G/T]TTGAAGTAGTTGAAT | 55779 |
rs190305974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418104 | GAGACACAATTTATT[C/T]ATTGAGACTCTGTCA | 55779 |
rs190307717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342210 | TGGTGGTGCATTCCT[A/G]TAATCTCAGCTACTT | 55779 |
rs190361407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370443 | ACACAAATCAATAAA[C/T]GTAATCCATCACATA | 55779 |
rs190375449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301368 | GGCTATCTCTGAATA[C/T]GGGGAGACAGAGAAT | 55779 |
rs190411383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415674 | GAAGTTGTGTGGTTT[C/T]TAGTGAGTTTCTTAA | 55779 |
rs190454485 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365636 | ACTATATTTTTGCAA[A/C]CCCTATCAAAACCAC | 55779 |
rs190469345 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287702 | CAGGAAAAACAGGTT[C/T]ATAGTTCTCTTACCA | 55779 |
rs190512930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326821 | AAATTTTATAATTCC[C/T]TTGTAAAAATCAGTC | 55779 |
rs190544775 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443932 | ATAAGAATGATTATA[C/T]GATAACTGTGGATGT | 55779 |
rs190551440 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361501 | AAGACCTGTTTTGTT[G/T]TTTTTTTTTTTGAGA | 55779 |
rs190553643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395562 | TGAGGAGAGAGCAAG[C/G]CTCCTGAGTGATGCT | 55779 |
rs190620811 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322473 | CTACAAGCAGGCAAC[A/C]AACATGAAAAAAATA | 55779 |
rs190649334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424530 | TTAAAAGAGTACTTA[A/G]GGAATACCTGATGGC | 55779 |
rs190706275 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345869 | CTTTTAAACTCTATG[A/T]CTGCTTTTAAAATGA | 55779 |
rs190746585 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412161 | GTTGGAAGTTCTGGC[C/T]GGGCAATCAGGCAAG | 55779 |
rs190754848 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435656 | ATCACTTGAGCCCAG[A/G]AGTTTGAGGCTGCAG | 55779 |
rs190775694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306457 | TCTAGCCAGCTTTTA[A/G]GACACTTATGGCTTA | 55779 |
rs190787338 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377394 | TGTAGCTTAATGGTT[A/G]AGGGCATGAACTCTG | 55779 |
rs190790955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347820 | CATTTTGGGGGCATA[A/T]CATCTTTATAGGACA | 55779 |
rs190791388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405458 | ATTTCCTTGACTCCA[C/G]ATTTCCCTTCTAATC | 55779 |
rs190795704 | snp | C/T | 0.000759178 | 0.0194682 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330197 | ACTGTTGCATGTACA[C/T]GTGTTTAATCTCGTC | 55779 |
rs190798091 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356934 | ACATATACACATACA[C/T]ACATGTCATATACGT | 55779 |
rs190804487 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309213 | CCACTTCTCCCAATG[C/G]AGAGAACTTGATATC | 55779 |
rs190833251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425390 | TGTTTTCTAACTACC[C/T]GCATTGCAAACCTAA | 55779 |
rs190842767 | snp | G/T | 0.00010068 | 0.00709434 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291754 | AGGCATTGCCCTGTT[G/T]AAAGAAAACAGCTCC | 55779 |
rs190901749 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358493 | AAATAATTCATCAAA[A/G]CAAAGTAAATATGTA | 55779 |
rs190918744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426827 | GAGCCATTATGCCCA[C/T]GTGCATCAGGAGTAA | 55779 |
rs190928538 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440372 | AGCCTATTATTATTA[C/T]TTTTGAGACAAAGTC | 55779 |
rs190932484 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379792 | ATTTGGTCATTTTTT[C/T]CATAATAGAGAAGCT | 55779 |
rs190936342 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407931 | AATTAACTGTTCAAT[A/G]TCTGCCTTTTCCCCA | 55779 |
rs190941170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352194 | AGATTGTAAATGCAC[A/T]ATCAGCACTCTGTAA | 55779 |
rs190947237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334259 | CCAGAAAATTAAACT[C/T]TGTAATTGCATAAGT | 55779 |
rs190950287 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313655 | GAAATAATTTGAATC[A/C]TGGGGGCGGTTTCCC | 55779 |
rs190974384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371312 | GCTGGAGGCATCACA[C/T]TACCTGACTTCAAAC | 55779 |
rs191014780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292195 | CCATGGACTAGGTTA[A/G]GATTTCCTGCTTTCT | 55779 |
rs191034431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425927 | TCTCTGTCACAACTA[C/T]TTATCCCTGTCCTTG | 55779 |
rs191116551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378580 | ATCTTCCACACACAC[C/T]TTTATGAAATTATTT | 55779 |
rs191124755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338932 | CTCCTCTGCTGGGGG[C/T]GCCTCTGAGACTCAT | 55779 |
rs191146474 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421242 | CAAACATGAAAAACG[C/G]TCCACATCACTAATC | 55779 |
rs191260437 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335256 | AATTCTTGAGAAAAG[G/T]AAAAAGACATGATCC | 55779 |
rs191268495 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361848 | GAAGACCTGCTATTC[G/T]GACCACAATTTTTTT | 55779 |
rs191280298 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292667 | CTAGCCAAGTCAAGC[G/T]GGAAGCAGAGTTAGA | 55779 |
rs191290517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406059 | ATTCTAATAGGAAGC[C/T]ATGTAAAATATTGAT | 55779 |
rs191328373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318721 | CCATCAGGCTAGCAG[C/T]AGACCTCTGAGCAGA | 55779 |
rs191366499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357633 | AACTGCGAGACAGTA[A/G]ATAACCAGTTTTAAG | 55779 |
rs191418148 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318252 | AGAAAAAAGAAAACC[G/T]AACTCCTAGAGCTAA | 55779 |
rs191503680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382339 | CAAGAAAGATAAGAA[C/T]TAAATGTTAAATGGA | 55779 |
rs191512490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315443 | TGAAGCAAAAACTGA[C/T]AGAAATAAAAGAAGA | 55779 |
rs191521221 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342888 | ACTCAGGAGGCTGAA[A/G]TACCAGAATTGCTTG | 55779 |
rs191528013 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389149 | AAGTCTTAAAACATT[C/T]CAAAAATTGAAATTA | 55779 |
rs191540006 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365060 | GTTTCTGTAGGAGGG[A/T]TATTGACTGCAGCTG | 55779 |
rs191574129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437999 | TTAAATGAGATCTTT[C/T]ATATACAGAGTTCTC | 55779 |
rs191599156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345417 | TATGTGTGTGTTTCC[A/G]TACATGTGGCAATGC | 55779 |
rs191600324 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324670 | TAATATTGAAAATAA[A/G]GCAAGAATGTCAGCT | 55779 |
rs191659906 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338228 | CACCACTGCATGCCA[C/G]CCTGGACAACACACG | 55779 |
rs191662601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394057 | ATTTTGAAATAAGTA[C/T]AGATTTACAGGAAGT | 55779 |
rs191665743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369746 | AGCAGAACTGAAGGA[A/G]ATAGAGACAAAAAAA | 55779 |
rs191668395 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348656 | GAAGGAAATAAGCAA[A/G]GAAATCTCCAAGGGA | 55779 |
rs191675171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297351 | TCCCCGCTGCTTTCT[C/T]ATGCCTCTCCTCCTT | 55779 |
rs191683236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416949 | TTATTAAAATATAGA[C/T]TGCAAGCCCTAACAC | 55779 |
rs191688955 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113442213 | ATTTCTTAAATGGGC[A/G]AAGGATTTGAATACT | 55779 |
rs191710910 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441780 | AAATGGCCCAACGGA[A/G]CCCTGATCGCGGCGT | 55779 |
rs191714912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300027 | CAGAGTGAGACCCTG[C/T]CTCAAAGAGAGAGAG | 55779 |
rs191722617 | snp | C/G | 0.000410298 | 0.0143172 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330551 | GCTTGGATATGTGAA[C/G]AGTCGACTGAATGTT | 55779 |
rs191765468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393313 | GTGTTTTGGTCTTGT[A/G]CGTTACAGGATGTTT | 55779 |
rs191783551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343781 | AAGTATCAGGACAGC[A/G]GTTTCAGAATTTATC | 55779 |
rs191794629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324248 | GGAAAAGAAAATTTT[A/C]TGATTCATATTAAGA | 55779 |
rs191802371 | snp | C/T | 0.00153917 | 0.0276987 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305073 | ACAACTAGCAGTTCA[C/T]TCAGCCGCTGCTGCT | 55779 |
rs191851815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419478 | TTATAACAAACTCTC[C/T]GAGGACATGGACTTT | 55779 |
rs191856651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385223 | CATTAAACCTCTTTT[C/T]ATTTATAAATTACCC | 55779 |
rs191881361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304837 | GCTAATGGGCCACAG[A/G]GAAATATCCATGTTT | 55779 |
rs191909418 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343474 | AACCATTTCATCATA[A/T]TTCATATTTCAAATT | 55779 |
rs191966962 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416166 | TGTCAGAGACTAAGA[C/T]TGCAACCCTTGGTGT | 55779 |
rs191980539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368388 | CAGACTAACAGCAGA[A/T]CTCTCGGCAGAAACC | 55779 |
rs192037425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287296 | CTGGATCCGGTGCTA[C/T]GGGAAACATTTTCCT | 55779 |
rs192038990 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329667 | ATTTCCTAGAAATAA[A/G]AATAGTCGCCATTCC | 55779 |
rs192055334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422800 | CTCTTCACTACTTTA[A/G]ATGAAAATTAGGAAT | 55779 |
rs192065238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401483 | TAAGCAATCTCATAA[C/T]ACTTACAGTCAAATG | 55779 |
rs192066767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374459 | TTGTTACATATATGT[G/T]GCAGCTGAGAGGCTA | 55779 |
rs192070799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416662 | ACCAAAATATTAAAA[G/T]AAAGATTTTTGTATA | 55779 |
rs192087438 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368615 | TGGAAAGGAACAACC[A/G]GTACCAGCCACTGCA | 55779 |
rs192160066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446377 | CTGTTGAATATCCTA[C/T]TGAATTTTACCTTAT | 55779 |
rs192203261 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370530 | CAACAAAATTCAACA[G/T]CCCTTCATGCTAAAA | 55779 |
rs192204629 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408208 | GGGAAGCTCTGGGGT[C/G]GTAGAAGATTGTTAC | 55779 |
rs192209599 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428051 | AGCTGGGCCAAGCCA[A/G]TTAGTTGCGGAACAG | 55779 |
rs192212592 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398377 | ACCTGAGCTGAGTCA[C/T]AAAAACTGATGTGTA | 55779 |
rs192214893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362656 | GTGCAGGGATGCACA[G/T]AGGAATCACAAATCA | 55779 |
rs192219195 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350096 | CAGTCTTACACTGCC[A/G]AAGCCATGAAAAGGG | 55779 |
rs192238895 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396339 | CTCCAGCTCTCTTCT[G/T]ATTAAAAAGAGGGTT | 55779 |
rs192290176 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418057 | TATTTATTGAGACAC[A/T]ATTTATTTATTTATT | 55779 |
rs192313689 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392736 | TAAAGACCAGAATAA[C/T]TCTCAAGATTCTGGC | 55779 |
rs192347372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308790 | TTTGTTTGTTTTGTA[A/G]AGACAGGGTTTCGCC | 55779 |
rs192348073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438773 | GAACAAGTTTTTCTG[C/T]GTACTTCAACCATTC | 55779 |
rs192352290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373342 | AAAAATTGACAATAT[C/T]CATGATGAACAAAAG | 55779 |
rs192356629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354052 | ACTAAAGGCTGCTCT[A/G]ATCTCACCTAACAAA | 55779 |
rs192369244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335903 | ATTTTCTATTACCAC[A/G]AACAACTAAATTAGA | 55779 |
rs192383306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347643 | GACCAACTATCCTTT[C/T]AGGATCCTTCCTCAG | 55779 |
rs192394970 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400253 | ATTTGCCATAAGTTA[A/T]GAAGGAAGAAAGGAG | 55779 |
rs192425216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316381 | ACAACAAAACCTAAA[C/T]ATGGAAGTATAAAAT | 55779 |
rs192432186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295221 | AGCTGGCTTGAGTGG[C/T]CACACATCTGTATAA | 55779 |
rs192435054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399714 | GCAAAAAATTTCACT[A/G]AAAACAAGACCAAAC | 55779 |
rs192478797 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316087 | AAAGAATTGAAATAA[C/T]ACAGAATATGTTCTC | 55779 |
rs192508896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339443 | GCCATAGGTACCACT[A/G]CGGTATGTACCAATG | 55779 |
rs192510763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353566 | TGAGAGTTCTTCCTG[A/G]GAGGAACTTCTTCAC | 55779 |
rs192541937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429697 | ATAAGTTATTTTCTG[G/T]TTTTCTCCTCCTACC | 55779 |
rs192579943 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341010 | GGTCAATGGCCTGCC[A/G]GCGTGCTGGCATCTG | 55779 |
rs192581256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319593 | CAATTGGACCTAATA[C/T]GCATCTACAGAACAC | 55779 |
rs192588042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113298321 | CCATGGCTGTGAGCT[A/G]TGCTCTCCCTAGAAT | 55779 |
rs192620528 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380457 | TTTTCTTGAGACAGG[G/T]TCTCACTCTGTCACC | 55779 |
rs192659261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309572 | ATACATCTGTCCCTA[A/G]GGGTTTTGGATAAGG | 55779 |
rs192710743 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295708 | CAAGGCTCATCTCAT[C/G]GCTCAGGGAACAATA | 55779 |
rs192728947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413024 | ATTTCTCCAGAGCCT[C/T]GCCAGCATCTACTGT | 55779 |
rs192730334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336297 | GTTCTTTGAAAAGAT[C/T]TATAACATGGGTAAA | 55779 |
rs192731659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363793 | TGCAAAATGTTAATA[C/T]CCCCATAATTTCCCC | 55779 |
rs192808258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373027 | GCTATTATATTGGGT[C/T]GTCAGAAGAATAACT | 55779 |
rs192811375 | snp | C/T | 0.000103109 | 0.0071794 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306372 | CAGCCTCATTTGTTA[C/T]GGAATGTGGTAGTAC | 55779 |
rs192813203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335386 | AGATCAGAGTACAGG[C/G]AGGCCAAATTTGGTG | 55779 |
rs192852439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408850 | CCTGGGCAACAAAAG[C/T]GAAACTCCATTTCAA | 55779 |
rs192860897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360809 | GCAGGGCAGAGAGAC[C/T]AACTGTTTCATAGGA | 55779 |
rs192887666 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288029 | GAATTAGATGGAGAC[G/T]GATGCTTGCAATGAA | 55779 |
rs192926085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354767 | CCCTGCCCACTGCCT[A/G]AGAAACCTGAATACT | 55779 |
rs192934604 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385835 | TTTTGGTAGAGACAG[A/G]GTTTCACCATGTTGA | 55779 |
rs192936380 | snp | A/C/T | 0.0115144 | 0.0749975 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316800 | CTTGAATCTGGGAGG[A/C/T]GGAGGTTGCAGTGAG | 55779 |
rs192968591 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444098 | AATCTCAGTTTGAAT[G/T]GTTCACTCAGGTTGA | 55779 |
rs192990998 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359607 | AACTATTTTGACCTG[G/T]TTTTTTTAACCAACA | 55779 |
rs192999505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321127 | AAAAATATTCAAAAC[A/T]TACTAGCAAACCAAA | 55779 |
rs193042520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422235 | AGAGTTGAAGGATCA[C/T]TGGAGGAATTTGTAT | 55779 |
rs193043785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390296 | TGATAAAATTCAACA[C/T]CCCATCATGACAAAA | 55779 |
rs193097305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331195 | TGATTCTGAATTTCA[G/T]TAGCATGTCACACCA | 55779 |
rs193098887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436093 | CACATTCTGTCATCC[C/T]TTTAGTTATCCACAT | 55779 |
rs193102249 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289505 | GCCCAGGAAGATAAC[A/G]TAACTTCTCCTGATT | 55779 |
rs193107173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369963 | ACACCTCTATGCAAA[C/T]AAACTAGAAAATCTA | 55779 |
rs193186565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418114 | TTATTTATTGAGACT[C/T]TGTCACTCTGTCACC | 55779 |
rs193193322 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299099 | CATCAAAAGCCACCA[C/T]AAAACAATCAACAAA | 55779 |
rs193200248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339978 | CAGACTAGATTGAAT[A/T]CCTTGGCCAGGGGAG | 55779 |
rs193207616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415555 | CCTAGAGATTCTGGT[A/T]TATCCTCTCTTTGTT | 55779 |
rs193255915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310821 | AAAGTGTGGTGTGTA[C/G]TGCCTTCTCTCTCAC | 55779 |
rs193261582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394778 | AAAGTTTATGAATTT[A/G]TGTTGCGCCTCATTC | 55779 |
rs193263258 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349460 | CAGGCTTAGTCATGG[C/T]CCTCAGACAAACCTC | 55779 |
rs199518927 | snp | C/T | 9.9832e-05 | 0.00706442 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379369 | GGGAGAGGGGGTTGA[C/T]GGAATAAATATTTCA | 55779 |
rs199527424 | in-del | -/ACAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353454 | TATATATGTATGAAT[-/ACAC]ACACACACACACACA | 55779 |
rs199597930 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336217 | AAGAAATTATAAAAA[-/T]AATAGTAAATCAATG | 55779 |
rs199602135 | snp | A/G/T | 0.000123038 | 0.00784252 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363556 | AGGGAAGTAAAAGGT[A/G/T]AGCCCTTTAAAATTG | 55779 |
rs199623142 | in-del | -/A | 0.0528381 | 0.153711 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412538 | TCACCCCCACCCCCC[-/A]ACAGGCCCTGGTGTG | 55779 |
rs199653080 | in-del | -/T | 0.449979 | 0.150028 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312074 | CTGTGTGTGTGTGTG[-/T]TTTTTTTTTTTTTTT | 55779 |
rs199660349 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364926 | TCTGTTGTTTTTTTT[-/A]AAAAAAAATCTTTCT | 55779 |
rs199684213 | in-del | -/TTTACT | 0.0119091 | 0.0762411 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327414 | ACCAAATTTACTAAA[-/TTTACT]AAATCTGAATCATTT | 55779 |
rs199688506 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416197 | TTTTTTGTTTTTTTT[C/T]CCTTTCCATTTACTT | 55779 |
rs199690120 | in-del | -/G | 0.176861 | 0.239062 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370945 | GCAGTAACAGACAAA[-/G]AGAAAGCCAAATCAT | 55779 |
rs199690254 | snp | A/T | 0.000739241 | 0.0192113 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366000 | TCACTATTTTTAAAT[A/T]CAGTTTGTTATTAAT | 55779 |
rs199704225 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336439 | ATATAAACTACCTTA[C/T]GCCAATAAAATTGAC | 55779 |
rs199710959 | snp | G/T | 0.000166525 | 0.00912331 | splice-acceptor-variant, intron-variant | CFAP44 | GRCh38.p7 | 3:113401741 | TCAAAATCCCATATC[G/T]TGTAAAATGAAAAGA | 55779 |
rs199722807 | snp | A/G | 1.64955e-05 | 0.00287184 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427270 | TCTTCTTCTAAATAT[A/G]ATCCTTCCCCTTTGG | 55779 |
rs199758390 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403096 | AGACTCTTAAAAAAG[A/G]AAAAAAAAAGAATCT | 55779 |
rs199771759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401198 | ATAACAAAAGTTTTT[A/C]CTATGAAAGTTAGGA | 55779 |
rs199780511 | snp | G/T | 0.200182 | 0.244986 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320453 | ATATATGATATATAT[G/T]ACATCTATATATCAT | 55779 |
rs199814107 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384058 | TTCCAAATAGTTGAC[-/T]TTTTTTTTTTTTTCT | 55779 |
rs199841703 | snp | A/C | 0.00299542 | 0.0385842 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291612 | TGAATGGGTGGGAGG[A/C]TAAGACTGCCTTTCC | 55779 |
rs199869411 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359735 | TATGGGTTTTTACTT[-/G]ATCAGATGGTTAATT | 55779 |
rs199896690 | snp | C/T | 0.000792406 | 0.0198891 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403865 | ACCCTAACATATCCA[C/T]CTGACCCAACAGTGA | 55779 |
rs199927736 | snp | C/T | 8.29428e-05 | 0.0064393 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381023 | GGAGCTTCAAGAATA[C/T]AGCCATTTTCACAGA | 55779 |
rs199946937 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320415 | GCAGATATATACATG[-/AT]ATATATATGATATAT | 55779 |
rs199952449 | in-del | -/A | 0.02016 | 0.0983543 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308571 | GCTCTAAAATCAGAC[-/A]AAAAATTTTTTTTTC | 55779 |
rs199967870 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355224 | AACCTATTGAAATTG[-/A]AAAAAAAAAATTTAA | 55779 |
rs199993078 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433639 | GATTTCTCCCCATCA[A/G]TATCCTGATCATCTG | 55779 |
rs200002067 | snp | A/G | 3.29533e-05 | 0.00405901 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403968 | GCTCCACTTTGATCA[A/G]ACCACCTTCCCAAAG | 55779 |
rs200020186 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320466 | ATTACATCTATATAT[-/C]ATATATGATATATAT | 55779 |
rs200044234 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367839 | GAAGCTAAAAACCTT[C/G]AAAAAAAGGTTAGAT | 55779 |
rs200044376 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411583 | GTTAGGTAGCATGAT[A/G]CCTCCAGCTTTGTTC | 55779 |
rs200049487 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413455 | TGCCCATGCCTATGT[C/T]CTGAATGGTATTGCC | 55779 |
rs200061990 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392729 | ATAATAATAAAGACC[A/C]GAATAACTCTCAAGA | 55779 |
rs200091032 | in-del | -/A | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380752 | CTACTGCCTTCTAAT[-/A]GCTGCTTTCCTACCA | 55779 |
rs200097595 | in-del | -/A | 0.0892195 | 0.191441 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343010 | AATAAATAAAAAATT[-/A]AAAAAAAATGGCTGT | 55779 |
rs200103970 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431097 | ATCCCAGAGTAAAAA[-/C]TTGCTGGATGTGCTA | 55779 |
rs200117088 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394725 | AACAGCTGACGAGCT[-/A]AAAAAAAAAATTGCA | 55779 |
rs200122065 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413521 | TTACATTTAAGTCTT[A/T]AATCCATCTTGAGTT | 55779 |
rs200132327 | snp | A/G | 0.000291338 | 0.0120658 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373371 | AGCATAGACACTAAC[A/G]GGATATGGTTTTTTT | 55779 |
rs200135990 | snp | A/G | 0.00175032 | 0.0295313 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327778 | TTTCTGATGTCTAAG[A/G]AGACGGAGTTCTGCA | 55779 |
rs200181184 | in-del | -/A | 0.180702 | 0.240204 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369767 | AAACCCTTCAAAAAA[-/A]TCAATGAATCCAGGA | 55779 |
rs200230306 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375157 | TAAGAAAGAAAGTAT[A/G]GTTGCCAGGGGCTGA | 55779 |
rs200266515 | in-del | -/A | 0.127026 | 0.217663 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412417 | TCTTTTATTTCTTCT[-/A]AAAAAAAAAAGATAC | 55779 |
rs200271647 | snp | G/T | 0.000103966 | 0.00720919 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419985 | AAAGATAGGGTTTTT[G/T]GGGGTTTTTTTCTAA | 55779 |
rs200309504 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410572 | TTTGGGTTGGTTCCA[A/G]GTCTTTGCTATTGTG | 55779 |
rs200372032 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370949 | TAACAGACAAAGAGA[A/G]AGCCAAATCATGAGT | 55779 |
rs200395263 | snp | A/C | 0.0758449 | 0.17936 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344632 | TACTTAGAGGGCTGC[A/C]CCAGCCTGTAAGAGG | 55779 |
rs200415177 | in-del | -/AA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327394 | TCTACCTTACAGAAT[-/AA]ATCAGACCAAATTTA | 55779 |
rs200421776 | in-del | -/TC | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430469 | TTAGCAAAGCCAAAA[-/TC]TCAGTCTTTGAAAAG | 55779 |
rs200432951 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370923 | AAATCACAAGCATTC[C/T]TATACAGCAGTAACA | 55779 |
rs200461029 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406959 | CCATGTAGCCTTCTA[C/T]ATCAGTAGTGATTGT | 55779 |
rs200463114 | in-del | -/AGTAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375151 | AATCATAAGAAAGAA[-/AGTAG]AGTATGGTTGCCAGG | 55779 |
rs200469577 | in-del | -/AG | 0.0221141 | 0.102801 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388620 | TGGATTTAAAAAACA[-/AG]ACTCAGTGATCTGTT | 55779 |
rs200486725 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336635 | GTAAAGCAGAAGAAA[-/G]AAAACAGAAATCCAA | 55779 |
rs200514436 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422601 | ATATGTGATCCAAAG[A/T]TGTAAATGAAGCTAT | 55779 |
rs200541138 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401698 | CAACAATCCAGTCTC[A/T]TCTATTACATCAGCA | 55779 |
rs200557858 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361662 | ACCACACCTGGCTAA[-/T]TTTTTTTTGTATTTT | 55779 |
rs200586609 | snp | A/G | 0.180702 | 0.240204 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370867 | TCCTTAAGCTGATAA[A/G]CAACTTCGGCAAAGT | 55779 |
rs200593093 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410960 | TTCTTTTGAGAAGTG[A/T]CTGTTCATATCCTTC | 55779 |
rs200606551 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406142 | ATAAGAGAAAGAAAG[A/G]AAAGAAACTAACAAT | 55779 |
rs200617587 | snp | A/C | 0.00769736 | 0.0615584 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326638 | AGTTTCATTTATTTT[A/C]CACTAAATGAATAAA | 55779 |
rs200623858 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318967 | AAAACAAAAAAAAAC[-/A]AAAAAAAAAACAATA | 55779 |
rs200624773 | in-del | -/AGGG | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421835 | CACTAGGGATTCCAA[-/AGGG]AGGGAGGGAGGGAGG | 55779 |
rs200634366 | in-del | -/GGAGGTGGG | 0.0644693 | 0.167566 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300222 | TCTGGGAAGGATAGT[-/GGAGGTGGG]GGATGTGGGAATGGT | 55779 |
rs200637877 | in-del | -/ATGAAAA | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338311 | TTAAGGGAATGAAAA[-/ATGAAAA]GACAAGCTACAGACT | 55779 |
rs200678347 | in-del | -/TGTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411938 | CATGATTTGGCTCTC[-/TGTT]TGTCTGTTATTGGTG | 55779 |
rs200691785 | snp | A/G | 8.35806e-05 | 0.006464 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366049 | CATACCCTGGGAGAT[A/G]GAACTTTGGCCTTCA | 55779 |
rs200739238 | snp | C/T | 0.000181292 | 0.0095191 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427200 | ACCTGTAGTGCTTTG[C/T]AAATCACCATACTGA | 55779 |
rs200751823 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373587 | GTAACATAGAAGGTG[A/G]TACTTGAATATAACA | 55779 |
rs200771612 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351751 | GGCTTCTCCCCTTTC[A/T]GGTCCCGTGACAGCC | 55779 |
rs200776776 | in-del | -/TT | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394492 | ATCTGTAGCTATCTC[-/TT]ATTCATTTGGTCATA | 55779 |
rs200789419 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411382 | TAGCCAGTTTTCCCA[C/G]CACCATTTATTAAAT | 55779 |
rs200793628 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372401 | TGCAGCCATAAAAAA[-/A]GGATGAGTTCATGTC | 55779 |
rs200795132 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372913 | CTGTGAGAAAAAAAA[A/T]TCTGCTGTATAAGCC | 55779 |
rs200831295 | snp | A/G | 1.81338e-05 | 0.00301108 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446658 | TGGAGAACAAGAATT[A/G]CCAGTAGCCCCGGAA | 55779 |
rs200840699 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320489 | ATATATATGATATAT[-/AG]ATGTAATATATATCT | 55779 |
rs200853107 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405721 | TTTAAAATGGCTTAT[A/T]TCTTCCCTATATCTA | 55779 |
rs200855344 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413469 | TCCTGAATGGTATTG[A/C]CTAGGTTTTCTTCTA | 55779 |
rs200861952 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444357 | ATACACAAATTAGCT[G/T]GGCGTGGTGGCATGA | 55779 |
rs200892539 | snp | A/G | 1.72418e-05 | 0.00293609 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395877 | TAAGGAAAAAGAGAC[A/G]CACCGACGAAATATA | 55779 |
rs200900144 | snp | C/T | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296877 | GCTGCCGGACTGTTT[C/T]CTCCATTTCTAAAAG | 55779 |
rs200919084 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324043 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs200920984 | in-del | -/AA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408864 | GCGAAACTCCATTTC[-/AA]AAAAAAAAAAAAAAA | 55779 |
rs200935553 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320423 | ATACATGATATATAT[-/A]TGATATATATTGATA | 55779 |
rs200946828 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328695 | GAAATTTAGAGAGCT[-/T]AAAAAAAAAAAAAAA | 55779 |
rs200949157 | in-del | -/CTA | 0.189576 | 0.242588 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320443 | TATATTGATATATAT[-/CTA]GATATATATTACATC | 55779 |
rs200952370 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368698 | TAACAGGCAAAATAA[-/C]CAGCTAACATCCTAA | 55779 |
rs200955458 | in-del | -/ATATATGAT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320467 | TTACATCTATATATC[-/ATATATGAT]ATATATGATATATAG | 55779 |
rs200964456 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374396 | TTATTTATTTATTTA[-/T]TTATTATTATACTTT | 55779 |
rs201032621 | snp | G/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441682 | CAAACAGAAAAGCCC[G/T]ACGAGTTTATTATCC | 55779 |
rs201058510 | snp | C/G | 0.16618 | 0.23553 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370930 | AAGCATTCCTATACA[C/G]CAGTAACAGACAAAG | 55779 |
rs201080398 | in-del | -/TAAAAT | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376811 | GAGAGGTTCAGGAAA[-/TAAAAT]TAAGATTAGTACTAG | 55779 |
rs201089471 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370926 | TCACAAGCATTCCTA[C/T]ACAGCAGTAACAGAC | 55779 |
rs201122506 | snp | A/C/T | 0.0039921 | 0.0444985 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327792 | GGAGACGGAGTTCTG[A/C/T]ATCGAAAGTGACAAC | 55779 |
rs201160705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373370 | AAGCATAGACACTAA[C/G]AGGATATGGTTTTTT | 55779 |
rs201194900 | snp | A/G | 0.00299557 | 0.0385851 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396561 | TCATAAGCTAAAGCA[A/G]TGACACAAGCAGTAT | 55779 |
rs201234676 | in-del | -/AGA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336627 | ATTCCTTAGTAAAGC[-/AGA]AGAAAGAAAACAGAA | 55779 |
rs201245249 | snp | C/T | 0.000100629 | 0.00709256 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304041 | ATTCGTTCTTGCAGC[C/T]GTCTCAAGGCATGGT | 55779 |
rs201287301 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407062 | AACAAGAAAGAGACT[A/G]AATGTACCTCAAAGA | 55779 |
rs201300380 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403095 | CAGACTCTTAAAAAA[A/G]AAAAAAAAAAGAATC | 55779 |
rs201307501 | in-del | -/A | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425110 | TGTCCAAAGATAAGG[-/A]AAAAAAAAAGCCATG | 55779 |
rs201311146 | in-del | -/ATAGA | 0.0883596 | 0.190715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353339 | TTTCCTATCTTCTTG[-/ATAGA]ATAGAAGCCCAGAGT | 55779 |
rs201328237 | in-del | -/A | 0.0581099 | 0.160244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371881 | TTTACAGGAAAAAAA[-/A]CAAATAATCCCATCA | 55779 |
rs201330970 | snp | C/T | 6.61255e-05 | 0.00574964 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286718 | AGTTGAAGAGGTGGA[C/T]AGTCCTGACTCCTGC | 55779 |
rs201331393 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379187 | TAATAAATGAAATCT[-/A]AAAAAAAAATAAATA | 55779 |
rs201344088 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410403 | AACATGCAGTGTTTG[G/T]TTTTTTGTCCTTGCA | 55779 |
rs201353779 | in-del | -/TTCT | 0.0174175 | 0.0916809 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401349 | CAGATTTTTTAAATG[-/TTCT]TTCTATGTTTTATTA | 55779 |
rs201363993 | in-del | -/AT | 0.195837 | 0.244062 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320508 | GTAATATATATCTAG[-/AT]ATACAGTACTTAATG | 55779 |
rs201396812 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409239 | TCCAGATAGTCAGTG[C/T]GTAGTCAGGGTTACT | 55779 |
rs201406682 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411388 | GTTTTCCCAGCACCA[C/T]TTATTAAATAGGGAA | 55779 |
rs201418383 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113435735 | CTCTGCTTCTAAAAT[A/T]AAAAAAAAAAAAAAA | 55779 |
rs201418516 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334665 | TTAATTAAAGGATTG[-/A]AAAAAAAAATGCTTA | 55779 |
rs201489070 | snp | A/G | 0.000710997 | 0.0188413 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426286 | TGAGGTACTAAAAAA[A/G]TAAAATAATTTAAGA | 55779 |
rs201525752 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318967 | AAAAACAAAAAAAAA[A/C]AAAAAAAAAACAATA | 55779 |
rs201540015 | in-del | -/TTTTCATT | 0.0876345 | 0.190099 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412288 | AGCTTAATAAACTTG[-/TTTTCATT]TTACTCTATGGATTC | 55779 |
rs201544892 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364918 | AGTTGTTTTCTGTTG[-/T]TTTTTTTTAAAAAAA | 55779 |
rs201564695 | snp | A/G | 0.000362337 | 0.013455 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406978 | AGTAGTGATTGTTTT[A/G]CCAAATCGACCTAGT | 55779 |
rs201574279 | snp | A/G | 0.00274119 | 0.0369199 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344732 | AAAAATAAAACAAGT[A/G]TTTGCAGTAGTCACC | 55779 |
rs201576281 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430429 | GCTGGAAAAATAAAT[A/G]AAAAAAAAAAAAAAA | 55779 |
rs201576396 | in-del | -/GAAAAATAAAT | 0.364609 | 0.222182 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430418 | CACCTCAAGAAGCTG[-/GAAAAATAAAT]GAAAAAAAAAAAAAA | 55779 |
rs201588091 | in-del | -/GATA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353338 | CTTTCCTATCTTCTT[-/GATA]GAATAGAAGCCCAGA | 55779 |
rs201601049 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302792 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 55779 |
rs201601718 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384195 | TCCCAAGTAGGTGGG[A/G]CTGCAGGTGCCCGCC | 55779 |
rs201609818 | snp | C/T | 0.000678679 | 0.0184087 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427299 | GGTAAATGTTTCATC[C/T]GTGTCATCTTCTAAA | 55779 |
rs201614884 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411029 | TGTTTGAGTTCTTTG[G/T]AGATTCTGGATATTA | 55779 |
rs201622357 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320493 | ATATGATATATAGAT[-/G]TAATATATATCTAGA | 55779 |
rs201626498 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413519 | TTTTACATTTAAGTC[G/T]TTAATCCATCTTGAG | 55779 |
rs201626739 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318968 | AAAACAAAAAAAAAC[A/C]AAAAAAAAACAATAC | 55779 |
rs201662786 | in-del | -/TTTA | 0.300169 | 0.244914 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374364 | CAACTGTCAATTTCT[-/TTTA]TTTATTTATTTATTT | 55779 |
rs201665444 | snp | C/G | 0.00299542 | 0.0385842 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291611 | CTGAATGGGTGGGAG[C/G]ATAAGACTGCCTTTC | 55779 |
rs201677861 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430316 | AATTGAGATATAGCT[-/A]AAGCAGTCCTTGGAA | 55779 |
rs201692129 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361500 | AAGACCTGTTTTGTT[-/G]TTTTTTTTTTTTGAG | 55779 |
rs201694980 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320433 | TATATATGATATATA[-/T]TGATATATATGATAT | 55779 |
rs201713461 | snp | C/T | 0.00272381 | 0.0368034 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341723 | TTAAAAAGATAAGAG[C/T]TTAGGTAAAAAAAAA | 55779 |
rs201738569 | snp | C/T | 0.0019981 | 0.0315445 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379296 | TAAAAATTATTACAT[C/T]GTTACTTACCAAAGA | 55779 |
rs201747437 | in-del | -/T | 0.0876345 | 0.190099 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421994 | TAAATATATTTTTTT[-/T]AAAAAAGAGGTATAA | 55779 |
rs201754449 | snp | C/G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416189 | CTTGGTGTTTTTTTG[C/G/T]TTTTTTTTCCTTTCC | 55779 |
rs201762471 | in-del | -/AATT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327395 | CTACCTTACAGAATA[-/AATT]TCAGACCAAATTTAC | 55779 |
rs201797786 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298802 | CAAGTTCACAGAGAC[-/AG]AAAGTAGAGTGGCAG | 55779 |
rs201875306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419989 | ATAGGGTTTTTTGGG[G/T]TTTTTTTCTAATTTA | 55779 |
rs201886712 | snp | C/T | 0.000437904 | 0.0147905 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296840 | TCTAGATTTACCACA[C/T]GGCCAAACTTGCTGA | 55779 |
rs201916710 | in-del | -/ATCCAATGA | 0.0618563 | 0.164627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315159 | GTGAATGAAAAACAT[-/ATCCAATGA]TATCCAATCATACGC | 55779 |
rs201922076 | in-del | -/CCTGAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320322 | CCAGTGCAGCTGGAA[-/CCTGAC]CCTGACCCTGACCCT | 55779 |
rs201940225 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375156 | ATAAGAAAGAAAGTA[G/T]GGTTGCCAGGGGCTG | 55779 |
rs201941809 | snp | C/T | 9.90589e-05 | 0.00703702 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406911 | TTTAATATTGTAGAA[C/T]AGTAGCTGTACTCAC | 55779 |
rs201963188 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361499 | TAAAGACCTGTTTTG[-/T]TTTTTTTTTTTTTGA | 55779 |
rs201969879 | snp | A/T | 0.00199806 | 0.0315443 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427271 | CTTCTTCTAAATATG[A/T]TCCTTCCCCTTTGGT | 55779 |
rs202001075 | snp | C/T | 0.000671817 | 0.0183155 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326425 | GAAAATAAGATCATA[C/T]GCAAGAAAGAAATAC | 55779 |
rs202007639 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330837 | CTTTAATATTGAGGA[-/T]TTTTTTCCATTTAGG | 55779 |
rs202039075 | snp | A/G | 1.68855e-05 | 0.00290559 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401229 | GAAAATAAGAATAAT[A/G]GGCAACTTACAATAT | 55779 |
rs202052076 | in-del | -/TTGT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411941 | GATTTGGCTCTCTGT[-/TTGT]CTGTTATTGGTGTAT | 55779 |
rs202098667 | snp | C/T | 0.000101714 | 0.00713068 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291643 | TACGCAAAAGAGCAA[C/T]CTCCTCCTTTAAGGC | 55779 |
rs202129117 | snp | A/C/G | 5.22993e-05 | 0.00511345 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379329 | CCCAGAACTTCCCTG[A/C/G]CTCTGAGTAAAATCC | 55779 |
rs202142813 | snp | C/T | 0.000135105 | 0.00821794 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445377 | TGTTGAACAAAGACA[C/T]GGAAAAAATTTAGAT | 55779 |
rs202156507 | in-del | -/C | 0.0872718 | 0.189788 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342814 | CTGGGCATGGTGAAA[-/C]CCCCGTCTCTGCTAA | 55779 |
rs202163588 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297990 | AAGTAATGCCCCACG[G/T]ACATGTATAATGTGG | 55779 |
rs202186235 | in-del | -/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416188 | CCTTGGTGTTTTTTT[-/G]TTTTTTTTTCCTTTC | 55779 |
rs202190591 | in-del | -/AAAA | 0.0376037 | 0.131863 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368702 | GGCAAAATAACCAGC[-/AAAA]TAACATCCTAATGAC | 55779 |
rs202191835 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320481 | CATATATGATATATA[-/T]GATATATAGATGTAA | 55779 |
rs202211743 | snp | A/G | 0.00195463 | 0.0312009 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333394 | ATTGTCATAAAATCT[A/G]TAGATAAGTACCAAA | 55779 |
rs367644538 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369320 | TATTCTAAAACTGAC[C/T]ACATAATTGGAAGTA | 55779 |
rs367646075 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386007 | AGTGGGATACTGAAA[A/T]CTGCTATCATTGTAT | 55779 |
rs367648757 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360320 | GTAGAAACATGTAGA[C/T]TGTATCACATCCTAT | 55779 |
rs367650180 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351001 | TCCTCCTGGGCGATT[A/G]AGGGAAAAAGACTCA | 55779 |
rs367658461 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328036 | GTGTAACTAGAAGTC[C/T]TTCCACCTATTTCTT | 55779 |
rs367673124 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335248 | AAAACTGTAATTCTT[A/G]AGAAAAGTAAAAAGA | 55779 |
rs367701452 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438580 | TTATTGATATATTCC[C/T]GAATAGATGAAAGAA | 55779 |
rs367715248 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396453 | GACATGATGAAGTAG[C/G]AGGACTTATAAGGCA | 55779 |
rs367778165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429441 | TATAGCCACTCCAGC[C/T]GTGTTATGCTTACTG | 55779 |
rs367848483 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364828 | TCTTGGGTGGGCTCT[A/G]GCATCTGTACTTCTA | 55779 |
rs367865069 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310552 | AGATACAAAGTCTCA[C/T]AATACAACATGAAAG | 55779 |
rs367874518 | snp | C/G | 0.000104226 | 0.00721819 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305007 | GACTCTTCTCGGACA[C/G]GATGGAGCAGCCTCC | 55779 |
rs367894445 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357429 | CAGGGAAACCTATAT[G/T]AAGAGACACAGGGAG | 55779 |
rs367902643 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399396 | AACTCCCTATCTCAG[C/T]CTAATTTTTTTCTAT | 55779 |
rs367919758 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294266 | GCAAGTTGAAACCCA[C/T]ACAAAGTGACAAGCA | 55779 |
rs367922743 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346774 | ACCAATCAGCAGGAA[A/G]TGGGCAGGGACAAAT | 55779 |
rs367954181 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399580 | GCCTGGCACATTGTC[A/G/T]GCACTCTGTAAATAT | 55779 |
rs367962018 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300410 | TTGAGGTGAGGATAT[A/C]CCATTTACCCTGATA | 55779 |
rs367987241 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379599 | CAATTATGACTCATT[C/T]GTTCATTTACACCAT | 55779 |
rs368003060 | in-del | -/GT | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443992 | GTAATTTGGAAAACT[-/GT]AAATTTCAGGTTGAG | 55779 |
rs368003969 | in-del | -/TAGAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353345 | ATCTTCTTGATAGAA[-/TAGAA]GCCCAGAGTCAAAGT | 55779 |
rs368018010 | snp | C/T | 1.97521e-05 | 0.00314256 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396765 | GGACCTGAAACTAGT[C/T]AAATTGAGAAAGTTG | 55779 |
rs368080560 | snp | C/T | 0.000115784 | 0.00760779 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395768 | AGACATGGGAGACCA[C/T]ATTAACTGACACACA | 55779 |
rs368095798 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373075 | CTCAATTATTAAAGG[G/T]CTAATGATTCATTTG | 55779 |
rs368150514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389993 | ATACTTCCAAACTCA[C/T]TCAACAAGGCCAGTA | 55779 |
rs368172404 | snp | A/G | 4.94874e-05 | 0.00497406 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286782 | CCCGTAGGGGCCTAC[A/G]TAGGACAGGAACCTG | 55779 |
rs368175355 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306981 | AAGATAAAAACTTTA[G/T]CTGAAATTAAACTTT | 55779 |
rs368188272 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423290 | TGGCTAATTTTTGTA[C/T]TTCTTGTAAAGACAG | 55779 |
rs368199106 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323686 | ATGTATTAATTTGGC[A/G]TCTTAGATGAAATAT | 55779 |
rs368203048 | snp | C/T | 0.000133572 | 0.00817116 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363344 | AATAACAGGTTGTGA[C/T]ACAGAAACAGCAGAG | 55779 |
rs368223245 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333094 | CGACCTAGATTACCA[A/G]ATATCCTTGATGACC | 55779 |
rs368243828 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409006 | GTTAACCAAAACAGC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs368255317 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443671 | GTTTACTCTCCAACA[A/G]GAGGCAGCACAGCAT | 55779 |
rs368268711 | snp | A/G | 8.65284e-05 | 0.00657698 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401785 | GATCAGTAGTTTCTG[A/G]ACATTTATTTTCTAA | 55779 |
rs368325155 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326967 | TTTTGCATGTGTAGT[A/C]TCAAAAACCAATGAA | 55779 |
rs368352621 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434925 | AGGACAAAGGAGAGT[A/G]TAGTATGATGACTGT | 55779 |
rs368357533 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421398 | TATCAGTGAGAATGT[-/GT]AAATCAGTTCAGCCA | 55779 |
rs368361223 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346789 | ATGGGCAGGGACAAA[G/T]AAGGGAATAAAAGCT | 55779 |
rs368365555 | in-del | -/T/TT | 0 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416197 | TTTTTGTTTTTTTTT[-/T/TT]CCTTTCCATTTACTT | 55779 |
rs368393292 | snp | C/T | 0.000102569 | 0.0071606 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296867 | CTGATCATGAGCTGC[C/T]GGACTGTTTCCTCCA | 55779 |
rs368405158 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302023 | TAAGTGATGTCATGT[C/G]GTATTTTCTTTCTGT | 55779 |
rs368435319 | snp | C/T | 1.79181e-05 | 0.00299311 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366355 | CCATTAATCTGAAAA[C/T]AATGCTTAATTTCAA | 55779 |
rs368436860 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406947 | CATCTGGGAGCTCCA[C/T]GTAGCCTTCTATATC | 55779 |
rs368480421 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425718 | AGCCTTTCCACTTGT[A/G]CAAAGGACAGCCAGA | 55779 |
rs368482862 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369041 | AGAAGAGCTAACTAT[C/T]CTAAATATATATGCA | 55779 |
rs368491621 | in-del | -/GGAGGGGTGTCTGCCATTACTGAGGCTTGACT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367037 | TACTGAGGCTTGACT[lengthTooLong]AAGTAAACAAAGCGG | 55779 |
rs368494570 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313545 | TTGGAGGGGCAAGGG[A/G]GCGGAATGATATGGT | 55779 |
rs368495959 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297413 | TGTGCTTCTCAAACA[A/T]GCCAGGCTCACCCCA | 55779 |
rs368520320 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336994 | AAGAAAAGGAAATAA[A/G]ATGCAAACAGATTAG | 55779 |
rs368536490 | snp | C/T | 3.43448e-05 | 0.00414382 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401202 | CAAAAGTTTTTACTA[C/T]GAAAGTTAGGAGAAA | 55779 |
rs368536792 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334327 | AGATGATAGCATGAG[-/C]ATACATATTTGCCTC | 55779 |
rs368553947 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426143 | GTGTGAGAAGATCCA[A/G]TGGTATGTTTGAATC | 55779 |
rs368581699 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400733 | GCAAAGATAAAAATA[A/T]AACACATGTGATTTT | 55779 |
rs368585172 | in-del | -/TGTG | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419614 | TATGTCTACATCCTA[-/TGTG]TGTGTCTCACATTTT | 55779 |
rs368604740 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366065 | GAACTTTGGCCTTCA[C/T]GTCTTTCCTTAGCAT | 55779 |
rs368620724 | snp | A/C/G | 4.99815e-05 | 0.00499887 | missense, stop-gained, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379386 | GAATAAATATTTCAG[A/C/G]TAATGGCTCTTCTTC | 55779 |
rs368655521 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427587 | TAAATACTTACAAGA[A/G]GTAAAAGATAAAAAG | 55779 |
rs368696742 | snp | A/C | 0.000124977 | 0.00790397 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326453 | TACAAACCAGCATCT[A/C]CTTCAACTTCTTTTT | 55779 |
rs368767874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347918 | AAGGGCCACTAAATC[C/T]GATTTTTCTCGGTCC | 55779 |
rs368773423 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411944 | TTTGGCTCTCTGTCT[A/G]TTATTGGTGTATAAG | 55779 |
rs368776455 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411092 | TTCTCCCATTCTGTA[A/G]GTTGCCTGTTCACTC | 55779 |
rs368790155 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311546 | CCAGCCATGTGGAAG[C/T]GTAAGTCCAATTAAA | 55779 |
rs368807168 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360444 | CAACTTCACTGCATG[A/G]ATAGTGAAGAAATTC | 55779 |
rs368835603 | snp | C/T | 5.0844e-05 | 0.00504177 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446716 | TAAGAGAGTGAGCTA[C/T]CATTATTAACCTTAA | 55779 |
rs368835653 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355284 | CCAGCACTTTGGGAG[C/G]CCTAGGCGGGTGGAT | 55779 |
rs368836016 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318328 | CAGAATAGACTAAGA[C/T]GAGGAAAGAATCTCA | 55779 |
rs368873366 | snp | C/T | 1.94926e-05 | 0.00312185 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400656 | GGGTCTGAGAATAGA[C/T]AGACAGCTTACTAGA | 55779 |
rs368879252 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420615 | ACATGGGAGAAAGTC[C/T]GTATCTTCATCACCT | 55779 |
rs368885257 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346116 | ACCAATCAGTGCTCC[A/G]TGTCTAGCTAAAGGA | 55779 |
rs368893634 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417794 | TCAAGCCAAGTATCA[-/G]AGTCAAGAAGCAAAC | 55779 |
rs368909908 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301770 | CATACTTTCTTTTTC[A/G]TGTTGTGAGAACACT | 55779 |
rs368934127 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378036 | TGCGTGGAGTTTTCT[A/G]TTTGTGTTTTGTTGT | 55779 |
rs368941955 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390262 | ACACCACCATTTCAA[C/T]TGATGCTGAAAATGC | 55779 |
rs368946246 | snp | A/C | 0.000109081 | 0.00738435 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400673 | GACAGCTTACTAGAT[A/C]TCAAAGACAGAGTAA | 55779 |
rs368960449 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340260 | TCGGAGGCTGAGCCT[A/G]ATGCTCATTTAGCTT | 55779 |
rs368964911 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400225 | TCAATTTCACCTTGC[A/G]TAGTCCATATAGATT | 55779 |
rs369011724 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406442 | ATCCTGGCTAACACG[G/T]TGAAACCCCGTCTCT | 55779 |
rs369043411 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374640 | CAAGTGTCTATTTTT[A/G]TGTGTTTGTTTTGAG | 55779 |
rs369048426 | snp | C/T | 0.000437904 | 0.0147905 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330407 | CTGTCTGTTCCACTC[C/T]GGGGGACTTTTCATC | 55779 |
rs369115738 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412547 | CCCCCCAACAGGCCC[C/T]GGTGTGTGTTGTTCC | 55779 |
rs369127806 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403340 | AATGTTCCAGCTTAG[A/C]CCAGGCTTTGGGCAA | 55779 |
rs369171364 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343848 | GAAGAAGATAAACCA[A/G]TATTAATGTTCGTAT | 55779 |
rs369194398 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447058 | TTCTGCTTTTGCTTC[G/T]TCCTCATTTTCTCTT | 55779 |
rs369202893 | snp | A/G | 0.000283316 | 0.0118986 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380854 | TATTTTATATTCTAA[A/G]GAAAGGAAATTATTA | 55779 |
rs369205486 | snp | A/G | 0.000347939 | 0.0131852 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426072 | AGTTTGCTGACCTCT[A/G]ACCTAAGAAATGAAA | 55779 |
rs369264062 | snp | C/T | 1.72047e-05 | 0.00293293 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396478 | AAGGCAATTTAACTA[C/T]AAAATTTCAACAAGA | 55779 |
rs369288050 | snp | C/G | 1.64808e-05 | 0.00287057 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366153 | GAAACGATCATCAAA[C/G]CTATTAGCAATACTT | 55779 |
rs369297839 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445394 | GAAAAAATTTAGATG[G/T]TAATTAGAAACATGA | 55779 |
rs369312343 | in-del | -/ATT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296088 | TCCCCAGTGTTTATT[-/ATT]TTCATCTTTATGTCC | 55779 |
rs369317273 | snp | A/G | | | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294809 | GTTCCCATCGCATTT[A/G]AGCAATCTTTTCCTA | 55779 |
rs369317378 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418096 | TATTTATTGAGACAC[A/T]ATTTATTTATTGAGA | 55779 |
rs369321946 | in-del | -/GATT | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302391 | AACCATAAATAAGTA[-/GATT]GATTAAAAAAATTAC | 55779 |
rs369324621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386839 | ATTGCTGACACCACT[C/T]TGGTGGCTGTGTGGC | 55779 |
rs369327267 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325484 | GGGTCTTGCTCTGTC[A/G]CCCAGACTGGAGTGC | 55779 |
rs369328591 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295929 | AAAATGTAGGTTCAG[A/G]TGTACATGTACAAGT | 55779 |
rs369352324 | in-del | -/GTTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437808 | TTTGTTTGTTTGTTT[-/GTTT]TGTTTTAATAACAAA | 55779 |
rs369369755 | in-del | -/AG | 0.170408 | 0.236992 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350356 | GACAAAGAGAGAGTC[-/AG]AGAGAGAGAGAGAGA | 55779 |
rs369386205 | snp | A/C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416423 | CTGTCTTCCACTAGT[A/C/T]CTGTTTCTCTGGAGA | 55779 |
rs369387228 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315264 | CAAATTTTAATCAAA[G/T]CAAAGCAGGAGCAGC | 55779 |
rs369405916 | in-del | -/TTATA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386142 | ACTTATCTTTTATTA[-/TTATA]AGATGTTATTCTTTG | 55779 |
rs369436402 | snp | C/T | | | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113298301 | ACACTCACTACCCAC[C/T]TTCCCCATGGCTGTG | 55779 |
rs369453821 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416348 | CTTTTAATTGGGGCA[C/T]TTAGCCCATTTACAT | 55779 |
rs369486585 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370079 | GTTCTGAAATTGAGG[C/T]AATAATTAATACCCT | 55779 |
rs369571239 | snp | A/C/G | 0.000205809 | 0.0101425 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291606 | GGAGACTGAATGGGT[A/C/G]GGAGGATAAGACTGC | 55779 |
rs369577399 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308423 | AAAGAACACAAACCC[A/G]AATGCCTGCAGAGGG | 55779 |
rs369587760 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295376 | CAGCTAATTTTTTAT[G/T]TTTTGTAGAGACAGG | 55779 |
rs369589077 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404606 | AGCACTGGTTCAGTA[C/T]TTTATATATGTTAAG | 55779 |
rs369646830 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325569 | CCTGTCTCAGCCTCC[C/T]TAGTAGCTCGGACTA | 55779 |
rs369660409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412162 | TTGGAAGTTCTGGCC[A/G]GGCAATCAGGCAAGA | 55779 |
rs369705436 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289571 | ACCTTTCTCAGAGAC[C/T]AGCCACTCTCTCCAG | 55779 |
rs369723026 | snp | C/T | 0.000522664 | 0.0161573 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420001 | GGGGTTTTTTTCTAA[C/T]TTATTGAAGGCATAC | 55779 |
rs369765794 | snp | C/T | 8.79716e-05 | 0.0066316 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395891 | CACACCGACGAAATA[C/T]ATATTACTATGAAAT | 55779 |
rs369768264 | in-del | -/CT | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374035 | GCTATATTGCTCCAA[-/CT]CTAATTTCCTTATTA | 55779 |
rs369806513 | snp | C/T | 0.0037605 | 0.0431985 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291704 | TTCAGTGACCTCCTC[C/T]CTTGCCACAACATCT | 55779 |
rs369812490 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329946 | TCAGCTTTCCAAAAC[-/A]AAAAAAAAAGTTTAA | 55779 |
rs369819622 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337489 | AGACAAAGTAATTAT[A/T]ATGTCTAAAATAATT | 55779 |
rs369841368 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437630 | GTTCTGATGTAGCAA[C/T]ACCGGACAATAAATA | 55779 |
rs369907197 | snp | G/T | 0.000214839 | 0.0103621 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396655 | TCGTGAGCCCTTTTG[G/T]ATCATAAAGTTCAAG | 55779 |
rs369939143 | snp | A/G | 0.000465658 | 0.0152516 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333618 | CCCCCCCACACACAA[A/G]TATGACAATAAACTC | 55779 |
rs369940586 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349797 | ACTTCCTCCTGGACA[C/G]TGGTGCAGCTTTCTC | 55779 |
rs369983128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357781 | CCGTTTTGAAAAACT[A/G]ACAGGATCTAACAAA | 55779 |
rs370018156 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319811 | TAAACAAGATTGCTA[A/T]ATCACTAGTTAGATT | 55779 |
rs370035542 | in-del | -/GGTGGGGGA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300225 | GGGAAGGATAGTGGA[-/GGTGGGGGA]TGTGGGAATGGTTAA | 55779 |
rs370044735 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425943 | TTATCCCTGTCCTTG[C/T]TGTGTGATGGCAGCC | 55779 |
rs370060574 | in-del | -/GATA | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441716 | AAAGGACGTCATGTA[-/GATA]ATTAAATGACATGAA | 55779 |
rs370063538 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353527 | CTGTGAATACTTATT[A/G]AAGCCAAACATAGGC | 55779 |
rs370083148 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346769 | AATGGACCAATCAGC[A/G]GGAAATGGGCAGGGA | 55779 |
rs370101635 | snp | A/G | 2.11513e-05 | 0.00325195 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400515 | AACAAAACAAGGCCA[A/G]ACATATTTTTATTAA | 55779 |
rs370109904 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411427 | CCATTTCTTGTTTTT[C/G]TCAGGTTTGTCAAAG | 55779 |
rs370115901 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374498 | GACAAAGCTATCTGC[A/G]GTCTCATAGACTTAT | 55779 |
rs370169331 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336278 | AATCTATGACCAAAA[A/G]CTAGTTCTTTGAAAA | 55779 |
rs370212794 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303533 | ACACATCCATATGTA[G/T]GTGTGCATACCTGGT | 55779 |
rs370266163 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323064 | AATAGCAGCATGAGG[A/G]TAACCACTCCCATGA | 55779 |
rs370266709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346824 | ACCCCAGCCAGCAGC[A/G]GCAAACCACTCGGGT | 55779 |
rs370276008 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326002 | GAAAAGGCAAGCTAC[A/G]CACTAGGAAAAAATA | 55779 |
rs370284655 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329955 | AAAACAAAAAAAAAA[-/A]GTTTAAAAGCTCTGT | 55779 |
rs370294371 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403895 | ATAACTTCACCCTCA[C/T]ACAGCATTATCTGGT | 55779 |
rs370302958 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323152 | TCAAGATGAGATTTC[A/G]GTAGGGACACAGCCA | 55779 |
rs370316396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316558 | CCAGACTGAAAAAAA[A/G]AGACACAAGTTACCA | 55779 |
rs370318076 | snp | C/T | 3.30797e-05 | 0.00406679 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420118 | CAGCTATGTATATGG[C/T]GATACTGTCGTCCAG | 55779 |
rs370323058 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446940 | CGCCCATGTTGTGGG[A/T]GGGACTCATGGGGAG | 55779 |
rs370342578 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414542 | ATATTCCATCAATAC[A/C]TAGTTTATTGAGAGT | 55779 |
rs370352293 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391223 | TTTTTGACAAAGATG[A/C]CAAGAACGTACATTG | 55779 |
rs370362007 | snp | C/G | 9.8044e-05 | 0.00700089 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306190 | ATAAATAAGTAAACA[C/G]ATCACCATACTTTTT | 55779 |
rs370412863 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428755 | CAAGGATGGGTGCAG[A/G]AGGAAGCAAAGGAAG | 55779 |
rs370420002 | in-del | -/A | | | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428925 | TTTGGGACCTCTCCT[-/A]CTCCAGCTATCTGAG | 55779 |
rs370441262 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427375 | AACTTCTAAATTTTG[A/G]TTAAACATTTTCTTA | 55779 |
rs370453892 | snp | C/G | 0.000437904 | 0.0147905 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333446 | TCTTCCTTCTTGGCA[C/G]CATTTATTCTCATGT | 55779 |
rs370484707 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363192 | TTTCATTCATTTCTA[A/G]TAGATTACAAAATTC | 55779 |
rs370502460 | snp | C/T | 0.00012285 | 0.00783645 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446582 | ACAATTACATTTTAA[C/T]GTGTACCTTTGCTCT | 55779 |
rs370519839 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399635 | CAGATGGATCGAGGC[C/T]AGATACACAAAGTTC | 55779 |
rs370527051 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445821 | TTAATATCTTTCCCC[-/T]ATCATTTAATTTGGG | 55779 |
rs370529653 | snp | A/C/T | 5.12136e-05 | 0.0050601 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286677 | TTTCTCCCCTCAGGG[A/C/T]CCCCATGCTGCTTGG | 55779 |
rs370535016 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382895 | AGCTTTGTGGAGAAG[A/T]AAAGTTCTAAAATGG | 55779 |
rs370562535 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365076 | TATTGACTGCAGCTG[C/T]AAATAAAAGGACATG | 55779 |
rs370563038 | snp | C/T | 0.000329468 | 0.0128306 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379458 | CTTTTTCTCCATCTT[C/T]TCCCATCTCTGCTGC | 55779 |
rs370566069 | in-del | -/CCC | | | cds-indel, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330604 | GTATTTCCTCAACAA[-/CCC]CAGCCACTTTAAGGT | 55779 |
rs370571219 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430390 | GTCAAAAAAAATCAA[C/T]GACCTAAAGTTCCAC | 55779 |
rs370611402 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304394 | AACATTTCAGGGCTG[C/G]CATACTAGGCAAACC | 55779 |
rs370612403 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330190 | ACCAAATACTGTTGC[A/G]TGTACACGTGTTTAA | 55779 |
rs370636558 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315160 | GTGAATGAAAAACAT[-/T]ATCCAATCATACGCT | 55779 |
rs370696607 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400336 | TTTCATGAGCAATTT[A/G]CAGATTTTGTCCTTC | 55779 |
rs370719601 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333572 | TAGTCATCACCAGGT[G/T]TACTCTTGTATCTAT | 55779 |
rs370726465 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380524 | CAGCCATAAACTCCC[A/G]GGCTCAAGCGATCCT | 55779 |
rs370743214 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113291872 | CAGCCACTGTTCCTT[A/C]ATCTCGGGAGCCTTC | 55779 |
rs370752390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308577 | AAAATCAGACAAAAA[A/T]TTTTTTTTCTTTTTT | 55779 |
rs370760895 | snp | C/T | 0.000213995 | 0.0103418 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327847 | AAATATTTGCGGATA[C/T]GTTAGAAGACTAGAT | 55779 |
rs370768140 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368877 | TACACATAGGCTCAA[A/G]ATAAAGGGATGGAGG | 55779 |
rs370800616 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333752 | TTTAAAAGTCAATTA[C/T]TATTTTTAAAGTATC | 55779 |
rs370818243 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396151 | AGTGCATAAAGAATT[-/T]ACACAGTTATTCTCT | 55779 |
rs370831974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389637 | AATAAGAGAGAGAAG[C/G]CTAAAATATATGAAA | 55779 |
rs370835898 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355050 | CAACCTGGAGCCCGG[C/T]AGCTCTGCTGGGACC | 55779 |
rs370880081 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441587 | GGGCGCATGCGCGGC[A/C]GGCGTCCAGCTCTCC | 55779 |
rs370893360 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442451 | TTTGGAAAACTATTT[C/G]AGAGGTTTCTTCAAA | 55779 |
rs370926067 | in-del | -/ACACAC | 0.492582 | 0.0604491 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353454 | TATATATGTATGAAT[-/ACACAC]ACACACACACACACA | 55779 |
rs370934331 | snp | C/T | 3.65711e-05 | 0.004276 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446659 | GGAGAACAAGAATTA[C/T]CAGTAGCCCCGGAAG | 55779 |
rs370991394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346546 | TAAGTGCACCAATCA[A/G]CACTCTGTAAAAACG | 55779 |
rs370996979 | snp | C/T | 5.02374e-05 | 0.0050116 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399861 | AGCATTGATATACCA[C/T]ATTTACCAATAGATT | 55779 |
rs370997916 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424028 | TCTAACTCCCTTTAG[G/T]TTATAGTTCACCATG | 55779 |
rs371001516 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330064 | TCAGGGTTTGGGAAA[A/G]GTTCATGCAGAGAAA | 55779 |
rs371016513 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364737 | TCAATCCTAGCTACA[C/T]AGTAGAATCACATGA | 55779 |
rs371022518 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383013 | ACTAAATTATAGAGG[A/C]GCTAATCTTCATTGA | 55779 |
rs371029096 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376507 | AGCTTGTTCTGCACA[A/T]GAGAAGCCAGCAAAA | 55779 |
rs371081988 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286523 | AGACCTTGGAGGGAA[A/C]AGAAGTGCCCTTGTC | 55779 |
rs371101760 | snp | C/G | 0.000443663 | 0.0148874 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420186 | AAAGAATGTCTGAGG[C/G]AAAGTTGCTAAGGAA | 55779 |
rs371109612 | in-del | -/TAAAAAAAAAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328696 | GAAATTTAGAGAGCT[-/TAAAAAAAAAA]AAAAAAAAAAAAAAA | 55779 |
rs371136985 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430102 | ATACATTTAAATGGA[C/T]TGAAATCATATAGAA | 55779 |
rs371155957 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426203 | CCATATAATCATAGA[A/G]GAAGCTCTCTGATAT | 55779 |
rs371164920 | snp | A/G | 0.00473102 | 0.0484059 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291589 | GTATCTCTTTCTCTC[A/G]TGGAGACTGAATGGG | 55779 |
rs371184854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347955 | TGGTCTAAGAGGACA[A/G]GCAAGAGTGCAGGTT | 55779 |
rs371192800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366777 | CCTCACCTGGGAAGC[A/G]CAAGGGGTCAGGAGA | 55779 |
rs371220476 | in-del | -/ATT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440371 | CAGCCTATTATTATT[-/ATT]TTTGAGACAAAGTCT | 55779 |
rs371224567 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390410 | GAATGAAGAAATACA[A/G]AAAGCCTTTCCTCTA | 55779 |
rs371243085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395528 | CAACTAATAAGCCCA[C/T]GGAAGAGAAAGGAGG | 55779 |
rs371245159 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318580 | AAATACAAAGAGCCC[-/C]AGCTAGATATGATAC | 55779 |
rs371254002 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411195 | TTGCCATTGCTTTTG[C/G]TGTTTTACACATGAA | 55779 |
rs371271361 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384018 | TGGTTTTCTGTTCCT[A/G]TGTTAGTTTGCTGAG | 55779 |
rs371277413 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367906 | TTAAATGACCTCCTG[G/T]AGCTGAAAACCACAG | 55779 |
rs371295685 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312519 | TTGCATAAGTAAATT[A/G]AGGAATGTTAATTCC | 55779 |
rs371317417 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364040 | AAATGCAAAGAACAA[C/T]ATAATCCCCCTCCTT | 55779 |
rs371341542 | snp | C/T | 0.000172132 | 0.00927558 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326421 | GAGAGAAAATAAGAT[C/T]ATATGCAAGAAAGAA | 55779 |
rs371347543 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328300 | CAAAAAACCTGTTCA[A/T]TCTCTTTCTAAGATT | 55779 |
rs371387551 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301843 | TATTAACTATAGTCA[C/T]CATAGTATACAATAG | 55779 |
rs371387557 | in-del | -/ATG | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373690 | TTCTACATAATTTCT[-/ATG]ATTATAGATTTATTA | 55779 |
rs371409607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325585 | TAGTAGCTCGGACTA[C/T]GGCATATTGTGCTTT | 55779 |
rs371441432 | in-del | -/A | 0.000954072 | 0.0218203 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409360 | AATAAATAAGGACAC[-/A]TTTATTTCATTTTCA | 55779 |
rs371471296 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440067 | ATTATTATTTTATTT[A/G]TGTATTTATGTATTG | 55779 |
rs371474074 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340182 | CTGAGCCATGCATGC[-/C]TGCAGCTGTCAAAGT | 55779 |
rs371489806 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391493 | GAAAATGGACAAATG[A/G]AATCACATCAACTTA | 55779 |
rs371495216 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409030 | AAAAAAAAAAAAAAA[A/G]TCTCCAGCTCTTAGA | 55779 |
rs371545575 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413718 | TGCTCCATTGGTCTA[C/T]ATGTCTGTTTTGGTA | 55779 |
rs371547701 | snp | A/G | 0.000155988 | 0.00883003 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401210 | TTTACTATGAAAGTT[A/G]GGAGAAAATAAGAAT | 55779 |
rs371556138 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322358 | TATTCACAAGCTATG[C/T]ATCCAACAAAAGACC | 55779 |
rs371563497 | in-del | -/GAGACAC | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418089 | ATTTATTTATTTATT[-/GAGACAC]AATTTATTTATTGAG | 55779 |
rs371595791 | snp | A/G | 1.65356e-05 | 0.00287533 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401650 | GAGATTCACATTCTT[A/G]TCTACTTGAAGTTCA | 55779 |
rs371596377 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289013 | AGAGGTGAGGCTGCT[C/T]CTCTGGGAGCACAGC | 55779 |
rs371643537 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300662 | CAATTTTTTTAAAGG[C/T]AAACAAATCAAGAGA | 55779 |
rs371652370 | snp | A/G | 0.00013185 | 0.00811835 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409124 | ATGTGGCCTGATCCC[A/G]ATGTAGTAAGCTGCT | 55779 |
rs371703878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315376 | TCAATTTACCAAGAC[A/G]ACATGACACTCCTAA | 55779 |
rs371720496 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436697 | GCAGGTCCCAAATAA[A/G]TGAAGGCAAGGCAGT | 55779 |
rs371740231 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346780 | CAGCAGGAAATGGGC[A/T]GGGACAAATAAGGGA | 55779 |
rs371742264 | snp | C/T | 0.000437904 | 0.0147905 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344597 | TTCTCTCTGATTGAC[C/T]AGCTCGTTTGAATTT | 55779 |
rs371767176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360330 | GTAGATTGTATCACA[C/T]CCTATGGCTCAAAGA | 55779 |
rs371783894 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365964 | ACTTTTAATTTATAA[C/T]GAATATGAACAATTT | 55779 |
rs371784109 | snp | C/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306272 | CAACTAAAGCCTCCT[C/G]AATGTCCAGCCTTTT | 55779 |
rs371789629 | snp | C/T | 3.44068e-05 | 0.00414756 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416495 | TGTTATCCTTGAACA[C/T]GAAATATTTAAATAT | 55779 |
rs371809724 | in-del | -/AGTCTTTTTTC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437273 | CACTTTCTACTTTTC[-/AGTCTTTTTTC]TGAATAAATTTATTT | 55779 |
rs371833856 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342450 | AAGCCACATTTTTTG[A/C]TTTTAAAACCCTTAT | 55779 |
rs371890378 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298249 | ATGCTGAAGAGGCCA[A/G]CAGCTAATGCTCAGT | 55779 |
rs371932454 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407971 | GGCATAGAAAATACA[A/G]ATTTTACTAAATAAT | 55779 |
rs371937318 | snp | G/T | 0.000437904 | 0.0147905 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304090 | CAGAAAGATCGCTAG[G/T]TATTTCTCCAAATAC | 55779 |
rs371957326 | snp | C/T | 1.73363e-05 | 0.00294412 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433545 | ATACTTTTAAAAGTA[C/T]ACATATTATCTTTAC | 55779 |
rs371972695 | snp | C/T | 0.000225685 | 0.0106203 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395881 | GAAAAAGAGACACAC[C/T]GACGAAATATATATT | 55779 |
rs371988611 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375954 | TAGAAGGTAAAAAAA[-/A]GGGAAAGAAAATAAA | 55779 |
rs371998581 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289968 | GTGACTGCAACTCCA[C/T]GAAAGACCCTGAGCC | 55779 |
rs372013535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327394 | TTCTACCTTACAGAA[C/T]ATCAGACCAAATTTA | 55779 |
rs372032197 | in-del | -/ACAA | 0.00993419 | 0.0697739 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345767 | AATTATCACACACAC[-/ACAA]ACAAGCACTTCTTAG | 55779 |
rs372039244 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352224 | AAATGGACCAATCAG[C/T]GCTCTGTAAAATGGA | 55779 |
rs372051631 | snp | A/G | 2.26109e-05 | 0.00336228 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379274 | CTATATTGAAATATG[A/G]TTGAGGTAAAAATTA | 55779 |
rs372069922 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415749 | TGATTTCAACTCTTA[C/T]GCATTTGCTGAGGAG | 55779 |
rs372072452 | snp | A/C/T | 0.00010293 | 0.00717318 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373360 | TGATGAACAAAAGCA[A/C/T]AGACACTAACAGGAT | 55779 |
rs372109401 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310068 | CCACCCTCACAGGGC[A/T]GTAACGAGGTGTCCC | 55779 |
rs372134256 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319066 | ACATCATGATGACAG[A/G]ATCAAAAATCACACG | 55779 |
rs372139250 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423525 | TTCTGATGTACCTTC[A/G]GCTCCCTTTGTCTTA | 55779 |
rs372165226 | snp | C/G/T | 6.69602e-05 | 0.00578581 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409336 | ATCTGGAAGGATAAA[C/G/T]GGAAGCCTAATAAAT | 55779 |
rs372235730 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431037 | GTCTACTCCAACTTC[C/T]CTGCTTGGGTGGAAT | 55779 |
rs372236228 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310979 | GAGCCAATTAAACGT[C/T]TTTTCTTATAACTTA | 55779 |
rs372239613 | snp | C/T | 0.000384652 | 0.0138628 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113303948 | ATTTCTCTCTTTTCT[C/T]GGATGAGCTGTTTAC | 55779 |
rs372241597 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370134 | AGACAGATTCAAAGC[C/T]GAATTCTATCAGAGG | 55779 |
rs372243181 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343275 | ACCATGTTGGCCAGG[C/T]TGGCCTCGGACTCCT | 55779 |
rs372254962 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440021 | CATATTATCGTACAA[-/A]TTCTCAAAACGACCC | 55779 |
rs372276161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407217 | AAGGTTGTAGGCAAT[A/G]TGAATTCTGCAATGA | 55779 |
rs372285929 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307687 | AAGAAATAAATATCC[C/T]AGCTAGGCACGATGG | 55779 |
rs372289908 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387045 | CAGAACCTGAGTTCT[C/G]GTAAGCCTCACCACC | 55779 |
rs372293815 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289941 | CAGATGGCTGCAGCC[C/G]CAGCTCCTAGTGTGA | 55779 |
rs372301519 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334101 | GGACTACAGGCATGC[A/G]CCACCACACCCAGCT | 55779 |
rs372315627 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400735 | AAGATAAAAATATAA[-/T]CACATGTGATTTTAT | 55779 |
rs372385532 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406965 | AGCCTTCTATATCAG[C/T]AGTGATTGTTTTGCC | 55779 |
rs372420178 | in-del | -/CT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299377 | GATATCATCTCACCC[-/CT]GTTAAAATGGCTTTT | 55779 |
rs372423033 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315873 | CATTCTGAAGCCAAG[C/T]TAAGCTAAGCTACTA | 55779 |
rs372444343 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299284 | TCTTAAAAGAAGACA[C/T]ACAAATGGCAAACAG | 55779 |
rs372458530 | snp | A/G | 0.000220576 | 0.0104995 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400594 | AGGAGAAACAGCCAC[A/G]GCTTCAATAGCTCCA | 55779 |
rs372463501 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342973 | TGGGGAACAGAGAGA[C/G]ACTCTGTATCAAAAA | 55779 |
rs372468574 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312633 | CATCACAGGCCTGGA[A/G]GCCTAGAAGAAAATG | 55779 |
rs372475616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337041 | GTTTACAAATGACAT[A/G]GTTGTCTACACTTAA | 55779 |
rs372493912 | snp | A/C/G/T | 8.29383e-05 | 0.00643923 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399995 | AATCATAGATTCGAA[A/C/G/T]AGAGCCTATAGAAAG | 55779 |
rs372499079 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405352 | TTATGAAATGTGACT[C/T]ATATCTAGCTTCCCT | 55779 |
rs372511381 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381956 | GGTTGTATAAAGCTT[-/T]CAGAGAAAGTGGTAT | 55779 |
rs372528909 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391968 | TTAGTACAACCACTA[C/T]GGAGAACAGTTTGGG | 55779 |
rs372533070 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389792 | CACATACAACCTACC[A/C]AGACTGAACCATGAA | 55779 |
rs372561747 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356631 | AAATACTAGGTCAAT[C/T]GGATATCAATATAAA | 55779 |
rs372564772 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430990 | AATAGAACTCAGAGA[C/T]AGCAGAAACCTCTTG | 55779 |
rs372574755 | snp | A/G | 1.65201e-05 | 0.00287398 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420071 | GTAGATCTGTTCCTT[A/G]GTTTTCAAATTCAGA | 55779 |
rs372585130 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348338 | CCTGAAAAAGAGGTG[G/T]CTCATTTTTTTCTGC | 55779 |
rs372599964 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308052 | ATACATTTTGAACTA[C/T]CCTTTTTTTGAATTA | 55779 |
rs372603969 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430070 | AGATCACTTGCTGGG[A/G]CATAAGACCAGTTTT | 55779 |
rs372623639 | snp | A/C | 0.154993 | 0.231244 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375072 | TTATCCCAAGTGAAA[A/C]AAGCCAGTCATAAAG | 55779 |
rs372641604 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426338 | GTCCCCACCCAAATC[C/T]CAACTTGAATTGTAG | 55779 |
rs372644979 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333199 | ATTAGCTGACTAACC[A/G]TGGACAAATCTCGTG | 55779 |
rs372662705 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113362137 | ATCTTGGTTGAGGGA[A/G]AACATATCAATATGG | 55779 |
rs372668448 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325147 | TCTCTACTAAAAATA[G/T]AAAAATTAGCCAGGC | 55779 |
rs372672844 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365827 | TCTTTTTTAATCTGG[C/G]GAATTCCAATCTTTA | 55779 |
rs372702295 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326793 | GTTTGCAGAGCCATC[C/T]ATTTATTGGTTAAAA | 55779 |
rs372705945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296015 | ACCAGATAGCAAACG[A/T]TGTACCTAGTAGGTA | 55779 |
rs372706190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353697 | TAAGAAGTGCTATAA[C/T]TTTCAGAGTGAAGTA | 55779 |
rs372717511 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319360 | TCACATAATGATAAA[-/A]GAGTGCAATCCAACA | 55779 |
rs372726630 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325433 | ATAAATAGAGATATA[G/T]TGTGCCTTTTTTATT | 55779 |
rs372738947 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358227 | TGCTATAAATGTTCT[C/T]TATCTTAATCTGAGT | 55779 |
rs372745679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415192 | TAGTCTGTATTTCTG[C/T]GGGTTCAGTGGTGAT | 55779 |
rs372764457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315173 | ATTTCTGGTAGTCAG[C/T]GTATGATTGGATAAT | 55779 |
rs372765969 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386553 | GGAAGAGATGCCTAG[-/G]TTGTACAATCAATAA | 55779 |
rs372788857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357900 | TACACAATGTTCATA[A/G]TAGCATTATTTATGG | 55779 |
rs372827082 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367250 | CTGAAAACGGACAGA[C/G]TGCCTCCTCAAGTGG | 55779 |
rs372864767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313694 | TTCTCATGGCAGTGA[A/C]TATGTCTCACAAGAT | 55779 |
rs372872994 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408453 | AAAAAAGAAATTCAG[C/T]AGTGGATGTGAAAGC | 55779 |
rs372917724 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329069 | ACTGAATATCTATTA[C/T]ATGTTTGACATTGTC | 55779 |
rs372930453 | snp | C/T | 0.000255722 | 0.0113047 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308138 | ACTTCACAGAGAACA[C/T]GTGGTTTTATCTAAC | 55779 |
rs372936562 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357346 | TGAGATAATGACAGC[A/G]GGCCTTAATGAAACA | 55779 |
rs372953998 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305167 | CCTGTAGAAAGCCCC[A/G]TGTTGTGAAATGGTG | 55779 |
rs372962359 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382682 | AAAGTAGAAACAAAA[A/G]GGCAAGAGGCAGAAT | 55779 |
rs373004993 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332843 | AAATCTAAGTCTTTG[A/G]TGGTCCATGGCAACG | 55779 |
rs373007775 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346379 | CACCAATCAGCGCTC[C/T]GTGCCTAGCTAAAGG | 55779 |
rs373017693 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308507 | CAGATGTTGTAGTCC[A/C]CCTAAAACACAGTTA | 55779 |
rs373048284 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393708 | TTTTGTAGAGACAGG[A/G]TTTCACTATGTTGCC | 55779 |
rs373072303 | in-del | -/TGTTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437795 | GGTTTTTTGGGGTTT[-/TGTTT]GTTTGTTTGTTTTGT | 55779 |
rs373091330 | snp | A/G | 1.72009e-05 | 0.0029326 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396477 | TAAGGCAATTTAACT[A/G]TAAAATTTCAACAAG | 55779 |
rs373108247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384261 | AGACAGAGTTTCACC[A/G]TGTTAGCCAGGATGG | 55779 |
rs373129414 | snp | A/G | 4.99023e-05 | 0.00499486 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416538 | ACCTCGAAGGACTCT[A/G]TATGGTCTCAGAGAA | 55779 |
rs373132236 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438440 | AAGTATTTAATGGCT[A/G]TGTGCCTCAGTACTT | 55779 |
rs373132679 | snp | C/T | 3.31367e-05 | 0.00407029 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396675 | TAAAGTTCAAGAATT[C/T]GAACAACTCCATCTT | 55779 |
rs373140006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412943 | AGATCCTTGAGGAAT[C/T]GCCATACTGTCTTCA | 55779 |
rs373147710 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424813 | GAATAAAAGTTAAGG[C/T]TCTTCTGACTCTGAT | 55779 |
rs373165787 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394072 | TAGATTTACAGGAAG[C/T]TGAAAAGATAGTACA | 55779 |
rs373197426 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406474 | TAAAAATACAAAAAA[-/A]TTAGCCAGGCATGGT | 55779 |
rs373265076 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383541 | ATAAACATTCAGTCC[A/C]TAGTATTATTGAAAT | 55779 |
rs373274170 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353668 | ATTCAACTATTCAGG[G/T]ATTTAATACCTGGTA | 55779 |
rs373295277 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412725 | TTTTTATGGCTACAT[A/G]GTATTCCATGATGTA | 55779 |
rs373319496 | in-del | -/A/AAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324042 | GCAAGACTCCGTCTC[-/A/AAA]AAAAAAAAAAAAAAA | 55779 |
rs373355918 | snp | A/G | 0.000107421 | 0.00732796 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286632 | GGGTGTTGGCTCCTC[A/G]GTCAATCTGGATTTT | 55779 |
rs373366019 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287276 | GGAGACACCCACACA[C/G]ATGGCTGGATCCGGT | 55779 |
rs373391960 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348322 | AATTTGACCCACAAA[C/T]CCTGAAAAAGAGGTG | 55779 |
rs373397037 | snp | A/C | 0.000618557 | 0.0175754 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305102 | CTTCTCTCGCTGATA[A/C]GCCTCCAGGGCCTCC | 55779 |
rs373452725 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402472 | GCAGGACCTCCCCTG[G/T]GAGGGGCCAAAGCTC | 55779 |
rs373486767 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378415 | TCCATCCTTCTTTCT[A/G]CTTGCCTCCTTAGTA | 55779 |
rs373491404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413598 | CATTTGACTAGCCAC[C/T]TTTCCCAGCACCACT | 55779 |
rs373493806 | snp | C/T | 0.000142708 | 0.00844591 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381110 | GCAAATTTTTAAAAG[C/T]ATAGTTTAAAGAGAT | 55779 |
rs373513156 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297603 | TTCCATGGAGGCTTT[C/T]CCTGCCTCCCATGGA | 55779 |
rs373513191 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350220 | AGACAAAGACAGAGA[C/G]AAAGAGAAAGACAGG | 55779 |
rs373518668 | snp | C/T | 1.65214e-05 | 0.0028741 | splice-acceptor-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433671 | TTCCTTCATTTCCTC[C/T]GTAAGTACAAAATGG | 55779 |
rs373531690 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412341 | TTGCACAAGGTCTAA[C/G]AACCCTCTCTTGGGG | 55779 |
rs373544294 | snp | A/G | 5.00571e-05 | 0.00500261 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403840 | TACCATCCAAGTATC[A/G]AGAAAACTTACCCTA | 55779 |
rs373556696 | snp | C/T | 1.67016e-05 | 0.00288973 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380907 | TCCATACCAGAATCT[C/T]AGATTTGACACTTGA | 55779 |
rs373569684 | in-del | -/ACACACACAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353454 | TATATATGTATGAAT[-/ACACACACAC]ACACACACACACACA | 55779 |
rs373592077 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441205 | GTCTAAGCTGTGCTC[C/T]TGCTGCCTGGCTGGC | 55779 |
rs373603281 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403897 | AACTTCACCCTCATA[C/T]AGCATTATCTGGTTA | 55779 |
rs373605493 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387915 | GCCAGGGAGTACTTG[C/T]CACAGGTCTGGGGTA | 55779 |
rs373614251 | snp | C/T | 0.000275257 | 0.0117283 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401320 | TATTTTGTTTTATCA[C/T]TTTAAACTTTCATCA | 55779 |
rs373659043 | snp | C/T | 3.3083e-05 | 0.00406699 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401719 | TACATCAGCAGTGTC[C/T]ATTGTCTCAAAATCC | 55779 |
rs373669626 | snp | A/C/T | 0.00041231 | 0.0143523 | intron-variant, missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286742 | CTCCTGCCAAGTGAG[A/C/T]GGAGGAGACTGGTGT | 55779 |
rs373699466 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355399 | GGTGGCAGGTGCCTG[C/T]AATCCCAGCTATTCA | 55779 |
rs373702935 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390808 | GTGAAAGATTTCTAC[A/C]ATGACAACTATAAAA | 55779 |
rs373736803 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431222 | CAGCAACAAGGTACA[A/G]GATGTTCAGAATGCC | 55779 |
rs373749751 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367419 | ATTCTGCAGCCTCCA[C/T]TGGTGATACCCAGGC | 55779 |
rs373774028 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327881 | TGCATTTTTAAACTA[C/T]CTAACAGTACTAATT | 55779 |
rs373783530 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430584 | CAGATCCTACAAAGT[C/T]ATGTCAACAAATTTG | 55779 |
rs373794353 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421773 | TCTCACTTATAAGTG[A/G]GAGCTAAATCTTGAG | 55779 |
rs373797526 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346773 | GACCAATCAGCAGGA[A/T]ATGGGCAGGGACAAA | 55779 |
rs373838001 | snp | C/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304051 | GCAGCCGTCTCAAGG[C/G]ATGGTTAGAGAAGAC | 55779 |
rs373838778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339897 | AAAAAGAGGAGAGAG[C/T]CTGGGGGAAGAACCC | 55779 |
rs373863394 | in-del | -/TTTA/TTTATTTA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374363 | CAACTGTCAATTTCT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 55779 |
rs373887851 | snp | A/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396581 | ACAAGCAGTATGGGG[A/T]TTGAAAACCTGTTTC | 55779 |
rs373896325 | in-del | -/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418298 | TACCATGTTGGCCAG[-/G]CTTGTCTTGAACTCC | 55779 |
rs373907074 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368773 | AATGGGCTAAATGCT[C/G]CAATTAAAAGATACA | 55779 |
rs373982996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325586 | AGTAGCTCGGACTAC[A/G]GCATATTGTGCTTTC | 55779 |
rs373991185 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352264 | AGCATGTGGGCAGGG[A/T]CAAATAAGGGAATAA | 55779 |
rs374001041 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377778 | CTGCCTTGGCCTCCC[A/G]AGTAGCTGGGACTAC | 55779 |
rs374025558 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377129 | TGAGATGAGGTTATC[A/G]TTGAAGAGTAAGAGA | 55779 |
rs374064859 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310423 | CCCTTGGGTGACAAT[A/G]AAGTCTGAATGGGGA | 55779 |
rs374144167 | in-del | -/AGAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439259 | CACCAGTGTTAAGAA[-/AGAA]CCCTGACAAATAGAG | 55779 |
rs374166383 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327021 | AAACAAAGAGACATA[C/T]AATTTCTAGTGAAGC | 55779 |
rs374171513 | snp | A/G | 3.62417e-05 | 0.00425671 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400641 | GGCATTCTGGGTCCT[A/G]GGTCTGAGAATAGAT | 55779 |
rs374176665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389384 | AAAGCAGTACTAAGA[G/T]AAAAGTTTATAGCTA | 55779 |
rs374184902 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371824 | AATTTTTGCAATCTA[C/T]CCATCTGACAAAGGG | 55779 |
rs374186043 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410462 | CTTCACCCATGTCCC[G/T]GCAAAGGACATGAAC | 55779 |
rs374191397 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360309 | ACCTTATTATTGTAG[A/C]AACATGTAGATTGTA | 55779 |
rs374192691 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310138 | GAGCCAGTACATTTA[C/T]TCATGCTGGCTGGTA | 55779 |
rs374261867 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373002 | AAAAAAGGCCAATTT[C/G]AAATTTGAAGCTATT | 55779 |
rs374267559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331119 | CAAACTACAGGTTAG[A/C]CTATTTTCATTCTGT | 55779 |
rs374274613 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405830 | TTAATTCTTACAGTA[C/T]TGAGAATTTGAAGCT | 55779 |
rs374310665 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368993 | CAAAAGAGACAAAGG[C/T]CATTACATAATGGTA | 55779 |
rs374392021 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359148 | CAATATTTGGAGAGT[A/G]TACAGTTTTAAAGAC | 55779 |
rs374396991 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297288 | AATGACAATCCCTTT[A/G]GGAATTCAGGAGGCC | 55779 |
rs374397193 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313497 | GGACTGTTGGGAAGG[C/T]ACGACTGGTTTTGAA | 55779 |
rs374402328 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321592 | TAACTATCTTTGCTG[C/G]TGATATGATTCTATA | 55779 |
rs374410160 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286558 | TTGTAGGTTTCTGTC[C/T]CCTTTCCAGAGCCAG | 55779 |
rs374416374 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399913 | AAACTTACCATTCGG[G/T]GTACCCAAACAAGGG | 55779 |
rs374432176 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315101 | ACAATTGTATTAAAT[A/G]TAAATGGTTTAAATA | 55779 |
rs374443246 | snp | C/T | 3.64047e-05 | 0.00426626 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426319 | AGTGATATGGTTTGG[C/T]TGTGTCCCCACCCAA | 55779 |
rs374443405 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435287 | CAGTTTGGCATGGCT[A/G]GGGAGGCCTCAGGAC | 55779 |
rs374498972 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309796 | CACTGTGGCGAGTTC[C/G]TTGGATATTCTTTTA | 55779 |
rs374519599 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441959 | GGTTTTATGTTGTGG[A/G]TTTCTTGGTCGCAGC | 55779 |
rs374528157 | snp | C/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301641 | TGAAAATGATCTTTT[C/G/T]AAATGGACAAAAATT | 55779 |
rs374528658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410892 | TTTGCATTTCTCTGA[C/T]GGCCAGTGATGATGA | 55779 |
rs374534802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389730 | TACTATGAGCAACTT[C/T]ATGCAAGTAAATTTT | 55779 |
rs374555304 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346718 | GTAAAGGCACCAATC[A/C]GCACTCTGTAAAATG | 55779 |
rs374575670 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435544 | ATGGGATTTGGGTGG[A/G]GACACAGCCAAACTG | 55779 |
rs374591973 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424542 | TTAGGGAATACCTGA[C/T]GGCTGACTTGTTCTT | 55779 |
rs374599460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385877 | TCAAACTCCTGACCT[C/T]AGGTGATCTGCCTGC | 55779 |
rs374599536 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321161 | GCAGCACATCAAAAA[-/A]GTTAATTCCCCATGA | 55779 |
rs374635553 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289659 | ATTCACACCCTGTTC[A/G]GTCCCCTCCCACATC | 55779 |
rs374654216 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351221 | AAGAATAACTGAAAT[C/T]CCAAACTTACAAGGT | 55779 |
rs374674865 | in-del | -/ACT | 0.00119737 | 0.0244387 | cds-indel, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290225 | TCCAGTAGAGAAGTG[-/ACT]ACATCAGAAATTAAT | 55779 |
rs374680034 | in-del | -/AC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320512 | TATATATCTAGATAT[-/AC]AGTACTTAATGAAGT | 55779 |
rs374693809 | snp | G/T | 0.000201633 | 0.0100387 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330395 | GGCCTCCAGACCCTG[G/T]CTGTTCCACTCCGGG | 55779 |
rs374736447 | snp | C/G | 3.65851e-05 | 0.00427683 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446660 | GAGAACAAGAATTAC[C/G]AGTAGCCCCGGAAGA | 55779 |
rs374784933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366927 | CATGCCTGGCTCAGC[A/G]GGTCCCACGCCCATG | 55779 |
rs374821709 | in-del | -/TAAATG | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430424 | AAGAAGCTGGAAAAA[-/TAAATG]AAAAAAAAAAAAAAA | 55779 |
rs374865531 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333463 | ATTTATTCTCATGTG[C/T]TCAGGTATCTTGTAG | 55779 |
rs374868241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397319 | CTCAAGAAAAAGTTA[C/T]AGTCTGACTAGAGTA | 55779 |
rs374878125 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373439 | TTTGGATGGGATTGT[C/T]CTCTGTATCCGCAAG | 55779 |
rs374882576 | snp | G/T | | | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428950 | TCTGAGAGATACTGC[G/T]TCCCGCAAACAGTTT | 55779 |
rs374889333 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346831 | CCAGCAGCGGCAAAC[C/T]ACTCGGGTCCCCTTC | 55779 |
rs374900774 | snp | C/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113434164 | AACTTTATGGAGCTT[C/G]TTTATAAAGATAGAT | 55779 |
rs374917262 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401901 | AGCCAAAACCTGACC[C/T]CTGAAATTTTACTCT | 55779 |
rs374927233 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362787 | CGAAGCCAGCCACCG[C/G]ACGCTTCAGGCCAAT | 55779 |
rs375002039 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393509 | ATTAAAAAGAGCCTG[C/G]CACCTCCCCACTCCC | 55779 |
rs375019267 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346784 | AGGAAATGGGCAGGG[A/C]CAAATAAGGGAATAA | 55779 |
rs375031527 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385972 | TGATTTTCGATCTAT[-/AT]GTTTTATCCATTATT | 55779 |
rs375033634 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304573 | CTGCAATTTAATATA[A/C]GTTGCAATTCAAATA | 55779 |
rs375036163 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320919 | TAATCTCCTTTGGCA[A/G]CACCCTCACAGACAC | 55779 |
rs375040605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379157 | ATTCATCAAAACTCA[C/T]GACTTCAATAGTATT | 55779 |
rs375151140 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439132 | ACTAGCATAAATTTC[A/G]TTTCATTAGATCCAG | 55779 |
rs375159154 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328989 | AGTGTCCCTGCATAC[A/G]GAACATCCAATAAAT | 55779 |
rs375175415 | snp | C/T | 0.000460076 | 0.01516 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400689 | TCAAAGACAGAGTAA[C/T]AAAGAATTAAGATCA | 55779 |
rs375176500 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306752 | AAGAGCCACCTTTAT[C/T]CACCAAGTAATAGAG | 55779 |
rs375237094 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437772 | GTAAGGTAGAATAAG[A/G]TATTTTTGGTTTTTT | 55779 |
rs375239809 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430576 | AATGAAAACAGATCC[C/T]ACAAAGTTATGTCAA | 55779 |
rs375261683 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344592 | TGGTTTTCTCTCTGA[C/T]TGACTAGCTCGTTTG | 55779 |
rs375266635 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360398 | AATGAGTGGTGTCTA[C/T]TGGGGTTTGACAGTA | 55779 |
rs375285103 | in-del | -/AATTAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376814 | AGGTTCAGGAAATAA[-/AATTAA]GATTAGTACTAGAGC | 55779 |
rs375346132 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434686 | AATGGAACACTAGTT[C/G]TATTTGGATCAGATT | 55779 |
rs375360351 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294043 | TTTCCAGGGTTCTGA[A/G]AGAAAATATAAAGCA | 55779 |
rs375388777 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418379 | GGCAGGAGCCACCGC[A/G]CCAAGCCAGGAGTTT | 55779 |
rs375396494 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443573 | CACAGCTTATAGTAC[A/G]GTGTCTGCCACAGTA | 55779 |
rs375398979 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339424 | ACCCCTTATCCCTGA[A/G]CTGGCCATAGGTACC | 55779 |
rs375404347 | snp | A/C | 6.59554e-05 | 0.00574224 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427173 | ATTACTGACAGAAAA[A/C]TAATAATACCTACCT | 55779 |
rs375406731 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366407 | TTAATAACAAAGTTG[C/T]TATGGACTGAATTGT | 55779 |
rs375438342 | snp | C/T | 1.69037e-05 | 0.00290716 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416600 | TCCCTTTTTCAGCTA[C/T]TGTGAAATAAGTTTT | 55779 |
rs375452765 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355259 | GGCGTGGTGGCTCAC[A/G]CTTGTAATCCCAGCA | 55779 |
rs375467131 | snp | A/G | 1.65389e-05 | 0.00287562 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426118 | ATATTTAGCCAGGGT[A/G]GATACACAAGTGTGA | 55779 |
rs375511670 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437571 | TAATGTCAGGTTGTG[C/T]ACAATGTGGAAGAAA | 55779 |
rs375533322 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390420 | ATACAGAAAGCCTTT[A/C]CTCTAAGATCTGAAA | 55779 |
rs375543955 | snp | A/G | 6.37816e-05 | 0.00564683 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416673 | AAAAGAAAGATTTTT[A/G]TATAAATAGTCTGAT | 55779 |
rs375548339 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361118 | TGAATGAGTTACCCT[C/T]GGGTGGATTTAATGG | 55779 |
rs375569865 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323801 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCCG | 55779 |
rs375586953 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360382 | TGTCTGAGTATTTGA[A/G]AATGAGTGGTGTCTA | 55779 |
rs375643064 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430248 | CAAAGGGAAATCAAC[A/G]AAGAAATTAGAAAAG | 55779 |
rs375645807 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436404 | TTAAAACTATTGAGC[A/G]TATTATTATGCTAGG | 55779 |
rs375653631 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423285 | ACACCTGGCTAATTT[C/T]TGTATTTCTTGTAAA | 55779 |
rs375694168 | snp | A/C | 1.64879e-05 | 0.00287118 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363243 | GCTCTCTCTTCCGTG[A/C]CTTTATTTCTCCCAC | 55779 |
rs375699329 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320128 | GAAAAAAAGCCCTGC[A/C]TCAGATGAATTCACA | 55779 |
rs375719467 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393406 | GTGTTTGGGTCTTGC[A/G]GGTGGATGCCTCATG | 55779 |
rs375749962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343114 | TCACCTAGGCTAGAG[C/T]GCAATGATGCAATGT | 55779 |
rs375762123 | snp | C/T | 1.65203e-05 | 0.002874 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399942 | GGCAGTACCTCCTTG[C/T]TTGAATTTCATCTGG | 55779 |
rs375762294 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334140 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATCATGT | 55779 |
rs375783344 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427076 | TTTATCATTCCCACA[C/T]ATATGTACATCCTGC | 55779 |
rs375825127 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374331 | GCCTGGCATTTGGCA[C/T]TGCTTTACTCCCTGG | 55779 |
rs375827016 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324852 | CCACAATTACTTTTG[C/T]ACCAACCTAATCATC | 55779 |
rs375833488 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342789 | CTGAGCTCAGGAGTT[C/T]AAGACCAGCCTGGGC | 55779 |
rs375852916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303489 | GCACAGTTAAAAATA[A/T]GCAAGGTAGGTCTCC | 55779 |
rs375856160 | in-del | -/TTTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328308 | TGTTCAATCTCTTTC[-/TTTT]TAAGATTGAAGAAAT | 55779 |
rs375868466 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322963 | TCCTCCACATGGCAG[C/G]AGGAAGGAGAAGTGC | 55779 |
rs375920426 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418851 | CCGGGATTACAGGCG[C/T]GTGCCACCATGCCTG | 55779 |
rs375945883 | in-del | C/GTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411938 | TCATGATTTGGCTCT[C/GTT]TGTCTGTTATTGGTG | 55779 |
rs375946809 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325156 | AAAATAGAAAAATTA[C/G]CCAGGCGTGGTGGTG | 55779 |
rs375979167 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437369 | AATTTATTCACAAGA[C/T]AATCATAAGGTGGGT | 55779 |
rs375993271 | in-del | -/CAAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327009 | GATATATAACTAAAA[-/CAAA]GAGACATATAATTTC | 55779 |
rs376002206 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403959 | CTCGACAGAGCTCCA[C/T]TTTGATCAGACCACC | 55779 |
rs376021647 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346946 | TATAACACTCACCGC[A/G]AAGGCCCGTGGCTTC | 55779 |
rs376046412 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358059 | TAATCTTAGACATCA[C/T]ATGAGTTTTAAAAAA | 55779 |
rs376056498 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343323 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55779 |
rs376059924 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308850 | GGCTCAAGGGATCTG[C/T]ACAACTGGGCCCCAC | 55779 |
rs376072086 | snp | C/T | 3.30382e-05 | 0.00406423 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420074 | GATCTGTTCCTTGGT[C/T]TTCAAATTCAGAAAG | 55779 |
rs376084020 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429404 | TACTCTTTGCCTTGA[A/G]GTCTATTTTATCTGG | 55779 |
rs376099759 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344049 | CCTCTATTCTCTGAT[A/C]ATTCTATTTAAAGCA | 55779 |
rs376103383 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375244 | GGATGAGGAGGACGG[C/T]AGAACAGATGTTGGT | 55779 |
rs376105432 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435419 | CATCAGATTTTGTGA[A/G]AACTCACTTACTATC | 55779 |
rs376106162 | snp | C/G | 0.000437904 | 0.0147905 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330440 | TACTTTTCATTTGCT[C/G]TTGCTTAAAATTTAG | 55779 |
rs376157619 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300476 | CCATATATCTTATAA[-/AT]ATATATATATATATA | 55779 |
rs376179721 | snp | C/T | 0.00011611 | 0.00761851 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330189 | GACCAAATACTGTTG[C/T]ATGTACACGTGTTTA | 55779 |
rs376193610 | snp | C/T | 0.000437904 | 0.0147905 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113308212 | ATTCAGACTCATCTT[C/T]ATCACTCTCCAAGCT | 55779 |
rs376206774 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336903 | CTGAATGCTTCCTAA[A/G]ATAAGGAACAAAGTG | 55779 |
rs376257525 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339133 | TGCTGAATGGTATCA[A/G]AAATGAATGGTTCCT | 55779 |
rs376263758 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439596 | TATTCCATTGCAATG[A/C]CTTACTCCCGAATAA | 55779 |
rs376274792 | snp | C/G | 0.000437904 | 0.0147905 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291594 | TCTTTCTCTCGTGGA[C/G]ACTGAATGGGTGGGA | 55779 |
rs376300090 | snp | C/T | 4.94181e-05 | 0.00497057 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406971 | CTATATCAGTAGTGA[C/T]TGTTTTGCCAAATCG | 55779 |
rs376367986 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370911 | ATCAATGTACAAAAA[C/T]CACAAGCATTCCTAT | 55779 |
rs376368512 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333788 | CAAAATAATATACAA[C/T]TATATAAACAGGAAC | 55779 |
rs376374174 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429878 | CTACTTAAGAGTTAC[C/T]ATTTATTATAGTAAC | 55779 |
rs376375459 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421284 | GCAAATCAAAACCAC[A/G]ATGAGATACCATCTC | 55779 |
rs376376875 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413101 | TCTCATTGTAGTTTT[A/G]ATTTGCATTTCTCTG | 55779 |
rs376378314 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369199 | GGTTAACAACGATAT[C/G]CAGGATTTCAACTCA | 55779 |
rs376378932 | in-del | -/T | 0.11228 | 0.208646 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343008 | TAAATAAATAAAAAA[-/T]TAAAAAAAAATGGCT | 55779 |
rs376414863 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350264 | GAGAAGGAAAGAGAG[-/AG]GAAGAGACAGACAAA | 55779 |
rs376429241 | in-del | -/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362879 | TCTTGGGTTCTACTT[-/T]ATTTCTTCCCCATGT | 55779 |
rs376455781 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297971 | TTCACTTTCTATTCT[A/G]TGTAAGTAATGCCCC | 55779 |
rs376458166 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347086 | AGCTTGCTCTTCTGC[C/T]CTATTTTTCCTTAGA | 55779 |
rs376508565 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346731 | TCCGCACTCTGTAAA[A/G]TGGACCAATCAGCAC | 55779 |
rs376515443 | snp | C/T | 0.000120472 | 0.00776024 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446563 | TCACCCCTATATGCA[C/T]TTCACAATTACATTT | 55779 |
rs376537096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439469 | TTATTGTTGATCTTT[G/T]TAGCCAAGGATAATT | 55779 |
rs376593009 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411942 | GATTTGGCTCTCTGT[C/T]TGTTATTGGTGTATA | 55779 |
rs376601745 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286441 | GGTGTGGGCTCAGTG[C/T]GGGAGTCTCTACAGT | 55779 |
rs376611855 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350368 | AGTCAGAGAGAGAGA[C/G]AGAGACAGAAAGTCA | 55779 |
rs376684331 | snp | A/T | 0.000727429 | 0.0190574 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433694 | CAAAATGGGGATGAG[A/T]TATGGATAAAGCTGT | 55779 |
rs376705548 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425936 | CAACTACTTATCCCT[A/G]TCCTTGTTGTGTGAT | 55779 |
rs376708807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357000 | ATGTATATAAATAAC[C/G]AAAGCTCATATCCAG | 55779 |
rs376743627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302787 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 55779 |
rs376773330 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416430 | CCACTAGTTCTGTTT[C/T]TCTGGAGAACCTTGA | 55779 |
rs376778311 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298264 | GCAGCTAATGCTCAG[A/T]AGGGACATAAAGTCT | 55779 |
rs376807913 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361740 | CCTGACCTCATGATC[C/T]GCCCGCCTCGGCCTC | 55779 |
rs376842768 | snp | C/G | 0.000103611 | 0.00719685 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305129 | CTCCTCTGCTGCATT[C/G]AGATTAGTTGCCACA | 55779 |
rs376851890 | snp | A/C/T | 0.00027891 | 0.0118061 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395884 | AAAGAGACACACCGA[A/C/T]GAAATATATATTACT | 55779 |
rs376875025 | snp | C/T | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400602 | CAGCCACGGCTTCAA[C/T]AGCTCCAGAATGGAA | 55779 |
rs376905113 | snp | A/C | 0.0876345 | 0.190099 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411360 | GTTTCAGCTTTCTAC[A/C]TATGGCTAGCCAGTT | 55779 |
rs376912117 | snp | C/T | 0.000213288 | 0.0103247 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286650 | CAATCTGGATTTTAA[C/T]GGTTCCTACTCTTTC | 55779 |
rs376924006 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393727 | CACTATGTTGCCCAA[C/G]CTTGTCTCAACTGCT | 55779 |
rs376926821 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419871 | ACTGAATTGAAAATG[C/T]CTTGGAATAAAGACA | 55779 |
rs376936719 | snp | A/G | 0.000425035 | 0.0145718 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327842 | GGAAAAAATATTTGC[A/G]GATACGTTAGAAGAC | 55779 |
rs376940664 | snp | A/C | 1.69876e-05 | 0.00291436 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395701 | TACAAGATAGTTTCA[A/C]TATGTAGTAATTGAG | 55779 |
rs376966734 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318376 | TTGAATCAACTCAGA[A/C]AAAAGTAAAGAAAAA | 55779 |
rs376980445 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395991 | CAGATTATTCTAGGA[G/T]AATTCTTATTTCTAA | 55779 |
rs377001923 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302204 | TTGATTCCGTGTCTT[A/G]GCAATTGTGAATAAT | 55779 |
rs377017412 | snp | A/G | 0.000437904 | 0.0147905 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305052 | TGGTGGAGCTTGAGC[A/G]GAATCACAACTAGCA | 55779 |
rs377018131 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389043 | TAATAGATATTTATA[G/T]AACTTTTTATCCAAT | 55779 |
rs377059555 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382979 | CGATTTCATGGATTA[C/T]GTCCAGGCCATTTTA | 55779 |
rs377086240 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336750 | AATATACCATTGAAT[A/G]ACAGAAATGGGCAGC | 55779 |
rs377098363 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389055 | ATAGAACTTTTTATC[C/T]AATGGCTGCAGAATA | 55779 |
rs377114273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396860 | TTTATATCACTTTCT[C/G]GTAACCTCTATCCAT | 55779 |
rs377117658 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387236 | GTGTCTGTGCCACCT[C/G]TTGCCCAACCCCAGG | 55779 |
rs377118877 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316244 | TTAAAAACTACATTG[A/G]CCAGAGTGAAAATTA | 55779 |
rs377128612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408487 | GTATGAATTTGGAAA[C/T]ACCATCCCAATGTTA | 55779 |
rs377159479 | in-del | -/CAGGTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304437 | TCATCCAGTTTGGGT[-/CAGGTT]ACACAAAACATATAT | 55779 |
rs377173393 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391999 | GTTCCTCAAAAAAAC[C/T]AAAAATGGAGCTAAC | 55779 |
rs377179425 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411417 | AATCCTTTCCCCATT[G/T]CTTGTTTTTGTCAGG | 55779 |
rs377181390 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366492 | CTGCATTGTGATAGG[G/T]CTTTTAAAGAGGTAA | 55779 |
rs377184205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385146 | TGTAAGACATCCCTT[A/T]GCTCTTCCTTTGTCT | 55779 |
rs377185040 | snp | C/T | 9.88859e-05 | 0.00703087 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366199 | TTATTGTCATGCATA[C/T]TGAAGTGCCAGTAGT | 55779 |
rs377202177 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374895 | CCCGCCTTGACCTCC[C/T]AAAGTGCTAGGATTA | 55779 |
rs377209069 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299320 | TGAAAAGGTGCTCAA[-/C]ATTGCTGATCGTCAG | 55779 |
rs377231427 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304537 | AATACAATAAGCCTT[A/T]TCTCTTAATGATATG | 55779 |
rs377238758 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335376 | GAAGAGACAGAGATC[A/G]GAGTACAGGGAGGCC | 55779 |
rs377241050 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328233 | ATGTTGAAAATTTTC[A/G]AAACCACAGAATGGT | 55779 |
rs377245953 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407116 | TATGACCCAAACATT[C/T]ACATATTTCATAGTT | 55779 |
rs377298889 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441531 | GGTTACCGAGACAAC[A/G]CCACCCCTCTTCCAG | 55779 |
rs377300074 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299982 | GCTGCAGTAAGCCAT[C/G]ATTGCGCTACTGCAC | 55779 |
rs377303253 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363604 | AATATCTAGGAAGAA[C/G]TAAATTAAAAACTCA | 55779 |
rs377310096 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416912 | CTCTATCTTCAATGT[C/G]CATCAGAATCCACTA | 55779 |
rs377324527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390836 | AAATATGGATGAAAG[A/G]AATTGAAGAGGAACA | 55779 |
rs377369496 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406407 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCAA | 55779 |
rs377374818 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308707 | GCAATCCTCCCACCT[C/T]AGCCTTCTGAGTAGC | 55779 |
rs377377712 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422751 | AGAAGGCTAAAGCAT[A/G]TTAGTAGCTATGAGA | 55779 |
rs377380720 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394607 | CTCTAAATTCACAAC[A/C]CACATTCTCTATACC | 55779 |
rs377414577 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427987 | TAGATCTGAGATGAG[C/G]CTAAAAGATTAGGAA | 55779 |
rs377418753 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422189 | TTAAGCAGATAGATT[C/G]TTTGTTCACAATAAT | 55779 |
rs377423877 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359301 | TGTCTTCTTGACATC[A/C]CCAAGTTTTTGTTGA | 55779 |
rs377503102 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286958 | GGTATTTATTTTTCT[A/T]TTATAGCCATATTTA | 55779 |
rs377503120 | snp | A/G | 0.000176063 | 0.00938085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396732 | GTGAAGTTTACCTTG[A/G]AGAAAATTAAAGATA | 55779 |
rs377508018 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323141 | GGGACCAAAATTCAA[C/G]ATGAGATTTCGGTAG | 55779 |
rs377515456 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310007 | AGAAAAACTCTGGTA[C/T]AATCCCCAACTAAAT | 55779 |
rs377529770 | snp | C/T | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396641 | CCGTCCCGCAAAAAT[C/T]GTGAGCCCTTTTGGA | 55779 |
rs377537690 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436817 | AGCACTTTCTTCTGT[-/T]AAGTAGGTACTGTTT | 55779 |
rs377544187 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337783 | TAAGTCTGATAACTT[A/T]TTTAAAAATTAGCTT | 55779 |
rs377548017 | in-del | -/GAGAGAGAGAACCAGAGTCA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353748 | CGATAGAGACAGAGG[-/GAGAGAGAGAACCAGAGTCA]GAGAGAGAGAACCAG | 55779 |
rs377553503 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327528 | TAAGGGCTAGAACAA[A/G]TGGGAGATTTGAGTT | 55779 |
rs377561598 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311962 | ACTTTGAACTTGAGA[C/G]AGATGATTTAAGGTG | 55779 |
rs377565248 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340507 | TCACTCACACTCACC[C/T]TCCGCAATCCCCAGT | 55779 |
rs377567248 | snp | A/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113434061 | AATCAATTTCAGTTT[A/T]TAAAATATTTTTTGA | 55779 |
rs377574633 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358971 | ATGCTGCATCATAAC[A/T]CTTCCCCAAATATCA | 55779 |
rs377617720 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295255 | CTTTCTTTTGTTTTC[C/T]TATTGCTCCATCGGT | 55779 |
rs377623503 | snp | A/G/T | 0.000115551 | 0.00760024 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373450 | TTGTCCTCTGTATCC[A/G/T]CAAGATAACGGACAT | 55779 |
rs377654876 | snp | C/T | 0.00040032 | 0.0141421 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291671 | GGCCGAAATCCTTTC[C/T]GCCTGGAGTTGGATC | 55779 |
rs377694964 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349748 | ACCCTCACTGAGCCC[C/T]AGGTATGTTTAACCA | 55779 |
rs377721094 | snp | G/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296325 | CCGACTGGTGTGAGA[G/T]GATATTTCATTTTCT | 55779 |
rs377758996 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440398 | AAGTCTTGCTATCCA[C/T]TATTATTACTGTCAT | 55779 |
rs377762573 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409752 | GCACAAGATACAGGT[C/G]AAAAGACCCAACTGA | 55779 |
rs377764647 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387959 | GAAGAGACTTCTCTG[C/T]TTGTGGAAAAGGGAG | 55779 |
rs377766656 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364285 | ACTAAACTTTATTCC[C/T]TATTCTCTTTCACAG | 55779 |
rs386397650 | in-del | -/CA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353463 | TGAATACACACACAC[-/CA]ACACACACACACACA | 55779 |
rs386397651 | in-del | -/TT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430470 | TAGCAAAGCCAAAAT[-/TT]CAGTCTTTGAAAAGA | 55779 |
rs386430659 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441651 | GCTTTGAACCAGTGT[C/T]ATGAGGCGGAGAAGG | 55779 |
rs386664761 | multinucleotide-polymorphism | GC/TG | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290341 | CACCTCTAAGAATAT[GC/TG]TGATGTACAAAGAAA | 55779 |
rs386664762 | in-del | AAACCAA/TATGGATAAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303413 | AAACTATCTGTAGTT[AAACCAA/TATGGATAAC]TTAAAAATTGGTTTA | 55779 |
rs386664763 | multinucleotide-polymorphism | GC/TA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318865 | TAAAATCCTTCTCAG[GC/TA]AAGCAAATGCTGAGG | 55779 |
rs386664764 | multinucleotide-polymorphism | CA/TG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349716 | GGCTCCCGGGGCAAG[CA/TG]CCAGCTCATGTCATC | 55779 |
rs386664765 | multinucleotide-polymorphism | CGA/TGC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350073 | AGTGCAAAAACCCAA[CGA/TGC]GGTGGCAGTCTTACA | 55779 |
rs386664766 | in-del | AAT/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369814 | TGAAACAATCAAGAG[AAT/G]TGATAGAGAGAGCAC | 55779 |
rs386664767 | multinucleotide-polymorphism | CA/GC | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379998 | CTACTTCATTCTGTT[CA/GC]CCCTTCAGAATAATC | 55779 |
rs386664768 | in-del | AA/GAG | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420284 | CTTAGATGAAGATGT[AA/GAG]GTTGAAGTAGTTGAA | 55779 |
rs386664769 | multinucleotide-polymorphism | CA/TG | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427283 | ATGATCCTTCCCCTT[CA/TG]GTAAATGTTTCATCT | 55779 |
rs386664770 | in-del | GTAT/TA | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432706 | TGCTTACTATTTTTA[GTAT/TA]ACTGCCTTAATAACA | 55779 |
rs397756654 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295002 | GGTTTGATTAAAGAT[-/T]AAGAATATAAGTATG | 55779 |
rs397784896 | in-del | -/A | 0.5 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318966 | AAAAACAAAAAAAAA[-/A]CAAAAAAAAAACAAT | 55779 |
rs397804413 | in-del | -/AA | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444514 | AAAAAAAAAAAAAAA[-/AA]GAGAAATCTACCCTG | 55779 |
rs397875064 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346229 | CAGCACTTTGTAAAA[-/A]CACACCAATCAGCAC | 55779 |
rs397876321 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447145 | GCCATGTGAAACTGT[-/T]AAGTCCAATTCAACC | 55779 |
rs397958411 | in-del | -/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341358 | TGGATTTTTTTTTTT[-/T]AAAAGAAAGCAATTA | 55779 |
rs397977310 | in-del | -/GA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350373 | AGAGAGAGAGAGAGA[-/GA]CAGAAAGTCAAAGAG | 55779 |
rs397977552 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391713 | CTATGGGGGAAAAAA[-/A]TCTACTAATCCAATT | 55779 |
rs397990836 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338284 | TAACAGAGTTTGTTC[-/T]TTTTTTTTTTTTTTT | 55779 |
rs397990837 | in-del | -/A | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343079 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs397990838 | in-del | -/T | 0 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412427 | TTCTGCACATGTATC[-/T]TTTTTTTTTTTAGAA | 55779 |
rs398052199 | in-del | AA/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433454 | AAAAAAAAAAAAAAA[AA/G]GATCTATTTTATAAC | 55779 |
rs398091744 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328696 | GAAATTTAGAGAGCT[-/T]AAAAAAAAAAAAAAA | 55779 |
rs527248362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374270 | TGAAGGCATTGGCAA[C/G]CTACCAAAATAGCAA | 55779 |
rs527291720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380842 | CTTAACATAGGATAT[G/T]TTATATTCTAAGGAA | 55779 |
rs527306102 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384454 | TGAAGTCCTAACCCT[C/T]AATACTTCAGAATGT | 55779 |
rs527332605 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288087 | CTGGAGAGGGTGGGG[A/G]GAGCCTGTATTTTCT | 55779 |
rs527400570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341602 | CCAGCTGACCTGTTT[A/G]TAATATCTCCTTCTT | 55779 |
rs527403002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347795 | TCCCTCAGGGTATGG[A/T]CCTCTACTTCATTTT | 55779 |
rs527410764 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290312 | AATCTTAGGAAGACA[A/G]TAGGCCAAGTGGCCA | 55779 |
rs527424802 | in-del | -/TC | 0.130447 | 0.219561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320232 | ATATTAGTCTCTCTC[-/TC]TCTCTCTCTCTCTCT | 55779 |
rs527428270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380265 | GCTGGCATTTAAGGA[A/G]CTCCATGCATTGGTC | 55779 |
rs527441059 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388049 | GAACACCAGGCAAAT[C/T]CCTAAGGTTTCTGAC | 55779 |
rs527464628 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387362 | AGCTAAGCTACAGTA[C/G]GTAGGGCACCAGGAA | 55779 |
rs527477088 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309426 | CCCATCTCTCTTCCC[A/T]GCTACAAAACCCCAT | 55779 |
rs527479805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394589 | TTTCTTGATAGTTCC[C/G]TGCTCTAAATTCACA | 55779 |
rs527505037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393795 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 55779 |
rs527507806 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422364 | TAACAAGAAGAAAAT[A/G]TAGAATGTAAAAAGA | 55779 |
rs527525481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435100 | CAGTGGCTCATGCCT[A/G]TAATCCTGGCAGTTT | 55779 |
rs527542857 | snp | A/G | 0.000308996 | 0.0124259 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400051 | ATACATAATTTTTTT[A/G]AGTCTTGGCTCACTT | 55779 |
rs527589050 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441761 | ATACCTGCCTGATAT[C/T]CCAAAATGGCCCAAC | 55779 |
rs527619256 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351080 | GAAAATTGCCTAATA[A/G]TGGGTCCGCTCAAAT | 55779 |
rs527643070 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385010 | ACCTGGTGGAAGGTA[A/G]TCGGATCATTGGGGC | 55779 |
rs527643961 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414711 | ACCAGGGATGAAGGC[A/G]GCGTGATCATGGTGG | 55779 |
rs527653435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367622 | AAAACCACAAAGATG[C/G]GGAGAAACCAGAGCA | 55779 |
rs527662966 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327324 | TTAGGGAACCCAACT[C/T]ACCAGACTGGTGTAG | 55779 |
rs527678996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407147 | GCATATATTATTTCA[C/T]TCATTCATTCATTTA | 55779 |
rs527680224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312198 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 55779 |
rs527690273 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367144 | CAGGGCATAGCTGAA[A/C/T]AAAAGGCAGCAGACA | 55779 |
rs527721844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413747 | TACCAGTACCATGCT[A/G]TTTTGTTTACTGTAG | 55779 |
rs527759256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412944 | GATCCTTGAGGAATC[A/G]CCATACTGTCTTCAA | 55779 |
rs527793170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332858 | GTGGTCCATGGCAAC[A/G]AAAAACTACATCCAA | 55779 |
rs527834618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418838 | GGCTCCTGAGTAGCC[A/G]GGATTACAGGCGCGT | 55779 |
rs527840917 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289651 | CACCTGGCATTCACA[A/C]CCTGTTCAGTCCCCT | 55779 |
rs527906016 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289250 | TCAGTGTTAACTGTC[A/G]TCAATTCCCAAACAT | 55779 |
rs527933331 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332218 | TGATGTATGTAACAT[G/T]ATGAATAAATAAAAA | 55779 |
rs527997119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342401 | GAATTCAACCCCATA[A/G]TAAGTACTGTGGAAT | 55779 |
rs527999703 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313054 | CTCCAGACCCCAGAA[C/T]GGTAGATCCACCAAC | 55779 |
rs528005313 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434232 | AGGAAAATGGTACTG[A/T]GGGCATGTATAGCAA | 55779 |
rs528005683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425965 | ATGGCAGCCATAATA[A/T]ACAAAATGTAAGCAA | 55779 |
rs528012432 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346515 | AATCAGTGCTCTGTA[A/T]CTAGCTAAAGGATTT | 55779 |
rs528020747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295877 | AGAGGATAGCCACTC[A/C]ATTTCTAAAACTGTC | 55779 |
rs528043812 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363839 | CTAATGTTCATATGC[G/T]ATTAACACAGAATTC | 55779 |
rs528069091 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295220 | TAGCTGGCTTGAGTG[G/T]CCACACATCTGTATA | 55779 |
rs528080005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392631 | ACCCTCATATGATTA[C/T]TATGCATTATATGCC | 55779 |
rs528089024 | in-del | -/CA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408863 | AGCGAAACTCCATTT[-/CA]AAAAAAAAAAAAAAA | 55779 |
rs528099378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302752 | GACTCCAGCCTGGGC[A/G]ATAGAGTGAGACTCC | 55779 |
rs528099505 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424350 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGCAG | 55779 |
rs528111800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311575 | AACCTCTTTTTCTTC[C/G]CAGTCTTGGTTATGT | 55779 |
rs528127911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440209 | GCTGCGATTACAGGC[A/G]CACACCACCTCGCCC | 55779 |
rs528137456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446961 | TCATGGGGAGGTAAC[C/T]GAATCATGGGGGCCG | 55779 |
rs528157293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405600 | AGTCATACTTCTCCA[C/T]TGAAATTCTCCACTT | 55779 |
rs528169366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351328 | ACCCTATCAGTACCC[C/T]TCAAAGCTTAAGTCC | 55779 |
rs528205446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357758 | ACTGAAGAGTGTAAA[C/T]TTTCAAACCGTTTTG | 55779 |
rs528242843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376287 | ATGGTTTAAAAGTAA[C/T]GTCTTGGACAGGTTA | 55779 |
rs528294040 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371626 | TAAAGCCATAAAAAC[C/T]CTAGAAGAAAACCTA | 55779 |
rs528294572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404624 | TATATATGTTAAGTT[A/G]TTTAATGCAAAAAAC | 55779 |
rs528321032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323778 | GCTGGGTGCAGTGGC[A/T]CACGCCTGTAATCCC | 55779 |
rs528331565 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411286 | GGTTTTAGGTCTAAC[A/G]ATTAAGTCTTTAATC | 55779 |
rs528340871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331143 | ATTCTGTATTTTGGC[C/T]ACATGATTATTGTTA | 55779 |
rs528344354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322996 | AGTGAAGTTGGCGGC[A/G]GGGAAGCCCCTTATA | 55779 |
rs528364506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417338 | AAAATACAGTAAGTA[C/T]GCCCTGGATAAACTA | 55779 |
rs528368478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410692 | TGGGTCAAATGGTAT[C/T]TCTAGTTGTAGATCC | 55779 |
rs528409033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351493 | AAGAAATAATGAAAT[A/C]TATCCTTACTCTACA | 55779 |
rs528425215 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424509 | TAATAATCATTAAAG[C/G]GTTAATTAAAAGAGT | 55779 |
rs528437079 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113434085 | TTTTTGAGCACACCT[G/T]CAGTGTATCAAGTCT | 55779 |
rs528438659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377809 | AGGCACCTGCTACCA[C/T]GCCCGGCTAATGTTT | 55779 |
rs528444787 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287761 | ATTGAAGAAATAGAA[C/T]TAATCTTTTTTATAT | 55779 |
rs528498118 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287118 | CCGCACAGGCTGGCG[C/T]GGGACAGACTCCTAA | 55779 |
rs528512311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338448 | AACAATCCTATTCAA[A/G]TGTGAGAAAAAGACA | 55779 |
rs528513042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384281 | AGCCAGGATGGTCTC[A/G]ATCCCCTGACCTTGT | 55779 |
rs528537066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391071 | CAAAGCTGGAGAAAT[C/T]ACATTAGCTGACTTC | 55779 |
rs528540540 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430804 | CCAATTCTACACAAA[A/G]TATTTTTGAAAATAG | 55779 |
rs528542462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439131 | GACTAGCATAAATTT[C/T]GTTTCATTAGATCCA | 55779 |
rs528549593 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383753 | GTTTAATAGCTGACC[G/T]TTTTTAAAAAATTAT | 55779 |
rs528578424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431623 | GGAGATCTGGACAGG[A/C]AGACTGAGGTAGAAA | 55779 |
rs528639349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349802 | CTCCTGGACACTGGT[A/G]CAGCTTTCTCAGTGT | 55779 |
rs528668861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308896 | CAGGCTTGAGCCACT[A/G]TGCCTGGCCCTGAAA | 55779 |
rs528673063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397121 | TGCTAAAAGAAAGAA[A/C]TGTATTCTCTGAGAG | 55779 |
rs528706637 | snp | C/T | 6.86566e-05 | 0.00585863 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396723 | TGTGCTCCAGTGAAG[C/T]TTACCTTGGAGAAAA | 55779 |
rs528723384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403040 | ATATGGGTTAAACAA[C/T]ATTAAACACAGTAAG | 55779 |
rs528726019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446015 | ACTGTACTAGCACCA[C/G]AGAAAAAATGCCTTC | 55779 |
rs528739360 | in-del | -/AATT | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425164 | AGATAAATCAGCACG[-/AATT]AATTTAGTTACACCT | 55779 |
rs528760500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402529 | CTGCCATGTGATCCT[A/G]GACTGAATAACTGAG | 55779 |
rs528786387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445512 | TATTGGCAATGTTAA[A/T]TCTCTAACAGAGATA | 55779 |
rs528792061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356027 | GAATTACATATTATA[G/T]ATAAAATGTATATAA | 55779 |
rs528801337 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340181 | CCTGAGCCATGCATG[-/C]CTGCAGCTGTCAAAG | 55779 |
rs528830685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355246 | AAAATTTAAGCCAGG[C/T]GTGGTGGCTCACGCT | 55779 |
rs528846379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370188 | CCTTCTGAAACTATT[C/T]CAATCAATAGAAAAA | 55779 |
rs528875360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314963 | AAACACTACAAAAAA[C/T]TAAAATAGAATCCCC | 55779 |
rs528894302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409504 | TTATGTTATATGAAA[A/G]GGGAGGGTAAAGAAG | 55779 |
rs528912823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321862 | ATGCTGAGAGAAATC[A/G]GAGATGACAAAAATA | 55779 |
rs528986283 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321353 | TCCTTGACAGACTAG[A/G]CATTGAGGAAACATA | 55779 |
rs529001981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336352 | AAGAGAGAATATGAA[A/C]ATTAACAATATAAAT | 55779 |
rs529006192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327919 | AGTCATTTTTTATTA[C/T]GCCCTTATGGATGGA | 55779 |
rs529045078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291988 | GTACACTTTAAGCTA[C/G]CTATCAGTCATTCAT | 55779 |
rs529066940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389622 | TAGCCAGACTAACAA[A/C]ATAAGAGAGAGAAGC | 55779 |
rs529069463 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326399 | TACCTCTCTATTTCA[C/T]GTTAATGAGAGAAAA | 55779 |
rs529070682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381828 | TAAGAAAAACATATA[A/G]TATCTGCCATTATGT | 55779 |
rs529150480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429193 | ATGTATACTTTGGCT[A/G]TTATGAAGTAACTAG | 55779 |
rs529180126 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436337 | GTTTAGATACACACA[C/T]ACCTAAATATTATTT | 55779 |
rs529191890 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328791 | CTATATGTTTGGGCT[A/C]CCCTTTAAAGCTTGT | 55779 |
rs529206845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298800 | GTCAAGTTCACAGAG[A/G]CAGAAAGTAGAGTGG | 55779 |
rs529214380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437157 | GCATTCCTTGACTTA[C/T]GGTGCCCTTTAAAGC | 55779 |
rs529218423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428494 | CACACTTAGGCAACT[C/T]TGTGAAGGCTGGATA | 55779 |
rs529247320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347919 | AGGGCCACTAAATCC[A/G]ATTTTTCTCGGTCCT | 55779 |
rs529250799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306765 | ATCCACCAAGTAATA[A/G]AGAATGTAGAAATGG | 55779 |
rs529259243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395378 | AAAGTACATTCAGAC[C/T]TTAGAATTCAGCTTC | 55779 |
rs529285495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298059 | GATGATGTGCACGTG[C/T]GTGCTGGCCTGTGGC | 55779 |
rs529311272 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443593 | CTGCCACAGTAATGG[C/T]TCAATAAGGAACAGC | 55779 |
rs529312804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306801 | TAAAATAGAATTCAG[A/G]AAGCTTAGATCTAGC | 55779 |
rs529347226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353565 | TTGAGAGTTCTTCCT[A/G]AGAGGAACTTCTTCA | 55779 |
rs529351879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400858 | GGCTGTGTGATTTTG[C/T]GCAAGTCACCTCAAA | 55779 |
rs529360672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313452 | ACTGTGGACTTTTGG[A/G]TTAATGCTGAAATGA | 55779 |
rs529370935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408727 | AATTAGCCAAGCGTT[A/G]TGGTGGGTGCCTGTA | 55779 |
rs529384026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361095 | GATTTACTTGGTTAG[C/T]GGTTTTGTGAATGAG | 55779 |
rs529390895 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442704 | TATTTGTCAATAAAA[G/T]TGGCAAGAAAAAATT | 55779 |
rs529406745 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113382007 | TGTATAAATTATAAT[C/T]ATATAATGAGTTAAG | 55779 |
rs529431488 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368371 | CACAAAGGGAAGACC[A/G]TCAGACTAACAGCAG | 55779 |
rs529454959 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319768 | CATACAAAAGATTCA[G/T]GAAACCAAGAGGTTT | 55779 |
rs529465806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346914 | TCACTCTTTGGGTCC[A/G]CACCACCTTTATGAG | 55779 |
rs529492102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367833 | TGCAAAGAAGCTAAA[A/G]ACCTTGAAAAAAAGG | 55779 |
rs529494380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326717 | ATGTACTTTACAATA[C/T]AAGGTTACAGTTTAC | 55779 |
rs529511562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334288 | GTGCTTGCTGTAAAA[A/T]TTTCAGAAAAGGTAT | 55779 |
rs529550966 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351932 | ACCCACTGGCCCTTC[A/G]GCTGACCTAGAGAGT | 55779 |
rs529551599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414496 | ATATTGGCTGTGGGT[C/T]TGTCATAAATAGCAC | 55779 |
rs529557368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325991 | CTACAGTAAATGAAA[A/T]GGCAAGCTACGCACT | 55779 |
rs529565125 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384082 | TTTTTCTTCTGAGAC[A/G]GAGTCTTGCTCTGTC | 55779 |
rs529588944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413973 | CCATTTTCACAACAT[C/T]GATTCTTTCTATCCA | 55779 |
rs529620477 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290281 | TATTCTGACCTCTTA[A/T]ATAGGAATATGAAGG | 55779 |
rs529681465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341463 | ATAATTTTGAGATAG[A/G]AAAGCATTTCTTAAT | 55779 |
rs529705680 | in-del | -/A | 0.497959 | 0.0318836 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409007 | GTTAACCAAAACAGC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs529714346 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441731 | GATAATTAAATGACA[C/T]GAATACCGTCGAAGA | 55779 |
rs529714456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434380 | CTTTAAAGGGCTGCA[A/G]GCAGTCTATTGGCCA | 55779 |
rs529718513 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340835 | TGGTGTACTGGAAGA[A/G]TCGGATCACATGTGG | 55779 |
rs529731380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347340 | TGGTTGACCCTGTAG[C/T]CATGAGTGGAACTCT | 55779 |
rs529735400 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443316 | CAAGATTTCTGGTTT[C/T]AGTACTTGCATCCTT | 55779 |
rs529738680 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289813 | CACTTGCTCTGGGAG[A/G]AGTCATATCCCAAGC | 55779 |
rs529748198 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293196 | AGTCACCTCACTTTC[C/T]CCTTCTCCTCACCAG | 55779 |
rs529766239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386653 | GCAAGATGGCTGATT[A/G]GAAGCCTCCACCAAT | 55779 |
rs529775438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305505 | TTTTTGGTCATGACT[G/T]CAACAAATTAAAGAA | 55779 |
rs529780160 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417995 | AAGTTTCTGCCTCAT[A/G]TTGGAAACTGCTGTG | 55779 |
rs529797993 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393753 | CTGCTGCACTCAAGT[A/G]ATCTACTTGCCTTGG | 55779 |
rs529842037 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391231 | AAAGATGCCAAGAAC[A/G]TACATTGCACAAAGA | 55779 |
rs529842127 | snp | A/G | 0.000281245 | 0.0118551 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399984 | TTTGCTAGCAAAATC[A/G]TAGATTCGAACAGAG | 55779 |
rs529854793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312157 | ACTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 55779 |
rs529894562 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420279 | ATACTCTTAGATGAA[G/T]ATGTGAGGTTGAAGT | 55779 |
rs529895820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304918 | GTCATTCTACAGGTG[C/G]AATTCTCAACAAAGA | 55779 |
rs529898954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318347 | GAAAGAATCTCAGTT[C/T]GAGGAATGCTTCTTT | 55779 |
rs529930416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399579 | GGCCTGGCACATTGT[C/T]GGCACTCTGTAAATA | 55779 |
rs529942056 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412903 | CAGTAATGGTATTGC[A/T]GGGTCAAATGGCATT | 55779 |
rs530001610 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419359 | AACTCTGAATTCATA[C/G]AGGTCATGAGTTCTT | 55779 |
rs530004590 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359581 | TTAGAAAAATAGCAT[A/T]AAGGTCTTTTAACTA | 55779 |
rs530025838 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297802 | TGACCAGACTGTCCC[C/T]TAAGAGAAGTTTGAA | 55779 |
rs530031502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325328 | AAAAATCACTAAAAA[A/G]GGAAATAGGTGTAAA | 55779 |
rs530034093 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418950 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 55779 |
rs530067236 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371048 | GGACCTCTTCAAGGA[A/G]AACTACAAACCACTG | 55779 |
rs530075192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412126 | GGATGCCCTCTCTCA[C/T]CACTCCTATTCAACA | 55779 |
rs530175958 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322782 | AAAGACATATGCACT[C/T]ATGTTCATTGCCATG | 55779 |
rs530177881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332055 | CTTCTGACTTGTAGA[A/G]AAAGGTGTTCTATGT | 55779 |
rs530193143 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288560 | TTTGCTATCCAGAGG[C/G]CCCCCAATCTGAGCT | 55779 |
rs530196005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295775 | AACAGTCTATGCCTT[C/G]TTACAAAATTTATTA | 55779 |
rs530210039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377981 | TGTAAGTATGTACTA[C/T]GTAATTTTACTTGGA | 55779 |
rs530210767 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385676 | AGCTGGGGTCTTACT[C/G]TCACCCAGGCTGGAG | 55779 |
rs530218657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339889 | TAGGGGGCAAAAAGA[A/G]GAGAGAGTCTGGGGG | 55779 |
rs530234612 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418750 | TTGCCCTGTCGCCCA[C/G]GCTGAAGTGCAACGG | 55779 |
rs530243225 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446996 | TTCCCATGCTATTCT[C/T]GTGATAGTAAATAAG | 55779 |
rs530296618 | in-del | -/AACT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297665 | ATTTTTCTTCTTAGC[-/AACT]AACTAACATGTAAGA | 55779 |
rs530315055 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367839 | AAGCTAAAAACCTTG[-/A]AAAAAAAGGTTAGAT | 55779 |
rs530338460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295157 | AGCTAACTTTTCTGT[A/G]TTGCTTTTTCCCCAT | 55779 |
rs530338899 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432608 | ATTATGGGAAGATGA[A/G]GAATGTTAAATCTCT | 55779 |
rs530366335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433283 | AAAATACAAAAATTG[A/G]CTGGGTGTGGTAGCA | 55779 |
rs530429212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440094 | ATTGAGATGGAGTCT[C/G]GCTCTGTCACCCAGG | 55779 |
rs530454601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397239 | CTAGGTACAGGAAGG[C/T]GGCACAAGCACTCCT | 55779 |
rs530461833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302684 | GAGAATTGCTTGAGC[C/T]CAGGAGGCAGAGGTT | 55779 |
rs530491833 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446593 | TTAACGTGTACCTTT[A/G]CTCTTGGATTAAGAG | 55779 |
rs530494237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310793 | GGAGTCATCATGAGA[A/G]CTGGTTGTTTTAAAA | 55779 |
rs530518833 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365107 | ATTATTGAAATGTGG[A/C]ATAAACATTTTTCTA | 55779 |
rs530555848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364185 | TGTGCTGTAAAATGT[C/T]TTAGTCTGTGATATT | 55779 |
rs530558878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404517 | CCAAGTGCATGCCAC[C/T]AAACATTAGTTGTTA | 55779 |
rs530589039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411130 | AGTTTCTTTTGCTGT[A/G]CAGAAGCTCTTTAGT | 55779 |
rs530594572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370988 | ATTCACAATTGGTAC[G/T]AAGAGAATAAAATAC | 55779 |
rs530645695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322461 | TCAAAAGATTACCTA[A/C]AAGCAGGCAACAAAC | 55779 |
rs530680559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338395 | GACTAGTATCTAGAA[C/T]ATATAAAGAAGTCTA | 55779 |
rs530680879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329523 | GGGCATCACCACAGG[A/G]TGAAGCTGGAAAGAC | 55779 |
rs530683458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417248 | TTTTAAAATTTCACT[A/G]TGGAAAAAGTTACAA | 55779 |
rs530698600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423883 | AAGGAAAGTGACATA[C/T]AGAAAACGAAAGTGA | 55779 |
rs530715194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337659 | ACACAAATATGTCCA[A/G]ATGATTTCTGACAAA | 55779 |
rs530721451 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342073 | TGTGGTGGCTCTTGC[C/T]TGTAATCCCAGCACT | 55779 |
rs530743727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376975 | TGGGAACAGTGTCCT[C/T]GGAGAGTTGCAGGAG | 55779 |
rs530770100 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407386 | ATTTTAGTGTTTCAG[A/T]CACACTAGCCAATTT | 55779 |
rs530801434 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323020 | CCTTATAAAGCCATC[A/G]GATCTCATGAGAACT | 55779 |
rs530816358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431517 | AGTACAGAAACATGA[A/G]AAAGGAAAAACTAGG | 55779 |
rs530839188 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348963 | GAGATACCTGGTATC[G/T]TAGTCAAGTAAATGA | 55779 |
rs530854544 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430510 | TTGATAAGCTCCTAG[A/C]TACACCAATGAAGAA | 55779 |
rs530854730 | snp | C/T | 0.000161695 | 0.00899006 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287082 | GAAGCTGCCACCTAA[C/T]AGGAGTCACCCAGGA | 55779 |
rs530857237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344342 | TCATTCTCAGCTATA[A/C]CATACACTTTTGTCT | 55779 |
rs530882902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384208 | GGACTGCAGGTGCCC[A/G]CCACCACGCCTGGGT | 55779 |
rs530887661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445428 | TACTCAAGATTTACA[A/G]ATCATTTAGACCAAG | 55779 |
rs530910577 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298201 | CTGATCCCTGCCAGC[C/T]CCATTGTGGAGCCAG | 55779 |
rs530915125 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325573 | TCTCAGCCTCCCTAG[C/T]AGCTCGGACTACGGC | 55779 |
rs530922724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349236 | TAAGAAAATATACTC[C/T]CCTGTCAGCCGACTC | 55779 |
rs530950310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390251 | GGACAAAAATCACAC[C/T]ACCATTTCAATTGAT | 55779 |
rs530956064 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404522 | TGCATGCCACCAAAC[A/T]TTAGTTGTTAAGATA | 55779 |
rs530959264 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355206 | CACTACCTGTTCCCC[A/C]AAAAACCTATTGAAA | 55779 |
rs531061601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321643 | GCCAAGAGGCTACTA[A/C]AACTGGTAAATATTT | 55779 |
rs531079845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409463 | ACAATTCCAAAAACA[C/T]TCTCCATCTTTGGCT | 55779 |
rs531086507 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430447 | AAAAAAAAAAAAAAC[A/G]AAGTAAATTAGCAAA | 55779 |
rs531101567 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347288 | CAACGGTCAAGAGAG[A/C]GGAAAATCATTCAGT | 55779 |
rs531118938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395945 | CATGTAATAACATAA[C/T]GCTATCTCTATCTAC | 55779 |
rs531128484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402897 | AATATATCATATGAC[A/T]AAATAAAGGACACAA | 55779 |
rs531137587 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288238 | ACTCTGACTGTTTAG[A/G]GCAAGTGCATCCTCT | 55779 |
rs531166694 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422748 | CTCAGAAGGCTAAAG[C/T]ATGTTAGTAGCTATG | 55779 |
rs531198552 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349027 | TACCAGTCAGCAAGC[C/T]GTCACCAGTATGGAT | 55779 |
rs531218090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374903 | GACCTCCTAAAGTGC[C/T]AGGATTACAGGCGTG | 55779 |
rs531220829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362326 | CTAGAAGGCACTCCT[C/T]GTGATGCTCTGGGCT | 55779 |
rs531231783 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410214 | TGCAGGTTTGTTACA[C/T]ATGTATACATGTGTC | 55779 |
rs531273302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335449 | CACAAAGAAATGCTT[C/T]TGGAAATCTACATAG | 55779 |
rs531287347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428402 | AGAAGGGTTGTGCTA[C/T]AGACGGAAAACTAGA | 55779 |
rs531310144 | in-del | -/A | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338101 | AACCCTGTCTCTACT[-/A]AAAAAAAAATGCAAA | 55779 |
rs531324696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422164 | AAAGAAGCATATCCT[A/G]TAGTGTAGCTTAAGC | 55779 |
rs531330142 | snp | G/T | 0.000944287 | 0.0217083 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291512 | AGACAGAACTTCCAG[G/T]GAGTTATGTCAGAAA | 55779 |
rs531355120 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381722 | ACTTTATTTGAAATG[A/T]TTATTCATTTGGTTA | 55779 |
rs531366856 | in-del | -/TCTCTCTCTC | 0.0883596 | 0.190715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320225 | GAGGAGGTATATTAG[-/TCTCTCTCTC]TCTCTCTCTCTCTCT | 55779 |
rs531388042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388920 | TCAACCCCAATACAA[C/T]AATAGCTGGAGATTC | 55779 |
rs531393803 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290806 | ATGAGAAACTATGGG[A/G]AAAACTTAGAATTCT | 55779 |
rs531422819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395267 | TTAGTAATCAATACC[C/G]AATTACCAATTGCTA | 55779 |
rs531424781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388190 | GGACTTGAGCAAACA[C/T]AGGCAGTAGCCAGGG | 55779 |
rs531428146 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415641 | GAGTCATTCAGGAGC[A/G]GGTTGTTCAATTTCC | 55779 |
rs531437643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342937 | TGCAGTGAGCCTAGA[C/T]TGGACCACTTCACTC | 55779 |
rs531441032 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309695 | AAATACAACTAAACA[C/T]TATATGCAAAACAAA | 55779 |
rs531460832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394650 | TCTTTTTGCTTCCCT[A/G]GGCCACACTGCAAAA | 55779 |
rs531463429 | snp | A/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381373 | TTTCTGATGAATATA[A/T]GTGGTTGTGAAATCT | 55779 |
rs531514881 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289355 | TTAGCTTTCCTCTCA[A/G]TTGAAATGCACAGCA | 55779 |
rs531518489 | snp | A/G | 1.69083e-05 | 0.00290755 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380895 | CTTCAGGAATATTCC[A/G]TACCAGAATCTTAGA | 55779 |
rs531522919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298737 | AATAAGCCAGTCACA[A/G]AAAGACAAATACTGT | 55779 |
rs531524118 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353429 | ACCTAAGTTTGCGAG[C/T]TAGGATTCATATATA | 55779 |
rs531552913 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316867 | GAGCGAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 55779 |
rs531567272 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391089 | ATTAGCTGACTTCAA[C/G]TTATACTACAGAGAT | 55779 |
rs531577063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348207 | CTTGGGTCGGGGGGA[A/G]GTAAACAAATCAAAA | 55779 |
rs531580549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427882 | TACAATGCCAAGCAG[G/T]ATGGGTATACTTTCA | 55779 |
rs531622142 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414954 | CCAGCTCCTCTTTGT[A/T]TTTCTAGTAGAATTC | 55779 |
rs531640260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407969 | GGGGCATAGAAAATA[C/T]AGATTTTACTAAATA | 55779 |
rs531641230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435817 | GGAGGCATTCTTCTG[G/T]GTTACAAAAATAATG | 55779 |
rs531656034 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417112 | CAGCTAGTTTGGAGA[C/T]CTTGCTTTGAGAATC | 55779 |
rs531722208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325936 | TGACAAAGATCAAAG[C/T]AATTCAGTCGAAGAG | 55779 |
rs531724710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367737 | TGGAGAATGATTTTG[A/G]TGAGTTAGTTGACAG | 55779 |
rs531764832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400103 | CAAGAAATTTCTTAA[C/T]TAAATCAGTCAATAA | 55779 |
rs531822361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360527 | CAGACATGATCCTCA[C/T]CTTTTATACACTGTT | 55779 |
rs531849659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413905 | TGTGAAGAATGCTAA[C/T]GGTAGTTTGATGGGA | 55779 |
rs531850913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341279 | TACCCAGCACTTCCC[C/T]TCCTCCCTTCCATAT | 55779 |
rs531895164 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435040 | CAGTACATTGTCTAA[A/T]CATTTGTATTATAAA | 55779 |
rs531896485 | snp | C/T | 0.000248833 | 0.0111514 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420144 | TCCAGAAGTTGTAGG[C/T]TGGCTCGCTTTCTAC | 55779 |
rs531920970 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315990 | AAATCAAGGAGCATC[C/T]ATATATTCTTTGCAA | 55779 |
rs531923706 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288379 | AGCAGTATTTTAAAA[A/T]TATTATTTAAAAGGA | 55779 |
rs531932133 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427135 | CTTCCATTTGTCTGG[G/T]CTTTGTCTCTAAAAC | 55779 |
rs531965359 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421395 | TACTATCAGTGAGAA[-/TG]TGTAAATCAGTTCAG | 55779 |
rs531997601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332917 | AAAGTCCACAAAATA[A/T]AAGCTTACCCATGAA | 55779 |
rs532008967 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425124 | GGAAAAAAAAAGCCA[G/T]GAAGAGAGAAAATTC | 55779 |
rs532013958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426679 | GAGAACGGACTAATA[C/T]AAAGAGTGTCTGGTG | 55779 |
rs532021099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346880 | TTTTTTTGCTCTTCA[A/C]AATAAATCTTGCTGC | 55779 |
rs532025124 | in-del | -/CAG | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410762 | AATTTACACTCCCAC[-/CAG]TAGTGTAAAAGCATT | 55779 |
rs532063251 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419551 | AAACAAACATGATAG[A/T]ATCTTTCACTCCATA | 55779 |
rs532079804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440437 | AGATGAGAAAGCAGC[A/G]TATTTACTCTGAATC | 55779 |
rs532080675 | snp | C/T | 0.000399281 | 0.0141238 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379407 | GCTCTTCTTCCTCCT[C/T]CTCCTCCTCTTTCTC | 55779 |
rs532081710 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290825 | ACTTAGAATTCTGAC[A/G]GAGTTGCAGAAATCT | 55779 |
rs532086802 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441119 | CCAGCTGAGCGCAGG[C/G]CAGGTGTCTCACTGG | 55779 |
rs532089998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352160 | AAATGCACCAATCAG[C/T]GCTCTGTGTCTAGCT | 55779 |
rs532096366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351784 | CTTGCTATTACTCAC[C/T]TTCGGGCCCTGTGTT | 55779 |
rs532116954 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433587 | TTCTGATTTAGAAGA[C/T]CTCAGAGACTTCTTC | 55779 |
rs532134878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296574 | GAACAGTAAAGAAGC[C/T]GAGACAAGGCCTAAG | 55779 |
rs532179235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434256 | ATAGCAAGAAGCCTA[A/G]AACATGATGGGGGGT | 55779 |
rs532197762 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113303929 | ACTGTGTATGGTTTT[C/T]GTCATTTCTCTCTTT | 55779 |
rs532207894 | snp | A/C | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427305 | TGTTTCATCTGTGTC[A/C]TCTTCTAAAAATGTG | 55779 |
rs532245578 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289493 | TAATAAAATGAGGCC[C/T]AGGAAGATAACGTAA | 55779 |
rs532247103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324463 | TTCTGATTTAATAAT[A/C]CATAATTAGCCAATG | 55779 |
rs532284139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323816 | TGGGAGGCCAAGGCC[G/T]GTGGAACACAAGGTC | 55779 |
rs532312754 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411358 | CAGTTTCAGCTTTCT[A/C]CATATGGCTAGCCAG | 55779 |
rs532314893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331860 | ATTTGACCATGACAA[C/T]AAAGACCATTTATGG | 55779 |
rs532320567 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445692 | CTAAATTCCAGGAAC[C/T]AAGAATAATTTATAT | 55779 |
rs532333328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311664 | GCTGTTGAACAGATA[A/T]CCAAAAATATGGAAG | 55779 |
rs532336955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365356 | GGAAGCCAATATGTT[A/C]AAAGGAATTTTAGCT | 55779 |
rs532340522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399097 | AACCTAAGCCACATG[C/G]AGAGGGTGTTAGGTA | 55779 |
rs532372455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378358 | GGCAGAAAGGGTAGA[A/G]GAACTAATAAAGGAT | 55779 |
rs532406411 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411967 | TGTATAAGAATGCTT[C/G]TGATTTTTGCACACT | 55779 |
rs532485034 | snp | C/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330530 | GAATTTTGGGAATGG[C/G]TATGTGCTTGGATAT | 55779 |
rs532499837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113294874 | TACGAGAAGAAAGAA[A/G]GAAAAATGAGTGTCC | 55779 |
rs532559083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302618 | ACACAAAAATGAGCC[A/G]GGCGTGGTGGCAGGC | 55779 |
rs532579094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384402 | CTTATAGTTGTTATG[A/T]GCTGAATTGTGTCCC | 55779 |
rs532584337 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367021 | GGAGGGGTGTCTGCC[A/G]TTACTGAGGCTTGAC | 55779 |
rs532616970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432405 | AGTACATGCCCATAA[C/T]TTAAAAAGTCAAGTA | 55779 |
rs532620911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391171 | TAGAACAGAATACAG[A/C]ATGCAAAAACAAATC | 55779 |
rs532637436 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431846 | TTAGGATTAGAACCT[C/T]AAATAGTCAAGATTC | 55779 |
rs532674317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345929 | CTTTCATACATACTA[C/T]CTTTCTCATCTCTTT | 55779 |
rs532698896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377317 | CTGCAGGCACAGAGT[C/T]GTCATATTGTTGACT | 55779 |
rs532752331 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319457 | TCTTCCTGGCCTACA[A/G]AAAGACTTAGACAAC | 55779 |
rs532760623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403752 | GAGTAAATGACTACT[A/G]ATCTCCTTCACAAAA | 55779 |
rs532769393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309111 | TCTGAGTCCTTTTTC[G/T]GACTAGTTCCTGACC | 55779 |
rs532823732 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315651 | TTTCTGACTTAAAAC[A/G]TTTTGACTTATGATT | 55779 |
rs532849953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350566 | CCATGACCTTATAAC[A/G]CTCCAATACCACCTT | 55779 |
rs532857679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356965 | AGTCACTCATATATA[C/T]AAATAACCAAAAATA | 55779 |
rs532866886 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296203 | GCCTCCAGCTCCATT[C/T]GTGTTGCTGCAAAGG | 55779 |
rs532877907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416703 | TTAATGCAGTATTTA[A/G]CATCCATTATTTCAT | 55779 |
rs532890751 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379147 | TCCCACATTCATTCA[C/T]CAAAACTCACGACTT | 55779 |
rs532895959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370303 | TTTAGACCAATATCC[C/G]TGATGAACATAGACA | 55779 |
rs532896898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364062 | CCCCTCCTTGAAAGA[G/T]AAAGATATGAAATCA | 55779 |
rs532919594 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344834 | TATTGTGCTAGACTC[A/T]AATTTTAACATATAT | 55779 |
rs532940029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316351 | AGAAAAATATCATCA[A/G]TAATCTAAACTCCCA | 55779 |
rs532967213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375377 | AAAGCAATTGGAAAA[A/C]CAAACTTTAAAATAA | 55779 |
rs532992673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445574 | TCCTCTTACTGATTT[A/C]GGAGTCATAATTTTT | 55779 |
rs533069214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321932 | ATATCATTAAAATGG[C/T]ATATCCTCCAAAGCA | 55779 |
rs533085685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352741 | TCTCAGAAGAATACA[C/T]GTAAATGAACCACAG | 55779 |
rs533097168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343649 | CAGGAGCCTGGGTGA[C/G]GAAGTGTTAGACATA | 55779 |
rs533103833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286920 | TTAAAAAAAAAAAGA[A/G]GAAAAAAGAGACAGA | 55779 |
rs533103858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416032 | ACTTGTTTTATGAAT[C/T]GGGGTGCTCTGTATT | 55779 |
rs533121313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382640 | AGAAAAGAGAAATAA[A/T]GTAAAATATTGAAAA | 55779 |
rs533156845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389706 | GAAATTCAAAGGATC[A/G]GTAGAGGCTACTATG | 55779 |
rs533179147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292702 | GGTTGCCTGATGCTA[A/G]AAGTCCATACTTTTT | 55779 |
rs533203712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337422 | TTCTTATTGAAATTA[C/T]GGCAAGATTTTGTAT | 55779 |
rs533244743 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439682 | AACTCTAAGGAAGTA[C/T]AAAGAAAAAGGGAAA | 55779 |
rs533248756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348245 | CGGTTTTTCCTTTCA[C/T]ATGGGAAACACTCAG | 55779 |
rs533258203 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307339 | TCAACTGTCAATTGT[C/T]TGCATATTATTTGTC | 55779 |
rs533281303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423156 | GTCTCACTTTGTCAC[C/T]CAGCCTGGAGTGCAG | 55779 |
rs533283260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430293 | TTTATTAAAATACAA[C/G]ATATTAAAATTGAGA | 55779 |
rs533297215 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292109 | TTCTGTTTCCTCATC[C/G]GAGTTATTTCCCTGT | 55779 |
rs533310860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316305 | CCAAAGCAGAGTTAA[A/G]AGGGAATTTATAGCA | 55779 |
rs533367954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368999 | AGACAAAGGCCATTA[C/T]ATAATGGTAAAGGGA | 55779 |
rs533368861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298919 | ATGGTGGTGATGGTT[A/G]CACAATCATCTGAAT | 55779 |
rs533383059 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356749 | TGAATTGGGAGTAGG[-/C]AAAAGTTCTTTAAGT | 55779 |
rs533389207 | snp | C/T | 0.000109922 | 0.00741276 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395907 | ATATTACTATGAAAT[C/T]TAGCCTATAGATCAC | 55779 |
rs533396705 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408786 | GAGAATCGCTTGAAC[C/G]CAGGAGGCGGAGGTT | 55779 |
rs533416622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319989 | AAACCAGAAAATCTA[A/G]AGGAAATGGATAAAT | 55779 |
rs533421664 | in-del | -/GGGG | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441138 | GTGTCTCACTGGAGC[-/GGGG]AGCCCCAGCACCTTC | 55779 |
rs533425868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395441 | AAGCATTTCGACATG[C/T]TGTGCCTGTGGCCAA | 55779 |
rs533427719 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402132 | ACATACCAGCAGGCC[C/G]CTGGAAGGGGGAAAT | 55779 |
rs533431092 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443684 | CAAGAGGCAGCACAG[A/C]ATAGGCTTTGGAGAA | 55779 |
rs533436791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422002 | TAAATATATTTTTTT[A/T]AAAAAGAGGTATAAA | 55779 |
rs533442259 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411661 | AACTTTAAGGTAGTT[C/T]TTTCCAATTCTATGA | 55779 |
rs533458956 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347456 | AACTTCCTCCTGCCT[A/C]TCTTCTCTGAGGCTA | 55779 |
rs533467615 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335835 | ATAGACTGTATATGC[A/G]TGGCCATAACACAGT | 55779 |
rs533511128 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329926 | GGCTTCCCCTTCATT[C/G]TTTGTCAGCTTTCCA | 55779 |
rs533523353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367880 | CTAGAATGAACAGTG[C/T]AGAGAAGATCTTAAA | 55779 |
rs533527853 | in-del | -/TAAA | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297268 | CCATCTTACTCCAGG[-/TAAA]TAATGACAATCCCTT | 55779 |
rs533543340 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317386 | ACCTCCAAGCCAGGA[A/G]AGAGCAGGGCCGGCT | 55779 |
rs533578644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361202 | TAAAGATCACTGGAA[A/G]CCTTCACTGGATTGA | 55779 |
rs533597533 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290827 | TTAGAATTCTGACGG[A/T]GTTGCAGAAATCTTT | 55779 |
rs533609445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313533 | AGGACATGAGATTTG[A/G]AGGGGCAAGGGGGCG | 55779 |
rs533613780 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384420 | TGAATTGTGTCCCTT[A/C]AGAAAAAAATTCATA | 55779 |
rs533630912 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325546 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGTCTC | 55779 |
rs533656871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420366 | TTTAAATTAGGTGAG[A/G]AAAAAAAGGCCTGGG | 55779 |
rs533665091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333061 | AGAGATAGAGACATT[C/G]ATCAGAGAGTCAAAC | 55779 |
rs533687039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414529 | ATTATTTTAAGATAT[A/G]TTCCATCAATACCTA | 55779 |
rs533700119 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332593 | AGTAGTAGCTCAGAT[A/G]ACCTTTAAGCCTTTA | 55779 |
rs533707137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340922 | GAACCAGAAGGGAGA[C/T]GGTTTTTCCCTGGAG | 55779 |
rs533712026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374827 | TTTTAGTAGAGATGC[A/G]GTTTTGCCATGTTGG | 55779 |
rs533719250 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434276 | TGATGGGGGGTTAGA[A/C/G]AAGAGGTGTTTGAGA | 55779 |
rs533739020 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289868 | CGAGGAACTGAAGCC[C/T]TGCCTAATGGCCAAG | 55779 |
rs533743755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296668 | CACTTCCTGCTCCCT[A/G]GGATTTCTTGCCTCC | 55779 |
rs533749948 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360104 | AAAAAGTGTGGTAGG[G/T]AAATCCAATAGTAAA | 55779 |
rs533777435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426856 | AAATGCTGAGTTCTG[A/G]TCGGTCATGGCGCAA | 55779 |
rs533778119 | snp | C/T | 5.20179e-05 | 0.00509963 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373533 | GAACTCACAGTGATA[C/T]AGAAAACCAGAATCA | 55779 |
rs533803100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433761 | CATTAGCACCAAACA[C/G]CATGTGTGTCAATAA | 55779 |
rs533803214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296202 | GGCCTCCAGCTCCAT[C/T]CGTGTTGCTGCAAAG | 55779 |
rs533818131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406818 | TGTTCATTACATTTA[C/T]AATAATATCTGTTAT | 55779 |
rs533829808 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327505 | GGGGAAAGAAGACAA[A/G]AAAGAGATAAGGGCT | 55779 |
rs533831776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318800 | AAAGAAAATAAATTC[A/G]AACCAAGAATTTCAC | 55779 |
rs533864266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419931 | TGTGCATGGTGTTGG[C/T]ATCTAACAACCATGT | 55779 |
rs533895548 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304784 | TTAAATCATAGGCTC[C/T]TCATTTCTCTAGACT | 55779 |
rs533928114 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429591 | ATCTCTGCCTTTTTA[C/T]ATTAATGTTCAGTTA | 55779 |
rs533939787 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399782 | CTGACTAAAATAAAC[A/T]AACTTAAAACTTTTA | 55779 |
rs533969203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399221 | CAGGCCCAGCCATTC[A/G]TGTCTTCCCAGCTGA | 55779 |
rs533972961 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333552 | GAAGATCTTTGGGAT[C/T]TTCATAGTCATCACC | 55779 |
rs533986545 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309940 | GGAAGGGGCAGCCTA[G/T]CAGGAGAGAAAACTT | 55779 |
rs533996695 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289528 | TCCTGATTCTCTACA[A/T]TTACCAAGGGGATGG | 55779 |
rs533996794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379072 | ATAGATTTATCTGTA[C/T]AATTATCTGCACAAG | 55779 |
rs534003942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398607 | GAGCTAGGTCTGCCA[A/G]TCTAAATGCTCTGTC | 55779 |
rs534020190 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350999 | GTTCCTCCTGGGCGA[C/T]TGAGGGAAAAAGACT | 55779 |
rs534038867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405084 | GTTCCATAAAAATGC[A/C]CTTTGGGAAACTCTA | 55779 |
rs534044675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412267 | ATTAGAAAACCCCAT[C/T]GTCTCAGCTTAATAA | 55779 |
rs534061535 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410323 | CCCACGACAGGCCCC[A/G]GTGTGTGATGTTCCC | 55779 |
rs534089606 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340246 | TCTGATTTTCACCTT[C/G]GGAGGCTGAGCCTAA | 55779 |
rs534151492 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308526 | AAAACACAGTTAGTG[A/G]AACAGACCCACAATT | 55779 |
rs534151932 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357563 | ATTCTCCCCACCAAG[A/T]CCTCAGAAAGAACCA | 55779 |
rs534190915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351550 | TGACTCTCCAAAACC[A/G]CCAAGACCTAGATCT | 55779 |
rs534192528 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358769 | AGCTTCATTAGGCCG[A/C]GTTCATGTTTCTCTT | 55779 |
rs534205839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417612 | AGATATAGATTGCTA[A/G]TCCTGGTACCCAAGA | 55779 |
rs534206456 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421213 | TTTTCAAAAGAAGAC[A/C]TGCAAGCGACCAACA | 55779 |
rs534225060 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288410 | AGGACTGTAAGGAAC[A/G]GGTAAATGTTAGGAA | 55779 |
rs534230543 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383090 | ATAAAGTAGTTGGGG[A/G]AATTCAGAGATGGAC | 55779 |
rs534249911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339444 | CCATAGGTACCACTG[C/T]GGTATGTACCAATGA | 55779 |
rs534290776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328393 | AGACTTTAATCCATT[A/G]TGGTCCTACTAATTT | 55779 |
rs534308366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317340 | CCCCCAGAGTTCCTC[A/G]TCCCTCTCTGGGAGG | 55779 |
rs534335096 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358037 | CTGATACATGTAACA[A/T]CACTGATAATCTTAG | 55779 |
rs534401432 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345717 | AAATTTTTTTCATCA[A/G]TTGCCTTGTTATTTG | 55779 |
rs534423434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371942 | AGACACTTCTCAATA[A/G]AAGACATTTACGCAG | 55779 |
rs534445145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350686 | CCACAGATGGCCCAG[A/G]TGCATTCAATCTGTG | 55779 |
rs534452674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345059 | GAATCCATCTCCCTA[C/T]ATATTATATATAATA | 55779 |
rs534477292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331397 | CTGTACTTCCTGTGT[A/G]CAGTTAGGCTACTAG | 55779 |
rs534478596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350095 | GCAGTCTTACACTGC[C/T]GAAGCCATGAAAAGG | 55779 |
rs534482351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357077 | ACTGGAACAAACACC[C/T]AACAACAGAAAATAT | 55779 |
rs534507887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445679 | AAATTAAATGCTACT[A/G]AATTCCAGGAACTAA | 55779 |
rs534515307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390553 | AAGAAAGAAGTCAAA[G/T]TATCCTTGTTTGCAG | 55779 |
rs534522907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418356 | CCTCCCAAAGTGCCA[C/T]GATTACAGGCAGGAG | 55779 |
rs534567312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338719 | GTTGCCAAGATTTCT[C/G]TTCATTTGCTGTAAG | 55779 |
rs534601730 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288094 | GGGTGGGGGGAGCCT[A/G]TATTTTCTAGATTTC | 55779 |
rs534602134 | in-del | -/AAAAAAAAAAAAAAAAAAA | 0.499354 | 0.0179596 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433429 | GCAAAACTCCATCTC[-/AAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55779 |
rs534606616 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394719 | ACTAACAACAGCTGA[C/G]GAGCTAAAAAAAAAA | 55779 |
rs534643580 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325552 | TGGGTTCACGCCATT[C/T]TCCTGTCTCAGCCTC | 55779 |
rs534643757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432707 | GCTTACTATTTTTAG[C/T]ATACTGCCTTAATAA | 55779 |
rs534646620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424781 | ATCCAGCACGAATAG[A/G]GATAATTCATATATT | 55779 |
rs534675924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391520 | CTTAAAAACCTTCTG[C/T]GCAGCAAAGGAAGAC | 55779 |
rs534684083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439287 | ATAGAGCTGGGGAAG[A/G]CTATGAAGAATGGGT | 55779 |
rs534692748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362745 | GCAAAAGATCAAATC[A/G]GGATGACGTTTAGCC | 55779 |
rs534697815 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372074 | CATTAAAAAGTCAGG[A/T]AACAACAGATGCTGG | 55779 |
rs534705484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425162 | CAAGATAAATCAGCA[C/T]GAATTAATTTAGTTA | 55779 |
rs534713002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432074 | TTCCAAGATCAAGCA[C/T]CTCTAAATGGTAGAT | 55779 |
rs534726149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370003 | GATAAATTTCTGGAC[A/T]CATACACCCTCCCAA | 55779 |
rs534741232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329674 | AGAAATAAGAATAGT[C/T]GCCATTCCAGCTCCA | 55779 |
rs534745106 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307346 | TCAATTGTCTGCATA[-/T]TATTTGTCACTCATA | 55779 |
rs534791060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310313 | CTTTCATCATTATCC[A/G]TAAGTACTTGCCATC | 55779 |
rs534791101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301261 | GATGTAATATTTCTA[A/C]AAAGTTCTAAAGCAA | 55779 |
rs534851684 | snp | A/C | 0.000148262 | 0.00860865 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403950 | TGCTTGTCCCTCGAC[A/C]GAGCTCCACTTTGAT | 55779 |
rs534861271 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350377 | GAGAGAGAGAGACAG[A/G]AAGTCAAAGAGAGAG | 55779 |
rs534888969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316037 | TACCAAGATAGATCA[C/T]ATGTTAGACCATAAA | 55779 |
rs534889915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403420 | GAAGAATGTAGCATC[C/T]ATAGGCAAACTCCAT | 55779 |
rs534894223 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405019 | TTTTTAGATACAAAG[C/G]AATTTGACTTAAAAA | 55779 |
rs534900651 | in-del | -/AAAC | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327006 | ATTGATATATAACTA[-/AAAC]AAAGAGACATATAAT | 55779 |
rs534944370 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342399 | ATGAATTCAACCCCA[-/T]AATAAGTACTGTGGA | 55779 |
rs534960129 | snp | A/G | 8.41857e-05 | 0.00648735 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363507 | TCTTCAATGTCTTCT[A/G]GAATTGGCTCTGTTT | 55779 |
rs534977497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299179 | CTGACAAGGGGTTAA[A/T]AACCAGAATATATAA | 55779 |
rs534988113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437660 | ACTATTCCTACCTTT[C/G]CTGGGTCATAAAAGG | 55779 |
rs534997307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370503 | TATCTCAATAGACGC[A/T]GAAAAGGCCTTCAAC | 55779 |
rs535066732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409775 | CCAACTGATAAAACA[A/G]GATGTGGTAAATATG | 55779 |
rs535075273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375522 | GTAATACACATAAAG[C/T]TGGGGTCCCAGAACA | 55779 |
rs535075913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299560 | AGCAATCGCACTGCT[A/C]GATAAATACCCAAAA | 55779 |
rs535119445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401852 | TCTTTTTCTTTCATG[A/G]AAAGTAACAATGAAC | 55779 |
rs535123068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307261 | CCTGTAAAATATATA[C/T]GTAAATTACAGTCTG | 55779 |
rs535134816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424101 | CAGCTTTAGGCTAAA[C/T]TTGATTTAACATTGC | 55779 |
rs535146844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313613 | GTACTCCCGTAATTC[C/T]CACATGTTGTGGGAG | 55779 |
rs535156407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286464 | TCTACAGTCCCAGCA[C/T]GAGTGGGAAATGGGT | 55779 |
rs535208072 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301970 | TAACCATCATTCTAT[-/TC]TGTTTCTATGAGTTT | 55779 |
rs535216458 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292226 | GTTTTATCGAAACAT[C/G]CATTATACATATACA | 55779 |
rs535293760 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444768 | ATATAAACAAACACT[A/C]CCAGGCCTATTGTTT | 55779 |
rs535373707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405613 | CACTGAAATTCTCCA[C/T]TTTTTGCCAACATAA | 55779 |
rs535384168 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427548 | TCTCCATTTTCACTT[C/T]ATTTTCAGTCTATTT | 55779 |
rs535390731 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301345 | CTAAACATAAAATTG[C/G]GAATGGTGGCTATCT | 55779 |
rs535413702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354811 | CTAGGGCAAGTTTGC[A/C]TCCTCCCTACAGGAC | 55779 |
rs535449868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388227 | TACCACAGGCCTTGG[A/G]CAAGACTCGGTGCTA | 55779 |
rs535450009 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380463 | TGAGACAGGGTCTCA[C/G]TCTGTCACCTGAGCT | 55779 |
rs535452407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361949 | ATGAAACCAGCACAA[A/G]TGTTATAAGATTAAA | 55779 |
rs535464104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314232 | CCAAAACTCATCACA[A/G]TCAAACTTCTGAAAA | 55779 |
rs535475388 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290470 | TTCCTTTCTTCACCC[A/G]CCCTTCTCAGTGACC | 55779 |
rs535503144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321048 | GCCTAATATCAAAAT[G/T]TTTTGGCAGAGATAT | 55779 |
rs535507498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401145 | TTATGAGGACCATGA[C/T]GAAATATGGAGAAAG | 55779 |
rs535515968 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311869 | GAGAAGCTTGTTGGG[A/G]ACTGGAGCAAAGGAG | 55779 |
rs535542797 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441838 | TTAAGAGGGGTCCTG[A/G]GAGATAGTAGGCAGC | 55779 |
rs535575004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347630 | CATTGGGTGGGGAGA[C/G]CAACTATCCTTTTAG | 55779 |
rs535591706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361304 | GGTGAATATTCAGCC[C/T]GAGCTAGTAAGCTAG | 55779 |
rs535631202 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299304 | ATGGCAAACAGGTAC[A/G]TGAAAAGGTGCTCAA | 55779 |
rs535663096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359983 | ATAGAAGCACAGACA[A/G]TCAAATTATACATGC | 55779 |
rs535694889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373874 | TTATTCTGAATAAGC[A/G]GGAACAAATATTAGG | 55779 |
rs535726621 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437780 | GAATAAGGTATTTTT[A/G]GTTTTTTGGGGTTTT | 55779 |
rs535773138 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291004 | TCTGTTTGTATTTCC[C/T]GAATCCTGAGCCCTC | 55779 |
rs535778245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325530 | GCTCACTGCCAGCTC[C/T]GCCTCCTGGGTTCAC | 55779 |
rs535816483 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405587 | TACACTAGGACCAAG[G/T]CATACTTCTCCACTG | 55779 |
rs535823269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366823 | CAAGGGAAACTGTGA[C/T]AGACTGTACCTGGAA | 55779 |
rs535842779 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415278 | ATTAGTCTAGCTAGT[G/T]GTGTACCTATGTTGT | 55779 |
rs535868946 | in-del | -/TAGA | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441714 | CTAAAGGACGTCATG[-/TAGA]TAATTAAATGACATG | 55779 |
rs535877175 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289969 | TGACTGCAACTCCAC[A/G]AAAGACCCTGAGCCA | 55779 |
rs535877760 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439722 | CACATTGATGCAGAG[A/G]AGTGTGTTGCTAGAA | 55779 |
rs535883433 | snp | C/T | 0.000391382 | 0.0139835 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379594 | AAAAACAATTATGAC[C/T]CATTCGTTCATTTAC | 55779 |
rs535892597 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435858 | TAAAAAGTGTATGTA[C/T]GTGTGTGTGTGTGTG | 55779 |
rs535917740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419668 | TGGCCATGTGCCTGC[A/T]TCAGTCTTCAGATTA | 55779 |
rs535919022 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339242 | CCAGATTCTGAGGGT[C/T]AAACAGTCCCAGTGG | 55779 |
rs535922272 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332517 | CCCTCTCCAAAGTGA[G/T]GCCTTGAAATGTGCA | 55779 |
rs535926570 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388868 | GCTGGAGAACTCAGA[A/T]ATATAAGCCAAATAT | 55779 |
rs536048309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312981 | TGGGGTCAGAGCCCC[C/G]ACACAGAGTCCCTAC | 55779 |
rs536081422 | snp | C/G | 3.30989e-05 | 0.00406797 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433705 | TGAGATATGGATAAA[C/G]CTGTAAAATTGAAAC | 55779 |
rs536083430 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364442 | ATGACTTTAATAAAA[A/G]CAAAGTCATAAAACA | 55779 |
rs536086811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399821 | TAAAATTTTGAGTCA[G/T]CAAATATCTATATTT | 55779 |
rs536107735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439801 | ATTCATTCACCAGAG[C/T]CCAGGTTCTGGTCCT | 55779 |
rs536131467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406738 | AAATGGTAGGTAAGT[A/G]TGGATTATGACAATT | 55779 |
rs536144236 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440658 | ATTTTCTACACTATC[G/T]CTTGTATTTCTAAAA | 55779 |
rs536155359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351851 | GATGCCATCAAGCTA[C/T]AGATGGTCTTACAAA | 55779 |
rs536168435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413278 | ATATTAGACCTTTGT[C/G]AGATGGGTAGATTGC | 55779 |
rs536205292 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412589 | CCATGTGTTCTCAAT[A/C]TTCAACTCCCATTTA | 55779 |
rs536327083 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404151 | AATGGAAAAATAAAA[A/C]AATACAGAAATGAAG | 55779 |
rs536383588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371825 | ATTTTTGCAATCTAC[C/T]CATCTGACAAAGGGC | 55779 |
rs536390240 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444300 | AGGTCAGGAGTTCGA[C/G]ATCAGCCTGGCCAAC | 55779 |
rs536422412 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407904 | GGTTCCTTCATAGCA[C/T]TTCACACATGAAATT | 55779 |
rs536429602 | in-del | -/ACTCATTTTATGAGG | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370220 | AGGAAATCCTCCCTA[-/ACTCATTTTATGAGG]GCAGCATCATCCTGA | 55779 |
rs536443753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385924 | GCTGAGATTATAGGC[A/G]TGAGGCACTGCGCCC | 55779 |
rs536455712 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355476 | AGTGAGCCGTGATCA[C/T]GCCACTACACTCCAG | 55779 |
rs536482289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385442 | AGAGCCTCAAAGAAA[A/G]AGAGTTTATATTTTA | 55779 |
rs536513356 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392371 | AACTCATAGAGATGG[A/C]GAGTAGAATGATGGT | 55779 |
rs536580683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294197 | TTAATTAGGTATATC[C/T]ACCACATACAATGTA | 55779 |
rs536585024 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287297 | TGGATCCGGTGCTAC[A/G]GGAAACATTTTCCTA | 55779 |
rs536586099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351525 | TCCCAAATAGACTCT[C/T]TGGCAGCAGTGACTC | 55779 |
rs536638136 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383901 | GCTATCCCTCCCCTA[G/T]CCCCCAACCCCCTGC | 55779 |
rs536642432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391423 | AAACTCTCCAGGACA[A/T]TAGACTGGGCAAAGA | 55779 |
rs536691252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404831 | TTAAGTAACTTGCCC[A/C]AAACTACCCAGTCAG | 55779 |
rs536719809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300141 | ATGCTCTCCCTTATT[C/T]GTGAGAGCTAAAAAT | 55779 |
rs536752433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396326 | TGTTATTCACATGCT[A/C]CAGCTCTCTTCTGAT | 55779 |
rs536774032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349549 | GTGTGGTTTGCAAGG[A/C]CACTTTAAAAAAGAT | 55779 |
rs536813623 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363281 | ATTAACTTGTCATGT[C/T]CTCTTTTTCTCCTAG | 55779 |
rs536814678 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395273 | ATCAATACCGAATTA[C/T]CAATTGCTAAGAAAG | 55779 |
rs536838475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308572 | GCTCTAAAATCAGAC[A/C]AAAATTTTTTTTTCT | 55779 |
rs536916836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438777 | AAGTTTTTCTGTGTA[A/C]TTCAACCATTCAAAT | 55779 |
rs536922211 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370213 | GAAAAAGAGGAAATC[C/T]TCCCTAACTCATTTT | 55779 |
rs536945852 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383574 | AGAATTATAAATTTT[-/A]AGCTGGATATGGAAG | 55779 |
rs536960834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345534 | CCTCAATTTTCCATG[C/T]TTAATGACATTTAAT | 55779 |
rs536962688 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338139 | GCACATGTTTGTAAT[A/C]CCAGCTACTTGGGAG | 55779 |
rs536964391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424680 | AAAAGCTCTCTAGTG[A/C]GCCGTCCAAAAGTGG | 55779 |
rs536969460 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318665 | GAAAAAAATCTTAAA[A/G]GCAGCTAAAGAGAAG | 55779 |
rs536997826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344868 | CCAACCAGGATGTCA[C/T]GAAAGTTGGATTGGA | 55779 |
rs537041088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438519 | ACAGGAAAGCTCTAA[C/G]AATGATACATGGCAG | 55779 |
rs537049627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113293332 | AGCAATGGAGTCAGC[A/G]TTGGAGGCAGACAGA | 55779 |
rs537061757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301038 | ACTCTTGTAAACATA[C/T]ACCATGTACAAGAAT | 55779 |
rs537064332 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375200 | ATCAGGAGTTATCAT[C/T]TGATGAGTATGGGAG | 55779 |
rs537079618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439267 | TTAAGAAAGAACCCT[A/G]ACAAATAGAGCTGGG | 55779 |
rs537101907 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445662 | AGTTATTTGGTCTTA[C/G]TAAATTAAATGCTAC | 55779 |
rs537103354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113382000 | TAAAAAATGTATAAA[A/T]TATAATTATATAATG | 55779 |
rs537123465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428653 | AAACTCCATTTTTTT[A/G]TATAACTAGAAGCAG | 55779 |
rs537154434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403332 | GCTGGAGCAATGTTC[C/T]AGCTTAGCCCAGGCT | 55779 |
rs537176771 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356443 | GCTGGAGGATTTACA[A/G]TATTAGATGTCAAGA | 55779 |
rs537200452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342819 | CATGGTGAAACCCCC[A/G]TCTCTGCTAAAAATA | 55779 |
rs537233997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315886 | AGCTAAGCTAAGCTA[A/C]TATGTTTGGTAGGTT | 55779 |
rs537242786 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443725 | TGTTCCCATTCTAAT[A/G]CCACCACTCCCTAGT | 55779 |
rs537249896 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398013 | TGTCTTGGAAGAGCC[G/T]GGGCATCCTGTAGAG | 55779 |
rs537271180 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315162 | GAATGAAAAACATTA[A/T]CCAATCATACGCTGA | 55779 |
rs537308740 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442892 | GAAAAGATAGAAAAC[A/G]TAGGGTAAACTTATT | 55779 |
rs537318221 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321964 | TATACAGATTCAATG[C/T]TACTCCTATCAAATT | 55779 |
rs537320068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409727 | ACTCACCAGATCAGA[C/T]AGGTGGTTGGCACAA | 55779 |
rs537328022 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416180 | ATTGCAACCCTTGGT[A/G]TTTTTTTGTTTTTTT | 55779 |
rs537346757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321291 | GATCATCGTAATAGA[C/T]GCAGAAAAAGTTTTC | 55779 |
rs537357252 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328806 | CCCCTTTAAAGCTTG[A/T]TTAACAAACTTGAAT | 55779 |
rs537369994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353733 | GAGGAGACAGCTGCA[C/T]GATAGAGACAGAGGG | 55779 |
rs537395648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415585 | TCTCATTGGTTTCAA[A/G]GAACTTCTTGATTTC | 55779 |
rs537432337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307962 | TCCACCCTGGGTGAC[A/G]CAGCTAAACTCTGTC | 55779 |
rs537467743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383008 | TAATCACTAAATTAT[A/G]GAGGAGCTAATCTTC | 55779 |
rs537476798 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320365 | AAGATATCCCAGTGT[C/T]TCCAGGGCTGTGGTG | 55779 |
rs537485391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408391 | GTTCCTTGTCAGGAA[C/T]GATAGTGTGATAATT | 55779 |
rs537500520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423212 | CTCAACTTCCCAGGC[G/T]CAAGAGATTCTCCCA | 55779 |
rs537545009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326159 | GATATACATATGGCA[A/C]ATAAACACATAAAAA | 55779 |
rs537564775 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414105 | TATTCCTAGGTATTT[C/G/T]ATTCTCTTTGTAGTG | 55779 |
rs537576746 | snp | A/G | 0.00069503 | 0.0186288 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291727 | CAACATCTGCTTCCC[A/G]AGGGCCCTGGAAGGC | 55779 |
rs537631279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389156 | AAAACATTCCAAAAA[C/T]TGAAATTATATCAAG | 55779 |
rs537641514 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291300 | TGAAACACAGCCTTC[C/T]GAGACTTCATATTCA | 55779 |
rs537667257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380404 | AGCCTTTATTGCCAT[C/T]GCCCTATTTTCACCT | 55779 |
rs537668084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388462 | CTAAAACGTAGATAA[A/G]AAGGAAGGAGAGAAG | 55779 |
rs537671933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395469 | CAAAAGTCCCGTTGG[A/G]GCAAAGCCTGATATA | 55779 |
rs537683126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333869 | CACTTCTAAGTAATT[C/T]ATATTAACATTGTTA | 55779 |
rs537694266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420420 | TAAATAAATCAGGTG[A/G]CTATCCCCATACTCT | 55779 |
rs537707575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394860 | ACACCATTGATATTT[C/T]AGTCACCAATTCCTT | 55779 |
rs537712574 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304761 | TCACCCTCTGAGCCA[C/T]TGCATTCTTAAATCA | 55779 |
rs537739703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354561 | TCAGCAGAGGCAGCC[A/G]TAATCCCCCTGGGAA | 55779 |
rs537758915 | snp | A/G | 1.77178e-05 | 0.00297634 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427339 | TCTTCTTGAACAGGA[A/G]CTATTAAAATTTGTT | 55779 |
rs537850988 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358168 | AGATTCAACTTTGAA[A/G]AGTATTTCCTGAAGT | 55779 |
rs537856245 | in-del | -/TGGCTGGAGGCCAACCA | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354860 | GAAAGCACCACCTCC[-/TGGCTGGAGGCCAACCA]ACACAAAACGAGCAC | 55779 |
rs537877169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393444 | TGATGATTTCCCTAG[A/G]TGGGGAAGGGGGTGG | 55779 |
rs537902253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312319 | CCATCACCTGACCTC[A/G]TGATCCGCCCACCTC | 55779 |
rs537915804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392947 | CACATCACAGCTGCC[A/C]AATAGATCCACCTGC | 55779 |
rs537925630 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407482 | TGTCAGAAAGTTCTA[C/T]TAGACAGTATTGTTT | 55779 |
rs537947216 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350514 | TTTAAAAGCCAGGGT[A/G]AATTTAAAACCTATA | 55779 |
rs537950881 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314931 | ACTTAAACAGTTATA[C/T]GAAGAGATGTATTCA | 55779 |
rs537958813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406613 | TGGGCAACAGAGCGA[A/G]ACCCTGTCTCAAAAA | 55779 |
rs538005661 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382762 | AGGAGCAGGTGAATA[C/T]AGAGGTAAATGGGAT | 55779 |
rs538046049 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410539 | CATTTTCTTAATCCC[A/G]TCTATCATTGATGGA | 55779 |
rs538051495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373257 | TTCAGTATTAGCTTT[A/G]ATTTTATTTATTCAT | 55779 |
rs538124363 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333154 | ATAACCCCCAGATAT[A/C]CTGTAAGTATTTGCA | 55779 |
rs538159404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332422 | AAAGACACCCCTTCC[C/T]CAGGACATTTCATTT | 55779 |
rs538172918 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411570 | AGTATAGTTTGAAGT[C/T]AGGTAGCATGATACC | 55779 |
rs538193950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372638 | AATTTAAATGATGAG[C/T]TGATAGGTGCAGCAA | 55779 |
rs538195918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365885 | TATTTGATATATAAG[C/T]ACCAGAAAGTCAAAT | 55779 |
rs538221572 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355822 | AGAAATATCTAGCAC[C/G]TACAATGTAAAATTT | 55779 |
rs538229019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386832 | GTCTTGAATTGCTGA[C/T]ACCACTCTGGTGGCT | 55779 |
rs538263380 | snp | A/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435000 | GTGACATCATAATGA[A/T]GCCTTCTTTTGATAT | 55779 |
rs538274846 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441788 | CAACGGAGCCCTGAT[C/G]GCGGCGTTCCTATGT | 55779 |
rs538298374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340078 | ATGGCTTTCTCCCGC[C/T]CTGCTCGTGACTGTT | 55779 |
rs538300913 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393324 | TTGTACGTTACAGGA[C/T]GTTTGTCCCCTCCAA | 55779 |
rs538303732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440826 | CACCCTCTCTCTCTC[C/T]CTAGCCTCCTTAGCC | 55779 |
rs538330319 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346791 | GGGCAGGGACAAATA[A/T]GGGAATAAAAGCTGG | 55779 |
rs538350442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311724 | TTGGAACAGTTTGGA[A/G]GGCTCAGAAGAAGAC | 55779 |
rs538355033 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339116 | CACAGAAAAATTCCA[A/G]CTGCTGAATGGTATC | 55779 |
rs538373978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338755 | TAGGGAGAAGGGGAC[C/T]TTGGCCTTACTGGGC | 55779 |
rs538402119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345674 | TTTTTAAAAGCTCTT[A/C]ATCTATCAACTAAAA | 55779 |
rs538431916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303004 | TAACTTCACCAGCAA[C/T]CAAAAAATGTGAATA | 55779 |
rs538474608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405968 | AGGTAGATGACTAGA[A/C]AACTTGGTTCCTTAA | 55779 |
rs538538755 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324058 | AAAAAAAAAAAAAAA[A/G]AGAGAGAAATAGATC | 55779 |
rs538540287 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363982 | TTTTTACATTTTAAG[C/T]AAGCATTTTATATCA | 55779 |
rs538664190 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286480 | GAGTGGGAAATGGGT[A/G]GCAAGTGGCCCTCCC | 55779 |
rs538672846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316104 | CAGAATATGTTCTCC[A/G]ACCACAATGAAATCA | 55779 |
rs538681310 | snp | C/T | 3.33712e-05 | 0.00408466 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426102 | AATCCCAAAATTATA[C/T]ATATTTAGCCAGGGT | 55779 |
rs538683295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418434 | AGTAAATCATTTACT[C/T]TACACTCAACATAGA | 55779 |
rs538687869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385409 | TGTAGAAAGAAAAGA[C/T]GTTATAGGTGAATGA | 55779 |
rs538699362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403537 | CCCATTCATATGGAG[C/T]CTTTTGGAAGGATAT | 55779 |
rs538701524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295310 | GGGCTCAAGTGATCC[C/T]CTGCCTAAGCCTCTC | 55779 |
rs538811350 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296019 | GATAGCAAACGTTGT[A/C]CCTAGTAGGTAATTT | 55779 |
rs538813424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294386 | CACCAAACCCAGGGC[A/G]TATAATGGTGTCGTT | 55779 |
rs538848453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113293272 | ATTTGACACATTTTT[A/G]TTGTCACCAACTATA | 55779 |
rs538859607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439726 | TTGATGCAGAGGAGT[A/G]TGTTGCTAGAAGGTT | 55779 |
rs538869928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391590 | AAAGTGAATTAAATT[C/T]TCTAAATAAAGTGAA | 55779 |
rs538889995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424129 | TGCTAAAATTTAGAA[G/T]ACATAAATTTAAAAA | 55779 |
rs538899148 | snp | C/T | 0.000102433 | 0.00715583 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291769 | GAAAGAAAACAGCTC[C/T]CTGTTGAAGCATCAT | 55779 |
rs538904412 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394029 | AAAAATTACTTTTAA[-/T]TTTTTTAAACTTATT | 55779 |
rs538926431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383337 | TTTTTCCTGCTGCAT[C/T]GATGGTGGTCTTGTA | 55779 |
rs538932060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404079 | TACATATTTATGCCT[C/G]AAATAGTAGGTGAAA | 55779 |
rs538934857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429702 | TTATTTTCTGTTTTT[C/T]TCCTCCTACCTGTCC | 55779 |
rs538940937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337013 | CAAACAGATTAGAAA[A/T]AAAACTGTTCCTGTT | 55779 |
rs538953996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423432 | GGCCTGAGCTGCTGC[A/G]CCTGGCCTGATCCTT | 55779 |
rs538995520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364475 | ATCAATATAAGAGAC[A/T]GTAATGGCTAATAAA | 55779 |
rs539061529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389952 | CCAATCATGCTCAAA[C/G]TATTATGAAAAATGA | 55779 |
rs539067241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410723 | TTGAGGAATCACCAC[A/G]CTGTCTTCCACAATG | 55779 |
rs539084477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299331 | TCAACATTGCTGATC[A/G]TCAGAAAAGTGCAAA | 55779 |
rs539094414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437768 | ACTGGTAAGGTAGAA[C/T]AAGGTATTTTTGGTT | 55779 |
rs539112774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307769 | GGTCAGGAGATCAAG[A/G]CCATCCTGGCTAACA | 55779 |
rs539117942 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402665 | CAGACTAACCCCTGG[A/G]AGTTGGGCTAGGTTT | 55779 |
rs539141443 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290253 | TTAATGGTGACAAGT[A/G]CAAACAATAAGGTAT | 55779 |
rs539158904 | in-del | -/C | 0.00243248 | 0.0347897 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446544 | ATCAGCCACCTTCTA[-/C]CCCTCACCCCTATAT | 55779 |
rs539171314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314312 | TAACTATAGGGGATA[C/T]ACAACTTGTATAGCA | 55779 |
rs539184447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370715 | ATTCAACATAGTGTT[G/T]GAAGTCCTGGCCAGG | 55779 |
rs539197962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405060 | TATGGAGCTTCTGTA[C/T]AGACTGATGTTCCAT | 55779 |
rs539246003 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441204 | GGTCTAAGCTGTGCT[C/G]CTGCTGCCTGGCTGG | 55779 |
rs539246367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383798 | GATACATGTGCAGAA[C/T]GTGCAGGTTTGTTAC | 55779 |
rs539257257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369247 | TCTAATAGACATCTA[C/T]AGAACTCTCCATCTC | 55779 |
rs539258735 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375632 | AAATTTAGAGTGCTA[C/G/T]GAACTGCAAACAAAA | 55779 |
rs539276851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390363 | AACACAATAAAACCC[A/G]TATATGACAGACCTA | 55779 |
rs539291744 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438458 | TGCCTCAGTACTTCC[A/C]TCTTTAAAATGCAGC | 55779 |
rs539317195 | snp | C/T | 0.000212067 | 0.0102951 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344707 | CTTTCCAGTGGATCT[C/T]GAAATCTGAAAAAAT | 55779 |
rs539334148 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421415 | AATCAGTTCAGCCAC[C/T]GTGGAAAGCAGTTTG | 55779 |
rs539335878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415456 | TTAATTGTGATGTTA[C/G]GGTGTCAATCTGAGA | 55779 |
rs539395534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375061 | ACTTGGGGAAATTAT[C/G]CCAAGTGAAACAAGC | 55779 |
rs539399289 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324289 | TATTACCCTGATACT[-/A]AAACCAGACAAAGAC | 55779 |
rs539411029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334971 | TCTATTGTATTAACT[C/G]ATAATCATTTATTTG | 55779 |
rs539431872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374592 | CTCATTCATAGCAGC[A/C]TTATTCACAATAGCC | 55779 |
rs539455852 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291121 | CTGCATCCTCTCAGA[C/G]AACACTTAATAACAT | 55779 |
rs539492389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315065 | ATAAAAATTAAATAA[C/T]AGACAAGCTCTAAAA | 55779 |
rs539505171 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388330 | TGTTAAGTTGTCATC[A/C]GTTAAAATAACAGGT | 55779 |
rs539528101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409654 | CATCTGGAATAGGAG[C/G]TGGGTAAAATGAGGC | 55779 |
rs539532801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348741 | GAATTTGGCCCAACC[C/T]GGGTACATGTCCCCT | 55779 |
rs539550518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362610 | CTCTGGTAAGATCCA[C/T]AGTTAACGCTCATCA | 55779 |
rs539577310 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347957 | GTCTAAGAGGACAGG[A/C]AAGAGTGCAGGTTTT | 55779 |
rs539692510 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357240 | TGGATTTGTGTCCCC[C/G]CAAAAAGCTATGTTG | 55779 |
rs539693442 | snp | A/G | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330933 | CCCTCCAGCTGGCTC[A/G]TGTGGCTGAGTTCCC | 55779 |
rs539717265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313097 | GCACCTGGAAAAGCC[G/T]CAGACGCTCAATGCC | 55779 |
rs539725576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422298 | TTTTAGAGAATTCCA[C/T]TTATTCATAAGTAAA | 55779 |
rs539731838 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320536 | AATGAAGTTATATAT[A/G]TATATATATAATGAA | 55779 |
rs539736282 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406082 | ATATTGATAGAGAAC[A/T]AATCCTAATTAACTA | 55779 |
rs539739281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414845 | GTTATGTCTCTTTCC[A/G]GTTTTGGTATCAGGA | 55779 |
rs539767814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368686 | AACTGCATCAATTAA[C/T]AGGCAAAATAACCAG | 55779 |
rs539768094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327341 | CCAGACTGGTGTAGA[A/G]TGGCACAATCAAAGG | 55779 |
rs539785848 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380428 | TTCACCTCTCAAAAT[G/T]CCCCCTATTTTTTTT | 55779 |
rs539846385 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407995 | AAATAATCAGAAAAT[A/G]TAAGAAATTGGAAAA | 55779 |
rs539851235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359254 | ACATCCCCCCTGGTG[A/T]GACCCCACCCAGGAA | 55779 |
rs539897040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311948 | TAGAGATTTGTGGAA[A/C]TTTGAACTTGAGAGA | 55779 |
rs539907982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298142 | CACCCCCATACAAGG[A/G]GTTGCCCTCTTGCAT | 55779 |
rs539938058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342193 | CAAAAATTAGCCAGC[C/T]GTGGTGGTGCATTCC | 55779 |
rs539939270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318121 | TGTCAAGGAAGCTCA[C/T]CAAGATTCAGGAGAT | 55779 |
rs539944958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428087 | AGTTCCTTAGGATGC[A/G]TGTATTTGGATGGCA | 55779 |
rs539962752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325212 | GAGGCTGAGTCAGGA[G/T]AGTGGTGTGAACCCG | 55779 |
rs539963570 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431845 | TTTAGGATTAGAACC[-/T]TAAATAGTCAAGATT | 55779 |
rs539998872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324302 | CTAAAACCAGACAAA[C/G]ACAGTACCAAAAATG | 55779 |
rs539999976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366897 | TAGCAACTGGCAGAC[C/T]AGGAGATTCCCTCCC | 55779 |
rs540017947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306908 | CATTAGGTTTGTGTG[C/T]TCTATTTCACTCATA | 55779 |
rs540023742 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387663 | CTGCTTGAGAAGTAC[A/G]GAGAGGGAAGAGTCA | 55779 |
rs540038411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394786 | TGAATTTGTGTTGCG[C/T]CTCATTCAAAGCCCA | 55779 |
rs540056081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394292 | TCCTTCAAGCTACTT[A/C]TTTAATGTCACACCT | 55779 |
rs540074053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400933 | TGCTTGTCTACTAAA[C/T]AGGGTAGTGATGAGG | 55779 |
rs540085458 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315743 | CATACAGCCATTCTG[G/T]TTCATTTTCAGTACT | 55779 |
rs540107964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400405 | TGGCCTCTCCTCTCC[A/G]CAGCTCAACTCGCTT | 55779 |
rs540123095 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288886 | TTTCTTTTTCTTCCA[A/G]TGCTGAGATTGATCA | 55779 |
rs540133553 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331854 | TTTTCAATTTGACCA[A/T]GACAATAAAGACCAT | 55779 |
rs540136524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312427 | GAGCATAAAAGTTTG[C/G]AAAATTTGCAGCATG | 55779 |
rs540191690 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303272 | ACAGGGAGATGTGTA[C/G]AAGAAGGTTTCCTGT | 55779 |
rs540192327 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339748 | GTATCTATTTAGAGT[C/G]TCTCAAATGTGCCCT | 55779 |
rs540212715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295521 | AGTACAGTGGTACAT[C/T]TTGGATTAGAAAAGT | 55779 |
rs540215460 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331199 | TCTGAATTTCAGTAG[C/T]ATGTCACACCAAGAG | 55779 |
rs540235827 | in-del | -/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408881 | AAAAAAAAAAAAAAA[-/G]AGCCCTTATTTTATC | 55779 |
rs540244343 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441114 | CGCACCCAGCTGAGC[G/T]CAGGGCAGGTGTCTC | 55779 |
rs540256767 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439903 | ATAAAACAGACTCTC[A/G]GTTTTTACTTTGCAA | 55779 |
rs540260327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433215 | AGGTGGATCACCTGA[A/G]GTCAGGAGTTCGAGA | 55779 |
rs540261648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424979 | AGTAGGTCCCGGAAG[G/T]CATCAGAGCATTGTG | 55779 |
rs540276912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399495 | CCCTCCCACTAAAGC[A/G]TAAGGTCCATGAGGG | 55779 |
rs540281839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302556 | AGATCACCTGGGAGT[C/T]TGAGACCAGCCTGGC | 55779 |
rs540304930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392466 | GAGTAAGAAAAAATA[C/T]ATAGAATGAATAAGA | 55779 |
rs540309937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311630 | CTAATACAGTAAATT[A/G]GAACCAGTAGAGTGG | 55779 |
rs540313290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406292 | TTTGACCCAATAAGT[C/T]TTCTTGGATCACGAT | 55779 |
rs540327922 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403117 | AAAAGAATCTTACTT[G/T]TGATAACATTTCTTA | 55779 |
rs540336945 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397904 | TTCGAGGTCCCCTTG[A/C]GATTTTAAAATAAAG | 55779 |
rs540343193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301657 | AAATGGACAAAAATT[G/T]TATATATTATCATAT | 55779 |
rs540345011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310654 | TCCCACCAAATCTCA[G/T]GTTGAACTGTAATCC | 55779 |
rs540346797 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306512 | TATTACTAATAACCA[C/T]AAAATAATAATAGTA | 55779 |
rs540379500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411810 | GTTTGTGTCCTCTTT[C/T]AATTCATTGAGCAGT | 55779 |
rs540408931 | snp | A/C/T | 0.000103045 | 0.00717718 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344467 | ACAGACAATTCACTT[A/C/T]TGAAGTCTTAGTAAA | 55779 |
rs540412151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372736 | AGTATAATAATAAAA[A/C]AAAAGAAGAAGAGGA | 55779 |
rs540430777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353051 | ATAACAAGGACGGTA[A/G]GGAGGCAGAGGTGAA | 55779 |
rs540436418 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406354 | TAAATACTGCAACTC[G/T]GTGACATAACTGAAA | 55779 |
rs540455575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446031 | AGAAAAAATGCCTTC[C/T]GCAAAAATTTTGAAT | 55779 |
rs540495279 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372531 | GGGAATTGAACAATG[A/G]GAACACATGGACACA | 55779 |
rs540498185 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352380 | AATCTTGCTGCTGCT[C/T]ACTCTTTGGGTCTGC | 55779 |
rs540509475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403713 | ACCACAAGAGAAGCA[C/T]TATTTAAAGTGAGTT | 55779 |
rs540526641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418612 | CTACCCAGGCTTCAA[C/T]AGCTCCAGCACACAT | 55779 |
rs540567889 | in-del | -/ATGATCACCATTCTAAC | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410828 | TTTCCTGACTTTTTA[-/ATGATCACCATTCTAAC]TGGTGTGAGATGGTA | 55779 |
rs540579141 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315441 | TTTGAAGCAAAAACT[A/G]ATAGAAATAAAAGAA | 55779 |
rs540627078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377839 | TTGTATTTTAGTAGA[C/G]ACAGGGTTTCACCAT | 55779 |
rs540675206 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287408 | CATATCTCTGTAAAA[A/G]CAAACACTGTAACTT | 55779 |
rs540691613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370241 | TTTATGAGGGCAGCA[C/T]CATCCTGAAACCAAA | 55779 |
rs540713897 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341518 | AGTATTATTAGCAAA[A/G]TGGAATTCCTGGACC | 55779 |
rs540785220 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295297 | ACCTCTAACTTCTGG[G/T]CTCAAGTGATCCTCT | 55779 |
rs540797909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350536 | AAACCTATAATTGAT[A/C]ATTGACAGTCTTCTC | 55779 |
rs540797991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357503 | GCCAAGAAAACCAAA[A/G]GTTGCTGGCAAACCA | 55779 |
rs540821880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383519 | AAATTGGAGTGTCAG[A/G]AGGAGCATAAACATT | 55779 |
rs540834625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356907 | TGTGTAAACACACAC[A/G]CACATACACACACAT | 55779 |
rs540843505 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446745 | AAAAGATTATGCAAA[A/C]AACTGACAATTCTCA | 55779 |
rs540878427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343635 | AGAGGTCACTCTGGC[A/G]GGAGCCTGGGTGAGG | 55779 |
rs540923946 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422619 | TAAATGAAGCTATTC[A/C]AGCCTCCTGGAGGAA | 55779 |
rs540943641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322909 | TGGGGACGCCTCAGG[A/T]AACTTAAAATCACAG | 55779 |
rs541002896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370892 | CAAAGTCTCAGGATA[A/C]AAAATCAATGTACAA | 55779 |
rs541013446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348992 | GATAGAATGACAGCC[A/G]AAGAAAGGGACAAAT | 55779 |
rs541022590 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441765 | CTGCCTGATATTCCA[A/G]AATGGCCCAACGGAG | 55779 |
rs541046649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362128 | TTTTAGAAGATCTTG[A/G]TTGAGGGAGAACATA | 55779 |
rs541069850 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414825 | CCTGAGGTTTTCTTT[A/T]TTTTGTTATGTCTCT | 55779 |
rs541096190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431152 | TTTCAGGGGTGGGGG[A/G]AATGCAGCTATGATC | 55779 |
rs541100248 | in-del | -/A | 0.31503 | 0.241394 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325301 | GCCAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs541131097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424276 | CCCAATCTCTACTAA[A/C]AATACAAAAATTAGC | 55779 |
rs541146994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328231 | TTATGTTGAAAATTT[A/T]CAAAACCACAGAATG | 55779 |
rs541163680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337303 | ACTGATGAAAGAAAT[A/C]AAAAATCTAAATAAA | 55779 |
rs541166911 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385132 | TTGCCTGCCGCCATG[-/T]TAAGACATCCCTTAG | 55779 |
rs541201177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292563 | GTGCTTTGCATATGC[G/T]CTCTCATCTAATCCC | 55779 |
rs541211404 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438056 | TGGAAAACTTAAAAA[C/T]GTACTGTTAACAGGG | 55779 |
rs541225947 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414946 | GAATGGTACCAGCTC[C/T]TCTTTGTATTTCTAG | 55779 |
rs541230548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349601 | CTCCCTTGCCCATGT[A/C]CACTATCCCGAGGCA | 55779 |
rs541256689 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390093 | ATATTGATGCAAAAC[C/G]TCAACAAAATACTAG | 55779 |
rs541280414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437291 | CTTTTTTCTGAATAA[A/C]TTTATTTTAACATAC | 55779 |
rs541282246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299551 | ATATGATCCAGCAAT[C/T]GCACTGCTAGATAAA | 55779 |
rs541282287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308578 | AAATCAGACAAAAAT[A/T]TTTTTTTCTTTTTTT | 55779 |
rs541293046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428293 | AGGAAAGGAGTTAGA[A/G]CTGGTAGATAAGGTG | 55779 |
rs541293832 | snp | C/G/T | 0.000155017 | 0.00880263 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396472 | ACTTATAAGGCAATT[C/G/T]AACTATAAAATTTCA | 55779 |
rs541348281 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446017 | GTACTAGCACCACAG[-/A]AAAAAATGCCTTCTG | 55779 |
rs541352918 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307904 | AGAATAGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 55779 |
rs541364569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421968 | AACAAACCTGCATGT[C/G]TACCCTCTGTATCTA | 55779 |
rs541375996 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293284 | TTTGTTGTCACCAAC[G/T]ATATCCCAATTCCTG | 55779 |
rs541431848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342396 | ACTATGAATTCAACC[C/T]CATAATAAGTACTGT | 55779 |
rs541440034 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290734 | TTCATTATCTCCTCA[C/T]CTATATCAAAACCAG | 55779 |
rs541453535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427695 | AAGACAAACAAGCCT[C/T]ATTGTCTTTCTTTCT | 55779 |
rs541455326 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436164 | GTGTTGGCCAGGGCT[A/G]AGAATATTTTCTATT | 55779 |
rs541467041 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347780 | CAGAGATCCCTTCCC[G/T]CCCTCAGGGTATGGT | 55779 |
rs541472175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369489 | GACTACTGGGTAAAT[A/G]ACAAAATGAAGGCAG | 55779 |
rs541485935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402126 | TTTTCTACATACCAG[C/G]AGGCCCCTGGAAGGG | 55779 |
rs541497072 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372947 | TAGTCTGTGGTGTTT[G/T]ATTGTGGCAGCCCTA | 55779 |
rs541520390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395650 | TCACTGCAGGAACCA[A/G]GAGTGGGCTAAAAAT | 55779 |
rs541539623 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295352 | ACTACTGGTGTGCAA[C/T]ACCACACCCAGCTAA | 55779 |
rs541559181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408739 | GTTGTGGTGGGTGCC[C/T]GTAGTCCCAGCTACT | 55779 |
rs541654247 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348203 | GGTTCTTGGGTCGGG[A/G]GGAAGTAAACAAATC | 55779 |
rs541667582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312600 | AGGGCATGTCGGAGG[A/C]CTTCACACAGCCCCT | 55779 |
rs541671648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407651 | AAAAATTCTTAGAAC[A/C]GTGCCTATCATATCA | 55779 |
rs541676864 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291416 | AGAGAGATTCTTAAA[A/G]TGACTTAACGTGACT | 55779 |
rs541713742 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367475 | GCAAACTCCAACAGA[A/C]CTGCAGCTGAGGGCC | 55779 |
rs541741384 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342833 | CGTCTCTGCTAAAAA[A/T]ACATAAAAAAAAAAA | 55779 |
rs541742177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318965 | AAAAAAACAAAAAAA[A/C]ACAAAAAAAAAACAA | 55779 |
rs541744875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413734 | ATGTCTGTTTTGGTA[A/C]CAGTACCATGCTGTT | 55779 |
rs541777046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325662 | AATATACAGTTTTAA[C/G]ACAATTACTATCAAA | 55779 |
rs541783280 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396248 | ACTAGCATGGTCCCC[A/T]GTTGAAATTTTCAAT | 55779 |
rs541795834 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375464 | AAAAAGGATGGAAAA[C/T]CTTCTTGAATGATGT | 55779 |
rs541843684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380834 | CATCAGCACTTAACA[C/T]AGGATATTTTATATT | 55779 |
rs541843717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388795 | AGGTCATTATATAAT[G/T]ATAAAGAGGTCAATT | 55779 |
rs541887796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386879 | TAATCTGGGTACTTG[C/G]GGGAAGGACAGAGCA | 55779 |
rs541896064 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350982 | GGACAGGACAATAGA[C/T]GGTTCCTCCTGGGCG | 55779 |
rs541897678 | snp | C/G/T | 3.307e-05 | 0.00406622 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420033 | CCAATGACGCCAATT[C/G/T]CTTCACCACTGCTAC | 55779 |
rs541922844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386291 | AACCAAGTTGGGTCT[C/T]ATTTTTTTTATTCAT | 55779 |
rs541928484 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289617 | GGCTGCCAGCTCCCA[C/T]GAAGGCCCCGGTGAC | 55779 |
rs541960857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426924 | AAGTTGAACTCCCAC[A/T]AATCTGTAGTGGAGC | 55779 |
rs542028061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360903 | GAAACTGGCTCTCTT[A/G]GGGAAGCTTGATGCT | 55779 |
rs542040511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296468 | CTCCATAATCTTTCA[C/T]CCATTTTACATAATA | 55779 |
rs542064850 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360354 | TCAAAGAAAGATGAT[G/T]ATGAATACTATATGT | 55779 |
rs542069141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352055 | CAGTTGGGGTGTCCT[A/G]TTTAGAGGGGGGATT | 55779 |
rs542098088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392988 | GCTCCCTTGTATCTT[A/C]TCCACACTGCTGCCA | 55779 |
rs542163532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359077 | CAATTAACAATAATA[A/C]AAATAAAGCTACACA | 55779 |
rs542164362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325346 | AAATAGGTGTAAATC[C/T]AACAAAACATGAACA | 55779 |
rs542192230 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436615 | TGACTATGATTGATC[A/G]ATAATGATTTCTTTG | 55779 |
rs542215646 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290020 | CCCAGATTCCTGGAC[C/T]TCAGAAACCCTCTCA | 55779 |
rs542223384 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313480 | TGAGTTAAGACTTTG[A/G]GGGACTGTTGGGAAG | 55779 |
rs542226118 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383666 | CTCTGTGTCGTGAAA[G/T]AACTACTTGGAGATA | 55779 |
rs542269183 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365122 | AATAAACATTTTTCT[A/T]TCCAATATGGGTTTC | 55779 |
rs542273716 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426446 | TTCTCATGATGGTGT[A/T]TGAGTTCTCACAAGA | 55779 |
rs542280386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313182 | AGCTGCCCAAGACCA[C/T]GGGAACCCACCTCTT | 55779 |
rs542283054 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286538 | CAGAAGTGCCCTTGT[C/T]TCGGTTGTAGGTTTC | 55779 |
rs542302912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317517 | CAGCCTTTGCAGCCC[A/G]GCCTGAGTGCATTGC | 55779 |
rs542305499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434878 | AGATAGACTGGTATG[C/T]CTAAAGCAGATATGG | 55779 |
rs542309093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347015 | AACCAACTCTGGACA[C/T]ATCTTGGCGACCCAG | 55779 |
rs542312408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419421 | GTAGTGTTGGATGCA[C/T]AGTATTACATAATAA | 55779 |
rs542334706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331661 | CTGAAGGACTGCAGA[G/T]TAGGCCACCAAGAAC | 55779 |
rs542336228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332846 | TCTAAGTCTTTGGTG[G/T]TCCATGGCAACGAAA | 55779 |
rs542379039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340563 | CCCTCGCAGGGTGTG[C/T]GATGGGGGTGTGGCT | 55779 |
rs542416741 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346364 | CACTCTGTAAAAACG[C/T]ACCAATCAGCGCTCC | 55779 |
rs542450129 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378285 | TCTTTATCCCTTTAT[C/T]CTTTGAACTCCATAC | 55779 |
rs542451591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295798 | ATTTATTACTTAGAG[A/G]TGTTTCATAATTTCC | 55779 |
rs542468800 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113434137 | AACCTGGAGAAGAGA[A/T]ATATGGTCCCTAACT | 55779 |
rs542481952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392605 | TGCTTGAGGTGACGG[A/C]TATCCCATTTACCCT | 55779 |
rs542496726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425459 | ATCATCCTGTTTCTA[C/T]ATATCTTAAAAGACT | 55779 |
rs542496902 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337774 | ATCTCAACCTAAGTC[C/T]GATAACTTATTTAAA | 55779 |
rs542497509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440141 | CGATCTCAGCTCACC[A/G]CAAACTCCACCTCCC | 55779 |
rs542509727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311886 | CTGGAGCAAAGGAGA[C/T]TTTTGTTAGTTTTAG | 55779 |
rs542512054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338930 | GACTCCTCTGCTGGG[A/G]GTGCCTCTGAGACTC | 55779 |
rs542519200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398938 | CACCCAATCAAGTAT[A/G]GTAGAAGTGATATTT | 55779 |
rs542555741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351712 | TTTCAAACTCTCATA[A/C]CAACCTCTGGAGTTG | 55779 |
rs542600677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438988 | TGGACACTTTCCAGA[A/T]GAGCGGAACTACCAA | 55779 |
rs542630532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350947 | AGGGGTCTGACCAGA[C/G]CTAGGAGGAACTCCC | 55779 |
rs542639558 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439440 | GCCTGTCCAACCTCA[C/G]ACTAGCATCACACTT | 55779 |
rs542669558 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349225 | ATGGGAGGCCTTAAG[A/G]AAATATACTCCCCTG | 55779 |
rs542670018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309814 | GGATATTCTTTTAGC[C/T]TCATCTACCTCAGAC | 55779 |
rs542679347 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441212 | CTGTGCTCCTGCTGC[C/T]TGGCTGGCTTCCGCC | 55779 |
rs542681343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431535 | AGGAAAAACTAGGGG[A/G]GAACAAACTAAAGTT | 55779 |
rs542689122 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381256 | ACTAATTATTGTTAT[-/A]TCATTATTAAGTGAT | 55779 |
rs542717277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316237 | AAAAATTTTAAAAAC[G/T]ACATTGACCAGAGTG | 55779 |
rs542726725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316957 | CTGAGAGAGCCTAAA[C/T]TATGGAGTAAACCAC | 55779 |
rs542728081 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323753 | ACCCAATATGAAATA[G/T]ATCATTTGGGCTGGG | 55779 |
rs542732805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411734 | AAATTACCTTGGGCA[C/G]TATGGCCATGTTCAT | 55779 |
rs542767757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411188 | GCTTTTGTTGCCATT[C/G]CTTTTGGTGTTTTAC | 55779 |
rs542797633 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371615 | AATGTAAGACCTAAA[A/G]CCATAAAAACTCTAG | 55779 |
rs542805922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402981 | ATGTAAAAAACATAC[A/T]CTGGGGCTCAAAAAG | 55779 |
rs542836015 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323437 | ACATGGACATAAGCA[C/T]GGGAACAACAGACAC | 55779 |
rs542856405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315529 | GATAGAACAACTACA[C/T]AGAAAAGCAGCAAGA | 55779 |
rs542888750 | snp | C/T | 1.6633e-05 | 0.00288378 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416567 | AAGGATATTCATAGA[C/T]GATAATATCTGGAAA | 55779 |
rs542895903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322900 | CAGCATGGCTGGGGA[C/T]GCCTCAGGAAACTTA | 55779 |
rs542901302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410009 | ACCCGTTTCCTGTCC[A/G]GAAACCTCATGAATA | 55779 |
rs542925681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416930 | TCAGAATCCACTAAA[G/T]AACTTATTAAAATAT | 55779 |
rs542926187 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313960 | TAGAAAGGAGACAGA[A/C]GAGAATCAATAAATG | 55779 |
rs542947623 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384215 | AGGTGCCCGCCACCA[C/T]GCCTGGGTAATTTTT | 55779 |
rs543010292 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328452 | TACAGCTTTCCCCCA[G/T]CTTTCCCCCCCAGTA | 55779 |
rs543018087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350266 | AGAAGGAAAGAGAGG[A/G]AGAGACAGACAAAGA | 55779 |
rs543024022 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361865 | CCACAATTTTTTTTT[-/A]ACCAGAAAACAAACA | 55779 |
rs543052740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301494 | CTGCTTATATGTATG[C/T]TCCACATATCAAATA | 55779 |
rs543108002 | in-del | -/GCTCC | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419192 | CCTGAAACCTCATAG[-/GCTCC]GCTCCGACTGACTTC | 55779 |
rs543109727 | in-del | -/CA | 0.00318978 | 0.0398085 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419625 | CCTATGTGTGTGTCT[-/CA]CATTTTCCTCACCTT | 55779 |
rs543114891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429095 | AAAATTTATAAGAAC[C/T]AAATTATAATTTATT | 55779 |
rs543118774 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302633 | GGGCGTGGTGGCAGG[-/C]GCCTGTAATCCTAGC | 55779 |
rs543119277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382429 | AGAGCACATAAAGGA[G/T]AGAGTGATAGATAAG | 55779 |
rs543119818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389581 | TTAAAAAGTTGTTTT[C/T]TTCAAAAGATAAATT | 55779 |
rs543120390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403683 | AAATTAATTTTGACA[A/G]GAATGCAAATATTTA | 55779 |
rs543143179 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391040 | GAATAGACAAAGCTA[C/T]GCTGAACAGAAAGAA | 55779 |
rs543150721 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293680 | CTTGATCCTTCACTC[A/C]AAAGTTCTTCAGTGG | 55779 |
rs543152828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422762 | GCATGTTAGTAGCTA[C/T]GAGAATAGAAATTGG | 55779 |
rs543155226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356833 | AAAGAAAAAACTTCT[A/G]TTCAACAAACAACTC | 55779 |
rs543168745 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291189 | TCTCATGAATTGCTG[A/C]ATGATAGTTTTTCTT | 55779 |
rs543212916 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290676 | TTTAAAATGTTATGC[A/G]TAATCAAAGGTGATT | 55779 |
rs543245965 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379248 | AAGAATGAAGTTACA[A/G]TAACTATAAACTATA | 55779 |
rs543256676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388984 | CAGGCAGAAAATGAA[C/T]AAGGAAACATTGGAC | 55779 |
rs543262050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348224 | TAAACAAATCAAAAC[C/T]GCGGGCGGTTTTTCC | 55779 |
rs543265611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362887 | TCTACTTTATTTCTT[C/T]CCCATGTATTCCTTT | 55779 |
rs543296237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370159 | CAGAGGTACAAAGAG[A/G]AGCCAGTACCACTCC | 55779 |
rs543298877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314501 | AAGAACATTTGTCAC[C/T]AGCATGCCTATCCTA | 55779 |
rs543310802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307441 | TTTCCCTGACCATAC[A/T]ATTGGAAATAGCAAT | 55779 |
rs543322315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329213 | ACATGAGATGCTTAT[C/T]ACAGGTGCAACTGGA | 55779 |
rs543331504 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426771 | TAAGTACTACTACTG[A/G]CTGGAAGATAGGAAG | 55779 |
rs543356297 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441334 | AGCTACCGCAGGGAG[G/T]ACGAAGGCTATAACA | 55779 |
rs543362407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362027 | CCTCAAGGATAACTG[A/C]CACCAGAGCTGCTGC | 55779 |
rs543396108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375691 | CCACGCGTGTTGGCA[C/T]ACACCTGTAATCTCA | 55779 |
rs543404475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429895 | TTTATTATAGTAACA[C/T]GTATCTTTCAGCAAT | 55779 |
rs543405031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408682 | CCAGCCTGACCAACA[C/T]GGAGAAACCCAACTC | 55779 |
rs543408424 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389394 | TAAGAGAAAAGTTTA[C/T]AGCTATAAGCAACTA | 55779 |
rs543425877 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368700 | ACAGGCAAAATAACC[A/G]GCTAACATCCTAATG | 55779 |
rs543426241 | in-del | -/ACAGAAA | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331526 | TTTACTATCTGCAAC[-/ACAGAAA]ACAGAAAACTGTATC | 55779 |
rs543428155 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419404 | CCCATTATATGTTCT[C/G]TGTAGTGTTGGATGC | 55779 |
rs543462923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368311 | ACCAAGGTTGCAATG[A/G]AGGAAAAAATTGTAA | 55779 |
rs543534098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344138 | CCCAGGAATCTAAAA[A/C]GAACCACTGCCTAGA | 55779 |
rs543547844 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368775 | TGGGCTAAATGCTCC[A/C]ATTAAAAGATACAAA | 55779 |
rs543563563 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316856 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 55779 |
rs543568195 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326578 | TGCCTTTTCTTGCTC[C/T]TGGAGTTTGGTGATT | 55779 |
rs543576887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343471 | AATAACCATTTCATC[A/T]TATTTCATATTTCAA | 55779 |
rs543580504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393218 | GTAATTTACTTTTTA[C/T]TTTAGTAATTTGCAA | 55779 |
rs543614493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354982 | GGTATCCATGGCTTC[A/C]AGACCTGAAGACGGA | 55779 |
rs543633207 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436308 | ATAAATGACCACATA[C/G]TGTGGGTAAAATTGT | 55779 |
rs543633418 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444170 | AACAAGTTTAAAATA[G/T]AAATAAACATCTCAG | 55779 |
rs543648690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307805 | AAACCCTGAAACCCC[A/G]TCTCTACTAAAAAAA | 55779 |
rs543655174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427559 | ACTTCATTTTCAGTC[C/T]ATTTCCTATCATTAA | 55779 |
rs543670168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437095 | AGTGGTCCCTGCTTT[C/T]TTGCTGGCTGTTGCC | 55779 |
rs543677189 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444163 | TTCAAAAAACAAGTT[G/T]AAAATAGAAATAAAC | 55779 |
rs543694551 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443567 | TGATACCACAGCTTA[C/T]AGTACGGTGTCTGCC | 55779 |
rs543696887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342315 | TCCAGCCTGGGGAAC[A/G]GAGTGAGACTCTGTC | 55779 |
rs543706162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314421 | TCAACCTAGGATTCT[A/G]TACCAAGTGAAAATG | 55779 |
rs543715475 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409145 | GTAAGCTGCTCTTCC[C/T]TATCAGGATTGAAAG | 55779 |
rs543722040 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292771 | GGGTTACCCAACACC[C/T]TCTGCCTCTTCTCCC | 55779 |
rs543734910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347695 | TATTCCTGAAGCTAG[A/G]ATGTGGGGAGCTTCA | 55779 |
rs543744749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313771 | CTCTTGCCACCACCA[C/T]GTAAGAAGTGCCTTT | 55779 |
rs543756855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342087 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAAG | 55779 |
rs543769565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347277 | TTGGGCTGAGCCAAC[A/G]GTCAAGAGAGAGGAA | 55779 |
rs543848628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374664 | TTTTGAGATGGGGTC[C/T]TACTCTGTCACCCAG | 55779 |
rs543863625 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336428 | ATAAGGGAGTAATAT[A/T]AACTACCTTATGCCA | 55779 |
rs543877847 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320563 | TGAAGTTATATATAT[A/G]TATATATAATGAAGT | 55779 |
rs543889361 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395511 | TGAGAGAAGATCATG[G/T]TCAACTAATAAGCCC | 55779 |
rs543907146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312025 | TTCAAGAAGTGACTT[C/G]GATACTGTTAAAGGC | 55779 |
rs543915892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319648 | ATTCTTCTCATCTGC[A/G]CACAGAATATAGTCT | 55779 |
rs543918795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305393 | TATAAAGTTTTGTGA[A/G]TAAGAGCCCAGAAGA | 55779 |
rs543924015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414916 | CTTTTCAAATGTCTG[C/G]AATAGTTTCAGAAGG | 55779 |
rs543966415 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312344 | CACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 55779 |
rs543988684 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407014 | CTGCAGCTTGAGACC[A/G]GTGAACGTAAAAGCC | 55779 |
rs544004978 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346275 | AGGATTGTAAATGCA[C/G]TAATCAGCACTCTGT | 55779 |
rs544058106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380109 | AGTTACATATGTATA[C/T]ATGTGTCATGCTGGT | 55779 |
rs544066293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297710 | ATATATTTTACTTTT[A/G]TTTTTGTCTTTCCCC | 55779 |
rs544092811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387728 | GGGCACAGTGGAATA[C/G]AGCACTAAGTGGGCA | 55779 |
rs544103021 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290189 | ACACAGAAAGTGATT[A/T]AAAAAAAAAAGTGGG | 55779 |
rs544119154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324532 | GATCATGAATCAATG[C/T]AGACAGGCATCTGAC | 55779 |
rs544133134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394465 | GCAGCTATCACTCCC[C/T]TCACCTGAACCATCT | 55779 |
rs544158543 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353046 | ATTTAATAACAAGGA[C/T]GGTAGGGAGGCAGAG | 55779 |
rs544197985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332702 | GGGCATCAGAATGAT[C/G]AGGATGATTGAAAGT | 55779 |
rs544199000 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289558 | GTATCGCCTCAAGAC[C/T]TTTCTCAGAGACCAG | 55779 |
rs544209000 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289057 | GTGTGCCAGGAGCAG[G/T]ATAGCTTCCCAGCCA | 55779 |
rs544210057 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430166 | TAGAAACCAATAATG[A/G]TAAGATACCTTGAAA | 55779 |
rs544211021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296347 | TCATTTTCTCATTGT[A/G]GTTTTAATTTGCATT | 55779 |
rs544218058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435045 | CATTGTCTAAACATT[C/T]GTATTATAAACTATG | 55779 |
rs544235369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418714 | TTTTTGTTTTTTGGG[G/T]TTTTTTTTTGAGACA | 55779 |
rs544268054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393706 | TTTTTTGTAGAGACA[C/G]GGTTTCACTATGTTG | 55779 |
rs544274728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295607 | GCTAATGAGATAAGA[C/T]AGGAAACTGGAGAAG | 55779 |
rs544279330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433916 | TTGTGGTGCACTTTG[A/G]TTTTCCAGAGGTCCA | 55779 |
rs544307857 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386166 | GTTATTCTTTGTATC[C/T]TATGATAGTTTTTTA | 55779 |
rs544308549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399577 | AAGGCCTGGCACATT[A/G]TCGGCACTCTGTAAA | 55779 |
rs544320140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406580 | AGTGAGCGGAGATCG[C/T]GCCACTGCACTCCAG | 55779 |
rs544344987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406349 | TAACATAAATACTGC[A/G]ACTCTGTGACATAAC | 55779 |
rs544388667 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295005 | TTTGATTAAAGATAA[A/G]AATATAAGTATGCTC | 55779 |
rs544432151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366951 | GCCCATGGAGCTTTG[C/T]TCACTGCTAGCACAG | 55779 |
rs544446786 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391933 | TGTGGAGTAAATTAT[A/G]CTGTTGGTAGGAATG | 55779 |
rs544465927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303455 | AAAGTGAACCACAAA[A/G]TGATATAAATATCAT | 55779 |
rs544480231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358123 | TCTATTTATATGGAA[C/T]TCACAAACAAAACTA | 55779 |
rs544480928 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332007 | AAAGTTCACATGGCT[A/G]TTAAGTGGCAGAGAT | 55779 |
rs544483988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398079 | AAAAAGCTGTACACC[A/G]TTCAACTTCAGTTGA | 55779 |
rs544484079 | in-del | -/TT | 0.495016 | 0.0496707 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343060 | TTCTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 55779 |
rs544506484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311508 | AAGTGCCTTTCACCT[C/T]CTGCCATGTTTCTGA | 55779 |
rs544543014 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113442063 | ACTGTGGTCATATTG[C/T]TTTTTAAAGTACCTA | 55779 |
rs544550220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331914 | ATGAGGTATACCAGA[C/T]ATGTCTTATTGTTAA | 55779 |
rs544551714 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316240 | AATTTTAAAAACTAC[A/G]TTGACCAGAGTGAAA | 55779 |
rs544568009 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386559 | GATGCCTAGGTTGTA[A/C]AATCAATAAGTCTTC | 55779 |
rs544591914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364906 | CAGTGCTGAGCTTAG[A/T]TGTTTTCTGTTGTTT | 55779 |
rs544605509 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341533 | ATGGAATTCCTGGAC[A/C]GGAAACTCTAAGAAT | 55779 |
rs544617084 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410248 | TTGGTGTGCTTCACC[C/T]ATTAACTCAACATTT | 55779 |
rs544621853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378364 | AAGGGTAGAGGAACT[A/G]ATAAAGGATGTCCTA | 55779 |
rs544629034 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371602 | GATTAAAGACTTAAA[C/T]GTAAGACCTAAAGCC | 55779 |
rs544656283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433226 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 55779 |
rs544658452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385651 | TTTGTTTGTTTGTTT[G/T]TTTGTTTTGAGCTGG | 55779 |
rs544662289 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382221 | GAAAGAATGACAAGA[C/T]GTGGGAGAGGGAACC | 55779 |
rs544669054 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435629 | AGCTACTCAGGAGGC[C/T]GAGGCAGGAGGATCA | 55779 |
rs544753369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330917 | CTTCCCACGATTTGT[G/T]CCCTCCAGCTGGCTC | 55779 |
rs544782516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345934 | ATACATACTATCTTT[C/T]TCATCTCTTTAAGAC | 55779 |
rs544802485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376895 | TGATGATACAGGAGA[C/T]CAAGTGGTTTATCTC | 55779 |
rs544806076 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439578 | AGTTTACCATGGCAC[A/G]CATATTCCATTGCAA | 55779 |
rs544837788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302665 | ACTCGGGAGGCTGAG[C/G]CAGGAGAATTGCTTG | 55779 |
rs544869319 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321156 | ATCCAGCAGCACATC[-/A]AAAAAGTTAATTCCC | 55779 |
rs544883879 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358118 | AACACTCTATTTATA[C/T]GGAATTCACAAACAA | 55779 |
rs544896011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345136 | ATAATAGATTATTAT[A/G]TAAAATGTATAATAG | 55779 |
rs544917973 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384234 | TGGGTAATTTTTTTG[C/T]ATTTTTAGTAGAGAC | 55779 |
rs544925044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316844 | ACTGCACTCCAGCCT[G/T]GGCAACAGAGCGAGA | 55779 |
rs544926946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344294 | TTAAAGAGGAAAGTG[A/G]ACATGGAGCATTTCT | 55779 |
rs544928818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350140 | GAACAGCAGCATAAG[C/T]GGCTGGCAGAGGCAG | 55779 |
rs544944458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411111 | GCCTGTTCACTCTGA[C/T]GGTAGTTTCTTTTGC | 55779 |
rs544955354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323926 | GCACGTGCCTATAGT[C/G]CCAGCTACTTGGGAG | 55779 |
rs544966362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446879 | AGTGATATGGTTTGG[C/T]TGTGTCCCCACCAAA | 55779 |
rs545060258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323475 | TATTAGAGTGGTGAG[A/G]GAAGGAGGGGGGCAT | 55779 |
rs545060709 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409978 | AGGGAGGAACCCTAA[C/G]TTCCAGGAATTGCCC | 55779 |
rs545095827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424860 | TATTTGTCTAATACA[A/G]ACCCTCCCATCCTGG | 55779 |
rs545096634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438170 | CACTCAGAAATGGCA[A/G]TTGTTTTTACTATAC | 55779 |
rs545099549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322145 | TAGTAACCAAAACAG[C/T]ACAGTACTGGTACAA | 55779 |
rs545132878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417805 | ATCAGAGTCAAGAAG[A/C]AAACGGGCCTAAGAA | 55779 |
rs545138070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338342 | AACAGAAAATATTTG[C/T]AAACTATATATCCAA | 55779 |
rs545172256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314743 | TATACAAGTATATTA[C/T]AAATGGGGGAGGGTA | 55779 |
rs545212686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355074 | TGGGACCCAGGGGAA[A/C]GGGTGGGGGATGGTG | 55779 |
rs545223646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384172 | TACACCATTCTCCTG[C/G]CTCAGCCTCCCAAGT | 55779 |
rs545227272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409408 | AAAGAGAGGGAGTCA[G/T]CCCATGGTGATGTAA | 55779 |
rs545234481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321601 | TTGCTGGTGATATGA[G/T]TCTATACTTAGAAGA | 55779 |
rs545239420 | in-del | -/TAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342837 | CTGCTAAAAATACAT[-/TAA]AAAAAAAAAAAAATT | 55779 |
rs545247928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362236 | GTGTACCGGAGTGCT[C/T]TGTGAAGAATCCTTT | 55779 |
rs545257261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424360 | AGAATTGCTTGAACC[C/T]GGCAGGCGGAGGTTG | 55779 |
rs545275026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328360 | TGATAAGAGCCGAAG[C/T]ATCCCAAGTCCTGGT | 55779 |
rs545289975 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390849 | AGAAATTGAAGAGGA[A/T]CAAAAAAAGGAAAGA | 55779 |
rs545296317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292719 | AGTCCATACTTTTTC[C/T]ATTACTCCTATGTAC | 55779 |
rs545308171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327605 | GCTAGGATTCTTCTG[C/T]CCACTCATACTTGCA | 55779 |
rs545308263 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308937 | AAGTTATCTGAAATA[A/C]AGTAATGACATTTCT | 55779 |
rs545371850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291877 | ACTGTTCCTTAATCT[C/T]GGGAGCCTTCAATTC | 55779 |
rs545391288 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428342 | GCGAGTGAATACAGA[A/T]GAAGGAGAAGACGTA | 55779 |
rs545403090 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353991 | GACATAGGATATTCT[G/T]CTCAGAAGAGTGTTG | 55779 |
rs545406663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300386 | GTTTGTAACATAAAA[C/G]ATAAATGCTTGAGGT | 55779 |
rs545428054 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422025 | GGTATAAAAATCTAA[A/G]TTATATAAAACATCT | 55779 |
rs545444283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298707 | GATAAACCTGAAAGA[C/T]ATTATCCTAAATAGA | 55779 |
rs545460396 | snp | G/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396592 | GGGGTTTGAAAACCT[G/T]TTTCAACTGAATATC | 55779 |
rs545463496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389034 | AAATTGACCTAATAG[A/G]TATTTATAGAACTTT | 55779 |
rs545506972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297914 | TGAATTAGAATAGTA[C/T]AATTGGCATGGCTGC | 55779 |
rs545513331 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414483 | CCCATTCAATATGAT[A/G]TTGGCTGTGGGTTTG | 55779 |
rs545536910 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436248 | ACTGTTTTTTTTTTT[A/T]AATAAAGAATTATGC | 55779 |
rs545603464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370112 | CAACCAAAAAAAGTC[C/T]AGAACCAGACAGATT | 55779 |
rs545625739 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386958 | AGCAGCTTTGGGCAC[A/T]ACTCAGCCAGTGCCC | 55779 |
rs545639518 | snp | C/T | 0.000237901 | 0.0109038 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401219 | AAAGTTAGGAGAAAA[C/T]AAGAATAATAGGCAA | 55779 |
rs545696146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366865 | TTCTGCCCAAATACT[A/G]CGCTTTTCAAAAGTC | 55779 |
rs545697859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336032 | AGTGATAATAAATGT[C/T]TACCATATGAAAATG | 55779 |
rs545766039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313310 | TTTTGGTCAATTTAT[C/T]CCATTTGCAATGGCT | 55779 |
rs545779409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437031 | GAAGAATCTACTTCT[G/T]GGCTCATTCAAGCTG | 55779 |
rs545801125 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351056 | AAACTCTTGTAGAGG[A/C]AGGGTTAGGAAAATT | 55779 |
rs545820313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389501 | TCAAAATTAGTAGAA[G/T]AAAATAAATGAAAAA | 55779 |
rs545852889 | snp | C/T | 1.7177e-05 | 0.00293056 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373364 | GAACAAAAGCATAGA[C/T]ACTAACAGGATATGG | 55779 |
rs545862101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368245 | ATACAGAGAACACCA[C/T]AAAGATTCTCCTTGA | 55779 |
rs545868464 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425861 | TGGGTTGGCACACAT[A/T]TTTTTATAAAGGGAA | 55779 |
rs545875415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328117 | AGCTTATGAGCTCTC[C/T]GAGTGGGTAGTGTTT | 55779 |
rs545896197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307394 | ACAGATAATAAATCA[C/T]CCAGAGAGCCCCCAA | 55779 |
rs545981690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361328 | AAGCTAGATTCACTG[A/G]GGCAAAAGTTGCGTA | 55779 |
rs545987274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354010 | AGAAGAGTGTTGTCT[C/T]AGTAGCTGGAAAAAA | 55779 |
rs546035557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341246 | GATGGAGCCCCAGCC[C/T]GGGACCACGCCTTTC | 55779 |
rs546040036 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427643 | AATTTCAACTAAATT[C/T]AATTTTACTAACTTT | 55779 |
rs546056012 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290135 | TGACTAGCATATTTT[A/T]AAAAATACTTGAAAG | 55779 |
rs546071246 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375914 | AGAGGAAGAAAACTG[C/T]GGAAAAAATTACCTA | 55779 |
rs546077183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434927 | GACAAAGGAGAGTGT[A/G]GTATGATGACTGTCT | 55779 |
rs546079876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347214 | CTCTCTAACAACCCC[C/T]GACTCTGGAGTTGGG | 55779 |
rs546106403 | snp | A/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402774 | CTTAGGAAATACTGG[A/T]GTCCATGAAGGGATC | 55779 |
rs546118974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352430 | AACACTTGCTGCAAA[A/G]GTCTGCGGCTTCATT | 55779 |
rs546138439 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441612 | CTCTCCGGGAACCCG[A/G]TACCTATCCGCCCTT | 55779 |
rs546192827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351757 | TCCCCTTTCTGGTCC[C/T]GTGACAGCCATCTTG | 55779 |
rs546244908 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113291911 | TGCTAAAATCCCACC[A/G]TTAGAAATGTGTGCC | 55779 |
rs546258042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319037 | CAAAATCAAGTCTAC[A/G]TAACAACCAGCTAAC | 55779 |
rs546271425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413781 | TGTAGTATAGTTTGA[A/C]GTCAGGTAGTGTGAT | 55779 |
rs546288597 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420105 | ATCAGTTGGTTCCCA[C/G]CTATGTATATGGCGA | 55779 |
rs546290391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427531 | CCTTTTCTGTTTGTT[A/T]ATCTCCATTTTCACT | 55779 |
rs546296695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325792 | AAGTAGGAGGAGTTA[A/G]TCTACCTGATTTAAG | 55779 |
rs546297365 | snp | A/G | 3.4046e-05 | 0.00412576 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433548 | CTTTTAAAAGTATAC[A/G]TATTATCTTTACTTA | 55779 |
rs546312920 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301536 | TTTTAAAAGATAATT[A/C]TCTTTATACCATACA | 55779 |
rs546324060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392657 | ATGCCTTATCAAAAT[A/G]TCTCATGTACCCCAT | 55779 |
rs546327257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420683 | ACAGTAAAAATATTA[C/T]GTAGGCCTTTTCCTT | 55779 |
rs546403364 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311005 | ACTTACCCAATATCA[A/G]GTATTTCTTTATAGC | 55779 |
rs546434992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434240 | GGTACTGTGGGCATG[C/T]ATAGCAAGAAGCCTA | 55779 |
rs546440127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317030 | ATTGAGAGGCAACAG[C/T]GAAGGTGAGGCTGAA | 55779 |
rs546451969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427077 | TTATCATTCCCACAC[A/G]TATGTACATCCTGCA | 55779 |
rs546467670 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340656 | GCTCCGACCCCATGG[C/T]AGTGTCTAGGGGTGA | 55779 |
rs546470719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305268 | GAATCTGCTTTGTTG[C/G]GCTGTGATTAAGTGC | 55779 |
rs546472612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296537 | CTCTCACTCCAAGAT[A/G]AACAAGTCCCTCTAA | 55779 |
rs546502868 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323022 | TTATAAAGCCATCAG[A/C]TCTCATGAGAACTCA | 55779 |
rs546525899 | snp | C/T | 1.67553e-05 | 0.00289437 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399856 | AAAATAGCATTGATA[C/T]ACCATATTTACCAAT | 55779 |
rs546536292 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435189 | ATAGTAAGACCCTGT[C/T]TGTATTAGTTTGTTC | 55779 |
rs546543221 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339454 | CACTGCGGTATGTAC[A/C]AATGAAGTAGGGGAA | 55779 |
rs546546678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418169 | CTCTGCTGTCTGCAA[A/C]CTCTGCCTCCCAGGC | 55779 |
rs546580002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346115 | CACCAATCAGTGCTC[C/T]GTGTCTAGCTAAAGG | 55779 |
rs546584534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424520 | AAAGGGTTAATTAAA[A/G]GAGTACTTAGGGAAT | 55779 |
rs546620976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385270 | TTATCAGTAGTGTGA[A/G]AACAGACTAATACAA | 55779 |
rs546628419 | in-del | -/G | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432706 | TGCTTACTATTTTTA[-/G]TATACTGCCTTAATA | 55779 |
rs546631677 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301274 | TACAAAGTTCTAAAG[C/T]AATATATTATTTAGA | 55779 |
rs546645937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424124 | AACATTGCTAAAATT[C/T]AGAAGACATAAATTT | 55779 |
rs546650037 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405440 | CAGCTTCTGTTCTAG[C/T]TCATTTCCTTGACTC | 55779 |
rs546659529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392198 | TGTAGTACATATACA[C/G]AATGTGTACTCTTCA | 55779 |
rs546715769 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374346 | CTGCTTTACTCCCTG[A/G]AGCAACTGTCAATTT | 55779 |
rs546716111 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287860 | CATATGGTGCATAAT[A/T]AATTCACTTCCCTTC | 55779 |
rs546720816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372679 | CATATGTATACCTAC[A/G]TAACAAATGTGCACG | 55779 |
rs546769236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338456 | TATTCAAATGTGAGA[A/G]AAAGACACGAAGAGT | 55779 |
rs546777014 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349569 | TTAAAAAAGATTGTC[C/T]AATGAGAAACAAGCT | 55779 |
rs546785435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446976 | TGAATCATGGGGGCC[A/G]GTCTTTCCCATGCTA | 55779 |
rs546785753 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391113 | CAGAGATACAGGAAC[A/C]AAAACAGCATGGTAC | 55779 |
rs546818789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300681 | CAAATCAAGAGAAAA[A/G]TGAACAAAATACATG | 55779 |
rs546832548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364332 | TTGCTGTCATTTGTT[A/G]TAAGTAAATAAAGAT | 55779 |
rs546833499 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318289 | CACTACAAGAATTTC[A/G]TAATATGATTGGAAT | 55779 |
rs546876451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299987 | AGTAAGCCATGATTG[C/T]GCTACTGCACTCCAG | 55779 |
rs546878367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308905 | GCCACTGTGCCTGGC[C/G]CTGAAAAGATTTTCA | 55779 |
rs546890468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308393 | AATATAAGAGTTTAA[A/G]ATGGTTAAGGACACA | 55779 |
rs546900088 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317477 | GGCCCATGCCTCACC[A/G]CCCTGCAGGAGCAGC | 55779 |
rs546900183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439141 | AATTTCGTTTCATTA[A/G]ATCCAGGCTTATTCG | 55779 |
rs546903995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410698 | AAATGGTATTTCTAG[C/T]TGTAGATCCTTGAGG | 55779 |
rs546911006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403063 | ACAGTAAGCTCAATC[A/G]GTGGCAACAGAGTGA | 55779 |
rs546947734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410044 | ACTCCTTGTTTAGCA[C/T]ATAATCAAGAATAAC | 55779 |
rs546950908 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343378 | ACTAACAAGTTCCTA[-/T]TTGGGGAATTACTCT | 55779 |
rs546998495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396017 | TCTAAAACTTGCTCA[A/T]TTTTCCCCATTAGAG | 55779 |
rs547000523 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315630 | AACAGCAGAATATAC[A/G]GACAGTTTCTGACTT | 55779 |
rs547031970 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312914 | AGGCAGAAGTTTGCT[C/G]CAGGGGTGGGGCACT | 55779 |
rs547053047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377229 | GTAGAATTGGCCTGC[A/T]GTGTGAGTATTGATT | 55779 |
rs547088436 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444769 | TATAAACAAACACTC[A/C]CAGGCCTATTGTTTT | 55779 |
rs547091216 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384373 | CCCAAATAGTTGACT[A/T]TTAAGCTTGAGCTCT | 55779 |
rs547106218 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291231 | AAAATTCAGGATACC[C/T]CCAAATCAAATTTTC | 55779 |
rs547109487 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441143 | TCACTGGAGCGGGGA[-/G]CCCCAGCACCTTCCC | 55779 |
rs547119563 | snp | A/G | | | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429024 | AGAACACTATAAGAA[A/G]GCCTACAAATGCTAT | 55779 |
rs547127960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383758 | ATAGCTGACCTTTTT[A/T]AAAAAATTATACTTT | 55779 |
rs547154429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438297 | GCAGGTCACACATCT[A/C]AACATCCACCCCAGC | 55779 |
rs547217059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390337 | GACTGGGTAGAGAAG[A/G]AATATACCTCAACAC | 55779 |
rs547218293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349862 | AGGTCTGTTACCATC[C/T]GAGGAATCCTGGGAC | 55779 |
rs547222682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375010 | TATTATTTGGCCTTG[A/G]AAGGAAATTCTGACA | 55779 |
rs547223952 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439609 | TGCCTTACTCCCGAA[A/T]AAACATCATCTTCTT | 55779 |
rs547286979 | snp | C/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393582 | CCAAGCTGGATGGAG[C/G/T]GCAGTGGCACGATCT | 55779 |
rs547330972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315002 | TCAAGTAACCCACAG[A/G]AAAGCAGGAAAAATT | 55779 |
rs547360257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349414 | CAAGAGGAACATGCC[A/G]AAAAGGAAAAGCGAG | 55779 |
rs547365810 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367114 | TACTGCCTCTATAGA[C/T]TCCACCTCTGTGGGC | 55779 |
rs547385871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362569 | AGGCATCAGAAACCC[C/T]AGGGCCTCCACAGAT | 55779 |
rs547388937 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291028 | AGCCCTCAAAACACT[C/G]CTTTATGAAGTCAAC | 55779 |
rs547394506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355291 | TTTGGGAGGCCTAGG[C/T]GGGTGGATCACGAGG | 55779 |
rs547415638 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433265 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 55779 |
rs547426821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369834 | ATAGAGAGAGCACTG[G/T]CAAGACTAATAAAGA | 55779 |
rs547430768 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441522 | GTTTACTCCGGTTAC[C/T]GAGACAACGCCACCC | 55779 |
rs547436970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416006 | CTAAGTCTCTTAGTA[G/T]GTCTCTAAGAACTTG | 55779 |
rs547439920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342638 | CACATACCAACTGAA[A/G]TGCTCTGAAGCCAAC | 55779 |
rs547478309 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347929 | AATCCGATTTTTCTC[A/G/T]GTCCTCATTGTGGTC | 55779 |
rs547500822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298067 | GCACGTGTGTGCTGG[C/T]CTGTGGCTGCCTGCC | 55779 |
rs547523625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388235 | GCCTTGGGCAAGACT[C/T]GGTGCTATTCTGGCT | 55779 |
rs547587601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336358 | GAATATGAAAATTAA[C/T]AATATAAATAAAACA | 55779 |
rs547601295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422998 | CTTCTCTCCATCTCT[A/G]TTTCCCAGAATGCCT | 55779 |
rs547602349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360732 | CACTGTGGTAGTTTT[A/G]TCAGCATACAGAATT | 55779 |
rs547605005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429196 | TATACTTTGGCTATT[A/G]TGAAGTAACTAGTAC | 55779 |
rs547624490 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389717 | GATCAGTAGAGGCTA[A/C]TATGAGCAACTTTAT | 55779 |
rs547661418 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444145 | GCCAGGGAGCAGAGA[C/T]CATTCAAAAAACAAG | 55779 |
rs547666765 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386300 | GGGTCTTATTTTTTT[A/T]ATTCATTCAGCTTCT | 55779 |
rs547675921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389042 | CTAATAGATATTTAT[A/G]GAACTTTTTATCCAA | 55779 |
rs547716226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343010 | AATAAATAAAAAATT[A/T]AAAAAAAATGGCTGT | 55779 |
rs547729796 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352788 | GCTGAACCCCACCAA[C/T]AATAAAAAGGATGCA | 55779 |
rs547731191 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367835 | CAAAGAAGCTAAAAA[A/C]CTTGAAAAAAAGGTT | 55779 |
rs547748798 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443612 | ATAAGGAACAGCTAT[G/T]CTTATTATTATGCTG | 55779 |
rs547753149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348231 | ATCAAAACCGCGGGC[A/G]GTTTTTCCTTTCACA | 55779 |
rs547756894 | snp | A/T | 0.000115587 | 0.00760132 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333614 | ACAACCCCCCCACAC[A/T]CAAATATGACAATAA | 55779 |
rs547773215 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369177 | TTATTAGATCAACGA[G/T]ACAGAAGGTTAACAA | 55779 |
rs547774450 | snp | A/G | 8.24137e-05 | 0.00641873 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427241 | AACTTCCTTCCAAAC[A/G]TTCCTCATCTGAGTC | 55779 |
rs547794323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333011 | CTAACTCAACAAAGA[C/T]GTATTAATACTTCTA | 55779 |
rs547807415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414008 | CATGAATGTTTTTCC[A/G]TTTGTTTGTGTCCTC | 55779 |
rs547813007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326001 | TGAAAAGGCAAGCTA[C/T]GCACTAGGAAAAAAT | 55779 |
rs547828427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436441 | AGAGGATACAAAGGT[A/G]AGCAATATACAGTCC | 55779 |
rs547833087 | in-del | -/TTAAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392272 | TGGAACTGGAGGTTA[-/TTAAG]TTAAGTGAAAAAAGC | 55779 |
rs547839911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307546 | TTAATTGACTTCTTA[C/T]ATTTATTGTCTTTCT | 55779 |
rs547895024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401479 | ACAATAAGCAATCTC[A/G]TAACACTTACAGTCA | 55779 |
rs547901553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306817 | AAGCTTAGATCTAGC[C/T]CTAGTGCTATCACCA | 55779 |
rs547906407 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420319 | TTACCCTGAAACTCA[A/T]GATTTTTCTACATAT | 55779 |
rs547932989 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289829 | AGTCATATCCCAAGC[A/G]GCCCTATGGAGAGGC | 55779 |
rs547969544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408087 | TGCTCAATTAGTCTA[C/T]ATTTCTAATAAATGA | 55779 |
rs547971760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313062 | CCCAGAATGGTAGAT[A/C]CACCAACAGCTTGCA | 55779 |
rs548011611 | snp | C/T | 0.000315408 | 0.0125541 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304996 | TTGGGTGTGATGACT[C/T]TTCTCGGACAGGATG | 55779 |
rs548027273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374189 | CACTTTTGACAACAG[C/G]AGACTAGATTGTTTC | 55779 |
rs548037594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421160 | AACAAGAAAAAAATA[A/T]TCCCACTAAAAAGCA | 55779 |
rs548065454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414498 | ATTGGCTGTGGGTTT[G/T]TCATAAATAGCACTT | 55779 |
rs548101431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311698 | CTTTGGAACTGGGTA[A/G]CAGGCAGAGGTTGGA | 55779 |
rs548101803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406410 | TGGGCGGATCACGAG[G/T]TCAGGAGATCAAGAC | 55779 |
rs548104143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352218 | TCTGTAAAATGGACC[A/T]ATCAGCGCTCTGTAA | 55779 |
rs548106487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407310 | CCTAATGCAGTACCC[C/T]CCAGCTATGTGTGAC | 55779 |
rs548170719 | in-del | -/A | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441986 | CAGCGCTCTGGGCAC[-/A]AAAGTATAGGCCTCC | 55779 |
rs548175869 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341498 | AAAAATCATTCTGAC[C/T]ATACAGTATTATTAG | 55779 |
rs548210256 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290283 | TTCTGACCTCTTAAA[C/T]AGGAATATGAAGGAA | 55779 |
rs548224592 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426821 | AAGGAAGAGCCATTA[G/T]GCCCACGTGCATCAG | 55779 |
rs548241573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380144 | TGCACCCACTAACTC[A/G]TCATCTAGCATTAGG | 55779 |
rs548245181 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447144 | CAGCCATGTGAAACT[C/G]TAAGTCCAATTCAAC | 55779 |
rs548277744 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387312 | GGAGAGGAGGGGGAA[A/C]AATAAAGAGGACTTG | 55779 |
rs548379361 | in-del | -/CAC | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393843 | TCTTGCTTCCTCTCT[-/CAC]CACATGATCTCTATA | 55779 |
rs548381764 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441742 | GACATGAATACCGTC[C/G]AAGATACCTGCCTGA | 55779 |
rs548445403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385225 | TTAAACCTCTTTTTA[C/T]TTATAAATTACCCAG | 55779 |
rs548449314 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337274 | AGAACTTTTTATGCT[A/G]AAAACAGCAAAACAC | 55779 |
rs548460984 | in-del | -/TAT | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345153 | AAAATGTATAATAGA[-/TAT]TATAATAGATATATA | 55779 |
rs548460995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359590 | TAGCATAAAGGTCTT[A/T]TAACTATTTTGACCT | 55779 |
rs548482506 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391949 | CTGTTGGTAGGAATG[C/T]AAATTAGTACAACCA | 55779 |
rs548485336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318415 | GAACCAAATCTCTGA[A/G]ACATATGAGATTCTA | 55779 |
rs548488742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399152 | GCTTAGCCTAGCCTT[C/T]AAGTCATCCAACCCA | 55779 |
rs548536759 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320209 | ACTATTCCAGAAAAT[A/T]GAGGAGGTATATTAG | 55779 |
rs548594192 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300699 | AACAAAATACATGAA[A/C]AGACATTTTATAGAA | 55779 |
rs548616297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391424 | AACTCTCCAGGACAT[C/T]AGACTGGGCAAAGAT | 55779 |
rs548648037 | snp | C/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296366 | TTAATTTGCATTTCT[C/G]CAATGATTAGTGATG | 55779 |
rs548684902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351233 | AATCCCAAACTTACA[A/C]GGTTTTCAACAAAAG | 55779 |
rs548700324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323930 | GTGCCTATAGTCCCA[G/T]CTACTTGGGAGGCTG | 55779 |
rs548737221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332124 | TTAAGTTGAAGATAT[C/G]ATACCTGCCCATCTC | 55779 |
rs548758387 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371846 | GACAAAGGGCTAATA[C/T]CCAGAATCTACAAAG | 55779 |
rs548793055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433346 | AGGCAGGAGAATCAC[G/T]TGAACCCAGAAGACG | 55779 |
rs548793361 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418350 | CCTCAGCCTCCCAAA[A/G]TGCCATGATTACAGG | 55779 |
rs548797550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378046 | TTTCTGTTTGTGTTT[C/T]GTTGTTGTTGTTTGA | 55779 |
rs548798378 | snp | C/T | 6.70668e-05 | 0.00579042 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363352 | GTTGTGATACAGAAA[C/T]AGCAGAGAAAGAGAA | 55779 |
rs548807341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339427 | CCTTATCCCTGAGCT[G/T]GCCATAGGTACCACT | 55779 |
rs548905891 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429084 | CTACTTTATAAAAAA[-/T]TTATAAGAACTAAAT | 55779 |
rs548936980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371094 | GAGGACACAAACAAA[C/T]GGAAGAACATTCCAT | 55779 |
rs548946599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345542 | TTCCATGTTTAATGA[C/T]ATTTAATGAAAGTCC | 55779 |
rs548957507 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412315 | TCTATGGATTCACCT[A/C]AAATTATTTCTTGCA | 55779 |
rs548971755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424415 | CACTCCAGCCTGGAC[A/G]ACAGAGCAAGACTCC | 55779 |
rs548972651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336741 | AATGGTCTAAATATA[A/C]CATTGAATGACAGAA | 55779 |
rs548977198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344460 | TCTGTCCACAGACAA[C/T]TCACTTTTGAAGTCT | 55779 |
rs548985492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350666 | GAGATCCTTGGCCCA[G/T]TGGCCCACAGATGGC | 55779 |
rs549000704 | snp | A/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330403 | GACCCTGTCTGTTCC[A/G]CTCCGGGGGACTTTT | 55779 |
rs549076034 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322970 | CATGGCAGCAGGAAG[A/G]AGAAGTGCAGAGTGA | 55779 |
rs549098091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423236 | TCTCCCACCTCAGCC[C/T]CCCAGGTAGCTGAGA | 55779 |
rs549139290 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434526 | GGGTTTTAAAGAGGG[G/T]AGCGACACAACAGGT | 55779 |
rs549140678 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444684 | ATTACCATTATTGAT[A/G]ACATTTTCACATTTA | 55779 |
rs549151271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375429 | GATCAGAAAAAATAG[A/G]CTAAAGCATGGAGAA | 55779 |
rs549160238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410628 | TGCATGTGTCTTTAT[A/G]GTAGCATGATTTATA | 55779 |
rs549165719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300605 | TATTTGGAAAACCCA[C/T]AACCAACAAAGGATT | 55779 |
rs549165978 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412853 | GTGCATGTCTCTTTA[C/T]AGCAGAATGATTTAT | 55779 |
rs549195861 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113308227 | CATCACTCTCCAAGC[C/T]AGATTCTTCTTCACT | 55779 |
rs549229249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370470 | CATAAACAGAACCAA[C/T]GACAAAAATCACATG | 55779 |
rs549244491 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290043 | CCCTCTCACTCCTGG[G/T]TGAGATCACAAGTTT | 55779 |
rs549246954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314925 | GCAACAACTTAAACA[G/T]TTATACGAAGAGATG | 55779 |
rs549259110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307708 | GGCACGATGGCTCAC[A/G]CCTGTAATCCTAGCA | 55779 |
rs549264063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376033 | AAACTAAAATATATT[A/G]GTAATTACATTAAAT | 55779 |
rs549264475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416748 | TACTCTAATAGAAAA[C/T]TCAAAAATGGGCATC | 55779 |
rs549285766 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314201 | TCCAAACAGGAGACA[A/C]CCAAATAAATTTATG | 55779 |
rs549289940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409480 | CTCCATCTTTGGCTT[C/T]AGAATGAATTATGTT | 55779 |
rs549292555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329631 | GAACATCCTGCCCAA[A/C]AGGCCCTAGTCTGGT | 55779 |
rs549297277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410310 | CCCCCTCTCCCACCC[C/G]ACGACAGGCCCCGGT | 55779 |
rs549301207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417265 | GGAAAAAGTTACAAA[C/T]GAATGTAAACTTACC | 55779 |
rs549312786 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113338739 | TTTGCTGTAAGTCCT[G/T]TAGGGAGAAGGGGAC | 55779 |
rs549396517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395490 | GCCTGATATAACCCT[C/G]GTTTTTGAGAGAAGA | 55779 |
rs549431451 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321692 | ACAAAATCAATATAC[A/C]AAAATCAGTAGCATT | 55779 |
rs549434629 | snp | C/T | 1.7416e-05 | 0.00295088 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401789 | AGTAGTTTCTGAACA[C/T]TTATTTTCTAAGCCA | 55779 |
rs549443662 | in-del | -/CTTAG | 0.000140795 | 0.00838916 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294014 | CAAACTGTTGGAACA[-/CTTAG]CTTAGACCATTTCCA | 55779 |
rs549478158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383083 | GGCAAATATAAAGTA[A/G]TTGGGGAAATTCAGA | 55779 |
rs549501676 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414726 | GGCGTGATCATGGTG[G/T]ATACGTTTTTCGATG | 55779 |
rs549514950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389766 | CTTGAAGAAATAGTA[A/C]AATTCCTAGACACAT | 55779 |
rs549546748 | snp | C/T | 0.000103697 | 0.00719984 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291568 | AAACTCAAAGGTCTG[C/T]GGGCTGTATCTCTTT | 55779 |
rs549574883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355207 | ACTACCTGTTCCCCC[A/C]AAAACCTATTGAAAT | 55779 |
rs549598210 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288213 | ATAAACAGGGTCCTA[A/G]GGAAGAGTCACTCTG | 55779 |
rs549610339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290824 | AACTTAGAATTCTGA[C/T]GGAGTTGCAGAAATC | 55779 |
rs549614562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374454 | CAGGTTTGTTACATA[C/T]ATGTGGCAGCTGAGA | 55779 |
rs549618364 | snp | A/G | | | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417270 | AAGTTACAAACGAAT[A/G]TAAACTTACCAGAAG | 55779 |
rs549638144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402416 | ATACTATAGGAAGAG[G/T]GAAGGAGCACAGTTT | 55779 |
rs549645133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327220 | AGCTGTCATACTTAA[G/T]AAACTCACCAGCTTC | 55779 |
rs549657923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362428 | AGGGGCCACCACCAA[C/T]CACCTCTTCTTGAAG | 55779 |
rs549679533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394701 | CACATAAAATACACT[A/G]ACACTAACAACAGCT | 55779 |
rs549681480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387481 | AGAAGGACTCAATCC[C/T]GGCAGGATTCATCAC | 55779 |
rs549698277 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424561 | TGACTTGTTCTTCCT[A/G]GAATTCCTCACAAGA | 55779 |
rs549707530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320947 | CACACCCAGGATCAA[C/T]ACTTTGCATCCTTCA | 55779 |
rs549750318 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380974 | ATAGGAGACTACATC[A/G]TGATCATCCTCTTCT | 55779 |
rs549756945 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308351 | GTAAACTATTTTTCA[A/G]TGAGTTAGTCACTAG | 55779 |
rs549794018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369762 | ATAGAGACAAAAAAA[A/C]CCTTCAAAAAATCAA | 55779 |
rs549811888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422183 | TGTAGCTTAAGCAGA[C/T]AGATTCTTTGTTCAC | 55779 |
rs549814100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374926 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCCCAAAT | 55779 |
rs549849129 | in-del | -/TAAA | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325415 | AAGAAACCGAGGTTC[-/TAAA]TAAATAGAGATATAT | 55779 |
rs549854635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381752 | ATTTCATTCTACAAT[C/T]ATTTGTTGTGTACCT | 55779 |
rs549930106 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352779 | AAAGGAAATGCTGAA[A/C]CCCACCAATAATAAA | 55779 |
rs549971908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334838 | GCTATCATAGTACCT[G/T]GGTACTAATAAAAGG | 55779 |
rs549973428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428407 | GGTTGTGCTACAGAC[A/G]GAAAACTAGAGTTAG | 55779 |
rs549997269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400112 | TCTTAACTAAATCAG[C/T]CAATAACTTTCTTTT | 55779 |
rs549998403 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391852 | ATAAAAACTATGATA[A/T]ATCATCTCATTCCTG | 55779 |
rs550075489 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355468 | GAGGTTGCAGTGAGC[C/T]GTGATCACGCCACTA | 55779 |
rs550101302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400818 | ATTAGGAGAACCAGA[C/T]AGAGTCCTGGGCTTT | 55779 |
rs550114196 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397081 | TAATCACATAAATGA[C/G]TGTGAAATTGTGAAC | 55779 |
rs550171994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340080 | GGCTTTCTCCCGCCC[G/T]GCTCGTGACTGTTGG | 55779 |
rs550172001 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346906 | GCTGCTGCTCACTCT[C/G/T]TGGGTCCACACCACC | 55779 |
rs550185470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347619 | GCCCAAAGCCCCATT[C/G]GGTGGGGAGACCAAC | 55779 |
rs550212462 | snp | C/T | 0.000181478 | 0.00952397 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379513 | TATTTTCTCCTTCAA[C/T]TCCCTTTGTCTCTCC | 55779 |
rs550214905 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441120 | CAGCTGAGCGCAGGG[A/C]AGGTGTCTCACTGGA | 55779 |
rs550240798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313423 | GACTTGCCTTGCCTC[A/C]GATGAGACTTAGGAC | 55779 |
rs550241537 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334074 | CTCCTGCCTCAGCCT[C/T]CCAAGCAGCTGGGAC | 55779 |
rs550279476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312932 | GGGGTGGGGCACTCA[C/T]GGAGAACCTCTGGGG | 55779 |
rs550282907 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366528 | TTAAAATTAGAACAT[C/T]AGGGTAGGTTCTAAT | 55779 |
rs550304297 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325945 | TCAAAGCAATTCAGT[A/C/T]GAAGAGAGACAACCT | 55779 |
rs550308935 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346589 | CTCTGGGTCTAGCTA[A/C]AGGATTGTAAATGCA | 55779 |
rs550315966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312326 | CTGACCTCATGATCC[A/G]CCCACCTCAGCCTCC | 55779 |
rs550347329 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359931 | TTTGTAGATCAACCG[G/T]GTACTGTCTTTTCAA | 55779 |
rs550354730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318705 | ACATACAGAGAGAAA[C/T]CCATCAGGCTAGCAG | 55779 |
rs550360843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413937 | TAGCATTGAATCTAT[A/T]AATTACTTTGGGCAG | 55779 |
rs550376332 | snp | G/T | 1.71102e-05 | 0.00292486 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373380 | ACTAACAGGATATGG[G/T]TTTTTTAAAGCTTTT | 55779 |
rs550376380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440471 | TCCTCTCACCCAATT[C/T]ATGTAGATGATTTCC | 55779 |
rs550405713 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344293 | ATTAAAGAGGAAAGT[A/G]GACATGGAGCATTTC | 55779 |
rs550439830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317630 | AAGATATCCCAGTGT[A/C]TCCAGGGCCGTGGTG | 55779 |
rs550454995 | snp | C/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443966 | TATCAATCCAGTATC[C/T]CTGCCAACCTGTAAT | 55779 |
rs550479346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317133 | GGATGAGTAAGAGAA[C/G]TGAGGGATGGCTCAC | 55779 |
rs550503891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447005 | TATTCTCGTGATAGT[A/C]AATAAGTCTCATGAG | 55779 |
rs550514266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323870 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAC | 55779 |
rs550521298 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425717 | CAGCCTTTCCACTTG[C/T]GCAAAGGACAGCCAG | 55779 |
rs550521903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332456 | TTTGTCAGAAAATTA[C/T]AAAATATTCAAAAAT | 55779 |
rs550538165 | snp | G/T | 1.65343e-05 | 0.00287521 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426119 | TATTTAGCCAGGGTG[G/T]ATACACAAGTGTGAG | 55779 |
rs550541395 | snp | G/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113442118 | ACTTGTTTTAAAATG[G/T]TCATTCCAATATGTG | 55779 |
rs550543381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311668 | TTGAACAGATATCCA[A/G]AAATATGGAAGCGAC | 55779 |
rs550642098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296581 | AAAGAAGCCGAGACA[A/T]GGCCTAAGATCCTGG | 55779 |
rs550703520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373012 | AATTTGAAATTTGAA[G/T]CTATTATATTGGGTC | 55779 |
rs550745863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399101 | TAAGCCACATGGAGA[C/G]GGTGTTAGGTATAAA | 55779 |
rs550760746 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377902 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 55779 |
rs550774023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351460 | TACCACACACTCTCA[A/G]AGGATTTCTCAGTTT | 55779 |
rs550785918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424563 | ACTTGTTCTTCCTAG[A/C]ATTCCTCACAAGATA | 55779 |
rs550789254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331269 | AGCCAAGCTGTGCCT[C/T]TGCTTCCAGGCACAG | 55779 |
rs550797683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385202 | AGCCATGAGGAACTG[G/T]GAGTCCATTAAACCT | 55779 |
rs550810591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294136 | GTTTGGAATATGCTA[C/T]ACATGTGTTAGGTTT | 55779 |
rs550820469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113293322 | CATTGTAAGAAGCAA[C/T]GGAGTCAGCGTTGGA | 55779 |
rs550831862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311202 | AAAATGCAAAGCCTC[A/T]GCAAATAAATAGAAA | 55779 |
rs550875701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390394 | TAGCTAGTATCATAC[C/T]GAATGAAGAAATACA | 55779 |
rs550876931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404809 | AGAACATTGAAGCAC[A/C]AAACAGTTAAGTAAC | 55779 |
rs550896250 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356621 | TTTCAACAAAAAATA[C/T]TAGGTCAATCGGATA | 55779 |
rs550909975 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382186 | AACTTAATACTCAAT[A/G]ACTGAGTGAAGGAGA | 55779 |
rs550912801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396794 | TGTACTATATAACAG[A/C]TATTTTATTTAGACT | 55779 |
rs550933976 | in-del | -/A | 0.184521 | 0.241273 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355769 | AGAATTTAAAGTATT[-/A]AAAAAAAAAAAGTTA | 55779 |
rs550953109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301739 | GATTGAGCTAATTAA[C/T]TTAAGCATTGCCTCA | 55779 |
rs551012496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310079 | GGGCTGTAACGAGGT[A/G]TCCCAACACTCCCAC | 55779 |
rs551021728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371683 | GGGCAAAGACTTCAC[A/G]TCTAAAACACCAAAA | 55779 |
rs551057493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352840 | TATATTTTGCCTATT[A/G]GATTGGTAAAGATGA | 55779 |
rs551065429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356988 | CAAAAATAACTCATG[C/T]ATATAAATAACCAAA | 55779 |
rs551083394 | snp | C/T | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330533 | TTTTGGGAATGGGTA[C/T]GTGCTTGGATATGTG | 55779 |
rs551095453 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407786 | ATAAAATAGATAATG[C/G]AGAGTATCAACAAGC | 55779 |
rs551096234 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379158 | TTCATCAAAACTCAC[A/G]ACTTCAATAGTATTT | 55779 |
rs551106053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438469 | TTCCATCTTTAAAAT[A/G]CAGCACCTACTGGAT | 55779 |
rs551119882 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338563 | GATTTTTTTTTTAAT[A/C]CCCAAATCTCTCTGC | 55779 |
rs551137849 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433495 | CTTTCCATTCTACTA[C/T]AAAAATTAATTATTT | 55779 |
rs551138745 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431859 | CTTAAATAGTCAAGA[G/T]TCCACTAAGATACCT | 55779 |
rs551140388 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288616 | TTTTTACATTTTTTC[C/T]TTTTTCTCCTTGATG | 55779 |
rs551170513 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441117 | ACCCAGCTGAGCGCA[-/G]GGCAGGTGTCTCACT | 55779 |
rs551188908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369902 | ATATAGGGGATATCA[C/T]CACTGATCCCACAGA | 55779 |
rs551197844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345462 | TAGTAACTATAAAAA[C/G]AGCAGACCTTGAGCA | 55779 |
rs551243070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329452 | CAAGAACAGTGAGAA[A/C]ACAGGGCTGGACAAA | 55779 |
rs551286062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362623 | CATAGTTAACGCTCA[A/T]CACATATGTGCATCA | 55779 |
rs551304879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439238 | TTGTCAGAATTAGAA[C/T]GGAGTCACCAGTGTT | 55779 |
rs551334718 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350581 | ACTCCAATACCACCT[A/T]GTTGTCAGTGTAAAC | 55779 |
rs551345363 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327941 | ATGGATGGAGAATTG[C/T]GTGTGTGTGTATAGT | 55779 |
rs551364615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343174 | TCAAGTGATTCTCCC[A/G]CCACAGCCTCCTGGG | 55779 |
rs551402998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350636 | GGCCACTGACAACCC[A/G]TAGCCTTCCTATCAG | 55779 |
rs551404429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446201 | TGAGAGGAAAAGTGA[C/T]TGGACCCAGTGCTCT | 55779 |
rs551419926 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427903 | TATACTTTCATATAG[A/C]GCTAGGTGAACTTTC | 55779 |
rs551481081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410198 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA | 55779 |
rs551495904 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329355 | GGAAGGAAGTCATTA[C/T]TGGTAGAAGGAAACA | 55779 |
rs551500338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348318 | GACCAATTTGACCCA[C/T]AAACCCTGAAAAAGA | 55779 |
rs551504543 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444362 | CAAATTAGCTGGGCG[C/T]GGTGGCATGAACCTA | 55779 |
rs551518151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315083 | ACAAGCTCTAAAATA[C/T]CAACAATTGTATTAA | 55779 |
rs551518162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322436 | GGCAAAGGACATGAA[C/T]ATACACTTCTCAAAA | 55779 |
rs551523158 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381941 | TCATAAGAACAAGTA[C/G]GTTGTATAAAGCTTT | 55779 |
rs551554901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321938 | TTAAAATGGCATATC[C/T]TCCAAAGCAATATAC | 55779 |
rs551560906 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389114 | TTCTTAAGAACAGAC[A/C]ATATGTTAGTCCACA | 55779 |
rs551599627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423809 | TCGGCAGCCTTCTGA[A/G]CCAGAGTAGGCCCAG | 55779 |
rs551609498 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332221 | TGTATGTAACATGAT[C/G]AATAAATAAAAATTA | 55779 |
rs551609782 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304318 | CACATCACGTCTCTG[A/T]GGGGATAGCAAATCC | 55779 |
rs551636777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416713 | ATTTAGCATCCATTA[C/T]TTCATAATTTATTAG | 55779 |
rs551637173 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311131 | TAAAGTATTTAAAAC[A/G]GCCATGATAAAAATG | 55779 |
rs551646524 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328730 | AAAAAAAAAAAAAAC[A/G]GAGAGAGAAGAAAAA | 55779 |
rs551659143 | snp | A/C | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434202 | AAGCAATTAAAAATA[A/C]TGAGTGCTACAAAAA | 55779 |
rs551671649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320210 | CTATTCCAGAAAATT[C/G]AGGAGGTATATTAGT | 55779 |
rs551684225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113336537 | AACATCTGGATAGCA[C/T]TATAACAACAAAAAT | 55779 |
rs551722049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306911 | TAGGTTTGTGTGCTC[C/T]ATTTCACTCATAAAT | 55779 |
rs551738443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361232 | AGAGAGATAAACCGC[A/G]TATGTAATTTCATCT | 55779 |
rs551751805 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421226 | ACATGCAAGCGACCA[A/G]CAAACATGAAAAACG | 55779 |
rs551764955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313547 | GGAGGGGCAAGGGGG[C/T]GGAATGATATGGTTT | 55779 |
rs551804376 | in-del | -/A | 0.124144 | 0.21601 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302773 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs551807098 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290792 | AAATGGCAGGGGACA[C/T]GAGAAACTATGGGGA | 55779 |
rs551818602 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113435971 | CTTCCCTTCCTTCCT[A/C]TTTCCTTCCACCTAA | 55779 |
rs551820765 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410278 | TACATTAGGTATATC[G/T]CCTAATGCTATCCCT | 55779 |
rs551827516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425140 | GAAGAGAGAAAATTC[C/T]AGGTTACAAGATAAA | 55779 |
rs551847859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326152 | CAAATAAGATATACA[C/T]ATGGCAAATAAACAC | 55779 |
rs551849192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299580 | AATACCCAAAAGAAA[A/G]GAAATCAGTATATTG | 55779 |
rs551859481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298993 | CATAAATGTTATGAT[A/G]TGTACATTTTACTGC | 55779 |
rs551884574 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395917 | GAAATCTAGCCTATA[G/T]ATCACAAAAAAGCAT | 55779 |
rs551891956 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350542 | ATAATTGATAATTGA[C/T]AGTCTTCTCCATGAC | 55779 |
rs551918520 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362327 | TAGAAGGCACTCCTC[A/G]TGATGCTCTGGGCTC | 55779 |
rs551923248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395443 | GCATTTCGACATGCT[A/G]TGCCTGTGGCCAAAA | 55779 |
rs551965191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361744 | ACCTCATGATCCGCC[C/T]GCCTCGGCCTCCCAA | 55779 |
rs551982316 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447175 | CTCTTTTTCTTCCCA[A/G]TCTCAGTTATGTTTT | 55779 |
rs551989874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313988 | ATGTAAAGACTGAAC[A/G]ATAGACATCATCCAA | 55779 |
rs552014961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296669 | ACTTCCTGCTCCCTG[C/G]GATTTCTTGCCTCCA | 55779 |
rs552015060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305680 | AATGAAGTTAAGTGA[C/T]GTTGCTCTAGACAAG | 55779 |
rs552029957 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394165 | CAACCACCCAGGACA[C/T]TGACATTAGTATAGA | 55779 |
rs552031338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393805 | CAGGCGTGAGCCACC[A/G]CGCCTGATCTCCCCA | 55779 |
rs552042769 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408834 | TGCCATTGCACTCCA[C/G]CCTGGGCAACAAAAG | 55779 |
rs552048696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341607 | TGACCTGTTTATAAT[A/C]TCTCCTTCTTTGTTT | 55779 |
rs552064489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369092 | ATTCATAAAGCAAAT[C/G]CTTAGAAACCTACAA | 55779 |
rs552070045 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400073 | GGCTCACTTTTTACA[G/T]GTTGAATATTATAAC | 55779 |
rs552095297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400942 | ACTAAATAGGGTAGT[A/G]ATGAGGATCACATGA | 55779 |
rs552128202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387371 | ACAGTAGGTAGGGCA[C/G]CAGGAAGAGTTGTGA | 55779 |
rs552159577 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323045 | AGAACTCACTCATCA[C/T]GAGAATAGCAGCATG | 55779 |
rs552221976 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421244 | AACATGAAAAACGCT[C/T]CACATCACTAATCAT | 55779 |
rs552223161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380844 | TAACATAGGATATTT[A/T]ATATTCTAAGGAAAG | 55779 |
rs552237591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334722 | CCACCTACACACATA[C/T]GAAACAGTGGCAATC | 55779 |
rs552245530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406581 | GTGAGCGGAGATCGC[A/G]CCACTGCACTCCAGC | 55779 |
rs552258244 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388119 | TGACGATCTCACCAC[C/G]CTGAAGGGAATACAA | 55779 |
rs552303230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380278 | GAGCTCCATGCATTG[A/G]TCACAGACTCTTGCA | 55779 |
rs552328412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312245 | CCTGGCTAATTTTTT[G/T]TTTTTTTTTTTGTAT | 55779 |
rs552358029 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298643 | GTACATATAATGGAA[C/T]ATTATTTGCCTTAAA | 55779 |
rs552371572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300465 | TATAAGAATATCCCA[C/T]ATATCTTATAAATAT | 55779 |
rs552390513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372596 | GAGTGGGGGGCAGAG[A/G]GAGGGATAGCATTAG | 55779 |
rs552401419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347370 | TCAAAGTCACGTCGC[C/T]CAAGCAAGGCTCACC | 55779 |
rs552446550 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312880 | ATTTCAGAGGATGTA[G/T]GGAAATGCCTGGATA | 55779 |
rs552451365 | in-del | -/ACACATACACACACATAT | 0.00953873 | 0.0683987 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356906 | TGTGTAAACACACAC[-/ACACATACACACACATAT]ACACATACACACACA | 55779 |
rs552462798 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393392 | GGGCCTAATGGGAGG[G/T]GTTTGGGTCTTGCGG | 55779 |
rs552542765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347036 | GGCGACCCAGATGGG[A/C]CATCGCCATGCAGTG | 55779 |
rs552547776 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289268 | AATTCCCAAACATGC[A/G]GAATGAAGCCCTGAA | 55779 |
rs552694457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338748 | AGTCCTGTAGGGAGA[A/G]GGGGACCTTGGCCTT | 55779 |
rs552726709 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350726 | GCTTTGCTAGCAGAA[G/T]AAAGTGGGAAAATAA | 55779 |
rs552741392 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288104 | AGCCTGTATTTTCTA[G/T]ATTTCTGTAAAATTG | 55779 |
rs552782619 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347402 | GTCTATCCTATCTAT[A/C]CTGACACTTGCCTCC | 55779 |
rs552799026 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426612 | TGTGAGTCAAGTAAA[C/T]CTCTTTCCTTTATAA | 55779 |
rs552800266 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331561 | TAGAGGAAATGTTCT[-/G]CAACTTGAAAATAAA | 55779 |
rs552801795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356586 | AGCATCACTACAATC[C/T]AGTAAGGAACAGATG | 55779 |
rs552829053 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377110 | TATTTTTTTCTGTGA[A/C]ATGTGAGATGAGGTT | 55779 |
rs552831406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345641 | GTTCATCTTTCTCTC[A/T]TAGCCCACAGAGTCT | 55779 |
rs552836132 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419458 | GCTGAACTTATTAAT[G/T]AGTCTTATAACAAAC | 55779 |
rs552862616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425977 | ATAAACAAAATGTAA[A/G]CAAATGGATGTGGCT | 55779 |
rs552903114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439308 | AAGAATGGGTTCTCA[C/T]GCTTGTATGCTGGAT | 55779 |
rs552936251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397232 | GAATTAGCTAGGTAC[A/G]GGAAGGTGGCACAAG | 55779 |
rs552946912 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369930 | AGAAATACAAACTAC[C/T]ATCAGAGAATACTAT | 55779 |
rs552955126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417623 | GCTAATCCTGGTACC[C/T]AAGATAACATTATTT | 55779 |
rs552972914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330799 | TCATCTGATCATACC[C/T]TTTTACCACCAAGTT | 55779 |
rs552989483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424798 | ATAATTCATATATTG[A/G]AATAAAAGTTAAGGT | 55779 |
rs553060281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410386 | TCCCACCTATGAGTG[A/G]GAACATGCAGTGTTT | 55779 |
rs553068714 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427467 | ACTCAAAAATTTCTA[A/G]AAGAATCATTTTATT | 55779 |
rs553076260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328990 | GTGTCCCTGCATACA[G/T]AACATCCAATAAATA | 55779 |
rs553086065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390624 | CAAAAAACTATTAGA[A/G]CTGGTAAACAAATTT | 55779 |
rs553088721 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401131 | GTTAGGCAAGTTTTT[C/T]ATGAGGACCATGATG | 55779 |
rs553133286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429626 | ATAATTAATGTAATT[A/G]TTGATATGGTTAGAT | 55779 |
rs553152839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432174 | GTAGCTCTCACAGGA[A/G]AACTCTAGACCAGAC | 55779 |
rs553172229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423352 | ACTCCTGAGCTCAAG[C/T]GATCTGGCTGCCTCC | 55779 |
rs553198129 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425201 | ATTTAACAACATGTT[C/T]TATTTTTATGTTTTT | 55779 |
rs553205684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286500 | GTGGCCCTCCCTGTT[C/T]TGATGAGAGACCTTG | 55779 |
rs553206941 | in-del | -/TC/TCTC | 0.0162398 | 0.0886349 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320224 | GAGGAGGTATATTAG[-/TC/TCTC]TCTCTCTCTCTCTCT | 55779 |
rs553216062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431261 | ATTTCACATTATCAT[C/T]TGGGAGTCTAAGACA | 55779 |
rs553253812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299282 | GTTCTTAAAAGAAGA[A/C]ATACAAATGGCAAAC | 55779 |
rs553265551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445796 | CGGGTATCTATCATT[A/C]CCCTATCATTTAATA | 55779 |
rs553274794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422649 | AGTTTTGCCCACCGG[C/T]TTTTTTCTTTCCTTC | 55779 |
rs553284246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315301 | AATGTCAGACAAATA[G/T]ACTTTAGAGCAAAGA | 55779 |
rs553314537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308591 | ATTTTTTTTTCTTTT[C/T]TTTTTCTTTTTTCTT | 55779 |
rs553319701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292246 | ATACATATACATCAC[C/T]ATAATTTACAGAATA | 55779 |
rs553349736 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417564 | ATTATTTCACATCCC[-/CT]GATTACATATAAGAC | 55779 |
rs553379543 | snp | C/T | 0.00524345 | 0.0509336 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327566 | AAAAGAAATCAAGTT[C/T]CTCCATAACTAAGGG | 55779 |
rs553390350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416440 | TGTTTCTCTGGAGAA[A/C]CTTGACTTATGAAAT | 55779 |
rs553406616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370010 | TTCTGGACACATACA[A/C]CCTCCCAAGACTAAA | 55779 |
rs553450364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307354 | CTGCATATTATTTGT[C/T]ACTCATAAATGGCTG | 55779 |
rs553480865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401178 | AAAGAATACTTTAAA[A/G]ACAAATAACAAAAGT | 55779 |
rs553483076 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408949 | TAGAAAAGGTGCATT[A/C/G]CTAGTTAGCTTTTAA | 55779 |
rs553493754 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311574 | AAACCTCTTTTTCTT[C/T]CCAGTCTTGGTTATG | 55779 |
rs553499139 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413270 | AATTCTGGATATTAG[A/C]CCTTTGTCAGATGGG | 55779 |
rs553502282 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348118 | TTGCAGGTTCTTGGG[A/C]AAGAGGGGTTTCTGC | 55779 |
rs553516195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375577 | GCAACACTGTGGTAG[A/G]TAATGGCTGAGAATT | 55779 |
rs553517941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408541 | CTTTTAGGAGGTGGA[A/G]CCTATAAGAAGGCAG | 55779 |
rs553572901 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388569 | TTGAAAGTAAATGGA[C/T]TAAACTCTCTAAACA | 55779 |
rs553577923 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395091 | AAGCTTAAAGTGGAT[C/T]ACCAACGTTACTCCA | 55779 |
rs553606766 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441150 | AGCGGGGAGCCCCAG[C/T]ACCTTCCCAGCTGAC | 55779 |
rs553619517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291809 | GAAAAACTCCATGCC[C/T]TTATACTGTGTATCT | 55779 |
rs553650197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383186 | ATTGATCCTTGTTTG[C/T]CTTAGTCAGTTCAGG | 55779 |
rs553651587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389448 | CAAATAACTAATGGC[A/G]TATCTTAAAGAACTA | 55779 |
rs553688866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382220 | AGAAAGAATGACAAG[A/C]TGTGGGAGAGGGAAC | 55779 |
rs553708933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348670 | AAGAAATCTCCAAGG[A/G]ACCACAAAAACTCCC | 55779 |
rs553791720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373883 | ATAAGCAGGAACAAA[C/T]ATTAGGGTTTTGCAG | 55779 |
rs553809871 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337714 | AAATGTCTTTTCAAC[A/C]AAAATGCTAGAGTAA | 55779 |
rs553819786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354827 | TCCTCCCTACAGGAC[C/G]ACAGCTGATGGGCTC | 55779 |
rs553824242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414231 | TGAGACTTTGCTGAA[G/T]TTGCTTATCAGCTTA | 55779 |
rs553835271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387564 | AGTACACACTGTGGG[C/T]CTTGGATGAGACTCT | 55779 |
rs553845570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313633 | TGTTGTGGGAGGGAC[C/G]TGGTGGGAAATAATT | 55779 |
rs553854669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353914 | AAAGGAACAGACAGA[A/C]TAATCCACAGATCTC | 55779 |
rs553860843 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413969 | ATGGCCATTTTCACA[A/G]CATTGATTCTTTCTA | 55779 |
rs553871878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386880 | AATCTGGGTACTTGG[C/G]GGAAGGACAGAGCAA | 55779 |
rs553884435 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320480 | TCATATATGATATAT[A/C]TGATATATAGATGTA | 55779 |
rs553895847 | snp | C/T | 0.000316456 | 0.0125749 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287036 | GAGACATAAGGAGTC[C/T]TACCCGTTGAGGTTG | 55779 |
rs553899408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420603 | TCATACTGTATAACA[C/T]GGGAGAAAGTCTGTA | 55779 |
rs553927908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352861 | GTAAAGATGAAAACA[C/T]TGGTAATACCCAGTG | 55779 |
rs553943188 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391545 | GAAGACATCAATAAA[A/G]TGAAGAGAATTTCTT | 55779 |
rs553961670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352412 | CCACCTTTAAGAGCT[A/G]TAAACACTTGCTGCA | 55779 |
rs553990454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421411 | TGTAAATCAGTTCAG[A/C]CACTGTGGAAAGCAG | 55779 |
rs553998194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360028 | TTTTGGCTAAGTACA[A/G]TAAGAGTTGATAACC | 55779 |
rs553999627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361309 | ATATTCAGCCTGAGC[C/T]AGTAAGCTAGATTCA | 55779 |
rs554015573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341207 | CTTGGGCAGGAAATG[C/T]CTGTCCTCACCTAGG | 55779 |
rs554024952 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339634 | ACATTGTGCCTGTTG[C/T]CTGGCTTTGGATCCC | 55779 |
rs554032956 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406062 | CTAATAGGAAGCTAT[A/G]TAAAATATTGATAGA | 55779 |
rs554038292 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333977 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTGTGTT | 55779 |
rs554045143 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372699 | AAATGTGCACGTTGT[A/G]CACATGTACCCTAGA | 55779 |
rs554062176 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364028 | ACATAAAGTGGAAAA[C/T]GCAAAGAACAATATA | 55779 |
rs554070011 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349037 | CAAGCCGTCACCAGT[A/G]TGGATCACCACTGGG | 55779 |
rs554097428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327276 | ACATATAATCAAAAC[C/T]CAATTTTATATCATA | 55779 |
rs554121973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368179 | CTTCAGGATATCATC[C/T]AGGAGAACTTCCCCA | 55779 |
rs554135964 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334958 | GAAACCCATACCATC[G/T]ATTGTATTAACTGAT | 55779 |
rs554162181 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290499 | CCAGCTTATCCTGGA[A/C]CAGCCTCAATGAGTA | 55779 |
rs554176724 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316411 | TAAACCAAAAGCAAG[C/T]AGGAAAAAATGTAAT | 55779 |
rs554190957 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427461 | ATACATACTCAAAAA[A/T]TTCTAGAAGAATCAT | 55779 |
rs554228028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428059 | CAAGCCAATTAGTTG[C/T]GGAACAGGGCAGAGT | 55779 |
rs554282756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347641 | GAGACCAACTATCCT[G/T]TTAGGATCCTTCCTC | 55779 |
rs554308642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331665 | AGGACTGCAGATTAG[A/G]CCACCAAGAACAAAC | 55779 |
rs554309842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306046 | AAAAGCAATGTCCCC[A/C]ACCACAATTTAGGGA | 55779 |
rs554322838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433742 | ATTTCCCCCTAACAT[A/G]TTTCATTAGCACCAA | 55779 |
rs554324507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419139 | ATGTGATAATTAGAT[A/G]TTTCTTGGTCCCCTG | 55779 |
rs554327209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340199 | GCAGCTGTCAAAGTG[A/G]AGGCATACATGGCAT | 55779 |
rs554354516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435389 | AGCGAAGGGGAAGAA[A/T]ACCCCTTATAAAACC | 55779 |
rs554366076 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367327 | AACAGACACCTCATA[A/C]AGGCGGGTGCCCTTC | 55779 |
rs554413859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434895 | TAAAGCAGATATGGT[A/G]CACTACACGATCAAA | 55779 |
rs554426559 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418297 | TTACCATGTTGGCCA[-/G]GCTTGTCTTGAACTC | 55779 |
rs554445791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303162 | TGTTCAACCACTTTG[C/G]GGGCAACCTGGCAAT | 55779 |
rs554466792 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308703 | CAAGCAATCCTCCCA[-/C]CCTCAGCCTTCTGAG | 55779 |
rs554467215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394950 | CTCCTTGAGAGACTA[C/T]TTTGTACTGCTTATT | 55779 |
rs554481189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399420 | TTTCTATAGTTCTTA[A/T]AATTATCTAACATAA | 55779 |
rs554494113 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288769 | GCACATGGCTCACAG[A/G]CCTCCCTAAGCTGGG | 55779 |
rs554502965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311410 | TTCTCATGGTAGTGA[A/G]TAAGTCTCATGAGCT | 55779 |
rs554504039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312375 | GGTATGAGCCACCCC[A/G]CCCAGCCTAAAGGAA | 55779 |
rs554513299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439465 | ACACTTATTGTTGAT[C/G]TTTGTAGCCAAGGAT | 55779 |
rs554521933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325540 | AGCTCCGCCTCCTGG[G/T]TTCACGCCATTCTCC | 55779 |
rs554526154 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415334 | GGATTCATTGATTTT[C/T]TTGGAGGGTTTTTCT | 55779 |
rs554535790 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442633 | ATGGGTATATACAAC[C/T]GCCAAAAGCCAATAA | 55779 |
rs554536870 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406741 | TGGTAGGTAAGTATG[G/T]ATTATGACAATTTCA | 55779 |
rs554542220 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419707 | TAAAATCTCCTCACT[A/C]ATCTCCACTTCTAAT | 55779 |
rs554546201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367317 | AGTAGGGGCCAACAG[A/G]CACCTCATACAGGCG | 55779 |
rs554552093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439821 | GTTCTGGTCCTCATG[C/T]TCACAAGCTCACTCA | 55779 |
rs554557435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295461 | CGCCAACATTCCCTT[A/G]ATAGGGACCAGTCCC | 55779 |
rs554575362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413294 | AGATGGGTAGATTGC[A/G]AAAATTTTCTCCCTC | 55779 |
rs554583362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373081 | TATTAAAGGGCTAAT[G/T]ATTCATTTGTGATTT | 55779 |
rs554612231 | snp | A/G | 0 | 0 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412643 | GTTTTCTGTTCCTGT[A/G]TTAGTTTGCTGAGGA | 55779 |
rs554621284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310544 | TTTAAATAAGATACA[A/T]AGTCTCATAATACAA | 55779 |
rs554639802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405031 | AAGGAATTTGACTTA[A/G]AAAGTCTTATTTTTA | 55779 |
rs554646859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351541 | TGGCAGCAGTGACTC[A/T]CCAAAACCGCCAAGA | 55779 |
rs554660597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372317 | CACAATAGCAAAGAC[C/T]TGGAACCAACCCAAA | 55779 |
rs554676879 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411461 | AGATGGTTGTAGATG[C/T]GTGGTATTATTTCTG | 55779 |
rs554713473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410898 | TTTCTCTGATGGCCA[C/G]TGATGATGAGCATTT | 55779 |
rs554768923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418487 | TAGGGTGCCCAAACA[C/T]TTTTCTCATAGGTTT | 55779 |
rs554770949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346654 | GCTCTGTGTCTAGCT[A/G]AAGGATTGTAAGTGC | 55779 |
rs554797163 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288083 | GGGGCTGGAGAGGGT[C/G]GGGGGAGCCTGTATT | 55779 |
rs554837086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323173 | GACACAGCCAAACCA[C/T]AACACTGTGCTATAC | 55779 |
rs554850562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384717 | AGCCTCCAGAATTGT[A/G]AGGAAAGAAATTATG | 55779 |
rs554860602 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287312 | GGGAAACATTTTCCT[A/C]AGATGCCCATGAGAA | 55779 |
rs554862216 | in-del | -/A | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288362 | AGCATGGTTTTCAGG[-/A]AAGCAGTATTTTAAA | 55779 |
rs554893691 | in-del | -/CTCTTTTCTTCA | 0.0908922 | 0.192833 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435336 | AGGGGAAGCAAACAC[-/CTCTTTTCTTCA]CATGGTGACAGCAAG | 55779 |
rs554896394 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371299 | GCAAAAGAACAAAGC[C/T]GGAGGCATCACATTA | 55779 |
rs554907443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391754 | GAAAAGTTCTGAAGA[C/G]ACATTTCTGAAAAGA | 55779 |
rs554941259 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300975 | CACTTATATGCCCTA[A/C]GACCCAGCTGTTCTA | 55779 |
rs554966544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350985 | CAGGACAATAGATGG[A/T]TCCTCCTGGGCGATT | 55779 |
rs554975300 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294251 | AAATATTATGTAATA[C/G]CAAGTTGAAACCCAC | 55779 |
rs554975874 | snp | C/T | 4.96364e-05 | 0.00498154 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286812 | GGAATGCAGCTCTCC[C/T]CGGGGCCACTGGTGC | 55779 |
rs554988513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383911 | CCCTAGCCCCCAACC[C/T]CCTGCCAGGCCCCAG | 55779 |
rs555004312 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397364 | CCCCAGGAGGCTGGA[A/G]AGGAAGAGAGGCAGG | 55779 |
rs555027632 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383368 | TGCTCACAGGACAGA[C/G]AGAAGAAACTCTGGT | 55779 |
rs555041373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397889 | TTTGGAAACACGGAG[C/T]TCGAGGTCCCCTTGA | 55779 |
rs555056989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365524 | TGAACCCTCAAACTT[A/C]ATCATAAAGCCAAAA | 55779 |
rs555067596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390069 | ACTATAGGCCACTAT[C/T]ACAGATGAATATTGA | 55779 |
rs555088759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344928 | AATGAAAATACTAAA[C/T]AACTCATTATTAATC | 55779 |
rs555121029 | snp | A/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432900 | TTCTACATGCATCTA[A/T]CAGATAATCTATTAT | 55779 |
rs555126568 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395684 | ACCTGCTATTTTCTA[C/T]CTACAAGATAGTTTC | 55779 |
rs555129175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350074 | GTGCAAAAACCCAAC[A/G]AGGTGGCAGTCTTAC | 55779 |
rs555136989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356470 | AAGATTTAATTAAGA[C/T]AGAATGATACTGGCA | 55779 |
rs555156650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322901 | AGCATGGCTGGGGAC[A/G]CCTCAGGAAACTTAA | 55779 |
rs555158379 | snp | A/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113303924 | TACTCACTGTGTATG[A/G]TTTTTGTCATTTCTC | 55779 |
rs555175694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355378 | ACAAAAAAATTCGCC[A/G]GGCATGGTGGCAGGT | 55779 |
rs555204686 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374080 | TTATAGGAAACAAAT[C/T]AAGGGTCAGAACAAC | 55779 |
rs555250509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376620 | TCTGTTAAATGTTCC[A/G]AAAAGTCAAATGGAC | 55779 |
rs555347094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338646 | AACATAACATCTCTC[C/T]AGGAACGTTCAAACA | 55779 |
rs555348960 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370297 | GAGAATTTTAGACCA[A/C]TATCCCTGATGAACA | 55779 |
rs555360677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424177 | GCGCGGTGGCTCACA[C/T]CTGTAATCCCAGCAT | 55779 |
rs555387897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338145 | GTTTGTAATCCCAGC[C/T]ACTTGGGAGGCTGAG | 55779 |
rs555406936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402034 | TATTTCAAGGTTTCT[A/G]TTAGGTCTCTTTTTA | 55779 |
rs555407105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321966 | TACAGATTCAATGCT[A/C]CTCCTATCAAATTAC | 55779 |
rs555424803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337162 | TTTCTATGCTAGCAG[C/T]GAATGTGAACACATA | 55779 |
rs555440726 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429946 | AACTTAGTAAAGACA[C/T]AGATGATCTGAACAT | 55779 |
rs555444793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300142 | TGCTCTCCCTTATTC[A/G]TGAGAGCTAAAAATT | 55779 |
rs555489758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335834 | GATAGACTGTATATG[C/T]GTGGCCATAACACAG | 55779 |
rs555506399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309387 | ATAAATCTCCACTTG[A/T]CCTTGTTGTATTCAG | 55779 |
rs555522702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436745 | AAATCAAACTGATAT[G/T]CTACTGCTGCTAATC | 55779 |
rs555527179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335076 | GAAAGAAAAAGGAAG[C/G]AAAGAAAAAGGGAGG | 55779 |
rs555534100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349594 | CAAGCTGCTCCCTTG[C/T]CCATGTCCACTATCC | 55779 |
rs555539820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357055 | CAGTTTTAAAAATGG[A/T]CAAAAGACTGGAACA | 55779 |
rs555542789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429916 | TTTCAGCAATTGATA[A/G]AACAACTAGTCAAAA | 55779 |
rs555594557 | in-del | -/T | 0.0013465 | 0.0259121 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346865 | GCTGTGGAAGCTTTG[-/T]TTTTTTGCTCTTCAC | 55779 |
rs555651269 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383133 | GGTATGAAGAAAAGA[A/C]AGAGGGATAAAGGAA | 55779 |
rs555697238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313565 | AATGATATGGTTTGG[C/T]TCTGTGTCCCCATTG | 55779 |
rs555731141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381477 | CCCATCCTACTTTAA[C/T]GGCTCATCCTCTATC | 55779 |
rs555744363 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442995 | TCAGGTGAAATACCT[C/T]TAAATTTCAAGCACT | 55779 |
rs555800477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375221 | AGTATGGGAGTTTCA[A/G]TGTTACAGGATGAGG | 55779 |
rs555840122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408456 | AAAGAAATTCAGTAG[C/T]GGATGTGAAAGCTCA | 55779 |
rs555844437 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434576 | TAATGCAGCTTTTCA[C/T]ATATTTGAAAACACC | 55779 |
rs555853325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306393 | GTGGTAGTACTAAAA[C/T]TGTGAACTTTGGAGA | 55779 |
rs555853885 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339812 | TTCCTGTTAACTTTC[A/G]TATCAGAAACAGAGC | 55779 |
rs555914198 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291744 | GGGCCCTGGAAGGCA[C/T]TGCCCTGTTGAAAGA | 55779 |
rs555928301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420462 | TATTTTAATTTTCCT[A/G]GGGAAATCCTGAGAG | 55779 |
rs555953683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410547 | TAATCCCGTCTATCA[C/T]TGATGGACATTTGGG | 55779 |
rs555982804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348050 | GGAAAACTAGTGTTT[C/T]TGCTGCTGCATTGGT | 55779 |
rs555989145 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439760 | TAGACGCCAGACAGA[A/G]TGCTGTCTAAGGTGA | 55779 |
rs556019247 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407570 | ACTTTTCTAGATCAC[C/G/T]CTGTGCCTTCATTTT | 55779 |
rs556030010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307147 | CAGTGAAAACAGTGA[A/G]TGTAAATTGTCAAGC | 55779 |
rs556078063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388576 | TAAATGGACTAAACT[C/G]TCTAAACAAAAGAAA | 55779 |
rs556083683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401007 | AACTATAAAGTACTA[C/T]ATAATGTTAGGTATT | 55779 |
rs556100754 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288954 | TTATATGAACAATTG[A/G]CCCACAAGTAACTCA | 55779 |
rs556120331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353766 | AGAGAGAACCAGAGT[C/G]AGAGAGAGAGAACCA | 55779 |
rs556157466 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394498 | AGCTATCTCTTATTC[A/T]TTTGGTCATATCCTA | 55779 |
rs556168544 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289596 | CTCCAGGCAGCTGCT[G/T]CTTGTGGCTGCCAGC | 55779 |
rs556200950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379794 | TTGGTCATTTTTTTC[A/G]TAATAGAGAAGCTAA | 55779 |
rs556223716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386188 | AGTTTTTTATGTAAA[C/G]TCTATGTTGTCTCAT | 55779 |
rs556228846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361279 | GCATGCCTGAAGAAG[G/T]GCTTCAGAGGGTGAA | 55779 |
rs556229431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333260 | AAAAAGAGGACATTC[G/T]AGATAATCATGGAAG | 55779 |
rs556260163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434577 | AATGCAGCTTTTCAT[A/G]TATTTGAAAACACCT | 55779 |
rs556260961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392949 | CATCACAGCTGCCCA[A/G]TAGATCCACCTGCCC | 55779 |
rs556297109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426865 | GTTCTGGTCGGTCAT[A/G]GCGCAACAGTCTCCA | 55779 |
rs556298196 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367938 | ACGAGAACTTCGTGA[C/T]GCATGCACAAGCTTC | 55779 |
rs556331247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333927 | TGGAAATTAGGTGGG[G/T]TTTTTAATGACTAAA | 55779 |
rs556366095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373787 | ATGATTTGTTTTCAT[C/T]TAAAAGCCAATACAA | 55779 |
rs556374857 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296377 | TTCTCCAATGATTAG[A/T]GATGCTGAGCATTTT | 55779 |
rs556388850 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304583 | ATATAAGTTGCAATT[A/C]AAATAGAAATGAACA | 55779 |
rs556400960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380421 | CCCTATTTTCACCTC[A/T]CAAAATTCCCCCTAT | 55779 |
rs556440488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367403 | TTCTGCAATATTTGC[C/T]ATTCTGCAGCCTCCA | 55779 |
rs556476066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352015 | CAGGAAGTAGCTGGA[A/G]CAGTCATTGCCCAAT | 55779 |
rs556580933 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372215 | ACCATTTGACCCAGC[A/C]ATCCCATTACTGGGT | 55779 |
rs556600753 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439665 | TTTAGGTTGACAGGG[C/T]CAACTCTAAGGAAGT | 55779 |
rs556615393 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337526 | AATAAAATGAGAGGA[A/G]TCACTCTACTGGATT | 55779 |
rs556618658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347106 | TTTTCCTTAGAATTC[A/G]GGGGCTAAATACTGG | 55779 |
rs556655288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324111 | TAAGAAAGTTGAATT[C/T]GTAATTTAAAAACTC | 55779 |
rs556691838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331637 | AATGGACAACCACCT[A/G]TGAAGTGTCTGAAGG | 55779 |
rs556715012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439749 | AGAAGGTTGGCTAGA[C/T]GCCAGACAGAGTGCT | 55779 |
rs556723849 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290095 | GGGTAATTTTTTACC[A/G]CAATAAATAAGACAC | 55779 |
rs556725010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338856 | GAGGGGGCAAGTGAG[A/G]GGCTGAAGCTGGATA | 55779 |
rs556732483 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441487 | GGCTCCTCTCTTCAC[A/G]GCGTCTGCCGGAGGC | 55779 |
rs556750439 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408812 | AGGTTGCAGTGAGCT[A/G]AGATCATGCCATTGC | 55779 |
rs556777995 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324161 | ATCCAAAAGCTTTCA[C/G]TGGTGAATTCTACTA | 55779 |
rs556779297 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440350 | ACAGGCGTCAGCCAC[C/T]GCGCACAGCCTATTA | 55779 |
rs556790499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428555 | CAGATGGAAGACTTA[C/T]GGTTTGAAGAATAAA | 55779 |
rs556798099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385414 | AAAGAAAAGATGTTA[C/T]AGGTGAATGACAAGA | 55779 |
rs556801687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440863 | TCTCAAAGATTTTCA[C/T]CAGTACGCACCCTTA | 55779 |
rs556850221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324854 | ACAATTACTTTTGCA[C/T]CAACCTAATCATCTA | 55779 |
rs556852736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405357 | AAATGTGACTCATAT[C/G]TAGCTTCCCTTTTCC | 55779 |
rs556853052 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418589 | CAGTGGAGGCAAGGC[C/T]TCTGTCACTACCCAG | 55779 |
rs556868009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398544 | CAATTACCTGGATTG[C/T]AGTTTTAAGACTTCA | 55779 |
rs556876358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439379 | AAGCCATCACAACCT[C/T]ACACATAAAAAAAAA | 55779 |
rs556890052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311510 | GTGCCTTTCACCTCC[C/T]GCCATGTTTCTGAGG | 55779 |
rs556891007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316638 | CTTTGAGAGACCGAG[A/G]TGGGTGGATCACTTG | 55779 |
rs556891689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317859 | CATGGCCTGGAACAC[C/T]CAACAACAACAAAAA | 55779 |
rs556892435 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432989 | GTTCTCTGCATGGCT[G/T]CCCAAGTGTCATCCT | 55779 |
rs556905201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445886 | CTCAGTAATAAGAAA[C/T]GCAAAGATTTTCCCA | 55779 |
rs556917271 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375812 | GGCAACAGAGTGAGT[C/G]AGACTCTGTCTCAAA | 55779 |
rs556919014 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345317 | CATTCCCCAGAGACT[-/A]AAAAAATGTTCATTC | 55779 |
rs556928488 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317436 | CATCTTCTCTGCAAG[C/G]CCTCCTGCCTGCCAG | 55779 |
rs556937081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350806 | CCTAAGTCAAAAAAA[C/G]AGGAAAGGCAAAGGG | 55779 |
rs556940790 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416081 | AATAGTTAGCTCTTC[G/T]TGAATTGTTCCTGTT | 55779 |
rs556971427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411608 | TTGTTCTTTTGGCTT[A/T]GGATTGTCTTGGCAA | 55779 |
rs556982311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310434 | CAATGAAGTCTGAAT[A/G]GGGAATATAGACTTC | 55779 |
rs556985255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418461 | TAGAGGTTCACCCTA[C/T]CTTTTCCAGGTAGGG | 55779 |
rs557018304 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347741 | CTATTCAAGTGAGGA[C/T]AAAAGGCGTCACTCT | 55779 |
rs557027966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316136 | ACTAGAAATCAATAA[A/C]AGAAAGATAACAGAA | 55779 |
rs557037290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404109 | AATTATTTTTTAAGG[C/T]TATCTTTATTGATTA | 55779 |
rs557063909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331025 | CTCCAGGGAGGAAGG[A/G]AAAGGCAATTAATTC | 55779 |
rs557072440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384955 | ACCCAAGTTTCATCT[G/T]GAATTGTAGCCCCCA | 55779 |
rs557075961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357236 | ATTATGGATTTGTGT[A/C]CCCCCAAAAAGCTAT | 55779 |
rs557077953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410830 | TCCTGACTTTTTAAT[A/G]ATCACCATTCTAACT | 55779 |
rs557113966 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288153 | ACTTGAGACAATCTC[G/T]TTAAGTGGGGGGCCA | 55779 |
rs557135457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424862 | TTTGTCTAATACAGA[C/T]CCTCCCATCCTGGAG | 55779 |
rs557144694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392288 | TAAGTTAAGTGAAAA[A/G]AGCCAGGTACAGAAA | 55779 |
rs557154442 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353849 | CAGTTAAGCACTAAT[C/T]AGCACTGCATAAGAA | 55779 |
rs557156787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416871 | CAATTTCTTTCATTG[C/T]CATTGGAAGAGCTAG | 55779 |
rs557229530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301402 | ATGGAAAAAATGCAC[A/C]CAGATAGATGTTACA | 55779 |
rs557259102 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429080 | AGAGCTACTTTATAA[A/C]AAATTTATAAGAACT | 55779 |
rs557264876 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330251 | CATCCGTTGGCTCTG[C/T]TTTTTCAAATTCCAA | 55779 |
rs557281960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391680 | TAATAACCAGAATAT[A/G]TAAGGAGCCCAAACA | 55779 |
rs557282088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338056 | TCACTTGAGGTCAGG[G/T]GTTCCAAACCAGCCT | 55779 |
rs557320608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397782 | TGACAGAAAACACTG[A/G]AAGGGAGCCAGGTGT | 55779 |
rs557323565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430927 | CAGTCCTTCACCATC[A/G]TGAGAAATGATGGAT | 55779 |
rs557353255 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401082 | TTTTATGTAAAATCA[-/T]TAACGAGAGAGAGAA | 55779 |
rs557360017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356802 | TAAAAAAAGACTAAT[A/G]AGTTGAACTTCAGTA | 55779 |
rs557418258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364487 | GACAGTAATGGCTAA[C/T]AAATTGTACTGACTA | 55779 |
rs557466854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410420 | TTTTTGTCCTTGCAA[C/T]AGTTTGCTCAGAATG | 55779 |
rs557492401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401897 | CACCAGCCAAAACCT[A/G]ACCCCTGAAATTTTA | 55779 |
rs557493633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370740 | GCCAGGGCAAACAGG[C/T]AAGAGAAAGAGATAA | 55779 |
rs557531401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355336 | TCAACCTGGCCAAGA[C/T]GGTGAAACCCTGTCT | 55779 |
rs557551907 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360080 | CTTATCTTGTTACCA[-/A]AAAAAAAAAAAAAGT | 55779 |
rs557559866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389509 | AGTAGAAGAAAATAA[A/G]TGAAAAAGATCAGAA | 55779 |
rs557594714 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402689 | TAGGTTTTTTCTATG[A/G]GGTAAGAGGTAAAGA | 55779 |
rs557606940 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437040 | ACTTCTGGGCTCATT[C/T]AAGCTGCTGGCAGAA | 55779 |
rs557628372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370121 | AAAGTCCAGAACCAG[A/G]CAGATTCAAAGCCGA | 55779 |
rs557666671 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302435 | TTTAAAACATCTGTA[G/T]CCAAAGATACACTAG | 55779 |
rs557666901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375680 | ACACCTTTTAACCAC[A/G]CGTGTTGGCACACAC | 55779 |
rs557713581 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437781 | AATAAGGTATTTTTG[G/T]TTTTTTGGGGTTTTG | 55779 |
rs557730278 | snp | C/T | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304084 | AAGTACCAGAAAGAT[C/T]GCTAGGTATTTCTCC | 55779 |
rs557760438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313697 | TCATGGCAGTGAATA[C/T]GTCTCACAAGATCTA | 55779 |
rs557805435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408638 | GGGAGGCTGAGGCGG[G/T]TGGATCACATGAGGT | 55779 |
rs557809972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343437 | AAATTAAATAATATG[A/G]GATATTTATATAGTT | 55779 |
rs557849515 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393927 | CACCAGAAGAAGATG[C/T]TGGCACCATGCTTCT | 55779 |
rs557888785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314358 | GAAACCATGGAAGCC[A/G]AAAGGAAATGACACA | 55779 |
rs557908672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347968 | CAGGCAAGAGTGCAG[G/T]TTTTCAAGAATGCAT | 55779 |
rs557927670 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420860 | ATATAAATATATATG[C/T]AATTAATAGACTAAC | 55779 |
rs557932035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354933 | CTCACAGAGTCCACT[A/T]CACTCCCCTGCTACC | 55779 |
rs557934375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409012 | CCAAAACAGCAAAAA[A/C]AAAAAAAAAAAAAAA | 55779 |
rs557984264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380571 | AAAGTGCTGGGATGA[C/T]AGGCATGAGCCAATG | 55779 |
rs558010553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334116 | GCCACCACACCCAGC[C/T]AATTTTTGTATTTTT | 55779 |
rs558019990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387670 | AGAAGTACGGAGAGG[A/G]AAGAGTCAAGGGTAT | 55779 |
rs558042375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435565 | AGCCAAACTGTCTCT[A/T]AAAAAAAATTTTAAA | 55779 |
rs558043417 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408062 | TCCCCAAAGATTACA[A/G]TTAAAAATCTGCTCA | 55779 |
rs558053216 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305504 | TTTTTTGGTCATGAC[G/T]TCAACAAATTAAAGA | 55779 |
rs558054372 | snp | A/T | | | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445028 | TAAAAATGTATTAAT[A/T]AAAAAAACCCTTAAA | 55779 |
rs558078182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321137 | AAAACATACTAGCAA[A/C]CCAAATCCAGCAGCA | 55779 |
rs558084896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319335 | AAAATTAAGAAGGAT[A/G]ATGAAGAGCATCACA | 55779 |
rs558113015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328150 | ATCTGTCTCCTCTTT[A/T]TTCTCCATAGTATCT | 55779 |
rs558115052 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320538 | TGAAGTTATATATGT[A/G]TATATATAATGAAGT | 55779 |
rs558123290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415549 | CTGTGTCCTAGAGAT[C/T]CTGGTATATCCTCTC | 55779 |
rs558137119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335010 | TGCACTAAAATGAAG[C/G]ATTACTATTTTTAAA | 55779 |
rs558149920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327378 | TGTGAAAATTTTATT[C/T]TTCTACCTTACAGAA | 55779 |
rs558161067 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342536 | TGGTGGACCACTAAC[A/T]TGTTGGGAAAGAGTG | 55779 |
rs558163776 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358263 | ATATATTTATACATC[A/T]GTAAAAAATTTTCAA | 55779 |
rs558201899 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113442126 | TAAAATGGTCATTCC[A/T]ATATGTGACAAAGGA | 55779 |
rs558222081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318824 | ATTTCACATCCTGCC[A/G]TACTGTTTCATAAGT | 55779 |
rs558222195 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343472 | ATAACCATTTCATCA[C/T]ATTTCATATTTCAAA | 55779 |
rs558224865 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357371 | GAAACATGACTGGTG[C/T]TCTTATAAAAAGGGA | 55779 |
rs558245434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388343 | TCAGTTAAAATAACA[G/T]GTTATAAGATATTAT | 55779 |
rs558261026 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325557 | TCACGCCATTCTCCT[C/G]TCTCAGCCTCCCTAG | 55779 |
rs558285874 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364839 | CTCTGGCATCTGTAC[C/T]TCTAGGGCTCCCTAG | 55779 |
rs558306233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360119 | TAAATCCAATAGTAA[A/G]CTTTGTATTACGTAA | 55779 |
rs558307357 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290589 | AATGTCAGTGAGATT[A/G]TCCTGCAATGGTTAT | 55779 |
rs558315992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419198 | AACCTCATAGGCTCC[A/G]ACTGACTTCCCTCCA | 55779 |
rs558333241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428107 | TTTGGATGGCAAGAA[A/G]GTAATCCTGGGTGCC | 55779 |
rs558339517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394803 | TCATTCAAAGCCCAC[A/T]TGCATGCAGCCCACA | 55779 |
rs558341996 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436005 | TAGAATATATACCTT[C/T]TGGGGTTTATGGAGG | 55779 |
rs558350553 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345604 | AAAAAACATTAAGCT[A/C]AGGAAATCATACTAA | 55779 |
rs558352996 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419942 | TTGGCATCTAACAAC[C/G]ATGTTGGCTGGTCCA | 55779 |
rs558394729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427547 | ATCTCCATTTTCACT[G/T]CATTTTCAGTCTATT | 55779 |
rs558401917 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386534 | AGAACAAAGAAGATA[C/T]AGAGGAAGAGATGCC | 55779 |
rs558409851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413464 | CTATGTCCTGAATGG[C/T]ATTGCCTAGGTTTTC | 55779 |
rs558425706 | snp | A/G | 0.000102244 | 0.00714924 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306274 | ACTAAAGCCTCCTCA[A/G]TGTCCAGCCTTTTCT | 55779 |
rs558443033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313102 | TGGAAAAGCCGCAGA[C/T]GCTCAATGCCAGCCC | 55779 |
rs558470779 | snp | A/G | 3.38576e-05 | 0.00411432 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426285 | CTGAGGTACTAAAAA[A/G]ATAAAATAATTTAAG | 55779 |
rs558477605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332657 | ATTAAGGAATTAATA[C/T]AGCAGGAAGAGGAAC | 55779 |
rs558482322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394344 | CCAACCCCTGCCAAA[C/T]GTTGGTTGATCTTTT | 55779 |
rs558515606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400417 | TCCACAGCTCAACTC[A/G]CTTGCATTCAAGAGG | 55779 |
rs558532944 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289547 | CCAAGGGGATGGTAT[C/T]GCCTCAAGACCTTTC | 55779 |
rs558551986 | snp | C/T | 4.97401e-05 | 0.00498674 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399910 | AACAAACTTACCATT[C/T]GGGGTACCCAAACAA | 55779 |
rs558563013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295581 | TAGGAAGCTCTCCTC[C/T]TACCCCATCTGCTAA | 55779 |
rs558592709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386027 | TATCATTGTATTACT[A/G]TCTATTTCTCCCTTC | 55779 |
rs558617568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340257 | CCTTCGGAGGCTGAG[C/T]CTAATGCTCATTTAG | 55779 |
rs558620328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399251 | AGTTCCCAGACACTC[C/T]GAAGCAGAGACAATC | 55779 |
rs558624642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303246 | TAGGATTCACCTTCT[C/T]ACACATGTGCACAGG | 55779 |
rs558652450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440781 | GTCCCTTGTCAGAGG[A/G]TCTGTAGCTTATTGC | 55779 |
rs558655118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405939 | CCATGCTTTTGAATT[C/G]AGAATATTCAGTCAG | 55779 |
rs558677520 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441344 | GGGAGGACGAAGGCT[A/G]TAACACTGGTCCAGC | 55779 |
rs558686449 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333098 | CTAGATTACCAGATA[A/T]CCTTGATGACCCTGC | 55779 |
rs558693277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405216 | TATTTTTTAACAACC[C/G]TACCGACTTTACTGA | 55779 |
rs558718555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340966 | CAGCCCCAGCCCGAC[C/T]GTCCCGCCAAACTCT | 55779 |
rs558763623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289899 | GGAGTGAATTTGCTA[A/G]TAGCCCCTCCAGCTC | 55779 |
rs558793545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386789 | CTTTACATCACTGAA[A/G]GAGGCACTGCAGAGG | 55779 |
rs558798763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311479 | CTCATTTTCTCTTGC[C/T]GCCACCATGTAAGAA | 55779 |
rs558826248 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372804 | ACCCAGAGAAAAGAT[C/G]ATGCAAGAAGGCAAA | 55779 |
rs558828365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379696 | ACCAATGCGAGAATA[C/T]ATTTTTATCATTAAA | 55779 |
rs558834572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378122 | CTCAAGCAATCTTCC[C/G]AATCTTCCCAATTAT | 55779 |
rs558837005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317388 | CTCCAAGCCAGGAGA[A/G]AGCAGGGCCGGCTTC | 55779 |
rs558888719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411526 | GTTTTAGTACCAGTA[C/T]CATGCTGTTTTGGTT | 55779 |
rs558920706 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401817 | CCAGAAAAACCCTGA[-/T]TTTTTTTTCAAAAGT | 55779 |
rs558923356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365786 | TTAATATACAAACTT[C/T]TAACTACATAGAAAA | 55779 |
rs558937704 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289699 | CAGCCTGTGACCCAT[A/G]TGACAATAGTGACGC | 55779 |
rs558944891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418359 | CCCAAAGTGCCATGA[C/T]TACAGGCAGGAGCCA | 55779 |
rs558961098 | in-del | -/TAAATGAAAAA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430424 | AAGAAGCTGGAAAAA[-/TAAATGAAAAA]AAAAAAAAAAACAAA | 55779 |
rs558969966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346762 | TCTGTAAAATGGACC[A/C]ATCAGCAGGAAATGG | 55779 |
rs558970897 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426880 | GGCGCAACAGTCTCC[A/G/T]AGGGGAACTCCCAAT | 55779 |
rs559001462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392483 | TAGAATGAATAAGAT[A/G]TAGTATTTATTAGCA | 55779 |
rs559031733 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425163 | AAGATAAATCAGCAC[A/G]AATTAATTTAGTTAC | 55779 |
rs559035790 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375848 | AAATAAATAAATAAA[A/T]AAAATCACCTCTAAA | 55779 |
rs559050185 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291360 | TTCAGTTTCATAACA[A/G]AGGTTGGGTGCTGCA | 55779 |
rs559114385 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335038 | AAAGAAAAGGAAAGG[A/C/G]GAAAGGGAGAAAGGA | 55779 |
rs559172836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349650 | GCCGCAGAGGACAAA[G/T]GTTCTCTGGGCCAGA | 55779 |
rs559178669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364876 | CTAAAGTACAGTAAG[G/T]TAAGAACCTCAGACC | 55779 |
rs559185321 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396117 | CAAAAAAATTATACC[A/G]TGCATATGCTCACCT | 55779 |
rs559193035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316801 | TTGAATCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55779 |
rs559209859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382593 | ACTGAAGGAAACAAT[C/G]CAATAAACAGGTATG | 55779 |
rs559262891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337310 | AAAGAAATCAAAAAT[C/T]TAAATAAATGGAAAG | 55779 |
rs559307935 | in-del | -/AAC | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370866 | CTCCTTAAGCTGATA[-/AAC]AACTTCGGCAAAGTC | 55779 |
rs559318406 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331415 | GTTAGGCTACTAGAT[G/T]GTCCAAAGGCCATTA | 55779 |
rs559318734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323358 | CTAAGCGAATTCACA[C/T]AGGAACAGAAAACCA | 55779 |
rs559320806 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347964 | AGGACAGGCAAGAGT[A/G]CAGGTTTTCAAGAAT | 55779 |
rs559349624 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363019 | AAATAAATGGCTATT[G/T]AAATTTTGAAAGAAA | 55779 |
rs559358821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322922 | GGAAACTTAAAATCA[C/G]AGTAGAAAGGGAAGC | 55779 |
rs559375346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370275 | TGGCAGAGACACAAC[A/C]AAAAAAGAGAATTTT | 55779 |
rs559379793 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390134 | TCAACAACACATTAA[A/G]AAGATCATTCATCAT | 55779 |
rs559382122 | snp | A/C | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445332 | TGGGTAGAAAGAGCA[A/C]ACCAGCCTTCTTCAT | 55779 |
rs559534041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329319 | ATGATAACTCAACTC[G/T]GGAAGGAAGTCATTA | 55779 |
rs559538379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424316 | TGGTGCATGCCTATA[A/G]TCCCAGCTACTCGGG | 55779 |
rs559552447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362226 | GTCTGATACAGTGTA[C/T]CGGAGTGCTCTGTGA | 55779 |
rs559559327 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366999 | GTGAGGCTGCAGCCC[A/G]GCGGGTGGAGGGGTG | 55779 |
rs559563801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430124 | CATATAGAATAGATA[C/T]GTTCTCTGAAAACAA | 55779 |
rs559581949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314549 | AATTCTCTAAACAGA[A/G]AGCAAACAATAAAAG | 55779 |
rs559597437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437442 | TGAACCACAACAAAA[A/G]GTAAGTTGGTCTCAA | 55779 |
rs559598521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423785 | TTGAGCAAAGAACCA[C/T]TCAAGAATTCGGCAG | 55779 |
rs559662809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326845 | ATCAGTCATGTTTAG[A/G]ATTAGAAAATCAGCT | 55779 |
rs559686263 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300327 | TATGGTGAATAATAA[C/G]TTAATTGTACATTTT | 55779 |
rs559689047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436223 | TTTCTATGTTACTCT[A/G]CAGTGAGTAACTGTT | 55779 |
rs559692963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427727 | TGAGTATGCTGATTT[A/C]TCTTGGAAGTGATAT | 55779 |
rs559719070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429375 | TGATCCTTTTACCCT[C/T]ATGTCACTGGTAGTA | 55779 |
rs559725644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428313 | TAGATAAGGTGATCA[A/C]AGATTAATGAATTGC | 55779 |
rs559749249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414511 | TTGTCATAAATAGCA[A/C]TTATTATTTTAAGAT | 55779 |
rs559756003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307922 | GAGGTGGAGGTTGCA[C/G]TGAGCCGAGATCGTA | 55779 |
rs559792577 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318835 | TGCCATACTGTTTCA[C/T]AAGTGAAGGAGAAAT | 55779 |
rs559796969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361683 | TTTGTATTTTTTAGT[A/G]GAGACAGGGTTTCAC | 55779 |
rs559814733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297765 | TCCAAGAAAACATAA[A/T]CTTGTAACAGGACTT | 55779 |
rs559851574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435716 | CCTGAGTGACAGACC[A/T]AGACTCTGCTTCTAA | 55779 |
rs559854483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388806 | TAATGATAAAGAGGT[C/T]AATTCAGTAAAAGGA | 55779 |
rs559863885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383613 | GAAAAGAGTGAACTA[C/T]TAAGTTAGGAAAAGC | 55779 |
rs559870563 | snp | G/T | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307549 | ATTGACTTCTTATAT[G/T]TATTGTCTTTCTCCA | 55779 |
rs559890260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305598 | GTCCTAGAAAACCTG[A/G]AAGTTTTCCAAATCA | 55779 |
rs559977308 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406774 | GAAATATTTTAATTA[C/T]AATTGATAATTGAAG | 55779 |
rs560040978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313264 | CTGCCCTGCTGGATT[C/T]CAGACTTGCATGGGC | 55779 |
rs560057268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393786 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 55779 |
rs560074362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374826 | TTTTTAGTAGAGATG[C/T]GGTTTTGCCATGTTG | 55779 |
rs560077499 | snp | C/T | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347364 | GAACTCTCAAAGTCA[C/T]GTCGCCCAAGCAAGG | 55779 |
rs560078353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299890 | AAAAAAGTTACCCAG[A/G]CATGGTGGTGTATGC | 55779 |
rs560092828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406421 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55779 |
rs560106147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342397 | CTATGAATTCAACCC[C/T]ATAATAAGTACTGTG | 55779 |
rs560123865 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297593 | TGTGCTGTCTTTCCA[C/T]GGAGGCTTTCCCTGC | 55779 |
rs560144495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358294 | GATGTTAAGATTTAC[A/G]TATTTTATGTAAATT | 55779 |
rs560177397 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287758 | CATATTGAAGAAATA[G/T]AACTAATCTTTTTTA | 55779 |
rs560231152 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412764 | ACATTTTCTTCATCC[A/G]GTCTATCATTGATGG | 55779 |
rs560235840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379295 | GTAAAAATTATTACA[C/T]TGTTACTTACCAAAG | 55779 |
rs560241707 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332559 | CACATTAGGTTACGA[C/T]GTATCGAGTTCTCCT | 55779 |
rs560252781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318589 | GAGCCCCAGCTAGAT[A/G]TGATACAAGATGACC | 55779 |
rs560274511 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386318 | TCATTCAGCTTCTCT[A/C]TGTCTTTAGATTGTG | 55779 |
rs560276585 | snp | A/C | 0.000205973 | 0.0101461 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344501 | GAATTTAAAAGCCTT[A/C]TTGTCATAGGCTACC | 55779 |
rs560333893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367102 | CTCAGCAAGGCCTAC[C/T]GCCTCTATAGACTCC | 55779 |
rs560367919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352064 | TGTCCTGTTTAGAGG[A/G]GGGATTGAGAGGTGA | 55779 |
rs560378470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353118 | AGCTGTGGGCACTTG[A/G]TCCCTGCATCTGGAA | 55779 |
rs560385314 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312683 | GGGTCCCCGTGCTGT[C/G]TGCAGCCTAGGGACT | 55779 |
rs560404813 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335072 | GAAAGAAAGAAAAAG[A/G]AAGGAAAGAAAAAGG | 55779 |
rs560422328 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318966 | AAAAAACAAAAAAAA[A/C]CAAAAAAAAAACAAT | 55779 |
rs560446147 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289227 | TGTCCAATTCAAAAT[A/T]AAGTAATTCAGTGTT | 55779 |
rs560481800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325725 | GATTATTCTAAAATA[C/T]GGAAATATCAAGGAA | 55779 |
rs560490498 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288791 | TAAGCTGGGGAGCCC[A/G]CTGTGGTGGGACAGG | 55779 |
rs560490585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325362 | AACAAAACATGAACA[C/T]GAATTATATACTGAA | 55779 |
rs560506803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362445 | ACCTCTTCTTGAAGC[C/T]GTATTTTTTGCATTC | 55779 |
rs560518061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413735 | TGTCTGTTTTGGTAC[A/C]AGTACCATGCTGTTT | 55779 |
rs560528121 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438481 | AATGCAGCACCTACT[A/G]GATAAGGTTGTTCTG | 55779 |
rs560534522 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386992 | GACAGAGTATTTAGA[A/C]CAGCCCGAGTCAGAG | 55779 |
rs560569485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414676 | TTTATTGATCTGTGT[A/G]TGTTGAACCAGCCTT | 55779 |
rs560578599 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358304 | TTTACGTATTTTATG[C/T]AAATTATATCTCAGT | 55779 |
rs560579315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346398 | CCTAGCTAAAGGATT[A/G]TAAGTGCCCCAATCA | 55779 |
rs560599285 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295845 | CAAAAACCATACAGT[A/C]ATACAATTCAAGCCT | 55779 |
rs560630771 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299069 | TTAATAAATTAAAAT[-/CA]CACAGTTATTGTTCA | 55779 |
rs560638830 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289627 | TCCCACGAAGGCCCC[A/G]GTGACCCCCACCTGG | 55779 |
rs560656358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392624 | CCCATTTACCCTCAT[A/G]TGATTATTATGCATT | 55779 |
rs560659177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365153 | TATAGAGAGGGTTGG[A/C]ACCAGGTAGAAAGGC | 55779 |
rs560676433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426488 | ATAAGGGACATTTCC[C/T]TCCTTCGCTCTGCAC | 55779 |
rs560686490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339946 | GCCTTTCTAATCCTT[G/T]TATCTGTCCCCCAGT | 55779 |
rs560693073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398975 | CTGGGGAATGGGCCA[C/T]AAAAGGTCATCAGCT | 55779 |
rs560695951 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361556 | CTGGAGTGCAGTGAC[A/G]TGATCTCGGCTCACT | 55779 |
rs560700153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296471 | CATAATCTTTCATCC[A/G]TTTTACATAATATTT | 55779 |
rs560756817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346844 | ACCACTCGGGTCCCC[C/T]TCCATGCTGTGGAAG | 55779 |
rs560836614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393045 | GACAGAATGGCTCTG[C/T]GTGTACATGGGACGC | 55779 |
rs560842165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302750 | GAGACTCCAGCCTGG[C/G]CGATAGAGTGAGACT | 55779 |
rs560845980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316979 | GTAAACCACCATAAT[C/T]TAAAAATGTCTCCAG | 55779 |
rs560858062 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288294 | GCTATTCCTGACTTC[C/T]GCATCCTTTTTCCAT | 55779 |
rs560865916 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439223 | TTTGAGTTGTAAAAG[C/T]TGTCAGAATTAGAAT | 55779 |
rs560871726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441072 | GATGAGGAAGCCGAA[A/G]TGCAGAGGGCCCAGC | 55779 |
rs560875033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405560 | AGTTCTGCCTACCTA[C/T]TAAACTCCTTGTACA | 55779 |
rs560884754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323758 | ATATGAAATAGATCA[A/T]TTGGGCTGGGTGCAG | 55779 |
rs560890332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338931 | ACTCCTCTGCTGGGG[A/G]TGCCTCTGAGACTCA | 55779 |
rs560904105 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443801 | CTGCAAAATGAGGAT[A/G]ATAGTACCTATCCCA | 55779 |
rs560918859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431538 | AAAAACTAGGGGGGA[A/G]CAAACTAAAGTTTCT | 55779 |
rs560952905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310936 | GAAGCAGGTGCTGCC[A/G]TGCCTCCTTTATAGC | 55779 |
rs560955861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432259 | ACACAGACAGCTCTT[A/C]AGGAACTTAGAGCTT | 55779 |
rs560965709 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351238 | CAAACTTACAAGGTT[A/T]TCAACAAAAGTAAAG | 55779 |
rs560972944 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371621 | AGACCTAAAGCCATA[A/C]AAACTCTAGAAGAAA | 55779 |
rs561003683 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384390 | AAGCTTGAGCTCTTA[-/T]TAGTTGTTATGTGCT | 55779 |
rs561008101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404589 | GTACTGACTCTGTAC[C/T]AAGCACTGGTTCAGT | 55779 |
rs561026771 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317547 | CTGCACCTGAGTAGT[C/T]TCCTGGCAACCACGA | 55779 |
rs561042110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438215 | TTTGACACATGTAGG[A/G]TTCAATAAATAAAAT | 55779 |
rs561051583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392800 | TACGGGAGGAAGAAC[A/G]TGTCTTAGAGAAACT | 55779 |
rs561057557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446957 | GGACTCATGGGGAGG[C/T]AACTGAATCATGGGG | 55779 |
rs561065569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324250 | AAAAGAAAATTTTCT[C/G]ATTCATATTAAGAAG | 55779 |
rs561089532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293879 | CCCCGGGAAGGCTGG[C/T]TAATGCAGACTGCTG | 55779 |
rs561156088 | in-del | -/TAAT | 0.00398564 | 0.0444627 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407347 | AATTTAGATTTAAAG[-/TAAT]TAACATTAAATAAAA | 55779 |
rs561156409 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288271 | TGGCCAAAATAAGTA[A/T]AGCACCTGCTATTCC | 55779 |
rs561160258 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312365 | TGGGATTACAGGTAT[A/G]AGCCACCCCGCCCAG | 55779 |
rs561166655 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418570 | AAAGATGAGGTAACA[C/T]GGACAGTGGAGGCAA | 55779 |
rs561190033 | snp | A/C | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327688 | CTGTTTTTCAAAATT[A/C]TTCAGGAGAAGTATT | 55779 |
rs561201940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301512 | CACATATCAAATATT[A/G]CTAAAGTATTTTAAA | 55779 |
rs561203865 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289267 | CAATTCCCAAACATG[C/T]GGAATGAAGCCCTGA | 55779 |
rs561224602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445994 | CACTCAAAGGAACTA[C/T]ATTTTACTGTACTAG | 55779 |
rs561259312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397082 | AATCACATAAATGAG[C/T]GTGAAATTGTGAACT | 55779 |
rs561280538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417266 | GAAAAAGTTACAAAC[A/G]AATGTAAACTTACCA | 55779 |
rs561295294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314959 | TCAAAAACACTACAA[A/G]AAATTAAAATAGAAT | 55779 |
rs561336642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365688 | ATCAGCCCTTACAAC[A/G]AGTGAATGAATAAAT | 55779 |
rs561339187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367276 | AGTGGGTCCCTGACC[A/C]CCATGTAGCCTGAGA | 55779 |
rs561362737 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391058 | TGAACAGAAAGAACA[A/T]AGCTGGAGAAATCAC | 55779 |
rs561365425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416638 | TGAACCTACAAAAGA[C/T]AAAATTTCACCAAAA | 55779 |
rs561438832 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391080 | AGAAATCACATTAGC[C/T]GACTTCAAGTTATAC | 55779 |
rs561449263 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342607 | AGTCCAATTCGATAC[A/G]TACAATTTGAGGTTG | 55779 |
rs561457881 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356886 | ACTACAGCAAGGTAT[C/T]TTATATGTGTAAACA | 55779 |
rs561470081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113382471 | TGAGAATAGTCAATC[C/T]TTCTGAGAAAGTTGG | 55779 |
rs561470334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300644 | AAAAAAATTCATACA[C/T]ATCAATTTTTTTAAA | 55779 |
rs561494846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445471 | AGTCATCCTGTGCCA[C/T]TGAATGGTACTGGAA | 55779 |
rs561506817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423648 | TTAAAATTGTTTAAA[C/T]ACTGTTAAGTTCTGT | 55779 |
rs561508174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389609 | ATTGACAAACCTTTA[C/G]CCAGACTAACAAAAT | 55779 |
rs561512924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329256 | GGACAGCATAAGTAA[C/T]GTGGGCGGAAAATGC | 55779 |
rs561521049 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402298 | TGGCATTTCCCCAAG[C/T]GCATACCACCAAACA | 55779 |
rs561525633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349795 | TGACTTCCTCCTGGA[C/T]ACTGGTGCAGCTTTC | 55779 |
rs561532146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362894 | TATTTCTTCCCCATG[C/T]ATTCCTTTCATGTGT | 55779 |
rs561539209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403026 | ACCCACTGTGGGAGA[C/T]ATGGGTTAAACAATA | 55779 |
rs561585708 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317475 | GGGGCCCATGCCTCA[C/T]CGCCCTGCAGGAGCA | 55779 |
rs561630672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113291944 | TGGGCTAATAAACAA[C/T]TCTTCAAGTGCAAAT | 55779 |
rs561648124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388988 | CAGAAAATGAACAAG[A/G]AAACATTGGACTTAA | 55779 |
rs561677623 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337621 | AGATCAACAGACTTG[A/G]AAGTAAACCCAGAAA | 55779 |
rs561696840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299479 | GGGAATGTAAATTAG[G/T]GCAACCACTTGGAGA | 55779 |
rs561710254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321720 | ATTTCTATACATCAA[C/T]AATGTACAGTCTGAA | 55779 |
rs561746852 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328461 | CCCCCAGCTTTCCCC[C/G/T]CCAGTATCACAAAGG | 55779 |
rs561750519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348957 | GAGTTGGAGATACCT[C/G]GTATCTTAGTCAAGT | 55779 |
rs561769324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369776 | ACCCTTCAAAAAATC[A/G]ATGAATCCAGGAGCT | 55779 |
rs561804274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375308 | CTACTGAGCTGTACA[C/G]TTAAAAATGGTTAAG | 55779 |
rs561817219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368709 | ATAACCAGCTAACAT[C/G]CTAATGACAGGATCA | 55779 |
rs561829967 | snp | A/T | 4.97352e-05 | 0.00498649 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395757 | TGACTTACATGAGAC[A/T]TGGGAGACCACATTA | 55779 |
rs561837177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437135 | TTCTAAGTTCCAGAG[A/G]CCACTCGCATTCCTT | 55779 |
rs561882238 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352624 | CAATATGTAGAATAA[A/G]AGGCAAATATCTGTA | 55779 |
rs561905364 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351645 | CAGTCAGGGATAGTA[C/T]GAGATGCCAACCGGC | 55779 |
rs561944606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400834 | AGAGTCCTGGGCTTT[A/G]TCCTTAATGGCTGTG | 55779 |
rs561948543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320581 | TATATAATGAAGTTA[C/T]ATATATCTAGATGTA | 55779 |
rs561960281 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443570 | TACCACAGCTTATAG[G/T]ACGGTGTCTGCCACA | 55779 |
rs561967713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334275 | TGTAATTGCATAAGT[C/G]CTTGCTGTAAAATTT | 55779 |
rs561970682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353464 | TGAATACACACACAC[A/C]CACACACACACACAC | 55779 |
rs561974776 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314747 | CAAGTATATTATAAA[C/T]GGGGGAGGGTAAAGG | 55779 |
rs561993228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298777 | CTCATTATGAAGTAC[G/T]TCGAGTAGTCAAGTT | 55779 |
rs561996537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436310 | AAATGACCACATACT[A/G]TGGGTAAAATTGTTT | 55779 |
rs561996925 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444222 | AATCTATCCTGAGCC[A/G]GGTGCAGTGGCTCAC | 55779 |
rs562002590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342374 | AAAATGTATTTATTG[A/G]CCAACTACTATGAAT | 55779 |
rs562002770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307486 | CCACTCCTGCACTCC[C/T]TTCATTTCTTTTCCC | 55779 |
rs562006205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333586 | TTTACTCTTGTATCT[A/G]TTAGAAAAACAGACA | 55779 |
rs562074803 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408683 | CAGCCTGACCAACAC[A/G]GAGAAACCCAACTCT | 55779 |
rs562075120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313427 | TGCCTTGCCTCAGAT[A/G]AGACTTAGGACTGTG | 55779 |
rs562082814 | snp | C/T | 1.69232e-05 | 0.00290883 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401281 | TCCATATGGCTCCAT[C/T]GGCATCCTAAAAAAA | 55779 |
rs562092556 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436681 | CCTAAGTTTCCAAGA[C/T]GCAGGTCCCAAATAA | 55779 |
rs562110813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435052 | TAAACATTTGTATTA[C/T]AAACTATGATCAAGA | 55779 |
rs562175607 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433361 | TTGAACCCAGAAGAC[A/G]GAGGTTATAGTAAGC | 55779 |
rs562209773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414939 | TCAGAAGGAATGGTA[C/T]CAGCTCCTCTTTGTA | 55779 |
rs562228727 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373420 | GCTCACTTGAAAGTG[A/G]TAGTTTGGATGGGAT | 55779 |
rs562256824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319684 | TGACCACATGCTTGG[A/T]CATAAAGCAAGAAGA | 55779 |
rs562271739 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441704 | TTATTATCCCCTAAA[G/T]GACGTCATGTAGATA | 55779 |
rs562286721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420284 | CTTAGATGAAGATGT[A/G]AGGTTGAAGTAGTTG | 55779 |
rs562314191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312078 | GTGTGTGTGTGTTTT[C/T]TTTTTTTTTTTTTGA | 55779 |
rs562387728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387784 | AGCTCTTGGACACCA[C/T]TTCTGGTCCTGGGCC | 55779 |
rs562403396 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288049 | CTTGCAATGAAAGCC[G/T]TACTACGCTTTGTGT | 55779 |
rs562409735 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410952 | TAAATGTCTTCTTTT[A/G]AGAAGTGTCTGTTCA | 55779 |
rs562424989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387065 | GCCTCACCACCATAG[C/T]CTAAAGTGCTCTGCG | 55779 |
rs562438994 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381129 | GTTTAAAGAGATTAT[A/T]AATAAAAATATAATT | 55779 |
rs562440461 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440019 | CACATATTATCGTAC[-/A]AATTCTCAAAACGAC | 55779 |
rs562451011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352190 | TAAAAGATTGTAAAT[A/G]CACAATCAGCACTCT | 55779 |
rs562490908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317688 | CTATGGCCAGCACTT[C/G]AGCTGGGGAGGAGCC | 55779 |
rs562514170 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399578 | AGGCCTGGCACATTG[A/T]CGGCACTCTGTAAAT | 55779 |
rs562577221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360228 | AGATAAAAAGAAGCT[C/T]AAAGATGATTTTGGC | 55779 |
rs562582346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305397 | AAGTTTTGTGAATAA[C/G]AGCCCAGAAGACATG | 55779 |
rs562602367 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347202 | TCTGGGAAAGGGCTC[G/T]CTAACAACCCCCGAC | 55779 |
rs562610494 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347923 | CCACTAAATCCGATT[A/T]TTCTCGGTCCTCATT | 55779 |
rs562633375 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289206 | CCTAAAGCTATCAAC[A/G]TATTTTGTCCAATTC | 55779 |
rs562639191 | snp | C/T | 1.65209e-05 | 0.00287405 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399954 | TTGTTTGAATTTCAT[C/T]TGGGCCAAAGGAGTT | 55779 |
rs562663883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385673 | TTGAGCTGGGGTCTT[A/G]CTCTCACCCAGGCTG | 55779 |
rs562691502 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329344 | TCATTACTGGTGGAA[A/G]GAAGTCATTACTGGT | 55779 |
rs562711222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295008 | GATTAAAGATAAGAA[C/T]ATAAGTATGCTCAAG | 55779 |
rs562740834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366996 | CCTGTGAGGCTGCAG[C/G]CCGGCGGGTGGAGGG | 55779 |
rs562763879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331967 | AGATGAAATAAAAGG[C/T]TTAGGGAGATTTATA | 55779 |
rs562778436 | snp | C/T | 6.59652e-05 | 0.00574267 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366256 | TTTTGATTTAGGACA[C/T]AGACTCGAATTGCTC | 55779 |
rs562801055 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332044 | AGAACTCCAGTCTTC[C/T]GACTTGTAGAAAAAG | 55779 |
rs562850391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325295 | GACAGAGCCAGACTC[C/T]GTCTCAAAAAAAAAA | 55779 |
rs562879971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398123 | AATAAAAATTTACTA[C/T]GTGTCTAAATGTACC | 55779 |
rs562880694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426371 | CCCATAATCTCCACA[A/T]GTCATGGGAGAGACC | 55779 |
rs562885824 | snp | C/T | 0.000204499 | 0.0101098 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358820 | TCCACTTGTTGAATT[C/T]TGAAAGCTGTTTTTC | 55779 |
rs562914496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372526 | TAGGTGGGAATTGAA[C/T]AATGAGAACACATGG | 55779 |
rs562923898 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384306 | CCTTGTGATCCACCC[A/T]CCTTGACCTCCCAAA | 55779 |
rs562926543 | in-del | -/ATATC | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309510 | AATGATTTATTTATA[-/ATATC]ATATCATATATAATA | 55779 |
rs562926921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339826 | CATATCAGAAACAGA[A/G]CTAGGGGGAGCCCTC | 55779 |
rs562946111 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291229 | TAAAAATTCAGGATA[C/T]CCCCAAATCAAATTT | 55779 |
rs562977960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435756 | AAAAAAAAAAGATAT[A/G]GTCTAACATGATACT | 55779 |
rs562986652 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364927 | TCTGTTGTTTTTTTT[A/T]AAAAAAATCTTTCTC | 55779 |
rs563009865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351088 | CCTAATAATGGGTCC[A/G]CTCAAATGTGTGAGC | 55779 |
rs563020039 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302671 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAGCCCA | 55779 |
rs563024890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364144 | AAAAAGTAAATCACT[C/T]AAAAGTACTCTGTTT | 55779 |
rs563047012 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357584 | GAAAGAACCAACTTG[A/C/T]CTGACACTTTGATTT | 55779 |
rs563057866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385216 | GTGAGTCCATTAAAC[C/T]TCTTTTTATTTATAA | 55779 |
rs563071164 | in-del | -/G | 0.00212903 | 0.0325574 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419977 | ACAAGCAAAAAGATA[-/G]GGTTTTTTGGGGTTT | 55779 |
rs563080557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310727 | CAGGGAGGAATCCCT[C/T]GAATAGTTTAGCACC | 55779 |
rs563203448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439584 | CCATGGCACGCATAT[A/T]CCATTGCAATGCCTT | 55779 |
rs563205577 | in-del | -/TA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300493 | ATATATATATATATA[-/TA]CCTACTATGTACCCA | 55779 |
rs563245738 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316870 | CGAGACTCCATCTCA[A/G]AAAAAAAAAAAAAGC | 55779 |
rs563280171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323613 | TTTTTTAGAAAAAAA[A/G]AATGCAACAGGTGAT | 55779 |
rs563282591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411112 | CCTGTTCACTCTGAT[C/G]GTAGTTTCTTTTGCT | 55779 |
rs563316521 | in-del | -/TTGGGGATTAAATGAAA | 0.0640965 | 0.167152 | intron-variant | CFAP44 | GRCh38.p7 | 3:113293435 | TTAGAAAGTACTGTT[-/TTGGGGATTAAATGAAA]TTGGGGATTAAATGA | 55779 |
rs563323904 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348752 | AACCCGGGTACATGT[-/C]CCCTTCTTCCTCTCT | 55779 |
rs563339272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356989 | AAAAATAACTCATGT[A/C]TATAAATAACCAAAG | 55779 |
rs563357019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338363 | ATATATCCAACTAGC[A/G]TATAGTATATATCCA | 55779 |
rs563365917 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423608 | AGCTTTCAATGTTTT[C/T]TCATGGCCATCTAGA | 55779 |
rs563411461 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349167 | TGATGTCCACCATAA[C/G]TCAGGGAAAGGAAGA | 55779 |
rs563440023 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398784 | CAACCCAAAATAGTA[A/G]AGATTAAATATTTCC | 55779 |
rs563452308 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445520 | ATGTTAATTCTCTAA[C/T]AGAGATACTACCAAA | 55779 |
rs563467676 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426495 | ACATTTCCCTCCTTC[A/G]CTCTGCACTTCTCCT | 55779 |
rs563472724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431498 | CTGTGTCAGAAATGT[A/G]GGGAGTACAGAAACA | 55779 |
rs563486576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350996 | ATGGTTCCTCCTGGG[C/T]GATTGAGGGAAAAAG | 55779 |
rs563487953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417155 | TGTCTACCCTACATA[C/T]AAATCAACCTAAATT | 55779 |
rs563510677 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314776 | GGGATGTAATGGTAA[A/G]TAAGGTTTTTGTACT | 55779 |
rs563547896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321618 | CTATACTTAGAAGAC[A/C]CCAAAGATTGCCAAG | 55779 |
rs563561355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337653 | AGACCCACACAAATA[C/T]GTCCAAATGATTTCT | 55779 |
rs563571030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293777 | CCAATCCTCCTAATT[C/T]ACTTTTCATGGAATA | 55779 |
rs563591033 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415819 | ATCATGTGGCACTGA[A/G]AAGAATGTATATTCT | 55779 |
rs563612821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308733 | GTAGCTGGAATTACA[A/G]GCACACACCATTATG | 55779 |
rs563616151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423865 | AAGATTTATGGACTG[A/C]AAAAGGAAAGTGACA | 55779 |
rs563621308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383633 | TTAGGAAAAGCAAAT[A/G]GTAAATGAAATACAG | 55779 |
rs563633871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390190 | TGCAAGGATGGTTCA[A/C]CATATGCAAATCAAT | 55779 |
rs563667758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402863 | ATTTTGGGGTAACGT[A/G]TATCTTGGAAAGATA | 55779 |
rs563669034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438174 | CAGAAATGGCAGTTG[C/T]TTTTACTATACTCCT | 55779 |
rs563685142 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320851 | CAGCTAATTAGAGGT[G/T]CCCACCCAGATTAAG | 55779 |
rs563706327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409930 | TTATAAATACCATGG[C/T]CACATCAGTAAGTTA | 55779 |
rs563732289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342090 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAAGCGG | 55779 |
rs563761384 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297813 | TCCCCTAAGAGAAGT[C/T]TGAAGGCCTTAATAT | 55779 |
rs563770309 | snp | A/T | 3.30115e-05 | 0.00406259 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396602 | AACCTGTTTCAACTG[A/T]ATATCAGCATCCAAA | 55779 |
rs563783835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113299699 | GATAAAGAAAATGTG[G/T]TACATGTAGACAATG | 55779 |
rs563813012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355101 | GGTGAAGGATTAAAG[A/G]CTACACATTGGGTAC | 55779 |
rs563834008 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291479 | TTTAAAGTAATAAGA[C/T]TGTTGGAGGTGATGA | 55779 |
rs563846225 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290805 | CATGAGAAACTATGG[A/G]GAAAACTTAGAATTC | 55779 |
rs563851191 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322887 | TTGACTCACAGCTCA[G/T]CATGGCTGGGGACGC | 55779 |
rs563877968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402293 | AAATCTGGCATTTCC[C/T]CAAGTGCATACCACC | 55779 |
rs563931766 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297340 | CCTGCTTTCTCTCCC[C/T]GCTGCTTTCTCATGC | 55779 |
rs563942556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394629 | CTCTATACCAGGGGT[A/G]TCCAATCTTTTTGCT | 55779 |
rs564070455 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424308 | GGATGTGGTGGTGCA[G/T]GCCTATAGTCCCAGC | 55779 |
rs564073819 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305554 | CAATGAAACTGCTAA[C/T]TATAGTATTTCTAAA | 55779 |
rs564091262 | snp | C/G | 0.00195503 | 0.0312041 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327729 | AGGTGACATGGTGCA[C/G]GTCAGATAATTTCAT | 55779 |
rs564092029 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388170 | TGCTGACTGTAGAGA[C/T]CTAGGGACTTGAGCA | 55779 |
rs564096005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307404 | AATCACCCAGAGAGC[A/C]CCCAAAAGTATTCAT | 55779 |
rs564180129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368250 | GAGAACACCACAAAG[A/T]TTCTCCTTGAAAAGA | 55779 |
rs564199252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381678 | CATTTAATCATGAAT[A/G]GGAAATCTCCATCTT | 55779 |
rs564220118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367712 | TCACCAGCAATGGAA[C/T]AAAGCTGAATGGAGA | 55779 |
rs564237425 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443492 | AGGTGCTGGGAGAGG[A/G]GGAAGCATTTACATA | 55779 |
rs564272350 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348202 | AGGTTCTTGGGTCGG[G/T]GGGAAGTAAACAAAT | 55779 |
rs564306066 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436261 | TTAAATAAAGAATTA[G/T]GCAGCCAATTCAGTT | 55779 |
rs564309204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347849 | CAGGGGTAAAGTCCC[A/G]ATACTAACAGGAGAA | 55779 |
rs564334954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407198 | TATCTACTACCTGCC[C/T]GGCAAGGTTGTAGGC | 55779 |
rs564338183 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430608 | AAATTTGACAATTGA[C/G]AAGAGAAGTGGGCAA | 55779 |
rs564370912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360497 | ACATGAGTTTGGTAG[A/T]ATAAGTGCTAATATC | 55779 |
rs564379437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353262 | CCACAGAATGAAAGG[A/G]CTAAAAGAATCAGGC | 55779 |
rs564387646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306591 | ATGTATGTTATCTCA[C/G]TCAAGGCTCATAGAC | 55779 |
rs564399220 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442536 | AAGTGGTTGCCTAGG[A/C]CTTAGTGAGATGCAC | 55779 |
rs564416247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360986 | TTTGATGGTGGATTT[G/T]GTTGCAGACCAGGTT | 55779 |
rs564444539 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349113 | CCTGTGTTCTAGAAG[G/T]ACTAAGGACAATTAA | 55779 |
rs564476682 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326534 | AATTTATTGTTTTCT[C/T]CAATGGCTGCTTGAA | 55779 |
rs564478812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319065 | AACATCATGATGACA[C/G]GATCAAAAATCACAC | 55779 |
rs564481841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407943 | AATGTCTGCCTTTTC[C/T]CCAAAGATATGGGGC | 55779 |
rs564488575 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289795 | TCTCCCTCACTCTTG[A/G]ATCACTTGCTCTGGG | 55779 |
rs564518026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414344 | TTCCTATTTGAATAC[A/G]CTTCATTTCTTTCTC | 55779 |
rs564550957 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346988 | CAGCGAGACCAAGAA[-/C]CCACTGGAAGGAACC | 55779 |
rs564616031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325837 | CTACAATAATCAAGA[C/T]TGTAGTATTGGTGAA | 55779 |
rs564617333 | snp | A/C | 1.66189e-05 | 0.00288256 | missense, stop-gained, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379377 | GGGTTGACGGAATAA[A/C]TATTTCAGGTAATGG | 55779 |
rs564619139 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289712 | ATATGACAATAGTGA[C/T]GCTATGTCACTTCTG | 55779 |
rs564620162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420701 | AGGCCTTTTCCTTGA[C/T]GTTGAAAGACAAGAT | 55779 |
rs564646679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427089 | CACATATGTACATCC[C/T]GCACATTTTTCTTTC | 55779 |
rs564657015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113380013 | CACCCTTCAGAATAA[A/T]CTTCCTAACTTATTT | 55779 |
rs564657267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386606 | CAAGGTGGTTAGAGG[C/T]AGGGACAAGGCTAGA | 55779 |
rs564668022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318197 | GAAAGATGAAATAAG[A/G]AAGAAGAAAACCAAA | 55779 |
rs564670217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341241 | GTGGGGATGGAGCCC[C/G]AGCCCGGGACCACGC | 55779 |
rs564670699 | in-del | -/TCACTGGA | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441128 | CGCAGGGCAGGTGTC[-/TCACTGGA]GCGGGGAGCCCCAGC | 55779 |
rs564686220 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333483 | GTATCTTGTAGTCTG[A/G]GGCTGTCTTCAGATT | 55779 |
rs564691544 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441115 | GCACCCAGCTGAGCG[C/G]AGGGCAGGTGTCTCA | 55779 |
rs564725055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341273 | TTTCGCTACCCAGCA[C/T]TTCCCTTCCTCCCTT | 55779 |
rs564766641 | snp | A/C | 0.000102939 | 0.00717348 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296898 | TTTCTAAAAGAAGAC[A/C]GTCACTGGCTCAGGT | 55779 |
rs564779044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296557 | AGTCCCTCTAACTAA[A/G]TGAACAGTAAAGAAG | 55779 |
rs564794076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386984 | TGCCCACAGACAGAG[C/T]ATTTAGACCAGCCCG | 55779 |
rs564795420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393646 | TCAACCTCCCGAGTA[A/G]CTGGGACTAGAGGCA | 55779 |
rs564806243 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316290 | ATCTGTGAGATGCAG[A/C]CAAAGCAGAGTTAAG | 55779 |
rs564821904 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289463 | ACCCATTCTACCAAT[C/G]CTTCATTTGTCAGAT | 55779 |
rs564826490 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377811 | GCACCTGCTACCATG[A/C]CCGGCTAATGTTTTG | 55779 |
rs564838887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434995 | CTGCAGTGACATCAT[A/C]ATGATGCCTTCTTTT | 55779 |
rs564840913 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384403 | TTATAGTTGTTATGT[A/G]CTGAATTGTGTCCCT | 55779 |
rs564859144 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312676 | GGGCCCAGGGTCCCC[A/G]TGCTGTGTGCAGCCT | 55779 |
rs564859547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311649 | CCAGTAGAGTGGGGC[A/G]CTGTTGAACAGATAT | 55779 |
rs564878173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323782 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55779 |
rs564881467 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287703 | AGGAAAAACAGGTTC[A/C]TAGTTCTCTTACCAA | 55779 |
rs564899262 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441613 | TCTCCGGGAACCCGG[C/T]ACCTATCCGCCCTTT | 55779 |
rs564899998 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317605 | GAACCTGACCCTGAC[C/G/T]CTGAATCTCAAGATA | 55779 |
rs564909048 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425032 | GGACTCTAATATACC[A/T]CCCCATCCCATTTGG | 55779 |
rs564915955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331180 | GTGTAGGCAAGGCCA[C/T]GATTCTGAATTTCAG | 55779 |
rs564948947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425574 | ATGTGAAAGTACTAA[C/T]GCCTTACAATGGACA | 55779 |
rs564967250 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359272 | CCCCACCCAGGAAAG[A/C]TAGCAGTATCTGGTG | 55779 |
rs564977683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412434 | AAAAAAAAAGATACA[C/T]GTGCAGAACGTGCAA | 55779 |
rs565012747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399086 | TGTTCTGATGAAACC[C/T]AAGCCACATGGAGAG | 55779 |
rs565031934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406331 | AAAATGGGGAAAAGT[A/G]AGTAACATAAATACT | 55779 |
rs565036781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113294862 | AGATGTAGTGAATAC[A/G]AGAAGAAAGAAAGAA | 55779 |
rs565046698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294023 | GGAACACTTAGCTTA[G/T]ACCATTTCCAGGGTT | 55779 |
rs565060132 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385165 | CTTCCTTTGTCTTCC[A/T]CCATGATTGTGAGGC | 55779 |
rs565067076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412773 | TCATCCAGTCTATCA[C/T]TGATGGGCACTTGGG | 55779 |
rs565076691 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386552 | AGGAAGAGATGCCTA[-/G]GTTGTACAATCAATA | 55779 |
rs565105058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397915 | CTTGAGATTTTAAAA[G/T]AAAGATATCATAGTC | 55779 |
rs565107275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301710 | ACACACATTGTGGAA[C/T]GGCTAGATTGATAGA | 55779 |
rs565133219 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324139 | CTCCCCCAAAAGAAA[C/T]GTTCAAATCCAAAAG | 55779 |
rs565134985 | in-del | -/ATTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418058 | ATTTATTGAGACACA[-/ATTT]ATTTATTTATTTATT | 55779 |
rs565142297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404422 | GAATTAAGTAGATTA[C/T]AGCATAATAGTATCC | 55779 |
rs565151484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339155 | ATGGTTCCTTCCTGA[A/G]GCCAAGCCATCCTTC | 55779 |
rs565155198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372421 | AGGATGAGTTCATGT[C/T]CTTTGCAGGGACATG | 55779 |
rs565191547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378353 | CGACAGGCAGAAAGG[A/G]TAGAGGAACTAATAA | 55779 |
rs565193371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371652 | ACCTAGGCAATACCA[C/T]TCAGGACATAGGCAT | 55779 |
rs565222620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385126 | CTTCTTCTTGCCTGC[C/T]GCCATGTAAGACATC | 55779 |
rs565229518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377859 | GGTTTCACCATGTTG[A/G]CGAGAATGGTCTTGA | 55779 |
rs565234533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385536 | AGAGAAAGTTCCATA[C/T]CACTTGAGAAGAATG | 55779 |
rs565255056 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433219 | GGATCACCTGAGGTC[A/T]GGAGTTCGAGACCAG | 55779 |
rs565267270 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393282 | ACTGCCCAAAATGAC[-/TT]TTAAATTATGCTGAG | 55779 |
rs565276460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403739 | GAGTTGGCCTTGGGA[A/G]TAAATGACTACTGAT | 55779 |
rs565349821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402659 | TAGGATCAGACTAAC[C/T]CCTGGGAGTTGGGCT | 55779 |
rs565388921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401885 | GTGTGATAAGAACAC[C/T]AGCCAAAACCTGACC | 55779 |
rs565423128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309990 | TTCCAACCAAACACC[A/C]CAGAAAAACTCTGGT | 55779 |
rs565437540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446751 | TTATGCAAACAACTG[A/G]CAATTCTCAATACTG | 55779 |
rs565440768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363929 | GAATCATTTGTCCAA[A/T]TACCTCAGTGTGTCC | 55779 |
rs565448282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310672 | TGAACTGTAATCCCC[A/C]GTGTTGGAGGAGGGG | 55779 |
rs565473933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345403 | GTGTGGTGTATATAT[A/G]TGTGTGTGTTTCCAT | 55779 |
rs565497202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308424 | AAGAACACAAACCCA[A/T]ATGCCTGCAGAGGGT | 55779 |
rs565500648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357524 | TGGCAAACCACTAGA[A/G]GCTTGGAGACAGGTA | 55779 |
rs565544708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315045 | ACAGAGAACATAAAC[A/G]GAAAATAAAAATTAA | 55779 |
rs565564281 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359100 | CTACACAGTTTAAGA[-/T]TTTTTTCCCACAATA | 55779 |
rs565565424 | in-del | -/GA | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296140 | CTCCCACTTATAAGT[-/GA]GAACATGCAGTATTT | 55779 |
rs565567994 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388710 | GAAAGATGTTCCATG[C/T]AAACAGAAATCAAAA | 55779 |
rs565600426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446053 | ATTTTGAATATACTG[C/T]GAAATGCTTAGCTTC | 55779 |
rs565607975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319397 | CTTAACTATCCGAAA[A/T]ATATATGCACCCAAC | 55779 |
rs565625620 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362606 | GCACCTCTGGTAAGA[A/T]CCATAGTTAACGCTC | 55779 |
rs565627128 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375033 | TTCTGACATATGCTG[C/T]ATCACGGATGAAACT | 55779 |
rs565651985 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441583 | CGTGGGGCGCATGCG[A/C]GGCCGGCGTCCAGCT | 55779 |
rs565656412 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359929 | ATTTTGTAGATCAAC[C/T]GGGTACTGTCTTTTC | 55779 |
rs565789885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335702 | TCAAAGAGAGAAAGG[C/T]ATAGAAGATATGAAA | 55779 |
rs565790513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361993 | TGTTCTGATAGCTTC[C/T]CACCACACACTGAAG | 55779 |
rs565810692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314278 | AAGTCTTGAAAGCAT[C/T]AACAGAAAAGTGACA | 55779 |
rs565821039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369245 | GATCTAATAGACATC[C/T]ATAGAACTCTCCATC | 55779 |
rs565849030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353581 | AGAGGAACTTCTTCA[C/G]CACTTTCATCTTTTA | 55779 |
rs565854103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423069 | TGTTGAACTAATGAA[C/T]TCATTAATTTGTGCA | 55779 |
rs565855685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408953 | AAAGGTGCATTACTA[G/T]TTAGCTTTTAAAATA | 55779 |
rs565892339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415343 | GATTTTTTTGGAGGG[G/T]TTTTCTGTCTCTATC | 55779 |
rs565896573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436585 | ACAAGGATGGTCTGA[C/T]AGTCGTGACTGAAGT | 55779 |
rs565898453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328005 | ACATAAATTAATTTA[C/T]TAAGTGGTAGGAATT | 55779 |
rs565925537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343024 | TAAAAAAAAATGGCT[A/G]TATCAACTAACAAGT | 55779 |
rs565946254 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395431 | ATCCAGGTGAAAGCA[C/T]TTCGACATGCTGTGC | 55779 |
rs565983363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352884 | ACCCAGTGTTATTTG[A/G]TACAACTTTATCCTC | 55779 |
rs566035540 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291063 | CCAAAACTGAAATTT[C/G]CATTTCTATTCTAAG | 55779 |
rs566044119 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428086 | GAGTTCCTTAGGATG[A/C/T]GTGTATTTGGATGGC | 55779 |
rs566052620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298897 | ATGAAAAGTGTTCTG[A/G]AGATGGATGGTGGTG | 55779 |
rs566056410 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397561 | ATAGATATGAGGTGG[G/T]TTGGATAGGATGCTG | 55779 |
rs566070638 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388303 | TGCTTATTAGTTTGT[G/T]TATAAAATCAGTGTT | 55779 |
rs566070886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334969 | CATCTATTGTATTAA[C/T]TGATAATCATTTATT | 55779 |
rs566106300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313514 | CGACTGGTTTTGAAA[C/T]GTAAGGACATGAGAT | 55779 |
rs566112646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326038 | AAACCACATATCTGA[C/T]ACAAGACTAGTATAC | 55779 |
rs566161106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298081 | GCCTGTGGCTGCCTG[A/C]CTGGCCTCTCTCAGT | 55779 |
rs566185662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333037 | TTCTAATAAGGCCAC[A/G]GCAAAAAAAGAGATA | 55779 |
rs566192543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361164 | AGCAGGTGTATGCTA[C/T]TCATGGTGGGTGTTG | 55779 |
rs566192857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435997 | CCTAATTGTAGAATA[C/T]ATACCTTTTGGGGTT | 55779 |
rs566224274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306860 | GTCATTCTTCAAGCC[A/G]TTTAATTATCCTGCT | 55779 |
rs566228124 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318067 | TTTTTTAACAGTCTA[A/C]AATGACTGAAATGAC | 55779 |
rs566232960 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350193 | AGAGAGAGAGAGAGG[-/A]AAGAGACAGAGAGAC | 55779 |
rs566235813 | snp | C/G | 0.000399281 | 0.0141238 | splice-donor-variant | CFAP44 | GRCh38.p7 | 3:113306200 | AAACAGATCACCATA[C/G]TTTTTTTGACAATGT | 55779 |
rs566241282 | snp | C/T | 0.00145389 | 0.0269227 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294690 | TAAAGAACATACCTG[C/T]TGATTCTGTAGTGTA | 55779 |
rs566289320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400364 | TTCTTTTAATCTCTC[A/G]CAATAACCATGGCTG | 55779 |
rs566290708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434448 | GTACCATATCATAAA[A/G]TTGTCTCTAAGCTTT | 55779 |
rs566299537 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296343 | TATTTCATTTTCTCA[C/T]TGTGGTTTTAATTTG | 55779 |
rs566322903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318786 | TTCAGTGTCCTTATA[A/G]AGAAAATAAATTCGA | 55779 |
rs566328181 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369038 | ACAAGAAGAGCTAAC[C/T]ATCCTAAATATATAT | 55779 |
rs566329931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407314 | ATGCAGTACCCTCCA[A/G]CTATGTGTGACTATT | 55779 |
rs566377399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367862 | GGTTAGATGAATGGC[A/T]AACTAGAATGAACAG | 55779 |
rs566395146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341530 | AAAATGGAATTCCTG[G/T]ACCGGAAACTCTAAG | 55779 |
rs566414890 | snp | C/T | 0.000102939 | 0.00717348 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305028 | AGCAGCCTCCCCAGA[C/T]GCATCACCTGGTGGA | 55779 |
rs566426150 | snp | C/T | 5.11269e-05 | 0.00505577 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373525 | CAAGGGGGGAACTCA[C/T]AGTGATATAGAAAAC | 55779 |
rs566435594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373105 | GTGATTTCTCCAGAA[A/T]AACTGTAACCCTGAA | 55779 |
rs566436791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420320 | TACCCTGAAACTCAT[A/G]ATTTTTCTACATATT | 55779 |
rs566452992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414014 | TGTTTTTCCGTTTGT[C/T]TGTGTCCTCTCTTAC | 55779 |
rs566473955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399581 | CCTGGCACATTGTCG[A/G]CACTCTGTAAATATT | 55779 |
rs566476245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304263 | CTTACTGAGTAACAG[C/T]AGCCAGGCAAACACA | 55779 |
rs566531255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311441 | CTAATGGTTTTATCA[G/T]GGGTTTCTGCTTTTG | 55779 |
rs566543331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405928 | CCTCCTATATACCAT[A/G]CTTTTGAATTGAGAA | 55779 |
rs566563136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380212 | CCCCTCCTCACAAAC[G/T]CACAATGGATCCCAG | 55779 |
rs566574164 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289856 | AGGCCCACATGGCGA[A/G]GAACTGAAGCCCTGC | 55779 |
rs566577808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340242 | TTGGTCTGATTTTCA[C/G]CTTCGGAGGCTGAGC | 55779 |
rs566597257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379633 | GGATGACAATGAAAA[C/T]AGAAAGAAGATACAC | 55779 |
rs566637903 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375399 | TTAAAATAAAAGTTA[C/G/T]GAAGCTGGAACAGAG | 55779 |
rs566639198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296108 | CATCTTTATGTCCAC[A/G]TGTACCCATTGTTTA | 55779 |
rs566648049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340869 | TGGAGAATGAGTACA[A/G]ATTTTTATAGAGTGG | 55779 |
rs566672543 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385964 | TTCTTTATTGATTTT[C/T]GATCTATATGTTTTA | 55779 |
rs566688643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307616 | TTTATACTTTGATGT[A/C]TCCTTAGCATCAGAT | 55779 |
rs566773255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351925 | TGGATTGACCCACTG[A/G]CCCTTCGGCTGACCT | 55779 |
rs566784752 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312950 | AGAACCTCTGGGGCA[C/G]TGTGGATGGGAAATG | 55779 |
rs566787281 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408063 | CCCCAAAGATTACAA[C/T]TAAAAATCTGCTCAA | 55779 |
rs566813337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378079 | TGGGATCTCACTATA[G/T]TACACAGGCTGGTCT | 55779 |
rs566852009 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377525 | TAAAATGCAAAAAAA[A/T]CCAGCACTTATTTTA | 55779 |
rs566852010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385247 | ATTACCCAGTCTTGG[C/G]TATGTCTTTATCAGT | 55779 |
rs566860129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317750 | ATGCATGAGTTCCTG[G/T]GCTGGGGTGAGAATG | 55779 |
rs566861045 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382564 | AAGTGGGAGAAACAG[G/T]AACATATTTAAATAC | 55779 |
rs566865875 | in-del | -/T | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432709 | TTACTATTTTTAGTA[-/T]ACTGCCTTAATAACA | 55779 |
rs566886171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384757 | CCATCCACTTTGTTG[C/T]ATTTTGTTATGGTAG | 55779 |
rs566893306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317300 | CATTGGGCAGCTCTG[A/G]CAGAGAGCGGCCATA | 55779 |
rs566899756 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410312 | CCCTCTCCCACCCCA[C/T]GACAGGCCCCGGTGT | 55779 |
rs566903264 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371932 | GGATATGAACAGACA[A/C]TTCTCAATAGAAGAC | 55779 |
rs566930911 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359788 | AAAATGAAAAAAAGC[C/T]AACCACTAGCAGGTA | 55779 |
rs566932293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323932 | GCCTATAGTCCCAGC[C/T]ACTTGGGAGGCTGAG | 55779 |
rs566942875 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366578 | CATAAGAAGAAGATA[C/T]CAAAGGGGGTCACTT | 55779 |
rs566958388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357960 | TATTAACAGTAGAAG[A/G]GATAAACTGTGGTAT | 55779 |
rs566972854 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384929 | ATCTAATATGGTTTG[G/T]CTGTGTCCCCACCCA | 55779 |
rs566979005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372583 | AGGGCCTGTTGGGGA[G/T]TGGGGGGCAGAGGGA | 55779 |
rs566992920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324713 | ATAGTACTGGATGTT[C/T]TAGCCATGCAATAAG | 55779 |
rs567087664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425197 | TGGGATTTAACAACA[A/T]GTTCTATTTTTATGT | 55779 |
rs567123992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294244 | GCTGGCTAAATATTA[C/T]GTAATAGCAAGTTGA | 55779 |
rs567125447 | snp | C/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330618 | AACAGCCACTTTAAG[C/G]TCTCTAAGAGAGAGA | 55779 |
rs567127048 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419984 | AAAAGATAGGGTTTT[C/T]TGGGGTTTTTTTCTA | 55779 |
rs567134119 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304929 | GGTGGAATTCTCAAC[A/C]AAGAACCACGATTCT | 55779 |
rs567151568 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288607 | CCCCACTGGTTTTTA[C/T]ATTTTTTCCTTTTTC | 55779 |
rs567199725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363373 | AGAAAGAGAAAATTA[A/G]TATTCAATAATTTGA | 55779 |
rs567215523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350674 | TGGCCCAGTGGCCCA[C/T]AGATGGCCCAGGTGC | 55779 |
rs567219334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391988 | AACAGTTTGGGGTTC[C/T]TCAAAAAAACTAAAA | 55779 |
rs567233065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431964 | TCCATTGCAGCCTAT[A/G]AAGTCCTTCCACATG | 55779 |
rs567233159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439606 | CAATGCCTTACTCCC[A/G]AATAAACATCATCTT | 55779 |
rs567241892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346100 | AGAGGATTGTAAACA[A/C]ACCAATCAGTGCTCC | 55779 |
rs567250366 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444067 | GTTATCAAAATATAT[A/G]AGTCTAAACACAAGT | 55779 |
rs567336988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328865 | TAGGTCTCCAAGTCT[A/G]TAAGGATTACACTTG | 55779 |
rs567351797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315941 | TTGTGATATTTTCAA[C/T]TTAAGATAGGTTTAT | 55779 |
rs567357026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113301992 | CTATGAGTTTAACTT[C/T]TTTATACTCTGCATA | 55779 |
rs567418005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316471 | TTAAAAGGAGAAAAA[C/G]AATAAAGAAAATCCC | 55779 |
rs567428911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309440 | CTGCTACAAAACCCC[A/G]TTATAGTAGCCCCCC | 55779 |
rs567436093 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396859 | CTTTATATCACTTTC[G/T]GGTAACCTCTATCCA | 55779 |
rs567441093 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113353948 | CAGTTGAAATAGCTT[G/T]TGTTCCCATAAACCT | 55779 |
rs567449146 | snp | A/C | 3.29489e-05 | 0.00405874 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403946 | GACTTGCTTGTCCCT[A/C]GACAGAGCTCCACTT | 55779 |
rs567453488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430661 | GCAAAACTTAGTAAA[A/G]AAGAAATAGAGAGCC | 55779 |
rs567477618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437649 | GGACAATAAATACTA[C/T]TCCTACCTTTCCTGG | 55779 |
rs567486454 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410633 | GTGTCTTTATAGTAG[C/G]ATGATTTATAATCCT | 55779 |
rs567488322 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288071 | GCTTTGTGTTTTGGG[G/T]CTGGAGAGGGTGGGG | 55779 |
rs567489943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322517 | ATCATCAGAGAAGTG[C/T]AAATCAAAACCACAA | 55779 |
rs567511695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376050 | TAATTACATTAAATA[C/T]AAATGAACATAGTAC | 55779 |
rs567521269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410322 | CCCCACGACAGGCCC[C/T]GGTGTGTGATGTTCC | 55779 |
rs567523930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423935 | GTTACAGCTTGGCAT[C/T]TGCCTTATTTTAACA | 55779 |
rs567577314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389128 | CCATATGTTAGTCCA[C/T]AAAACAAGTCTTAAA | 55779 |
rs567643273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436780 | GATAACTAAATGAAA[A/G]TTTTTCATCTGTGAG | 55779 |
rs567658126 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387518 | ACTAAAGAGCGCTTG[C/G]GCCCCGAATAATCAA | 55779 |
rs567658223 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360627 | TTCCAAGTCTATGGA[-/AAG]AAGATGTTTCTCTTG | 55779 |
rs567682454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314217 | CCAAATAAATTTATG[C/T]CAAAACTCATCACAA | 55779 |
rs567693498 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292211 | GATTTCCTGCTTTCT[G/T]TTTTATCGAAACATC | 55779 |
rs567719474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313574 | GTTTGGCTCTGTGTC[C/T]CTACCCAAATCTCAT | 55779 |
rs567735324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408860 | AAAAGCGAAACTCCA[C/T]TTCAAAAAAAAAAAA | 55779 |
rs567748056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375491 | ATGTAAGATACATAC[A/G]GAACATGAGAAGGAT | 55779 |
rs567760736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383693 | GATAACAGTGGCAAA[C/T]AAATTGTCTCAAAAA | 55779 |
rs567772528 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364309 | TTCACAGAAGATAGG[C/T]CTCTGTTTTGCTGTC | 55779 |
rs567847313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438584 | TGATATATTCCTGAA[C/T]AGATGAAAGAACAAG | 55779 |
rs567907008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414757 | TGCTGCTGGATTTGG[C/T]TTGCCAGTATTTTAT | 55779 |
rs567926513 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355235 | AATTGAAAAAAAAAA[A/T]TTAAGCCAGGCGTGG | 55779 |
rs567980346 | in-del | -/TTC | 0.00755907 | 0.0610114 | cds-indel, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443611 | AATAAGGAACAGCTA[-/TTC]TTATTATTATGCTGC | 55779 |
rs568028024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401805 | TTATTTTCTAAGCCA[A/G]AAAAACCCTGATTTT | 55779 |
rs568034163 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349637 | TGGAAGGTGCACTGC[C/T]GCAGAGGACAAAGGT | 55779 |
rs568048269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369194 | CAGAAGGTTAACAAC[A/G]ATATCCAGGATTTCA | 55779 |
rs568058439 | in-del | -/A | 0.103438 | 0.202533 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372400 | ATACTATGCAGCCAT[-/A]AAAAAAGGATGAGTT | 55779 |
rs568155408 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347495 | TCTAAAAACTACCCC[A/G]TCTCTGGTGCTTTTC | 55779 |
rs568164223 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374352 | TACTCCCTGGAGCAA[C/T]TGTCAATTTCTTTTA | 55779 |
rs568168508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422184 | GTAGCTTAAGCAGAT[A/G]GATTCTTTGTTCACA | 55779 |
rs568184524 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368499 | CAAACTAAGCTTCAT[A/C]AGTGAAGGAGAAATA | 55779 |
rs568216256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421303 | AGATACCATCTCACA[C/T]CAGTCAGAATGGCTA | 55779 |
rs568223900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327224 | GTCATACTTAAGAAA[C/T]TCACCAGCTTCTTTT | 55779 |
rs568275898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334922 | CTAGCCAACATGAGC[A/G]TGTACACATAGCTCT | 55779 |
rs568304090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298035 | GTGACGCAAATGAAA[C/T]GATGAATAGATGATG | 55779 |
rs568312649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333952 | ACTAAAAAGTCAATT[A/G]AACTTTTTTTTTTTT | 55779 |
rs568316527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342556 | GGGAAAGAGTGTTTG[C/T]GAGATGATGGTGGGG | 55779 |
rs568317763 | in-del | -/G | | | intron-variant, splice-donor-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429062 | CATACAGAAAAATCC[-/G]TAAGAGCTACTTTAT | 55779 |
rs568332331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394747 | AAAATTGCAAAATAT[A/C]TCATAAAGTTTTAAG | 55779 |
rs568358300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113435847 | GTTTTACTTTTTAAA[A/T]AGTGTATGTACGTGT | 55779 |
rs568375810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427935 | GAAGAATAAGGAAGA[A/C]ATGGCAAATGTACTA | 55779 |
rs568393713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297307 | ATTCAGGAGGCCCTG[C/T]ATGGTCAGCCTGCCT | 55779 |
rs568399416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367228 | CTCCCAGCACAGCGT[C/T]CAAGCTCTGAAAACG | 55779 |
rs568402410 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434412 | AGTGGGAGAGTAAAA[C/T]GGATATTGAAGAGAA | 55779 |
rs568421783 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442679 | TGGATGTCATTTATT[A/G]TATATAAATTATTTG | 55779 |
rs568455767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305908 | AATAGTTCATAAATA[C/G]AATTTATAAATACAT | 55779 |
rs568465576 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352392 | GCTCACTCTTTGGGT[C/G]TGCACCACCTTTAAG | 55779 |
rs568472630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347629 | CCATTGGGTGGGGAG[A/G]CCAACTATCCTTTTA | 55779 |
rs568486071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305172 | AGAAAGCCCCGTGTT[A/G]TGAAATGGTGACAAG | 55779 |
rs568547150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340826 | TTCTTGCCTTGGTGT[A/C]CTGGAAGAATCGGAT | 55779 |
rs568565784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113340084 | TTCTCCCGCCCTGCT[C/T]GTGACTGTTGGGCTC | 55779 |
rs568586620 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400149 | AATTTCAGGTACAAC[A/C]TCAAACAGGTAATTC | 55779 |
rs568588213 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441801 | ATCGCGGCGTTCCTA[G/T]GTTGAGGTTTTAACT | 55779 |
rs568669490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440484 | TTCATGTAGATGATT[C/T]CCAAGTCCTGTTACT | 55779 |
rs568669709 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407637 | TCATAGAATTGTTGA[A/C]AAATTCTTAGAACAG | 55779 |
rs568691114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413949 | TATAAATTACTTTGG[A/G]CAGTATGGCCATTTT | 55779 |
rs568698052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325514 | CAGTGGCATGATCTC[A/G]GCTCACTGCCAGCTC | 55779 |
rs568721089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311680 | CCAAAAATATGGAAG[C/T]GACTTTGGAACTGGG | 55779 |
rs568729744 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325471 | TTTTTTGGAGACAGG[G/T]TCTTGCTCTGTCGCC | 55779 |
rs568736016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325025 | CACTAAAAAAGGGGC[C/T]GGGCACAGTGGCTCA | 55779 |
rs568793410 | snp | C/T | 4.94947e-05 | 0.00497443 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379514 | ATTTTCTCCTTCAAC[C/T]CCCTTTGTCTCTCCC | 55779 |
rs568837734 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289812 | TCACTTGCTCTGGGA[A/G]AAGTCATATCCCAAG | 55779 |
rs568839650 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419072 | TTATTTTATAACAAA[A/T]TATTAAAATAGAAAT | 55779 |
rs568860508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311312 | AAATCTCATCTTGAA[C/T]TGTACTCCAATAATG | 55779 |
rs568935032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316646 | GACCGAGGTGGGTGG[A/G]TCACTTGAGGTCAGG | 55779 |
rs568949118 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289360 | TTTCCTCTCAGTTGA[A/G]ATGCACAGCAAGTCC | 55779 |
rs568967772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410891 | ATTTGCATTTCTCTG[A/G]TGGCCAGTGATGATG | 55779 |
rs568967824 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314509 | TTGTCACCAGCATGC[C/T]TATCCTAAAATAATG | 55779 |
rs568972634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296061 | CCCCCACCATCCTCC[A/C]CGCTGCTGGAGTCCC | 55779 |
rs568986662 | snp | C/T | 0.000299177 | 0.012227 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304029 | TGGAGCTCATGGATT[C/T]GTTCTTGCAGCCGTC | 55779 |
rs569005438 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412876 | TGATTTATATTCCTT[C/T]GGGTATATAACCAGT | 55779 |
rs569010331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385890 | CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAG | 55779 |
rs569019359 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438912 | CCACCCTGAGAGCTC[-/AAG]AAGTTAATTCCCAAT | 55779 |
rs569042870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392722 | ACAAATAATAATAAT[A/G]AAGACCAGAATAACT | 55779 |
rs569051627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418314 | CTTGTCTTGAACTCC[C/T]GGCCTCAAGTGATCC | 55779 |
rs569062744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357893 | AAAAACGTACACAAT[A/G]TTCATAGTAGCATTA | 55779 |
rs569101386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358638 | TTTCAAGTCAGTGGG[C/T]ACTTCCAGAGCCCTC | 55779 |
rs569101644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398466 | CATATGATCATTACT[C/T]GAATATAAGCCTAAA | 55779 |
rs569115417 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302399 | ATAAGTAGATTGATT[A/T]AAAAAATTACTATAT | 55779 |
rs569142459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404816 | TGAAGCACAAAACAG[C/T]TAAGTAACTTGCCCA | 55779 |
rs569187705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294179 | ACTTGGATTGGGTAA[A/T]TATTAATTAGGTATA | 55779 |
rs569216189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323151 | TTCAAGATGAGATTT[C/T]GGTAGGGACACAGCC | 55779 |
rs569233158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392418 | GGGTGGTGGGTGTGG[C/T]GGGGGGTGGGGTGCA | 55779 |
rs569247596 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391399 | AACAATTAAAAGAAA[A/G]CATTGGGGAAACTCT | 55779 |
rs569252039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113293331 | AAGCAATGGAGTCAG[C/T]GTTGGAGGCAGACAG | 55779 |
rs569262920 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380173 | GGTATATCTCCCAAA[C/T]TTATATGATATCATC | 55779 |
rs569285076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390409 | TGAATGAAGAAATAC[A/G]GAAAGCCTTTCCTCT | 55779 |
rs569285114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397234 | ATTAGCTAGGTACAG[C/G]AAGGTGGCACAAGCA | 55779 |
rs569296285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331286 | GCTTCCAGGCACAGG[A/G]GCTATACAATCTCAT | 55779 |
rs569309911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377408 | TGAGGGCATGAACTC[G/T]GGAGCCAGATTGCTT | 55779 |
rs569311051 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431244 | CAGAATGCCAGAAAA[C/T]TATTTCACATTATCA | 55779 |
rs569356483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371769 | GCACAGCAAAAGAAA[A/C]TATCATCAGAGTGAA | 55779 |
rs569356778 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113364544 | GAATTTTATTTATTT[A/T]TTATTCTTTTATTGG | 55779 |
rs569375802 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358089 | AAGGCCAGATGCAAA[A/G]GAATCCATACTGTAA | 55779 |
rs569396464 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371237 | AAAAACTACTTTAAA[C/G]TTCATATGGAGCCAA | 55779 |
rs569445966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384476 | TCAGAATGTGACTGA[C/T]AGATCTTTGGGGATA | 55779 |
rs569478867 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431891 | ACATCGTGATAGTCA[G/T]TCAGAAAGAGCCAGC | 55779 |
rs569541462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350609 | AACAAGGGTGTAGCC[C/T]GAAAGCACTGAGGCC | 55779 |
rs569557635 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362624 | ATAGTTAACGCTCAT[A/C]ACATATGTGCATCAG | 55779 |
rs569566080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383898 | AATGCTATCCCTCCC[C/T]TAGCCCCCAACCCCC | 55779 |
rs569569804 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346871 | GAAGCTTTGTTTTTT[C/T]GCTCTTCACAATAAA | 55779 |
rs569595306 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385868 | AGGCTTGTCTCAAAC[G/T]CCTGACCTCAGGTGA | 55779 |
rs569657367 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420685 | AGTAAAAATATTACG[C/T]AGGCCTTTTCCTTGA | 55779 |
rs569698226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403226 | TCACAAGGCTACAGG[C/T]TGACCAGCCACAGCA | 55779 |
rs569702986 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441834 | GATTTTAAGAGGGGT[C/T]CTGGGAGATAGTAGG | 55779 |
rs569811576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328782 | CTCTATAGACTATAT[A/G]TTTGGGCTCCCCTTT | 55779 |
rs569816501 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402697 | TTCTATGGGGTAAGA[A/C/G]GTAAAGATTTACTGT | 55779 |
rs569822111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348383 | CCAATATTCTCTCTC[C/T]GATGGGGAAAAATGG | 55779 |
rs569845109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416714 | TTTAGCATCCATTAT[A/T]TCATAATTTATTAGG | 55779 |
rs569872072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375402 | AAATAAAAGTTACGA[A/G]GCTGGAACAGAGATC | 55779 |
rs569886148 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318547 | ATCTTATTAGAGAGT[A/T]TGAAATACAAACTCA | 55779 |
rs569888992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321961 | CAATATACAGATTCA[A/G]TGCTACTCCTATCAA | 55779 |
rs569910056 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426868 | CTGGTCGGTCATGGC[A/G]CAACAGTCTCCAAGG | 55779 |
rs569918733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429442 | ATAGCCACTCCAGCC[A/G]TGTTATGCTTACTGT | 55779 |
rs569989924 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375159 | AGAAAGAAAGTATGG[G/T]TGCCAGGGGCTGAGA | 55779 |
rs570006654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416176 | TAAGATTGCAACCCT[C/T]GGTGTTTTTTTGTTT | 55779 |
rs570030677 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442879 | TATCTAGGTGCCAGA[A/C]AAGATAGAAAACATA | 55779 |
rs570031804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328162 | TTTATTCTCCATAGT[A/G]TCTCTACAATCCCTT | 55779 |
rs570036066 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425753 | ATATTTCTCTGTATG[A/G]TTATTTGGCATCAAA | 55779 |
rs570045288 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371484 | AGAAATGGGGAAAGG[-/AT]TCCCTATTTAATAAA | 55779 |
rs570047656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294326 | CACTCAAGATGCCCA[C/T]TTCAAGTCAAATGAA | 55779 |
rs570068471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335797 | GCATACTCTTTTCAA[A/G]CACATATTGAATTTT | 55779 |
rs570081318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437576 | TCAGGTTGTGTACAA[C/T]GTGGAAGAAAATACT | 55779 |
rs570096640 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296399 | GAGCATTTTTAAATA[C/T]AATTTTTGGCTGCAG | 55779 |
rs570097655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320263 | CTCTCTCAATATATA[C/T]AGATCTATATTTGTT | 55779 |
rs570128652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436661 | TAAAGTATTGGAAAG[A/T]ACTCCCTAAGTTTCC | 55779 |
rs570133973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319358 | GCATCACATAATGAT[A/G]AAGAGTGCAATCCAA | 55779 |
rs570160484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428626 | AACATTGAGAATAAA[C/T]ACCAAAAACACAAAC | 55779 |
rs570164819 | snp | C/T | 0.000463024 | 0.0152085 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401718 | TTACATCAGCAGTGT[C/T]TATTGTCTCAAAATC | 55779 |
rs570169804 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326154 | AATAAGATATACATA[G/T]GGCAAATAAACACAT | 55779 |
rs570175972 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345655 | CATAGCCCACAGAGT[A/C]TTATTTTTAAAAGCT | 55779 |
rs570199997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354512 | GCAAGGTCAGGCCTA[A/T]GACTACCAGCTTTCC | 55779 |
rs570213662 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364762 | ACATGAAGGATAGTG[C/T]ATACAATACTGAAGA | 55779 |
rs570235226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395461 | CCTGTGGCCAAAAGT[C/T]CCGTTGGAGCAAAGC | 55779 |
rs570315824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420374 | AGGTGAGAAAAAAAA[C/G]GCCTGGGCAGGAAAA | 55779 |
rs570377107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400981 | ACATGAAAATTCTAT[A/G]TATTTATAAAAACTA | 55779 |
rs570408847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334730 | ACACATACGAAACAG[C/T]GGCAATCTTTATATC | 55779 |
rs570411898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408290 | CATCCCGGAAATAGA[C/G]GAGGGTATGATATAA | 55779 |
rs570415115 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372058 | CAGTTAGAATGGCAC[C/T]CATTAAAAAGTCAGG | 55779 |
rs570416702 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368424 | AGCCAGAAGAGAGTG[G/T]GGGCCAATATTCAAT | 55779 |
rs570447794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393806 | AGGCGTGAGCCACCG[C/T]GCCTGATCTCCCCAC | 55779 |
rs570453729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320694 | GCAAGAAAAGCCAGT[C/T]CAAGCCCCAAAACTG | 55779 |
rs570455884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296698 | CAGCCAGATTCAACC[A/G]AAGATCAACCCCCTT | 55779 |
rs570483717 | snp | A/T | 3.51296e-05 | 0.00419089 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380870 | GAAAGGAAATTATTA[A/T]AAGATAATGCTTCAG | 55779 |
rs570484622 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393415 | TCTTGCGGGTGGATG[C/G]CTCATGAATAGATTG | 55779 |
rs570529765 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350192 | GAGAGAGAGAGAGAG[-/A]GAAGAGACAGAGAGA | 55779 |
rs570554957 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374441 | ATGTGCACACGTGCA[G/T]GTTTGTTACATATAT | 55779 |
rs570555598 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408536 | AAACTCTTTTAGGAG[G/T]TGGAGCCTATAAGAA | 55779 |
rs570591236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373694 | ACATAATTTCTATGA[A/T]TATAGATTTATTATT | 55779 |
rs570591967 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380374 | CAACTCTGCATTCTC[A/T]TGGGATGTTCTTCCA | 55779 |
rs570624859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341009 | TGGTCAATGGCCTGC[C/T]GGCGTGCTGGCATCT | 55779 |
rs570629243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387425 | CCCAGATGATATCTC[C/T]AGACACACCCTGGGA | 55779 |
rs570662966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352746 | GAAGAATACATGTAA[A/G]TGAACCACAGGCATA | 55779 |
rs570663216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341677 | AATAAATATAAAGAT[G/T]TTTAAGATATATTAT | 55779 |
rs570731285 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356624 | CAACAAAAAATACTA[-/G]GTCAATCGGATATCA | 55779 |
rs570749661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435236 | GGCATACCTGAGAAT[A/G]GGTAATTTATAAAGG | 55779 |
rs570767474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347089 | TTGCTCTTCTGCCCT[A/G]TTTTTCCTTAGAATT | 55779 |
rs570781310 | snp | C/T | 0.000102971 | 0.00717459 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305094 | CGCTGCTGCTTCTCT[C/T]GCTGATAAGCCTCCA | 55779 |
rs570801249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372637 | TAATTTAAATGATGA[A/G]TTGATAGGTGCAGCA | 55779 |
rs570838116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378663 | TTTGCAGTAGATCAA[C/T]AGAATATTTCAAGCA | 55779 |
rs570839145 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415088 | TTTCTGGTTTAGCCT[-/TG]GTAGGGTGTATGCAT | 55779 |
rs570876030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378167 | GAGTAATTTTTGCAT[C/G]TATATTTCCAGGACA | 55779 |
rs570876610 | snp | A/G | 0.000101312 | 0.00711658 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358851 | TGTGCATCTCAGCAC[A/G]GATTTGGGAATCTAC | 55779 |
rs570889094 | snp | A/G | | | intron-variant, synonymous-codon | CFAP44 | GRCh38.p7 | 3:113363138 | ATCAAGTTTATATTA[A/G]GCTTACTGTTCGTTT | 55779 |
rs570907777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359786 | ACAAAATGAAAAAAA[A/G]CTAACCACTAGCAGG | 55779 |
rs570911131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366727 | GACAGTGGGTGCAGC[C/T]GATGGAGGGCAAGCC | 55779 |
rs570942050 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367178 | TCTGCAGACTTAAAC[A/G/T]TTCTTGTCTGACAGC | 55779 |
rs570943945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405943 | GCTTTTGAATTGAGA[A/T]TATTCAGTCAGGTAG | 55779 |
rs570980698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412355 | AGAACCCTCTCTTGG[A/G]GTCTGGATCGGGACC | 55779 |
rs571012197 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413061 | ACTTTTTAATAATTG[C/T]CATTCTGACTGGCAT | 55779 |
rs571013714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374849 | CCATGTTGGCCAGGC[C/T]GGTCTGGAACTCCTG | 55779 |
rs571031303 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436990 | AAGGTGTTGGCAGTG[C/T]TGCCTTCACTTTCAG | 55779 |
rs571039015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317818 | GTTGCATATCTCCCT[C/G]CTACAGTCTTTTTGC | 55779 |
rs571041009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325452 | GCCTTTTTTATTTTT[A/T]ATTTTTTTTGGAGAC | 55779 |
rs571065741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446986 | GGGCCGGTCTTTCCC[A/G]TGCTATTCTCGTGAT | 55779 |
rs571078593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113324802 | GCAGACGAAATTATT[A/T]GGTGAAATTATTTTC | 55779 |
rs571082020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332306 | ATTGTCCATTTTGAT[A/G]AGAAACACACAGTTA | 55779 |
rs571100325 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379186 | TTTAATAAATGAAAT[C/G]TAAAAAAAAATAAAT | 55779 |
rs571120397 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311533 | TTCTGAGGCATCCCC[A/T]GCCATGTGGAAGTGT | 55779 |
rs571126127 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314865 | GGATAAATGATGACA[-/T]TGGTAGACTGGGATA | 55779 |
rs571126400 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288696 | AGGTGAAACATCTGC[G/T]TTCTGCACAGCACTG | 55779 |
rs571133276 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289319 | ATTTAGTCCAGCTCA[A/G]TTTGGGAATAATTAT | 55779 |
rs571145929 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412942 | TAGATCCTTGAGGAA[C/T]CGCCATACTGTCTTC | 55779 |
rs571157332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350730 | TGCTAGCAGAAGAAA[A/G]TGGGAAAATAACTTT | 55779 |
rs571190872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339457 | TGCGGTATGTACCAA[C/T]GAAGTAGGGGAAACC | 55779 |
rs571200045 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418879 | CTGGCTAATTTTTTG[A/T]ATCTTTAGTAGAGAC | 55779 |
rs571231579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295940 | TCAGGTGTACATGTA[C/G]AAGTCTGTGACTTGG | 55779 |
rs571240211 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310635 | ATATGGTTTGGATCT[C/G]TGTTCCCACCAAATC | 55779 |
rs571258974 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399653 | ATACACAAAGTTCTG[C/T]TGGGAAATTGCTTTG | 55779 |
rs571266193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425990 | AAGCAAATGGATGTG[A/G]CTGTGTTGCAATAAA | 55779 |
rs571290286 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323062 | AGAATAGCAGCATGA[C/G]GGTAACCACTCCCAT | 55779 |
rs571327054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322740 | TTAGTGGGTATATAC[A/G]CAAAGGAAAATAGAT | 55779 |
rs571338558 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350854 | ATCTTGAAGTGTGGG[A/G]CTGGTTCTGTTGGAA | 55779 |
rs571348162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113295228 | TTGAGTGGCCACACA[C/T]CTGTATAATGGCTTT | 55779 |
rs571348306 | in-del | -/CCC | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371487 | AATGGGGAAAGGATT[-/CCC]TATTTAATAAATGGT | 55779 |
rs571371555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310365 | ACTACATGTGGAGCT[A/G]GAACCCACACCCATA | 55779 |
rs571388796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311053 | ATGCAATCTCCAACT[C/G]AGTGAAAAAAGAAAA | 55779 |
rs571410653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113302848 | TTTGCAGTGCATTCA[A/G]TGGACAAAAAGGATA | 55779 |
rs571436065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357147 | ACTCATCAGGGAGAT[A/G]CCAATTTAAACCATA | 55779 |
rs571446521 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429588 | ATAATCTCTGCCTTT[C/T]TATATTAATGTTCAG | 55779 |
rs571508177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424125 | ACATTGCTAAAATTT[A/G]GAAGACATAAATTTA | 55779 |
rs571508229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431811 | GGTGAACAGTCAAAA[A/T]TAAATTTCTCAAATC | 55779 |
rs571526003 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417400 | AAGTTGGATAAAATA[G/T]TATGGTCATTTCTGT | 55779 |
rs571544615 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350703 | GCATTCAATCTGTGG[C/T]GGTGGCTGCTTTGCT | 55779 |
rs571557648 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332885 | CCAATGAGGATTTGT[C/T]TGAATTTCAGAGGTT | 55779 |
rs571622830 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371151 | ATGAACATGGCCATA[C/T]TGTCCAAGGTAATTC | 55779 |
rs571658175 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287222 | CACATGGTTCATCAC[A/G]AGCATGAGGGAACAG | 55779 |
rs571659323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428329 | AGATTAATGAATTGC[A/G]AGTGAATACAGATGA | 55779 |
rs571661437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413637 | AGGAAATCCTTTCCC[C/T]GTTGCTTGTTTTTGT | 55779 |
rs571708016 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287880 | CACTTCCCTTCTTTC[A/C]AAAGATACACCAACA | 55779 |
rs571723045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395589 | TGCTCTACGGGCCAA[A/C]CCCAGCAGCAGCCAC | 55779 |
rs571729043 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307768 | AGGTCAGGAGATCAA[G/T]ACCATCCTGGCTAAC | 55779 |
rs571729202 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298690 | ACACATGCTACAACA[A/C]GGATAAACCTGAAAG | 55779 |
rs571743986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384401 | TCTTATAGTTGTTAT[A/G]TGCTGAATTGTGTCC | 55779 |
rs571749669 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410718 | GATCCTTGAGGAATC[A/G]CCACACTGTCTTCCA | 55779 |
rs571761494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370705 | CACCATGCCTATTCA[A/T]CATAGTGTTGGAAGT | 55779 |
rs571783515 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344695 | ACAATAGTATCACTT[C/T]CCAGTGGATCTCGAA | 55779 |
rs571800151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113376429 | AAAGCCATGAGACTG[C/T]GTAGTTACCTTAGCA | 55779 |
rs571823490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385740 | TGCCTCCCGGGTTCA[A/G]GCGATTCTCCCACCT | 55779 |
rs571839940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445543 | CTACCAAATAACTGA[A/T]TACTTGGTCAACAGA | 55779 |
rs571840580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307389 | AGAGAACAGATAATA[A/C]ATCACCCAGAGAGCC | 55779 |
rs571882600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343859 | ACCAATATTAATGTT[C/T]GTATTATATCACTGT | 55779 |
rs571897591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436968 | CTTAGAGTTTCAGGA[C/G]GTTGCTAAGGTGTTG | 55779 |
rs571898934 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113437720 | GCAGGTCAGGTGGGA[A/C/G]AGACTCCTGTTCTCC | 55779 |
rs571902550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306468 | TTTAAGACACTTATG[A/G]CTTAATTGTTCCAGG | 55779 |
rs571933065 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400591 | GAGAGGAGAAACAGC[C/T]ACGGCTTCAATAGCT | 55779 |
rs571942798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349889 | GGACAGCCTGTAGCC[A/G]GGTATTTCTCCCACC | 55779 |
rs571971724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407714 | CTTATTAATAGTCTA[A/C]ACAAATGGACAGGAT | 55779 |
rs571981807 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356086 | AAGGTAGAGGAAAGC[A/G]TACATTAAAGTGAGG | 55779 |
rs571981842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349446 | TCAGAGAAAGGCCGC[A/G]GGCTTAGTCATGGCC | 55779 |
rs572030962 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412775 | ATCCAGTCTATCATT[G/T]ATGGGCACTTGGGTT | 55779 |
rs572058145 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323031 | CATCAGATCTCATGA[A/G]AACTCACTCATCATG | 55779 |
rs572076038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374031 | AAGAGCTATATTGCT[C/T]CAACTCTAATTTCCT | 55779 |
rs572083195 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443355 | TACTGTATTAGTTCC[C/T]GTAAATTAGGAGAAA | 55779 |
rs572113782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380487 | CTGAGCTGGAGTGCA[C/T]TGGTGCAATCACAGC | 55779 |
rs572119283 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436247 | AACTGTTTTTTTTTT[A/T]AAATAAAGAATTATG | 55779 |
rs572157484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348141 | GTTTCTGCTGCTGCA[C/T]TGGTGAGTGCAACTA | 55779 |
rs572209539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414844 | TGTTATGTCTCTTTC[C/T]GGTTTTGGTATCAGG | 55779 |
rs572220625 | snp | C/G | | | utr-variant-5-prime, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441489 | CTCCTCTCTTCACAG[C/G]GTCTGCCGGAGGCCT | 55779 |
rs572236372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368648 | AACATTCCAAATTGT[A/G]AAGAACATCAAGGCT | 55779 |
rs572239146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113361347 | AAAAGTTGCGTACTA[C/T]AGTATAATTTTGCCA | 55779 |
rs572260829 | in-del | -/CT | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339943 | TGAGCCTTTCTAATC[-/CT]TGTATCTGTCCCCCA | 55779 |
rs572263040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113319581 | TCAACACTTGACCAA[C/T]TGGACCTAATACGCA | 55779 |
rs572301975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360958 | GTTGAATTTGTTTTA[C/T]CTGTGTATGAATTTT | 55779 |
rs572309543 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315842 | CCCAACTCCAGGCTA[-/AC]ATAAGTGTTCTGAGC | 55779 |
rs572340148 | in-del | -/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289081 | CAGCCACCCTGCCCA[-/T]TGCCACACCCTGCTG | 55779 |
rs572368142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420666 | AAGTTTGTTGACTAA[A/C]CACAGTAAAAATATT | 55779 |
rs572388198 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358042 | ACATGTAACAACACT[A/G]ATAATCTTAGACATC | 55779 |
rs572392802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352428 | TAAACACTTGCTGCA[A/G]AAGTCTGCGGCTTCA | 55779 |
rs572427222 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442583 | GAATCTTAGAAATGA[C/T]AGAAATGCTGTGTCT | 55779 |
rs572466645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359164 | TACAGTTTTAAAGAC[A/G]CTATCTCAAAGAAAC | 55779 |
rs572475080 | snp | C/G | 1.65266e-05 | 0.00287455 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420097 | TCAGAAAGATCAGTT[C/G]GTTCCCAGCTATGTA | 55779 |
rs572490981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387662 | TCTGCTTGAGAAGTA[C/T]GGAGAGGGAAGAGTC | 55779 |
rs572506480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325747 | ATCAAGGAACTAGAA[G/T]AGCTACAACAATTTT | 55779 |
rs572506572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334037 | GCTCACTACAACCTC[C/T]ACCTCCCAGGTTCAA | 55779 |
rs572510654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395515 | AGAAGATCATGGTCA[A/T]CTAATAAGCCCACGG | 55779 |
rs572557951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325203 | GCTACTTGGGAGGCT[C/G]AGTCAGGAGAGTGGT | 55779 |
rs572558659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427043 | CTAAAGTACCCTACC[A/G]AAATATGTACTTGTC | 55779 |
rs572560575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435395 | GGGGAAGAAAACCCC[C/T]TATAAAACCATCAGA | 55779 |
rs572579679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386913 | ACTGTGAGACTGCAT[C/T]AGAACACAGTGCTGC | 55779 |
rs572594886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419159 | TTGGTCCCCTGCAGA[C/T]GGTGTGGACCTCAGG | 55779 |
rs572598784 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427484 | AGAATCATTTTATTT[C/G]GTCAGTCTTGTAACT | 55779 |
rs572602193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393074 | GCACCCTTACCAGAA[C/T]CACTCAAAGCCATCA | 55779 |
rs572614599 | snp | A/C | 0 | 0 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393628 | TCAAGCGATCCTCCC[A/C]CCTCAACCTCCCGAG | 55779 |
rs572621294 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292153 | ACTCATGTTTCACAC[A/G]TCACTTTCAGGGAGG | 55779 |
rs572625340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434904 | TATGGTACACTACAC[A/G]ATCAAAGGACAAAGG | 55779 |
rs572637148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346859 | TTCCATGCTGTGGAA[A/G]CTTTGTTTTTTTGCT | 55779 |
rs572693064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113332576 | TATCGAGTTCTCCTA[A/G]AAGTAGTAGCTCAGA | 55779 |
rs572697949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296526 | TAGTGCTGGTGCTCT[C/T]ACTCCAAGATAAACA | 55779 |
rs572712850 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441589 | GCGCATGCGCGGCCG[A/G]CGTCCAGCTCTCCGG | 55779 |
rs572728150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399831 | AGTCAGCAAATATCT[A/G]TATTTCCAGAAAATA | 55779 |
rs572729730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | CFAP44 | GRCh38.p7 | 3:113331770 | TCAAATACCACACAA[A/G]CCTAAATACTGGCTG | 55779 |
rs572809401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304699 | TGATTAGTCCATGTA[C/T]AGATAAAGATGGTGT | 55779 |
rs572814632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317996 | GCAAACACTAGGAAA[C/T]ACTAAAGAGCTGTGC | 55779 |
rs572852034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411754 | GCCATGTTCATGATA[C/T]TGATTCTTCCTATCC | 55779 |
rs572859449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412712 | ATGATCTCATTCCTT[G/T]TTATGGCTACATAGT | 55779 |
rs572861315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303196 | CAGGAGAGCTGAAAA[C/T]GTACATATCCCTCTG | 55779 |
rs572866729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406804 | GAAGTAAAATTAAAT[A/G]TTCATTACATTTACA | 55779 |
rs572866826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399494 | TCCCTCCCACTAAAG[C/T]GTAAGGTCCATGAGG | 55779 |
rs572884132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366888 | CAAAAGTCTTAGCAA[C/T]TGGCAGACCAGGAGA | 55779 |
rs572912965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418515 | TTTCTCATAGCCTTG[C/T]TAAAGTATTTCTGAA | 55779 |
rs572916641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372322 | TAGCAAAGACTTGGA[A/G]CCAACCCAAATGTCC | 55779 |
rs573027093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406167 | AACAATATTAAAGAA[C/T]AAATTAACAGATTAC | 55779 |
rs573034043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310576 | ATGAAAGTTTTTAGG[A/G]TTCAATTAAAAGTCA | 55779 |
rs573037444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379026 | TGGAACATGTATGAT[C/T]GACAAGCAGATAATA | 55779 |
rs573086818 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308483 | GGCTGAGACCAAGTT[C/T]CCAAGCTGCAGATGT | 55779 |
rs573095467 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346232 | CACTTTGTAAAAACA[C/T]ACCAATCAGCACTCT | 55779 |
rs573165565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410490 | AACTCATCCTTTTTT[A/G]TGGCTGCATAGTATT | 55779 |
rs573168421 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391790 | TGAGAATGGCAAACA[C/G]GTATATGAAAAGGTG | 55779 |
rs573188996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354415 | TCAGCCCTGCTCAGC[A/T]GCTGCCTGGAAATAG | 55779 |
rs573204933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345919 | TTTCCCTTTTCTTTC[A/C]TACATACTATCTTTC | 55779 |
rs573207238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113397892 | GGAAACACGGAGTTC[A/G]AGGTCCCCTTGAGAT | 55779 |
rs573207514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398605 | GTGAGCTAGGTCTGC[C/G]AATCTAAATGCTCTG | 55779 |
rs573212327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385503 | TGTATGTGGTAAAAA[A/C]AACATTTGATCTATC | 55779 |
rs573234420 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286530 | GGAGGGAACAGAAGT[C/G]CCCTTGTCTCGGTTG | 55779 |
rs573236268 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439829 | CCTCATGCTCACAAG[A/C/T]TCACTCAATCCCAGC | 55779 |
rs573249448 | snp | A/G | | | intron-variant, splice-acceptor-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286674 | CTCTTTCTCCCCTCA[A/G]GGCCCCCATGCTGCT | 55779 |
rs573255138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385089 | CTGACAGATTTATAA[A/G]GAGGAGTTCCCCTTC | 55779 |
rs573274543 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287385 | CCAGAATCAATAATC[C/T]GTGGCAACATATCTC | 55779 |
rs573323117 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433103 | TTTTTATGGAGCCCA[C/T]CTTCCTACAGCTTTC | 55779 |
rs573359829 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334132 | AATTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT | 55779 |
rs573364721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316791 | CAAGAATTGCTTGAA[C/T]CTGGGAGGCGGAGGT | 55779 |
rs573399251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357421 | GACATACACAGGGAA[A/G]CCTATATGAAGAGAC | 55779 |
rs573401613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323253 | GGACAAAGAAAATCT[A/G]CATATACACCATTGA | 55779 |
rs573410670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322908 | CTGGGGACGCCTCAG[A/G]AAACTTAAAATCACA | 55779 |
rs573421624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113312908 | ATACCCAGGCAGAAG[C/T]TTGCTGCAGGGGTGG | 55779 |
rs573436157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356900 | TTTTATATGTGTAAA[C/T]ACACACACACATACA | 55779 |
rs573513753 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430158 | AGGTAAGTTAGAAAC[C/T]AATAATGATAAGATA | 55779 |
rs573566746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363903 | TTTTTCAGTATATAC[C/G]TTTATCACATGAATC | 55779 |
rs573575502 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355381 | AAAAAATTCGCCGGG[A/C]ATGGTGGCAGGTGCC | 55779 |
rs573575507 | in-del | -/TCTCTCTC | 0.00171637 | 0.0292445 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320225 | GAGGAGGTATATTAG[-/TCTCTCTC]TCTCTCTCTCTCTCT | 55779 |
rs573611752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362682 | AATCACACACTTGCC[A/G]TCACATTTTTCACAC | 55779 |
rs573611767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113354989 | ATGGCTTCAAGACCT[A/G]AAGACGGATCACATC | 55779 |
rs573622946 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347041 | CCCAGATGGGACATC[A/G]CCATGCAGTGAGTAC | 55779 |
rs573645543 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344933 | AAATACTAAACAACT[C/T]ATTATTAATCACTAT | 55779 |
rs573660326 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349109 | TTGACCTGTGTTCTA[A/G]AAGGACTAAGGACAA | 55779 |
rs573703865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292527 | AGACATAATACTTGC[A/G]TGGTGCCCACTTTGT | 55779 |
rs573707495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329263 | ATAAGTAATGTGGGC[A/G]GAAAATGCTGGAGAG | 55779 |
rs573714022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113300216 | CTAGAGTCTGGGAAG[G/T]ATAGTGGAGGTGGGG | 55779 |
rs573733203 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362877 | ACTCTTGGGTTCTAC[-/T]TTATTTCTTCCCCAT | 55779 |
rs573745547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113337228 | TGCTCAAAAAAGAAA[C/T]GCATATGTGCAAATC | 55779 |
rs573765027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429976 | TCACTATCAACCATC[C/G]TGACCTGACATTTAT | 55779 |
rs573765127 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438648 | TAAGAGGGTGAGCAC[A/C]TTCTGTTCATGCTCA | 55779 |
rs573835573 | snp | C/T | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395802 | CCAGGAGTATTAATA[C/T]AACCAATCGGCTTAT | 55779 |
rs573854793 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373618 | CACATAAATGCATGA[G/T]AATTTTTTGATTATT | 55779 |
rs573856631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348979 | TAGTCAAGTAAATGA[C/T]AGAATGACAGCCGAA | 55779 |
rs573857075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428735 | CAAAATTAGTGGAGA[A/C]TGAACAAGGATGGGT | 55779 |
rs573879760 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288630 | CCTTTTTCTCCTTGA[A/T]GATCTAAGGTAGCTG | 55779 |
rs573889679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335837 | AGACTGTATATGCGT[A/G]GCCATAACACAGTTC | 55779 |
rs573927057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335168 | TCCTCATAATATAAA[C/G]AACCAGAAAACTGAA | 55779 |
rs573936627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402804 | CCTCTGTGAAATATT[C/T]AACTTCTTTTCTCCT | 55779 |
rs573952519 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357673 | TTGTAGTACTTTTTT[-/A]CAGTAGCCCTAAGAC | 55779 |
rs573957936 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333939 | GGGTTTTTTAATGAC[-/T]AAAAAGTCAATTAAA | 55779 |
rs573959030 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342832 | CCGTCTCTGCTAAAA[A/T]TACATAAAAAAAAAA | 55779 |
rs573964603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113321358 | GACAGACTAGGCATT[A/G]AGGAAACATACCTCA | 55779 |
rs573981432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113436116 | ATCCACATCTCAACA[A/T]CCACTCCAGCACTGT | 55779 |
rs573988068 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354885 | CCAACCAACACAAAA[C/T]GAGCACACTAAACAA | 55779 |
rs574004975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113328222 | CCCAACTTCTTATGT[G/T]GAAAATTTTCAAAAC | 55779 |
rs574018531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307852 | GGGCGTGATGGCATG[C/T]GCCTGTAGTCCCAAC | 55779 |
rs574024569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315290 | GCAGCTATATTAATG[C/T]CAGACAAATAGACTT | 55779 |
rs574041040 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406391 | AATATTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 55779 |
rs574047708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422611 | CAAAGATGTAAATGA[A/G]GCTATTCAAGCCTCC | 55779 |
rs574049690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369487 | ATGACTACTGGGTAA[A/C]TAACAAAATGAAGGC | 55779 |
rs574073285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409761 | ACAGGTCAAAAGACC[C/G]AACTGATAAAACAGG | 55779 |
rs574132332 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323148 | AAATTCAAGATGAGA[C/T]TTCGGTAGGGACACA | 55779 |
rs574137134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421750 | ACAGAAAACCAAATA[C/T]TGCATGTTCTCACTT | 55779 |
rs574141198 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374762 | GCCTCGGCCTCCCGG[C/G]TAGCTAGGATTGCAG | 55779 |
rs574164323 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295336 | CTCTCAAGTAGCTGG[A/G]ACTACTGGTGTGCAA | 55779 |
rs574237565 | snp | C/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291392 | TCAGTTCTAAGATAA[C/G/T]CAAATTGTAGAGAGA | 55779 |
rs574250408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113382040 | AGGGTTTGAGGGAGC[A/C]AGTCCTCAAGGGAAA | 55779 |
rs574251988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113348103 | AGGGTCCAGGGACCA[C/T]TGCAGGTTCTTGGGC | 55779 |
rs574269634 | in-del | -/AGG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435361 | CACATGGTGACAGCA[-/AGG]AGAAGTGCAGAGCGA | 55779 |
rs574283861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407642 | GAATTGTTGAAAAAT[G/T]CTTAGAACAGTGCCT | 55779 |
rs574298398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428287 | TTCCCCAGGAAAGGA[A/G]TTAGAACTGGTAGAT | 55779 |
rs574302068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113298638 | GGCATGTACATATAA[C/T]GGAATATTATTTGCC | 55779 |
rs574321932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414116 | ATTTTATTCTCTTTG[C/T]AGTGATTGTGAATGG | 55779 |
rs574330302 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418695 | TTAGGATTAGCTTTT[-/G]TTTTTTTTGTTTTTT | 55779 |
rs574346836 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346020 | GACCCAGATTAACAT[C/T]GAGAAGTGAACCCAG | 55779 |
rs574355337 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443826 | ATCCCATAAGGTGTC[A/G]TGAAGCACATAAAGT | 55779 |
rs574357666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413638 | GGAAATCCTTTCCCC[A/G]TTGCTTGTTTTTGTC | 55779 |
rs574365593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401054 | TGGTAAATTGTGTTA[C/T]GAGATAGATTCTTTT | 55779 |
rs574405499 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343799 | TTCAGAATTTATCCT[A/G]GAAGCAAAAAGGAGA | 55779 |
rs574455297 | in-del | -/A | 0.229136 | 0.249128 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318957 | CAAAAATAAAAAAAC[-/A]AAAAAAAAACAAAAA | 55779 |
rs574486588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373332 | ATGGATCTTTAAAAA[C/T]TGACAATATCCATGA | 55779 |
rs574502780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113386869 | CATGAAGAGATAATC[C/T]GGGTACTTGGGGGAA | 55779 |
rs574559522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326336 | ACAGTGTCTCTACAT[C/T]GTCCATGTTATAGTG | 55779 |
rs574589540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113318874 | TCTCAGTAAAGCAAA[C/T]GCTGAGGGAATAAGT | 55779 |
rs574646624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113368015 | ATCAAATTAATGAAA[C/T]AAAGCAAGAAGACAA | 55779 |
rs574665268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425305 | TGGTGGTTTAGGCCA[C/T]GTGGTGATAAGTACT | 55779 |
rs574677528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420509 | GCAAAAATAAATAAG[G/T]TTAAACCTATTTGGG | 55779 |
rs574687069 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352018 | GAAGTAGCTGGAGCA[A/G]TCATTGCCCAATTCC | 55779 |
rs574734776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426867 | TCTGGTCGGTCATGG[C/T]GCAACAGTCTCCAAG | 55779 |
rs574749298 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379847 | TCACTGTTAACCCAG[A/G]AATTAGGTAGACTGA | 55779 |
rs574753062 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296746 | CATCTTCATCTCTTT[C/T]GCATTTGCTAGCTCC | 55779 |
rs574770552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113359061 | GGAGAAATGTTCTTC[A/G]CAATTAACAATAATA | 55779 |
rs574782697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367404 | TCTGCAATATTTGCC[A/G]TTCTGCAGCCTCCAT | 55779 |
rs574805620 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347118 | TTCGGGGGCTAAATA[C/T]TGGACACCTGTCAGC | 55779 |
rs574808540 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358293 | AGATGTTAAGATTTA[C/T]GTATTTTATGTAAAT | 55779 |
rs574810960 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396149 | TTAGTGCATAAAGAA[-/T]TTACACAGTTATTCT | 55779 |
rs574814748 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366806 | GATTTTCCTTTCCTA[A/G]CCAAGGGAAACTGTG | 55779 |
rs574817892 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427533 | TTTTCTGTTTGTTAA[C/T]CTCCATTTTCACTTC | 55779 |
rs574854044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113365958 | TAAATAACTTTTAAT[C/T]TATAACGAATATGAA | 55779 |
rs574877076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346823 | CACCCCAGCCAGCAG[C/T]GGCAAACCACTCGGG | 55779 |
rs574916584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341080 | TGTCTTCTTCTGCCA[A/G]TGTGTCCCTCATGAT | 55779 |
rs574929173 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325145 | TGTCTCTACTAAAAA[C/T]AGAAAAATTAGCCAG | 55779 |
rs574930697 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331360 | ATGCCATTCTGAGAG[A/C]CTGAGAGCACATGCA | 55779 |
rs574965770 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350525 | GGGTAAATTTAAAAC[C/T]TATAATTGATAATTG | 55779 |
rs574995576 | snp | A/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362918 | CATGTGTTCTATAAC[A/T]ACAGTTGATGTAAAA | 55779 |
rs575010199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351693 | TCTGAAATCAGACAA[C/T]GCCTTTCAAACTCTC | 55779 |
rs575016794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352043 | AATTCCCAACAGCAG[C/T]TGGGGTGTCCTGTTT | 55779 |
rs575086892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311876 | TTGTTGGGAACTGGA[C/G]CAAAGGAGACTTTTG | 55779 |
rs575087508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339552 | TACCTTGGGCCTGTT[C/T]ATGCCATGAAGCATG | 55779 |
rs575105349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405660 | TGCCCTCTAAAAATT[C/T]GATATTTATTTCTAA | 55779 |
rs575123858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405388 | ATTTGTTCTGAGAAG[G/T]CTAGGCCCTTGATCA | 55779 |
rs575163747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345774 | ACACACAAACAAGCA[A/C]TTCTTAGAATTTAAT | 55779 |
rs575176484 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439397 | ACATAAAAAAAAATA[A/C/T]TTCTACAAGGACATC | 55779 |
rs575219211 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300180 | CTGAACTCATGGAGA[C/T]AGAGAGTAGAATGAC | 55779 |
rs575222943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310463 | TCTACCTCCACCAAC[A/T]GTAAGGAGACTCCCA | 55779 |
rs575246804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311517 | TCACCTCCTGCCATG[A/T]TTCTGAGGCATCCCC | 55779 |
rs575251667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113331647 | CACCTGTGAAGTGTC[C/T]GAAGGACTGCAGATT | 55779 |
rs575279308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113438838 | TCCTCTCTTTTCCCA[C/G]AGAAAGTATCCCAAT | 55779 |
rs575279950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113371608 | AGACTTAAATGTAAG[A/G]CCTAAAGCCATAAAA | 55779 |
rs575287793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317486 | CTCACCGCCCTGCAG[A/G]AGCAGCTATACAACA | 55779 |
rs575292299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425419 | AACATCATAATGTGA[A/T]GACGAACACAAAATC | 55779 |
rs575296964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316231 | CTCAATAAAAATTTT[A/C]AAAACTACATTGACC | 55779 |
rs575299125 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328072 | TTAACTAAGCCATCA[A/G]TCAAGAATGCCCTTC | 55779 |
rs575318416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377754 | ACCTCCCGGGTTCAA[A/G]CAATTCCCCTGCCTT | 55779 |
rs575333545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113378272 | AGGAACCATGTTTTC[A/T]TTATCCCTTTATCCT | 55779 |
rs575341977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411629 | GTCTTGGCAATGTGG[C/T]CTTTTGGTTCCATAT | 55779 |
rs575346570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445913 | CCCAATGTCAGACAC[G/T]TATTGGCTCAAGTCT | 55779 |
rs575402648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416908 | GGTTCTCTATCTTCA[A/G]TGTGCATCAGAATCC | 55779 |
rs575411901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294555 | CAGTGTCCTCGGGGA[C/T]GCAGATGGTCTGGAA | 55779 |
rs575449861 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288755 | TAAAGAGAAATTTAG[C/T]ACATGGCTCACAGAC | 55779 |
rs575484072 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113385430 | AGGTGAATGACAAGA[A/G]CCTCAAAGAAAGAGA | 55779 |
rs575504565 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340653 | GGGGCTCCGACCCCA[C/T]GGCAGTGTCTAGGGG | 55779 |
rs575516332 | in-del | -/C | 0.00452114 | 0.04733 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296909 | AGACAGTCACTGGCT[-/C]AGGTTGTTCAATGGC | 55779 |
rs575520332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113384976 | GTAGCCCCCACAATT[A/C]CCACATGTCATGGGA | 55779 |
rs575551276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113309666 | GAACTACAGATCACC[A/C]ATTTACAATTTATAA | 55779 |
rs575564248 | snp | A/G | 0.000150599 | 0.00867621 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416517 | TTTAAATATGCTTCT[A/G]GACTCACCTCGAAGG | 55779 |
rs575584554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113292488 | CAATAACATTTGAAT[A/G]CATGAATACATCTGT | 55779 |
rs575592400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350196 | AGAGAGAGAGAGGAA[A/G]AGACAGAGAGACAAA | 55779 |
rs575593256 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377886 | TTGATCTTCTGACCT[C/T]GTGATCCACCCGCCT | 55779 |
rs575611652 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315292 | AGCTATATTAATGTC[A/C]GACAAATAGACTTTA | 55779 |
rs575613799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404135 | GATTATAAAATTTTT[A/T]AATGGAAAAATAAAA | 55779 |
rs575627346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356816 | TAAGTTGAACTTCAG[C/T]AAAAGAAAAAACTTC | 55779 |
rs575637012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293801 | TGGAATAAACAACAT[G/T]GTTTCTTACTTTGGG | 55779 |
rs575655280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113391685 | ACCAGAATATATAAG[A/G]AGCCCAAACAACTCT | 55779 |
rs575692260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390957 | CAATGCCTATCAAAA[C/T]AGCAATCACATTCTT | 55779 |
rs575774434 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379097 | CACAAGAAGACATAT[-/A]AAAGAGATGTTAAGA | 55779 |
rs575778162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396225 | AAATACTGATTATAA[A/G]TAATACAACTAGCAT | 55779 |
rs575780693 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113389558 | AAAGAAAACAAAAGA[G/T]CAACAAATTAAAAAG | 55779 |
rs575794146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113322874 | GAAAGAGGTTTAATT[C/G]ACTCACAGCTCAGCA | 55779 |
rs575799939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329159 | TAATTTTCAAGACAA[C/T]ACTAATACCCATGAA | 55779 |
rs575860828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113362886 | TTCTACTTTATTTCT[C/T]CCCCATGTATTCCTT | 55779 |
rs575871750 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350206 | AGGAAGAGACAGAGA[-/G]ACAAAGACAGAGAGA | 55779 |
rs575883782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375681 | CACCTTTTAACCACG[C/T]GTGTTGGCACACACC | 55779 |
rs575921598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113383349 | CATCGATGGTGGTCT[C/T]GTATGCTCACAGGAC | 55779 |
rs575937968 | in-del | -/TAAAAGAATAG | 0.0023933 | 0.0345097 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375860 | AAATAAAATCACCTC[-/TAAAAGAATAG]TAAAAGAATGTATAA | 55779 |
rs575951500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369303 | CAGGACCACATCATA[C/T]TTATTCTAAAACTGA | 55779 |
rs575987687 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415480 | TCTGAGATCTTTCTG[C/G]CTTTTTGATGTGGGT | 55779 |
rs576055658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349496 | TTAGAGAGGACAGAA[A/C]ATGGAGCAGGCCAAT | 55779 |
rs576108912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429083 | GCTACTTTATAAAAA[A/T]TTTATAAGAACTAAA | 55779 |
rs576146853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113307785 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGAAA | 55779 |
rs576162207 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113374130 | TAAATAAGAAAGAGA[A/C]TGTAACATCATGATC | 55779 |
rs576167616 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314261 | AACTAAAGACAAAGA[A/C]AAAGTCTTGAAAGCA | 55779 |
rs576172965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343447 | ATATGAGATATTTAT[A/G]TAGTTATAAATAACC | 55779 |
rs576216609 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349399 | TTCTATAATAGGTAC[C/T]AAGAGGAACATGCCG | 55779 |
rs576276475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113342248 | TGAGGCAGGAGAATT[G/T]CTTGAAACCAGGAGG | 55779 |
rs576312697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113347676 | AAGCGGGCCTAACAA[A/G]AGCTATTCCTGAAGC | 55779 |
rs576352803 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444143 | GAGCCAGGGAGCAGA[A/G]ATCATTCAAAAAACA | 55779 |
rs576366927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113313732 | TTTTATCAGGGGTTT[C/T]CACTTTTGCATCTTT | 55779 |
rs576379798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408671 | GGAGTTCGAGACCAG[C/T]CTGACCAACACGGAG | 55779 |
rs576394486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327387 | TTTATTCTTCTACCT[C/T]ACAGAATATCAGACC | 55779 |
rs576396245 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426828 | AGCCATTATGCCCAC[C/G]TGCATCAGGAGTAAA | 55779 |
rs576433318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113335034 | TTTTAAAGAAAAGGA[A/G]AGGAGAAAGGGAGAA | 55779 |
rs576454657 | snp | C/G | 0.000200844 | 0.0100191 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326541 | TGTTTTCTCCAATGG[C/G]TGCTTGAAAACCAGC | 55779 |
rs576482744 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422054 | CTTTTAAATGTATAT[C/T]GTTAGTATGTTTAAG | 55779 |
rs576491200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113334192 | CCTGACTTCATGATC[C/T]GCCCACCTCAGCCTC | 55779 |
rs576492667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381301 | TATTAAAATTAGATT[C/T]ACATTTGGTTCCTTT | 55779 |
rs576493942 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316968 | TAAATTATGGAGTAA[A/G]CCACCATAATTTAAA | 55779 |
rs576504713 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP44 | GRCh38.p7 | 3:113320561 | AATGAAGTTATATAT[A/G]TGTATATATAATGAA | 55779 |
rs576531399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113388401 | AAAAAACATACAATG[C/G]ATATACAAGAAATTT | 55779 |
rs576534208 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP44 | GRCh38.p7 | 3:113441087 | GTGCAGAGGGCCCAG[C/T]GTGCCAAGCGTCGCA | 55779 |
rs576539582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414873 | GGATGATGCTGGCTT[C/T]GTAAAATGAGTTAGG | 55779 |
rs576576735 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408838 | ATTGCACTCCAGCCT[G/T]GGCAACAAAAGCGAA | 55779 |
rs576585483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113387681 | GAGGGAAGAGTCAAG[A/G]GTATTTTGTCTTGCA | 55779 |
rs576594425 | snp | G/T | 1.74631e-05 | 0.00295487 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419979 | AAGCAAAAAGATAGG[G/T]TTTTTTGGGGTTTTT | 55779 |
rs576596232 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315719 | GTAGAAACCAGACTT[-/C]CAAGTACTCATACAG | 55779 |
rs576598744 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401030 | TAGGTATTGACACGG[C/T]CACTTTTCTGGTAAA | 55779 |
rs576609081 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361136 | GTGGATTTAATGGAA[A/G]GCCAGGGAAGTTAGC | 55779 |
rs576664167 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290598 | GAGATTATCCTGCAA[C/T]GGTTATAGCCATGAA | 55779 |
rs576664826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113325232 | GTGTGAACCCGAGGG[C/T]GGAGCTTGCAGTGAG | 55779 |
rs576690984 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435578 | CTAAAAAAAAATTTT[A/T]AATGGCCAGGCATAG | 55779 |
rs576692190 | snp | C/G | 0.000102907 | 0.00717238 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306311 | GGTGAAGGGCCAGCT[C/G]AAAAAGAGCCACATC | 55779 |
rs576720630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360820 | AGACCAACTGTTTCA[C/T]AGGATGGGAAAAATC | 55779 |
rs576727187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113297706 | TGCAATATATTTTAC[C/T]TTTGTTTTTGTCTTT | 55779 |
rs576767855 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289548 | CAAGGGGATGGTATC[A/G]CCTCAAGACCTTTCT | 55779 |
rs576786082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407451 | TTGTATTAGACAGCA[C/T]AGAACATTCCCAGTC | 55779 |
rs576813934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113352532 | TGGTTTTGATCACAT[A/G]AAAATTAAAAATTCT | 55779 |
rs576834835 | snp | C/T | 0.00195543 | 0.0312073 | intron-variant | CFAP44 | GRCh38.p7 | 3:113296933 | CAATGGCTCCCATTG[C/T]TATAAATGAACACCA | 55779 |
rs576852205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113360130 | GTAAACTTTGTATTA[C/T]GTAAAGAGGTTCATC | 55779 |
rs576858500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113394395 | TGAATGAAGGATGCA[C/T]ATAATATTATATGTT | 55779 |
rs576869622 | in-del | -/TATT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374398 | ATTTATTTATTTATT[-/TATT]ATTATACTTTAAGTT | 55779 |
rs576889455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113393681 | CCACCATACCTGGCT[A/G]ATTTTTGTATTTTTT | 55779 |
rs576933013 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442966 | ATGTTTTCTTTCAAT[C/T]TCTAGACATCTTTTC | 55779 |
rs576934632 | snp | C/T | 1.65203e-05 | 0.002874 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399943 | GCAGTACCTCCTTGT[C/T]TGAATTTCATCTGGG | 55779 |
rs576947326 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292979 | TTGAAGGAAACTTTA[A/G]GAAAATCACAGAGAT | 55779 |
rs576964861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413533 | CTTTAATCCATCTTG[A/C]GTTAATTTTTGTATA | 55779 |
rs576971969 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399258 | AGACACTCTGAAGCA[C/G]AGACAATCCATCTCT | 55779 |
rs576972201 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113392518 | CGGGAGATTATAGTC[A/G]ATAATAACTTATTGC | 55779 |
rs577010727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113398676 | CTTCCCTGGACTAAG[C/T]TCTCTTTCTGATCTT | 55779 |
rs577032279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113367378 | AAGGATCAGGCAGCA[A/G]TATTTGCTGTTCTGC | 55779 |
rs577058101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379709 | TATATTTTTATCATT[A/G]AAACTTTTAAATCAT | 55779 |
rs577071069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373192 | ACAATTCAATTGTGC[A/G]ATAAACAAAAATACT | 55779 |
rs577101586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379105 | GACATATAAAAGAGA[A/T]GTTAAGATTATTTAA | 55779 |
rs577148999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113372121 | TAGGAATGCTTTTAC[A/G]CTGCTGGTGGGAATG | 55779 |
rs577177742 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434839 | ACTTAAACTGCCACA[-/CT]GTTATATCTTCCTGG | 55779 |
rs577186125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304476 | GCTGATCTTGTTGTT[C/G]TTGTTTTCCTAAAAT | 55779 |
rs577214072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113339792 | TTCTCAGCCAGCAGG[A/G]GCCATTCCTGTTAAC | 55779 |
rs577223468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113377665 | CAAAAACATATATAT[A/T]TTTTTTGAGACAGAG | 55779 |
rs577245698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113440030 | CGTACAATTCTCAAA[A/G]CGACCCTATGAGGTA | 55779 |
rs577258137 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432906 | ATGCATCTATCAGAT[A/C]ATCTATTATTTAACA | 55779 |
rs577297015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303335 | ATCCTAAATATCCAT[A/C]AATAGGAGGCTAAAT | 55779 |
rs577325716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358100 | CAAAAGAATCCATAC[G/T]GTAACACTCTATTTA | 55779 |
rs577330307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113345643 | TCATCTTTCTCTCAT[A/G]GCCCACAGAGTCTTA | 55779 |
rs577351861 | in-del | -/A | 0.00042924 | 0.0146436 | splice-acceptor-variant | CFAP44 | GRCh38.p7 | 3:113401289 | CTCCATTGGCATCCT[-/A]AAAAAAATTAAATAG | 55779 |
rs577352170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113311480 | TCATTTTCTCTTGCT[A/G]CCACCATGTAAGAAG | 55779 |
rs577359336 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339815 | CTGTTAACTTTCATA[C/T]CAGAAACAGAGCTAG | 55779 |
rs577369331 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP44 | GRCh38.p7 | 3:113310680 | AATCCCCAGTGTTGG[A/G]GGAGGGGCCTGTTGG | 55779 |
rs577401172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113346309 | AATGCACCAATCAGC[A/G]CTCTGTGTCTAGCTA | 55779 |
rs577401264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113351992 | GCCCCTTCTTCACCC[A/C]TACCCAGCAGGAAGT | 55779 |
rs577424560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113316812 | AGGCGGAGGTTGCAG[C/T]GAGCCAAGATCACGC | 55779 |
rs577426374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404430 | TAGATTATAGCATAA[C/T]AGTATCCAATTTCAA | 55779 |
rs577427813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411535 | CCAGTACCATGCTGT[G/T]TTGGTTACTGTAGCC | 55779 |
rs577461343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113357538 | AAGCTTGGAGACAGG[C/T]ATGGAACAGATTCTC | 55779 |
rs577498259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350129 | AGGAGAGGGGAGAAC[A/T]GCAGCATAAGCGGCT | 55779 |
rs577534785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113317394 | GCCAGGAGAGAGCAG[A/G]GCCGGCTTCCCTTTG | 55779 |
rs577536111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113349707 | AGTACTGAGGGCTCC[C/T]GGGGCAAGTGCCAGC | 55779 |
rs577562481 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411073 | TGAGTAGATTGCAAA[A/C]ATTTTCTCCCATTCT | 55779 |
rs577575000 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113355499 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 55779 |
rs577585427 | in-del | -/TG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297398 | CACACTGGCCACCTC[-/TG]TGCTTCTCAAACATG | 55779 |
rs577587269 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324484 | TTAGCCAATGTAATC[C/T]ACCATATTAATAGGC | 55779 |
rs577615350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446775 | AATACTGGCAAGAGC[C/T]TGAAAACATATGGCT | 55779 |
rs577628676 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360315 | TTATTGTAGAAACAT[A/G]TAGATTGTATCACAT | 55779 |
rs577641646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113338751 | CCTGTAGGGAGAAGG[A/G]GACCTTGGCCTTACT | 55779 |
rs577677143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338303 | CAAACTCTGTTAAGG[A/G]AATGAAAAGACAAGC | 55779 |
rs577707373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113323438 | CATGGACATAAGCAC[A/G]GGAACAACAGACACT | 55779 |
rs577715960 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309351 | TTTTCTGTCCACTGA[C/T]GCCCACTCTGTTCCT | 55779 |
rs577718051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113439318 | TCTCACGCTTGTATG[C/T]TGGATAACTATCCCA | 55779 |
rs577718791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431349 | TCTGCGCCTAACAGC[A/G]TCTGACATAAGGAAG | 55779 |
rs577755608 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357917 | AGCATTATTTATGGT[A/G]GCCAAAAATAGAAAC | 55779 |
rs577778599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423431 | AGGCCTGAGCTGCTG[C/T]GCCTGGCCTGATCCT | 55779 |
rs577805901 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383524 | GGAGTGTCAGGAGGA[A/G]CATAAACATTCAGTC | 55779 |
rs577811907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113329014 | ATAAATATTTGCTAA[A/G]TTAATAAATTAGTTA | 55779 |
rs577851156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344292 | CATTAAAGAGGAAAG[C/T]GGACATGGAGCATTT | 55779 |
rs577889314 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113356629 | AAAAATACTAGGTCA[A/T]TCGGATATCAATATA | 55779 |
rs577916154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113390146 | TAAAAAGATCATTCA[A/T]CATGGCCAAGTGGGA | 55779 |
rs577922259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363602 | AAAATATCTAGGAAG[A/G]AGTAAATTAAAAACT | 55779 |
rs577928589 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333956 | AAAAGTCAATTAAAC[-/T]TTTTTTTTTTTTTTT | 55779 |
rs577945573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422684 | CACTGCTCTCACATC[C/T]CCTTCTTCCCTTTCT | 55779 |
rs577971353 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337532 | ATGAGAGGAATCACT[C/G]TACTGGATTTCAAGA | 55779 |
rs577974912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113315336 | TACCAGAAACAGAAA[A/G]AAACCTTACATAATG | 55779 |
rs577989540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410394 | ATGAGTGAGAACATG[C/T]AGTGTTTGGTTTTTT | 55779 |
rs577997869 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290221 | GCTCTCCAGTAGAGA[A/G]GTGACTACATCAGAA | 55779 |
rs578015357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113314616 | TAAGCAAAAATATGG[A/G]TAAATACAACAGGCT | 55779 |
rs578028766 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344194 | TTTAAGAATAGCTAG[A/C]TGTGGCAAGTAAGAA | 55779 |
rs578055480 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311945 | CCCTAGAGATTTGTG[A/G]AACTTTGAACTTGAG | 55779 |
rs578055943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113370085 | AAATTGAGGCAATAA[C/T]TAATACCCTACCAAC | 55779 |
rs578059192 | snp | A/G | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396544 | GAATTTCCCCATCAC[A/G]TTCATAAGCTAAAGC | 55779 |
rs578060127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403507 | ATGTTCAGCACCTTT[A/G]TTCCTACAAAATGGC | 55779 |
rs578072184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP44 | GRCh38.p7 | 3:113362228 | CTGATACAGTGTACC[A/G]GAGTGCTCTGTGAAG | 55779 |
rs578079011 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | CFAP44 | GRCh38.p7 | 3:113350258 | AAGAAAGAGAAGGAA[-/AG]AGAGAGGAAGAGACA | 55779 |
rs578088013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402843 | CTCCCACTTGGTATT[C/T]AGACATTTTGGGGTA | 55779 |
rs578099585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113369589 | AAGCAGTGTGTAGAG[A/G]GAAATTTATAGCACT | 55779 |
rs578101164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286502 | GGCCCTCCCTGTTTT[A/G]ATGAGAGACCTTGGA | 55779 |
rs578111345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416445 | CTCTGGAGAACCTTG[A/C]CTTATGAAATAATGT | 55779 |
rs578122433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409404 | AAAAAAAGAGAGGGA[A/G]TCAGCCCATGGTGAT | 55779 |
rs578150433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415786 | ACTTCCAATTATGTG[A/G]TCGATTTTAGTATAA | 55779 |
rs578191818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113375608 | TTCTAAAACTGAAGA[G/T]ATATGTTGAAATTTA | 55779 |
rs578195636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP44 | GRCh38.p7 | 3:113343351 | TACAAGTGTGAGCCA[C/T]CACACCTGGTCTACT | 55779 |
rs745314438 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342022 | ACACAGAGAATATAT[C/T]GAATTTGTAAATCAA | 55779 |
rs745318829 | snp | C/T | 1.65414e-05 | 0.00287583 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433580 | ATCTTGATTCTGATT[C/T]AGAAGACCTCAGAGA | 55779 |
rs745367872 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434457 | CATAAAGTTGTCTCT[A/G]AGCTTTGCTAAGAAG | 55779 |
rs745401233 | snp | C/T | 1.65176e-05 | 0.00287376 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366277 | CGAATTGCTCCATTT[C/T]TCATTCCACAAAACA | 55779 |
rs745410894 | in-del | -/AGTG | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403379 | CCCCAAGAGAAAGCA[-/AGTG]AGGTCCCTAGCATAA | 55779 |
rs745451007 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386747 | AGAATCAAAAATCAG[A/G]TGAGTGATGACAATA | 55779 |
rs745467952 | snp | A/G | 0.000140835 | 0.00839034 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113293996 | TGCTCTTCTTCAGAG[A/G]ACCAAACTGTTGGAA | 55779 |
rs745501826 | snp | A/T | 1.69347e-05 | 0.00290982 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396493 | TAAAATTTCAACAAG[A/T]AAAGAAAGGAAATGT | 55779 |
rs745531272 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403880 | TCTGACCCAACAGTG[A/G]TAACTTCACCCTCAT | 55779 |
rs745545532 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385119 | CACAAGACTTCTTCT[C/T]GCCTGCCGCCATGTA | 55779 |
rs745569824 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360063 | TCAAACCTATACTTA[C/T]GTCTTATCTTGTTAC | 55779 |
rs745582197 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396584 | AGCAGTATGGGGTTT[A/G]AAAACCTGTTTCAAC | 55779 |
rs745591378 | snp | A/G | 9.69039e-05 | 0.00696007 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296806 | AAGTGTTGTATTAAC[A/G]GAAAGCGTTTGAAGG | 55779 |
rs745595829 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293912 | CCCCTCCCCTCAGGC[C/T]TCTGAAGCAGTACAA | 55779 |
rs745622321 | snp | A/G | 0.000231623 | 0.0107591 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420128 | TATGGCGATACTGTC[A/G]TCCAGAAGTTGTAGG | 55779 |
rs745625700 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290823 | AAACTTAGAATTCTG[A/C]CGGAGTTGCAGAAAT | 55779 |
rs745650781 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441286 | GTGTCTAGCTCCGAG[C/T]CTGAGAATACTCGTG | 55779 |
rs745673128 | snp | G/T | 0.000111888 | 0.00747874 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308285 | TATGGAAAGAGGAGG[G/T]CATTGTTAACAAAGA | 55779 |
rs745677213 | snp | G/T | 1.65455e-05 | 0.00287619 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426116 | ACATATTTAGCCAGG[G/T]TGGATACACAAGTGT | 55779 |
rs745677428 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319615 | ACAGAACACTCAATC[A/C]AACAACTTAGAATAT | 55779 |
rs745683727 | snp | A/C | 0.000105457 | 0.00726069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358713 | CACATGTGCTCTCAA[A/C]CATCTTAGCTTGTAG | 55779 |
rs745693251 | in-del | -/AGTC | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431886 | ACCTAACATCGTGAT[-/AGTC]AGTCAGAAAGAGCCA | 55779 |
rs745700059 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361016 | TCTGAATTCCATGCT[A/G]GGCACATTTATTGTT | 55779 |
rs745726918 | in-del | -/AAA | 0.000334975 | 0.0129374 | intron-variant, cds-indel, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286907 | TATTGTTTTTTTTTT[-/AAA]AAAAAAAAGAAGAAA | 55779 |
rs745732087 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395305 | AGAAATAAAAGGATA[G/T]AAGAGAAAATAGATG | 55779 |
rs745734842 | snp | C/T | 3.51828e-05 | 0.00419406 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380868 | AGGAAAGGAAATTAT[C/T]ATAAGATAATGCTTC | 55779 |
rs745783667 | snp | A/G | 2.28271e-05 | 0.00337832 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446704 | AATAAAACAGAGTAA[A/G]AGAGTGAGCTATCAT | 55779 |
rs745795538 | snp | G/T | 2.23691e-05 | 0.00334426 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400497 | AAATTTTATTGCAAA[G/T]AAAACAAAACAAGGC | 55779 |
rs745804855 | snp | C/T | 3.46789e-05 | 0.00416392 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379331 | CAGAACTTCCCTGGC[C/T]CTGAGTAAAATCCAC | 55779 |
rs745805853 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395566 | GAGAGAGCAAGGCTC[C/T]TGAGTGATGCTCTAC | 55779 |
rs745839989 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382405 | AATGATGAGACTAGA[A/C]GTCAGGTAAGAGCAC | 55779 |
rs745843246 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379469 | TCTTCTCCCATCTCT[A/G]CTGCTAGCTTGTTCC | 55779 |
rs745892193 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387513 | TGCTGACTAAAGAGC[A/G]CTTGGGCCCCGAATA | 55779 |
rs745905862 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315172 | CATTATCCAATCATA[C/T]GCTGACTACCAGAAA | 55779 |
rs745916520 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287800 | GTTGAAGACCAAATA[G/T]TTTCTCCAAAATACT | 55779 |
rs745952692 | snp | C/T | 0.00010237 | 0.00715363 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305062 | TGAGCGGAATCACAA[C/T]TAGCAGTTCATTCAG | 55779 |
rs745953249 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438590 | ATTCCTGAATAGATG[A/G]AAGAACAAGATTGTC | 55779 |
rs745961284 | snp | A/T | 4.94173e-05 | 0.00497053 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406990 | TTTGCCAAATCGACC[A/T]AGTGATCCCTGCAGC | 55779 |
rs745964678 | in-del | -/TAT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422839 | TTATCATTTATCTAA[-/TAT]TATTATCTTTAATTT | 55779 |
rs745980541 | snp | C/G | 1.69533e-05 | 0.00291142 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363519 | TCTGGAATTGGCTCT[C/G]TTTCAATTCCAAACT | 55779 |
rs745982497 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332614 | TAAGCCTTTAAGTAT[A/T]AAAAGTCACTTGTCA | 55779 |
rs746008539 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391173 | GAACAGAATACAGAA[G/T]GCAAAAACAAATCCA | 55779 |
rs746014694 | in-del | -/ATC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360272 | CATGGCCATGTTATT[-/ATC]ATCAAGTGAGATACA | 55779 |
rs746040778 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425462 | ATCCTGTTTCTACAT[A/G]TCTTAAAAGACTCTT | 55779 |
rs746067426 | snp | G/T | 4.96956e-05 | 0.00498451 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426265 | ACAGCTGGAGCAGGG[G/T]TTTGCTGAGGTACTA | 55779 |
rs746075058 | snp | A/G | 1.81952e-05 | 0.00301617 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381071 | TCAGGCTAAAAAAGA[A/G]AAATTGAACATATTT | 55779 |
rs746095711 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437693 | ACTGAAGAACCTGTA[A/T]AAAGCAGTGGAGCAG | 55779 |
rs746115361 | snp | C/T | 1.66879e-05 | 0.00288855 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363339 | AAAACAATAACAGGT[C/T]GTGATACAGAAACAG | 55779 |
rs746183942 | snp | A/T | 1.75668e-05 | 0.00296363 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400629 | GGAAGGAGAAGAGGC[A/T]TTCTGGGTCCTGGGT | 55779 |
rs746194275 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293292 | CACCAACTATATCCC[A/T]ATTCCTGCCTACATC | 55779 |
rs746195547 | snp | A/G | 1.89838e-05 | 0.00308083 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416630 | TATGTGGATGAACCT[A/G]CAAAAGATAAAATTT | 55779 |
rs746237104 | snp | A/G | 3.43271e-05 | 0.00414275 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401204 | AAAGTTTTTACTATG[A/G]AAGTTAGGAGAAAAT | 55779 |
rs746269289 | snp | C/T | 1.65531e-05 | 0.00287686 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286813 | GAATGCAGCTCTCCC[C/T]GGGGCCACTGGTGCG | 55779 |
rs746273294 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294131 | ATAGAGTTTGGAATA[C/T]GCTATACATGTGTTA | 55779 |
rs746317674 | snp | A/T | 1.70726e-05 | 0.00292164 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373386 | AGGATATGGTTTTTT[A/T]AAAGCTTTTTGAAAT | 55779 |
rs746333429 | snp | C/T | 1.6869e-05 | 0.00290417 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416504 | TGAACATGAAATATT[C/T]AAATATGCTTCTGGA | 55779 |
rs746344744 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398295 | AGGGGAAGAAAATCA[C/T]AGAGGAAGGAGGCCC | 55779 |
rs746355068 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389778 | GTAAAATTCCTAGAC[A/C]CATACAACCTACCAA | 55779 |
rs746382803 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353242 | GCTCCAGCAGAGCAC[A/C]AAAACCACAGAATGA | 55779 |
rs746406433 | in-del | -/CCCT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347332 | CAAAAAGTTGGTTGA[-/CCCT]GTAGCCATGAGTGGA | 55779 |
rs746419615 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309586 | AAGGGTTTTGGATAA[A/G]GGGTTGTAGACCTTT | 55779 |
rs746430527 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311929 | GGGCATTTTGCCCCT[G/T]CCCTAGAGATTTGTG | 55779 |
rs746460918 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322341 | TACAGAATGGAAGAA[A/C]ATATTCACAAGCTAT | 55779 |
rs746474731 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310539 | GAAAATTTAAATAAG[A/C]TACAAAGTCTCATAA | 55779 |
rs746483589 | snp | A/C | 6.6865e-05 | 0.0057817 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401747 | TCCCATATCTTGTAA[A/C]ATGAAAAGAAAATAC | 55779 |
rs746496866 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445476 | TCCTGTGCCATTGAA[C/T]GGTACTGGAAATTAA | 55779 |
rs746502385 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397141 | TTCTCTGAGAGCATA[C/T]AACAAAGAAGGCTGA | 55779 |
rs746523789 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432934 | ACATTTTTAACTTTC[C/T]TGGAGGTGAAAATTC | 55779 |
rs746552275 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352300 | GGCCACCCCAGCCAG[C/G]AGCAGCAACCTGCTC | 55779 |
rs746571898 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440266 | GGGTTTCCCCATGTT[A/G]GCCAGACTTGTCTCG | 55779 |
rs746588474 | snp | C/T | 1.73003e-05 | 0.00294106 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427334 | TGTTATCTTCTTGAA[C/T]AGGAGCTATTAAAAT | 55779 |
rs746590516 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398199 | TTGTCACCATGAAAA[A/C]CAGTCTAGTGGGAAG | 55779 |
rs746602640 | snp | G/T | 0.000102854 | 0.00717053 | intron-variant | CFAP44 | GRCh38.p7 | 3:113341924 | ACACTCCCACCTACA[G/T]AGAGAATCAACATTT | 55779 |
rs746613875 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434288 | AGAGAAGAGGTGTTT[A/G]AGACATGGATGATGG | 55779 |
rs746626045 | snp | G/T | 1.65548e-05 | 0.002877 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401622 | CAGTTTCATTCATTT[G/T]TATCATAGAGAAGAG | 55779 |
rs746629391 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339913 | CTGGGGGAAGAACCC[C/T]TTGCTTAGTGCAACT | 55779 |
rs746663994 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318831 | ATCCTGCCATACTGT[G/T]TCATAAGTGAAGGAG | 55779 |
rs746671613 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429844 | TCAGAGATTACAATA[C/T]ATAACAACTTTCTAC | 55779 |
rs746678899 | in-del | -/TT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406284 | TATAACCTTTGACCC[-/TT]AATAAGTCTTCTTGG | 55779 |
rs746729585 | snp | C/T | 0.000391262 | 0.0139813 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344749 | TTGCAGTAGTCACCA[C/T]TTTGATCATTCTGCA | 55779 |
rs746737545 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329244 | GTTTAGAAACAAGGA[C/T]AGCATAAGTAATGTG | 55779 |
rs746781518 | in-del | -/CTGT | 0.000102981 | 0.00717496 | frameshift-variant, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344529 | CCTGCATCTCTCTGG[-/CTGT]CTGTCCTTTCTTCCA | 55779 |
rs746815697 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289828 | AAGTCATATCCCAAG[C/T]GGCCCTATGGAGAGG | 55779 |
rs746827989 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375038 | ACATATGCTGCATCA[C/T]GGATGAAACTTGGGG | 55779 |
rs746830679 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368917 | CAAGCAAATGGAAAG[-/C]AAAAAAAGCAGAGGT | 55779 |
rs746836033 | snp | C/T | 1.65323e-05 | 0.00287505 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420035 | AATGACGCCAATTCC[C/T]TCACCACTGCTACTT | 55779 |
rs746836556 | in-del | -/TT/TTTT | 0.000145618 | 0.00853177 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286909 | TGTTTTTTTTTTAAA[-/TT/TTTT]AAAAAAAAGAAGAAA | 55779 |
rs746860911 | in-del | -/CAGA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439752 | AGGTTGGCTAGACGC[-/CAGA]CAGAGTGCTGTCTAA | 55779 |
rs746894709 | snp | C/T | 0.000132846 | 0.00814896 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308118 | TATTGCCAATCAATA[C/T]TCACACTTCACAGAG | 55779 |
rs746935694 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418561 | TGTTTCAGAAAAGAT[A/G]AGGTAACACGGACAG | 55779 |
rs746936708 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359857 | AGAATACAAAATTGG[A/C]TTAAACAATTTTGTG | 55779 |
rs746942917 | snp | C/T | 3.31939e-05 | 0.0040738 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409089 | CTACTGGCACCTCTA[C/T]TGGTTACCCAACCTA | 55779 |
rs746953712 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420849 | TGATTTATAGCATAT[-/AA]ATATATATGTAATTA | 55779 |
rs746959006 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306602 | CTCACTCAAGGCTCA[C/T]AGACCCTGCAAGGCA | 55779 |
rs746968115 | snp | A/T | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379690 | ATACTCACCAATGCG[A/T]GAATATATTTTTATC | 55779 |
rs746991195 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393634 | GATCCTCCCACCTCA[A/G]CCTCCCGAGTAGCTG | 55779 |
rs746993808 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426145 | GTGAGAAGATCCAGT[A/G]GTATGTTTGAATCCA | 55779 |
rs746996957 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441228 | TGGCTGGCTTCCGCC[C/G]GGTCAGACTGACAGG | 55779 |
rs747011698 | snp | C/T | 1.72406e-05 | 0.00293599 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373531 | GGGAACTCACAGTGA[C/T]ATAGAAAACCAGAAT | 55779 |
rs747018486 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338431 | TCAACAGTAAAAGAG[C/T]GAACAATCCTATTCA | 55779 |
rs747036205 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361842 | TATTTTGAAGACCTG[C/T]TATTCTGACCACAAT | 55779 |
rs747064253 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431207 | AGAGACCTCTTCACG[C/T]AGCAACAAGGTACAG | 55779 |
rs747072531 | in-del | -/A | 1.67492e-05 | 0.00289384 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445269 | GGAAAGGGAAGTAAT[-/A]AATTATTAAGAACAA | 55779 |
rs747082328 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350205 | AGGAAGAGACAGAGA[-/G]GACAAAGACAGAGAG | 55779 |
rs747093350 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296478 | TTTCATCCATTTTAC[A/G]TAATATTTATATGCA | 55779 |
rs747114623 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363223 | ACTCCTCAAAGCTTT[A/G]ATTTGCTCTCTCTTC | 55779 |
rs747118096 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417500 | TAAGCTGTTATAAGG[A/G]TAAGCTATTTAAAAC | 55779 |
rs747123391 | in-del | -/AAAG | 1.65594e-05 | 0.0028774 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416659 | TTCACCAAAATATTA[-/AAAG]AAAGATTTTTGTATA | 55779 |
rs747138511 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286638 | TGGCTCCTCGGTCAA[A/T]CTGGATTTTAATGGT | 55779 |
rs747140119 | snp | A/G | 1.74848e-05 | 0.0029567 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381059 | AGTAAAGTACTTTCA[A/G]GCTAAAAAAGAAAAA | 55779 |
rs747166992 | snp | C/G | 1.64972e-05 | 0.00287199 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426254 | CTGCTTCTTCCACAG[C/G]TGGAGCAGGGGTTTG | 55779 |
rs747173009 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401432 | AATTGAAATTTAATA[A/T]AAACAACTTCTATAT | 55779 |
rs747176442 | in-del | -/AAAAATAAATGA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430419 | ACCTCAAGAAGCTGG[-/AAAAATAAATGA]AAAAAAAAAAAAAAA | 55779 |
rs747188084 | snp | A/G | 1.6715e-05 | 0.00289089 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286692 | CCCCCATGCTGCTTG[A/G]GCCTTGTGCCAGTTG | 55779 |
rs747195998 | snp | A/C | 1.70093e-05 | 0.00291622 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400599 | AAACAGCCACGGCTT[A/C]AATAGCTCCAGAATG | 55779 |
rs747232824 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314889 | TGGGATAAATTATGT[A/G]TATATAATGAAATAT | 55779 |
rs747234772 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304883 | ATAACAATCTGACAG[A/T]GGATAAGACAAGTGT | 55779 |
rs747237565 | in-del | -/TTTA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374367 | TGTCAATTTCTTTTA[-/TTTA]TTTATTTATTTATTT | 55779 |
rs747238280 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314099 | AGATCTAATATTTAT[G/T]CCATCAGAGTACCAG | 55779 |
rs747240002 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357510 | AAACCAAAGGTTGCT[A/G]GCAAACCACTAGAAG | 55779 |
rs747240980 | snp | G/T | 1.69994e-05 | 0.00291538 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380892 | ATGCTTCAGGAATAT[G/T]CCATACCAGAATCTT | 55779 |
rs747249360 | snp | C/T | 1.65332e-05 | 0.00287512 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286806 | GAACCTGGAATGCAG[C/T]TCTCCCCGGGGCCAC | 55779 |
rs747255907 | snp | A/C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390218 | AATCAATGTGGTACA[A/C/T]CATATCAACAGAATG | 55779 |
rs747278567 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293566 | GCTGTTTCCTCTCCA[A/T]TGTATCTGGACTGAT | 55779 |
rs747283841 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303601 | AAAGAGATGGGGCTT[C/T]GATTGTATCTCAACG | 55779 |
rs747296667 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351218 | GCAAAGAATAACTGA[A/C]ATCCCAAACTTACAA | 55779 |
rs747337890 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389511 | TAGAAGAAAATAAAT[A/G]AAAAAGATCAGAACA | 55779 |
rs747352740 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316447 | AGATAAGAGCAGAAA[C/T]CAATGAAATTAAAAG | 55779 |
rs747357047 | snp | A/G | 1.65332e-05 | 0.00287512 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433688 | TAAGTACAAAATGGG[A/G]ATGAGATATGGATAA | 55779 |
rs747382822 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292019 | TACCTAAAGAGCTCA[C/T]CACTGGAATAATAAA | 55779 |
rs747384919 | snp | A/G | 1.72107e-05 | 0.00293343 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416494 | TTGTTATCCTTGAAC[A/G]TGAAATATTTAAATA | 55779 |
rs747408137 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304614 | AGAAAAGTAAAAAAG[A/G]GAAAATATTTTCCTT | 55779 |
rs747410095 | snp | C/T | 1.95589e-05 | 0.00312715 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400522 | CAAGGCCAGACATAT[C/T]TTTATTAAGAGTTCC | 55779 |
rs747414272 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425359 | TACATTGCCAGCTAA[A/G]GACCTCAATGAAAAC | 55779 |
rs747444080 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391104 | GTTATACTACAGAGA[C/T]ACAGGAACCAAAACA | 55779 |
rs747502899 | snp | C/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396571 | AAGCAGTGACACAAG[C/G]AGTATGGGGTTTGAA | 55779 |
rs747503079 | snp | A/T | 1.65042e-05 | 0.0028726 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366105 | AAAAATGTTGAAAAC[A/T]AAGATATTGCCATCT | 55779 |
rs747508849 | snp | C/T | 0.000103087 | 0.00717866 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327787 | TCTAAGGAGACGGAG[C/T]TCTGCATCGAAAGTG | 55779 |
rs747518714 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333703 | TATGATTTCAAATCT[G/T]TGATGCCACTTTTGT | 55779 |
rs747534432 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363629 | AACTCAAATTGGTTC[A/G]GTTTTCTTTTTCTGC | 55779 |
rs747556063 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366262 | TTTAGGACATAGACT[C/T]GAATTGCTCCATTTT | 55779 |
rs747556453 | snp | A/G/T | 0.000598847 | 0.0172954 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330210 | CACGTGTTTAATCTC[A/G/T]TCTCTCTTCATAATT | 55779 |
rs747585352 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443738 | ATGCCACCACTCCCT[A/G]GTTGTGTGACCTTGA | 55779 |
rs747591094 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332718 | AGGATGATTGAAAGT[C/G]GTTTGGAAGAATGCA | 55779 |
rs747617519 | snp | A/T | 1.65353e-05 | 0.00287531 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420032 | CCCAATGACGCCAAT[A/T]CCTTCACCACTGCTA | 55779 |
rs747623754 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319892 | AAAGATGGCATTACA[A/G]CTCATCCCACAGAAA | 55779 |
rs747626948 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425294 | AAGAGGCCAGTTGGT[A/G]GTTTAGGCCACGTGG | 55779 |
rs747632417 | in-del | -/CAGTACT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320513 | ATATATCTAGATATA[-/CAGTACT]TAATGAAGTTATATA | 55779 |
rs747633181 | snp | C/T | 0.000102844 | 0.00717016 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341874 | TAGGCCGAAATTTCT[C/T]CCCTTTTTCTATTAT | 55779 |
rs747641652 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322790 | ATGCACTCATGTTCA[C/T]TGCCATGTGTATTAG | 55779 |
rs747660159 | snp | A/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363114 | GAAATAGCATATGTT[A/T]AAATAAAAATCAAGT | 55779 |
rs747672710 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401581 | GACAAGAATGCAACA[C/T]ACCTGAGCCAACCAA | 55779 |
rs747690788 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297776 | ATAATCTTGTAACAG[A/G]ACTTTCTCAATGACC | 55779 |
rs747717602 | snp | A/C | 0.000154595 | 0.00879055 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287013 | TGTATATGTTTTATA[A/C]TTCTGGAGAGACATA | 55779 |
rs747782208 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381985 | TCTGAGCTTCAAGGT[-/A]AAAAAATGTATAAAT | 55779 |
rs747786811 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321066 | TTGGCAGAGATATGA[A/T]GAAGAAAGAAAACTT | 55779 |
rs747786890 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426552 | GTTTGCTTCCCTTTC[C/T]GCCATAATTGTAAGT | 55779 |
rs747787988 | snp | A/T | 3.38181e-05 | 0.00411192 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373520 | CATCACAAGGGGGGA[A/T]CTCACAGTGATATAG | 55779 |
rs747810124 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352189 | CTAAAAGATTGTAAA[C/T]GCACAATCAGCACTC | 55779 |
rs747813752 | snp | C/T | 2.19657e-05 | 0.00331397 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446574 | TGCATTTCACAATTA[C/T]ATTTTAACGTGTACC | 55779 |
rs747844035 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445249 | AAACTTAAAAGTCAG[A/G]GCAGGGAAAGGGAAG | 55779 |
rs747847768 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311619 | GTGAAAATGGACTAA[C/T]ACAGTAAATTGGAAC | 55779 |
rs747856471 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383682 | AACTACTTGGAGATA[A/G]CAGTGGCAAATAAAT | 55779 |
rs747873222 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310352 | GTTGATCACAGAAAC[C/T]ACATGTGGAGCTGGA | 55779 |
rs747875540 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332873 | GAAAAACTACATCCA[A/G]TGAGGATTTGTTTGA | 55779 |
rs747877093 | snp | A/C | 0.000111676 | 0.00747164 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333608 | AAACAGACAACCCCC[A/C]CACACACAAATATGA | 55779 |
rs747883111 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431730 | AAGACATGTCTGCGA[A/T]AGATTAAAAGAATTT | 55779 |
rs747908617 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418994 | TAGGCATGAGCCACC[A/G]TGCTTGGCCAGGATT | 55779 |
rs747921809 | snp | A/G | 3.3189e-05 | 0.0040735 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366295 | ATTCCACAAAACATC[A/G]TAACTTTGTTAATGC | 55779 |
rs747930649 | in-del | -/ACT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318275 | AGAGCTAAAAAACTC[-/ACT]ACAAGAATTTCATAA | 55779 |
rs747945567 | snp | C/T | 6.67847e-05 | 0.00577822 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396778 | GTTAAATTGAGAAAG[C/T]TGTACTATATAACAG | 55779 |
rs747945670 | snp | A/G | 1.65274e-05 | 0.00287462 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373437 | AGTTTGGATGGGATT[A/G]TCCTCTGTATCCGCA | 55779 |
rs747955857 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336291 | AAGCTAGTTCTTTGA[A/C]AAGATCTATAACATG | 55779 |
rs747956482 | snp | A/G | 1.66147e-05 | 0.0028822 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445329 | ACATGGGTAGAAAGA[A/G]CAAACCAGCCTTCTT | 55779 |
rs748001531 | in-del | -/TTTA | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113380037 | CTTATTTTTTTAAAT[-/TTTA]TTTATTATTATTATA | 55779 |
rs748002527 | in-del | -/T | 0.000203223 | 0.0100782 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381100 | TTACATTTAGGCAAA[-/T]TTTTAAAAGCATAGT | 55779 |
rs748022850 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418285 | AGATACGGGGTTTTA[C/T]CATGTTGGCCAGGCT | 55779 |
rs748024029 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327923 | ATTTTTTATTATGCC[C/T]TTATGGATGGAGAAT | 55779 |
rs748035663 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404550 | ATATTTAACAAGTGT[C/G]ACAAATAAAGTAATA | 55779 |
rs748057384 | snp | A/C | 1.66721e-05 | 0.00288717 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363332 | GAAATTTAAAACAAT[A/C]ACAGGTTGTGATACA | 55779 |
rs748076094 | snp | C/T | 8.65164e-05 | 0.00657653 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420195 | CTGAGGGAAAGTTGC[C/T]AAGGAAAAGAAGTGA | 55779 |
rs748077131 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316715 | CTCTACTAAAAATAT[A/T]AAAATTAGCTGGGTG | 55779 |
rs748081341 | snp | A/G | 1.81572e-05 | 0.00301302 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373545 | ATATAGAAAACCAGA[A/G]TCATAGCCACCCTAG | 55779 |
rs748084304 | snp | A/C | 1.66568e-05 | 0.00288585 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404033 | TGGCAGGTATGTGGA[A/C]AAAAGAAATGTGCAT | 55779 |
rs748089435 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357299 | TGACCTTATTTGAAA[A/G]TAGGGTCTTGATAGA | 55779 |
rs748143885 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288702 | AACATCTGCTTTCTG[C/T]ACAGCACTGGAATCA | 55779 |
rs748155638 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369614 | AGCACTAAATGCCCG[-/C]AAGAGAAAGCAGGAA | 55779 |
rs748161563 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328967 | TGTATCCCTAATCCT[A/G]TCTATCAGTGTCCCT | 55779 |
rs748162574 | snp | A/T | 0.000463553 | 0.0152172 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291527 | TGAGTTATGTCAGAA[A/T]TCTTGTATGGGTTTG | 55779 |
rs748163260 | snp | C/T | 0.000102475 | 0.0071573 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305037 | CCCAGACGCATCACC[C/T]GGTGGAGCTTGAGCG | 55779 |
rs748187987 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294538 | TGTGGCTAACACCAA[C/T]TCAGTGTCCTCGGGG | 55779 |
rs748223456 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441930 | TATCTCTGTTGGCTT[C/T]TAAGAGTAAATCAGG | 55779 |
rs748240845 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295437 | ATTATTTTAGATTGC[A/G]TATATTATCGCCAAC | 55779 |
rs748244843 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379477 | CATCTCTGCTGCTAG[C/T]TTGTTCCTCCTTTCT | 55779 |
rs748253757 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428008 | AGATTAGGAACAAAG[A/C]CCAAGACTAATATGA | 55779 |
rs748264101 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293317 | TACATCATTGTAAGA[A/G]GCAATGGAGTCAGCG | 55779 |
rs748281411 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416401 | TGAATTTGAATAAAT[C/T]TCTTTTCTGTCTTCC | 55779 |
rs748287314 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409214 | AGTATGGGTTGTTCT[C/T]CTTTCCAGTTCCAGA | 55779 |
rs748310072 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336704 | ATGTAAGCCCTAAAT[A/G]TAAATAAGTACATTA | 55779 |
rs748318406 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354649 | CCCGCCCAAGGAGAG[C/G]GTGAGCTCAGACACA | 55779 |
rs748356432 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113382090 | GTGGAACATTTGCTT[C/T]TATAAGAAAATTGTG | 55779 |
rs748356496 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368280 | AGCAACCCCAAGACA[C/T]ATAATTGTCAGATTC | 55779 |
rs748365185 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324994 | CTGAGATTAAAAATA[A/C]AGTATCATTTAAAAT | 55779 |
rs748372828 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370162 | AGGTACAAAGAGGAG[A/C]CAGTACCACTCCTTC | 55779 |
rs748394826 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323914 | CTGGGCATGGTGGCA[C/T]GTGCCTATAGTCCCA | 55779 |
rs748396974 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392850 | TACCTCAAAATTGTC[-/T]TCACAAAAATAAAAG | 55779 |
rs748434148 | snp | C/T | 0.000522125 | 0.016149 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330176 | CCCTTACCCTGTTGA[C/T]CAAATACTGTTGCAT | 55779 |
rs748442220 | snp | C/G | 1.66829e-05 | 0.00288811 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427318 | TCATCTTCTAAAAAT[C/G]TGTTATCTTCTTGAA | 55779 |
rs748451268 | in-del | -/A | 1.76081e-05 | 0.00296711 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419968 | GTCCACAGAACAAGC[-/A]AAAAGATAGGGTTTT | 55779 |
rs748490667 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302351 | ATTTCTTAAGCAAGA[C/T]ACACACACATACACA | 55779 |
rs748497409 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435593 | AAATGGCCAGGCATA[G/T]TGAGGTATGCCTGTA | 55779 |
rs748524052 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301870 | ATAGATCTCTTGAAA[C/T]TGTTCTTTGGATCTC | 55779 |
rs748525915 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314713 | GTGGTTCTAGATGTA[C/T]GGAGAGGAAATATTT | 55779 |
rs748550204 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436944 | AAGTGTGACTCAGCT[A/G]GCTCTCTGCTTAGAG | 55779 |
rs748565207 | snp | A/G | 1.77704e-05 | 0.00298075 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433542 | TTAATACTTTTAAAA[A/G]TATACATATTATCTT | 55779 |
rs748586583 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388108 | CTGGACCTGCCTGAC[A/G]ATCTCACCACCCTGA | 55779 |
rs748592704 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402551 | ATAACTGAGACTTTG[A/G]GAAAGGAACTCTGGG | 55779 |
rs748601404 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409121 | TTGATGTGGCCTGAT[C/T]CCGATGTAGTAAGCT | 55779 |
rs748602121 | snp | A/G | 1.65198e-05 | 0.00287395 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395819 | ACCAATCGGCTTATA[A/G]TCCCTTTCCACTTCA | 55779 |
rs748605040 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389791 | ACACATACAACCTAC[A/C]AAGACTGAACCATGA | 55779 |
rs748608937 | in-del | -/AATT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408077 | ATTAAAAATCTGCTC[-/AATT]AGTCTATATTTCTAA | 55779 |
rs748620634 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346250 | CAATCAGCACTCTGT[A/G]TCTAGCTAAAGGATT | 55779 |
rs748621414 | in-del | -/ACAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353456 | TATATGTATGAATAC[-/ACAC]ACACACACACACACA | 55779 |
rs748625950 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376099 | TAATCCTATAGGATT[A/C]TTTTAAGCCTAACCA | 55779 |
rs748639591 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350915 | CAGGGGATCTAGGTC[C/T]TGATTGGTTGCCATA | 55779 |
rs748654269 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345022 | TAATGGTAAATAGAT[C/T]ATATCAAATTCTGAG | 55779 |
rs748656157 | snp | G/T | 3.31049e-05 | 0.00406834 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401723 | TCAGCAGTGTCTATT[G/T]TCTCAAAATCCCATA | 55779 |
rs748657244 | snp | G/T | 3.50459e-05 | 0.0041859 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363553 | GGAAGGGAAGTAAAA[G/T]GTTAGCCCTTTAAAA | 55779 |
rs748717363 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331659 | GTCTGAAGGACTGCA[A/G]ATTAGGCCACCAAGA | 55779 |
rs748720178 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303298 | CCTGTAACATTGTCT[A/G]TAATAATGAAAAATA | 55779 |
rs748726819 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301663 | ACAAAAATTGTATAT[A/G]TTATCATATACAACA | 55779 |
rs748739316 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422923 | AAACCCAGAATGGAT[C/G]AGATTGTAACTTCTC | 55779 |
rs748761689 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408216 | CTGGGGTGGTAGAAG[A/G]TTGTTACGCAAATGC | 55779 |
rs748763612 | snp | C/T | 2.15929e-05 | 0.00328572 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416646 | CAAAAGATAAAATTT[C/T]ACCAAAATATTAAAA | 55779 |
rs748770248 | snp | A/T | 1.66131e-05 | 0.00288206 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445321 | CTTATGATACATGGG[A/T]AGAAAGAGCAAACCA | 55779 |
rs748779980 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291023 | TCCTGAGCCCTCAAA[A/G]CACTGCTTTATGAAG | 55779 |
rs748784041 | snp | C/T | 1.6684e-05 | 0.00288821 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373510 | TCACTGCTTTCATCA[C/T]AAGGGGGGAACTCAC | 55779 |
rs748789684 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436781 | ATAACTAAATGAAAA[C/T]TTTTCATCTGTGAGT | 55779 |
rs748793444 | snp | C/T | 6.66889e-05 | 0.00577408 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416527 | CTTCTGGACTCACCT[C/T]GAAGGACTCTGTATG | 55779 |
rs748828708 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380257 | ATGTCTTGGCTGGCA[-/T]TTAAGGAGCTCCATG | 55779 |
rs748839091 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376001 | CAAATAGAAATAATT[A/C]GTAAGATAGTAGATT | 55779 |
rs748840382 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424220 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGTTCGA | 55779 |
rs748857913 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362706 | TTCACACAGTCTTCC[A/G]ATAGCAATACCAGTC | 55779 |
rs748864899 | snp | A/T | 0.00010188 | 0.00713649 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330589 | TCTTGTACCAGGCAC[A/T]GTATTTCCTCAACAA | 55779 |
rs748880227 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319249 | GAGAAAGATCTACCA[C/T]GTAAATGGAAAACAA | 55779 |
rs748886974 | snp | G/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443658 | CACTGTAAAACAGGT[G/T]TACTCTCCAACAAGA | 55779 |
rs748926464 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409717 | GGGCTTTCTAACTCA[C/T]CAGATCAGATAGGTG | 55779 |
rs748936185 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331243 | TCCTTCATTCCTTCT[A/C]CATTTATCAAAGCCA | 55779 |
rs748996514 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426211 | TCATAGAAGAAGCTC[C/T]CTGATATTTTCTTCT | 55779 |
rs749014083 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319762 | AAAATCCATACAAAA[G/T]ATTCATGAAACCAAG | 55779 |
rs749018450 | snp | G/T | 1.65332e-05 | 0.00287512 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373433 | TGATAGTTTGGATGG[G/T]ATTGTCCTCTGTATC | 55779 |
rs749034941 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309027 | GATTTTGGGATTCTG[C/T]ACCAGAACTTGCTAG | 55779 |
rs749039093 | snp | C/G | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379993 | TTTTACTACTTCATT[C/G]TGTTCACCCTTCAGA | 55779 |
rs749041019 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354461 | GAGGGTATGGTAGGA[A/G]TGAGACCAGCCTTTA | 55779 |
rs749041779 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310107 | CACTGGATGGTGTTA[C/G]AGAAGGGCAAGCAGG | 55779 |
rs749059989 | snp | A/G | 0.000100215 | 0.00707797 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296828 | GTTTGAAGGGCTTCT[A/G]GATTTACCACACGGC | 55779 |
rs749066820 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395604 | CCCCAGCAGCAGCCA[C/G]CTGAGCTTTCTGTTG | 55779 |
rs749093203 | snp | C/G | 1.64961e-05 | 0.00287189 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403996 | AAGCAGCATGTTGCC[C/G]CATTCTGACCCTGAG | 55779 |
rs749095455 | snp | C/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396596 | TTTGAAAACCTGTTT[C/G]AACTGAATATCAGCA | 55779 |
rs749165764 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382661 | ATATTGAAAAAAAAC[G/T]GGGAGAAAGTAGAAA | 55779 |
rs749171251 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417645 | ACATTATTTCCTTTA[A/C]ATTTTATACCAACCT | 55779 |
rs749174550 | snp | C/T | 3.43885e-05 | 0.00414645 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400549 | TTCCTACTTACAGTC[C/T]AAGGCAGTTGTGGCC | 55779 |
rs749225113 | snp | A/C | 1.65198e-05 | 0.00287395 | splice-donor-variant, intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426123 | TAGCCAGGGTGGATA[A/C]ACAAGTGTGAGAAGA | 55779 |
rs749240090 | snp | C/T | | | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286778 | GCACCCCGTAGGGGC[C/T]TACGTAGGACAGGAA | 55779 |
rs749274495 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310867 | CCTGCATTATAAGAT[A/G]CCTGCTCCTGTTTTG | 55779 |
rs749275834 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380751 | CTACTGCCTTCTAAT[-/A]AGCTGCTTTCCTACC | 55779 |
rs749281594 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297468 | GCTCTTCCCCAGAGA[G/T]CCACACGGCTTGCTC | 55779 |
rs749288658 | snp | A/G | 0.000508324 | 0.0159343 | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294673 | GAAAAAGGGTCTGAA[A/G]GTAAAGAACATACCT | 55779 |
rs749339544 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347527 | AGTTTCTCCTATAAT[G/T]ATTTCTAGTATAAAC | 55779 |
rs749380370 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427114 | TCTTTCTATGGATTT[A/G]TAACTCTTCCATTTG | 55779 |
rs749384603 | snp | A/G | 0.000102812 | 0.00716906 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306293 | CCAGCCTTTTCTCTC[A/G]AAGGTGAAGGGCCAG | 55779 |
rs749397215 | snp | C/T | 0.000107302 | 0.00732389 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327592 | AAGGGACCAGCCAGC[C/T]AGGATTCTTCTGCCC | 55779 |
rs749408832 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379614 | CGTTCATTTACACCA[C/T]TAGGGATGACAATGA | 55779 |
rs749410449 | in-del | -/G | 3.50189e-05 | 0.00418428 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363553 | GGAAGGGAAGTAAAA[-/G]GTTAGCCCTTTAAAA | 55779 |
rs749438030 | snp | C/G | 5.32789e-05 | 0.00516107 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446608 | GCTCTTGGATTAAGA[C/G]GTGTGAATCTCCCAC | 55779 |
rs749476268 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430318 | TTGAGATATAGCTAA[-/A]GCAGTCCTTGGAAGG | 55779 |
rs749487367 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357160 | TGCCAATTTAAACCA[-/G]TACTGAGATGCTACT | 55779 |
rs749492755 | snp | C/G/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407013 | CCTGCAGCTTGAGAC[C/G/T]GGTGAACGTAAAAGC | 55779 |
rs749499786 | snp | A/G | 1.72231e-05 | 0.0029345 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363538 | CAATTCCAAACTATA[A/G]GAAGGGAAGTAAAAG | 55779 |
rs749500799 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366926 | CCATGCCTGGCTCAG[C/T]GGGTCCCACGCCCAT | 55779 |
rs749505207 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365762 | AAACCTTTGATTAAG[-/A]AAGTTTTTTTAATAT | 55779 |
rs749515093 | snp | C/T | 0.000103003 | 0.0071757 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113308186 | AGAATCATCAAAAAC[C/T]TCATCTTCTGATTCA | 55779 |
rs749519752 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415271 | CTTCCTTATTAGTCT[A/G]GCTAGTGGTGTACCT | 55779 |
rs749521632 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417840 | TAGATCTCAAGGAGG[A/T]GGGGGACATGGATTA | 55779 |
rs749522796 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334386 | GACAATATAGAAGTA[C/T]AAAACATTGTAAATT | 55779 |
rs749524905 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335394 | GTACAGGGAGGCCAA[A/G]TTTGGTGCTAAGAAT | 55779 |
rs749547392 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350111 | GAAGCCATGAAAAGG[A/G]GAAGGAGAGGGGAGA | 55779 |
rs749570028 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408280 | AAGATCATTCCATCC[C/T]GGAAATAGACGAGGG | 55779 |
rs749589578 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323560 | AATGTAACAATCCTG[C/T]ACATATACCGCCTGT | 55779 |
rs749606081 | snp | A/G | 1.90235e-05 | 0.00308406 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381083 | AGAAAAATTGAACAT[A/G]TTTACATTTAGGCAA | 55779 |
rs749616303 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323759 | TATGAAATAGATCAT[C/T]TGGGCTGGGTGCAGT | 55779 |
rs749618390 | snp | A/G | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426215 | AGAAGAAGCTCTCTG[A/G]TATTTTCTTCTTAAC | 55779 |
rs749635142 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415025 | TAGGCTATTAATTAC[C/T]GCCTCAATTTCAGAG | 55779 |
rs749647304 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295282 | CGGTTGCTCACTGCA[A/G]CCTCTAACTTCTGGG | 55779 |
rs749659118 | snp | C/T | 1.67489e-05 | 0.00289381 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363346 | TAACAGGTTGTGATA[C/T]AGAAACAGCAGAGAA | 55779 |
rs749668671 | snp | C/T | 1.65149e-05 | 0.00287353 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395810 | ATTAATATAACCAAT[C/T]GGCTTATAATCCCTT | 55779 |
rs749669144 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324876 | AATCATCTACATAGA[A/G]ATCCCCAAGGAATCT | 55779 |
rs749677890 | in-del | -/AAACA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342333 | GTGAGACTCTGTCTC[-/AAACA]AAACAAAACAAAACA | 55779 |
rs749686721 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400740 | TAAAAATATAACACA[C/T]GTGATTTTATTTGGA | 55779 |
rs749700773 | snp | C/T | 0.000103109 | 0.0071794 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333544 | GATGGCTTGAAGATC[C/T]TTGGGATCTTCATAG | 55779 |
rs749706480 | in-del | -/ATT | 0.000261172 | 0.0114244 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446718 | AGAGAGTGAGCTATC[-/ATT]ATTAACCTTAAAAGA | 55779 |
rs749707722 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368170 | GAAAACACTCTTCAG[A/G]ATATCATCCAGGAGA | 55779 |
rs749717625 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399927 | GGGTACCCAAACAAG[A/G]GCAGTACCTCCTTGT | 55779 |
rs749718619 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353703 | GTGCTATAACTTTCA[C/G]AGTGAAGTACCAGAG | 55779 |
rs749740208 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386758 | TCAGGTGAGTGATGA[C/T]AATACTTGGTTTTAA | 55779 |
rs749757705 | snp | A/G | 6.64308e-05 | 0.0057629 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286828 | CGGGGCCACTGGTGC[A/G]TGTGTCTTTTGAAAC | 55779 |
rs749769022 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371116 | ACATTCCATGTTCAT[A/G]GATAGGAAGAATCAA | 55779 |
rs749770965 | in-del | -/GAAACCCC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307796 | ACACGGTGAAACCCT[-/GAAACCCC]GAAACCCCGTCTCTA | 55779 |
rs749784972 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387872 | GCTGACTGAAGAGCC[C/G]TTGGGCCTTGAGTGA | 55779 |
rs749840140 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435404 | AACCCCTTATAAAAC[C/G]ATCAGATTTTGTGAG | 55779 |
rs749873759 | in-del | -/TCC | 0.00119811 | 0.0244463 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379399 | GGTAATGGCTCTTCT[-/TCC]TCCTCCTCCTCCTCC | 55779 |
rs749878311 | snp | C/T | 2.54534e-05 | 0.00356736 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286976 | ATAGCCATATTTATA[C/T]ATTTATGCACTTGTA | 55779 |
rs749879766 | snp | A/G | 0.000112189 | 0.0074888 | intron-variant | CFAP44 | GRCh38.p7 | 3:113304167 | AAAAACACAGATTTT[A/G]TATGGCAACAGAAAG | 55779 |
rs749889377 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337647 | AGAAATAGACCCACA[C/T]AAATATGTCCAAATG | 55779 |
rs749926245 | in-del | -/GAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328919 | GCCTATAAGCTTTGT[-/GAA]GATAGAGAACATGTC | 55779 |
rs749942655 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307462 | AAATAGCAATGTGCC[C/T]CTCCATCCCCACTCC | 55779 |
rs749948006 | in-del | -/TT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343061 | TCTTTCTTTCTTTCT[-/TT]TTTTTTTTTTTTTTT | 55779 |
rs749952567 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406948 | ATCTGGGAGCTCCAT[A/G]TAGCCTTCTATATCA | 55779 |
rs749958316 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313663 | TTGAATCATGGGGGC[A/G]GTTTCCCCCATACTG | 55779 |
rs749977674 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388811 | ATAAAGAGGTCAATT[C/T]AGTAAAAGGATATAA | 55779 |
rs749983786 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401941 | TATGATAAGCTATTA[C/T]AGTTTCCTTTATATT | 55779 |
rs750022266 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387714 | TTAGGTACCAGCTTG[C/G]GCACAGTGGAATAGA | 55779 |
rs750035941 | snp | C/G | 1.65765e-05 | 0.00287888 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363171 | ACTGCATATGCTTTG[C/G]TAATTTTTCATTCAT | 55779 |
rs750039859 | snp | C/T | 1.6525e-05 | 0.00287441 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380978 | GAGACTACATCATGA[C/T]CATCCTCTTCTTGCT | 55779 |
rs750072011 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291402 | GATAACCAAATTGTA[C/G]AGAGATTCTTAAAGT | 55779 |
rs750079641 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353053 | AACAAGGACGGTAGG[A/G]AGGCAGAGGTGAACC | 55779 |
rs750092086 | snp | C/T | 0.000197707 | 0.00994053 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403971 | CCACTTTGATCAGAC[C/T]ACCTTCCCAAAGCAG | 55779 |
rs750110286 | snp | C/T | 1.65455e-05 | 0.00287619 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363290 | TCATGTTCTCTTTTT[C/T]TCCTAGCATTCTCGA | 55779 |
rs750110605 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389013 | ACTTAATCTGCACTA[C/T]AGACCAAATTGACCT | 55779 |
rs750118937 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327131 | AGTATAATTTATTTT[C/T]TGAAATTTAATATAC | 55779 |
rs750123683 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439313 | TGGGTTCTCACGCTT[C/G]TATGCTGGATAACTA | 55779 |
rs750151318 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424042 | GGTTATAGTTCACCA[C/T]GTACAGAGAAACCTG | 55779 |
rs750158158 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356952 | ATGTCATATACGTAG[G/T]CACTCATATATATAA | 55779 |
rs750160528 | in-del | -/GAAAA | 1.67181e-05 | 0.00289115 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401750 | CATATCTTGTAAAAT[-/GAAAA]GAAAATACTTTAATC | 55779 |
rs750164768 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345953 | TCTCTTTAAGACTTA[C/T]TTCCTTTATGTATTT | 55779 |
rs750201681 | snp | A/C | 1.64912e-05 | 0.00287147 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286760 | AGGAGACTGGTGTCC[A/C]CAGCACCCCGTAGGG | 55779 |
rs750213559 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302962 | AATAAAATAAATAAA[C/T]GGCAAATATATGTAT | 55779 |
rs750231312 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113338854 | AAGAGGGGGCAAGTG[-/A]GGGGCTGAAGCTGGA | 55779 |
rs750248541 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332190 | TTGTGGTCATAAGAA[C/T]ATTTCTCTACAATGA | 55779 |
rs750254918 | snp | A/G | 0.000299506 | 0.0122337 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304030 | GGAGCTCATGGATTC[A/G]TTCTTGCAGCCGTCT | 55779 |
rs750272157 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376643 | AAATGGACAGAGAAT[C/T]GACCTCTGAGCTTAT | 55779 |
rs750276806 | snp | A/G/T | 5.29847e-05 | 0.00514684 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380860 | ATATTCTAAGGAAAG[A/G/T]AAATTATTATAAGAT | 55779 |
rs750294799 | snp | C/T | 0.00018134 | 0.00952036 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330132 | TCCCTTCTCTTCTCT[C/T]TTTCAGCTTTAACTA | 55779 |
rs750296726 | snp | C/T | 1.79926e-05 | 0.00299933 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366358 | TTAATCTGAAAATAA[C/T]GCTTAATTTCAACTT | 55779 |
rs750320856 | snp | C/T | 3.39893e-05 | 0.00412232 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409347 | TAAATGGAAGCCTAA[C/T]AAATAAGGACACATT | 55779 |
rs750345122 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446448 | TTTTTCCTAAAAAGG[C/T]AAATTAGTATTTCTT | 55779 |
rs750351856 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329164 | TCAAGACAATACTAA[-/T]TACCCATGAAACAGC | 55779 |
rs750358305 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377490 | TGCCTAACATTTCCA[C/T]GCCTTGGTTTCTTCA | 55779 |
rs750388106 | snp | C/G | 1.75857e-05 | 0.00296522 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286661 | TTAATGGTTCCTACT[C/G]TTTCTCCCCTCAGGG | 55779 |
rs750389878 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351154 | AATCAGGAAGGAGCC[A/G]TCTATACAAATTCTA | 55779 |
rs750400526 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340953 | TTGGGCCACTCGGCA[A/G]CCCCAGCCCGACTGT | 55779 |
rs750405340 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412962 | ATACTGTCTTCAACA[A/G]TGGTTGAATTAATTT | 55779 |
rs750434192 | snp | C/G | 1.68972e-05 | 0.0029066 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400580 | ATGAGATAAGTGAGA[C/G]GAGAAACAGCCACGG | 55779 |
rs750450757 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367985 | AAGTGGAAGAAAGGA[C/T]ATCAGTGATTGAAGA | 55779 |
rs750471893 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298670 | TAAAAAGGAAGAAAA[C/T]TCTGACACATGCTAC | 55779 |
rs750523307 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288652 | AGGTAGCTGTCAAAA[G/T]GAAGTCTGGTGAACT | 55779 |
rs750544743 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394665 | GGGCCACACTGCAAA[-/AAG]AAGAATTGTCTTGGC | 55779 |
rs750572643 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435072 | TATGATCAAGAAAGA[C/T]ATAGACCGAGCTCAG | 55779 |
rs750574059 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406272 | CCACATGGTTGTATA[C/T]AACCTTTGACCCAAT | 55779 |
rs750577137 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386292 | ACCAAGTTGGGTCTT[A/G]TTTTTTTTATTCATT | 55779 |
rs750586672 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289529 | CCTGATTCTCTACAA[G/T]TACCAAGGGGATGGT | 55779 |
rs750609141 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403505 | AAATGTTCAGCACCT[C/T]TGTTCCTACAAAATG | 55779 |
rs750610134 | snp | C/T | 0.000103056 | 0.00717755 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341815 | TAATATAAGTTTTCT[C/T]GTTTTCTCAATTTGA | 55779 |
rs750631438 | snp | C/T | 3.34437e-05 | 0.0040891 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401560 | TGTAATGTTAAAGAG[C/T]CAAGAGACAAGAATG | 55779 |
rs750643275 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384519 | AGATAAGTTAAAACA[-/G]GGTTGTTAGGGTGGG | 55779 |
rs750645978 | snp | C/G | 1.65266e-05 | 0.00287455 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420092 | CAAATTCAGAAAGAT[C/G]AGTTGGTTCCCAGCT | 55779 |
rs750660695 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297278 | CCAGGTAAATAATGA[C/G]AATCCCTTTGGGAAT | 55779 |
rs750663618 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407294 | TTTTAGGGCTGTGCT[A/C]CCTAATGCAGTACCC | 55779 |
rs750670295 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359399 | ATCCCTGGAAAAATA[C/T]CAGAGCCAATATTTG | 55779 |
rs750683978 | snp | A/G | 1.6516e-05 | 0.00287362 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395801 | TCCAGGAGTATTAAT[A/G]TAACCAATCGGCTTA | 55779 |
rs750684225 | snp | C/T | 1.65312e-05 | 0.00287495 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401656 | CACATTCTTGTCTAC[C/T]TGAAGTTCATTAATA | 55779 |
rs750709393 | snp | C/T | 2.58742e-05 | 0.00359673 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446549 | GCCACCTTCTACCCT[C/T]ACCCCTATATGCATT | 55779 |
rs750713543 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360504 | TTTGGTAGAATAAGT[A/G]CTAATATCAGACATG | 55779 |
rs750719115 | snp | A/T | 0.00011753 | 0.00766492 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291516 | AGAACTTCCAGTGAG[A/T]TATGTCAGAAATCTT | 55779 |
rs750745065 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317640 | AGTGTCTCCAGGGCC[A/G]TGGTGCACAGCTCAA | 55779 |
rs750745546 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348181 | GCAGGGTCCAGGGAC[C/T]ATTGCAGGTTCTTGG | 55779 |
rs750758895 | snp | A/G | 1.67789e-05 | 0.00289641 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420004 | GTTTTTTTCTAATTT[A/G]TTGAAGGCATACCCC | 55779 |
rs750775241 | snp | C/T | 2.31677e-05 | 0.00340343 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379264 | TAACTATAAACTATA[C/T]TGAAATATGATTGAG | 55779 |
rs750789406 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393291 | AATGACTTTTAAATT[A/T]TGCTGAGTGTTTTGG | 55779 |
rs750798154 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318736 | CAGACCTCTGAGCAG[A/C]AATCTTACAAGCAAG | 55779 |
rs750810173 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440353 | GGCGTCAGCCACCGC[A/G]CACAGCCTATTATTA | 55779 |
rs750828637 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441712 | CCCTAAAGGACGTCA[C/T]GTAGATAATTAAATG | 55779 |
rs750843046 | snp | A/G | 0.000102981 | 0.00717496 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333475 | GTGCTCAGGTATCTT[A/G]TAGTCTGGGGCTGTC | 55779 |
rs750906729 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349308 | GTCAGCCACAGGTAT[C/T]AGGAGAAAGCTCCAA | 55779 |
rs750917098 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335381 | GACAGAGATCAGAGT[A/G]CAGGGAGGCCAAATT | 55779 |
rs750925565 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394463 | TTGCAGCTATCACTC[C/G]CCTCACCTGAACCAT | 55779 |
rs750929712 | snp | A/G | 1.86869e-05 | 0.00305665 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396750 | AAAATTAAAGATAAG[A/G]GACCTGAAACTAGTT | 55779 |
rs750934710 | snp | A/C | 0.000149859 | 0.00865488 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399897 | AGTTCATTATAACAA[A/C]AAACTTACCATTCGG | 55779 |
rs750940301 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381681 | TTAATCATGAATGGG[A/G]AATCTCCATCTTGAT | 55779 |
rs750940366 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441152 | CGGGGAGCCCCAGCA[C/T]CTTCCCAGCTGACTC | 55779 |
rs750970434 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336330 | ACTAGCTGGAATGAT[C/T]AAGAAAAAGAGAGAA | 55779 |
rs750997922 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409825 | ATCAAGATGGTGATG[-/A]AAGCGACCTCTGGTC | 55779 |
rs751009539 | snp | C/T | 9.95751e-05 | 0.00705533 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373501 | TCTTTGAAATCACTG[C/T]TTTCATCACAAGGGG | 55779 |
rs751039024 | snp | A/G | 5.01987e-05 | 0.00500967 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403837 | TGCTACCATCCAAGT[A/G]TCGAGAAAACTTACC | 55779 |
rs751044546 | snp | C/G/T | 5.07475e-05 | 0.00503703 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363149 | ATTAGGCTTACTGTT[C/G/T]GTTTAAACTGCATAT | 55779 |
rs751061145 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427692 | TTAAAGACAAACAAG[C/T]CTTATTGTCTTTCTT | 55779 |
rs751064505 | in-del | -/TTTTTTTTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423106 | GAATCTGATCCTTCC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs751086066 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428458 | AGGAAGTAGGCACAT[C/T]AAATCAAGCTGGCAA | 55779 |
rs751089766 | snp | A/G | 4.94262e-05 | 0.00497098 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426195 | AGCAAGCTCCATATA[A/G]TCATAGAAGAAGCTC | 55779 |
rs751091920 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323196 | TGCTATACACAACAG[C/T]AAAGACATGGAATCA | 55779 |
rs751093631 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295098 | TTACTATGCATACTG[A/G]TTGCTGGTACTCATT | 55779 |
rs751109945 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312075 | TGTGTGTGTGTGTGT[-/T]TTTTTTTTTTTTTTT | 55779 |
rs751115099 | snp | C/G | 1.68972e-05 | 0.0029066 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400576 | GGCCATGAGATAAGT[C/G]AGAGGAGAAACAGCC | 55779 |
rs751133767 | in-del | -/CT | 1.64738e-05 | 0.00286995 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403933 | ACCATTGTGACATGA[-/CT]TGCTTGTCCCTCGAC | 55779 |
rs751156511 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399212 | GGATTATTCCAGGCC[C/T]AGCCATTCATGTCTT | 55779 |
rs751163572 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379447 | CTCCTGAAATTCTTT[C/T]TCTCCATCTTCTCCC | 55779 |
rs751166288 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380397 | TTCTTCCAGCCTTTA[C/T]TGCCATCGCCCTATT | 55779 |
rs751188402 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354258 | TTTGCTCCAAGAACT[A/G]TCACAGGAACATACC | 55779 |
rs751209318 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292673 | AAGTCAAGCTGGAAG[C/T]AGAGTTAGAAACAGG | 55779 |
rs751219652 | snp | A/G | 5.32713e-05 | 0.0051607 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286652 | ATCTGGATTTTAATG[A/G]TTCCTACTCTTTCTC | 55779 |
rs751235459 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374011 | GAAGATGAATGATCA[A/C]CTGGAAGAGCTATAT | 55779 |
rs751252439 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367760 | GTTGACAGAAGTAGG[C/T]TTCAGAAGGTTGGTA | 55779 |
rs751274581 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369343 | TGGAAGTAAAACACT[A/C]CTCAGCAAATGTAAA | 55779 |
rs751329025 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355048 | ACCAACCTGGAGCCC[A/G]GTAGCTCTGCTGGGA | 55779 |
rs751341906 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341383 | CAATTAACTTCAGAT[A/G]GTTAAAGATAAAGGT | 55779 |
rs751371050 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435164 | GGAGTTCAAGACCAA[C/T]ATGAGAAACATAGTA | 55779 |
rs751379285 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313571 | ATGGTTTGGCTCTGT[A/G]TCCCCATTGAAATCT | 55779 |
rs751396872 | snp | A/T | 3.41227e-05 | 0.0041304 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366033 | ACTGGTTAATTAATT[A/T]CATACCCTGGGAGAT | 55779 |
rs751402711 | snp | A/G | 2.03279e-05 | 0.00318803 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400040 | AAAAAAATTATATAC[A/G]TAATTTTTTTAAGTC | 55779 |
rs751434000 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409312 | ATAAGCATATCCCTT[C/G]TCAGTCCCATCTGGA | 55779 |
rs751451853 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290756 | CAAAACCAGCAAATG[A/G]CCCAAGTAAAACCTG | 55779 |
rs751456381 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376560 | AAGAGTGTAATGTCT[C/T]AGAAGCCAAGAGAAG | 55779 |
rs751460783 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436081 | TCTTTTAAAATTCAC[A/G]TTCTGTCATCCTTTT | 55779 |
rs751479197 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423889 | AGTGACATACAGAAA[A/G]CGAAAGTGAGGTACA | 55779 |
rs751486066 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388779 | GATTTTAAGACATAG[A/G]AGGTCATTATATAAT | 55779 |
rs751510380 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443039 | AATCTGAGAAAGATA[C/G]AATAAATTCACTATA | 55779 |
rs751521473 | snp | C/G | 0.000334616 | 0.0129304 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326687 | ATATTTCTGATAAAC[C/G]AAGTTCAGAGAGCAA | 55779 |
rs751521893 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384924 | TTAATATCTAATATG[G/T]TTTGGCTGTGTCCCC | 55779 |
rs751550672 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360843 | GAAAAATCTACTTTT[A/T]TAAAGTAGGGGGAAA | 55779 |
rs751554299 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351914 | CCAAGGACTCCTGGA[C/T]TGACCCACTGGCCCT | 55779 |
rs751573529 | snp | G/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424707 | GTGGGGTAAGCTACT[G/T]TGTGATTTTCCTGGT | 55779 |
rs751574396 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403179 | ATGAAAGGCCCCACT[A/G]AAAATATCTACCAAG | 55779 |
rs751616465 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386058 | ATCTTTCTCAATGTT[C/T]GCTTTATATATTTAG | 55779 |
rs751616674 | in-del | -/T | 1.65033e-05 | 0.00287252 | frameshift-variant, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379518 | TCTCCTTCAACTCCC[-/T]TTGTCTCTCCCTCTT | 55779 |
rs751621042 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321895 | TGGAAAAACATCCCA[C/T]GCTCATAGATTAGAA | 55779 |
rs751621126 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310016 | CTGGTACAATCCCCA[A/C]CTAAATCAGCAAAGG | 55779 |
rs751623611 | snp | C/T | 2.35098e-05 | 0.00342846 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286898 | AAGACTATATATTGT[C/T]TTTTTTTTAAAAAAA | 55779 |
rs751624576 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297306 | AATTCAGGAGGCCCT[A/G]CATGGTCAGCCTGCC | 55779 |
rs751632655 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383452 | TGACCTAATTCCCTC[A/G]AAGGCCCCACCTCCA | 55779 |
rs751648090 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319443 | TTCATAAAACAAGTT[A/C]TTCCTGGCCTACAAA | 55779 |
rs751661226 | snp | G/T | 0.000102517 | 0.00715876 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330491 | GAAATCTCTTTTCTG[G/T]AACTTCTTCTGGGTG | 55779 |
rs751672278 | snp | C/T | 1.95624e-05 | 0.00312743 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401334 | ATTTTAAACTTTCAT[C/T]AGATTTTTTAAATGT | 55779 |
rs751699116 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432513 | TTTTAGCTTTTAATC[C/T]TTTTTCTTCTGATAT | 55779 |
rs751712962 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354031 | CTGGAAAAAAATTAG[C/T]CCTAGACTAAAGGCT | 55779 |
rs751723756 | in-del | -/AA/AAA/AAAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328696 | AAATTTAGAGAGCTT[-/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 55779 |
rs751726833 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397570 | AGGTGGTTTGGATAG[C/G]ATGCTGGGAGAACTT | 55779 |
rs751752261 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425367 | CAGCTAAGGACCTCA[A/G]TGAAAACTGTTTTCT | 55779 |
rs751763628 | snp | C/T | 3.30513e-05 | 0.00406504 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373481 | CAATAGGTTCATCTT[C/T]TTGTTCTTTGAAATC | 55779 |
rs751778587 | snp | C/T | 3.33195e-05 | 0.0040815 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416575 | TCATAGATGATAATA[C/T]CTGGAAAACTCCCTT | 55779 |
rs751803545 | snp | A/G | 6.80573e-05 | 0.00583301 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445391 | ACGGAAAAAATTTAG[A/G]TGGTAATTAGAAACA | 55779 |
rs751831958 | snp | A/G | 3.82782e-05 | 0.00437466 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400714 | AGATCAAGTTTAAAA[A/G]AATGCAAAGATAAAA | 55779 |
rs751870967 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400072 | TGGCTCACTTTTTAC[A/G]TGTTGAATATTATAA | 55779 |
rs751876154 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317568 | GCAACCACGAAGCAA[A/G]TTGGATCCCCCAGTG | 55779 |
rs751884529 | snp | A/G | 1.66438e-05 | 0.00288472 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445299 | AACTCAGTGAGACTT[A/G]ACTTCACTTATGATA | 55779 |
rs751886321 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439399 | ATAAAAAAAAATACT[C/T]CTACAAGGACATCTG | 55779 |
rs751897008 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419886 | CCTTGGAATAAAGAC[A/C]GCTGTGCATCTCATG | 55779 |
rs751955215 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380291 | TGGTCACAGACTCTT[C/G]CAACATCCTTCAACA | 55779 |
rs751956940 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309481 | CTGCCTTATTGTTTT[C/T]AATAAGTGTCAGGAA | 55779 |
rs751959447 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332347 | AAATGGATTTGTGAA[C/T]ATGAATTGCCAAGCC | 55779 |
rs751994270 | snp | A/T | 1.71566e-05 | 0.00292883 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373367 | CAAAAGCATAGACAC[A/T]AACAGGATATGGTTT | 55779 |
rs751999264 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363260 | TTTATTTCTCCCACT[C/T]CTTTCATTAACTTGT | 55779 |
rs752004440 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334285 | TAAGTGCTTGCTGTA[A/G]AATTTTCAGAAAAGG | 55779 |
rs752006930 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437217 | ATTTGAATCTCATGA[G/T]TTTCTTCCCTGCTAT | 55779 |
rs752007006 | in-del | -/GTGTGTGT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113435859 | AAAAAGTGTATGTAC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 55779 |
rs752016366 | snp | A/C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298948 | ATGTACTTAGTGCCA[A/C/T]TGAACTGTCCACTTA | 55779 |
rs752018447 | snp | C/G | 9.47822e-05 | 0.00688347 | missense, nc-transcript-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296776 | CTTTCGAAGTTTTCT[C/G]ATCTTCAGTTCTTCA | 55779 |
rs752032494 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359283 | AAAGATAGCAGTATC[C/T]GGTGTCTTCTTGACA | 55779 |
rs752070470 | in-del | -/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286897 | AAAGACTATATATTG[-/T]TTTTTTTTTAAAAAA | 55779 |
rs752092804 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347476 | CTCTGAGGCTAATCC[C/T]GCTTCTAAAAACTAC | 55779 |
rs752109047 | snp | A/C | 1.87047e-05 | 0.0030581 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446666 | AAGAATTACCAGTAG[A/C]CCCGGAAGATCTATT | 55779 |
rs752109790 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438993 | ACTTTCCAGAAGAGC[A/G]GAACTACCAATTCAC | 55779 |
rs752118519 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347989 | AAGAATGCATTGGTA[A/T]GGGCCACTAAATCCA | 55779 |
rs752143509 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379037 | TGATTGACAAGCAGA[C/T]AATAGATAATCTATA | 55779 |
rs752145184 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372166 | CATTGTGGAAGACAG[C/T]GTGGCGATTCCTCAA | 55779 |
rs752149726 | snp | A/C | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396636 | TTCTTCCGTCCCGCA[A/C]AAATCGTGAGCCCTT | 55779 |
rs752153537 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356211 | AAAAATATTAAAACT[G/T]CTTCTTTTTAAGATA | 55779 |
rs752166997 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318603 | TATGATACAAGATGA[C/T]CACCCCAAGGCACAC | 55779 |
rs752177867 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304385 | GATGTGACAAACATT[G/T]CAGGGCTGGCATACT | 55779 |
rs752220399 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439302 | GCTATGAAGAATGGG[G/T]TCTCACGCTTGTATG | 55779 |
rs752224552 | snp | C/T | 1.65583e-05 | 0.00287731 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379398 | CAGGTAATGGCTCTT[C/T]TTCCTCCTCCTCCTC | 55779 |
rs752231001 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305542 | AGTGCTTTAAAGCAA[G/T]GAAACTGCTAACTAT | 55779 |
rs752249906 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392728 | ATAATAATAAAGACC[-/A]AGAATAACTCTCAAG | 55779 |
rs752264279 | snp | A/G | 1.65329e-05 | 0.0028751 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420112 | GGTTCCCAGCTATGT[A/G]TATGGCGATACTGTC | 55779 |
rs752272828 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347927 | TAAATCCGATTTTTC[A/T]CGGTCCTCATTGTGG | 55779 |
rs752283035 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409171 | GAAAGTAACCTTAAA[A/C]ACTTCCTGAGAAAAA | 55779 |
rs752283979 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413324 | CTCTGTAGGTTGCTT[A/G]TTCACTCTAATGATA | 55779 |
rs752285704 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292869 | AGAGAGAGCTAAGTG[A/G]ATATAATCTGAAACT | 55779 |
rs752292330 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293831 | GACTTTTGTTTAGAC[C/T]AGTGATTCTTAAACT | 55779 |
rs752336084 | snp | C/T | 9.99151e-05 | 0.00706736 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400004 | TTCGAACAGAGCCTA[C/T]AGAAAGACAGTTTTA | 55779 |
rs752337230 | snp | A/G | 1.65732e-05 | 0.00287859 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399911 | ACAAACTTACCATTC[A/G]GGGTACCCAAACAAG | 55779 |
rs752342860 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288481 | ACTGTGATTTCAGAC[A/C]ACCTGGCATCACGGC | 55779 |
rs752384202 | snp | C/T | 1.89238e-05 | 0.00307596 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379306 | TACATTGTTACTTAC[C/T]AAAGAAACCCAGAAC | 55779 |
rs752387221 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398928 | GTGACTGCTTCACCC[-/A]ATCAAGTATGGTAGA | 55779 |
rs752389896 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446934 | AGAATTCGCCCATGT[C/T]GTGGGAGGGACTCAT | 55779 |
rs752411914 | in-del | -/A | 1.64798e-05 | 0.00287047 | frameshift-variant, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409297 | GTAGTTAAAGTCCAC[-/A]TAAGCATATCCCTTC | 55779 |
rs752417003 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393613 | TGGCACACTGCAGCC[C/T]CAAGCGATCCTCCCA | 55779 |
rs752435687 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335139 | CCATGTGAGAGTAAC[A/G]GGGCCCATTATTATC | 55779 |
rs752487115 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323118 | CTCCCATACATGTGG[A/G]GATTATGGGGACCAA | 55779 |
rs752489992 | snp | A/C/T | 3.29686e-05 | 0.00405998 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427249 | TCCAAACGTTCCTCA[A/C/T]CTGAGTCTTCTTCTA | 55779 |
rs752514551 | snp | A/C | 1.75857e-05 | 0.00296522 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366002 | ACTATTTTTAAATAC[A/C]GTTTGTTATTAATTA | 55779 |
rs752517603 | snp | A/C | 0.000411989 | 0.0143466 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306348 | TGCCAAGAGAATTAA[A/C]ATAAAAACCAGCCTC | 55779 |
rs752535745 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301753 | ACTTAAGCATTGCCT[-/C]ACATACTTTCTTTTT | 55779 |
rs752537064 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312647 | AGGCCTAGAAGAAAA[C/T]GGTTTCTTGGGGAGG | 55779 |
rs752542727 | snp | A/G | 1.64912e-05 | 0.00287147 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427164 | ACAGTGACAATTACT[A/G]ACAGAAAACTAATAA | 55779 |
rs752544939 | snp | A/G | 1.67458e-05 | 0.00289355 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409069 | GAAAAATACTCCTGT[A/G]ATATCTACTGGCACC | 55779 |
rs752602922 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354173 | ATACAGAGATTAAGA[C/T]GGCAGATAGGAGGCA | 55779 |
rs752642428 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435105 | GCTCATGCCTGTAAT[C/T]CTGGCAGTTTGACAG | 55779 |
rs752652367 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431922 | CATCTTTCAAAAATC[A/C]TAGTTATAAAATTCC | 55779 |
rs752675256 | in-del | -/C | 0.00336116 | 0.0408569 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446551 | CACCTTCTACCCTCA[-/C]CCCTATATGCATTTC | 55779 |
rs752720664 | snp | C/T | 1.6628e-05 | 0.00288335 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416563 | AGAGAAGGATATTCA[C/T]AGATGATAATATCTG | 55779 |
rs752722282 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308745 | ACAGGCACACACCAT[C/T]ATGCCCAGCTAATTT | 55779 |
rs752723486 | snp | C/T | 1.67393e-05 | 0.00289299 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445273 | AGGGAAGTAATAAAT[C/T]ATTAAGAACAAACTC | 55779 |
rs752723571 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331955 | TACTCTTTTTACAGA[C/T]GAAATAAAAGGCTTA | 55779 |
rs752727141 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324244 | AAATGGAAAAGAAAA[A/T]TTTCTGATTCATATT | 55779 |
rs752745387 | in-del | -/A | 3.29813e-05 | 0.00406073 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427169 | GACAATTACTGACAG[-/A]AAACTAATAATACCT | 55779 |
rs752758278 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113341087 | TTCTGCCAATGTGTC[C/T]CTCATGATGTCCAGC | 55779 |
rs752761111 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394899 | CTTATTATTCAATGA[C/T]AAGGTATATTTAACT | 55779 |
rs752769975 | snp | G/T | 1.85517e-05 | 0.00304557 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409373 | ACATTTATTTCATTT[G/T]CAAAAACATATTGTA | 55779 |
rs752776730 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443428 | CTTACAAGCACTCTG[G/T]CATTAGACAACTTTC | 55779 |
rs752779258 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113362037 | AACTGCCACCAGAGC[A/T]GCTGCAAGAATATGT | 55779 |
rs752808122 | snp | A/T | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366238 | CTGGTCAATGAAGGA[A/T]CATTTTGATTTAGGA | 55779 |
rs752823318 | snp | A/G | 1.69198e-05 | 0.00290854 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400589 | GTGAGAGGAGAAACA[A/G]CCACGGCTTCAATAG | 55779 |
rs752863847 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410251 | GTGTGCTTCACCCAT[G/T]AACTCAACATTTACA | 55779 |
rs752885039 | snp | A/G | 0.000148575 | 0.00861774 | missense, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433654 | GTATCCTGATCATCT[A/G]GTTCCTTCATTTCCT | 55779 |
rs752938727 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350936 | GGTTGCCATACAGGG[A/G]TCTGACCAGACCTAG | 55779 |
rs752954245 | snp | C/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338633 | CTGATTGAAAAGTAA[C/T]ATAACATCTCTCCAG | 55779 |
rs752976562 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423412 | CCCAAGGTGCTAGGA[A/G]TACAGGCCTGAGCTG | 55779 |
rs753005059 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363884 | CATTTATTTCAAAAT[A/G]CTGTTTTTCAGTATA | 55779 |
rs753009355 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337892 | TTAGACTTGACACCA[A/G]AATCAAGATTTATAT | 55779 |
rs753019207 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309700 | CAACTAAACATTATA[C/T]GCAAAACAAACATAA | 55779 |
rs753027624 | snp | A/C | 3.43253e-05 | 0.00414264 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373363 | TGAACAAAAGCATAG[A/C]CACTAACAGGATATG | 55779 |
rs753028128 | in-del | -/A | 0.000389674 | 0.013953 | intron-variant | CFAP44 | GRCh38.p7 | 3:113303909 | GCTGTGGGCTTAGAT[-/A]ACTCACTGTGTATGG | 55779 |
rs753029114 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298528 | ACATAAAGAGATATT[C/T]GTACACTCATGTTCA | 55779 |
rs753039101 | snp | C/T | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396554 | ATCACGTTCATAAGC[C/T]AAAGCAGTGACACAA | 55779 |
rs753056131 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437032 | AAGAATCTACTTCTG[C/G]GCTCATTCAAGCTGC | 55779 |
rs753057151 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353378 | GTCAGATTTAAGTTA[C/G]TTTAAATAAAATAAA | 55779 |
rs753062172 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326109 | GCAAATGATCCTATT[C/G]AAACATGGGCAAAAG | 55779 |
rs753069427 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339093 | TTCAGACCATCTGTC[C/T]TCACATCCACAGAAA | 55779 |
rs753078986 | in-del | -/A/AA/TA | 0.181183 | 0.241356 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286906 | TATTGTTTTTTTTTT[-/A/AA/TA]AAAAAAAAAAAGAAG | 55779 |
rs753116854 | in-del | -/TG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373109 | TTTCTCCAGAATAAC[-/TG]TAACCCTGAACCTTC | 55779 |
rs753130819 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287332 | GCCCATGAGAACAGA[A/C]CAAGATGTGTACAGC | 55779 |
rs753147586 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435272 | GGTTTAATTGACTTA[C/T]AGTTTGGCATGGCTA | 55779 |
rs753199785 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373032 | TATATTGGGTCGTCA[G/T]AAGAATAACTGGCAT | 55779 |
rs753216924 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368135 | TACCTGAAAGTGATG[A/G]GGAAAATGGAACCAA | 55779 |
rs753249320 | snp | C/T | 1.78112e-05 | 0.00298417 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420218 | AGAAGTGAAAAACAC[C/T]ACCATCCTAGGGATT | 55779 |
rs753261027 | snp | C/T | 1.91064e-05 | 0.00309077 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363103 | ATCTCTATCCAGAAA[C/T]AGCATATGTTAAAAT | 55779 |
rs753265775 | in-del | -/GT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113435865 | TGTATGTACGTGTGT[-/GT]GTGTGTGTGTGTGTG | 55779 |
rs753289982 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390926 | ATAGTATCTAAAGCA[A/G]TCTACAAATTCAATG | 55779 |
rs753293775 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326956 | TCAGCTAATATTTTT[A/G]CATGTGTAGTCTCAA | 55779 |
rs753293888 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314506 | CATTTGTCACCAGCA[G/T]GCCTATCCTAAAATA | 55779 |
rs753305361 | snp | G/T | 9.94678e-05 | 0.00705153 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291731 | ATCTGCTTCCCGAGG[G/T]CCCTGGAAGGCATTG | 55779 |
rs753344367 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357073 | AAAGACTGGAACAAA[C/T]ACCTAACAACAGAAA | 55779 |
rs753380250 | snp | A/C/T | 6.63431e-05 | 0.00575915 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399908 | ACAACAAACTTACCA[A/C/T]TCGGGGTACCCAAAC | 55779 |
rs753423405 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390668 | GATACAAAATCAACA[C/T]ACAAAAATCAATAGC | 55779 |
rs753427680 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427240 | AAACTTCCTTCCAAA[C/T]GTTCCTCATCTGAGT | 55779 |
rs753455075 | snp | A/G | 2.42539e-05 | 0.00348229 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446562 | CTCACCCCTATATGC[A/G]TTTCACAATTACATT | 55779 |
rs753465010 | snp | C/T | 0.000103204 | 0.00718273 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305023 | GATGGAGCAGCCTCC[C/T]CAGACGCATCACCTG | 55779 |
rs753471669 | snp | A/G | 1.68207e-05 | 0.00290001 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363460 | GCCTAGTCAGTATTT[A/G]TCAAAAATTCCCATA | 55779 |
rs753478925 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332145 | TGCCCATCTCCTCTA[G/T]CTAGAGTATGAAATT | 55779 |
rs753503185 | in-del | -/TT | 0.000204436 | 0.0101082 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327634 | CATGTACTGTTCCTC[-/TT]TGTCTAAGGAATTAA | 55779 |
rs753531773 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320908 | GACTCAAAAGTTAAT[C/G]TCCTTTGGCAGCACC | 55779 |
rs753533562 | snp | C/T | 1.66799e-05 | 0.00288785 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407085 | CTCAAAGATATTTTA[C/T]TGATTTTTATTTTAA | 55779 |
rs753536100 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406683 | GAAAATGCTCACATA[C/T]TTTATATGTGTGTAC | 55779 |
rs753539765 | snp | A/C | 7.68462e-05 | 0.00619816 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396758 | AGATAAGGGACCTGA[A/C]ACTAGTTAAATTGAG | 55779 |
rs753546326 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292654 | AGGGAGTCATTAACT[A/G]GCCAAGTCAAGCTGG | 55779 |
rs753565071 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349551 | GTGGTTTGCAAGGAC[A/T]CTTTAAAAAAGATTG | 55779 |
rs753580748 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364550 | TATTTATTTTTTATT[A/C]TTTTATTGGCCAGAG | 55779 |
rs753587917 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332580 | GAGTTCTCCTAAAAG[A/T]AGTAGCTCAGATGAC | 55779 |
rs753608544 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347078 | ACCCCTTTAGCTTGC[C/T]CTTCTGCCCTATTTT | 55779 |
rs753617207 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378714 | TGGAGGATATACTCC[C/T]ACAGCCTTGTGATAG | 55779 |
rs753641339 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333327 | TTATTGACCAGATAG[A/G]GAAATGAGTGGTTTT | 55779 |
rs753643925 | snp | A/G | | | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426183 | AAAAGGCATCGAAGC[A/G]AGCTCCATATAATCA | 55779 |
rs753657698 | in-del | -/TTC | 2.61742e-05 | 0.00361752 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427385 | TTTTGATTAAACATT[-/TTC]TTATTTCTAAAGTAG | 55779 |
rs753679774 | snp | A/C | 6.59652e-05 | 0.00574267 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427147 | TGGGCTTTGTCTCTA[A/C]AACAGTGACAATTAC | 55779 |
rs753680549 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446147 | TACCATAACCTATCT[A/C]ACCAATGGCACAGTC | 55779 |
rs753687420 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324112 | AAGAAAGTTGAATTT[A/G]TAATTTAAAAACTCC | 55779 |
rs753705389 | snp | C/T | 1.66671e-05 | 0.00288674 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395745 | GACAAATAATAATGA[C/T]TTACATGAGACATGG | 55779 |
rs753711694 | snp | C/T | 3.31818e-05 | 0.00407306 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363303 | TTCTCCTAGCATTCT[C/T]GATACTGAAAACAGA | 55779 |
rs753730823 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413132 | ATGATCAGTGATGTT[A/G]AGCTTTTTTTCATAT | 55779 |
rs753735134 | snp | C/T | 0.00013195 | 0.00812143 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286781 | CCCCGTAGGGGCCTA[C/T]GTAGGACAGGAACCT | 55779 |
rs753739848 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287273 | CCTGGAGACACCCAC[A/G]CAGATGGCTGGATCC | 55779 |
rs753767009 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397793 | ACTGGAAGGGAGCCA[C/G]GTGTGTGTGTGGTTT | 55779 |
rs753774246 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400065 | TAAGTCTTGGCTCAC[-/T]TTTTACATGTTGAAT | 55779 |
rs753775673 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351994 | CCCTTCTTCACCCCT[A/G]CCCAGCAGGAAGTAG | 55779 |
rs753785048 | snp | A/G | 3.68582e-05 | 0.00429275 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286891 | TCCCAGAAAGACTAT[A/G]TATTGTTTTTTTTTT | 55779 |
rs753792888 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323283 | ATACTACACAGCCAT[-/A]AAAAAAAGAATGAAA | 55779 |
rs753817806 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330112 | AAAAACCCGACCCAA[A/T]TTTTTCCCTTCTCTT | 55779 |
rs753828126 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301240 | ATGTTTCAAAAGGCT[A/G]CATATGATGTAATAT | 55779 |
rs753840741 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421860 | GGAGGGAGGGGGCAC[A/G]GCTGAAAAACTTCCT | 55779 |
rs753853749 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361133 | TGGGTGGATTTAATG[A/G]AAGGCCAGGGAAGTT | 55779 |
rs753861485 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398817 | AAATACTTCCATGGC[A/G]TTTTAAAAATATGGC | 55779 |
rs753871519 | snp | A/G | 1.65534e-05 | 0.00287688 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381009 | TTATGGTTGGAAGTG[A/G]AGCTTCAAGAATATA | 55779 |
rs753873448 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433645 | TCCCCATCAGTATCC[C/T]GATCATCTGGTTCCT | 55779 |
rs753901272 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335816 | ATATTGAATTTTTAC[A/G]TAGATAGACTGTATA | 55779 |
rs753905424 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305984 | TTATACAGTCATCAG[-/A]AAAGTCTGGAGACCA | 55779 |
rs753911746 | snp | C/T | 2.07179e-05 | 0.00321846 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433520 | TTATTTAAATGTTTA[C/T]CTAAGTTTAATACTT | 55779 |
rs753916864 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419617 | GTCTACATCCTATGT[A/G]TGTGTCTCACATTTT | 55779 |
rs753920625 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375679 | AACACCTTTTAACCA[C/T]GCGTGTTGGCACACA | 55779 |
rs753934634 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407355 | TTTAAAGTAATTAAC[A/G]TTAAATAAAATCAAC | 55779 |
rs753939652 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290567 | CTCTGTTACTAACAG[C/G]ATTCCAAATGTCAGT | 55779 |
rs753994983 | snp | A/C | 1.79686e-05 | 0.00299733 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395903 | ATATATATTACTATG[A/C]AATCTAGCCTATAGA | 55779 |
rs754005849 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393562 | TAGGGTCTCACTCTT[A/G]ACACCCAAGCTGGAT | 55779 |
rs754074273 | snp | C/T | 1.69232e-05 | 0.00290883 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403812 | GTGAGCTACAAGTCT[C/T]AAACGTGGGTGCTAC | 55779 |
rs754122525 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358723 | CTCAAACATCTTAGC[C/T]TGTAGAGAATATGGA | 55779 |
rs754131517 | snp | A/T | 3.30256e-05 | 0.00406346 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396540 | GCTAGAATTTCCCCA[A/T]CACGTTCATAAGCTA | 55779 |
rs754143581 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349473 | GGCCCTCAGACAAAC[C/G]TCGGTGGTTAGAGAG | 55779 |
rs754161731 | in-del | -/CAGC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374204 | CAGACTAGATTGTTT[-/CAGC]CAAACTCTCCCACTG | 55779 |
rs754162372 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428142 | TAGGCCAAACAGATT[-/CCC]CAAGAGGGGGCCCTG | 55779 |
rs754205860 | snp | A/T | 1.65272e-05 | 0.0028746 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420100 | GAAAGATCAGTTGGT[A/T]CCCAGCTATGTATAT | 55779 |
rs754222219 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428792 | AAGGAGAAAGGAATG[C/T]CATAACTGTAGATAT | 55779 |
rs754232585 | snp | C/T | 0.000115161 | 0.00758731 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291531 | TTATGTCAGAAATCT[C/T]GTATGGGTTTGAGAA | 55779 |
rs754245535 | in-del | -/G | 1.67105e-05 | 0.0028905 | frameshift-variant, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373512 | CTGCTTTCATCACAA[-/G]GGGGGGAACTCACAG | 55779 |
rs754283713 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296252 | TGGCTGCGTAGTAAT[C/T]CATGGTATTCTATAT | 55779 |
rs754291408 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369863 | GAAGAAAAGAGAGGA[A/C]TCAAATAGATGCAAT | 55779 |
rs754317354 | snp | A/G | 2.17512e-05 | 0.00329774 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379282 | AAATATGATTGAGGT[A/G]AAAATTATTACATTG | 55779 |
rs754332561 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417199 | TTCATGGAATGTATG[A/G]GATTCTTGTTTCCAG | 55779 |
rs754336666 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297074 | CATTCGGTATTGTCT[G/T]TTCACCTTCTGAATC | 55779 |
rs754348506 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315589 | CAACAGGATTTAAAT[A/G]ACAGTAATTAAAACA | 55779 |
rs754363411 | snp | C/T | 1.65963e-05 | 0.0028806 | splice-donor-variant, intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420016 | TTTATTGAAGGCATA[C/T]CCCAATGACGCCAAT | 55779 |
rs754394996 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402145 | CCCCTGGAAGGGGGA[A/G]ATATACCTTCTTGCT | 55779 |
rs754404269 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440496 | TTTCCAAGTCCTGTT[-/A]ACTTGGTGTCCAGTG | 55779 |
rs754414906 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288320 | TCCATCAAGCTCAAC[A/G]TCAGAGAGAACTTCA | 55779 |
rs754417094 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438137 | GGAATCATGAGTTTA[C/T]ATAAAACACCTACTA | 55779 |
rs754435998 | snp | A/T | 0.000102981 | 0.00717496 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341856 | TGATTTCACTTAGGG[A/T]TTTAGGCCGAAATTT | 55779 |
rs754448178 | snp | A/G | 1.67553e-05 | 0.00289437 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373515 | GCTTTCATCACAAGG[A/G]GGGAACTCACAGTGA | 55779 |
rs754457034 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376718 | AAGATCAAATAGGAG[A/G]TGAATAAGTTAAGCC | 55779 |
rs754490808 | in-del | -/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341363 | TTTTTTTTTTTAAAA[-/G]AAAGCAATTAACTTC | 55779 |
rs754534981 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403701 | ATGCAAATATTTACC[A/G]CAAGAGAAGCATTAT | 55779 |
rs754561908 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344863 | ATATACCAACCAGGA[G/T]GTCATGAAAGTTGGA | 55779 |
rs754583545 | snp | A/G | 0.000298879 | 0.0122209 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291738 | TCCCGAGGGCCCTGG[A/G]AGGCATTGCCCTGTT | 55779 |
rs754584003 | snp | C/T | 6.62098e-05 | 0.00575331 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420025 | GGCATACCCCAATGA[C/T]GCCAATTCCTTCACC | 55779 |
rs754639351 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445764 | GCAAAGAACAAATCT[C/G]CTAGAACTGGACAAT | 55779 |
rs754653840 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304242 | CCTTTGGGCTTCTAC[A/G]TCTTCCTTACTGAGT | 55779 |
rs754678751 | snp | C/T | 1.6777e-05 | 0.00289624 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409062 | CCTCTTAGAAAAATA[C/T]TCCTGTGATATCTAC | 55779 |
rs754683433 | snp | A/G | | | utr-variant-3-prime, utr-variant-5-prime, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445116 | TCACAGGGAGCTGTA[A/G]GTCAGTTGGTTGTTG | 55779 |
rs754712205 | snp | A/T | 3.29853e-05 | 0.00406098 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427148 | GGGCTTTGTCTCTAA[A/T]ACAGTGACAATTACT | 55779 |
rs754717396 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309336 | CCTACTTCTTAGTAA[C/T]TTTCTGTCCACTGAC | 55779 |
rs754718553 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413250 | ACATGTTTAAGTTCC[C/T]TGTAAATTCTGGATA | 55779 |
rs754737068 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397987 | CCAATGTTGGAATGT[A/C]CCAAATCTACTGTCT | 55779 |
rs754746139 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310111 | GGATGGTGTTAGAGA[A/G]GGGCAAGCAGGGAGC | 55779 |
rs754778450 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299538 | AAACAGAGCTATCAT[A/G]TGATCCAGCAATCGC | 55779 |
rs754782428 | snp | G/T | 1.66449e-05 | 0.00288482 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363322 | ACTGAAAACAGAAAT[G/T]TAAAACAATAACAGG | 55779 |
rs754785641 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322124 | CTAACTTCAGCTATA[A/C]AGCTGTAGTAACCAA | 55779 |
rs754824774 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339609 | ACTCCGCAGGAATTG[C/G]TCCTGCTTTACATTG | 55779 |
rs754828598 | in-del | -/C | 1.64741e-05 | 0.00286998 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407034 | ACGTAAAAGCCATTT[-/C]CCAGAACCTACAAAC | 55779 |
rs754831283 | snp | C/T | 1.67908e-05 | 0.00289743 | splice-donor-variant, intron-variant | CFAP44 | GRCh38.p7 | 3:113363476 | TCAAAAATTCCCATA[C/T]CTGTAGGCTTTGGGA | 55779 |
rs754832526 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352045 | TTCCCAACAGCAGTT[A/G]GGGTGTCCTGTTTAG | 55779 |
rs754845303 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432769 | TATTTCCTTCTTGAA[C/T]AACTCGCTTTTCTAA | 55779 |
rs754863599 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347199 | CTTTCTGGGAAAGGG[A/C]TCTCTAACAACCCCC | 55779 |
rs754893583 | snp | A/G | 1.91867e-05 | 0.00309725 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286893 | CCAGAAAGACTATAT[A/G]TTGTTTTTTTTTTAA | 55779 |
rs754924799 | snp | C/T | 0.000149218 | 0.00863636 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381021 | GTGGAGCTTCAAGAA[C/T]ATAGCCATTTTCACA | 55779 |
rs754931385 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298677 | GAAGAAAATTCTGAC[A/T]CATGCTACAACACGG | 55779 |
rs754947400 | snp | C/T | 3.29549e-05 | 0.00405911 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426222 | GCTCTCTGATATTTT[C/T]TTCTTAACTTCCTCC | 55779 |
rs754971808 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340970 | CCCAGCCCGACTGTC[A/C]CGCCAAACTCTGCCT | 55779 |
rs754977408 | in-del | -/AG | 3.50902e-05 | 0.00418854 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380872 | AAGGAAATTATTATA[-/AG]ATAATGCTTCAGGAA | 55779 |
rs754983161 | in-del | -/AAAAA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430429 | CTGGAAAAATAAATG[-/AAAAA]AAAAAAAAAAAAAAA | 55779 |
rs754989315 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419879 | GAAAATGCCTTGGAA[G/T]AAAGACAGCTGTGCA | 55779 |
rs755011203 | snp | A/G | 0.000210482 | 0.0102565 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327604 | AGCTAGGATTCTTCT[A/G]CCCACTCATACTTGC | 55779 |
rs755015228 | snp | A/C | 3.29663e-05 | 0.00405981 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366215 | TGAAGTGCCAGTAGT[A/C]CACCAAACTGGTCAA | 55779 |
rs755066167 | snp | C/T | 0.00017481 | 0.00934743 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330140 | CTTCTCTCTTTCAGC[C/T]TTAACTAGGAACAGG | 55779 |
rs755136363 | snp | C/T | 0.000115585 | 0.00760126 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396541 | CTAGAATTTCCCCAT[C/T]ACGTTCATAAGCTAA | 55779 |
rs755139714 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318849 | ATAAGTGAAGGAGAA[A/T]TAAAATCCTTCTCAG | 55779 |
rs755141997 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380621 | TTTAGGTACTAAATG[C/T]CACTTCCATGCAGTC | 55779 |
rs755147758 | in-del | -/A | 1.67171e-05 | 0.00289107 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445283 | TAAATTATTAAGAAC[-/A]AACTCAGTGAGACTT | 55779 |
rs755156897 | snp | A/T | 1.86055e-05 | 0.00304999 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433538 | AAGTTTAATACTTTT[A/T]AAAGTATACATATTA | 55779 |
rs755174677 | snp | A/T | 1.66991e-05 | 0.00288951 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366051 | TACCCTGGGAGATGG[A/T]ACTTTGGCCTTCATG | 55779 |
rs755175745 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394296 | TCAAGCTACTTCTTT[A/G]ATGTCACACCTACTC | 55779 |
rs755184590 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417881 | TATCTAGATTCCCAT[C/T]TGTAAAGAAATATGG | 55779 |
rs755224850 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301500 | ATATGTATGTTCCAC[A/G]TATCAAATATTACTA | 55779 |
rs755254090 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350704 | CATTCAATCTGTGGC[A/G]GTGGCTGCTTTGCTA | 55779 |
rs755294857 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443350 | TACTGTACTGTATTA[C/G]TTCCCGTAAATTAGG | 55779 |
rs755298837 | in-del | -/GA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324234 | CCAGAAAATCAAATG[-/GA]AAAGAAAATTTTCTG | 55779 |
rs755313397 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430939 | ATCGTGAGAAATGAT[A/G]GATGGTTTAGCTGGT | 55779 |
rs755319151 | snp | C/T | 0.000101859 | 0.00713576 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344660 | AGGATATCTTGTGGT[C/T]ACTCAGTATGGCATG | 55779 |
rs755324990 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296342 | ATATTTCATTTTCTC[A/G]TTGTGGTTTTAATTT | 55779 |
rs755345657 | snp | A/G | 0.000113167 | 0.00752135 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291536 | TCAGAAATCTTGTAT[A/G]GGTTTGAGAAAATAG | 55779 |
rs755395756 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324891 | AATCCCCAAGGAATC[A/T]ATCAAAACCTCTTAG | 55779 |
rs755410376 | snp | A/G/T | 0.00102896 | 0.0226604 | synonymous-codon, missense, intron-variant, stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341865 | TTAGGGTTTTAGGCC[A/G/T]AAATTTCTTCCCTTT | 55779 |
rs755421212 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400836 | AGTCCTGGGCTTTGT[A/C]CTTAATGGCTGTGTG | 55779 |
rs755429010 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417376 | CAGTATTTTCAAAGA[C/T]AGCCATATAAGTTGG | 55779 |
rs755439998 | snp | A/T | 1.81269e-05 | 0.00301051 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395905 | ATATATTACTATGAA[A/T]TCTAGCCTATAGATC | 55779 |
rs755442246 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355379 | CAAAAAAATTCGCCG[A/G]GCATGGTGGCAGGTG | 55779 |
rs755469724 | snp | C/T | 1.66518e-05 | 0.00288542 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401574 | GCCAAGAGACAAGAA[C/T]GCAACACACCTGAGC | 55779 |
rs755484081 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350358 | CAAAGAGAGAGTCAG[-/AG]AGAGAGAGAGAGAGA | 55779 |
rs755509326 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314625 | ATATGGGTAAATACA[A/G]CAGGCTTTTCTCCTC | 55779 |
rs755521325 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313794 | GTGCCTTTTGCCTCC[C/T]ACCATGATTCTGAGG | 55779 |
rs755553884 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369780 | TTCAAAAAATCAATG[A/G]ATCCAGGAGCTGGTT | 55779 |
rs755561307 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344805 | TACAATACACTATTC[C/T]TATTATATCATTATA | 55779 |
rs755563915 | snp | A/G | 1.81823e-05 | 0.0030151 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400642 | GCATTCTGGGTCCTG[A/G]GTCTGAGAATAGATA | 55779 |
rs755569257 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374256 | TTGTAAATGTGTTTG[-/A]AAGGCATTGGCAAGC | 55779 |
rs755573256 | snp | C/T | 1.65296e-05 | 0.00287481 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420101 | AAAGATCAGTTGGTT[C/T]CCAGCTATGTATATG | 55779 |
rs755585393 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287309 | TACGGGAAACATTTT[C/T]CTAAGATGCCCATGA | 55779 |
rs755596121 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402455 | GGTGGCAGGGAGGCT[C/T]AGCAGGACCTCCCCT | 55779 |
rs755624497 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443456 | TTCTTCACCTCTAGG[G/T]CTCAGCATCCTCATC | 55779 |
rs755647581 | snp | A/G | 1.87254e-05 | 0.00305979 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396751 | AAATTAAAGATAAGG[A/G]ACCTGAAACTAGTTA | 55779 |
rs755718166 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375892 | AATGTATAACTAATA[A/G]TCTAGTAGAGGAAGA | 55779 |
rs755718406 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373403 | AAGCTTTTTGAAATA[C/T]TGCTCACTTGAAAGT | 55779 |
rs755723850 | in-del | -/A | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286905 | ATATTGTTTTTTTTT[-/A]TAAAAAAAAAAAGAA | 55779 |
rs755765335 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363298 | TCTTTTTCTCCTAGC[A/G]TTCTCGATACTGAAA | 55779 |
rs755770345 | snp | G/T | 0.000102992 | 0.00717533 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344518 | TGTCATAGGCTACCT[G/T]CATCTCTCTGGCTGT | 55779 |
rs755787985 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314446 | AAAATGTCTTTCAAA[A/G]AGGGAAAAATTAAGA | 55779 |
rs755793674 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403984 | ACCACCTTCCCAAAG[C/T]AGCATGTTGCCCCAT | 55779 |
rs755804572 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424911 | CTGCCAAACCAACTC[A/G]GAGTTTCTTCAGAGT | 55779 |
rs755808361 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329288 | GGAGAGGGTTTGGAA[C/T]TGAGCCATGCTTTGA | 55779 |
rs755812639 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386563 | CCTAGGTTGTACAAT[A/C]AATAAGTCTTCCTGA | 55779 |
rs755844582 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318734 | AGCAGACCTCTGAGC[-/AG]AAATCTTACAAGCAA | 55779 |
rs755860805 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346008 | GCCTTTCCATGAGAC[A/C]CAGATTAACATTGAG | 55779 |
rs755862698 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388823 | ATTCAGTAAAAGGAT[A/G]TAACAATTGTAAATA | 55779 |
rs755878114 | snp | C/T | 0.000111816 | 0.00747631 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400502 | TTATTGCAAATAAAA[C/T]AAAACAAGGCCAGAC | 55779 |
rs755891626 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426554 | TTGCTTCCCTTTCTG[-/C]CATAATTGTAAGTTT | 55779 |
rs755911294 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427676 | TAGGGAACCTGTTAC[A/G]TTAAAGACAAACAAG | 55779 |
rs755921587 | snp | C/T | 1.6528e-05 | 0.00287467 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363186 | GTAATTTTTCATTCA[C/T]TTCTAATAGATTACA | 55779 |
rs755921774 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332551 | TCCACAACCACATTA[C/G]GTTACGATGTATCGA | 55779 |
rs755921882 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362636 | CATCACATATGTGCA[A/T]CAGAGTGCAGGGATG | 55779 |
rs755938318 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351279 | GTTAACAGTGTAACA[C/T]GTATTATTCTAACTC | 55779 |
rs755949642 | snp | A/C | 3.29511e-05 | 0.00405887 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426205 | ATATAATCATAGAAG[A/C]AGCTCTCTGATATTT | 55779 |
rs755974919 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320767 | ATGGGAGAAAGATGT[A/T]GGCTGGGAGGCTAGG | 55779 |
rs755989309 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368084 | TCCAAGAAATATGGG[A/G]CTATGTGAAAAGACC | 55779 |
rs756009483 | in-del | -/ATA | 1.64817e-05 | 0.00287064 | cds-indel, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427209 | GCTTTGCAAATCACC[-/ATA]CTGAAATGAACTCAA | 55779 |
rs756034722 | snp | A/G | 3.30929e-05 | 0.0040676 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381006 | GCTTTATGGTTGGAA[A/G]TGGAGCTTCAAGAAT | 55779 |
rs756048359 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292038 | GGAATAATAAAAGAC[-/A]AGAGTATGTCTTTCT | 55779 |
rs756071987 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310032 | CTAAATCAGCAAAGG[C/T]TAAGTGGAGAGGCTA | 55779 |
rs756074708 | snp | G/T | 0.00030754 | 0.0123966 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286676 | CTTTCTCCCCTCAGG[G/T]CCCCCATGCTGCTTG | 55779 |
rs756099419 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351947 | GGCTGACCTAGAGAG[C/T]TACCCTCTGGAGGAC | 55779 |
rs756114964 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431212 | CCTCTTCACGCAGCA[A/G]CAAGGTACAGGATGT | 55779 |
rs756118892 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299565 | TCGCACTGCTAGATA[A/G]ATACCCAAAAGAAAG | 55779 |
rs756121139 | snp | A/T | 1.76668e-05 | 0.00297205 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395894 | ACCGACGAAATATAT[A/T]TTACTATGAAATCTA | 55779 |
rs756141951 | snp | C/G | 1.69017e-05 | 0.00290699 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400583 | AGATAAGTGAGAGGA[C/G]AAACAGCCACGGCTT | 55779 |
rs756145439 | snp | C/G | 3.40078e-05 | 0.00412344 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363523 | GAATTGGCTCTGTTT[C/G]AATTCCAAACTATAG | 55779 |
rs756160740 | snp | C/T | 1.65263e-05 | 0.00287452 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420046 | TTCCTTCACCACTGC[C/T]ACTTCGCAGGTAGAT | 55779 |
rs756177698 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421711 | GCAGCAGGAGGCCAT[C/T]ATCCTAAGCAAATTA | 55779 |
rs756213094 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406286 | ATAACCTTTGACCCA[A/G]TAAGTCTTCTTGGAT | 55779 |
rs756222943 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359404 | TGGAAAAATATCAGA[A/G]CCAATATTTGTGATA | 55779 |
rs756227781 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439262 | CAGTGTTAAGAAAGA[A/C]CCCTGACAAATAGAG | 55779 |
rs756228077 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386422 | CCTATTAGTCTGTAG[G/T]TCTTTTGTCTGTCTT | 55779 |
rs756245998 | snp | A/C | 3.38604e-05 | 0.00411449 | splice-donor-variant, intron-variant | CFAP44 | GRCh38.p7 | 3:113366038 | TTAATTAATTACATA[A/C]CCTGGGAGATGGAAC | 55779 |
rs756263549 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329982 | CTGTAGTTCTGGGAA[A/G]AGCACAGTGATTTCC | 55779 |
rs756270479 | snp | A/C | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379756 | TGTTTTACCCCCATC[A/C]ATCTTGGTTTTATAG | 55779 |
rs756303468 | snp | A/T | 9.94481e-05 | 0.00705083 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409094 | GGCACCTCTATTGGT[A/T]ACCCAACCTACTTGA | 55779 |
rs756312526 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401678 | TCATTAATAGGCTCA[A/G]TCTCCAACAATCCAG | 55779 |
rs756320784 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356841 | AACTTCTATTCAACA[A/C]ACAACTCTATTAAGA | 55779 |
rs756337159 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392421 | TGGTGGGTGTGGCGG[C/G]GGGTGGGGTGCAAAT | 55779 |
rs756374500 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407313 | AATGCAGTACCCTCC[A/G]GCTATGTGTGACTAT | 55779 |
rs756401749 | snp | A/G | 0.000117158 | 0.00765279 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291520 | CTTCCAGTGAGTTAT[A/G]TCAGAAATCTTGTAT | 55779 |
rs756427990 | snp | A/T | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306259 | ATTTTCTTTTCTTCA[A/T]CTAAAGCCTCCTCAA | 55779 |
rs756444958 | snp | C/T | 1.67595e-05 | 0.00289473 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420005 | TTTTTTTCTAATTTA[C/T]TGAAGGCATACCCCA | 55779 |
rs756474294 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333065 | ATAGAGACATTCATC[-/AG]AGAGTCAAACTCCGA | 55779 |
rs756477508 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441718 | AGGACGTCATGTAGA[C/T]AATTAAATGACATGA | 55779 |
rs756481510 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307553 | ACTTCTTATATTTAT[C/T]GTCTTTCTCCACTAG | 55779 |
rs756507810 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290590 | ATGTCAGTGAGATTA[C/T]CCTGCAATGGTTATA | 55779 |
rs756517914 | in-del | -/GC | 9.71865e-05 | 0.00697021 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304018 | AATTTTCCTCCTGGA[-/GC]TCATGGATTCGTTCT | 55779 |
rs756518577 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380523 | GCAGCCATAAACTCC[C/T]GGGCTCAAGCGATCC | 55779 |
rs756539907 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335384 | AGAGATCAGAGTACA[A/G]GGAGGCCAAATTTGG | 55779 |
rs756556223 | snp | C/T | 3.32591e-05 | 0.0040778 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373505 | TGAAATCACTGCTTT[C/T]ATCACAAGGGGGGAA | 55779 |
rs756565220 | snp | C/T | 0.000103024 | 0.00717644 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341838 | CAATTTGATTTTCCA[C/T]GATGATTTCACTTAG | 55779 |
rs756567970 | snp | C/T | 5.01509e-05 | 0.00500729 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401561 | GTAATGTTAAAGAGC[C/T]AAGAGACAAGAATGC | 55779 |
rs756593049 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323737 | CAAACTACCATGACT[C/T]ACCCAATATGAAATA | 55779 |
rs756593492 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336376 | TATAAATAAAACAGA[A/G]GGCATCAAAACAGAT | 55779 |
rs756611095 | snp | A/G | 5.81615e-05 | 0.00539234 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416634 | TGGATGAACCTACAA[A/G]AGATAAAATTTCACC | 55779 |
rs756615313 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415857 | TGGAGTAGGGGAGAG[C/T]TCTGTAGAGGTCTAT | 55779 |
rs756627555 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296220 | TGTTGCTGCAAAGGA[C/T]ATGATATCATTTTTT | 55779 |
rs756664016 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426196 | GCAAGCTCCATATAA[A/T]CATAGAAGAAGCTCT | 55779 |
rs756710790 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414874 | GATGATGCTGGCTTC[A/G]TAAAATGAGTTAGGA | 55779 |
rs756723383 | snp | C/T | 2.55242e-05 | 0.00357232 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446553 | CCTTCTACCCTCACC[C/T]CTATATGCATTTCAC | 55779 |
rs756774049 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323382 | AAAACCAAATACTAC[A/G]TATTTTCATTTGTAA | 55779 |
rs756791001 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399261 | CACTCTGAAGCAGAG[A/G]CAATCCATCTCTGCT | 55779 |
rs756796404 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366568 | CTGGTGTACTCATAA[A/G]AAGAAGATATCAAAG | 55779 |
rs756800029 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380426 | TTTTCACCTCTCAAA[A/G]TTCCCCCTATTTTTT | 55779 |
rs756822026 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415631 | ATTTACACAGGAGTC[A/T]TTCAGGAGCAGGTTG | 55779 |
rs756848454 | in-del | -/AAACA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342337 | ACTCTGTCTCAAACA[-/AAACA]AAACAAAACAAAACA | 55779 |
rs756867407 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354324 | GAACTGGATCACCCA[G/T]GCAGGTTCCCTGAGA | 55779 |
rs756870742 | snp | C/T | 0.000105983 | 0.00727875 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358702 | TATGTTATTCACACA[C/T]GTGCTCTCAAACATC | 55779 |
rs756892179 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396574 | CAGTGACACAAGCAG[C/T]ATGGGGTTTGAAAAC | 55779 |
rs756905606 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351777 | CAGCCATCTTGCTAT[C/T]ACTCACCTTCGGGCC | 55779 |
rs756905786 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324314 | AAAGACAGTACCAAA[A/T]ATGAAAACTACAGAA | 55779 |
rs756907662 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324461 | AATTCTGATTTAATA[A/C]TCCATAATTAGCCAA | 55779 |
rs756912353 | snp | C/T | 1.77165e-05 | 0.00297623 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380849 | TAGGATATTTTATAT[C/T]CTAAGGAAAGGAAAT | 55779 |
rs756935892 | snp | G/T | 1.66944e-05 | 0.0028891 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400047 | TTATATACATAATTT[G/T]TTTAAGTCTTGGCTC | 55779 |
rs756940634 | in-del | -/C | 0.00111198 | 0.0235532 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333602 | TAGAAAAACAGACAA[-/C]CCCCCCCACACACAA | 55779 |
rs756941392 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312820 | TAGTGTTGAACCTGT[A/G]AGTGCACAGAAGTCA | 55779 |
rs756948171 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436159 | CTAGTGTGTTGGCCA[C/G]GGCTGAGAATATTTT | 55779 |
rs756952650 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386638 | TAGGGAGGAGGCAGA[A/G]CAAGATGGCTGATTA | 55779 |
rs756956308 | snp | C/T | 0.000188377 | 0.00970325 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330126 | ATTTTTTCCCTTCTC[C/T]TCTCTCTTTCAGCTT | 55779 |
rs756959205 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409829 | AGATGGTGATGAAAG[C/T]GACCTCTGGTCGTCC | 55779 |
rs756996247 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313606 | TTGAATTGTACTCCC[A/G]TAATTCCCACATGTT | 55779 |
rs756996447 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299915 | GTATGCCTGTAGTCC[C/T]AGTTACCCAGGAGGC | 55779 |
rs757011114 | snp | A/C | 1.76474e-05 | 0.00297042 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286659 | TTTTAATGGTTCCTA[A/C]TCTTTCTCCCCTCAG | 55779 |
rs757017180 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375743 | GGAGAATCACTTGAG[C/T]CTGGGAAGTAGAGGC | 55779 |
rs757044319 | snp | A/T | 1.95052e-05 | 0.00312285 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446675 | CAGTAGCCCCGGAAG[A/T]TCTATTCATGAAAAA | 55779 |
rs757091214 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443162 | GAGCCAAGCTCTGAT[A/C]TCAGCCCATTTACAT | 55779 |
rs757109721 | snp | C/T | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330297 | TAGGCTGAATGTTGA[C/T]GCCTTTGATGATCTA | 55779 |
rs757111768 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397814 | GTGTGGTTTGTAGTT[-/G]GCTATTGTTGATTTA | 55779 |
rs757113796 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425422 | ATCATAATGTGATGA[C/T]GAACACAAAATCCCC | 55779 |
rs757125153 | snp | A/G | | | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341825 | TTTCTCGTTTTCTCA[A/G]TTTGATTTTCCACGA | 55779 |
rs757125795 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290757 | AAAACCAGCAAATGG[C/T]CCAAGTAAAACCTGA | 55779 |
rs757144501 | in-del | -/CTTAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324607 | ACAGAGGTGAACTTC[-/CTTAA]CTTAATAGAGTATCT | 55779 |
rs757153226 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423890 | GTGACATACAGAAAA[C/T]GAAAGTGAGGTACAG | 55779 |
rs757164917 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331048 | ATTAATTCATTTTCC[G/T]CCTGGAACTTTGAAT | 55779 |
rs757180240 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376611 | GGGGTCAACTCTGTT[A/C]AATGTTCCGAAAAGT | 55779 |
rs757200550 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386073 | TGCTTTATATATTTA[C/G]GTGCTCTGAGGTGGG | 55779 |
rs757215558 | snp | A/T | 1.77502e-05 | 0.00297905 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381063 | AAGTACTTTCAGGCT[A/T]AAAAAGAAAAATTGA | 55779 |
rs757216076 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319566 | ACTCTGGACTTAAAC[C/T]CAACACTTGACCAAT | 55779 |
rs757244785 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441982 | GTCGCAGCGCTCTGG[A/G]CACAAAAGTATAGGC | 55779 |
rs757247431 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361955 | CCAGCACAAGTGTTA[C/T]AAGATTAAATGCCTA | 55779 |
rs757256113 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291569 | AACTCAAAGGTCTGC[A/G]GGCTGTATCTCTTTC | 55779 |
rs757257139 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432609 | TTATGGGAAGATGAA[C/G]AATGTTAAATCTCTA | 55779 |
rs757261147 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311421 | GTGAATAAGTCTCAT[A/G]AGCTCTAATGGTTTT | 55779 |
rs757263081 | snp | C/T | 1.6808e-05 | 0.00289892 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401537 | CTACTACTTTAATTT[C/T]TGGTCCATGTAATGT | 55779 |
rs757263282 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297401 | ACTGGCCACCTCTGT[A/G]CTTCTCAAACATGCC | 55779 |
rs757284330 | snp | A/C/G | 6.58896e-05 | 0.00573943 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409199 | AAAGCTTTTGTCCTT[A/C/G]GTATGGGTTGTTCTT | 55779 |
rs757291572 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297205 | TTTCAAATATGGCAC[A/T]TTACAGCATCTAGTA | 55779 |
rs757331282 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354054 | TAAAGGCTGCTCTGA[C/T]CTCACCTAACAAAGA | 55779 |
rs757335186 | snp | A/G/T | 3.33652e-05 | 0.00408432 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363336 | TTTAAAACAATAACA[A/G/T]GTTGTGATACAGAAA | 55779 |
rs757348195 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418731 | TTTTTTTTGAGACAG[A/G]GTCTTGCCCTGTCGC | 55779 |
rs757356041 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383480 | CCAAATACTATCACA[A/T]GGGGAATTTAGGCTT | 55779 |
rs757413676 | snp | A/G | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395779 | ACCACATTAACTGAC[A/G]CACAGGTCCAGGAGT | 55779 |
rs757416172 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400396 | TGTGTTTTGTGGCCT[C/G]TCCTCTCCACAGCTC | 55779 |
rs757455647 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316498 | TCCCTTATAACACAA[A/G]CTGATTTGTTCTTGA | 55779 |
rs757458864 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298652 | ATGGAATATTATTTG[C/T]CTTAAAAAGGAAGAA | 55779 |
rs757459403 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427168 | TGACAATTACTGACA[C/G]AAAACTAATAATACC | 55779 |
rs757466055 | snp | G/T | 2.11129e-05 | 0.003249 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286899 | AGACTATATATTGTT[G/T]TTTTTTTAAAAAAAA | 55779 |
rs757495043 | snp | C/G | 1.65392e-05 | 0.00287564 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286808 | ACCTGGAATGCAGCT[C/G]TCCCCGGGGCCACTG | 55779 |
rs757495866 | snp | A/G | 5.15371e-05 | 0.00507601 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401201 | ACAAAAGTTTTTACT[A/G]TGAAAGTTAGGAGAA | 55779 |
rs757531703 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327588 | AACTAAGGGACCAGC[C/T]AGCTAGGATTCTTCT | 55779 |
rs757596427 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358350 | ACATTCCCCTGGAAG[C/T]CAAATTGGTGCATGA | 55779 |
rs757628367 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405984 | AACTTGGTTCCTTAA[A/G]TATTTGTGTGCTGGC | 55779 |
rs757628685 | snp | A/T | 1.66405e-05 | 0.00288443 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445300 | ACTCAGTGAGACTTG[A/T]CTTCACTTATGATAC | 55779 |
rs757633486 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439425 | ATCTGCCCAACAATT[C/G]CCTGTCCAACCTCAG | 55779 |
rs757644735 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392183 | AATGGATAAAGAAAA[C/T]GTAGTACATATACAC | 55779 |
rs757661773 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368614 | ATGGAAAGGAACAAC[C/T]GGTACCAGCCACTGC | 55779 |
rs757663679 | snp | A/C | 9.99534e-05 | 0.00706871 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416576 | CATAGATGATAATAT[A/C]TGGAAAACTCCCTTT | 55779 |
rs757665389 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426819 | GGAAGGAAGAGCCAT[G/T]ATGCCCACGTGCATC | 55779 |
rs757686266 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347165 | GCGTGGCCGCCGGAC[C/T]AAAGACATGGGTGTC | 55779 |
rs757688187 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359285 | AGATAGCAGTATCTG[A/G]TGTCTTCTTGACATC | 55779 |
rs757704633 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348107 | TCCAGGGACCATTGC[A/C]GGTTCTTGGGCAAGA | 55779 |
rs757707464 | snp | C/T | 3.30781e-05 | 0.00406669 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373488 | TTCATCTTTTTGTTC[C/T]TTGAAATCACTGCTT | 55779 |
rs757709573 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335313 | GGAAATTACCAGCCT[A/G]TGGAGTAGGATCAGG | 55779 |
rs757716094 | in-del | -/TAAC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369718 | GCAGAAGGCAAGAAA[-/TAAC]TAAGATCAGAGCAGA | 55779 |
rs757748430 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427719 | TCTTTCTCTGAGTAT[A/G]CTGATTTCTCTTGGA | 55779 |
rs757763071 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420915 | TATGTATTGGTGTGT[A/G]GGTAACTAGTGTGTG | 55779 |
rs757833486 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305609 | CCTGAAAGTTTTCCA[A/C]ATCATTTCCTGTTTG | 55779 |
rs757834189 | snp | A/C | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330333 | TGAATCACGGGTTGT[A/C]AAATCCCCATCCTTT | 55779 |
rs757847579 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426704 | CTGGTGAATCCAAAA[C/T]TGTATTTCCCAGAGA | 55779 |
rs757852322 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332440 | GGACATTTCATTTTC[A/G]TTTGTCAGAAAATTA | 55779 |
rs757860294 | snp | C/G/T | 3.29626e-05 | 0.00405961 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379445 | TCCTCCTGAAATTCT[C/G/T]TTTCTCCATCTTCTC | 55779 |
rs757889589 | snp | C/T | 1.81645e-05 | 0.00301362 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420224 | GAAAAACACTACCAT[C/T]CTAGGGATTGGAAAA | 55779 |
rs757902155 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364812 | ATTCTAATTTAATTG[C/T]TCTTGGGTGGGCTCT | 55779 |
rs757908791 | snp | C/T | 1.65351e-05 | 0.00287528 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420115 | TCCCAGCTATGTATA[C/T]GGCGATACTGTCGTC | 55779 |
rs757909999 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333516 | AATCTCCCATATACA[C/T]CTGGGCTTCTTTGAT | 55779 |
rs757913168 | snp | A/G | 0.000119225 | 0.00771999 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344730 | GAAAAAATAAAACAA[A/G]TATTTGCAGTAGTCA | 55779 |
rs757938835 | snp | A/G | 4.12771e-05 | 0.00454278 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446581 | CACAATTACATTTTA[A/G]CGTGTACCTTTGCTC | 55779 |
rs757939665 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413413 | CTTTTGTTGCAATTG[C/T]TTTTGGCTTTTTTGT | 55779 |
rs758021596 | snp | A/C | 1.83727e-05 | 0.00303085 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379312 | GTTACTTACCAAAGA[A/C]ACCCAGAACTTCCCT | 55779 |
rs758033778 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370766 | GATAAAGGATATTCA[A/G]TTAGGAAAAGAGGAA | 55779 |
rs758034500 | in-del | -/TCC | 0.00119811 | 0.0244463 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379400 | GGTAATGGCTCTTCT[-/TCC]TCCTCCTCCTCCTCT | 55779 |
rs758037721 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293897 | ATGCAGACTGCTGGG[A/C]CCCTCCCCTCAGGCT | 55779 |
rs758049624 | snp | C/G | 5.00622e-05 | 0.00500286 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400006 | CGAACAGAGCCTATA[C/G]AAAGACAGTTTTAAA | 55779 |
rs758073656 | snp | C/T | 1.67055e-05 | 0.00289006 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409075 | TACTCCTGTGATATC[C/T]ACTGGCACCTCTATT | 55779 |
rs758077868 | snp | A/G | 5.23793e-05 | 0.00511732 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366014 | TACAGTTTGTTATTA[A/G]TTAACTGGTTAATTA | 55779 |
rs758095276 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414806 | TGTTCATCAGGGATA[C/T]TGGCCTGAGGTTTTC | 55779 |
rs758095464 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312619 | CACACAGCCCCTCCC[A/G]TCACAGGCCTGGAGG | 55779 |
rs758107139 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300478 | ATATATCTTATAAAT[-/AT]ATATATATATATATA | 55779 |
rs758140898 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386551 | GAGGAAGAGATGCCT[A/G]GGTTGTACAATCAAT | 55779 |
rs758151424 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420209 | CTAAGGAAAAGAAGT[A/G]AAAAACACTACCATC | 55779 |
rs758152069 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298909 | CTGGAGATGGATGGT[A/G]GTGATGGTTGCACAA | 55779 |
rs758154887 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311648 | ACCAGTAGAGTGGGG[C/T]GCTGTTGAACAGATA | 55779 |
rs758198179 | snp | A/G | 1.65343e-05 | 0.00287521 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399925 | CGGGGTACCCAAACA[A/G]GGGCAGTACCTCCTT | 55779 |
rs758206087 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312659 | AAATGGTTTCTTGGG[A/G]AGGGCCCAGGGTCCC | 55779 |
rs758216021 | snp | A/C | 0.000103056 | 0.00717755 | intron-variant | CFAP44 | GRCh38.p7 | 3:113306355 | AGAATTAAAATAAAA[A/C]CCAGCCTCATTTGTT | 55779 |
rs758216653 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329121 | GAAGTATATGTGGCC[C/T]TTTGCTCAAGAATTG | 55779 |
rs758261688 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299768 | GCACAGTGACTCACA[A/C]CTGTAATCCTAGGGC | 55779 |
rs758266124 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361642 | CTGGGACTACAGGCA[A/C]CCACCACCACACCTG | 55779 |
rs758277154 | snp | A/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343255 | TTTAGTAGAGATGGG[A/G/T]TTTCACCATGTTGGC | 55779 |
rs758315305 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387396 | TTGTGAGGCCCCTAT[A/T]CCAGGCCCTAGGTCC | 55779 |
rs758319161 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289761 | CTGTGGCTCTTGTAT[A/G]CATCATTCTCTCTTG | 55779 |
rs758325441 | snp | C/T | 1.68015e-05 | 0.00289836 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363499 | CTTTGGGATCTTCAA[C/T]GTCTTCTGGAATTGG | 55779 |
rs758371444 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374874 | CTCCTGGCCTCAAGT[G/T]ATCCACCCGCCTTGA | 55779 |
rs758395593 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406979 | GTAGTGATTGTTTTG[C/T]CAAATCGACCTAGTG | 55779 |
rs758401736 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421972 | AACCTGCATGTGTAC[C/T]CTCTGTATCTAAAAT | 55779 |
rs758412574 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443507 | AGGAAGCATTTACAT[A/G]CCTCTAACTGATAGG | 55779 |
rs758413221 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396368 | TTATTCACAGACTAC[A/G]CTGAAAGAATATGAC | 55779 |
rs758433834 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431191 | GGCTGAGCCAGGAGG[A/G]AGAGACCTCTTCACG | 55779 |
rs758445540 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384877 | GTCAAGAAGTTCAGA[A/G]TCTGATGCTGTTTGA | 55779 |
rs758546738 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399840 | ATATCTATATTTCCA[G/T]AAAATAGCATTGATA | 55779 |
rs758548327 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309713 | TATGCAAAACAAACA[A/T]AAGAAGACTCTGAAA | 55779 |
rs758552506 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326262 | AAACAAACATGCACA[C/T]AGATTAACTCGAGGT | 55779 |
rs758567499 | snp | A/G | 5.1565e-05 | 0.00507739 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400690 | CAAAGACAGAGTAAC[A/G]AAGAATTAAGATCAA | 55779 |
rs758572504 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397509 | ACATGGTCAGATTTG[C/T]TCATTTTAAAATGAC | 55779 |
rs758579206 | in-del | -/G | 1.68342e-05 | 0.00290117 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433552 | AAAAGTATACATATT[-/G]ATCTTTACTTACATC | 55779 |
rs758614660 | snp | C/T | 0.000124139 | 0.00787743 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330181 | ACCCTGTTGACCAAA[C/T]ACTGTTGCATGTACA | 55779 |
rs758628790 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318179 | AAAATGATCCAAGAG[-/C]CCGAAAGATGAAATA | 55779 |
rs758632163 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315889 | TAAGCTAAGCTACTA[C/T]GTTTGGTAGGTTAGG | 55779 |
rs758642886 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337924 | AGGAAAATTGGTAAG[C/T]TGGACATCAACTAAA | 55779 |
rs758646460 | snp | A/G | 8.67852e-05 | 0.00658673 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416474 | GTCACACCTTCTTCA[A/G]AATGTTGTTATCCTT | 55779 |
rs758668309 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437034 | GAATCTACTTCTGGG[C/G]TCATTCAAGCTGCTG | 55779 |
rs758696301 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339127 | TCCAACTGCTGAATG[C/G]TATCAAAAATGAATG | 55779 |
rs758732407 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371634 | TAAAAACTCTAGAAG[A/G]AAACCTAGGCAATAC | 55779 |
rs758738438 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412839 | TAATAAACATACGTG[C/T]GCATGTCTCTTTACA | 55779 |
rs758743884 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314833 | AATGATGGCAAAATG[A/G]TGACATTGCTAGACT | 55779 |
rs758756999 | snp | C/T | 1.76052e-05 | 0.00296686 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433543 | TAATACTTTTAAAAG[C/T]ATACATATTATCTTT | 55779 |
rs758765401 | snp | A/C | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396556 | CACGTTCATAAGCTA[A/C]AGCAGTGACACAAGC | 55779 |
rs758822442 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357447 | GAGACACAGGGAGAA[C/T]ACTGAGTGAAAGCAG | 55779 |
rs758824628 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402609 | GGGGGAAGAGGGAAA[C/T]ATCTGAGGGTCAGGG | 55779 |
rs758827824 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414986 | GCTGTGAATCTATCT[A/G]GTCCTGGAGTTTTTT | 55779 |
rs758851970 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366248 | AAGGATCATTTTGAT[C/T]TAGGACATAGACTCG | 55779 |
rs758854274 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347152 | TTAAAAGTGACTAGC[A/G]TGGCCGCCGGACTAA | 55779 |
rs758877386 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295267 | TTCTTATTGCTCCAT[C/T]GGTTGCTCACTGCAA | 55779 |
rs758887887 | snp | C/T | 1.65124e-05 | 0.00287331 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396632 | AATTTTCTTCCGTCC[C/T]GCAAAAATCGTGAGC | 55779 |
rs758896310 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439316 | GTTCTCACGCTTGTA[A/T]GCTGGATAACTATCC | 55779 |
rs758900481 | snp | A/T | 4.9423e-05 | 0.00497082 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409148 | AGCTGCTCTTCCTTA[A/T]CAGGATTGAAAGTAA | 55779 |
rs758926958 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390942 | TCTACAAATTCAATG[C/T]AATGCCTATCAAAAT | 55779 |
rs758965149 | in-del | -/AAATT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422072 | AGTATGTTTAAGTCA[-/AAATT]AAATTAATATGCCCA | 55779 |
rs758988568 | snp | A/G | 0.000186794 | 0.0096624 | missense, nc-transcript-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296747 | ATCTTCATCTCTTTC[A/G]CATTTGCTAGCTCCT | 55779 |
rs758999668 | snp | G/T | 1.68727e-05 | 0.00290449 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403823 | GTCTTAAACGTGGGT[G/T]CTACCATCCAAGTAT | 55779 |
rs759056280 | snp | A/T | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358846 | TTTTCTGTGCATCTC[A/T]GCACGGATTTGGGAA | 55779 |
rs759071307 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288184 | GACCCTGGCTTTTAA[A/C]CATGAAGAATTTGAT | 55779 |
rs759072693 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391703 | CCCAAACAACTCTAT[A/G]GGGGAAAAAATCTAC | 55779 |
rs759096325 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393298 | TTTAAATTATGCTGA[A/G]TGTTTTGGTCTTGTA | 55779 |
rs759114815 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373936 | TGCAGTTTAAGGTAA[C/T]TGTAAACACTGTTAA | 55779 |
rs759123329 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357869 | AGAAATAAGCACTTA[C/T]ATCCATCAAAAAACG | 55779 |
rs759131433 | in-del | -/T | 1.69229e-05 | 0.00290881 | splice-acceptor-variant, intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420181 | AACCAAAAGAATGTC[-/T]GAGGGAAAGTTGCTA | 55779 |
rs759131732 | snp | A/C | 2.02128e-05 | 0.003179 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427361 | AAATTTGTTTTAATA[A/C]CTTCTAAATTTTGAT | 55779 |
rs759144544 | snp | C/T | 0.000106174 | 0.00728531 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327841 | TGGAAAAAATATTTG[C/T]GGATACGTTAGAAGA | 55779 |
rs759145758 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409262 | GGGTTACTACCAACA[A/G]AGGCCAGCAAGTTAC | 55779 |
rs759180075 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317172 | CAGACCTCTGGAATC[C/T]TGGCTATAGGGGACC | 55779 |
rs759214306 | snp | C/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293724 | AATATTCAAATTCTA[C/G]TCTTCCTTTCACATC | 55779 |
rs759220610 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418888 | TTTTTGTATCTTTAG[C/T]AGAGACAGGGTTTCA | 55779 |
rs759227192 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440031 | GTACAATTCTCAAAA[C/T]GACCCTATGAGGTAG | 55779 |
rs759228402 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378757 | TCTTCCTAATATCCA[C/T]TTTTCCCTTCTTCCT | 55779 |
rs759229138 | in-del | -/TATCAT | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381255 | TACTAATTATTGTTA[-/TATCAT]TATTAAGTGATTAAA | 55779 |
rs759233023 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305338 | TTTCTGCCAAGTTAT[G/T]ATCCACATCACTCTT | 55779 |
rs759284319 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306697 | TAACAGAATGGGATT[A/C]AAGTGCATTATCTCT | 55779 |
rs759362233 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324114 | GAAAGTTGAATTTGT[A/G]ATTTAAAAACTCCCC | 55779 |
rs759383217 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414621 | TATTGAGATAATCAT[G/T]TGGTTTTTGTCTTTG | 55779 |
rs759385400 | snp | C/T | | | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294657 | GAGCTTCCTCAATTC[C/T]GAAAAAGGGTCTGAA | 55779 |
rs759385472 | snp | A/C | 1.7303e-05 | 0.00294129 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395880 | GGAAAAAGAGACACA[A/C]CGACGAAATATATAT | 55779 |
rs759442578 | snp | C/G | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379821 | CTAAATATAACTTCT[C/G]TTAGAGCCTATCACT | 55779 |
rs759451649 | snp | C/T | 3.30447e-05 | 0.00406464 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420051 | TCACCACTGCTACTT[C/T]GCAGGTAGATCTGTT | 55779 |
rs759457363 | in-del | -/TC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320226 | GGAGGTATATTAGTC[-/TC]TCTCTCTCTCTCTCT | 55779 |
rs759458461 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335015 | TAAAATGAAGGATTA[A/C]TATTTTTAAAGAAAA | 55779 |
rs759473267 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398827 | ATGGCATTTTAAAAA[C/T]ATGGCTGCAAATCTT | 55779 |
rs759494562 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368801 | ACAAACTGGCAAATT[G/T]GATAAAAAGTCATGA | 55779 |
rs759504265 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388742 | AGAGTAGAAATAATT[A/G]CACTTACATCAGACA | 55779 |
rs759507167 | snp | C/T | 0.000324781 | 0.0127391 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287101 | AGTCACCCAGGAAAG[C/T]ACCGCACAGGCTGGC | 55779 |
rs759543525 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291389 | CAGTCAGTTCTAAGA[C/T]AACCAAATTGTAGAG | 55779 |
rs759564874 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323959 | TGAGGCAGGAGAATC[A/G]CTTGAACCTAGGAGG | 55779 |
rs759568851 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431709 | GTGGAGAAACTGTGG[A/G]TTTACAAGACATGTC | 55779 |
rs759574107 | snp | A/G | 5.02635e-05 | 0.0050129 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445267 | AGGGAAAGGGAAGTA[A/G]TAAATTATTAAGAAC | 55779 |
rs759594166 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443858 | GCTACAATATTGCCT[A/G]GTATGTAGTTAACAG | 55779 |
rs759594218 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376453 | CTTAGCAAGAAAGAG[A/G]GGGCCCAAGGCCGCA | 55779 |
rs759605728 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446949 | TGTGGGAGGGACTCA[C/T]GGGGAGGTAACTGAA | 55779 |
rs759624707 | snp | A/C/T | 6.60408e-05 | 0.00574601 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396627 | TCCAAAATTTTCTTC[A/C/T]GTCCCGCAAAAATCG | 55779 |
rs759629547 | snp | G/T | 1.81023e-05 | 0.00300846 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366361 | ATCTGAAAATAATGC[G/T]TAATTTCAACTTAAT | 55779 |
rs759652204 | in-del | -/ATTA | 1.7532e-05 | 0.00296069 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366010 | TAAATACAGTTTGTT[-/ATTA]ATTAACTGGTTAATT | 55779 |
rs759664024 | snp | A/G | 0.000196928 | 0.00992095 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296684 | GGATTTCTTGCCTCC[A/G]GCCAGATTCAACCAA | 55779 |
rs759666634 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331020 | ACTCTCTCCAGGGAG[A/G]AAGGGAAAGGCAATT | 55779 |
rs759667735 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384332 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 55779 |
rs759679115 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437499 | GCTATCTTAAACAAT[A/G]TATTCCCCAAATGGC | 55779 |
rs759721651 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331805 | AAAAGACAAATAATA[C/T]ACTATTTTAAAAATA | 55779 |
rs759726305 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422763 | CATGTTAGTAGCTAT[A/G]AGAATAGAAATTGGT | 55779 |
rs759747422 | in-del | -/AT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412433 | AAAAAAAAAAGATAC[-/AT]GTGCAGAACGTGCAA | 55779 |
rs759751302 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321322 | AAGAAAATCAAACAT[A/T]TCTTCATAATAAAAA | 55779 |
rs759777550 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403936 | ATTGTGACATGACTT[C/G]CTTGTCCCTCGACAG | 55779 |
rs759820701 | snp | A/C | 1.961e-05 | 0.00313123 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363087 | TGTTGGGAAAATAGT[A/C]ATCTCTATCCAGAAA | 55779 |
rs759840353 | snp | C/T | 1.70252e-05 | 0.00291759 | splice-acceptor-variant, utr-variant-5-prime, intron-variant | CFAP44 | GRCh38.p7 | 3:113379552 | AATTTCTATTAATCT[C/T]TTTTAAAATAAACAT | 55779 |
rs759867028 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292142 | AGCTGACTCCTACTC[A/T]TGTTTCACACATCAC | 55779 |
rs759907209 | in-del | -/C | 0.000105291 | 0.00725495 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294816 | TCGCATTTGAGCAAT[-/C]TTTTCCTACCAGGGT | 55779 |
rs759943902 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310881 | TGCCTGCTCCTGTTT[C/T]GGCTTCTGATGTGAG | 55779 |
rs759950414 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383330 | AAGGGCATTTTTCCT[C/G]CTGCATCGATGGTGG | 55779 |
rs759952686 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397237 | AGCTAGGTACAGGAA[A/G]GTGGCACAAGCACTC | 55779 |
rs759965448 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445618 | TTTATAGCTATCATA[C/G]GCATAAATTTTTAAA | 55779 |
rs759969041 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384770 | TGTATTTTGTTATGG[C/T]AGGTCTAGCAAACAA | 55779 |
rs760001882 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340784 | CTTCCTTATCACAAG[C/G]ACAGAGGGATTTCTG | 55779 |
rs760015329 | snp | A/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317309 | GCTCTGACAGAGAGC[A/G/T]GCCATAGACACTCAT | 55779 |
rs760058238 | snp | C/T | 1.68312e-05 | 0.00290092 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363455 | CTCAGGCCTAGTCAG[C/T]ATTTATCAAAAATTC | 55779 |
rs760095974 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340165 | GGGTAAGGAGAGGTG[A/C]CCTGAGCCATGCATG | 55779 |
rs760110273 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372923 | AAAAATTCTGCTGTA[G/T]AAGCCACCTAGTCTG | 55779 |
rs760113742 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298146 | CCCATACAAGGGGTT[A/G]CCCTCTTGCATGGCA | 55779 |
rs760116186 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427224 | ATACTGAAATGAACT[C/G]AAACTTCCTTCCAAA | 55779 |
rs760122426 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325604 | ATATTGTGCTTTCCA[C/T]TGGAAAACTCAATGT | 55779 |
rs760168560 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113384409 | TTGTTATGTGCTGAA[C/T]TGTGTCCCTTCAGAA | 55779 |
rs760208462 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383114 | GATGGACTTTTGCTA[A/G]ATGGGTATGAAGAAA | 55779 |
rs760217453 | snp | A/C | 1.69441e-05 | 0.00291063 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395871 | TTACTCTAAGGAAAA[A/C]GAGACACACCGACGA | 55779 |
rs760261257 | snp | A/G | 0.00015902 | 0.00891543 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287042 | TAAGGAGTCCTACCC[A/G]TTGAGGTTGGAGAGG | 55779 |
rs760264376 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418198 | GCTCAAGCAATTCTC[A/G]TGCCTCAGCCTCCCA | 55779 |
rs760281357 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298627 | AAACAAAATGTGGCA[C/T]GTACATATAATGGAA | 55779 |
rs760314063 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288055 | ATGAAAGCCTTACTA[C/T]GCTTTGTGTTTTGGG | 55779 |
rs760318654 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326859 | GAATTAGAAAATCAG[C/T]TTTTTAGTGCTAAGC | 55779 |
rs760411103 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320467 | TTACATCTATATATC[-/AT]ATATGATATATATGA | 55779 |
rs760447847 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416674 | AAAGAAAGATTTTTG[C/T]ATAAATAGTCTGATT | 55779 |
rs760458127 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439110 | GGTTTGGGAGTCTAT[C/T]TGCAGGACTAGCATA | 55779 |
rs760477055 | snp | C/T | 2.19734e-05 | 0.00331455 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400674 | ACAGCTTACTAGATC[C/T]CAAAGACAGAGTAAC | 55779 |
rs760532446 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393058 | TGTGTGTACATGGGA[C/T]GCACCCTTACCAGAA | 55779 |
rs760549801 | snp | A/G | 1.66994e-05 | 0.00288953 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286857 | ACACCACCTCTCACA[A/G]TTTAGGCAGAAGCTG | 55779 |
rs760555298 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334725 | CCTACACACATACGA[A/C]ACAGTGGCAATCTTT | 55779 |
rs760580468 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391477 | CACAGGCAACCAAAG[C/T]GAAAATGGACAAATG | 55779 |
rs760593381 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346917 | CTCTTTGGGTCCACA[C/T]CACCTTTATGAGCTA | 55779 |
rs760601472 | snp | G/T | 1.78733e-05 | 0.00298937 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401311 | ATTAAATAGTATTTT[G/T]TTTTATCATTTTAAA | 55779 |
rs760625105 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365764 | ACCTTTGATTAAGAA[A/G]GTTTTTTTAATATAC | 55779 |
rs760653649 | snp | C/T | 0.00010869 | 0.0073711 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330651 | GCACTTGTTCATGTG[C/T]CTTTTATTTCCATGG | 55779 |
rs760677084 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292643 | CATTGAGACTCAGGG[A/C]GTCATTAACTAGCCA | 55779 |
rs760687134 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321930 | CAATATCATTAAAAT[A/G]GCATATCCTCCAAAG | 55779 |
rs760723523 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403922 | TGGTTAATGGGACCA[C/T]TGTGACATGACTTGC | 55779 |
rs760736275 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293640 | GTGAAGATTTGGGTT[A/C]GGTATTAACCTTCTC | 55779 |
rs760739204 | snp | C/T | 1.74278e-05 | 0.00295188 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401787 | TCAGTAGTTTCTGAA[C/T]ATTTATTTTCTAAGC | 55779 |
rs760786680 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354830 | TCCCTACAGGACCAC[A/T]GCTGATGGGCTCTTG | 55779 |
rs760803051 | snp | A/C | 3.30491e-05 | 0.00406491 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396531 | ACCCCTGTGGCTAGA[A/C]TTTCCCCATCACGTT | 55779 |
rs760843818 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406624 | GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAG | 55779 |
rs760871160 | snp | C/T | 0.000115908 | 0.00761188 | intron-variant | CFAP44 | GRCh38.p7 | 3:113294861 | TAGATGTAGTGAATA[C/T]GAGAAGAAAGAAAGA | 55779 |
rs760872364 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301062 | CAAGAATTTTCATAG[C/T]AGAATCATCAAAGCA | 55779 |
rs760887434 | snp | C/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113331737 | CTCTTCACACATCAA[C/T]TCTTTCTTTCTAGTT | 55779 |
rs760908306 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441165 | CACCTTCCCAGCTGA[C/T]TCGCTGCTGCTCTGA | 55779 |
rs760910161 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375573 | AGAAGCAACACTGTG[G/T]TAGATAATGGCTGAG | 55779 |
rs760911839 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315381 | TTACCAAGACGACAT[A/G]ACACTCCTAAATTTG | 55779 |
rs760917456 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381463 | ATGGCGTAGTCAGTC[C/T]CATCCTACTTTAATG | 55779 |
rs760929513 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290540 | ACAGAGCTCTTAATC[G/T]AAAGAGCTATGCTCT | 55779 |
rs760953032 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349427 | CCGAAAAGGAAAAGC[A/G]AGATCAGAGAAAGGC | 55779 |
rs760968798 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443212 | CTCACAAGCCTCTAG[C/G]GAAGACATTATGTCT | 55779 |
rs760968842 | in-del | -/CCTCTAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316536 | AGTTGAATTGACAAA[-/CCTCTAG]CCAGACTGAAAAAAA | 55779 |
rs760970019 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360529 | GACATGATCCTCATC[A/T]TTTATACACTGTTAG | 55779 |
rs760973928 | snp | A/G | 3.32392e-05 | 0.00407658 | stop-gained, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420151 | GTTGTAGGTTGGCTC[A/G]CTTTCTACAGTCATA | 55779 |
rs760977397 | snp | C/G/T | 0.0010415 | 0.0227978 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344630 | AGTACTTAGAGGGCT[C/G/T]CACCAGCCTGTAAGA | 55779 |
rs760983812 | snp | G/T | 3.30546e-05 | 0.00406524 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420095 | ATTCAGAAAGATCAG[G/T]TGGTTCCCAGCTATG | 55779 |
rs760985142 | snp | A/G | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330869 | CCTCCAAGATGGAAG[A/G]ACAGACTACATATGA | 55779 |
rs761000460 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376324 | AGGTGCCAAGGAGCA[C/T]TGTCAAGTTGGATAT | 55779 |
rs761021622 | in-del | -/T | 6.8451e-05 | 0.00584985 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373379 | ACTAACAGGATATGG[-/T]TTTTTTTAAAGCTTT | 55779 |
rs761027247 | snp | C/G | 9.97556e-05 | 0.00706172 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291677 | AATCCTTTCCGCCTG[C/G]AGTTGGATCAATTCA | 55779 |
rs761029484 | snp | A/C | 0.000102443 | 0.0071562 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358879 | TACATCAAAATCCTG[A/C]AGATAAGAAGATCTG | 55779 |
rs761032749 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442369 | TTGCTAACACCAAAT[A/G]CAGAAGGATATGGAG | 55779 |
rs761033149 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324038 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 55779 |
rs761046015 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394728 | AGCTGACGAGCTAAA[A/G]AAAAAAATTGCAAAA | 55779 |
rs761060128 | snp | A/C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319403 | TATCCGAAATATATA[A/C/T]GCACCCAACATTGGA | 55779 |
rs761065062 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340594 | CGCTTCTTCAGTACC[A/C]CATTGCTCAAACCTC | 55779 |
rs761071601 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350446 | AGAGACAAAGAAGCC[A/G]AAGAGAAAGAAAGAG | 55779 |
rs761113654 | in-del | -/T | 4.18778e-05 | 0.00457571 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400044 | AAATTATATACATAA[-/T]TTTTTTAAGTCTTGG | 55779 |
rs761133990 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395956 | ATAACGCTATCTCTA[C/T]CTACAATGGTCATAT | 55779 |
rs761143760 | in-del | -/TA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438953 | TATACCTCCTAATTT[-/TA]TATGTTCTTCGTAGG | 55779 |
rs761160130 | snp | C/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424627 | AACTAAATCTAATGG[C/G]GGCCATCCCAGCAAG | 55779 |
rs761162801 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385648 | GGTTTTGTTTGTTTG[C/T]TTGTTTGTTTTGAGC | 55779 |
rs761190030 | snp | C/T | 1.65225e-05 | 0.00287419 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380972 | TCATAGGAGACTACA[C/T]CATGATCATCCTCTT | 55779 |
rs761224451 | snp | A/T | 1.66161e-05 | 0.00288232 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399902 | ATTATAACAACAAAC[A/T]TACCATTCGGGGTAC | 55779 |
rs761230374 | snp | C/T | 0.000299043 | 0.0122242 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326438 | TATGCAAGAAAGAAA[C/T]ACAAACCAGCATCTC | 55779 |
rs761243537 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309183 | AATCCTGCAAGTTAA[C/T]TTAGAAAAAATTTCC | 55779 |
rs761245186 | snp | C/T | 3.30093e-05 | 0.00406246 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363272 | ACTTCTTTCATTAAC[C/T]TGTCATGTTCTCTTT | 55779 |
rs761256061 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319992 | CCAGAAAATCTAGAG[A/G]AAATGGATAAATTCC | 55779 |
rs761258185 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308555 | TTCCTAACTCATAAG[A/G]TGCTCTAAAATCAGA | 55779 |
rs761294256 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412211 | TCAATTAGGAAAAGA[A/G]GAACTCAAATTGTCC | 55779 |
rs761313427 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309380 | CTTGGCTATAAATCT[C/G]CACTTGTCCTTGTTG | 55779 |
rs761324939 | in-del | -/GAG | 5.07988e-05 | 0.00503953 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379348 | TGAGTAAAATCCACA[-/GAG]GATGGGAGAGGGGGT | 55779 |
rs761359751 | snp | C/T | 0.000622148 | 0.0176263 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113308237 | CAAGCTAGATTCTTC[C/T]TCACTTGATTCCTCA | 55779 |
rs761359904 | snp | C/T | 0.000309231 | 0.0124306 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330639 | AAGAGAGAGAATGCA[C/T]TTGTTCATGTGCCTT | 55779 |
rs761360745 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350141 | AACAGCAGCATAAGC[A/G]GCTGGCAGAGGCAGA | 55779 |
rs761366388 | snp | A/C | 1.72466e-05 | 0.00293649 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401295 | TTGGCATCCTAAAAA[A/C]ATTAAATAGTATTTT | 55779 |
rs761381330 | snp | A/T | 1.74275e-05 | 0.00295186 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426298 | AAAATAAAATAATTT[A/T]AGAAGAGTGATATGG | 55779 |
rs761398742 | snp | A/C | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434350 | ATACATTAGGCACAT[A/C]AAAGAGGGCTGCATC | 55779 |
rs761400407 | snp | C/T | 0.000100271 | 0.00707992 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381112 | AAATTTTTAAAAGCA[C/T]AGTTTAAAGAGATTA | 55779 |
rs761425737 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337184 | GAACACATAGACACC[A/G]ATATTAAAAACACAA | 55779 |
rs761449418 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436396 | TTTAATTCTTAAAAC[C/T]ATTGAGCATATTATT | 55779 |
rs761508464 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316726 | ATATAAAAATTAGCT[A/G]GGTGTGGTGGTGGGT | 55779 |
rs761514737 | snp | C/G | 1.64917e-05 | 0.00287151 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286749 | CAAGTGAGTGGAGGA[C/G]ACTGGTGTCCCCAGC | 55779 |
rs761532720 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308643 | TTGCCCAGGCTGTAG[C/T]GCAGTGATGCAATCT | 55779 |
rs761534181 | snp | C/T | 1.89406e-05 | 0.00307733 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400652 | TCCTGGGTCTGAGAA[C/T]AGATAGACAGCTTAC | 55779 |
rs761551040 | snp | C/T | 5.16249e-05 | 0.00508033 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366331 | AACAAAAAATGTAAA[C/T]TGTTCTTCCCATTAA | 55779 |
rs761583110 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370518 | AGAAAAGGCCTTCAA[A/C]AAAATTCAACAGCCC | 55779 |
rs761606549 | snp | C/T | 0.000217794 | 0.0104331 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326613 | TCTTTTTCTCTTCCA[C/T]CTCTTTAAGAGTTTC | 55779 |
rs761608560 | snp | C/G | 1.65866e-05 | 0.00287976 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433716 | TAAAGCTGTAAAATT[C/G]AAACTAACAGATTTC | 55779 |
rs761634529 | snp | C/T | 1.66626e-05 | 0.00288635 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409332 | TCCCATCTGGAAGGA[C/T]AAATGGAAGCCTAAT | 55779 |
rs761641753 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357658 | TTTAAGCCAATCAGT[G/T]TGTAGTACTTTTTTA | 55779 |
rs761663946 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417908 | ATGGTGTAGAACATA[C/T]GGTCAAAGAAATCTG | 55779 |
rs761673690 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352719 | ACAAGAAATCTAAAC[-/AG]AGAATTCTCAGAAGA | 55779 |
rs761674016 | snp | A/G | 0.000101046 | 0.00710723 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330331 | ATTGAATCACGGGTT[A/G]TCAAATCCCCATCCT | 55779 |
rs761686533 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437891 | ACTTGGGTTCACATC[C/T]CTGCTTGCCCAAGAA | 55779 |
rs761702093 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390400 | GTATCATACTGAATG[A/G]AGAAATACAGAAAGC | 55779 |
rs761708225 | snp | A/C/T | 4.94444e-05 | 0.00497194 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366195 | ATAATTATTGTCATG[A/C/T]ATATTGAAGTGCCAG | 55779 |
rs761710369 | snp | A/T | 1.65048e-05 | 0.00287265 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396608 | TTTCAACTGAATATC[A/T]GCATCCAAAATTTTC | 55779 |
rs761758858 | snp | A/G | 1.68946e-05 | 0.00290638 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400578 | CCATGAGATAAGTGA[A/G]AGGAGAAACAGCCAC | 55779 |
rs761796971 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315510 | CACCCCTCTCTAAAC[A/T]TTTGATAGAACAACT | 55779 |
rs761800527 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331372 | GAGCCTGAGAGCACA[C/T]GCAACCCTACTGTAC | 55779 |
rs761838378 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352635 | ATAAAAGGCAAATAT[C/G]TGTAATATAGATAAA | 55779 |
rs761858657 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420137 | ACTGTCGTCCAGAAG[C/T]TGTAGGTTGGCTCGC | 55779 |
rs761871560 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388605 | AATGAGATGGCTGAA[A/T]GGATTTAAAAAACAA | 55779 |
rs761936996 | snp | C/T | 1.70151e-05 | 0.00291672 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379344 | GCTCTGAGTAAAATC[C/T]ACAGAGGATGGGAGA | 55779 |
rs761960511 | snp | A/G | 0.000326691 | 0.0127765 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287119 | CGCACAGGCTGGCGC[A/G]GGACAGACTCCTAAC | 55779 |
rs761977485 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414399 | TTCCAATACTATGTT[A/G]AATAGGAGTGGTGAG | 55779 |
rs762012724 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288760 | AGAAATTTAGCACAT[-/G]GCTCACAGACCTCCC | 55779 |
rs762016042 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407021 | TTGAGACCGGTGAAC[A/G]TAAAAGCCATTTCCC | 55779 |
rs762055916 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403321 | GGGACTTAGATGCTG[A/G]AGCAATGTTCCAGCT | 55779 |
rs762059878 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113434971 | CACTAGGGTTCATTC[A/C]ATGTTTTCCTGCAGT | 55779 |
rs762069661 | in-del | -/AAC | 0.000166398 | 0.00911982 | intron-variant, cds-indel, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286841 | GCGTGTGTCTTTTGA[-/AAC]ACCACCTCTCACAAT | 55779 |
rs762090194 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400067 | AGTCTTGGCTCACTT[C/T]TTACATGTTGAATAT | 55779 |
rs762098096 | snp | A/G | 2.27332e-05 | 0.00337136 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373586 | AGTAACATAGAAGGT[A/G]GTACTTGAATATAAC | 55779 |
rs762148298 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421398 | CTATCAGTGAGAATG[C/T]AAATCAGTTCAGCCA | 55779 |
rs762167333 | in-del | -/TA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320536 | ATGAAGTTATATATG[-/TA]TATATATATAATGAA | 55779 |
rs762186800 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360636 | TATGGAAAGAAGATG[G/T]TTCTCTTGCTGGAGA | 55779 |
rs762197226 | snp | C/T | 0.000117405 | 0.00766087 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308305 | GTTAACAAAGAAGCT[C/T]CTATATTAAACTAAA | 55779 |
rs762227261 | snp | A/T | 1.78213e-05 | 0.00298502 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396735 | AAGTTTACCTTGGAG[A/T]AAATTAAAGATAAGG | 55779 |
rs762277463 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307330 | AACTCTGAATCAACT[A/G]TCAATTGTCTGCATA | 55779 |
rs762285460 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298950 | GTACTTAGTGCCATT[A/G]AACTGTCCACTTACA | 55779 |
rs762328209 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427205 | TAGTGCTTTGCAAAT[C/G]ACCATACTGAAATGA | 55779 |
rs762331050 | snp | A/T | 1.69092e-05 | 0.00290763 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400572 | TTGTGGCCATGAGAT[A/T]AGTGAGAGGAGAAAC | 55779 |
rs762338539 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349140 | TTAAGAAAAAGCCCA[C/T]GAATTATTCAATGAT | 55779 |
rs762360235 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406936 | ACTCACCTTCCCATC[C/T]GGGAGCTCCATGTAG | 55779 |
rs762376963 | snp | C/G | 1.68789e-05 | 0.00290503 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363428 | CTGCACTGTTGATTT[C/G]TTTTGCAAAATCTCA | 55779 |
rs762401929 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373896 | AATATTAGGGTTTTG[C/T]AGTTCCTCGTTTTTA | 55779 |
rs762414664 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312257 | TTTTTTTTTTTTTTT[-/G]TATTTTTAGGAGAGA | 55779 |
rs762460445 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318448 | AAGAGAACAAATCTA[C/T]GACTCATTGGTACTC | 55779 |
rs762461356 | snp | C/T | 1.6504e-05 | 0.00287258 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379597 | AACAATTATGACTCA[C/T]TCGTTCATTTACACC | 55779 |
rs762462260 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319359 | CATCACATAATGATA[A/T]AGAGTGCAATCCAAC | 55779 |
rs762489970 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360243 | TAAAGATGATTTTGG[A/C]TCTTCACTCTTAGAC | 55779 |
rs762490493 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316607 | GCTGTAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 55779 |
rs762500349 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348991 | TGATAGAATGACAGC[C/T]GAAGAAAGGGACAAA | 55779 |
rs762510645 | snp | C/T | 4.99056e-05 | 0.00499503 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366299 | CACAAAACATCATAA[C/T]TTTGTTAATGCTACG | 55779 |
rs762546622 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294099 | CTTTTTGCAGGTAAT[A/G]TTGTTAAGTATATAA | 55779 |
rs762550192 | in-del | -/A | 3.34616e-05 | 0.00409019 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401751 | ATATCTTGTAAAATG[-/A]AAAGAAAATACTTTA | 55779 |
rs762565803 | snp | C/G | 9.70638e-05 | 0.00696581 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330244 | AGCTCCACATCCGTT[C/G]GCTCTGCTTTTTCAA | 55779 |
rs762566137 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393103 | CAGGCAGAAGCTTAA[C/T]ACGTTATGCTCAGAT | 55779 |
rs762586529 | snp | A/T | 1.64982e-05 | 0.00287208 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286738 | CTGACTCCTGCCAAG[A/T]GAGTGGAGGAGACTG | 55779 |
rs762637939 | snp | C/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294722 | TCAACCGAGAATCAA[C/G]TTTCTTCTTTTCAAT | 55779 |
rs762638045 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308397 | TAAGAGTTTAAAATG[A/G]TTAAGGACACAAAGA | 55779 |
rs762655642 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380292 | GGTCACAGACTCTTG[C/G]AACATCCTTCAACAA | 55779 |
rs762678373 | snp | A/G | 0.000213607 | 0.0103324 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327848 | AATATTTGCGGATAC[A/G]TTAGAAGACTAGATA | 55779 |
rs762690894 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296008 | ACCCATCACCAGATA[A/G]CAAACGTTGTACCTA | 55779 |
rs762747710 | snp | A/G | 1.77874e-05 | 0.00298218 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286649 | TCAATCTGGATTTTA[A/G]TGGTTCCTACTCTTT | 55779 |
rs762752016 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314649 | TCTCCTCTCTTCGAG[C/T]GTTTAAATTATGTTT | 55779 |
rs762760856 | snp | A/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396528 | CTTACCCCTGTGGCT[A/T]GAATTTCCCCATCAC | 55779 |
rs762780239 | snp | A/G | 2.75319e-05 | 0.00371015 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427390 | ATTAAACATTTTCTT[A/G]TTTCTAAAGTAGCTA | 55779 |
rs762790255 | snp | C/T | 0.00071323 | 0.0188708 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291630 | AGACTGCCTTTCCTA[C/T]GCAAAAGAGCAATCT | 55779 |
rs762820838 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400518 | AAAACAAGGCCAGAC[A/T]TATTTTTATTAAGAG | 55779 |
rs762827037 | in-del | -/AACCCCCGACTCTGG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347208 | AAAGGGCTCTCTAAC[-/AACCCCCGACTCTGG]AGTTGGGAGCGTTGG | 55779 |
rs762828211 | in-del | -/TTTTTTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423108 | ATCTGATCCTTCCTT[-/TTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs762848188 | snp | C/G | 8.56069e-05 | 0.00654187 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401775 | TACTTTAATCGATCA[C/G]TAGTTTCTGAACATT | 55779 |
rs762876203 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409177 | AACCTTAAAAACTTC[C/T]TGAGAAAAAGCTTTT | 55779 |
rs762880343 | in-del | -/CTTTTTTTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423105 | GGAATCTGATCCTTC[-/CTTTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs762912305 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344187 | TCCTAGATTTAAGAA[C/T]AGCTAGATGTGGCAA | 55779 |
rs762946186 | snp | A/G | 1.84609e-05 | 0.00303811 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373548 | TAGAAAACCAGAATC[A/G]TAGCCACCCTAGAAA | 55779 |
rs762963354 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333072 | CATTCATCAGAGAGT[A/C]AAACTCCGACCTAGA | 55779 |
rs763010065 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364051 | ACAATATAATCCCCC[A/T]CCTTGAAAGAGAAAG | 55779 |
rs763035964 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314159 | AACTTCCCTAATTTG[A/T]CAAAAGACAGGCTAA | 55779 |
rs763039505 | snp | A/G | 3.30109e-05 | 0.00406256 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373460 | TATCCGCAAGATAAC[A/G]GACATCAATAGGTTC | 55779 |
rs763047893 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343480 | TTCATCATATTTCAT[A/G]TTTCAAATTTCAAAT | 55779 |
rs763049174 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444334 | GTGAAACCCCGTCTC[C/T]ACTGAAAATACACAA | 55779 |
rs763065118 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307001 | AATTAAACTTTTAAA[A/T]TTTAATTAAAACTTT | 55779 |
rs763072792 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287905 | CCAACATTGCCAGAG[G/T]AGTTGACTCACTAGT | 55779 |
rs763076778 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292491 | TAACATTTGAATGCA[G/T]GAATACATCTGTGAA | 55779 |
rs763076780 | snp | C/T | 1.67203e-05 | 0.00289134 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399878 | TTTACCAATAGATTC[C/T]GGTAGTTCATTATAA | 55779 |
rs763078176 | in-del | -/A | 0.000105731 | 0.00727008 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287025 | TAATTCTGGAGAGAC[-/A]ATAAGGAGTCCTACC | 55779 |
rs763083543 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364620 | ATTTGATGCTGATAC[-/T]TGGGGCAATTGTCTC | 55779 |
rs763090282 | snp | A/G | 1.75136e-05 | 0.00295914 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419972 | ACAGAACAAGCAAAA[A/G]GATAGGGTTTTTTGG | 55779 |
rs763109455 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425585 | CTAATGCCTTACAAT[A/G]GACAGACACATAAGT | 55779 |
rs763116898 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113411956 | TCTGTTATTGGTGTA[-/T]AAGAATGCTTGTGAT | 55779 |
rs763134815 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298163 | CCTCTTGCATGGCAG[-/C]CTCATATACCAGAAC | 55779 |
rs763158107 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321824 | AAGAGGTGAAAGATC[G/T]CTACAAGGAGAATTA | 55779 |
rs763163778 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378309 | TCCATACAATAGTAG[C/T]CATTTACAATTGTTT | 55779 |
rs763191040 | snp | A/G | 1.66768e-05 | 0.00288758 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445290 | TTAAGAACAAACTCA[A/G]TGAGACTTGACTTCA | 55779 |
rs763191053 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446227 | GCTCTGGCTGTCCCA[A/G]ACCCCACCCAAGCAC | 55779 |
rs763211376 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322631 | ACTTATACACCATTA[C/G]TGGGAATGTAAATTA | 55779 |
rs763211898 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351867 | AGATGGTCTTACAAA[C/T]AGAACCTAATGAGTT | 55779 |
rs763233402 | snp | C/T | 1.69864e-05 | 0.00291426 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396718 | TAATTTGTGCTCCAG[C/T]GAAGTTTACCTTGGA | 55779 |
rs763242657 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299277 | AGACAGTTCTTAAAA[A/G]AAGACATACAAATGG | 55779 |
rs763287340 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385980 | GATCTATATGTTTTA[C/T]CCATTATTAGAAGTG | 55779 |
rs763288942 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311179 | TGAACATACTTGAAG[A/G]AAATGAAAAAATGCA | 55779 |
rs763321110 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405808 | TTCTATTGATCTTTA[C/T]CTTAGCTTAATTCTT | 55779 |
rs763339253 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298536 | AGATATTTGTACACT[C/T]ATGTTCATCACAGTA | 55779 |
rs763345969 | snp | A/G | 3.29484e-05 | 0.00405871 | stop-gained, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403947 | ACTTGCTTGTCCCTC[A/G]ACAGAGCTCCACTTT | 55779 |
rs763356001 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402900 | ATATCATATGACAAA[A/C]TAAAGGACACAAAAG | 55779 |
rs763432902 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438593 | CCTGAATAGATGAAA[C/G]AACAAGATTGTCAGT | 55779 |
rs763446112 | snp | A/G | 1.8731e-05 | 0.00306025 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363109 | ATCCAGAAATAGCAT[A/G]TGTTAAAATAAAAAT | 55779 |
rs763446288 | snp | A/C | 1.65419e-05 | 0.00287588 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380932 | ACTTGAAAAATGGAA[A/C]CATTTTATGCACATG | 55779 |
rs763473132 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359184 | CTCAAAGAAACTACT[A/G]TTACATAAAAATTGG | 55779 |
rs763473173 | snp | A/T | 4.97739e-05 | 0.00498844 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406903 | AACACAATTTTAATA[A/T]TGTAGAATAGTAGCT | 55779 |
rs763499350 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363246 | CTCTCTTCCGTGCCT[C/T]TATTTCTCCCACTTC | 55779 |
rs763509304 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347937 | TTTTCTCGGTCCTCA[C/T]TGTGGTCTAAGAGGA | 55779 |
rs763511555 | in-del | -/AAGA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321068 | GGCAGAGATATGATG[-/AAGA]AAGAAAACTTCAGGC | 55779 |
rs763525002 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113405910 | ATCCAAGGCTTTTTA[A/C]TTCCTCCTATATACC | 55779 |
rs763541397 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426191 | TCGAAGCAAGCTCCA[C/T]ATAATCATAGAAGAA | 55779 |
rs763552086 | snp | A/T | 4.95757e-05 | 0.00497849 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380943 | GGAAACATTTTATGC[A/T]CATGTCTTTGATTTC | 55779 |
rs763561887 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421221 | AGAAGACATGCAAGC[A/G]ACCAACAAACATGAA | 55779 |
rs763562715 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373952 | TGTAAACACTGTTAA[C/T]TTTCCAGAAAGGGCT | 55779 |
rs763573064 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349863 | GGTCTGTTACCATCC[A/G]AGGAATCCTGGGACA | 55779 |
rs763581899 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307096 | CATCTATTGAGACTG[C/T]AAGAAATTGGTCTGG | 55779 |
rs763595476 | in-del | -/TAAAAAAAAAAAAAAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328696 | GAAATTTAGAGAGCT[-/TAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55779 |
rs763606379 | snp | C/T | 5.84516e-05 | 0.00540577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400035 | AAAGAAAAAAAATTA[C/T]ATACATAATTTTTTT | 55779 |
rs763620097 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289337 | TGGGAATAATTATCC[C/T]GATTAGCTTTCCTCT | 55779 |
rs763630108 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393105 | GGCAGAAGCTTAATA[C/T]GTTATGCTCAGATAT | 55779 |
rs763633625 | snp | A/G | 1.83764e-05 | 0.00303115 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363115 | AAATAGCATATGTTA[A/G]AATAAAAATCAAGTT | 55779 |
rs763641420 | snp | A/G/T | 5.55852e-05 | 0.00527163 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420227 | AAACACTACCATCCT[A/G/T]GGGATTGGAAAAGTG | 55779 |
rs763645839 | snp | A/G | 0.00011932 | 0.00772306 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379600 | AATTATGACTCATTC[A/G]TTCATTTACACCATT | 55779 |
rs763697339 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372342 | CCCAAATGTCCATCA[A/G]TGATAGACTGGATTA | 55779 |
rs763717583 | snp | A/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294787 | TGTTCTTTTGTCTTC[A/G]TCATCAGTTCCCATC | 55779 |
rs763721635 | in-del | -/A | 0.000102928 | 0.00717311 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306318 | GGCCAGCTCAAAAAG[-/A]GCCACATCACAATCT | 55779 |
rs763722122 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380395 | TGTTCTTCCAGCCTT[C/T]ATTGCCATCGCCCTA | 55779 |
rs763736666 | snp | A/G | | | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341854 | GATGATTTCACTTAG[A/G]GTTTTAGGCCGAAAT | 55779 |
rs763768932 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296062 | CCCCACCATCCTCCC[C/T]GCTGCTGGAGTCCCC | 55779 |
rs763773147 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323142 | GGACCAAAATTCAAG[A/T]TGAGATTTCGGTAGG | 55779 |
rs763774293 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428406 | GGGTTGTGCTACAGA[C/T]GGAAAACTAGAGTTA | 55779 |
rs763784285 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366175 | GCAATACTTTTAATA[C/T]ATCCATAATTATTGT | 55779 |
rs763791557 | snp | C/T | 4.94417e-05 | 0.00497176 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409298 | TAGTTAAAGTCCACA[C/T]AAGCATATCCCTTCT | 55779 |
rs763795493 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415270 | TCTTCCTTATTAGTC[C/T]AGCTAGTGGTGTACC | 55779 |
rs763809979 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113443012 | AAATTTCAAGCACTG[C/T]GTGCAATTGTTAATC | 55779 |
rs763812427 | snp | C/T | 1.69017e-05 | 0.00290699 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400575 | TGGCCATGAGATAAG[C/T]GAGAGGAGAAACAGC | 55779 |
rs763820017 | in-del | -/TCT | 1.65869e-05 | 0.00287979 | cds-indel, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427306 | GTTTCATCTGTGTCA[-/TCT]TCTAAAAATGTGTTA | 55779 |
rs763837756 | snp | C/T | 0.000111427 | 0.00746331 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327866 | AGAAGACTAGATAAA[C/T]GCATTTTTAAACTAT | 55779 |
rs763871752 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292526 | AAGACATAATACTTG[C/T]GTGGTGCCCACTTTG | 55779 |
rs763880370 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381440 | CCAAGGAAACTCTGC[A/G]TGTGTGGATGGCGTA | 55779 |
rs763888039 | snp | C/T | 0.000156974 | 0.00885789 | intron-variant | CFAP44 | GRCh38.p7 | 3:113326679 | AATGATAAATATTTC[C/T]GATAAACCAAGTTCA | 55779 |
rs763919813 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399508 | GCGTAAGGTCCATGA[-/G]GGGCAAGTATTTTTT | 55779 |
rs763946289 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290677 | TTAAAATGTTATGCA[C/T]AATCAAAGGTGATTG | 55779 |
rs763951648 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409191 | CCTGAGAAAAAGCTT[C/T]TGTCCTTAGTATGGG | 55779 |
rs763953889 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433617 | CCCATCACTCTTTGA[C/T]GTAACTGATTTCTCC | 55779 |
rs763966222 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324230 | TCTTCCAGAAAATCA[A/C]ATGGAAAAGAAAATT | 55779 |
rs763973078 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344241 | CCTCTCACCCACTCT[A/C]AGTCACATGACCAGG | 55779 |
rs763976845 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375721 | AGCTACTCGGGAAGC[C/T]AAGGCAGGAGAATCA | 55779 |
rs764019491 | snp | A/G | 0.000308912 | 0.0124242 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333382 | GGTGCCTTCTCCATT[A/G]TCATAAAATCTGTAG | 55779 |
rs764076863 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400058 | ATTTTTTTAAGTCTT[C/G]GCTCACTTTTTACAT | 55779 |
rs764078209 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314195 | TTGAATTCCAAACAG[A/G]AGACACCCAAATAAA | 55779 |
rs764078447 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412028 | GCTTATCAGCTTAAG[C/T]TATTCATGACAAACC | 55779 |
rs764087330 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365542 | CATAAAGCCAAAAAT[C/T]TAGTTCTGCTTTTAA | 55779 |
rs764121940 | snp | C/T | 1.72841e-05 | 0.00293969 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366023 | TTATTAATTAACTGG[C/T]TAATTAATTACATAC | 55779 |
rs764131000 | snp | A/G | 1.74903e-05 | 0.00295717 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419974 | AGAACAAGCAAAAAG[A/G]TAGGGTTTTTTGGGG | 55779 |
rs764131508 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299780 | ACACCTGTAATCCTA[-/G]GGCTTTCTGAGGCTG | 55779 |
rs764143970 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437724 | GTCAGGTGGGAGAGA[C/T]TCCTGTTCTCCTGGA | 55779 |
rs764160475 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388749 | AAATAATTACACTTA[C/T]ATCAGACAAAAATAG | 55779 |
rs764171667 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352599 | ATGGCAGAGCAGGAG[A/G]AACCATTTACAATAT | 55779 |
rs764184840 | snp | C/T | 2.79959e-05 | 0.00374128 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427391 | TTAAACATTTTCTTA[C/T]TTCTAAAGTAGCTAA | 55779 |
rs764196208 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444361 | ACAAATTAGCTGGGC[A/G]TGGTGGCATGAACCT | 55779 |
rs764209469 | snp | C/T | 5.73159e-05 | 0.00535301 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373553 | AACCAGAATCATAGC[C/T]ACCCTAGAAAAGAGA | 55779 |
rs764222043 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364199 | TCTTAGTCTGTGATA[C/T]TAAGGAAGGAGAATT | 55779 |
rs764222947 | snp | C/T | 4.5041e-05 | 0.00474536 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286894 | CAGAAAGACTATATA[C/T]TGTTTTTTTTTTAAA | 55779 |
rs764223848 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333123 | CCCTGCCATACCTGT[C/T]AGGCAATACCCATCT | 55779 |
rs764235468 | snp | A/T | 0.000100043 | 0.00707189 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445291 | TAAGAACAAACTCAG[A/T]GAGACTTGACTTCAC | 55779 |
rs764253346 | snp | G/T | 1.651e-05 | 0.0028731 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373472 | AACGGACATCAATAG[G/T]TTCATCTTTTTGTTC | 55779 |
rs764255669 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311259 | GAACTGAAAAATACA[A/T]TAACCAAGTGATATG | 55779 |
rs764282561 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445945 | CAAAATTAACTTTTA[C/T]AATTTTAAAGATATC | 55779 |
rs764297844 | snp | A/C | 0.000228754 | 0.0106923 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341738 | TTTAGGTAAAAAAAA[A/C]CTCACAGTTCCTCCC | 55779 |
rs764300887 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433360 | CTTGAACCCAGAAGA[C/T]GGAGGTTATAGTAAG | 55779 |
rs764337554 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446245 | CCCACCCAAGCACAA[C/G]GACTGGGGGAACCAA | 55779 |
rs764359874 | snp | C/T | 1.6989e-05 | 0.00291449 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445388 | GACACGGAAAAAATT[C/T]AGATGGTAATTAGAA | 55779 |
rs764360194 | snp | A/C | 1.66502e-05 | 0.00288527 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416574 | TTCATAGATGATAAT[A/C]TCTGGAAAACTCCCT | 55779 |
rs764384733 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373114 | CCAGAATAACTGTAA[C/T]CCTGAACCTTCATTT | 55779 |
rs764471939 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426193 | GAAGCAAGCTCCATA[C/T]AATCATAGAAGAAGC | 55779 |
rs764478319 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358259 | GTAGATATATTTATA[C/T]ATCTGTAAAAAATTT | 55779 |
rs764478381 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113374247 | AGAACAAATTTTGTA[A/C]ATGTGTTTGAAGGCA | 55779 |
rs764516737 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440231 | ACCTCGCCCGGCTAA[G/T]TTTTGTATTTTTAGT | 55779 |
rs764539290 | in-del | -/ATAA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303460 | GAACCACAAAATGAT[-/ATAA]ATATCATTTTGCACA | 55779 |
rs764565262 | snp | C/T | 5.14955e-05 | 0.00507396 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373366 | ACAAAAGCATAGACA[C/T]TAACAGGATATGGTT | 55779 |
rs764586551 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390912 | TTGTTAAAATGTCCA[C/T]AGTATCTAAAGCAAT | 55779 |
rs764603637 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328576 | TTTAATTAGTTTGTA[C/T]ATGATAGGTGGCCTC | 55779 |
rs764605240 | snp | A/G | 9.43619e-05 | 0.00686819 | stop-gained, nc-transcript-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296766 | TTGCTAGCTCCTTTC[A/G]AAGTTTTCTGATCTT | 55779 |
rs764605360 | snp | C/G | 1.64904e-05 | 0.00287139 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363254 | CGTGCCTTTATTTCT[C/G]CCACTTCTTTCATTA | 55779 |
rs764618070 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332342 | TATGAAAATGGATTT[A/G]TGAATATGAATTGCC | 55779 |
rs764619687 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298780 | ATTATGAAGTACTTC[C/G]AGTAGTCAAGTTCAC | 55779 |
rs764624661 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317314 | GACAGAGAGCGGCCA[C/T]AGACACTCATCCCCC | 55779 |
rs764639505 | snp | C/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328314 | AATCTCTTTCTAAGA[C/G/T]TGAAGAAATTAAGGT | 55779 |
rs764656749 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329806 | TCTCTGGAAAATTCT[C/T]AGCTATGTTCCATCC | 55779 |
rs764678885 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305656 | ACATCAAAAATATTT[A/C]TGAACATGAATGAAG | 55779 |
rs764698483 | in-del | -/ATAAGTTGGGTGGGTGGGTTC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301439 | GTAATAATATTGTTA[-/ATAAGTTGGGTGGGTGGGTTC]ATTCTGTTGTAATAC | 55779 |
rs764708636 | snp | A/G | 1.79175e-05 | 0.00299306 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286624 | GTGTCACTGGGTGTT[A/G]GCTCCTCGGTCAATC | 55779 |
rs764713204 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316103 | ACAGAATATGTTCTC[C/T]GACCACAATGAAATC | 55779 |
rs764737293 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309443 | CTACAAAACCCCATT[A/G]TAGTAGCCCCCCTGA | 55779 |
rs764753484 | snp | C/T | 1.67829e-05 | 0.00289675 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409063 | CTCTTAGAAAAATAC[C/T]CCTGTGATATCTACT | 55779 |
rs764755064 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392035 | ATCCAGCAATCCCAC[G/T]GCTAGGTATATACCC | 55779 |
rs764764165 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304311 | AGAAAGCCACATCAC[A/G]TCTCTGTGGGGATAG | 55779 |
rs764778092 | in-del | -/T | 1.97795e-05 | 0.00314473 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401337 | TAAACTTTCATCAGA[-/T]TTTTTTAAATGTTCT | 55779 |
rs764811390 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359149 | AATATTTGGAGAGTA[C/T]ACAGTTTTAAAGACG | 55779 |
rs764818073 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305380 | ATGACTCCAGAGTTA[C/T]AAAGTTTTGTGAATA | 55779 |
rs764849894 | in-del | -/AC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357395 | AAAGGGAAAATTTGG[-/AC]ACAGAGATGGACATA | 55779 |
rs764905222 | snp | C/T | 2.16172e-05 | 0.00328757 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427370 | TTAATAACTTCTAAA[C/T]TTTGATTAAACATTT | 55779 |
rs764916991 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427242 | ACTTCCTTCCAAACG[C/T]TCCTCATCTGAGTCT | 55779 |
rs764950219 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293750 | ACATCTAATCTTCAA[C/T]TATAAGCCTTCCCAA | 55779 |
rs764958494 | snp | C/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409151 | TGCTCTTCCTTATCA[C/G]GATTGAAAGTAACCT | 55779 |
rs764973543 | in-del | -/TCTTCCTCCTCCTCCTCCTCTTTCTCC | 1.65833e-05 | 0.00287948 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379396 | TCAGGTAATGGCTCT[-/TCTTCCTCCTCCTCCTCCTCTTTCTCC]TCTTCCTCCTCCTCC | 55779 |
rs764979221 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378776 | TCCCTTCTTCCTTAT[A/G]AGCCAAGTTCTGATT | 55779 |
rs764995192 | snp | A/C | | | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294678 | AGGGTCTGAAGGTAA[A/C]GAACATACCTGCTGA | 55779 |
rs765000269 | snp | G/T | 0.000101302 | 0.00711622 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326558 | GCTTGAAAACCAGCA[G/T]AGAGTGCCTTTTCTT | 55779 |
rs765044207 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312616 | CTTCACACAGCCCCT[C/T]CCATCACAGGCCTGG | 55779 |
rs765074849 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292327 | TTAAATCTAAAACAA[A/T]GGCAATTTAATATAG | 55779 |
rs765093424 | snp | A/G | 1.65444e-05 | 0.00287609 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401637 | TTATCATAGAGAAGA[A/G]ATTCACATTCTTGTC | 55779 |
rs765106804 | snp | A/C/G | 0.00010078 | 0.00709795 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363498 | GCTTTGGGATCTTCA[A/C/G]TGTCTTCTGGAATTG | 55779 |
rs765107096 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353959 | GCTTGTGTTCCCATA[A/T]ACCTGATAATACATG | 55779 |
rs765107594 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324173 | TCACTGGTGAATTCT[A/G]CTAAGTGTTTAAAGA | 55779 |
rs765137664 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415242 | ATTGCATCTATTTGA[G/T]TCTTCTCTTCCTTCT | 55779 |
rs765167986 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323114 | ATCCCTCCCATACAT[A/G]TGGGGATTATGGGGA | 55779 |
rs765175518 | snp | A/C | 1.86579e-05 | 0.00305428 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401325 | TGTTTTATCATTTTA[A/C]ACTTTCATCAGATTT | 55779 |
rs765207893 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409359 | TAATAAATAAGGACA[A/C]ATTTATTTCATTTTC | 55779 |
rs765218045 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422963 | CCCTCTAAATTACAA[C/T]TTACTGAGGGCAAAG | 55779 |
rs765222593 | snp | A/G | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395767 | GAGACATGGGAGACC[A/G]CATTAACTGACACAC | 55779 |
rs765225249 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323988 | GGTGGAGGTTGCAGT[A/G]AGCACAGATCGCGCC | 55779 |
rs765228934 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313518 | TGGTTTTGAAATGTA[A/G]GGACATGAGATTTGG | 55779 |
rs765243189 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351595 | AAGGAGGACTCTGAA[C/T]CTTCTTAGGGGAAGA | 55779 |
rs765261899 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113447003 | GCTATTCTCGTGATA[A/G]TAAATAAGTCTCATG | 55779 |
rs765278537 | snp | A/G | 1.67469e-05 | 0.00289364 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445271 | AAAGGGAAGTAATAA[A/G]TTATTAAGAACAAAC | 55779 |
rs765295115 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331021 | CTCTCTCCAGGGAGG[A/C]AGGGAAAGGCAATTA | 55779 |
rs765297151 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444018 | GTTGAGCAAGTTATT[A/G]GCAGCTTTCTGGGGC | 55779 |
rs765304418 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380711 | TAAAATTTCCTTCTT[C/T]GCATTTTGATTTCAG | 55779 |
rs765315177 | in-del | -/C | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431775 | ATGTGTATTGATTTT[-/C]CCAGGACCTGATCTT | 55779 |
rs765320838 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409149 | GCTGCTCTTCCTTAT[C/T]AGGATTGAAAGTAAC | 55779 |
rs765329459 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386445 | TCTGTCTTTTGTCTA[C/T]TGCTGTCTTCTTTTG | 55779 |
rs765338230 | snp | C/T | 0.000100801 | 0.00709863 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330399 | TCCAGACCCTGTCTG[C/T]TCCACTCCGGGGGAC | 55779 |
rs765344439 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292208 | TAGGATTTCCTGCTT[A/T]CTGTTTTATCGAAAC | 55779 |
rs765350972 | snp | C/G | 9.60107e-05 | 0.00692793 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113303956 | CTTTTCTCGGATGAG[C/G]TGTTTACGTCTCTCT | 55779 |
rs765356980 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410169 | TTTTTTTTTATTATA[C/T]TTTAAGTTCTAGGGT | 55779 |
rs765363799 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424881 | CCCATCCTGGAGCAG[C/T]GAGAAGGCAGTGCAC | 55779 |
rs765366411 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340819 | CCGGGGTTTCTTGCC[C/T]TGGTGTACTGGAAGA | 55779 |
rs765396243 | snp | A/G | 3.30098e-05 | 0.00406249 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373455 | CTCTGTATCCGCAAG[A/G]TAACGGACATCAATA | 55779 |
rs765406691 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319503 | TGAGACCTCAACATC[C/T]CACTGACAGCATTAG | 55779 |
rs765441488 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113362031 | AAGGATAACTGCCAC[A/C]AGAGCTGCTGCAAGA | 55779 |
rs765445737 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396313 | GAATATTTTTAAGTG[C/T]TATTCACATGCTCCA | 55779 |
rs765484643 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337766 | ACAAACAAATCTCAA[C/T]CTAAGTCTGATAACT | 55779 |
rs765506198 | snp | A/C | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433652 | CAGTATCCTGATCAT[A/C]TGGTTCCTTCATTTC | 55779 |
rs765511007 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439046 | TCCTTTAAGGCAGTC[A/G]AAGTTTGGGTTCTAG | 55779 |
rs765511584 | snp | C/G | 0.000576431 | 0.0169671 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403937 | TTGTGACATGACTTG[C/G]TTGTCCCTCGACAGA | 55779 |
rs765528448 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383336 | ATTTTTCCTGCTGCA[C/T]CGATGGTGGTCTTGT | 55779 |
rs765576084 | snp | A/G | 1.91137e-05 | 0.00309136 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363102 | CATCTCTATCCAGAA[A/G]TAGCATATGTTAAAA | 55779 |
rs765583252 | in-del | -/TATA | 1.77669e-05 | 0.00298046 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286888 | ATATCCCAGAAAGAC[-/TATA]TATTGTTTTTTTTTT | 55779 |
rs765608721 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113363822 | CCTCAAAATGTAAAT[C/T]ACTAATGTTCATATG | 55779 |
rs765608778 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350858 | TGAAGTGTGGGGCTG[A/G]TTCTGTTGGAAAAAG | 55779 |
rs765620452 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436842 | CTGTTTAGTTTTCCA[G/T]TGCTGCCATATAAAT | 55779 |
rs765654293 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339066 | GCTATACAAAGCCTG[A/C]ACATATGGGGCTTCA | 55779 |
rs765661948 | snp | A/G/T | 3.37611e-05 | 0.00410848 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403821 | AAGTCTTAAACGTGG[A/G/T]TGCTACCATCCAAGT | 55779 |
rs765663958 | snp | C/T | 0.000131791 | 0.00811655 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426177 | AGTCACAAAAGGCAT[C/T]GAAGCAAGCTCCATA | 55779 |
rs765669930 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376810 | AGAGAGGTTCAGGAA[A/G]TAAAATTAAGATTAG | 55779 |
rs765691560 | snp | C/T | 0.000102833 | 0.00716979 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344696 | CAATAGTATCACTTT[C/T]CAGTGGATCTCGAAA | 55779 |
rs765703270 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310889 | CCTGTTTTGGCTTCT[A/G]ATGTGAGTTAAAGCT | 55779 |
rs765705469 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327246 | GCTTCTTTTTCAGTT[A/G]TTTTCATAAGGATAA | 55779 |
rs765726272 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419477 | CTTATAACAAACTCT[C/G]CGAGGACATGGACTT | 55779 |
rs765744197 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418335 | CAAGTGATCCACCCA[A/C]CTCAGCCTCCCAAAG | 55779 |
rs765758271 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378571 | TTAGTAATGATCTTC[C/T]ACACACACTTTTATG | 55779 |
rs765761736 | snp | A/G | 1.75844e-05 | 0.00296511 | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379563 | ATCTCTTTTAAAATA[A/G]ACATTAAGTAGGTAT | 55779 |
rs765803740 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295151 | TTAAGCAGCTAACTT[C/T]TCTGTATTGCTTTTT | 55779 |
rs765818370 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391478 | ACAGGCAACCAAAGC[A/G]AAAATGGACAAATGG | 55779 |
rs765821300 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287318 | CATTTTCCTAAGATG[C/G]CCATGAGAACAGACC | 55779 |
rs765841288 | snp | A/G | 1.65165e-05 | 0.00287367 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407066 | AGAAAGAGACTGAAT[A/G]TACCTCAAAGATATT | 55779 |
rs765864129 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325726 | ATTATTCTAAAATAC[A/G]GAAATATCAAGGAAC | 55779 |
rs765865194 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287247 | GAACAGCAAGGGGCA[C/T]GGTATCACAGCCTGG | 55779 |
rs765877553 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329791 | AGAGGGTGCCCTGTT[G/T]CTCTGGAAAATTCTT | 55779 |
rs765911174 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308852 | CTCAAGGGATCTGCA[A/C]AACTGGGCCCCACAA | 55779 |
rs765927243 | in-del | -/G | 1.69115e-05 | 0.00290782 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403819 | ACAAGTCTTAAACGT[-/G]GGTGCTACCATCCAA | 55779 |
rs765927313 | snp | C/T | 1.81464e-05 | 0.00301212 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363574 | CCCTTTAAAATTGCA[C/T]AGCATTTTCCTTAAA | 55779 |
rs765948284 | snp | A/C | 1.85016e-05 | 0.00304145 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426328 | GTTTGGCTGTGTCCC[A/C]ACCCAAATCTCAACT | 55779 |
rs766001247 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438083 | AGGGTCTCACTCCCC[A/G]GATAATTCTTTCACA | 55779 |
rs766035563 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403613 | GAAGCTATTATTTCA[A/G]CAGAATCAGAATAAC | 55779 |
rs766065322 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355477 | GTGAGCCGTGATCAC[A/G]CCACTACACTCCAGC | 55779 |
rs766068279 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113304085 | AGTACCAGAAAGATC[A/G]CTAGGTATTTCTCCA | 55779 |
rs766076849 | snp | A/C/G | 4.94192e-05 | 0.00497067 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406963 | GTAGCCTTCTATATC[A/C/G]GTAGTGATTGTTTTG | 55779 |
rs766077211 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357814 | TAAACATGCATATAA[C/T]CTATGGCCCAGCAGT | 55779 |
rs766077594 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346016 | ATGAGACCCAGATTA[A/G]CATTGAGAAGTGAAC | 55779 |
rs766078197 | snp | C/T | 1.80377e-05 | 0.00300308 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401314 | AAATAGTATTTTGTT[C/T]TATCATTTTAAACTT | 55779 |
rs766093427 | snp | G/T | 1.68556e-05 | 0.00290302 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286876 | AGGCAGAAGCTGATA[G/T]CCCAGAAAGACTATA | 55779 |
rs766113265 | snp | C/G | 3.29641e-05 | 0.00405968 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427236 | ACTCAAACTTCCTTC[C/G]AAACGTTCCTCATCT | 55779 |
rs766125693 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390565 | AAATTATCCTTGTTT[G/T]CAGATTATATGATCT | 55779 |
rs766139283 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333261 | AAAAGAGGACATTCT[A/G]GATAATCATGGAAGT | 55779 |
rs766158972 | in-del | -/T | 8.62523e-05 | 0.00656648 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419990 | TAGGGTTTTTTGGGG[-/T]TTTTTTCTAATTTAT | 55779 |
rs766163287 | snp | A/G | 0.000100976 | 0.00710478 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363456 | TCAGGCCTAGTCAGT[A/G]TTTATCAAAAATTCC | 55779 |
rs766190003 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378667 | CAGTAGATCAATAGA[A/C]TATTTCAAGCAAATA | 55779 |
rs766191824 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364497 | GCTAATAAATTGTAC[C/T]GACTATTAATCACTT | 55779 |
rs766192571 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413088 | GCATGAGATGGTATC[A/T]CATTGTAGTTTTGAT | 55779 |
rs766206636 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293645 | GATTTGGGTTAGGTA[C/T]TAACCTTCTCAAACA | 55779 |
rs766239212 | snp | A/T | 1.66957e-05 | 0.00288922 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416675 | AAGAAAGATTTTTGT[A/T]TAAATAGTCTGATTA | 55779 |
rs766263985 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427786 | AGGACAAGCTGGGAA[C/T]GAGAACTGGTATAGG | 55779 |
rs766274876 | snp | A/G | 1.65523e-05 | 0.00287678 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113381008 | TTTATGGTTGGAAGT[A/G]GAGCTTCAAGAATAT | 55779 |
rs766295652 | snp | C/T | 1.66239e-05 | 0.00288299 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416561 | TCAGAGAAGGATATT[C/T]ATAGATGATAATATC | 55779 |
rs766303970 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334809 | TGGAAGCACTCAGGT[A/G]TCTAAAGGTATGGGC | 55779 |
rs766318781 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311439 | CTCTAATGGTTTTAT[C/T]AGGGGTTTCTGCTTT | 55779 |
rs766324910 | snp | C/T | 0.000120228 | 0.0077524 | splice-acceptor-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330669 | TTTATTTCCATGGAC[C/T]TGAAAAAAAGAAGAG | 55779 |
rs766329845 | snp | C/T | 0.000169253 | 0.00919772 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395712 | TTCACTATGTAGTAA[C/T]TGAGATTCAAACAGG | 55779 |
rs766344290 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292647 | GAGACTCAGGGAGTC[A/G]TTAACTAGCCAAGTC | 55779 |
rs766350766 | snp | A/T | 2.54676e-05 | 0.00356836 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400688 | CTCAAAGACAGAGTA[A/T]CAAAGAATTAAGATC | 55779 |
rs766395566 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414421 | AGTGGTGAGAGAGGG[A/C]ATCCTTGTCTTGTAC | 55779 |
rs766434831 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421857 | GAGGGAGGGAGGGGG[A/C]ACGGCTGAAAAACTT | 55779 |
rs766439948 | snp | A/G | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330910 | CTCTTGGCTTCCCAC[A/G]ATTTGTTCCCTCCAG | 55779 |
rs766443560 | snp | A/T | 3.3048e-05 | 0.00406484 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396532 | CCCCTGTGGCTAGAA[A/T]TTCCCCATCACGTTC | 55779 |
rs766478097 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397789 | AAACACTGGAAGGGA[A/G]CCAGGTGTGTGTGTG | 55779 |
rs766498797 | snp | A/C | 0.000181532 | 0.00952538 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396611 | CAACTGAATATCAGC[A/C]TCCAAAATTTTCTTC | 55779 |
rs766506851 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387263 | CAGGCAGCACAGCTC[A/G]CAGCTCTGGGAGATA | 55779 |
rs766538592 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441760 | GATACCTGCCTGATA[C/T]TCCAAAATGGCCCAA | 55779 |
rs766560220 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407328 | AGCTATGTGTGACTA[G/T]TTAAATTTAGATTTA | 55779 |
rs766594763 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419601 | TCCATAGTCAATCTA[C/T]GTCTACATCCTATGT | 55779 |
rs766596716 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375655 | AAACAAAATAAAAAT[A/G]AAGAAACTAACACCT | 55779 |
rs766615225 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323283 | AATACTACACAGCCA[-/T]AAAAAAAGAATGAAA | 55779 |
rs766623605 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291301 | GAAACACAGCCTTCC[A/G]AGACTTCATATTCAA | 55779 |
rs766647486 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324088 | CATTTGAACAACCCT[A/G]TAACTATTAAGAAAG | 55779 |
rs766657326 | in-del | -/AC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396152 | GTGCATAAAGAATTT[-/AC]ACAGTTATTCTCTTC | 55779 |
rs766666769 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410061 | TAATCAAGAATAACT[A/G]TGAGTATTCTCAGCC | 55779 |
rs766666826 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394784 | TATGAATTTGTGTTG[C/T]GCCTCATTCAAAGCC | 55779 |
rs766731724 | snp | A/G | 9.94481e-05 | 0.00705083 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291692 | GAGTTGGATCAATTC[A/G]GTGACCTCCTCTCTT | 55779 |
rs766754182 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376417 | TAAGTGATATTTAAA[A/G]CCATGAGACTGTGTA | 55779 |
rs766757460 | snp | G/T | 1.65976e-05 | 0.00288072 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379374 | AGGGGGTTGACGGAA[G/T]AAATATTTCAGGTAA | 55779 |
rs766775955 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350546 | TTGATAATTGACAGT[C/G]TTCTCCATGACCTTA | 55779 |
rs766786248 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381824 | ATAATAAGAAAAACA[C/T]ATAATATCTGCCATT | 55779 |
rs766802496 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320090 | TTCTGAAATTGAATC[A/C]GTCATAAAAAATAGA | 55779 |
rs766804155 | snp | A/G | 2.21521e-05 | 0.00332799 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379279 | TTGAAATATGATTGA[A/G]GTAAAAATTATTACA | 55779 |
rs766813369 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340690 | TTTGCAGCTGAAGCC[C/T]CAATGGGCGTGTCTT | 55779 |
rs766825874 | snp | A/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399907 | AACAACAAACTTACC[A/G]TTCGGGGTACCCAAA | 55779 |
rs766831859 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383253 | ATGACAGAAATTCAT[G/T]TCTCAGAGTTCTAGG | 55779 |
rs766837007 | snp | A/G | 0.000617983 | 0.0175673 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341839 | AATTTGATTTTCCAC[A/G]ATGATTTCACTTAGG | 55779 |
rs766890047 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308557 | CCTAACTCATAAGAT[A/G]CTCTAAAATCAGACA | 55779 |
rs766892154 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113292975 | GACTTTGAAGGAAAC[-/T]TTAGGAAAATCACAG | 55779 |
rs766937740 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414604 | AAGGCCTTTTCTGCA[-/T]CTATTGAGATAATCA | 55779 |
rs766980753 | snp | C/T | 1.68567e-05 | 0.00290312 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363446 | TTGCAAAATCTCAGG[C/T]CTAGTCAGTATTTAT | 55779 |
rs766985372 | snp | C/G/T | 3.59999e-05 | 0.00424251 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426313 | AAGAAGAGTGATATG[C/G/T]TTTGGCTGTGTCCCC | 55779 |
rs766987840 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430911 | ATGCCTTAGTAACTA[A/G]CAGTCCTTCACCATC | 55779 |
rs766994997 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296128 | CCCATTGTTTAGCTC[C/T]CACTTATAAGTGAGA | 55779 |
rs767004319 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417146 | GAGATGAACTGTCTA[C/T]CCTACATATAAATCA | 55779 |
rs767008309 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432089 | TCTCTAAATGGTAGA[C/T]CCAGGACTCAAAACC | 55779 |
rs767041703 | snp | A/T | 1.65203e-05 | 0.002874 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363278 | TTCATTAACTTGTCA[A/T]GTTCTCTTTTTCTCC | 55779 |
rs767057845 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386115 | TTCATAATTGTTATA[A/T]CTTTCTGGTGGACTT | 55779 |
rs767146489 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403434 | CCATAGGCAAACTCC[A/C]TCAGTTCACCTCTGG | 55779 |
rs767154029 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376530 | CAGCAAAAGAGGCTG[-/A]AATGGAATGGTCAGA | 55779 |
rs767176746 | snp | C/T | 1.66771e-05 | 0.00288761 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286848 | TCTTTTGAAACACCA[C/T]CTCTCACAATTTAGG | 55779 |
rs767178044 | in-del | -/GAA | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426525 | TTCCTGCCATTATGT[-/GAA]GAAGGACATGTTTGC | 55779 |
rs767188778 | in-del | -/AAAAAAA | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430423 | AAGAAGCTGGAAAAA[-/AAAAAAA]TAAATGAAAAAAAAA | 55779 |
rs767211122 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327612 | TTCTTCTGCCCACTC[A/T]TACTTGCATGTACTG | 55779 |
rs767213269 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314371 | CCGAAAGGAAATGAC[A/C]CAATGATTTTTCAAG | 55779 |
rs767216492 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426199 | AGCTCCATATAATCA[C/T]AGAAGAAGCTCTCTG | 55779 |
rs767254443 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401925 | TTACTCTGAACTGAG[G/T]TATGATAAGCTATTA | 55779 |
rs767261115 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437975 | TATTTGGTAGAGTTG[C/T]TGTAAATATTAAATG | 55779 |
rs767263825 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294465 | TTGATTAGTACTTAC[A/G]TGAGTTCATGGCACC | 55779 |
rs767283369 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315545 | AGAAAAGCAGCAAGA[A/G]TGTAAGAGACCTCAA | 55779 |
rs767283578 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286755 | AGTGGAGGAGACTGG[C/T]GTCCCCAGCACCCCG | 55779 |
rs767308005 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388825 | TCAGTAAAAGGATAT[A/G]ACAATTGTAAATATA | 55779 |
rs767309756 | in-del | -/TT | 0.000309518 | 0.0124364 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291580 | TGCGGGCTGTATCTC[-/TT]TTTCTCTCGTGGAGA | 55779 |
rs767325308 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370571 | AACTAGGTATTGAAG[C/G]AATGTACCTCAAAAT | 55779 |
rs767326612 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390463 | GCCCACTGTTACTGC[C/T]GTTATTCAACATAGT | 55779 |
rs767329242 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355201 | CCAAACACTACCTGT[A/T]CCCCCAAAAACCTAT | 55779 |
rs767340224 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344457 | GGTTCTGTCCACAGA[C/T]AATTCACTTTTGAAG | 55779 |
rs767342913 | in-del | -/AAG | 1.73561e-05 | 0.00294581 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426298 | AAAATAAAATAATTT[-/AAG]AAGAGTGATATGGTT | 55779 |
rs767388079 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307369 | CACTCATAAATGGCT[G/T]CCTAAGAGAACAGAT | 55779 |
rs767388785 | snp | A/G | 9.97656e-05 | 0.00706207 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416543 | GAAGGACTCTGTATG[A/G]TCTCAGAGAAGGATA | 55779 |
rs767388844 | snp | A/T | 1.69006e-05 | 0.00290689 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400579 | CATGAGATAAGTGAG[A/T]GGAGAAACAGCCACG | 55779 |
rs767395496 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288199 | ACATGAAGAATTTGA[C/T]AAACAGGGTCCTAGG | 55779 |
rs767399956 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444565 | GGCTGGGAAAATTAA[C/T]AGCAACTTTTTCTAT | 55779 |
rs767415145 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356859 | AACTCTATTAAGAGA[C/T]TAAAGCCACATACTA | 55779 |
rs767419732 | snp | C/T | 1.65067e-05 | 0.00287282 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433644 | CTCCCCATCAGTATC[C/T]TGATCATCTGGTTCC | 55779 |
rs767486026 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377453 | GTTTCACTTCTCATT[A/G]GTTATATGGCCTCAG | 55779 |
rs767488737 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302950 | CAAGTTACAGAAAAT[A/T]AAATAAATAAATGGC | 55779 |
rs767504184 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353895 | CTGGGAAAAGAAACA[C/T]CTGAAAGGAACAGAC | 55779 |
rs767534799 | in-del | -/ATT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299031 | AAAATAAACTTAGAA[-/ATT]ATTAACCCTAAAATA | 55779 |
rs767556156 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424793 | TAGAGATAATTCATA[C/T]ATTGGAATAAAAGTT | 55779 |
rs767592130 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342796 | CAGGAGTTCAAGACC[A/G]GCCTGGGCATGGTGA | 55779 |
rs767597967 | snp | A/G | 1.75013e-05 | 0.0029581 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446622 | AGGTGTGAATCTCCC[A/G]CTTCCTGAGGTGGCA | 55779 |
rs767628609 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435011 | ATGATGCCTTCTTTT[G/T]ATATGGGGGATAACA | 55779 |
rs767639004 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289504 | GGCCCAGGAAGATAA[C/T]GTAACTTCTCCTGAT | 55779 |
rs767648143 | snp | G/T | 0.000102928 | 0.00717311 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344612 | TAGCTCGTTTGAATT[G/T]GGAGTACTTAGAGGG | 55779 |
rs767717460 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419944 | GGCATCTAACAACCA[C/T]GTTGGCTGGTCCACA | 55779 |
rs767723795 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386172 | CTTTGTATCTTATGA[C/T]AGTTTTTTATGTAAA | 55779 |
rs767741701 | snp | A/G | 1.67279e-05 | 0.002892 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401558 | CATGTAATGTTAAAG[A/G]GCCAAGAGACAAGAA | 55779 |
rs767757782 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359380 | TCTCATGTTTCTTAC[A/C]CTCATCCCTGGAAAA | 55779 |
rs767772174 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419278 | TTGCCACATTATCAT[C/G]TACTTGTGTGTCTAG | 55779 |
rs767809011 | in-del | -/TT | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286897 | AAAGACTATATATTG[-/TT]TTTTTTTTAAAAAAA | 55779 |
rs767825520 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407254 | CAGGCGAAAAATAAA[A/G]TTTCCTGCTTTCATG | 55779 |
rs767886067 | snp | A/T | 0.000103056 | 0.00717755 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341810 | GCTTTTAATATAAGT[A/T]TTCTCGTTTTCTCAA | 55779 |
rs767906644 | snp | A/G | 1.7117e-05 | 0.00292544 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445397 | AAAATTTAGATGGTA[A/G]TTAGAAACATGAGAC | 55779 |
rs767908627 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375466 | AAAGGATGGAAAATC[C/T]TCTTGAATGATGTAA | 55779 |
rs767920992 | snp | C/T | 3.33517e-05 | 0.00408347 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399891 | TCTGGTAGTTCATTA[C/T]AACAACAAACTTACC | 55779 |
rs767927343 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360464 | TGAAGAAATTCTGAC[A/G]TTTATTAAGTCTTGC | 55779 |
rs767972682 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394390 | GGAAGTGAATGAAGG[A/G]TGCACATAATATTAT | 55779 |
rs767983815 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329891 | ATGACTTCAGTTAGA[C/T]GCCAAGTAACTGAAA | 55779 |
rs767987614 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408663 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 55779 |
rs767990330 | snp | C/T | 1.65762e-05 | 0.00287886 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373496 | TTTGTTCTTTGAAAT[C/T]ACTGCTTTCATCACA | 55779 |
rs768034781 | snp | A/G | 0.000103804 | 0.00720357 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305145 | AGATTAGTTGCCACA[A/G]TTTTCACCTGTAGAA | 55779 |
rs768038182 | snp | C/G | 1.85321e-05 | 0.00304396 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400647 | CTGGGTCCTGGGTCT[C/G]AGAATAGATAGACAG | 55779 |
rs768038941 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318718 | AACCCATCAGGCTAG[C/G]AGCAGACCTCTGAGC | 55779 |
rs768045345 | snp | A/G | 5.06881e-05 | 0.00503403 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373597 | AGGTGGTACTTGAAT[A/G]TAACACACATAAATG | 55779 |
rs768058161 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300553 | AATTATCTTTAAAAA[C/G]CCTCCATAAACGTGA | 55779 |
rs768074517 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295187 | TCTTTTCCCAGTCTT[G/T]GCCCAGGATCCTTAA | 55779 |
rs768082475 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407041 | AGCCATTTCCCAGAA[C/T]CTACAAACAAGAAAG | 55779 |
rs768107892 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375916 | GGAAGAAAACTGTGG[-/A]AAAAAATTACCTAAT | 55779 |
rs768145734 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408329 | GCATGGAGTTTGGAG[C/T]AAGACCTAAGATCAA | 55779 |
rs768155988 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291139 | CACTTAATAACATCT[A/G]AGTTTATTTTCTAAG | 55779 |
rs768175154 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319874 | AGTACAATTAGAAAT[G/T]ACAAAGATGGCATTA | 55779 |
rs768216131 | snp | A/G | 1.65302e-05 | 0.00287486 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373434 | GATAGTTTGGATGGG[A/G]TTGTCCTCTGTATCC | 55779 |
rs768224179 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309038 | TCTGTACCAGAACTT[C/G]CTAGTGGTATCATGT | 55779 |
rs768257326 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350115 | CCATGAAAAGGGGAA[C/G]GAGAGGGGAGAACAG | 55779 |
rs768270796 | snp | A/G | 0.000108737 | 0.0073727 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333598 | TCTATTAGAAAAACA[A/G]ACAACCCCCCCACAC | 55779 |
rs768276203 | snp | A/C | 6.73318e-05 | 0.00580184 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416649 | AAGATAAAATTTCAC[A/C]AAAATATTAAAAGAA | 55779 |
rs768301107 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340254 | TCACCTTCGGAGGCT[A/G]AGCCTAATGCTCATT | 55779 |
rs768324085 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337099 | TTACAACTGAGACAG[G/T]TCAGAAAGGTCACAG | 55779 |
rs768336074 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308440 | ATGCCTGCAGAGGGT[C/T]GTGCAGTTACTATCA | 55779 |
rs768341516 | snp | A/G | 1.66136e-05 | 0.00288211 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286830 | GGGCCACTGGTGCGT[A/G]TGTCTTTTGAAACAC | 55779 |
rs768342955 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383724 | ACAAAGGGTGAACTC[-/A]AGAGTAAAGGCTAGT | 55779 |
rs768346780 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415421 | TTTTGGATTCATTTG[C/T]TCTTGCCTCTCTAGT | 55779 |
rs768370329 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424475 | AAGCAAAAACTGAAG[G/T]AGAATCAATATAATA | 55779 |
rs768378245 | snp | C/T | 3.3134e-05 | 0.00407012 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433714 | GATAAAGCTGTAAAA[C/T]TGAAACTAACAGATT | 55779 |
rs768381106 | snp | C/T | 0.000197492 | 0.00993514 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330271 | TCAAATTCCAAACAC[C/T]TTGGTATATCTAGGC | 55779 |
rs768383943 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296599 | CCTAAGATCCTGGGG[C/T]AGCCAAAGGGGGCTC | 55779 |
rs768419832 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412818 | TGCTATTGTAAATAG[-/T]TGTTGTAATAAACAT | 55779 |
rs768425056 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404020 | CCCTGAGAGCACCTG[A/G]CAGGTATGTGGAAAA | 55779 |
rs768426729 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426141 | AAGTGTGAGAAGATC[C/T]AGTGGTATGTTTGAA | 55779 |
rs768428865 | snp | C/G | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396599 | GAAAACCTGTTTCAA[C/G]TGAATATCAGCATCC | 55779 |
rs768429457 | snp | A/G | 5.00037e-05 | 0.00499994 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416528 | TTCTGGACTCACCTC[A/G]AAGGACTCTGTATGG | 55779 |
rs768454856 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431561 | AAGTTTCTGAAGTAA[C/G]CGATATAATGATACT | 55779 |
rs768460266 | snp | A/G | 8.25798e-05 | 0.00642519 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395811 | TTAATATAACCAATC[A/G]GCTTATAATCCCTTT | 55779 |
rs768476248 | in-del | -/ACTGAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357162 | GCCAATTTAAACCAT[-/ACTGAG]ATGCTACTACAGAAT | 55779 |
rs768482323 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331126 | CAGGTTAGCCTATTT[C/T]CATTCTGTATTTTGG | 55779 |
rs768505392 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370444 | CACAAATCAATAAAC[A/G]TAATCCATCACATAA | 55779 |
rs768536423 | snp | C/T | 5.06547e-05 | 0.00503237 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366313 | ACTTTGTTAATGCTA[C/T]GAAACAAAAAATGTA | 55779 |
rs768536594 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113338471 | AAAAGACACGAAGAG[C/T]CATGTCACTAAAAAT | 55779 |
rs768554516 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417798 | GCCAAGTATCAGAGT[C/T]AAGAAGCAAACGGGC | 55779 |
rs768560129 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382704 | AGGCAGAATTGGCCT[C/T]AAGTAGGAAGGGAGA | 55779 |
rs768574631 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286963 | TTATTTTTCTATTAT[A/G]GCCATATTTATATAT | 55779 |
rs768576716 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297578 | CTACATATTATCAGA[C/T]GTGCTGTCTTTCCAT | 55779 |
rs768577831 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427140 | ATTTGTCTGGGCTTT[C/G]TCTCTAAAACAGTGA | 55779 |
rs768580148 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383638 | AAAAGCAAATGGTAA[A/G]TGAAATACAGGTCTC | 55779 |
rs768628030 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287867 | TGCATAATAAATTCA[C/G]TTCCCTTCTTTCCAA | 55779 |
rs768633256 | in-del | -/C | 1.69404e-05 | 0.00291031 | frameshift-variant, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363149 | ATTAGGCTTACTGTT[-/C]GTTTAAACTGCATAT | 55779 |
rs768642388 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418863 | GCGCGTGCCACCATG[C/T]CTGGCTAATTTTTTG | 55779 |
rs768646059 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403083 | CAACAGAGTGACCAG[A/G]CTCTTAAAAAAGAAA | 55779 |
rs768661406 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334502 | TACATTAATGAATAA[A/G]CCAGACCAAACTATA | 55779 |
rs768665667 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113293999 | TCTTCTTCAGAGGAC[C/T]AAACTGTTGGAACAC | 55779 |
rs768687377 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286931 | AAGAAGAAAAAAGAG[-/AC]AGAGAAAATTGGTAT | 55779 |
rs768691448 | snp | C/G | 1.7663e-05 | 0.00297173 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446611 | CTTGGATTAAGAGGT[C/G]TGAATCTCCCACTTC | 55779 |
rs768723685 | snp | A/C | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379636 | TGACAATGAAAATAG[A/C]AAGAAGATACACAGC | 55779 |
rs768725704 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297759 | CACCTCTCCAAGAAA[A/G]CATAATCTTGTAACA | 55779 |
rs768779373 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113305002 | GTGATGACTCTTCTC[A/G]GACAGGATGGAGCAG | 55779 |
rs768798883 | snp | C/T | 3.30431e-05 | 0.00406454 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399955 | TGTTTGAATTTCATC[C/T]GGGCCAAAGGAGTTT | 55779 |
rs768821786 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322657 | AATTAGTTCAGCCAC[G/T]GTGGAAAGCAGTTTG | 55779 |
rs768867901 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368267 | TCTCCTTGAAAAGAG[C/T]AACCCCAAGACACAT | 55779 |
rs768871536 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367066 | GGTTGGGAAGCTCTA[A/G]CTGGGCAGAGCCCAC | 55779 |
rs768873175 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323767 | AGATCATTTGGGCTG[G/T]GTGCAGTGGCTCACG | 55779 |
rs768883356 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446777 | TACTGGCAAGAGCTT[C/G]AAAACATATGGCTAA | 55779 |
rs768897400 | snp | A/G | 1.71779e-05 | 0.00293064 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379336 | CTTCCCTGGCTCTGA[A/G]TAAAATCCACAGAGG | 55779 |
rs768898839 | snp | A/C | 1.64825e-05 | 0.00287071 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427191 | ATAATACCTACCTGT[A/C]GTGCTTTGCAAATCA | 55779 |
rs768900338 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427955 | CAAATGTACTACTAG[G/T]TACCAGAGCTACATA | 55779 |
rs768900867 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350119 | AAAAGGGGAAGGAGA[-/G]GGGGAGAACAGCAGC | 55779 |
rs768913494 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306371 | CCAGCCTCATTTGTT[A/G]TGGAATGTGGTAGTA | 55779 |
rs768949729 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393344 | GTCCCCTCCAAATCT[-/C]ATGTTGGAATTTGAT | 55779 |
rs768955314 | snp | C/T | 3.30907e-05 | 0.00406746 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409101 | CTATTGGTTACCCAA[C/T]CTACTTGATGTGGCC | 55779 |
rs768958415 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390572 | CCTTGTTTGCAGATT[A/G]TATGATCTTATATTT | 55779 |
rs768959756 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354629 | CCACAGCAGCCACAG[C/T]AAGTCCCGCCCAAGG | 55779 |
rs768968553 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294423 | ACCTAAGTAACCTTA[A/C]ACCTCTCCAGGACCA | 55779 |
rs769013255 | in-del | -/ATAA | 6.35546e-05 | 0.00563678 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416675 | AAGAAAGATTTTTGT[-/ATAA]ATAGTCTGATTAATG | 55779 |
rs769030060 | snp | A/G | 1.67147e-05 | 0.00289086 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399880 | TACCAATAGATTCTG[A/G]TAGTTCATTATAACA | 55779 |
rs769031030 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408375 | CTGTTTCGTATTGAG[C/T]GTTCCTTGTCAGGAA | 55779 |
rs769031213 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353762 | GGAGAGAGAGAACCA[C/G]AGTCAGAGAGAGAGA | 55779 |
rs769076071 | in-del | -/CT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440407 | TATCCATTATTATTA[-/CT]GTCATTATTTTACAG | 55779 |
rs769077379 | snp | A/G | 1.73009e-05 | 0.00294111 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363540 | ATTCCAAACTATAGG[A/G]AGGGAAGTAAAAGGT | 55779 |
rs769116246 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430771 | AAATTCTACCAAGCA[C/T]TTAAGGAAGAAATAA | 55779 |
rs769183877 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323703 | CTTAGATGAAATATA[A/C]CAATTCCTCAAAAAA | 55779 |
rs769186901 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409268 | CTACCAACAGAGGCC[A/G]GCAAGTTACCGCTGT | 55779 |
rs769199818 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342586 | GAAAAGGAGAAAAAT[C/T]GAGTAAGTCCAATTC | 55779 |
rs769212276 | in-del | -/ACCTCTGT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297393 | CTAGACACACTGGCC[-/ACCTCTGT]GCTTCTCAAACATGC | 55779 |
rs769229204 | in-del | -/T | 2.03209e-05 | 0.00318748 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400521 | ACAAGGCCAGACATA[-/T]TTTTATTAAGAGTTC | 55779 |
rs769237393 | snp | A/G | 1.98426e-05 | 0.00314975 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381094 | ACATATTTACATTTA[A/G]GCAAATTTTTAAAAG | 55779 |
rs769256963 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286999 | CACTTGTAAATAAAT[A/G]TATATGTTTTATAAT | 55779 |
rs769262486 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385196 | CTCCCCAGCCATGAG[G/T]AACTGTGAGTCCATT | 55779 |
rs769283030 | snp | A/T | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330364 | CTAGAAGAGAGTTTG[A/T]GGAATCCTCCAACTG | 55779 |
rs769286823 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360112 | TGGTAGGTAAATCCA[A/G]TAGTAAACTTTGTAT | 55779 |
rs769292840 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300256 | ATGGTTAATGGGTAC[A/G]AAAACAGTTAGATAG | 55779 |
rs769305647 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422826 | GGAATTGGAGAAATT[A/G]TCATTTATCTAATAT | 55779 |
rs769325567 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342171 | AACCCCATCTCTACT[A/G]AAAATACAAAAATTA | 55779 |
rs769343213 | in-del | -/CTG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440723 | TCTAATGGCTCATCA[-/CTG]CTATCAAATAAGAGC | 55779 |
rs769343579 | snp | A/C/G | 3.30941e-05 | 0.0040677 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433703 | GATGAGATATGGATA[A/C/G]AGCTGTAAAATTGAA | 55779 |
rs769355431 | snp | A/G | 3.49412e-05 | 0.00417964 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395885 | AAGAGACACACCGAC[A/G]AAATATATATTACTA | 55779 |
rs769396702 | snp | G/T | 1.67728e-05 | 0.00289588 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416513 | AATATTTAAATATGC[G/T]TCTGGACTCACCTCG | 55779 |
rs769397073 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401841 | CAAAAGTCATTTCTT[C/T]TTCTTTCATGAAAAG | 55779 |
rs769408955 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424209 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACGAGGT | 55779 |
rs769443241 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319156 | AAACTGGATAAAAAG[A/G]CAAGAACCAACCATC | 55779 |
rs769453173 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407065 | AAGAAAGAGACTGAA[C/T]GTACCTCAAAGATAT | 55779 |
rs769563847 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290201 | ATTTAAAAAAAAAAG[C/T]GGGTGCTCTCCAGTA | 55779 |
rs769566832 | snp | C/T | 3.40727e-05 | 0.00412737 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401769 | AGAAAATACTTTAAT[C/T]GATCAGTAGTTTCTG | 55779 |
rs769573537 | snp | A/G | 7.18073e-05 | 0.00599153 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446710 | ACAGAGTAAGAGAGT[A/G]AGCTATCATTATTAA | 55779 |
rs769592524 | snp | A/G | 3.29641e-05 | 0.00405968 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366143 | CAGTCACCAAGAAAC[A/G]ATCATCAAAGCTATT | 55779 |
rs769592533 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362438 | ACCAATCACCTCTTC[C/T]TGAAGCCGTATTTTT | 55779 |
rs769617969 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403889 | ACAGTGATAACTTCA[C/T]CCTCATACAGCATTA | 55779 |
rs769654165 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393857 | TCACCACATGATCTC[C/T]ATACAGGCTAACTCC | 55779 |
rs769661493 | in-del | -/CTTTTTTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423105 | GGAATCTGATCCTTC[-/CTTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs769662656 | snp | C/T | 0.000190749 | 0.00976412 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380880 | TATTATAAGATAATG[C/T]TTCAGGAATATTCCA | 55779 |
rs769668953 | snp | A/G | 1.66073e-05 | 0.00288156 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396512 | GAAAGGAAATGTACT[A/G]CTTACCCCTGTGGCT | 55779 |
rs769673594 | snp | A/G | 1.65228e-05 | 0.00287422 | stop-gained, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420052 | CACCACTGCTACTTC[A/G]CAGGTAGATCTGTTC | 55779 |
rs769691942 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308816 | TCGCCATGTTGCCCA[G/T]GCCGATCTTGAACTC | 55779 |
rs769693163 | snp | A/G | 0.000140321 | 0.00837502 | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294652 | TGACAGAGCTTCCTC[A/G]ATTCCGAAAAAGGGT | 55779 |
rs769706611 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390263 | CACCACCATTTCAAT[C/T]GATGCTGAAAATGCA | 55779 |
rs769728207 | snp | A/G | 1.65531e-05 | 0.00287686 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420132 | GCGATACTGTCGTCC[A/G]GAAGTTGTAGGTTGG | 55779 |
rs769734983 | in-del | -/TTTTTTTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312238 | ACCATGCCTGGCTAA[-/TTTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs769743540 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295683 | TCTCTGAATCAGGCT[A/G]GAACCAGGCCAAGGC | 55779 |
rs769759057 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335820 | TGAATTTTTACGTAG[A/G]TAGACTGTATATGCG | 55779 |
rs769774506 | snp | C/T | 0.000131311 | 0.00810175 | intron-variant | CFAP44 | GRCh38.p7 | 3:113308125 | AATCAATATTCACAC[C/T]TCACAGAGAACACGT | 55779 |
rs769786212 | in-del | -/TTA | 0.000263622 | 0.0114779 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379497 | TCCTCCTTTCTTCCC[-/TTA]TTTTCTCCTTCAACT | 55779 |
rs769796819 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377133 | ATGAGGTTATCATTG[A/G]AGAGTAAGAGAAGGT | 55779 |
rs769802921 | snp | C/T | 3.34633e-05 | 0.0040903 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399871 | TACCATATTTACCAA[C/T]AGATTCTGGTAGTTC | 55779 |
rs769820919 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368971 | CAGACTTTAACCCAA[C/T]AAAGATCAAAAGAGA | 55779 |
rs769866498 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325204 | CTACTTGGGAGGCTG[A/G]GTCAGGAGAGTGGTG | 55779 |
rs769875201 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446168 | TGGCACAGTCAGATA[C/T]GGCACACAGGGATAA | 55779 |
rs769875510 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379470 | CTTCTCCCATCTCTG[C/T]TGCTAGCTTGTTCCT | 55779 |
rs769892146 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360080 | TCTTATCTTGTTACC[-/A]AAAAAAAAAAAAAGT | 55779 |
rs769900759 | snp | C/T | 1.68533e-05 | 0.00290282 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396712 | CTACAATAATTTGTG[C/T]TCCAGTGAAGTTTAC | 55779 |
rs769945724 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391177 | AGAATACAGAATGCA[A/C]AAACAAATCCATACA | 55779 |
rs769962761 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333015 | CTCAACAAAGATGTA[C/T]TAATACTTCTAATAA | 55779 |
rs769976064 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415231 | TATTACTTTTTATTG[A/C]ATCTATTTGATTCTT | 55779 |
rs769984016 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407004 | CTAGTGATCCCTGCA[A/G]CTTGAGACCGGTGAA | 55779 |
rs769985506 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413989 | GATTCTTTCTATCCA[G/T]GAGCATGAATGTTTT | 55779 |
rs769992533 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347368 | TCTCAAAGTCACGTC[A/G]CCCAAGCAAGGCTCA | 55779 |
rs770017779 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334232 | TGGGATTATAGGTGT[A/G]AGCCATCATGCCCAG | 55779 |
rs770033760 | snp | A/G | 1.66996e-05 | 0.00288956 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363342 | ACAATAACAGGTTGT[A/G]ATACAGAAACAGCAG | 55779 |
rs770053618 | snp | C/G | | | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379516 | TTTCTCCTTCAACTC[C/G]CTTTGTCTCTCCCTC | 55779 |
rs770066445 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321387 | CAAAATAATAAGAGC[A/G]CTATGTCAAATCCAC | 55779 |
rs770074731 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293335 | AATGGAGTCAGCGTT[A/G]GAGGCAGACAGACCT | 55779 |
rs770085531 | snp | A/T | 1.66507e-05 | 0.00288532 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380911 | TACCAGAATCTTAGA[A/T]TTGACACTTGAAAAA | 55779 |
rs770103851 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413923 | TAGTTTGATGGGAAT[A/C]GCATTGAATCTATAA | 55779 |
rs770105803 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439533 | TCCTTTAAAACCCTT[A/G]TTTTCCTTTACCTCC | 55779 |
rs770111618 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304823 | CTGATTTCCAAAGTG[C/T]TAATGGGCCACAGGG | 55779 |
rs770166401 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428384 | TGGGTATTCTGAGCC[C/T]GGAGAAGGGTTGTGC | 55779 |
rs770197438 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426989 | GTATCAGAGTACTCT[A/G]TGTGATCCTCAGAAA | 55779 |
rs770208543 | snp | C/T | 1.85321e-05 | 0.00304396 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381076 | CTAAAAAAGAAAAAT[C/T]GAACATATTTACATT | 55779 |
rs770212492 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322514 | CTAATCATCAGAGAA[C/G]TGCAAATCAAAACCA | 55779 |
rs770248505 | snp | A/G | 3.31148e-05 | 0.00406894 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286814 | AATGCAGCTCTCCCC[A/G]GGGCCACTGGTGCGT | 55779 |
rs770252931 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332506 | TGTGATTGGCACCCT[-/C]TCCAAAGTGATGCCT | 55779 |
rs770259599 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446556 | TCTACCCTCACCCCT[A/G]TATGCATTTCACAAT | 55779 |
rs770278619 | snp | A/G | 3.31384e-05 | 0.00407039 | stop-gained, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396676 | AAAGTTCAAGAATTC[A/G]AACAACTCCATCTTC | 55779 |
rs770317160 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315159 | GGTGAATGAAAAACA[-/T]TATCCAATCATACGC | 55779 |
rs770318749 | snp | C/G | 1.79664e-05 | 0.00299714 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400638 | AGAGGCATTCTGGGT[C/G]CTGGGTCTGAGAATA | 55779 |
rs770333558 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440280 | TGGCCAGACTTGTCT[C/T]GAACTCCTGACCTCA | 55779 |
rs770377441 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327630 | CTTGCATGTACTGTT[-/C]CTCTTTGTCTAAGGA | 55779 |
rs770387539 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353273 | AAGGACTAAAAGAAT[C/T]AGGCATTCTGGGAAA | 55779 |
rs770389788 | snp | A/G | 1.65252e-05 | 0.00287443 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286720 | TTGAAGAGGTGGACA[A/G]TCCTGACTCCTGCCA | 55779 |
rs770395255 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434487 | GTTTATACCTTATTT[C/T]CTTGACAACTGAAAA | 55779 |
rs770404311 | snp | A/G | 0.000102569 | 0.0071606 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330552 | CTTGGATATGTGAAG[A/G]GTCGACTGAATGTTC | 55779 |
rs770414749 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398205 | CCATGAAAAACAGTC[C/T]AGTGGGAAGACAATA | 55779 |
rs770431160 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385706 | GGGTGGTGGTGTGAC[C/T]TCAGCTCACTGAAAC | 55779 |
rs770439774 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373812 | ATACAAGAGAGATAT[C/G]ACCTCTGACTCCCTA | 55779 |
rs770440962 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288770 | CACATGGCTCACAGA[C/G]CTCCCTAAGCTGGGG | 55779 |
rs770459232 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299228 | TAGAAAAATATCTAC[A/T]AATCCAATTTTTAAA | 55779 |
rs770517298 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288926 | CTATGGATGACAGTT[C/G]AGAAGAGCCAAGTTA | 55779 |
rs770523782 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401749 | CCATATCTTGTAAAA[C/T]GAAAAGAAAATACTT | 55779 |
rs770527075 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328195 | ATATAGTAAGCACAA[A/G]TAAATACGTTTCCCA | 55779 |
rs770560532 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404942 | GTCAAACAACTTTAT[A/T]TTCTCTAGGACCCCT | 55779 |
rs770580418 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329287 | TGGAGAGGGTTTGGA[A/C]CTGAGCCATGCTTTG | 55779 |
rs770599155 | snp | A/G | | | stop-gained, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358746 | AATATGGATCCTACC[A/G]ATTCTTTAGCTTCAT | 55779 |
rs770608250 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360288 | ATCAAGTGAGATACA[C/T]CAGACACCTTATTAT | 55779 |
rs770628705 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366125 | TATTGCCATCTGCTC[C/T]AGCAGTCACCAAGAA | 55779 |
rs770673651 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298992 | TCATAAATGTTATGA[C/T]ATGTACATTTTACTG | 55779 |
rs770683197 | snp | A/G | 9.9226e-05 | 0.00704295 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420119 | AGCTATGTATATGGC[A/G]ATACTGTCGTCCAGA | 55779 |
rs770686171 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434396 | GCAGTCTATTGGCCA[A/G]AGTGGGAGAGTAAAA | 55779 |
rs770687940 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289992 | CTGAGCCAGAACACC[C/T]GGCCAAGCTGTCCCC | 55779 |
rs770692564 | in-del | -/TACAT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113395360 | AGAGATAAAGATGAG[-/TACAT]GAAAAGTACATTCAG | 55779 |
rs770705920 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406845 | TTATTGGCAGAGCTT[C/G]TTAGAATTTTCATAT | 55779 |
rs770731068 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382367 | GGATATTATTGGTGC[A/T]TTTAGAAGAGCTGAT | 55779 |
rs770757205 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375039 | CATATGCTGCATCAC[A/G]GATGAAACTTGGGGA | 55779 |
rs770774084 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420690 | AAATATTACGTAGGC[C/T]TTTTCCTTGATGTTG | 55779 |
rs770774689 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318073 | AACAGTCTAAAATGA[C/T]TGAAATGACAAACAT | 55779 |
rs770775610 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359960 | AACAGATCTGATAAA[C/T]TATAGAAATAGAAGC | 55779 |
rs770801430 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307929 | AGGTTGCAGTGAGCC[A/G]AGATCGTACCACTGT | 55779 |
rs770812321 | snp | A/G | 1.65523e-05 | 0.00287678 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401627 | TCATTCATTTTTATC[A/G]TAGAGAAGAGATTCA | 55779 |
rs770817539 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421075 | ACCTACAGAATGGGA[A/G]AAAATATTCCCAAAC | 55779 |
rs770823870 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113441238 | CCGCCCGGTCAGACT[C/G]ACAGGGTCTTGCAGG | 55779 |
rs770846693 | snp | A/C | | | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286726 | AGGTGGACAGTCCTG[A/C]CTCCTGCCAAGTGAG | 55779 |
rs770870500 | snp | C/T | 1.94e-05 | 0.00311442 | splice-donor-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446588 | ACATTTTAACGTGTA[C/T]CTTTGCTCTTGGATT | 55779 |
rs770875804 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306633 | GAAACTATTATTCCC[A/G]TATATAGGTGAATAC | 55779 |
rs770904679 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347687 | ACAAAAGCTATTCCT[A/G]AAGCTAGGATGTGGG | 55779 |
rs770912101 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370373 | AGCACATCAAAAAGC[G/T]TATCCACCACAATCC | 55779 |
rs770915352 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319326 | AAACCAATAAAAATT[-/AAG]AAGGATAATGAAGAG | 55779 |
rs770930757 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294561 | CCTCGGGGACGCAGA[C/T]GGTCTGGAAGTGGTC | 55779 |
rs770955857 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348512 | CTTTTCATTGAAGGA[A/G]AATACACAGCTATGC | 55779 |
rs770961014 | snp | A/T | 1.67086e-05 | 0.00289033 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404044 | TGGAAAAAAGAAATG[A/T]GCATTAAAACAGGTA | 55779 |
rs770973736 | snp | G/T | 1.64885e-05 | 0.00287123 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363230 | AAAGCTTTGATTTGC[G/T]CTCTCTTCCGTGCCT | 55779 |
rs770979643 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314101 | ATCTAATATTTATGC[C/T]ATCAGAGTACCAGAA | 55779 |
rs771010702 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410538 | ACATTTTCTTAATCC[A/C]GTCTATCATTGATGG | 55779 |
rs771015907 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355707 | AGCAAACCAACATGG[C/T]ACATGTATACCTATG | 55779 |
rs771026720 | in-del | -/G | 1.78163e-05 | 0.0029846 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396734 | GAAGTTTACCTTGGA[-/G]AAAATTAAAGATAAG | 55779 |
rs771035321 | snp | C/T | 1.64743e-05 | 0.00287 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403923 | GGTTAATGGGACCAT[C/T]GTGACATGACTTGCT | 55779 |
rs771074247 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402754 | ACTCTGAAAAGAGAA[A/G]CAAGCTTAGGAAATA | 55779 |
rs771077793 | snp | A/T | 0.000103815 | 0.00720395 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358898 | TAAGAAGATCTGTTC[A/T]TCAAAATGGGTACTG | 55779 |
rs771127513 | snp | A/G | 1.65206e-05 | 0.00287403 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426259 | TCTTCCACAGCTGGA[A/G]CAGGGGTTTGCTGAG | 55779 |
rs771135417 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433255 | CCAATATGATGAAAC[A/C]CCATCTCTACTAAAA | 55779 |
rs771159958 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314919 | TAAAGAGCAACAACT[G/T]AAACAGTTATACGAA | 55779 |
rs771201028 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326386 | TAGGTCCCTTAGTTA[A/C]CTCTCTATTTCATGT | 55779 |
rs771202902 | in-del | -/T | 1.75459e-05 | 0.00296186 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363555 | AAGGGAAGTAAAAGG[-/T]TAGCCCTTTAAAATT | 55779 |
rs771210467 | snp | G/T | 3.32901e-05 | 0.0040797 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286698 | TGCTGCTTGGGCCTT[G/T]TGCCAGTTGAAGAGG | 55779 |
rs771222648 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412403 | CCATTAAATATATCT[A/C]TTTTATTTCTTCTAA | 55779 |
rs771224972 | snp | C/G | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286570 | GTCCCCTTTCCAGAG[C/G]CAGTGTAACCACCTC | 55779 |
rs771243266 | snp | C/T | | | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379517 | TTCTCCTTCAACTCC[C/T]TTTGTCTCTCCCTCT | 55779 |
rs771243443 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424592 | TATAGAGATTATATA[C/T]GTCCATCTGCAGAGA | 55779 |
rs771267346 | snp | A/G | 3.65905e-05 | 0.00427714 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400532 | CATATTTTTATTAAG[A/G]GTTCCTACTTACAGT | 55779 |
rs771307361 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325797 | GGAGGAGTTAGTCTA[A/C]CTGATTTAAGGGCTC | 55779 |
rs771310913 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331794 | CTGGCTGAGAAAAAA[A/G]ACAAATAATACACTA | 55779 |
rs771340076 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438541 | ACATGGCAGTCAATA[C/T]GTAAAATGGTTGCAG | 55779 |
rs771384130 | in-del | -/AC | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443760 | TGACCTTGAGAAAAT[-/AC]CTCCTTGTACCTCAG | 55779 |
rs771419199 | snp | C/T | 3.39403e-05 | 0.00411934 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433549 | TTTTAAAAGTATACA[C/T]ATTATCTTTACTTAC | 55779 |
rs771430458 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409253 | GTGTAGTCAGGGTTA[C/T]TACCAACAGAGGCCA | 55779 |
rs771436137 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426600 | GCCATGCAGAACTGT[A/G]AGTCAAGTAAACCTC | 55779 |
rs771486712 | in-del | -/AG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334614 | AAAGAGGACAGGTAT[-/AG]AGAGTGGAATGGAAT | 55779 |
rs771517153 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397048 | ACAGAGTTTTGGTCT[A/G]GTGAAAGGTGCAGAC | 55779 |
rs771535185 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326192 | TGTGCTTATTAACTT[-/A]AACTACACTATGCTC | 55779 |
rs771542371 | snp | G/T | 1.65031e-05 | 0.00287251 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366268 | ACATAGACTCGAATT[G/T]CTCCATTTTTCATTC | 55779 |
rs771623663 | snp | C/T | 0.000309454 | 0.0124351 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291584 | GGGCTGTATCTCTTT[C/T]TCTCGTGGAGACTGA | 55779 |
rs771640161 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382939 | AAGAGGGAGTTGATA[A/G]GAGCAATGTCATAGG | 55779 |
rs771654723 | snp | A/C | 3.30486e-05 | 0.00406487 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395823 | ATCGGCTTATAATCC[A/C]TTTCCACTTCAAAGA | 55779 |
rs771669524 | snp | A/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443983 | TGCCAACCTGTAATT[A/T]GGAAAACTGTAAATT | 55779 |
rs771677195 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309295 | CTCAGCAAAAGTCCT[A/G]TTAAAACAGTCTAGA | 55779 |
rs771678684 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417987 | AAATTAAAAAGTTTC[C/T]GCCTCATATTGGAAA | 55779 |
rs771681329 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380135 | CTGGTGCACTGCACC[C/T]ACTAACTCGTCATCT | 55779 |
rs771687748 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404733 | GCTTTTTCTGACCCC[C/T]GCAAAGGAACCATAT | 55779 |
rs771691859 | snp | C/G | 1.65957e-05 | 0.00288055 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401593 | ACACACCTGAGCCAA[C/G]CAAAAGTTATTTCCA | 55779 |
rs771760052 | snp | A/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400565 | AAGGCAGTTGTGGCC[A/G]TGAGATAAGTGAGAG | 55779 |
rs771798583 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288000 | AAATTTTAAAATCTT[C/T]ATATGTGGAAGTGGA | 55779 |
rs771800322 | snp | G/T | 3.06876e-05 | 0.00391699 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416672 | TAAAAGAAAGATTTT[G/T]GTATAAATAGTCTGA | 55779 |
rs771808564 | snp | G/T | 1.65332e-05 | 0.00287512 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401651 | AGATTCACATTCTTG[G/T]CTACTTGAAGTTCAT | 55779 |
rs771818283 | snp | A/T | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113431849 | GGATTAGAACCTTAA[A/T]TAGTCAAGATTCCAC | 55779 |
rs771826626 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310400 | GCAGTATCAAAGAGG[C/T]CCCCTATCCCTTGGG | 55779 |
rs771832176 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419000 | TGAGCCACCGTGCTT[A/G]GCCAGGATTAGCATG | 55779 |
rs771853378 | snp | A/G | 1.74653e-05 | 0.00295505 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401301 | TCCTAAAAAAATTAA[A/G]TAGTATTTTGTTTTA | 55779 |
rs771865043 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391289 | AAAACTGGATATCCA[C/T]ATGCAGAAGAATAAA | 55779 |
rs771865120 | snp | A/G | 1.66252e-05 | 0.00288311 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445337 | AGAAAGAGCAAACCA[A/G]CCTTCTTCATTCTGT | 55779 |
rs771908466 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432902 | CTACATGCATCTATC[A/G]GATAATCTATTATTT | 55779 |
rs771915474 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439618 | CCCGAATAAACATCA[A/T]CTTCTTTTAGAAAGC | 55779 |
rs771920227 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404741 | TGACCCCCGCAAAGG[A/C]ACCATATGGGCCAAT | 55779 |
rs771923244 | snp | G/T | 0.000103783 | 0.00720282 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330641 | GAGAGAGAATGCACT[G/T]GTTCATGTGCCTTTT | 55779 |
rs771973113 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327992 | TGGCATTAAGTTTAC[A/T]TAAATTAATTTATTA | 55779 |
rs771981265 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415177 | GGTATTCTCTGATGG[C/T]AGTCTGTATTTCTGT | 55779 |
rs772002488 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113373569 | ACCCTAGAAAAGAGA[C/T]AAGTAACATAGAAGG | 55779 |
rs772012007 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299598 | AATCAGTATATTGAA[A/G]AGATACCTACACTCC | 55779 |
rs772033601 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391297 | ATATCCATATGCAGA[A/G]GAATAAAATGACCCC | 55779 |
rs772037402 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432835 | CTGGAATCTCCTGAT[-/A]AATATTCCCACATCT | 55779 |
rs772090593 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358640 | TCAAGTCAGTGGGTA[C/T]TTCCAGAGCCCTCTT | 55779 |
rs772090818 | snp | C/T | 1.69896e-05 | 0.00291454 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286679 | TCTCCCCTCAGGGCC[C/T]CCATGCTGCTTGGGC | 55779 |
rs772102740 | snp | A/G | 0.000102422 | 0.00715546 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305039 | CAGACGCATCACCTG[A/G]TGGAGCTTGAGCGGA | 55779 |
rs772124474 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429287 | TTTGTGTATTATGAT[A/G]CTGTTACTAGGTGAA | 55779 |
rs772149722 | in-del | -/TTT/TTTT | 0.0183021 | 0.093902 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286908 | TTGTTTTTTTTTTAA[-/TTT/TTTT]AAAAAAAAAGAAGAA | 55779 |
rs772205142 | in-del | -/T | 3.31755e-05 | 0.00407267 | frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399908 | ACAACAAACTTACCA[-/T]TCGGGGTACCCAAAC | 55779 |
rs772223437 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379503 | TTTCTTCCCTTATTT[C/T]CTCCTTCAACTCCCT | 55779 |
rs772261976 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287115 | GCACCGCACAGGCTG[A/G]CGCGGGACAGACTCC | 55779 |
rs772272919 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313541 | AGATTTGGAGGGGCA[A/C]GGGGGCGGAATGATA | 55779 |
rs772294499 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354670 | CTCAGACACACCTAT[C/T]CCTGCCCCCACCTGG | 55779 |
rs772295550 | in-del | -/T | 0.000398896 | 0.014117 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416546 | GGACTCTGTATGGTC[-/T]CAGAGAAGGATATTC | 55779 |
rs772304926 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400246 | CATATAGATTTGCCA[C/T]AAGTTAAGAAGGAAG | 55779 |
rs772309449 | in-del | -/A | 0.000380346 | 0.0137851 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416639 | GAACCTACAAAAGAT[-/A]AAATTTCACCAAAAT | 55779 |
rs772322422 | in-del | -/CC | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383457 | TAATTCCCTCAAAGG[-/CC]CCACCTCCAAATACT | 55779 |
rs772324384 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376260 | GATGGAGCAGGTTTG[C/T]ATGGGACATGTATGG | 55779 |
rs772343131 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314060 | AAACCCCAGAGCCTC[A/G]GGGACCTTTTGGATT | 55779 |
rs772367833 | snp | C/T | 2.08657e-05 | 0.00322993 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400517 | CAAAACAAGGCCAGA[C/T]ATATTTTTATTAAGA | 55779 |
rs772369484 | snp | A/G | 3.31082e-05 | 0.00406854 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399986 | TGCTAGCAAAATCAT[A/G]GATTCGAACAGAGCC | 55779 |
rs772379684 | snp | C/T | 0.000103003 | 0.0071757 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327770 | AGTTTTAGTTTCTGA[C/T]GTCTAAGGAGACGGA | 55779 |
rs772384769 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423544 | CCCTTTGTCTTATCT[C/T]ACCCTCTCTTCTGGC | 55779 |
rs772409709 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361597 | CCTCCCAGGTTTCAC[A/G]CCATTCTCCTGCCTC | 55779 |
rs772442799 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349141 | TAAGAAAAAGCCCAT[G/T]AATTATTCAATGATG | 55779 |
rs772442850 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372900 | CTAGCCTCCAGAACT[A/G]TGAGAAAAAAAATTC | 55779 |
rs772455469 | snp | A/C | 1.67612e-05 | 0.00289488 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379357 | TCCACAGAGGATGGG[A/C]GAGGGGGTTGACGGA | 55779 |
rs772457606 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343874 | CGTATTATATCACTG[G/T]CAATAGCCTAGATCT | 55779 |
rs772465600 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113401059 | AATTGTGTTATGAGA[C/T]AGATTCTTTTTTATG | 55779 |
rs772482254 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301888 | TTCTTTGGATCTCAC[C/T]GAAATTTTGTATCCT | 55779 |
rs772527110 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427218 | ATCACCATACTGAAA[C/T]GAACTCAAACTTCCT | 55779 |
rs772539468 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291207 | GATAGTTTTTCTTGC[C/T]AAGGGCTAAAAATTC | 55779 |
rs772545554 | in-del | -/TTAA | 1.73e-05 | 0.00294104 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366023 | TTATTAATTAACTGG[-/TTAA]TTAATTACATACCCT | 55779 |
rs772547685 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424462 | GAACAAAACAAAAAA[A/G]CAAAAACTGAAGTAG | 55779 |
rs772548864 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388142 | GAATACAAGCCTGGC[C/T]GGCTTCACCACCTGC | 55779 |
rs772551484 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362744 | AGCAAAAGATCAAAT[C/T]GGGATGACGTTTAGC | 55779 |
rs772578269 | snp | C/T | 1.6755e-05 | 0.00289435 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427322 | CTTCTAAAAATGTGT[C/T]ATCTTCTTGAACAGG | 55779 |
rs772581644 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443696 | CAGCATAGGCTTTGG[A/G]GAAAGACTGCCTATG | 55779 |
rs772581815 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376861 | CTCATGATAATAACT[A/G]AATAGAAAAGACAGA | 55779 |
rs772587866 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427094 | ATGTACATCCTGCAC[A/G]TTTTTCTTTCTATGG | 55779 |
rs772605566 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357448 | AGACACAGGGAGAAC[A/G]CTGAGTGAAAGCAGA | 55779 |
rs772608276 | snp | G/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330742 | AATATGATCTGCTCT[G/T]TTCTGTTGCTGAAAG | 55779 |
rs772633194 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327420 | ATTTACTAAAAAATC[G/T]GAATCATTTCTCTTT | 55779 |
rs772662107 | in-del | -/AATA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438219 | ACACATGTAGGGTTC[-/AATA]AATAAAATCATGGAA | 55779 |
rs772662276 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397089 | TAAATGAGTGTGAAA[C/T]TGTGAACTGAAATAA | 55779 |
rs772691098 | snp | C/T | 1.67091e-05 | 0.00289038 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286855 | AAACACCACCTCTCA[C/T]AATTTAGGCAGAAGC | 55779 |
rs772713111 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427222 | CCATACTGAAATGAA[C/T]TCAAACTTCCTTCCA | 55779 |
rs772716517 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319927 | AAAGATAATCAGAGA[C/T]TAATTATGAACACTT | 55779 |
rs772717331 | snp | A/G | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113338653 | CATCTCTCCAGGAAC[A/G]TTCAAACATTTGGGT | 55779 |
rs772733218 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333955 | AAAAGTCAATTAAAC[-/T]TTTTTTTTTTTTTTT | 55779 |
rs772759835 | snp | C/T | 1.6851e-05 | 0.00290263 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363447 | TGCAAAATCTCAGGC[C/T]TAGTCAGTATTTATC | 55779 |
rs772818620 | snp | C/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444033 | AGCAGCTTTCTGGGG[C/T]ATACTGGAGAAGTCA | 55779 |
rs772851985 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297814 | CCCCTAAGAGAAGTT[C/T]GAAGGCCTTAATATG | 55779 |
rs772869837 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310519 | TGAGAAATTTGAGTA[A/G]AACAGAAAATTTAAA | 55779 |
rs772909234 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113326727 | CAATACAAGGTTACA[C/G]TTTACAAATATATTT | 55779 |
rs772922229 | snp | C/T | 0.000158491 | 0.00890059 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287041 | ATAAGGAGTCCTACC[C/T]GTTGAGGTTGGAGAG | 55779 |
rs772935997 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439042 | GTATTCCTTTAAGGC[A/T]GTCGAAGTTTGGGTT | 55779 |
rs772939496 | snp | A/G | 3.50693e-05 | 0.00418729 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401303 | CTAAAAAAATTAAAT[A/G]GTATTTTGTTTTATC | 55779 |
rs772940579 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408911 | CTATGCTGTTTGCAG[-/A]AATAAAATCCCACAT | 55779 |
rs772946611 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403552 | CCTTTTGGAAGGATA[C/T]GTGGGTCTACTGTTC | 55779 |
rs772951195 | in-del | -/TTT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343060 | TTCTTTCTTTCTTTC[-/TTT]TTTTTTTTTTTTTTT | 55779 |
rs772957743 | snp | A/G | 0.000106129 | 0.00728376 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330648 | AATGCACTTGTTCAT[A/G]TGCCTTTTATTTCCA | 55779 |
rs772970700 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333144 | ATACCCATCTATAAC[A/C]CCCAGATATACTGTA | 55779 |
rs773000145 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393007 | ACACTGCTGCCAAAG[C/T]GAACATGGTAGTAGC | 55779 |
rs773030592 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315603 | TGACAGTAATTAAAA[C/T]ACTCCACCCAAAACA | 55779 |
rs773049321 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289634 | AAGGCCCCGGTGACC[C/T]CCACCTGGCATTCAC | 55779 |
rs773050317 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313905 | GAGAACAGACTAATA[-/C]ACCAAGATAAAAACT | 55779 |
rs773062344 | snp | C/T | 0.000165744 | 0.0091019 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401603 | GCCAACCAAAAGTTA[C/T]TTCCAGTTTCATTCA | 55779 |
rs773067100 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320866 | GCCCACCCAGATTAA[-/G]GGTGGGTCTACCTTT | 55779 |
rs773068411 | snp | C/T | 1.69666e-05 | 0.00291256 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395706 | GATAGTTTCACTATG[C/T]AGTAATTGAGATTCA | 55779 |
rs773074470 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357736 | TACATTGATGGTAAG[A/T]GTGTAAACTGAAGAG | 55779 |
rs773134644 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439663 | TATTTAGGTTGACAG[G/T]GTCAACTCTAAGGAA | 55779 |
rs773143531 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113378526 | TAGTCAGTGTCCTGG[A/C]CTGGCTAAAGACCTA | 55779 |
rs773149772 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392689 | AATACATATATCTAC[C/T]ATGTATCCACAAAAA | 55779 |
rs773160379 | snp | C/T | 0.000106389 | 0.00729267 | intron-variant | CFAP44 | GRCh38.p7 | 3:113358706 | TTATTCACACATGTG[C/T]TCTCAAACATCTTAG | 55779 |
rs773170416 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371385 | ACCAAAACAGATATA[C/G]AGACCAATGGAACAG | 55779 |
rs773192205 | snp | A/G | 3.35419e-05 | 0.00409509 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445264 | AGCAGGGAAAGGGAA[A/G]TAATAAATTATTAAG | 55779 |
rs773193445 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325045 | ACAGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 55779 |
rs773222987 | snp | C/T | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427210 | CTTTGCAAATCACCA[C/T]ACTGAAATGAACTCA | 55779 |
rs773249401 | snp | C/G | 3.32602e-05 | 0.00407786 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416547 | GACTCTGTATGGTCT[C/G]AGAGAAGGATATTCA | 55779 |
rs773302842 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410421 | TTTTGTCCTTGCAAT[A/G]GTTTGCTCAGAATGA | 55779 |
rs773304759 | snp | C/T | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401270 | AAGGTCAAGCTTCCA[C/T]ATGGCTCCATTGGCA | 55779 |
rs773311704 | snp | A/G | 1.73372e-05 | 0.0029442 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401786 | ATCAGTAGTTTCTGA[A/G]CATTTATTTTCTAAG | 55779 |
rs773314978 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375477 | AATCTTCTTGAATGA[C/T]GTAAGATACATACGG | 55779 |
rs773320371 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347621 | CCAAAGCCCCATTGG[G/T]TGGGGAGACCAACTA | 55779 |
rs773343157 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344005 | GCCAGAAGAAACAGG[C/T]TGCAGGGATTAGAGG | 55779 |
rs773353688 | snp | C/T | 4.9831e-05 | 0.00499129 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420150 | AGTTGTAGGTTGGCT[C/T]GCTTTCTACAGTCAT | 55779 |
rs773357862 | in-del | -/TA | 0.000146477 | 0.0085567 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287000 | ACTTGTAAATAAATG[-/TA]TATGTTTTATAATTC | 55779 |
rs773389786 | in-del | -/G | 2.33299e-05 | 0.00341532 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286895 | GAAAGACTATATATT[-/G]GTTTTTTTTTTAAAA | 55779 |
rs773431003 | snp | G/T | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113330812 | CCTTTTTACCACCAA[G/T]TTTCCCTTTTCTTTA | 55779 |
rs773507224 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437278 | TCTACTTTTCAGTCT[C/T]TTTTCTGAATAAATT | 55779 |
rs773561453 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387023 | GGGAATGGTTCAGCC[C/T]AGTAGTCAGAACCTG | 55779 |
rs773572661 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345228 | AAACATGTAAATTAT[A/G]TAAACAAATATGTTA | 55779 |
rs773618326 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291260 | TCCTAAAACAAAATA[C/T]ATTACAGGTGATTTG | 55779 |
rs773626116 | snp | A/G | | | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113331718 | GCCTACCTTTTTAAG[A/G]AGACTCTTCACACAT | 55779 |
rs773631063 | snp | A/G | 0.000617729 | 0.0175637 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344624 | ATTTGGAGTACTTAG[A/G]GGGCTGCACCAGCCT | 55779 |
rs773634028 | snp | C/G | 1.74628e-05 | 0.00295484 | stop-gained, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446629 | AATCTCCCACTTCCT[C/G]AGGTGGCATTTAGTG | 55779 |
rs773669788 | in-del | -/T | 0.000101748 | 0.00713186 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446555 | TTCTACCCTCACCCC[-/T]ATATGCATTTCACAA | 55779 |
rs773671645 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113291999 | GCTAGCTATCAGTCA[G/T]TCATTACCTAAAGAG | 55779 |
rs773691823 | snp | C/G | 1.70924e-05 | 0.00292334 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427331 | ATGTGTTATCTTCTT[C/G]AACAGGAGCTATTAA | 55779 |
rs773698043 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409844 | CGACCTCTGGTCGTC[C/T]TCACTACTCATTATA | 55779 |
rs773719081 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419979 | AGCAAAAAGATAGGG[-/T]TTTTTTGGGGTTTTT | 55779 |
rs773721569 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291163 | TTCTAAGGATCAAGA[A/T]AACAAAGTTTTCTCA | 55779 |
rs773742609 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361747 | TCATGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT | 55779 |
rs773747189 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409126 | GTGGCCTGATCCCGA[C/T]GTAGTAAGCTGCTCT | 55779 |
rs773748495 | in-del | -/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416198 | TTTTGTTTTTTTTTC[-/C]CTTTCCATTTACTTG | 55779 |
rs773762208 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377926 | AAAGTGCTGAGATTA[C/T]AGGTGTGAGCCACTG | 55779 |
rs773780159 | in-del | -/CCTG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334061 | GGTTCAAGCGATTCT[-/CCTG]CCTCAGCCTCCCAAG | 55779 |
rs773780647 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394068 | AGTATAGATTTACAG[A/G]AAGTTGAAAAGATAG | 55779 |
rs773783695 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113349135 | GACAATTAAGAAAAA[G/T]CCCATGAATTATTCA | 55779 |
rs773833370 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376871 | TAACTGAATAGAAAA[G/T]ACAGAAACTGATGAT | 55779 |
rs773839968 | snp | A/C | 9.9369e-05 | 0.00704802 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330281 | AACACTTTGGTATAT[A/C]TAGGCTGAATGTTGA | 55779 |
rs773863938 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442298 | TAGTCATAAGGGAAA[C/T]AGAAACCACAATACA | 55779 |
rs773873628 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350121 | AAAGGGGAAGGAGAG[C/G]GGAGAACAGCAGCAT | 55779 |
rs773880096 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352957 | TCCTTCCATATGTTC[A/C]CTGAAAACATGATGC | 55779 |
rs773909973 | snp | A/C/T | 3.33451e-05 | 0.0040831 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286846 | TGTCTTTTGAAACAC[A/C/T]ACCTCTCACAATTTA | 55779 |
rs773910944 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319970 | TGAACACTTCTATGC[A/C]CACAAACCAGAAAAT | 55779 |
rs773918824 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316332 | AGCACTAAATTAGAA[-/AAG]AAGAAAAATATCATC | 55779 |
rs773934833 | snp | C/T | 1.65203e-05 | 0.002874 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380960 | ATGTCTTTGATTTCA[C/T]AGGAGACTACATCAT | 55779 |
rs773957337 | snp | A/T | 3.30562e-05 | 0.00406534 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373436 | TAGTTTGGATGGGAT[A/T]GTCCTCTGTATCCGC | 55779 |
rs773964027 | in-del | -/GGCCGGGCGCGGTGGCTCACGCCTG | 1.6601e-05 | 0.00288101 | frameshift-variant, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420148 | AAGTTGTAGGTTGGC[-/GGCCGGGCGCGGTGGCTCACGCCTG]TCGCTTTCTACAGTC | 55779 |
rs773970504 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318761 | AGCAAGAAGAGACTG[G/T]GGGCCTATTTTCAGT | 55779 |
rs773985495 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430081 | TGGGACATAAGACCA[A/G]TTTTAATACATTTAA | 55779 |
rs773989571 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309072 | CAAAGACTCTCTCCT[C/T]TGACCCCACTTGAGT | 55779 |
rs774046504 | snp | A/T | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113326483 | TTCTTTACCCGTTTA[A/T]TCTTCTTCTTTAGGA | 55779 |
rs774050497 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417894 | ATTTGTAAAGAAATA[C/T]GGTGTAGAACATATG | 55779 |
rs774066525 | snp | A/G | 0.000102359 | 0.00715327 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330636 | TCTAAGAGAGAGAAT[A/G]CACTTGTTCATGTGC | 55779 |
rs774069563 | in-del | -/TTTTTTTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423107 | AATCTGATCCTTCCT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 55779 |
rs774074485 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416968 | AAGCCCTAACACCCA[C/G]AGTTTCTGACTTAAT | 55779 |
rs774092853 | snp | A/G | 1.87612e-05 | 0.00306272 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400649 | GGGTCCTGGGTCTGA[A/G]AATAGATAGACAGCT | 55779 |
rs774115573 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398429 | GTATGGAGAAGGGAC[A/G]TTTTAATTGTAGCTT | 55779 |
rs774120264 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436111 | TAGTTATCCACATCT[C/T]AACATCCACTCCAGC | 55779 |
rs774123882 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415695 | AGTTTCTTAATCCTG[A/C]GTTCTAATTTGATTG | 55779 |
rs774133139 | snp | A/T | 1.66421e-05 | 0.00288458 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416535 | CTCACCTCGAAGGAC[A/T]CTGTATGGTCTCAGA | 55779 |
rs774164217 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113382731 | GAGACAGCTTCTCTA[C/T]TGCAAAAGAGGGACG | 55779 |
rs774171615 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287069 | GAGGGAAAATAAAGA[A/C]GCTGCCACCTAACAG | 55779 |
rs774176557 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325521 | ATGATCTCAGCTCAC[C/T]GCCAGCTCCGCCTCC | 55779 |
rs774184684 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416665 | AAAATATTAAAAGAA[A/G]GATTTTTGTATAAAT | 55779 |
rs774213443 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308576 | TAAAATCAGACAAAA[A/T]TTTTTTTTTCTTTTT | 55779 |
rs774221236 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388554 | TTATCAACAATAGCA[C/T]TGAAAGTAAATGGAC | 55779 |
rs774221787 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345788 | ACTTCTTAGAATTTA[A/G]TTTATTTTTGTATAG | 55779 |
rs774230659 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335012 | CACTAAAATGAAGGA[-/T]TACTATTTTTAAAGA | 55779 |
rs774232971 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287871 | TAATAAATTCACTTC[C/G]CTTCTTTCCAAAGAT | 55779 |
rs774251084 | in-del | -/AC | 3.52268e-05 | 0.00419668 | intron-variant | CFAP44 | GRCh38.p7 | 3:113366000 | TCACTATTTTTAAAT[-/AC]AGTTTGTTATTAATT | 55779 |
rs774261291 | snp | A/C/T | 0.000317287 | 0.012592 | stop-gained, missense, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341753 | ACTCACAGTTCCTCC[A/C/T]ATTCTTTTTTTCGCT | 55779 |
rs774278183 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113390298 | ATAAAATTCAACATC[C/G]CATCATGACAAAAAT | 55779 |
rs774283478 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346777 | AATCAGCAGGAAATG[G/T]GCAGGGACAAATAAG | 55779 |
rs774284726 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403905 | CCTCATACAGCATTA[A/T]CTGGTTAATGGGACC | 55779 |
rs774289418 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433715 | ATAAAGCTGTAAAAT[C/T]GAAACTAACAGATTT | 55779 |
rs774318701 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355167 | CTCAGAAATCACCAC[C/T]AAAGAACTTTTCATG | 55779 |
rs774351742 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113428557 | GATGGAAGACTTATG[A/G]TTTGAAGAATAAATC | 55779 |
rs774357012 | in-del | -/AAT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416316 | CTTGACTCCTTATCC[-/AAT]TTGCCAGTCTGTGTC | 55779 |
rs774368855 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437733 | GAGAGACTCCTGTTC[C/T]CCTGGAGATTATCAG | 55779 |
rs774372015 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379688 | AAATACTCACCAATG[C/T]GAGAATATATTTTTA | 55779 |
rs774385047 | snp | A/G | 0.000101487 | 0.00712272 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294744 | CTTTTCAATACACAA[A/G]TCATTCATCTGATAA | 55779 |
rs774390087 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446784 | AAGAGCTTGAAAACA[C/T]ATGGCTAACTTAGGT | 55779 |
rs774405832 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372802 | GCACCCAGAGAAAAG[A/T]TCATGCAAGAAGGCA | 55779 |
rs774410481 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367097 | CTCAGCTCAGCAAGG[A/C]CTACTGCCTCTATAG | 55779 |
rs774411579 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357617 | GACTTCTAGCCTCCA[C/G]AACTGCGAGACAGTA | 55779 |
rs774436326 | snp | A/G | 0.000102569 | 0.0071606 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296868 | TGATCATGAGCTGCC[A/G]GACTGTTTCCTCCAT | 55779 |
rs774445732 | snp | C/G | 1.65209e-05 | 0.00287405 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420055 | CACTGCTACTTCGCA[C/G]GTAGATCTGTTCCTT | 55779 |
rs774446286 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365653 | CCTATCAAAACCACA[C/T]TTTATGGCATATGTC | 55779 |
rs774470635 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334537 | AGAATACCCACAAGA[C/T]AAGGCCACAAAAAGG | 55779 |
rs774483229 | snp | C/G | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433637 | CTGATTTCTCCCCAT[C/G]AGTATCCTGATCATC | 55779 |
rs774489216 | snp | A/C/T | 5.27972e-05 | 0.00513773 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446614 | GGATTAAGAGGTGTG[A/C/T]ATCTCCCACTTCCTG | 55779 |
rs774490752 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348742 | AATTTGGCCCAACCC[A/G]GGTACATGTCCCCTT | 55779 |
rs774527809 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440647 | TTCTGTAACCCATTT[C/T]CTACACTATCGCTTG | 55779 |
rs774550904 | snp | A/G | 1.71275e-05 | 0.00292634 | missense, synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379338 | TCCCTGGCTCTGAGT[A/G]AAATCCACAGAGGAT | 55779 |
rs774607124 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446250 | CCAAGCACAAGGACT[A/G]GGGGAACCAATAGCT | 55779 |
rs774620477 | snp | C/T | | | intron-variant, utr-variant-3-prime, splice-donor-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294464 | ATTGATTAGTACTTA[C/T]GTGAGTTCATGGCAC | 55779 |
rs774648794 | snp | A/G/T | 3.33641e-05 | 0.00408425 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399890 | TTCTGGTAGTTCATT[A/G/T]TAACAACAAACTTAC | 55779 |
rs774667803 | snp | C/G | 1.73141e-05 | 0.00294223 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363542 | TCCAAACTATAGGAA[C/G]GGAAGTAAAAGGTTA | 55779 |
rs774671780 | snp | A/G | 0.00010329 | 0.0071857 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305111 | CTGATAAGCCTCCAG[A/G]GCCTCCTCTGCTGCA | 55779 |
rs774699827 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113415085 | TTCTTTCTGGTTTAG[C/T]CTTGGTAGGGTGTAT | 55779 |
rs774699835 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398508 | GCTGTGAACATTACA[C/T]GATCATCTGAATAAA | 55779 |
rs774707875 | snp | G/T | 1.72725e-05 | 0.0029387 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426295 | AAAAAAATAAAATAA[G/T]TTAAGAAGAGTGATA | 55779 |
rs774715620 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354636 | AGCCACAGCAAGTCC[C/T]GCCCAAGGAGAGGGT | 55779 |
rs774716195 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113400007 | GAACAGAGCCTATAG[A/G]AAGACAGTTTTAAAA | 55779 |
rs774731968 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386794 | CATCACTGAAAGAGG[C/T]ACTGCAGAGGGTAGG | 55779 |
rs774747550 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300366 | TAAAAGAGTATAATC[A/G]GATTGTTTGTAACAT | 55779 |
rs774762913 | snp | G/T | 1.64933e-05 | 0.00287165 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406919 | TGTAGAATAGTAGCT[G/T]TACTCACCTTCCCAT | 55779 |
rs774764621 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113358261 | AGATATATTTATACA[C/T]CTGTAAAAAATTTTC | 55779 |
rs774771415 | snp | A/G | 4.47698e-05 | 0.00473105 | intron-variant | CFAP44 | GRCh38.p7 | 3:113373584 | TAAGTAACATAGAAG[A/G]TGGTACTTGAATATA | 55779 |
rs774780028 | snp | C/G | 1.65345e-05 | 0.00287524 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399977 | AAGGAGTTTTGCTAG[C/G]AAAATCATAGATTCG | 55779 |
rs774782183 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423033 | CACTGTCTTCAGCCT[A/G]TTGGCTATTCAGGAA | 55779 |
rs774801350 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407020 | CTTGAGACCGGTGAA[C/T]GTAAAAGCCATTTCC | 55779 |
rs774826443 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359182 | ATCTCAAAGAAACTA[C/T]TATTACATAAAAATT | 55779 |
rs774838736 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329630 | AGAACATCCTGCCCA[A/G]CAGGCCCTAGTCTGG | 55779 |
rs774850821 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113300271 | AAAAACAGTTAGATA[G/T]AATAAATAAAATCTG | 55779 |
rs774861751 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329875 | CCACTTCCCCTTTAC[G/T]ATGACTTCAGTTAGA | 55779 |
rs774896923 | snp | A/G | 3.364e-05 | 0.00410108 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363360 | ACAGAAACAGCAGAG[A/G]AAGAGAAAATTAGTA | 55779 |
rs774897337 | in-del | -/TGG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342564 | GTGTTTGTGAGATGA[-/TGG]TGGGGAAAAGGAGAA | 55779 |
rs774902922 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113408635 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACATGA | 55779 |
rs775030846 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | CFAP44, SPICE1 | GRCh38.p7 | 3:113442456 | AAAACTATTTGAGAG[C/G]TTTCTTCAAAAGTTA | 55779 |
rs775059701 | snp | A/T | | | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330606 | TATTTCCTCAACAAC[A/T]GCCACTTTAAGGTCT | 55779 |
rs775068649 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306903 | GTTGGCATTAGGTTT[A/G]TGTGCTCTATTTCAC | 55779 |
rs775091254 | snp | C/T | 6.76521e-05 | 0.00581562 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400571 | GTTGTGGCCATGAGA[C/T]AAGTGAGAGGAGAAA | 55779 |
rs775101365 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360131 | TAAACTTTGTATTAC[A/G]TAAAGAGGTTCATCT | 55779 |
rs775111132 | snp | A/G | 9.71204e-05 | 0.00696784 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330241 | TCCAGCTCCACATCC[A/G]TTGGCTCTGCTTTTT | 55779 |
rs775123221 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289334 | GTTTGGGAATAATTA[G/T]CCCGATTAGCTTTCC | 55779 |
rs775124777 | snp | C/G | 1.65471e-05 | 0.00287633 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396522 | GTACTGCTTACCCCT[C/G]TGGCTAGAATTTCCC | 55779 |
rs775137548 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113340007 | AGGAGAGGGTCAATT[A/G]GCGTGGTGGGCGAGA | 55779 |
rs775150983 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319247 | TGGAGAAAGATCTAC[C/T]ATGTAAATGGAAAAC | 55779 |
rs775151445 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113337036 | TTCCTGTTTACAAAT[G/T]ACATGGTTGTCTACA | 55779 |
rs775155650 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113316600 | ACAGCTGGCTGTAGT[C/G]GCTCACGCCTGTAAT | 55779 |
rs775168907 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396594 | GGTTTGAAAACCTGT[C/T]TCAACTGAATATCAG | 55779 |
rs775178369 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290206 | AAAAAAAAAGTGGGT[A/G]CTCTCCAGTAGAGAA | 55779 |
rs775200089 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320416 | AGATATATACATGAT[-/AT]ATATATATGATATAT | 55779 |
rs775204560 | in-del | -/AT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298466 | CCATATGGTCCAGCC[-/AT]ATATATCCCAATTCT | 55779 |
rs775248110 | snp | A/T | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441916 | TTTTAAAACTATATT[A/T]TCTCTGTTGGCTTTT | 55779 |
rs775251170 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409278 | AGGCCAGCAAGTTAC[C/T]GCTGTAGTTAAAGTC | 55779 |
rs775268858 | snp | C/T | 1.65127e-05 | 0.00287334 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433596 | AGAAGACCTCAGAGA[C/T]TTCTTCCCATCACTC | 55779 |
rs775304744 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335824 | TTTTTACGTAGATAG[A/G]CTGTATATGCGTGGC | 55779 |
rs775316416 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113295990 | GGTTTGGGTTTCTAG[C/T]AGACCCATCACCAGA | 55779 |
rs775333437 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113296311 | CACATTTTCTTTGCC[C/T]GACTGGTGTGAGATG | 55779 |
rs775349284 | snp | A/G | 1.65603e-05 | 0.00287747 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420136 | TACTGTCGTCCAGAA[A/G]TTGTAGGTTGGCTCG | 55779 |
rs775361634 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328169 | TCCATAGTATCTCTA[A/C]AATCCCTTTTATATA | 55779 |
rs775402954 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308533 | AGTTAGTGAAACAGA[A/C]CCACAATTCCTAACT | 55779 |
rs775430215 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324132 | TTAAAAACTCCCCCA[A/G]AAGAAATGTTCAAAT | 55779 |
rs775430437 | in-del | -/T | 3.38155e-05 | 0.00411176 | intron-variant, frameshift-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286682 | CCCTCAGGGCCCCCA[-/T]TGCTGCTTGGGCCTT | 55779 |
rs775430506 | snp | C/T | 2.71802e-05 | 0.00368637 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427389 | GATTAAACATTTTCT[C/T]ATTTCTAAAGTAGCT | 55779 |
rs775459825 | snp | C/G | 0.000102971 | 0.00717459 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113344565 | CTCTTTTTCAAACCT[C/G]TCCAATTTGCTTGGT | 55779 |
rs775467735 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354865 | CACCACCTCCTGGCT[A/G]GAGGCCAACCAACAC | 55779 |
rs775473602 | snp | A/G | 1.70507e-05 | 0.00291977 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401770 | GAAAATACTTTAATC[A/G]ATCAGTAGTTTCTGA | 55779 |
rs775496268 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391230 | CAAAGATGCCAAGAA[C/T]GTACATTGCACAAAG | 55779 |
rs775498181 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446223 | CAGTGCTCTGGCTGT[C/T]CCAGACCCCACCCAA | 55779 |
rs775507105 | snp | A/C/G | 0.000181392 | 0.00952204 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286770 | TGTCCCCAGCACCCC[A/C/G]TAGGGGCCTACGTAG | 55779 |
rs775515132 | snp | A/G | 0.00142668 | 0.0266703 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291620 | TGGGAGGATAAGACT[A/G]CCTTTCCTACGCAAA | 55779 |
rs775533935 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293415 | GTTACTCAGCTCCTC[C/T]GAGCTTTAGAAAGTA | 55779 |
rs775549526 | snp | A/G | 1.67758e-05 | 0.00289614 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445366 | GTTTCTCAATCTGTT[A/G]AACAAAGACACGGAA | 55779 |
rs775553339 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333071 | ACATTCATCAGAGAG[C/T]CAAACTCCGACCTAG | 55779 |
rs775553487 | in-del | -/A | 0.000120799 | 0.00777077 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400024 | AGACAGTTTTAAAAG[-/A]AAAAAAATTATATAC | 55779 |
rs775556094 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370411 | TTCACCCCTGGGATG[C/T]AAGGCTGGTTCAACA | 55779 |
rs775576813 | snp | A/G | 0.000102675 | 0.00716427 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113305080 | GCAGTTCATTCAGCC[A/G]CTGCTGCTTCTCTCG | 55779 |
rs775582423 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113346832 | CAGCAGCGGCAAACC[A/C]CTCGGGTCCCCTTCC | 55779 |
rs775594664 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377206 | TGGAAAGTGAATATG[G/T]CTGGGCAGTAGAATT | 55779 |
rs775605709 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397350 | AGAGAACAATGTTTC[C/T]CCAGGAGGCTGGAGA | 55779 |
rs775613245 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438746 | CCTTATTTTTTCTTC[C/T]GAGAACACACAGAAC | 55779 |
rs775655625 | in-del | -/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423062 | AAATGTTTGTTGAAC[-/T]AATGAATTCATTAAT | 55779 |
rs775687743 | snp | C/G | 1.67323e-05 | 0.00289239 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399877 | ATTTACCAATAGATT[C/G]TGGTAGTTCATTATA | 55779 |
rs775710413 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303857 | GGAGACAGTCACCTG[A/G]ATAATTCCCTTTCTT | 55779 |
rs775733956 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306793 | TGGAATACTAAAATA[C/G]AATTCAGGAAGCTTA | 55779 |
rs775747821 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321727 | TACATCAATAATGTA[C/T]AGTCTGAAAATCAAA | 55779 |
rs775800162 | snp | A/G | 1.67075e-05 | 0.00289023 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406893 | TGTACTTGAAAACAC[A/G]ATTTTAATATTGTAG | 55779 |
rs775800881 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322578 | CTATTATTAAAAAGT[A/C]AAAAAAGAGGCTGGT | 55779 |
rs775845940 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323132 | GGGATTATGGGGACC[A/C]AAATTCAAGATGAGA | 55779 |
rs775863230 | in-del | -/AAAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433430 | GCAAAACTCCATCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 55779 |
rs775877450 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386756 | AATCAGGTGAGTGAT[A/G]ACAATACTTGGTTTT | 55779 |
rs775895652 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113421208 | GACACTTTTCAAAAG[A/C]AGACATGCAAGCGAC | 55779 |
rs775918709 | snp | C/T | 5.0659e-05 | 0.00503259 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396713 | TACAATAATTTGTGC[C/T]CCAGTGAAGTTTACC | 55779 |
rs775922844 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407005 | TAGTGATCCCTGCAG[C/T]TTGAGACCGGTGAAC | 55779 |
rs775927390 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345492 | AGTTGAATAAAAGTG[C/G]AAACCTCTTCATTTC | 55779 |
rs775930871 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113352480 | AGAACCCACTGGAAG[A/G]AACCAACTCCAAACA | 55779 |
rs775950333 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311960 | GAACTTTGAACTTGA[A/G]AGAGATGATTTAAGG | 55779 |
rs775961449 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372891 | CTTGGAACTCTAGCC[C/T]CCAGAACTGTGAGAA | 55779 |
rs776001686 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299238 | TCTACTAATCCAATT[C/T]TTAAATGGGCAAAAG | 55779 |
rs776021056 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353589 | TTCTTCACCACTTTC[A/T]TCTTTTAGCAGGTAG | 55779 |
rs776033529 | snp | A/G | 3.31181e-05 | 0.00406914 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380926 | TTTGACACTTGAAAA[A/G]TGGAAACATTTTATG | 55779 |
rs776033769 | in-del | -/A | 1.65381e-05 | 0.00287555 | frameshift-variant, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366088 | TTAGCATAAATTCAG[-/A]AAAAAATGTTGAAAA | 55779 |
rs776044660 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426955 | AGTTTTTATACCTTC[C/T]TAAAACCCAGAAGAA | 55779 |
rs776094689 | snp | C/T | 1.65108e-05 | 0.00287317 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286728 | GTGGACAGTCCTGAC[C/T]CCTGCCAAGTGAGTG | 55779 |
rs776122768 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357824 | TATAACCTATGGCCC[A/G]GCAGTTCCACAACTG | 55779 |
rs776124894 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438581 | ATTGATATATTCCTG[-/A]AATAGATGAAAGAAC | 55779 |
rs776132422 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402266 | ATTTCACACTTTACT[A/G]TCTCATTGGGAAAAT | 55779 |
rs776148004 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409146 | TAAGCTGCTCTTCCT[C/T]ATCAGGATTGAAAGT | 55779 |
rs776191039 | snp | A/G | 8.23716e-05 | 0.00641709 | missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426178 | GTCACAAAAGGCATC[A/G]AAGCAAGCTCCATAT | 55779 |
rs776216393 | in-del | -/AGG | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435129 | TTGACAGGCTGAGGC[-/AGG]AGGACTGCTTGAGAC | 55779 |
rs776225333 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359993 | AGACAATCAAATTAT[A/G]CATGCATCTACCCAT | 55779 |
rs776241852 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113392788 | GTCCAAGAATAATAC[A/G]GGAGGAAGAACATGT | 55779 |
rs776246375 | snp | A/T | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366129 | GCCATCTGCTCCAGC[A/T]GTCACCAAGAAACGA | 55779 |
rs776277046 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360316 | TATTGTAGAAACATG[C/T]AGATTGTATCACATC | 55779 |
rs776282652 | snp | A/G | 0.000103024 | 0.00717644 | intron-variant | CFAP44 | GRCh38.p7 | 3:113344482 | TTGAAGTCTTAGTAA[A/G]TAAGAATTTAAAAGC | 55779 |
rs776283694 | snp | A/T | 1.68832e-05 | 0.00290539 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401763 | ATGAAAAGAAAATAC[A/T]TTAATCGATCAGTAG | 55779 |
rs776303870 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113289115 | TACTTGTGTTTGAAG[C/T]TTAACTTCCCAAAGA | 55779 |
rs776317299 | snp | C/T | 1.6549e-05 | 0.0028765 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401628 | CATTCATTTTTATCA[C/T]AGAGAAGAGATTCAC | 55779 |
rs776321850 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113419258 | TGGCTATCTGCACAC[A/T]GTTATTGCCACATTA | 55779 |
rs776323046 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317119 | AGCTACTGGGAAAGG[A/G]ATGAGTAAGAGAACT | 55779 |
rs776324896 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416502 | CTTGAACATGAAATA[C/T]TTAAATATGCTTCTG | 55779 |
rs776351701 | snp | A/G | 3.45363e-05 | 0.00415536 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395879 | AGGAAAAAGAGACAC[A/G]CCGACGAAATATATA | 55779 |
rs776363174 | snp | G/T | | | intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113294636 | TGTGAATAGCTACCT[G/T]TGACAGAGCTTCCTC | 55779 |
rs776377533 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414532 | ATTTTAAGATATATT[A/C]CATCAATACCTAGTT | 55779 |
rs776378746 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318227 | ATTTTTAAAGTTTTT[A/T]AACATTTTCAGAAAA | 55779 |
rs776392942 | snp | A/T | 1.88432e-05 | 0.00306941 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427348 | ACAGGAGCTATTAAA[A/T]TTTGTTTTAATAACT | 55779 |
rs776401045 | snp | A/C | 1.69864e-05 | 0.00291426 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396491 | TATAAAATTTCAACA[A/C]GAAAAGAAAGGAAAT | 55779 |
rs776403644 | snp | A/C | 0.00178152 | 0.0297924 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287094 | TAACAGGAGTCACCC[A/C]GGAAAGCACCGCACA | 55779 |
rs776405406 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113358768 | TAGCTTCATTAGGCC[A/G]AGTTCATGTTTCTCT | 55779 |
rs776408333 | in-del | -/AA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113369106 | TCCTTAGAAACCTAC[-/AA]AGAGACTTAGACTCC | 55779 |
rs776429081 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406956 | GCTCCATGTAGCCTT[C/T]TATATCAGTAGTGAT | 55779 |
rs776471089 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113293677 | TGCCTTGATCCTTCA[C/T]TCAAAAGTTCTTCAG | 55779 |
rs776472446 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357822 | CATATAACCTATGGC[C/T]CAGCAGTTCCACAAC | 55779 |
rs776476429 | snp | C/T | 3.66609e-05 | 0.00428125 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363577 | TTTAAAATTGCATAG[C/T]ATTTTCCTTAAAATA | 55779 |
rs776477857 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371870 | TACAAAGAACTTAAA[A/C]AAATTTACAGGAAAA | 55779 |
rs776487447 | in-del | -/CTT | 1.64923e-05 | 0.00287156 | cds-indel, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363258 | CCTTTATTTCTCCCA[-/CTT]CTTTCATTAACTTGT | 55779 |
rs776518176 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385728 | CACTGAAACCTCTGC[C/T]TCCCGGGTTCAAGCG | 55779 |
rs776527291 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431544 | TAGGGGGGAACAAAC[A/T]AAAGTTTCTGAAGTA | 55779 |
rs776538257 | snp | A/G | 1.78344e-05 | 0.00298611 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113446606 | TTGCTCTTGGATTAA[A/G]AGGTGTGAATCTCCC | 55779 |
rs776576526 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113334929 | ACATGAGCGTGTACA[C/T]ATAGCTCTCACAGGA | 55779 |
rs776599988 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396612 | AACTGAATATCAGCA[C/T]CCAAAATTTTCTTCC | 55779 |
rs776607566 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367280 | GGTCCCTGACCCCCA[C/T]GTAGCCTGAGAGACA | 55779 |
rs776614822 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416676 | AGAAAGATTTTTGTA[C/T]AAATAGTCTGATTAA | 55779 |
rs776622522 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402982 | TGTAAAAAACATACA[C/G]TGGGGCTCAAAAAGC | 55779 |
rs776629920 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113355806 | AAATTTAAGTATATA[C/T]AGAAATATCTAGCAC | 55779 |
rs776639489 | snp | A/G | 0.000149689 | 0.00864999 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341716 | TCACATATTAAAAAG[A/G]TAAGAGTTTAGGTAA | 55779 |
rs776674164 | snp | C/T | 1.81099e-05 | 0.00300909 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401317 | TAGTATTTTGTTTTA[C/T]CATTTTAAACTTTCA | 55779 |
rs776675459 | snp | A/T | 0.000100413 | 0.00708496 | missense, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380904 | TATTCCATACCAGAA[A/T]CTTAGATTTGACACT | 55779 |
rs776723665 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388676 | ATAAAGACACATATA[A/G]ACTGAAAGTAAAGGA | 55779 |
rs776728539 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363235 | TTTGATTTGCTCTCT[C/T]TTCCGTGCCTTTATT | 55779 |
rs776751014 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410111 | TCTGCCTATGGAGTA[C/G]CCATTCTTTTATTCC | 55779 |
rs776774018 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335770 | GAACACTATGCCAAG[A/C]AATGCAAGAAAGCAT | 55779 |
rs776783881 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331797 | GCTGAGAAAAAAGAC[A/G]AATAATACACTATTT | 55779 |
rs776791082 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302073 | ATATTGTCTTCCAAG[C/T]TTATCCATGTTGTTG | 55779 |
rs776791085 | snp | A/G | 1.68267e-05 | 0.00290053 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404061 | CATTAAAACAGGTAA[A/G]TGTACATATTTATGC | 55779 |
rs776807392 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113387402 | GGCCCCTATTCCAGG[A/C]CCTAGGTCCCAGATG | 55779 |
rs776819151 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113314131 | AGGAGTGAAGAAAGA[C/G]AATGAGGATGAAAAC | 55779 |
rs776819217 | snp | G/T | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327790 | AAGGAGACGGAGTTC[G/T]GCATCGAAAGTGACA | 55779 |
rs776820816 | in-del | -/C | 1.68505e-05 | 0.00290258 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401235 | AAGAATAATAGGCAA[-/C]TTACAATATTTGAAA | 55779 |
rs776821235 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303204 | CTGAAAATGTACATA[C/T]CCCTCTGTAACCCAG | 55779 |
rs776837479 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320322 | CCAGTGCAGCTGGAA[A/C]CTGACCCTGACCCTG | 55779 |
rs776846217 | snp | A/G | 9.71393e-05 | 0.00696851 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113303919 | TTAGATACTCACTGT[A/G]TATGGTTTTTGTCAT | 55779 |
rs776850747 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291320 | CTTCATATTCAATCT[A/C]GTAGGTTCGAAACAT | 55779 |
rs776869445 | snp | C/T | 1.9541e-05 | 0.00312572 | intron-variant, utr-variant-3-prime | CFAP44 | GRCh38.p7 | 3:113363083 | TACTTGTTGGGAAAA[C/T]AGTCATCTCTATCCA | 55779 |
rs776889611 | snp | A/G | 1.6473e-05 | 0.00286988 | stop-gained, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409209 | TCCTTAGTATGGGTT[A/G]TTCTTCTTTCCAGTT | 55779 |
rs776907642 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113306529 | AAATAATAATAGTAT[C/T]GATGTTGTGAGCAGT | 55779 |
rs776919739 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437485 | ACACTTTATTCTGTG[C/T]TATCTTAAACAATAT | 55779 |
rs776942542 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325967 | AGACAACCTTTTCAA[C/G]AAATGATACTACAGT | 55779 |
rs776947053 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425393 | TTTCTAACTACCCGC[A/G]TTGCAAACCTAACAT | 55779 |
rs776954093 | snp | A/C/G | 0.000206441 | 0.0101577 | missense, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113327796 | ACGGAGTTCTGCATC[A/C/G]AAAGTGACAACCAGT | 55779 |
rs776960709 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376440 | ACTGTGTAGTTACCT[C/T]AGCAAGAAAGAGGGG | 55779 |
rs777005495 | snp | C/G | 0.000121293 | 0.00778664 | intron-variant | CFAP44 | GRCh38.p7 | 3:113294871 | GAATACGAGAAGAAA[C/G]AAAGAAAAATGAGTG | 55779 |
rs777028574 | snp | C/G | 0.000148678 | 0.00862073 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379521 | CCTTCAACTCCCTTT[C/G]TCTCTCCCTCTTTTC | 55779 |
rs777030443 | snp | C/G | 3.30398e-05 | 0.00406434 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426260 | CTTCCACAGCTGGAG[C/G]AGGGGTTTGCTGAGG | 55779 |
rs777038814 | snp | A/G | 1.65348e-05 | 0.00287526 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286717 | CAGTTGAAGAGGTGG[A/G]CAGTCCTGACTCCTG | 55779 |
rs777068086 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409254 | TGTAGTCAGGGTTAC[C/T]ACCAACAGAGGCCAG | 55779 |
rs777072478 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446096 | TGGCACATCAAAATA[C/T]ATGAAGAACACATTA | 55779 |
rs777120452 | snp | G/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444110 | AATTGTTCACTCAGG[G/T]TGAGAATTCCTATCA | 55779 |
rs777123647 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322952 | CAAACATGTCCTCCT[-/C]CACATGGCAGCAGGA | 55779 |
rs777129029 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432100 | TAGATCCAGGACTCA[A/G]AACCAAAGTCCAGGT | 55779 |
rs777136412 | snp | A/G | 5.10504e-05 | 0.00505199 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420184 | CAAAAGAATGTCTGA[A/G]GGAAAGTTGCTAAGG | 55779 |
rs777211761 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113299666 | TGGAAGCGACTTACT[G/T]TCCCTCAACAGACAA | 55779 |
rs777217148 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413620 | AGCACCACTTACTGA[A/T]TAGGAAATCCTTTCC | 55779 |
rs777231159 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113338873 | GCTGAAGCTGGATAA[C/G]GAGGTCAAGGTGGAT | 55779 |
rs777247466 | in-del | -/AT | 6.76041e-05 | 0.00581356 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416679 | AAGATTTTTGTATAA[-/AT]AGTCTGATTAATGCA | 55779 |
rs777332180 | in-del | -/CT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429725 | ACCTGTCCTTTTTCC[-/CT]CTTTTTCTCTTTCCA | 55779 |
rs777334066 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113353021 | GAAAGCAGGAGTTAA[A/G]GAAAAGAGGATTTAA | 55779 |
rs777346573 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385607 | GTTAGGGCTATTTGG[C/G]CTATGGTGTTATACA | 55779 |
rs777352698 | snp | C/T | 0.000158519 | 0.00890137 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379325 | GAAACCCAGAACTTC[C/T]CTGGCTCTGAGTAAA | 55779 |
rs777366279 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347613 | ATTTTTGCCCAAAGC[C/T]CCATTGGGTGGGGAG | 55779 |
rs777374679 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398183 | GAAGAATAAGGCATG[C/G]TTGTCACCATGAAAA | 55779 |
rs777384130 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321105 | TATCTCTGATGAGCA[C/T]AGACGCAAAAATATT | 55779 |
rs777400320 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113361652 | AGGCACCCACCACCA[C/T]ACCTGGCTAATTTTT | 55779 |
rs777406064 | snp | A/G | 0.000102844 | 0.00717016 | synonymous-codon, intron-variant, missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113341917 | TATGGTAACACTCCC[A/G]CCTACATAGAGAATC | 55779 |
rs777407391 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324293 | ACCCTGATACTAAAA[C/T]CAGACAAAGACAGTA | 55779 |
rs777414606 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298921 | GGTGGTGATGGTTGC[A/G]CAATCATCTGAATGT | 55779 |
rs777420601 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324587 | AAAATTCATGAAAAA[-/G]AGGAACAGAGGTGAA | 55779 |
rs777441584 | in-del | -/AA | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286907 | TATTGTTTTTTTTTT[-/AA]AAAAAAAAAGAAGAA | 55779 |
rs777460152 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113399174 | TCCAACCCAGGTGAC[A/G]GCCTTGTGATCAAGA | 55779 |
rs777472716 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288761 | GAAATTTAGCACATG[A/G]CTCACAGACCTCCCT | 55779 |
rs777509389 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406980 | TAGTGATTGTTTTGC[C/T]AAATCGACCTAGTGA | 55779 |
rs777535398 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341401 | TAAAGATAAAGGTAC[A/G]AGCCAAAACTATAAG | 55779 |
rs777557004 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386565 | TAGGTTGTACAATCA[A/G]TAAGTCTTCCTGAAC | 55779 |
rs777572227 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113329170 | ACAATACTAATACCC[A/G]TGAAACAGCAAGGAA | 55779 |
rs777589127 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407518 | GACATAAAAGTTTTC[C/T]AAAGAATTCTAATTT | 55779 |
rs777596014 | snp | C/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113399940 | AGGGCAGTACCTCCT[C/T]GTTTGAATTTCATCT | 55779 |
rs777600466 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434281 | GGGGGTTAGAGAAGA[A/G]GTGTTTGAGACATGG | 55779 |
rs777625954 | snp | C/T | 3.35542e-05 | 0.00409585 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399859 | ATAGCATTGATATAC[C/T]ATATTTACCAATAGA | 55779 |
rs777627371 | snp | C/T | | | splice-donor-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330167 | CAGGTTCACCCCTTA[C/T]CCTGTTGACCAAATA | 55779 |
rs777644824 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375026 | AAGGAAATTCTGACA[C/T]ATGCTGCATCACGGA | 55779 |
rs777694615 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312677 | GGCCCAGGGTCCCCG[G/T]GCTGTGTGCAGCCTA | 55779 |
rs777745958 | snp | C/T | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441541 | ACAACGCCACCCCTC[C/T]TCCAGGGAGGCGGAA | 55779 |
rs777762013 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435150 | ACTGCTTGAGACCAG[C/G]AGTTCAAGACCAACA | 55779 |
rs777770787 | snp | C/T | 8.25416e-05 | 0.00642371 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286796 | CGTAGGACAGGAACC[C/T]GGAATGCAGCTCTCC | 55779 |
rs777786708 | snp | G/T | 1.64852e-05 | 0.00287094 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427257 | TTCCTCATCTGAGTC[G/T]TCTTCTAAATATGAT | 55779 |
rs777828849 | snp | A/G | 4.98062e-05 | 0.00499005 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409088 | TCTACTGGCACCTCT[A/G]TTGGTTACCCAACCT | 55779 |
rs777873614 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418546 | CCATAACTGGATAAC[C/T]GTTTCAGAAAAGATG | 55779 |
rs777882079 | snp | A/G | 1.7105e-05 | 0.00292441 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113380887 | AGATAATGCTTCAGG[A/G]ATATTCCATACCAGA | 55779 |
rs777883279 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431205 | GAAGAGACCTCTTCA[C/T]GCAGCAACAAGGTAC | 55779 |
rs777894715 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359805 | ACCACTAGCAGGTAC[A/G]TGGGGCTTTGCAATA | 55779 |
rs777902133 | snp | C/T | 1.72979e-05 | 0.00294086 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416480 | CCTTCTTCAGAATGT[C/T]GTTATCCTTGAACAT | 55779 |
rs777908758 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113372994 | GAATAGAGAAAAAAG[C/G]CCAATTTGAAATTTG | 55779 |
rs777951197 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113370238 | CATTTTATGAGGGCA[A/G]CATCATCCTGAAACC | 55779 |
rs777952433 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113365374 | AGGAATTTTAGCTAT[-/A]ATCTTTCTAATACAA | 55779 |
rs777974744 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336811 | TTGCCTAGTGAAGTT[A/G]GTAAAGACACTAACT | 55779 |
rs777994379 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327561 | GAAGAAAAAGAAATC[A/G]AGTTTCTCCATAACT | 55779 |
rs778000174 | snp | A/C | 1.6908e-05 | 0.00290753 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286682 | CCCCTCAGGGCCCCC[A/C]TGCTGCTTGGGCCTT | 55779 |
rs778009071 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113364748 | TACACAGTAGAATCA[C/T]ATGAAGGATAGTGTA | 55779 |
rs778034407 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383436 | AAGGGCTCCACCCTC[A/G]TGACCTAATTCCCTC | 55779 |
rs778040144 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438365 | GAGAATACTGGCTAC[A/G]GTCAGTCTGACTAGG | 55779 |
rs778047955 | snp | C/T | 0.00011753 | 0.00766492 | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330187 | TTGACCAAATACTGT[C/T]GCATGTACACGTGTT | 55779 |
rs778058764 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287528 | GTATTTGAAGAAAAT[A/G]CCCACTTACAATATT | 55779 |
rs778087433 | snp | C/T | 0.000101384 | 0.00711911 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330435 | ATCTTTACTTTTCAT[C/T]TGCTGTTGCTTAAAA | 55779 |
rs778088180 | snp | A/G | | | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286487 | AAATGGGTGGCAAGT[A/G]GCCCTCCCTGTTTTG | 55779 |
rs778094754 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386969 | GCACAACTCAGCCAG[C/T]GCCCACAGACAGAGT | 55779 |
rs778107821 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113397534 | AATGACATCCTAGCT[A/G]CAGTATGGAAAATAG | 55779 |
rs778129322 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409241 | CAGATAGTCAGTGTG[C/T]AGTCAGGGTTACTAC | 55779 |
rs778131554 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433677 | CATTTCCTCTGTAAG[C/T]ACAAAATGGGGATGA | 55779 |
rs778157900 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303544 | TGTATGTGTGCATAC[C/T]TGGTGGTGAACCCCG | 55779 |
rs778229858 | in-del | -/A | 0.000484555 | 0.0155577 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333610 | ACAGACAACCCCCCC[-/A]CACACAAATATGACA | 55779 |
rs778260331 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412268 | TTAGAAAACCCCATC[A/G]TCTCAGCTTAATAAA | 55779 |
rs778283363 | snp | A/C | 0.000447477 | 0.0149512 | intron-variant | CFAP44 | GRCh38.p7 | 3:113333603 | TAGAAAAACAGACAA[A/C]CCCCCCACACACAAA | 55779 |
rs778307685 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113377734 | CTCGGCTCACTGCAA[A/C]CTTCACCTCCCGGGT | 55779 |
rs778332613 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439331 | TGCTGGATAACTATC[C/T]CAAAAGACTGCAAAG | 55779 |
rs778336352 | snp | A/G | 0.000151458 | 0.00870092 | utr-variant-3-prime, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113287003 | TGTAAATAAATGTAT[A/G]TGTTTTATAATTCTG | 55779 |
rs778342530 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320511 | ATATATATCTAGATA[G/T]ACAGTACTTAATGAA | 55779 |
rs778351378 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426774 | GTACTACTACTGGCT[A/G]GAAGATAGGAAGCAG | 55779 |
rs778382324 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327544 | TGGGAGATTTGAGTT[-/AAG]AAGAAAAAGAAATCA | 55779 |
rs778386618 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354027 | GTAGCTGGAAAAAAA[C/T]TAGCCCTAGACTAAA | 55779 |
rs778388546 | snp | C/T | 1.67433e-05 | 0.00289333 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403836 | GTGCTACCATCCAAG[C/T]ATCGAGAAAACTTAC | 55779 |
rs778393254 | snp | C/T | 3.9514e-05 | 0.00444471 | intron-variant | CFAP44 | GRCh38.p7 | 3:113379298 | AAAATTATTACATTG[C/T]TACTTACCAAAGAAA | 55779 |
rs778433648 | snp | A/G | 3.3006e-05 | 0.00406226 | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396569 | TAAAGCAGTGACACA[A/G]GCAGTATGGGGTTTG | 55779 |
rs778467136 | snp | A/C | 2.31828e-05 | 0.00340453 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446568 | CCTATATGCATTTCA[A/C]AATTACATTTTAACG | 55779 |
rs778514724 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404205 | CCAATAACATTTTGA[C/T]GTATTTCCTTCCAGC | 55779 |
rs778539612 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331381 | AGCACATGCAACCCT[A/G]CTGTACTTCCTGTGT | 55779 |
rs778556119 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343011 | ATAAATAAAAAATTA[A/T]AAAAAAATGGCTGTA | 55779 |
rs778561104 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310201 | GCCTGTGGAGGCCAT[A/G]TGATAGCCTGGACTT | 55779 |
rs778591889 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417898 | GTAAAGAAATATGGT[A/G]TAGAACATATGGTCA | 55779 |
rs778644134 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113321019 | CCCTAAAACATTCTA[C/T]GAAACCAGCATCAGC | 55779 |
rs778653311 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426244 | ACTTCCTCCTCTGCT[C/T]CTTCCACAGCTGGAG | 55779 |
rs778654010 | snp | A/G | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443820 | GTACCTATCCCATAA[A/G]GTGTCATGAAGCACA | 55779 |
rs778660581 | snp | C/G | 1.66396e-05 | 0.00288436 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396691 | GAACAACTCCATCTT[C/G]AAATCCTACAATAAT | 55779 |
rs778678880 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445959 | ACAATTTTAAAGATA[G/T]CCTCACAATTTACCA | 55779 |
rs778692837 | snp | A/G | 3.32298e-05 | 0.004076 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445327 | ATACATGGGTAGAAA[A/G]AGCAAACCAGCCTTC | 55779 |
rs778697482 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113359302 | GTCTTCTTGACATCA[C/T]CAAGTTTTTGTTGAA | 55779 |
rs778697600 | snp | A/C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332869 | CAACGAAAAACTACA[A/C/T]CCAATGAGGATTTGT | 55779 |
rs778738217 | in-del | -/CAGC | | | | | GRCh38.p7 | 3:113295754 | CCTCTAAGACTGTAT[-/CAGC]CAAACAGTCTATGCC | 55779 |
rs778779845 | snp | C/T | 1.66203e-05 | 0.00288268 | intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404027 | AGCACCTGGCAGGTA[C/T]GTGGAAAAAAGAAAT | 55779 |
rs778802813 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339627 | CTGCTTTACATTGTG[C/G]CTGTTGCCTGGCTTT | 55779 |
rs778807014 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432833 | TTCTGGAATCTCCTG[A/G]TAAATATTCCCACAT | 55779 |
rs778815278 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113311529 | ATGTTTCTGAGGCAT[C/T]CCCAGCCATGTGGAA | 55779 |
rs778820928 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393592 | TGGAGCGCAGTGGCA[C/G]GATCTTGGCACACTG | 55779 |
rs778839680 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322547 | ATGAGACACCATCTC[A/G]CACCAGTCAGAATAA | 55779 |
rs778844145 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322168 | TGGTACAAAAACAGA[C/T]AGACACATAGACCGC | 55779 |
rs778856103 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327884 | ATTTTTAAACTATCT[A/G]ACAGTACTAATTTGT | 55779 |
rs778868501 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298687 | CTGACACATGCTACA[A/G]CACGGATAAACCTGA | 55779 |
rs778896694 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113418957 | GATCCACCCGCCTCA[C/G]CCTCCCAAAGTGCTG | 55779 |
rs778926063 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297761 | CCTCTCCAAGAAAAC[A/G]TAATCTTGTAACAGG | 55779 |
rs778926335 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325705 | TTTTTTGTAGATATA[-/AAG]AAGATTATTCTAAAA | 55779 |
rs778943334 | snp | A/C | 1.65048e-05 | 0.00287265 | missense, intron-variant, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409115 | ACCTACTTGATGTGG[A/C]CTGATCCCGATGTAG | 55779 |
rs778948456 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363210 | GATTACAAAATTCAC[C/T]CCTCAAAGCTTTGAT | 55779 |
rs778953085 | snp | C/T | 0.00015075 | 0.00868057 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113330161 | TAGGAACAGGTTCAC[C/T]CCTTACCCTGTTGAC | 55779 |
rs778972570 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427153 | TTGTCTCTAAAACAG[C/T]GACAATTACTGACAG | 55779 |
rs778995540 | snp | A/C | 8.33229e-05 | 0.00645403 | intron-variant | CFAP44 | GRCh38.p7 | 3:113363330 | CAGAAATTTAAAACA[A/C]TAACAGGTTGTGATA | 55779 |
rs778996756 | in-del | -/AGC/AGCTT | 8.77807e-05 | 0.00662447 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409360 | ATAAATAAGGACACA[-/AGC/AGCTT]TTTATTTCATTTTCA | 55779 |
rs779026888 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113315715 | ATTTGGTAGAAACCA[C/G]ACTTCAAGTACTCAT | 55779 |
rs779090865 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP44 | GRCh38.p7 | 3:113441911 | GTTATTTTTAAAACT[A/G]TATTATCTCTGTTGG | 55779 |
rs779112167 | snp | A/G | 2.17214e-05 | 0.00329549 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400511 | ATAAAACAAAACAAG[A/G]CCAGACATATTTTTA | 55779 |
rs779119233 | snp | C/T | 1.8121e-05 | 0.00301001 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395906 | TATATTACTATGAAA[C/T]CTAGCCTATAGATCA | 55779 |
rs779135074 | snp | A/C | 1.64819e-05 | 0.00287066 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433539 | AGTTTAATACTTTTA[A/C]AAGTATACATATTAT | 55779 |
rs779162876 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113325999 | AATGAAAAGGCAAGC[A/T]ACGCACTAGGAAAAA | 55779 |
rs779175721 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113394834 | GGCTATGGGATGGAC[A/C]AGCTTGGTCTACACC | 55779 |
rs779202601 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366223 | CAGTAGTCCACCAAA[C/T]TGGTCAATGAAGGAT | 55779 |
rs779229935 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293150 | CCTCATACACCAACT[A/C]ATGCCCAGTCATTCC | 55779 |
rs779236136 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350541 | TATAATTGATAATTG[A/G]CAGTCTTCTCCATGA | 55779 |
rs779243420 | in-del | -/TTCAT | 1.67089e-05 | 0.00289035 | intron-variant | CFAP44 | GRCh38.p7 | 3:113399884 | AATAGATTCTGGTAG[-/TTCAT]TATAACAACAAACTT | 55779 |
rs779252782 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113388107 | CCTGGACCTGCCTGA[C/T]GATCTCACCACCCTG | 55779 |
rs779270351 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313951 | ACAGCAGAATAGAAA[C/G]GAGACAGAAGAGAAT | 55779 |
rs779285578 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416233 | ATTTTCCTCCATTCC[C/T]TTGTTTTGAGCCTGT | 55779 |
rs779302516 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324926 | AATAAGTAAGGTTAC[A/G]GGATATCAGCTAAAC | 55779 |
rs779325629 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113301782 | TTCATGTTGTGAGAA[A/C]ACTTAAAATTTACTC | 55779 |
rs779333619 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436830 | TGTAAGTAGGTACTG[C/T]TTAGTTTTCCATTGC | 55779 |
rs779365864 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385212 | AACTGTGAGTCCATT[-/A]AACCTCTTTTTATTT | 55779 |
rs779373057 | in-del | -/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331390 | AACCCTACTGTACTT[-/C]CTGTGTGCAGTTAGG | 55779 |
rs779396543 | in-del | -/CAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327397 | TACCTTACAGAATAT[-/CAG]ACCAAATTTACTAAA | 55779 |
rs779401967 | snp | A/G | 1.65496e-05 | 0.00287655 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373428 | GAAAGTGATAGTTTG[A/G]ATGGGATTGTCCTCT | 55779 |
rs779427276 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424368 | TTGAACCCGGCAGGC[A/G]GAGGTTGCAGTAAGC | 55779 |
rs779460034 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432774 | CCTTCTTGAACAACT[C/T]GCTTTTCTAAAACTA | 55779 |
rs779491276 | snp | C/T | 0.00018182 | 0.00953293 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420109 | GTTGGTTCCCAGCTA[C/T]GTATATGGCGATACT | 55779 |
rs779493411 | snp | C/G | 1.66466e-05 | 0.00288496 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401576 | CAAGAGACAAGAATG[C/G]AACACACCTGAGCCA | 55779 |
rs779504165 | snp | A/G | 0.000105949 | 0.00727759 | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291554 | TTTGAGAAAATAGCA[A/G]ACTCAAAGGTCTGCG | 55779 |
rs779516865 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331201 | TGAATTTCAGTAGCA[C/T]GTCACACCAAGAGAC | 55779 |
rs779532800 | snp | G/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395812 | TAATATAACCAATCG[G/T]CTTATAATCCCTTTC | 55779 |
rs779534055 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113402499 | GCTCATTCTGGACAG[G/T]TCTGGCAACATACCC | 55779 |
rs779553068 | in-del | -/A | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113412416 | TCTTTTATTTCTTCT[-/A]AAAAAAAAAAAGATA | 55779 |
rs779555744 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424189 | ACACCTGTAATCCCA[A/G]CATTTTGGGAGGCCA | 55779 |
rs779587601 | snp | A/T | 1.91985e-05 | 0.0030982 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396757 | AAGATAAGGGACCTG[A/T]AACTAGTTAAATTGA | 55779 |
rs779615233 | snp | G/T | 1.64906e-05 | 0.00287142 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403993 | CCAAAGCAGCATGTT[G/T]CCCCATTCTGACCCT | 55779 |
rs779617428 | snp | A/C/G | 0.000102759 | 0.00716722 | intron-variant | CFAP44 | GRCh38.p7 | 3:113305029 | GCAGCCTCCCCAGAC[A/C/G]CATCACCTGGTGGAG | 55779 |
rs779617993 | snp | C/T | 1.65485e-05 | 0.00287645 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113401721 | CATCAGCAGTGTCTA[C/T]TGTCTCAAAATCCCA | 55779 |
rs779624748 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368098 | GACTATGTGAAAAGA[C/T]CAAATCTACATTTGA | 55779 |
rs779631389 | snp | A/G | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396672 | TCATAAAGTTCAAGA[A/G]TTCGAACAACTCCAT | 55779 |
rs779651702 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113422884 | TCCCTTTTACATGCT[A/G]CTGCCCTGATAAAAG | 55779 |
rs779697903 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343543 | GGCCTGTGTGGTCAT[C/G]GGAAGGCCTTATAAA | 55779 |
rs779699917 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307664 | TAGAAGTTGAATATT[A/C]TTGAATAAAGAAATA | 55779 |
rs779709462 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113319685 | GACCACATGCTTGGT[A/C]ATAAAGCAAGAAGAA | 55779 |
rs779714449 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113344720 | CTCGAAATCTGAAAA[A/C]ATAAAACAAGTATTT | 55779 |
rs779733415 | in-del | -/TCTT | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406221 | TATAAAGTGGTTTGC[-/TCTT]TCTGAGTAATAATCT | 55779 |
rs779736796 | snp | C/G | 1.66156e-05 | 0.00288228 | missense, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445320 | ACTTATGATACATGG[C/G]TAGAAAGAGCAAACC | 55779 |
rs779739939 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113437949 | AATATGTAAAATGAG[A/G]GTGATAGGGTTATTT | 55779 |
rs779752593 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113376680 | TAGTGAAGTGATGGA[A/G]ATATCCCAACTGGAA | 55779 |
rs779760160 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113424973 | TAGCACAGTAGGTCC[C/T]GGAAGGCATCAGAGC | 55779 |
rs779781088 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297488 | ACGGCTTGCTCCTCC[C/T]AGCCCATTTTCTAAA | 55779 |
rs779793040 | snp | A/G | | | utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113444749 | CTCTTACCTGCTTAA[A/G]CAAATATAAACAAAC | 55779 |
rs779802641 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113291016 | TCCTGAATCCTGAGC[A/C]CTCAAAACACTGCTT | 55779 |
rs779803075 | snp | A/C | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362645 | TGTGCATCAGAGTGC[A/C]GGGATGCACATAGGA | 55779 |
rs779813584 | snp | C/T | 1.69103e-05 | 0.00290773 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400587 | AAGTGAGAGGAGAAA[C/T]AGCCACGGCTTCAAT | 55779 |
rs779828370 | snp | A/G | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379801 | TTTTTTTCATAATAG[A/G]GAAGCTAAATATAAC | 55779 |
rs779844934 | snp | C/T | 8.23771e-05 | 0.0064173 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426210 | ATCATAGAAGAAGCT[C/T]TCTGATATTTTCTTC | 55779 |
rs779845733 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113410527 | TTATATGTGCCACAT[C/T]TTCTTAATCCCGTCT | 55779 |
rs779877379 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113308920 | CCTGAAAAGATTTTC[A/G]TAAGTTATCTGAAAT | 55779 |
rs779905944 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113431452 | TCCAGGAAAACACTG[C/T]CGAGGACTGGAAACC | 55779 |
rs779929601 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351281 | TAACAGTGTAACATG[A/T]ATTATTCTAACTCTA | 55779 |
rs779948250 | snp | C/T | 0.000100065 | 0.00707266 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296826 | GCGTTTGAAGGGCTT[C/T]TAGATTTACCACACG | 55779 |
rs779952280 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320883 | GTGGGTCTACCTTTC[C/G]CAGCCCACTGACTCA | 55779 |
rs779981703 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297445 | CCTCATTTCCTCCTA[C/T]CTGAACTGCTCTTCC | 55779 |
rs779993984 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113432681 | CACAAAAAAACTATA[A/G]TGAAGTCCATGCTTA | 55779 |
rs779996047 | snp | A/C | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113417622 | TGCTAATCCTGGTAC[A/C]CAAGATAACATTATT | 55779 |
rs779997628 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113328948 | TGTCTTTCTTAAGAA[C/T]TGTTGTATCCCTAAT | 55779 |
rs780047666 | snp | C/G | 3.31686e-05 | 0.00407225 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363301 | TTTTCTCCTAGCATT[C/G]TCGATACTGAAAACA | 55779 |
rs780050671 | snp | A/G | 0.000110284 | 0.00742495 | intron-variant | CFAP44 | GRCh38.p7 | 3:113327581 | TCTCCATAACTAAGG[A/G]ACCAGCCAGCTAGGA | 55779 |
rs780058882 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113335743 | ATCCTCTTGTCCTAA[C/T]TGACATTTATAGAAC | 55779 |
rs780086350 | snp | C/G/T | 4.94469e-05 | 0.00497206 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427187 | ACTAATAATACCTAC[C/G/T]TGTAGTGCTTTGCAA | 55779 |
rs780101411 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379473 | CTCCCATCTCTGCTG[A/C]TAGCTTGTTCCTCCT | 55779 |
rs780103395 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318410 | TAAATGAACCAAATC[C/T]CTGAAACATATGAGA | 55779 |
rs780103861 | snp | C/T | 1.68704e-05 | 0.00290429 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366040 | AATTAATTACATACC[C/T]TGGGAGATGGAACTT | 55779 |
rs780105667 | snp | G/T | 1.80166e-05 | 0.00300133 | intron-variant | CFAP44 | GRCh38.p7 | 3:113396739 | TTACCTTGGAGAAAA[G/T]TAAAGATAAGGGACC | 55779 |
rs780184916 | in-del | -/A | 0.000470588 | 0.0153321 | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341730 | GATAAGAGTTTAGGT[-/A]AAAAAAAACTCACAG | 55779 |
rs780199280 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113356947 | CATACATGTCATATA[C/T]GTAGTCACTCATATA | 55779 |
rs780209905 | snp | A/G | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395808 | GTATTAATATAACCA[A/G]TCGGCTTATAATCCC | 55779 |
rs780239162 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113310664 | TCTCATGTTGAACTG[C/T]AATCCCCAGTGTTGG | 55779 |
rs780253576 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318815 | GAACCAAGAATTTCA[C/T]ATCCTGCCATACTGT | 55779 |
rs780258914 | snp | A/C/T | 3.31319e-05 | 0.00407002 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409096 | CACCTCTATTGGTTA[A/C/T]CCAACCTACTTGATG | 55779 |
rs780259233 | snp | A/C/T | 3.33624e-05 | 0.00408415 | intron-variant | CFAP44 | GRCh38.p7 | 3:113401568 | TAAAGAGCCAAGAGA[A/C/T]AAGAATGCAACACAC | 55779 |
rs780270352 | snp | C/T | 3.53426e-05 | 0.00420357 | intron-variant | CFAP44 | GRCh38.p7 | 3:113395895 | CCGACGAAATATATA[C/T]TACTATGAAATCTAG | 55779 |
rs780270435 | snp | C/T | 1.70493e-05 | 0.00291965 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363528 | GGCTCTGTTTCAATT[C/T]CAAACTATAGGAAGG | 55779 |
rs780296838 | in-del | -/T | 1.65466e-05 | 0.00287628 | frameshift-variant, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433578 | ACATCTTGATTCTGA[-/T]TTAGAAGACCTCAGA | 55779 |
rs780302144 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113368023 | AATGAAATAAAGCAA[A/G]AAGACAAGATTAGAG | 55779 |
rs780317262 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393516 | AGAGCCTGGCACCTC[A/C]CCACTCCCTCTTTTG | 55779 |
rs780332505 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317756 | GAGTTCCTGGGCTGG[A/G]GTGAGAATGGGGCTT | 55779 |
rs780359254 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313096 | TGCACCTGGAAAAGC[C/T]GCAGACGCTCAATGC | 55779 |
rs780363277 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113313081 | CAACAGCTTGCACCG[C/T]GCACCTGGAAAAGCC | 55779 |
rs780364561 | snp | C/T | 1.90098e-05 | 0.00308294 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381082 | AAGAAAAATTGAACA[C/T]ATTTACATTTAGGCA | 55779 |
rs780370342 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113348199 | TGCAGGTTCTTGGGT[C/T]GGGGGGAAGTAAACA | 55779 |
rs780385377 | snp | C/T | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113306282 | CTCCTCAATGTCCAG[C/T]CTTTTCTCTCGAAGG | 55779 |
rs780394524 | snp | C/T | 1.64969e-05 | 0.00287196 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427275 | TTCTAAATATGATCC[C/T]TCCCCTTTGGTAAAT | 55779 |
rs780402631 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366772 | TGTTGCCTCACCTGG[A/G]AAGCGCAAGGGGTCA | 55779 |
rs780421986 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113323754 | CCCAATATGAAATAG[A/T]TCATTTGGGCTGGGT | 55779 |
rs780438195 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113347704 | AGCTAGGATGTGGGG[-/A]GCTTCAGAAATGATA | 55779 |
rs780450938 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113427871 | TGGTTAAAATATACA[A/G]TGCCAAGCAGGATGG | 55779 |
rs780473739 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113371096 | GGACACAAACAAATG[A/G]AAGAACATTCCATGT | 55779 |
rs780491998 | snp | A/G | 1.66466e-05 | 0.00288496 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420011 | TCTAATTTATTGAAG[A/G]CATACCCCAATGACG | 55779 |
rs780502962 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407958 | CCCAAAGATATGGGG[C/T]ATAGAAAATACAGAT | 55779 |
rs780555312 | snp | A/T | 7.28129e-05 | 0.00603334 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286909 | TTGTTTTTTTTTTAA[A/T]AAAAAAAAGAAGAAA | 55779 |
rs780562305 | snp | A/G | 1.66838e-05 | 0.00288818 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113373509 | ATCACTGCTTTCATC[A/G]CAAGGGGGGAACTCA | 55779 |
rs780608607 | in-del | -/TA | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113341601 | TCCAGCTGACCTGTT[-/TA]TAATATCTCCTTCTT | 55779 |
rs780621604 | snp | A/T | 3.72835e-05 | 0.00431745 | intron-variant | CFAP44 | GRCh38.p7 | 3:113400710 | ATTAAGATCAAGTTT[A/T]AAAAAATGCAAAGAT | 55779 |
rs780632889 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330292 | ATATCTAGGCTGAAT[A/G]TTGATGCCTTTGATG | 55779 |
rs780643205 | snp | C/T | 2.48185e-05 | 0.00352259 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446559 | ACCCTCACCCCTATA[C/T]GCATTTCACAATTAC | 55779 |
rs780658912 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302061 | ATTTCACTTAACATA[C/T]TGTCTTCCAAGTTTA | 55779 |
rs780661075 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113327070 | ATGTTACTATTTAGC[A/T]TATACTATCTGTTTA | 55779 |
rs780669248 | snp | C/G | 0.000580832 | 0.0170317 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113296805 | CAAGTGTTGTATTAA[C/G]AGAAAGCGTTTGAAG | 55779 |
rs780698384 | snp | G/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113416033 | CTTGTTTTATGAATC[G/T]GGGTGCTCTGTATTG | 55779 |
rs780698829 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113435249 | ATGGGTAATTTATAA[A/C]GGAAAGGGGTTTAAT | 55779 |
rs780714673 | snp | C/T | 0.000102981 | 0.00717496 | synonymous-codon, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113333514 | GAAATCTCCCATATA[C/T]ACCTGGGCTTCTTTG | 55779 |
rs780714903 | snp | A/G | 1.68661e-05 | 0.00290392 | stop-gained, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113363150 | TTAGGCTTACTGTTC[A/G]TTTAAACTGCATATG | 55779 |
rs780745079 | snp | C/G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354615 | CACACCTCCATCCCC[C/G/T]ACAGCAGCCACAGCA | 55779 |
rs780751479 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393902 | CATGACTACAAGCCC[A/G]TGAGGCCCTCACCAG | 55779 |
rs780752618 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304410 | CATACTAGGCAAACC[A/G]CTCCATTTAGCTCAT | 55779 |
rs780756828 | snp | A/G | 6.62241e-05 | 0.00575392 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113426114 | ATACATATTTAGCCA[A/G]GGTGGATACACAAGT | 55779 |
rs780757935 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113343446 | AATATGAGATATTTA[C/T]ATAGTTATAAATAAC | 55779 |
rs780767994 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375089 | AGCCAGTCATAAAGA[C/G]ACAGATACTATATAA | 55779 |
rs780785398 | snp | A/C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113324557 | TCTGACAAATTTTCA[A/C/T]CCCCATTCACGAAAA | 55779 |
rs780789774 | snp | A/C | | | synonymous-codon, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400585 | ATAAGTGAGAGGAGA[A/C]ACAGCCACGGCTTCA | 55779 |
rs780793496 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113386718 | ATCTACACACACACA[A/C]AAACACCTTGCTAAG | 55779 |
rs780794346 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113367871 | AATGGCTAACTAGAA[C/T]GAACAGTGTAGAGAA | 55779 |
rs780794644 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389294 | GTCAATGAAGAAATT[-/AAG]AAGAAAATTTAAAAA | 55779 |
rs780797405 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113434418 | AGAGTAAAATGGATA[C/T]TGAAGAGAAGGTGGG | 55779 |
rs780798708 | in-del | -/AT | 1.65248e-05 | 0.00287439 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113380945 | AAACATTTTATGCAC[-/AT]GTCTTTGATTTCATA | 55779 |
rs780850994 | snp | C/T | 0.000140875 | 0.00839152 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113293991 | GCTGATGCTCTTCTT[C/T]AGAGGACCAAACTGT | 55779 |
rs780880271 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354336 | CCATGCAGGTTCCCT[C/G]AGATGCCAAAAAACT | 55779 |
rs780909216 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113318215 | GAAGAAAACCAAATT[G/T]TTAAAGTTTTTAAAC | 55779 |
rs780934613 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113330299 | GGCTGAATGTTGATG[C/T]CTTTGATGATCTAGA | 55779 |
rs780955357 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113398105 | GTTGAATGTTGTTTA[A/T]CCAATAAAAATTTAC | 55779 |
rs780957030 | snp | C/T | | | intron-variant, utr-variant-5-prime | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113425436 | ACGAACACAAAATCC[C/T]CTTGTCAATCATCCT | 55779 |
rs780975006 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113375745 | AGAATCACTTGAGCC[G/T]GGGAAGTAGAGGCTG | 55779 |
rs780985141 | snp | A/T | 0.00015841 | 0.00889832 | intron-variant, downstream-variant-500B | CFAP44, BOC | GRCh38.p7 | 3:113286660 | TTTAATGGTTCCTAC[A/T]CTTTCTCCCCTCAGG | 55779 |
rs780990198 | snp | C/T | 3.30907e-05 | 0.00406746 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113420127 | ATATGGCGATACTGT[C/T]GTCCAGAAGTTGTAG | 55779 |
rs781005336 | snp | C/T | 3.48008e-05 | 0.00417123 | synonymous-codon, missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113379330 | CCAGAACTTCCCTGG[C/T]TCTGAGTAAAATCCA | 55779 |
rs781031925 | snp | C/T | | | intron-variant, downstream-variant-500B | CFAP44 | GRCh38.p7 | 3:113362293 | AGGGACAGGAGGGGG[C/T]GGCAAGGTGACAGTA | 55779 |
rs781062863 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113331142 | CATTCTGTATTTTGG[C/T]CACATGATTATTGTT | 55779 |
rs781074198 | in-del | -/TT | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113312074 | CTGTGTGTGTGTGTG[-/TT]TTTTTTTTTTTTTTT | 55779 |
rs781086676 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113407673 | ATCATATCAAAGCAA[A/T]CAATAAATGTTATTA | 55779 |
rs781103158 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339550 | AGTACCTTGGGCCTG[C/T]TTATGCCATGAAGCA | 55779 |
rs781104816 | in-del | -/AAACA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113342332 | GTGAGACTCTGTCTC[-/AAACA]AAACAAAACAAAACA | 55779 |
rs781127003 | snp | C/T | | | utr-variant-3-prime, intron-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113443519 | CATACCTCTAACTGA[C/T]AGGTCTACTATGAGA | 55779 |
rs781136397 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113339279 | ATACACTCCAGCTGG[A/G]GGTGGTGAAGAGAAC | 55779 |
rs781139323 | snp | C/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113429295 | TTATGATGCTGTTAC[C/T]AGGTGAATACACATT | 55779 |
rs781147522 | snp | A/G | 1.99463e-05 | 0.00315797 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446679 | AGCCCCGGAAGATCT[A/G]TTCATGAAAAATAAA | 55779 |
rs781151318 | snp | A/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113423796 | ACCATTCAAGAATTC[A/G]GCAGCCTTCTGAGCC | 55779 |
rs781154425 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113357525 | GGCAAACCACTAGAA[A/G]CTTGGAGACAGGTAT | 55779 |
rs781154881 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393719 | CAGGGTTTCACTATG[C/T]TGCCCAAGCTTGTCT | 55779 |
rs781192617 | in-del | -/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113351124 | GCACTCAGCCAAACA[-/T]TAAAGTACTTACAGA | 55779 |
rs781225240 | in-del | -/A | 1.6607e-05 | 0.00288153 | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113409088 | TCTACTGGCACCTCT[-/A]TTGGTTACCCAACCT | 55779 |
rs781242084 | snp | C/T | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113395800 | GTCCAGGAGTATTAA[C/T]ATAACCAATCGGCTT | 55779 |
rs781301776 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354200 | GGCAGGATTAGCTTG[C/T]GGATGGGGACAGAGC | 55779 |
rs781358249 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113385208 | GAGGAACTGTGAGTC[C/G]ATTAAACCTCTTTTT | 55779 |
rs781402539 | snp | A/G | 1.8e-05 | 0.00299995 | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381068 | CTTTCAGGCTAAAAA[A/G]GAAAAATTGAACATA | 55779 |
rs781453140 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113288529 | GGTGGGTAGGGCTGA[C/T]GCTCTCAGTCATTGC | 55779 |
rs781471527 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113404203 | TACCAATAACATTTT[C/G]ATGTATTTCCTTCCA | 55779 |
rs781476419 | in-del | -/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113302015 | CTGCATATAAGTGAT[-/G]GTCATGTGGTATTTT | 55779 |
rs781489565 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113391133 | CAGCATGGTACTGAC[A/G]TAAAAACAGAAACAC | 55779 |
rs781492648 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113322460 | CTCAAAAGATTACCT[A/G]CAAGCAGGCAACAAA | 55779 |
rs781503926 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113297208 | CAAATATGGCACTTT[A/T]CAGCATCTAGTATTA | 55779 |
rs781509749 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113438577 | AATTTATTGATATAT[C/T]CCTGAATAGATGAAA | 55779 |
rs781512164 | snp | A/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286905 | TATATTGTTTTTTTT[A/T]TAAAAAAAAAAAGAA | 55779 |
rs781516982 | snp | C/G | 6.93553e-05 | 0.00588837 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113400621 | TCCAGAATGGAAGGA[C/G]AAGAGGCATTCTGGG | 55779 |
rs781548123 | snp | A/T | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113413673 | TTGCCAAAGATCAGA[A/T]GTGTGGTGTTATTTC | 55779 |
rs781548215 | in-del | -/AA | 0.00010084 | 0.0071 | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113445370 | CTCAATCTGTTGAAC[-/AA]AGACACGGAAAAAAT | 55779 |
rs781567905 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113333892 | CATTGTTATTTATTC[A/T]CTTGATATAAATTAA | 55779 |
rs781568461 | in-del | -/AAG | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113336108 | ATGTTTATATTACAA[-/AAG]AAGAAGGGCATAGAA | 55779 |
rs781598969 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113389748 | GCAAGTAAATTTTAA[A/G]ACCTTGAAGAAATAG | 55779 |
rs781599836 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113439462 | ATCACACTTATTGTT[C/G]ATCTTTGTAGCCAAG | 55779 |
rs781610197 | snp | C/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113304728 | GTGAAAAGTGGCATG[C/G]GTATAAGAGCCAAGA | 55779 |
rs781615610 | snp | C/T | 1.66297e-05 | 0.0028835 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | SPICE1, CFAP44 | GRCh38.p7 | 3:113445306 | TGAGACTTGACTTCA[C/T]TTATGATACATGGGT | 55779 |
rs781647768 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113293209 | TCCCCTTCTCCTCAC[C/T]AGACTCAATCAAATT | 55779 |
rs781674805 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113309519 | TTTATAATATCATAT[C/T]ATATATAATATCTTC | 55779 |
rs781680660 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113317633 | ATATCCCAGTGTCTC[C/T]AGGGCCGTGGTGCAC | 55779 |
rs781683003 | snp | A/C/T | 4.9626e-05 | 0.00498106 | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1, MIR8076 | GRCh38.p7 | 3:113433697 | AATGGGGATGAGATA[A/C/T]GGATAAAGCTGTAAA | 55779 |
rs781687661 | snp | A/G | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396642 | CGTCCCGCAAAAATC[A/G]TGAGCCCTTTTGGAT | 55779 |
rs781717135 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113440351 | CAGGCGTCAGCCACC[A/G]CGCACAGCCTATTAT | 55779 |
rs781723779 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113414915 | CCTTTTCAAATGTCT[C/G]GAATAGTTTCAGAAG | 55779 |
rs781736933 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPICE1, CFAP44 | GRCh38.p7 | 3:113446372 | AAGGACTGTTGAATA[G/T]CCTATTGAATTTTAC | 55779 |
rs781745833 | snp | C/T | 1.651e-05 | 0.0028731 | missense, intron-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113366274 | ACTCGAATTGCTCCA[C/T]TTTTCATTCCACAAA | 55779 |
rs781750898 | snp | A/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113332493 | AATATAACCATGATG[A/T]GATTGGCACCCTCTC | 55779 |
rs781759814 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113379277 | TATTGAAATATGATT[A/G]AGGTAAAAATTATTA | 55779 |
rs781782759 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113366576 | CTCATAAGAAGAAGA[G/T]ATCAAAGGGGGTCAC | 55779 |
rs796115776 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113383759 | TAGCTGACCTTTTTT[-/A]AAAAATTATACTTTA | 55779 |
rs796171668 | in-del | -/AA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113354099 | CAAAAAAAAAAAAAA[-/AA]TCTTTTTCCATGTAA | 55779 |
rs796206817 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113436664 | AGTATTGGAAAGTAC[C/T]CCCTAAGTTTCCAAG | 55779 |
rs796218121 | in-del | -/TA | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CFAP44, BOC | GRCh38.p7 | 3:113286906 | ATATTGTTTTTTTTT[-/TA]AAAAAAAAAAGAAGA | 55779 |
rs796312328 | in-del | -/CT | | | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113441477 | TGACCGCCGCGGCTC[-/CT]CTCTTCACAGCGTCT | 55779 |
rs796326331 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113403105 | AAAAAGAAAAAAAAA[-/A]GAATCTTACTTTTGA | 55779 |
rs796332736 | snp | C/G | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113406494 | CCAGGCATGGTGGCA[C/G]GCGCCTGTAGTCCCA | 55779 |
rs796385666 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113298169 | GCATGGCAGCCTCAT[A/G]TACCAGAACATGTAC | 55779 |
rs796395357 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113290189 | CACAGAAAGTGATTT[-/A]AAAAAAAAAAGTGGG | 55779 |
rs796435685 | in-del | -/CA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320254 | TCTCTCTCTCTCTCT[-/CA]ATATATATAGATCTA | 55779 |
rs796444753 | in-del | -/A | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SPICE1, CFAP44 | GRCh38.p7 | 3:113444499 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55779 |
rs796456905 | in-del | -/TG | | | intron-variant | CFAP44, CFAP44-AS1 | GRCh38.p7 | 3:113430428 | AGCTGGAAAAATAAA[-/TG]AAAAAAAAAAAAAAA | 55779 |
rs796466056 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113396159 | AAGAATTTACACAGT[C/T]ATTCTCTTCATTTAT | 55779 |
rs796499538 | snp | G/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113303269 | TGCACAGGGAGATGT[G/T]TACAAGAAGGTTTCC | 55779 |
rs796532705 | in-del | -/T | | | intron-variant, utr-variant-5-prime | CFAP44 | GRCh38.p7 | 3:113379785 | GAAATTATTTGGTCA[-/T]TTTTTTTCATAATAG | 55779 |
rs796535666 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP44 | GRCh38.p7 | 3:113381805 | AAGTGGTAGGGATAA[A/G]TTTATAATAAGAAAA | 55779 |
rs796588240 | snp | C/T | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113350570 | GACCTTATAACACTC[C/T]AATACCACCTTGTTG | 55779 |
rs796611771 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113393641 | CCACCTCAACCTCCC[A/G]AGTAGCTGGGACTAG | 55779 |
rs796709291 | snp | A/G | | | missense, nc-transcript-variant | CFAP44 | GRCh38.p7 | 3:113396580 | CACAAGCAGTATGGG[A/G]TTTGAAAACCTGTTT | 55779 |
rs796757421 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113320423 | ATACATGATATATAT[A/G]TGATATATATTGATA | 55779 |
rs796838624 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307935 | CAGTGAGCCGAGATC[A/G]TACCACTGTACTCCA | 55779 |
rs796858618 | snp | A/G | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113307676 | ATTATTGAATAAAGA[A/G]ATAAATATCCTAGCT | 55779 |
rs796967486 | snp | A/C | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113345030 | AATAGATCATATCAA[A/C]TTCTGAGGAAATAGA | 55779 |
rs797004636 | in-del | -/TTA | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113296083 | TGGAGTCCCCAGTGT[-/TTA]TTATTTTCATCTTTA | 55779 |
rs797017796 | in-del | -/A | | | intron-variant | CFAP44 | GRCh38.p7 | 3:113360079 | TCTTATCTTGTTACC[-/A]AAAAAAAAAAAAAAG | 55779 |