SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8048 | snp | C/T | 0.462691 | 0.131387 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732949 | TCATGGAATCCACTG[C/T]TATGCAGCCACACTG | 7805 |
rs8056 | snp | A/C | 0.0349115 | 0.127424 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732942 | GCTGCATAACAGTGG[A/C]TTCCATGAAAGGAGT | 7805 |
rs9146 | snp | A/G | 0.11963 | 0.213316 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732548 | GAGAAGGCTCTGCAA[A/G]AGCTCCCTGGCAATA | 7805 |
rs1050663 | snp | A/G | 0.494598 | 0.051691 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742517 | GTTCATCGAGCACTC[A/G]GTAGAGGTGGCCCAT | 7805 |
rs1050731 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732616 | CAGGGAGCTGACCCA[A/G]AGGTGGAGGCCACGG | 7805 |
rs1050732 | snp | A/C | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732604 | CCAGAGGTGGAGGCC[A/C]CGGAGGCAGGGTCTC | 7805 |
rs1050733 | snp | C/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732589 | ACGGAGGCAGGGTCT[C/T]TGGGGACTGTCGGGG | 7805 |
rs1050739 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732567 | CTGTCGGGGGGTACA[A/G]AGGGAGAAGGCTCTG | 7805 |
rs1050746 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732561 | GGGGGTACAGAGGGA[A/G]AAGGCTCTGCAAGAG | 7805 |
rs1050748 | snp | C/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732554 | CAGAGGGAGAAGGCT[C/T]TGCAAGAGCTCCCTG | 7805 |
rs1050752 | snp | A/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732534 | AGAGCTCCCTGGCAA[A/T]ACCCCCTTGTGTAAT | 7805 |
rs1078609 | snp | A/G | 0.207864 | 0.246424 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740727 | TAGCTGAACCCTTTG[A/G]GTTTCTGCACAAGCA | 7805 |
rs1078610 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740761 | ACAGCCACCCTGCAC[A/C]AGGCAAACGGCCTCC | 7805 |
rs1188346 | snp | A/T | 0.470811 | 0.117228 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753528 | ttttctcatgattag[A/T]ctgggaatgtgcttt | 7805 |
rs1188347 | snp | A/G | 0.470715 | 0.117409 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753493 | aggaagaccacagag[A/G]tgatgtgccagtctc | 7805 |
rs1188348 | snp | A/G | 0.452103 | 0.147154 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751153 | CCCATGGCCCATCCC[A/G]CCCAGAGAGTGGCTG | 7805 |
rs1188349 | snp | C/T | 0.325327 | 0.238382 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750810 | TACCATTTGTGGCAC[C/T]GGAAAAATGGCAGCT | 7805 |
rs1188350 | snp | C/T | 0.490673 | 0.0676508 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749469 | tgtataatttaccta[C/T]agaaaagcacagcta | 7805 |
rs1188351 | snp | C/T | 0.279461 | 0.248258 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749071 | ccagcttggggctgt[C/T]acaaataaggcagcc | 7805 |
rs1188352 | snp | A/G | 0.200492 | 0.245049 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746442 | CTTGGAGGCTTGGAA[A/G]TGTTGACTGTCTGCA | 7805 |
rs1188353 | snp | G/T | 0.189576 | 0.242588 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745432 | AGGGGAGGGAGGGGG[G/T]ACTGCAGAGGGAGAG | 7805 |
rs1188355 | snp | A/G | 0.283421 | 0.247756 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737820 | CAGCGTGGCACAGCC[A/G]TCACCTTGGTCGACC | 7805 |
rs1188356 | snp | G/T | 0.306927 | 0.243432 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738235 | gctggacttagcaac[G/T]cacttctaactaaca | 7805 |
rs1188357 | snp | G/T | 0.435119 | 0.16802 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738435 | tgagccaccaggagt[G/T]catccttcagatcta | 7805 |
rs1188358 | snp | A/C | 0.304438 | 0.244001 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739394 | AGCCCTCAAGCCACC[A/C]CACAGTGGGCGCTCA | 7805 |
rs1188359 | snp | A/C | 0.309154 | 0.242901 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739467 | CAAAGAAGAAATAAT[A/C]CTGGGGGCTGGGGGC | 7805 |
rs1188360 | snp | A/G | 0.496649 | 0.0407971 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739529 | CAATTCACTCCCAGC[A/G]GCACTGACTGAGTGC | 7805 |
rs1323444 | snp | A/C | 0.0240643 | 0.107019 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759229 | CACTGCACTGTGTCA[A/C]CTTTCTATGATGTCA | 7805 |
rs1323445 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747442 | GGCTGGGACCGCAGC[C/T]TGAGCCTGGCTTGGA | 7805 |
rs1407881 | snp | C/T | 0.152001 | 0.229992 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759429 | TAGGAAATCGTCAAA[C/T]GGCTTCTGTGCACAA | 7805 |
rs1407882 | snp | A/G | 0.423413 | 0.180077 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757348 | ATGGGGCACAGCAGC[A/G]GCCGGAAGGTTATTT | 7805 |
rs1407883 | snp | A/G | 0.425894 | 0.177655 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757279 | AGGCAGGGATCTTGG[A/G]AGGAACGTGGGCTGG | 7805 |
rs1407884 | snp | C/T | 0.285519 | 0.247464 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757252 | CTGGGATTGTTTGAC[C/T]GGGATGTGAGGTCGG | 7805 |
rs1407885 | snp | C/T | 0.398174 | 0.201356 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757036 | CATTAGGGTAACTTG[C/T]CCGGCCCAAGCTCTT | 7805 |
rs1407886 | snp | A/C | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754963 | CTGGCAACAGGTGTG[A/C]TGATAGGACCTTGAG | 7805 |
rs1535637 | snp | A/G | 0.144969 | 0.226867 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735055 | ATGAGGGTTGGAACA[A/G]AAGAAATGTGTTCTC | 7805 |
rs1590340 | snp | C/G | 0.43598 | 0.167067 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738008 | agccaaaatgatctt[C/G]tagagaagagcatag | 7805 |
rs1614931 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753835 | ggcctagttcctcta[G/T]tgctaacgtctcaac | 7805 |
rs1623695 | snp | C/T | 0.306679 | 0.24349 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738005 | CACCTATGCTCTTCT[C/T]TACAAGATCATTTTG | 7805 |
rs1746056 | snp | A/G | 0.497829 | 0.0328757 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752875 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 7805 |
rs1804623 | snp | G/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733071 | AACAATTAGCTCCAG[G/T]AAATAACAGTTATTT | 7805 |
rs1853449 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743824 | AGTTGAGACCTGTGT[C/T]TGAGCTAAAAAAAAA | 7805 |
rs1882024 | snp | C/T | 0.439224 | 0.163383 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746868 | TGCACCTGCTGTGTG[C/T]CCGGCTCCGCGCACC | 7805 |
rs1920420 | snp | G/T | 0.420255 | 0.183066 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749644 | CTGAGCTCTGGGTGT[G/T]GACCCAGAGCCCTGT | 7805 |
rs1951782 | snp | A/G | 0.475789 | 0.107327 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754594 | ATTCTTTTTTTCAAA[A/G]TTCAGTAACTTGCCC | 7805 |
rs2178424 | snp | A/C/G | 0.163236 | 0.234461 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736537 | CTCCCAGGCTCAAGC[A/C/G]ATCCTCCCGCTTCAG | 7805 |
rs2273979 | snp | A/G | 0.384017 | 0.211044 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757821 | GGAGGGCAGCCAGCA[A/G]CTTCCCCTTCTCTGC | 7805 |
rs2377488 | snp | C/G | 0.28578 | 0.247426 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757160 | GAGGCACAAAGGGGA[C/G]ATCCCCACTTCTCAT | 7805 |
rs3748602 | snp | G/T | 0.141258 | 0.225111 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741522 | GAAGATCTCCAGAAC[G/T]CAGGTGGGACCGCCT | 7805 |
rs3748603 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742124 | GCAGAGGCTGGATCC[C/T]ATGGTGAGGAGTTTC | 7805 |
rs3762295 | snp | C/T | 0.0648419 | 0.167978 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758538 | GGCTCCAGACAAGGA[C/T]GGAAGAATAACCAGG | 7805 |
rs3762296 | snp | A/G | 0.497613 | 0.0344622 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758539 | GCTCCAGACAAGGAC[A/G]GAAGAATAACCAGGA | 7805 |
rs3762297 | snp | C/T | 0.384209 | 0.210922 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758833 | AGGGAATAGGAAGTA[C/T]ATGCAACATTTCTGG | 7805 |
rs3790495 | snp | C/T | 0.0916144 | 0.193427 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748668 | CCAGATACCACCAGA[C/T]GCCCCCATTCCTGGG | 7805 |
rs3790496 | snp | A/T | 0.432063 | 0.171327 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749144 | TTGTGGTAGATTCAT[A/T]CAATGGAGTATACAC | 7805 |
rs3790497 | snp | G/T | 0.255224 | 0.249945 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749323 | ATAGACAGGCAGAAG[G/T]CAGTGGGGGCGGGGC | 7805 |
rs3790500 | snp | A/C | 0.130694 | 0.219696 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749682 | CCGTAGGGGTCAGGG[A/C]GGGCTTCTCAGAGGA | 7805 |
rs3790501 | snp | C/T | 0.125528 | 0.21681 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749782 | GCAGAGGCCAGTGTG[C/T]ATGAGACGCATTCAG | 7805 |
rs3790502 | snp | G/T | 0.155656 | 0.231515 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755931 | CAAGCAAGGGCTCCC[G/T]GGGTCACCGCAGGCC | 7805 |
rs3790503 | snp | A/G | 0.372189 | 0.218105 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756228 | ACAGGGTACAGGGAC[A/G]CTCAAAGAGTGATTT | 7805 |
rs3795437 | snp | A/G | 0.433655 | 0.16962 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733959 | TTGGAATTGCAGGTC[A/G]TTCTTGACCATACTC | 7805 |
rs3795438 | snp | A/G | 0.345418 | 0.231074 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733790 | GTGCTGGGAGGGGTG[A/G]AGCTGCCTCATAATC | 7805 |
rs3795439 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732843 | AGTCATAGGCGAATC[G/T]GTTCTGCCCGAGGCT | 7805 |
rs3828053 | snp | A/T | 0.348574 | 0.229746 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750504 | CACTCTCTCGTGTCA[A/T]CCTCGCGCCAGTCTT | 7805 |
rs3833525 | in-del | -/AG | 0.0142054 | 0.0830717 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741767 | TGCCCCTGGGACCCC[-/AG]CCAGGCTCCCAGGAC | 7805 |
rs3833526 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742216 | CCTTTACCAGCTGGT[-/G]GGGATTTGCAAAGTG | 7805 |
rs4319383 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754101 | TGACAGTGGAATTCC[A/G]GGCACTCTGGGGAAG | 7805 |
rs4409706 | snp | A/G | 0.436976 | 0.165952 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751689 | GGTTGCAGTGAGCCA[A/G]GATCACGCCACTGCA | 7805 |
rs4614309 | snp | G/T | 0.489665 | 0.0711382 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758407 | TGAAGGTGCAAGGAT[G/T]TTAACTGAGGCTGAC | 7805 |
rs5773314 | in-del | -/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742762 | CTCTCTCCAGCTATG[-/T]GACCCTGGGCAAGCT | 7805 |
rs6671857 | snp | G/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758964 | TCATGGAGTTAGGAT[G/T]GGACACTGCTGCAGC | 7805 |
rs6684975 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733290 | TCTAAATGACTCATG[A/G]TTGGCTAATTGATTA | 7805 |
rs6685063 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755091 | GGACCACAGCCTGGA[C/G]ACAACCTGGGCCGAG | 7805 |
rs6685295 | snp | C/G | 0.286825 | 0.247273 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755351 | ATGAAGAATTATCCA[C/G]CCCAAAATATCAATG | 7805 |
rs6702831 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752799 | CTCCTTCTTCAAATA[C/T]TATGATTTGAATGCT | 7805 |
rs7415292 | snp | G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732315 | tgtggggggagtgtg[G/T]gtgtttgggtgtatt | 7805 |
rs7416874 | snp | C/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732184 | GTGTGTGGgggtggg[C/G]gtgtgtggaggggtg | 7805 |
rs7417219 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737943 | tgcttcccaggctgg[C/T]gcaccggcccatccc | 7805 |
rs7417251 | snp | A/C | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738083 | ctcccctaggggcag[A/C]ttgaaaccaatgact | 7805 |
rs7512767 | snp | A/G | 0.181022 | 0.240296 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750546 | TCTAACATGAGTCCC[A/G]TATTTTTCTGATTTT | 7805 |
rs7514358 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755863 | CGGCCACCAGGGCCC[A/G]CAATCCTTCGTGGCA | 7805 |
rs7549164 | snp | C/T | 0.424503 | 0.179021 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751346 | TCCAGCCCAGGGGCA[C/T]TGGACATAAAGGTGG | 7805 |
rs10914189 | snp | C/T | 0.410568 | 0.191619 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734934 | TGGCATCTTAGTTTT[C/T]TCTGCGCCTCCTGGA | 7805 |
rs10914190 | snp | C/T | 0.448195 | 0.152377 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736949 | ttgagtcctctattt[C/T]ccatgctgaataaac | 7805 |
rs10914192 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750602 | TACACATGGGCTCTG[G/T]GCTTCTCAGAACAAG | 7805 |
rs10914193 | snp | A/G | 0.497586 | 0.0346604 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758486 | CCTGAGCCGCAGGGA[A/G]AAGCTTGTTCTTCCT | 7805 |
rs11541205 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733215 | TTAAATGGTTTGGAG[A/G]CTAACGTGATTTTTT | 7805 |
rs11541206 | snp | C/G | 1.65701e-05 | 0.00287833 | missense | LAPTM5 | GRCh38.p7 | 1:30737604 | TGTCCTTATCTTCAA[C/G]GTGAGTGGATCCCTG | 7805 |
rs11585511 | snp | A/G | 0.21845 | 0.248001 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744122 | CTGGGGCAAGCTTAC[A/G]TGGTTCGGCAGTAGT | 7805 |
rs11586021 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745018 | CATGAGGTCACCTTG[A/G]ACATTACCCGACTTT | 7805 |
rs11586791 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739731 | GCCTGAGCACAGGGC[C/T]CGTGTCTGGTCCCCT | 7805 |
rs11801629 | snp | C/G | 0.398534 | 0.201091 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758279 | TGGATTCACTCCTTT[C/G]ATCCTCACCTCAATC | 7805 |
rs11808067 | snp | A/T | 0.0232847 | 0.105357 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759023 | AGAAAGTCCCTAAGC[A/T]CCTCCCACTTGGCAG | 7805 |
rs12032350 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732356 | tgggggtgggtgTGA[A/G]TGTGTGGAGGGGTGT | 7805 |
rs12077548 | snp | A/G | 0.0275645 | 0.114116 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749291 | taattctacagatgt[A/G]tgtattatagaacta | 7805 |
rs12078167 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741023 | GGTTCCTCTTCTGCA[A/G]GGGATTGAGCTACAG | 7805 |
rs12078854 | snp | A/G | 0.231189 | 0.249291 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750010 | AGAACCTAGACTCGG[A/G]CGGCTCAGATGGCGC | 7805 |
rs12079273 | snp | A/G | 0.216349 | 0.247725 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745004 | TGTCCTCCTGAGGCC[A/G]TGAGGTCACCTTGGA | 7805 |
rs12083195 | snp | A/G | 0.122411 | 0.214991 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752801 | CCTTCTTCAAATACT[A/G]TGATTTGAATGCTTT | 7805 |
rs12085079 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751225 | GAGGAGAACAACTCA[A/G]TTCTGACACTGAGGA | 7805 |