SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1180888 | snp | C/G | 0.288879 | 0.246958 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515473 | GTTTAAGTCTTTTGA[C/G]GAAGGGAAAACAGAG | 142684 |
rs1180895 | snp | A/T | 0.303826 | 0.244137 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500623 | TCGATCCCCCCGAGA[A/T]GGCTGTACGGGGACT | 142684 |
rs1180896 | snp | C/T | 0.438958 | 0.163691 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506318 | ctgagtttccagtgt[C/T]cattatTAATTATAA | 142684 |
rs2858077 | snp | A/T | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512981 | TACACATGTTATCAT[A/T]CCTAACGGTGAGCAA | 142684 |
rs2858078 | snp | C/T | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512980 | ACACATGTTATCATT[C/T]CTAACGGTGAGCAAC | 142684 |
rs5903216 | in-del | -/G | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513490 | AATATTAAACCGAAA[-/G]GAAAATATACACATG | 142684 |
rs5945784 | snp | C/T | 0.145864 | 0.227279 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506301 | actcccacctccccc[C/T]tctgagtttccagtg | 142684 |
rs5945785 | snp | A/C | 0.0142023 | 0.083063 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103516679 | AAAATATCAATAGCC[A/C]GCAATCCCATCATAA | 142684 |
rs5987466 | snp | C/G | 0.158238 | 0.232551 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103514597 | ctcaagtgatccacc[C/G]gtctcaacctcccag | 142684 |
rs5987535 | snp | C/G | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509321 | TCTCTCTCTCTCTCT[C/G]TCTCTCTGTCTCTCT | 142684 |
rs5987536 | snp | C/T | 0.286808 | 0.247275 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103511371 | aggcaggtgtggtgg[C/T]gggcgcctgtagtcc | 142684 |
rs6616477 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500984 | GCACAGAGTAGTGAC[A/G]CAGCAGTTAATTCAT | 142684 |
rs6652889 | snp | C/G | | | upstream-variant-2KB | RAB40A | GRCh38.p7 | X:103520705 | ATGCTTGCTCACCCT[C/G]TCACCACTCCAAATT | 142684 |
rs7061268 | snp | A/G | 0.0384368 | 0.133195 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103508907 | ATGAATATTCTGGAC[A/G]TATCCTGCAGTCACC | 142684 |
rs7063032 | snp | C/G | 0.0317957 | 0.122012 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103505658 | tgctcattttctTTT[C/G]TCCTTGTTTCCAAAA | 142684 |
rs7891217 | snp | A/C | 0.290597 | 0.246682 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502546 | CAACTCATACGGTCC[A/C]ACACCCAGTCTCTTG | 142684 |
rs10127233 | snp | C/G | 0.163909 | 0.234709 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512375 | GCAGGAGTAGCACAT[C/G]CTGGTTAGATAAATT | 142684 |
rs10521501 | snp | C/T | 0.102711 | 0.202005 | intron-variant, utr-variant-5-prime | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103503304 | CTGGGCAACTGTGTC[C/T]ATAGGATCCTAGAGA | 142684 |
rs11796780 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103505159 | ttaatattatccttg[C/T]gagatatatccatga | 142684 |
rs12171775 | snp | A/G | 0.158238 | 0.232551 | intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103518529 | ctggaccaaactatc[A/G]tgccagagagtgcgt | 142684 |
rs12852743 | snp | A/C | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512927 | TTGGAAGTGAAAAAA[A/C]CAATAAAAACAAAAT | 142684 |
rs12864165 | snp | A/C | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506480 | AAACAGATCTATTTA[A/C]AACATAATCCAACAT | 142684 |
rs16983958 | snp | A/G | 0.107889 | 0.205681 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512148 | ATATTCCTTGAGTTC[A/G]ATGTTTTGTAGACAG | 142684 |
rs17285130 | snp | C/T | 0.123219 | 0.215468 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515018 | CATGAAATGAGTTAT[C/T]AAATGATTCCAAGTT | 142684 |
rs17340328 | snp | C/T | 0.407578 | 0.194085 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103514934 | ATTATACTCTGTATG[C/T]ATGCATCATAATGTA | 142684 |
rs34408030 | in-del | -/T | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507226 | AATCTCATTCCTTTT[-/T]ATGGCTGCAGGTTTT | 142684 |
rs34471945 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103499359 | TCCCCAAATGTAGTA[-/G]AATAACATAGCAAAA | 142684 |
rs34521680 | in-del | -/A | | | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502258 | TAGAGAAAAAAAAAA[-/A]CCTTTAGATTAATTC | 142684 |
rs35908052 | in-del | -/T | | | upstream-variant-2KB | RAB40A | GRCh38.p7 | X:103519908 | ATGAATAATAATTTT[-/T]AAGATGACAGATATT | 142684 |
rs41304054 | snp | A/C | 0.0425 | 0.139441 | utr-variant-3-prime, nc-transcript-variant, intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103498757 | ACAATCACCCTATGA[A/C]AATGCACAAATAAAT | 142684 |
rs55653558 | in-del | -/T | | | upstream-variant-2KB | RAB40A | GRCh38.p7 | X:103521335 | ATTAGCAATTGTGTT[-/T]AACAAACAAAGCCAT | 142684 |
rs55670739 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103499418 | CTGGACAGATCTGTT[A/G]TATACAATCTCTATA | 142684 |
rs55718654 | in-del | -/C | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509662 | TTCACTTCCCACTGA[-/C]TCCTTATCCCACTGC | 142684 |
rs57824262 | in-del | -/CTTTAGT | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507403 | TTGTTTTAATACAGT[-/CTTTAGT]GGTTTTTTTTCCTTT | 142684 |
rs59159060 | snp | C/T | 0.108358 | 0.206004 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515714 | ATAGCACAGAGATGG[C/T]ACCTAACCTCCTACA | 142684 |
rs59511853 | in-del | -/CA | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513918 | ACACACACACACACA[-/CA]GACACATTGCAACAT | 142684 |
rs60492530 | in-del | -/GG | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507410 | AATACAGTCTTTAGT[-/GG]TTTTTTTTCCTTTGG | 142684 |
rs60506082 | in-del | -/TTTA | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507404 | TGTTTTAATACAGTC[-/TTTA]GTGGTTTTTTTTCCT | 142684 |
rs60551444 | snp | A/G | 0.258603 | 0.249852 | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502191 | CAATACAGAACAAAC[A/G]TGAATAAAGGATAAG | 142684 |
rs60612948 | snp | C/G | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507403 | TTGTTTTAATACAGT[C/G]TTTAGTGGTTTTTTT | 142684 |
rs60649805 | in-del | -/A | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507485 | TTTAAAAGGAAAAAA[-/A]CATTAAAAAACACCT | 142684 |
rs61528307 | in-del | -/A | | | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502258 | ATAGAGAAAAAAAAA[-/A]CCTTTAGATTAATTC | 142684 |
rs61571242 | in-del | -/A/AA | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507589 | TGAAAATAACAACTG[-/A/AA]AAAAAAAACCCTTAA | 142684 |
rs61735524 | snp | A/G | 0.0502271 | 0.150302 | missense, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500086 | TTAGCCATGGAGAAG[A/G]ACTTGAGGTGGCTTC | 142684 |
rs61735525 | snp | A/G | 0.00143474 | 0.0267453 | synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500085 | CTTAGCCATGGAGAA[A/G]GACTTGAGGTGGCTT | 142684 |
rs61739206 | snp | A/G | 0.0118725 | 0.0761269 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500632 | CCGAGATGGCTGTAC[A/G]GGGACTCAGCTGCAC | 142684 |
rs62591316 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510527 | GTAAATAGGATGAAA[A/G]TGAGTAGAATGAAAC | 142684 |
rs67128561 | in-del | -/C | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509663 | TCACTTCCCACTGAT[-/C]CCTTATCCCACTGCA | 142684 |
rs67719496 | snp | G/T | 0.407578 | 0.194085 | intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103517986 | ATACCCACTGGCCAC[G/T]CATGGCTATTTAAGT | 142684 |
rs72175174 | in-del | -/AGTCTTT | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507400 | CCCTTGTTTTAATAC[-/AGTCTTT]AGTGGTTTTTTTTCC | 142684 |
rs72541397 | snp | A/G | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513490 | AAATATTAAACCGAA[A/G]GAAAATATACACATG | 142684 |
rs72616821 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510196 | CAATTTCTCAGACTC[A/G]GGAGCATGATGTACT | 142684 |
rs73520351 | snp | C/G | 0.0993986 | 0.199548 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506529 | AGATCATTGCCAATT[C/G]TTTACTTGCCAGTTA | 142684 |
rs73520352 | snp | C/T | 0.161297 | 0.233735 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506893 | GCATCTTGTTAGTTC[C/T]TGTGGTTTTTGTAAT | 142684 |
rs73520355 | snp | A/G | 0.286116 | 0.247378 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509204 | AGACGACTTCTTCAC[A/G]TCAACTTTTAAACTT | 142684 |
rs73633875 | snp | C/T | 0.146755 | 0.227685 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103512847 | AATAAAATTTTAAGG[C/T]TTTTTAAAGATTTTA | 142684 |
rs74765911 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103519347 | AAAAGAGAAAGAAAT[A/C]CTTGGAATTTGATTT | 142684 |
rs77241510 | in-del | -/A/C | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509661 | CTTCACTTCCCACTG[-/A/C]ACCCTTATCCCACTG | 142684 |
rs79739139 | snp | C/G | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103509337 | TCTCTCTGTCTCTCT[C/G]TCTCTTCTTTCCCCT | 142684 |
rs79820963 | snp | A/G | 0.104508 | 0.203303 | synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500322 | CACACCCAGGCGCTC[A/G]GCGTAGGCCTGGGCC | 142684 |
rs111385536 | snp | A/G | 0 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513110 | CCGGGGGAAGGGCAA[A/G]CACGTCTCTCAGATG | 142684 |
rs111711166 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103505500 | GCCCCTTACTCTTTT[C/T]TTTAGTCCATGGGGT | 142684 |
rs111760830 | snp | A/G | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513492 | ATATTAAACCGAAAG[A/G]AAATATACACATGCC | 142684 |
rs112309833 | snp | C/T | 0.0689654 | 0.172414 | upstream-variant-2KB | RAB40A | GRCh38.p7 | X:103520812 | TCCCAGCTACTCAGA[C/T]GGCTGAGGTAGGAGG | 142684 |
rs112753774 | snp | G/T | 0.5 | 0 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103506626 | TTTATTCTCAAATAT[G/T]AAACTTCAAAAACTA | 142684 |
rs113570594 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103503573 | AAAATGTCCTCCTTT[-/A]AAAAAAAAAAAAATG | 142684 |
rs113619372 | snp | A/C | 0.0845627 | 0.187431 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515495 | AAAACAGAGGGGAGA[A/C]CAAATATATATTTAT | 142684 |
rs113735781 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103513919 | ACACACACACACACA[C/G]ACACATTGCAACATT | 142684 |
rs113737976 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime, intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103499294 | CTTGTAGAACATCTC[A/G]TACAAAAAAAGTAGA | 142684 |
rs113865852 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103503627 | TGGCCAGAACCCGGA[A/T]CACAGCTTTGAGAGT | 142684 |
rs137891150 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510892 | ATCTACATTATAACA[C/T]GGCATATTTTCCCCA | 142684 |
rs138078971 | snp | A/G | 0.0256233 | 0.11025 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103503740 | CACCTAACGATAGCA[A/G]TCTCTGTGTATTAGT | 142684 |
rs138220734 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510092 | TATAGGCATGAGCCA[C/T]CGTGCCCAACCGAAA | 142684 |
rs138527980 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515724 | GATGGCACCTAACCT[C/G]CTACATAATATAGAT | 142684 |
rs138556327 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103504634 | TCAAGCGATTCTCGT[A/G]CCTCAGCGTACTGAG | 142684 |
rs138568966 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103514975 | ATGTGAGTCTAATAT[A/G]TTGAGACATTCAAGA | 142684 |
rs139017752 | snp | C/T | 0.00235463 | 0.0342312 | missense, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500272 | AAAGACTCTATGATG[C/T]TGAAATTGCACAGAG | 142684 |
rs139170788 | snp | C/T | 0.000683589 | 0.018475 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500613 | CGTCTTGTAGTCGAT[C/T]CCCCCGAGATGGCTG | 142684 |
rs139389579 | snp | C/T | 0.00143501 | 0.0267479 | missense, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500099 | AGGACTTGAGGTGGC[C/T]TCTTAAGGTACTGGG | 142684 |
rs139889011 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103519262 | TTACATAGGTATACA[C/T]GTGCCATGGTGGTTT | 142684 |
rs140295269 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB | RAB40A | GRCh38.p7 | X:103520977 | ATTGCTTGAGCCTGG[A/G]AGTTCAAGGCTGCAG | 142684 |
rs140475786 | snp | C/T | | | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507957 | GTCTGCAGGTTTTTG[C/T]ATTTTTTAATGTTTA | 142684 |
rs140511113 | snp | C/T | 0.0047219 | 0.0483597 | missense, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103499988 | GTGGGCAGACGATCT[C/T]CACTTTGCAGAGGCT | 142684 |
rs140923310 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103514116 | TAAAGAGGCATATAT[A/G]GCAGGTCACAGTGTT | 142684 |
rs141189365 | snp | G/T | 0.0204488 | 0.0990265 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510659 | TTACCAGGACTTGTC[G/T]TTGAGTGTTCTGTTT | 142684 |
rs141221975 | snp | A/G | 2.30081e-05 | 0.00339168 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500516 | CACGAGAGTAGGAGC[A/G]GAATATGGTACAAAA | 142684 |
rs141296716 | snp | C/T | 0.0302564 | 0.119217 | intron-variant, utr-variant-5-prime | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502902 | TGGGACTTCAATGGC[C/T]CTTTAAATGCTGAGA | 142684 |
rs141359465 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103501859 | ATGCAAAAGAAAAAG[G/T]CTCTGTGTGTGTCTG | 142684 |
rs142215218 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103516296 | TGTGAAAGTGGTACA[C/T]ATTCAGTAGAAACTG | 142684 |
rs142225101 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103514795 | TTCTGATTATAAAAA[C/T]GATTTGTATCAATTT | 142684 |
rs142382786 | snp | C/T | 0.0384368 | 0.133195 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103510932 | TCACACTGATAATTA[C/T]CAATTTTAATTTTTG | 142684 |
rs142893565 | snp | A/G | 0.000254824 | 0.0112848 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500724 | CTTGAGCAGGAAGTC[A/G]TAGGCCTGGTCGGGG | 142684 |
rs143418229 | snp | A/G | 2.29268e-05 | 0.00338569 | synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500208 | CTTGCTCGGCCTCCC[A/G]AGCCAATTCATCCTG | 142684 |
rs143487548 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103515379 | ACAAAGAAATGTCAC[C/T]AAAGGTTCTATAACA | 142684 |
rs143662347 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103503795 | AGATTGGCTCCAGCC[C/G]CTGTCTGCATTAAAG | 142684 |
rs143676720 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103502697 | CCATCTTCTAAAAGG[A/G]GGTGCTCAGGGTCCT | 142684 |
rs143851190 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103507632 | TAACTGCTGATCAGG[A/C]GATTAAAAAGTTTTC | 142684 |
rs144417939 | snp | C/T | 0.0338441 | 0.125605 | intron-variant, upstream-variant-2KB | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103505223 | AATTGTGGTAGAGTA[C/T]TTCATTTTATGAATA | 142684 |
rs144592449 | snp | A/G | 0.000706359 | 0.0187798 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500625 | GATCCCCCCGAGATG[A/G]CTGTACGGGGACTCA | 142684 |
rs144613307 | snp | A/G | 2.29058e-05 | 0.00338414 | synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant | RAB40A, LL0XNC01-250H12.3 | GRCh38.p7 | X:103500325 | ACCCAGGCGCTCGGC[A/G]TAGGCCTGGGCCTGC | 142684 |