SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3156373 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45636724 | TTTTTCACTTGTAAA[C/T]ATGTCTTTGCTCCAA | 30838 |
rs3156374 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45636488 | AGAAGTGCAGGCAGT[A/G]GCTACACTTCGTTGA | 30838 |
rs3156375 | snp | A/T | 0.5 | 0 | intron-variant | Fbxw4 | Mm_Celera | 19:45636473 | AGCTACACTTCGTTG[A/T]TGTTTGTTTTGTTCC | 30838 |
rs3156376 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Fbxw4 | Mm_Celera | 19:45636403 | TTCTCTGTACCTATC[A/G]CAGGCTAATTTCATC | 30838 |
rs3156377 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45636050 | TTTATTTTCTCTCTC[A/G]GCTCTGTTAGCCTCA | 30838 |
rs3156378 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45636021 | CAAGTGTGCTGAAGA[A/G]GTAACTGTGTAAAAG | 30838 |
rs3156379 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45635486 | GGAGGAGTGGCCAGC[A/G]GCTGGGATGTGTGCC | 30838 |
rs3156380 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45635483 | GGAGTGGCCAGCAGC[C/T]GGGATGTGTGCCACT | 30838 |
rs3156381 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45635477 | GCCAGCAGCTGGGAT[A/G]TGTGCCACTCTCTGG | 30838 |
rs3156382 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45635186 | CATCAGTACCAGGTC[A/G]CCTGATCCACAGACT | 30838 |
rs3156383 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45635167 | GATCCACAGACTTCC[A/T]CCAGGACATGAAAGA | 30838 |
rs3156384 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634852 | AATAACTCTGACTCT[A/G]TGTAGCCTCTAGTGA | 30838 |
rs3156385 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45634731 | TGCCTTATATTTTAT[A/T]CTTAGAGAAAATGCA | 30838 |
rs3156386 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634730 | GCCTTATATTTTATA[C/T]TTAGAGAAAATGCAT | 30838 |
rs3156387 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45634529 | TCCCATCCCATATTC[A/T]TGTGGAATTGTTGTT | 30838 |
rs3156388 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634528 | CCCATCCCATATTCA[C/T]GTGGAATTGTTGTTT | 30838 |
rs3156389 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634259 | ATGCAAGTTTCTAAT[A/G]CATCCTGTTCCCCTG | 30838 |
rs3156390 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634228 | GCCCTATGTTGTTCC[C/T]TCCCACTCTCTCTGC | 30838 |
rs3156391 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45633647 | CTCTTTTGAAACAGC[A/G]TCTGGCTGTGTAGCA | 30838 |
rs3156392 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45633538 | CTAGCAATGTAGACT[A/G]TAACCAGGAGCTATG | 30838 |
rs3156393 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632978 | AGGCATGGCCCCCAT[C/T]CAATGCGCTGAAACC | 30838 |
rs3156394 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632963 | CCAATGCGCTGAAAC[C/T]GAGACCAAGAAGTTA | 30838 |
rs3156395 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45632917 | AAAATTCAGTAAGTC[A/T]CGGGTAGGGTTCAAA | 30838 |
rs3156396 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632915 | AATTCAGTAAGTCAC[A/G]GGTAGGGTTCAAACC | 30838 |
rs3156397 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632852 | TTCTGCAATAACAGG[C/T]TTCCACAAATATCTT | 30838 |
rs3156398 | snp | G/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632176 | TTGTTGTTGTTGTTG[G/T]ttttttttttttttt | 30838 |
rs3156399 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45631495 | CGCGAATACCTTTGG[A/G]TCCTGGGCATTATGA | 30838 |
rs3156400 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45631367 | CCCCCCCCCCCACTG[C/T]GCCTTGGTCTTCCCG | 30838 |
rs3156401 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45630541 | ACCTGAGAGGCAAGG[A/G]CAGCAGCTAGCCTGC | 30838 |
rs3156402 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45629683 | AGCCAGAGCTACACA[A/G]AGAAGTCCTGTATTG | 30838 |
rs3156403 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45629637 | TTGGCTATTAATTGT[C/T]ATTAAAAAACATTTT | 30838 |
rs3156404 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45628898 | GAGAATGGAGACCCC[A/G]TTCCTTAGCATATTG | 30838 |
rs3156405 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxw4 | Mm_Celera | 19:45627501 | ACCTTTAATCCCTGC[A/T]TTGGGAGGCAGAGGC | 30838 |
rs3156406 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45627178 | AAGCTTGGGCTTCCC[C/T]GGGCCTTCTGCCTCC | 30838 |
rs3156407 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45626736 | TCTGACCTGGCTCTA[A/C]GTATCACCTTTTGTT | 30838 |
rs3156408 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45624684 | CAACCTGCTGAAGTA[C/T]ATCTTTCTTTACCAA | 30838 |
rs3156409 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45621900 | TTAAAAGCACCTGCT[C/T]GCACAGCTAGATAGC | 30838 |
rs3156410 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Fbxw4 | GRCm38.p3 | 19:45621473 | AATACATATTTCTCC[C/T]TATCTCATTAAGCAA | 30838 |
rs3156411 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Fbxw4 | GRCm38.p3 | 19:45621465 | TTTCTCCCTATCTCA[C/T]TAAGCAACTCAAATC | 30838 |
rs3156412 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Fbxw4 | GRCm38.p3 | 19:45621062 | ACGGCACTGACCCAT[C/T]CCAGTGGCCCTGTCA | 30838 |
rs3156413 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45618591 | GTGGCAATGGCCAGA[A/G]ATGGCTGGGAATGGT | 30838 |
rs3156414 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45617705 | TCCTCTCTGACACAG[C/T]GTTGGTTGGGTCAAA | 30838 |
rs3156415 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45616209 | GGGATAGAGTGAGGG[A/G]TTCAGGGAGCGGTGT | 30838 |
rs3156416 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45616035 | GGAGACCAACAGGCC[G/T]CGTCTCTTGAGAGCC | 30838 |
rs3156417 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45613550 | TCCTGTCTGAAGTGC[A/G]TTGAGTTCTCAGAAA | 30838 |
rs3156418 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45611061 | CTGCTGCAGCCACCG[A/C]GAGGTCTGGGCCATA | 30838 |
rs3156419 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45599535 | GAAGCCAACAGAGAA[C/T]ATTGGATTCTCTCTC | 30838 |
rs3156498 | snp | A/C | 0.387812 | 0.208586 | upstream-variant-2KB | Fbxw4 | GRCm38.p3 | 19:45662520 | CCACGCATTATATCC[A/C]TCCTTGTCTTCTTGT | 30838 |
rs3156499 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Fbxw4 | Mm_Celera | 19:45661727 | GGTGTGTCCCACCAC[A/T]CCTTGGTTCTTATAT | 30838 |
rs3156500 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxw4 | GRCm38.p3 | 19:45661280 | GGCCCCACAGATCCA[A/G]TGGGACAGCATCGAT | 30838 |
rs3156501 | snp | A/C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45658981 | TTGTTGTAACATATG[A/C/T]GAATATAATAAAGTT | 30838 |
rs3156502 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45657422 | ATATTGAACTATAAT[A/T]GAAGTTGGCTAAAAT | 30838 |
rs3156503 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45656750 | TGAGGACTTTTCATT[A/T]TCCGCTGTCCCCCTT | 30838 |
rs3156504 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45656199 | TTTATGAAGCCTGGG[A/G]GAGTAGAAATATCTT | 30838 |
rs3156505 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxw4 | Mm_Celera | 19:45655996 | TGTAAACTCTGATGC[C/G]GAAAATTAGAATAAA | 30838 |
rs3156506 | snp | A/C | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45655662 | TGGTGATTAACATCC[A/C]GAGTGGTGAGATAGA | 30838 |
rs3156507 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45655208 | GTgctggatgagggt[A/G]cagagagtgaacttg | 30838 |
rs3156508 | snp | A/T | | | intron-variant | Fbxw4 | Mm_Celera | 19:45655124 | cAGGCCTTTTTTCTT[A/T]TTACTTTTTAAAAAG | 30838 |
rs3156509 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45654772 | ATTGAGAAAGCATTC[A/G]GGTCTTCAAGTAATT | 30838 |
rs3156510 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45654741 | ATTATAGTGCACTTG[A/G]CATAGAAAAGACTCT | 30838 |
rs3156511 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45645605 | TGGAGGCATTTCCAG[G/T]TCTCTGCTTTCTGTG | 30838 |
rs3156512 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45645506 | TAAAGAAACGTGCTC[A/G]TGACCCAAAGCACCA | 30838 |
rs3156513 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxw4 | Mm_Celera | 19:45645331 | TCTATTCCAAAGCGT[A/T]TGTGCGCCGCGCTCC | 30838 |
rs3156514 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45645120 | ACTATATAGAGGGGA[A/G]GCAGTGTTTAATACT | 30838 |
rs3156515 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45644677 | GGCTGGTTTGGGGCT[C/T]ACAATAAATTCTCCT | 30838 |
rs3156516 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45644655 | aattctcctgcctta[A/G]ccttttgagtgttac | 30838 |
rs3156517 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45644234 | AGACTGTGTCCTAAG[A/C]CTGCTTCATGAGCAC | 30838 |
rs3156518 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Fbxw4 | GRCm38.p3 | 19:45642992 | GAAGGTGTAAGTAGA[A/G]ACAAAGAGAAATGTC | 30838 |
rs3156519 | snp | C/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Fbxw4 | GRCm38.p3 | 19:45642773 | GGCCTTTGAACTTTT[C/T]GCTGTCTCTGCATCC | 30838 |
rs3156521 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxw4 | GRCm38.p3 | 19:45641698 | AACATGGTACATATA[C/T]GTGAATGTAGGCAGA | 30838 |
rs3156522 | snp | A/T | | | intron-variant, upstream-variant-2KB | Fbxw4 | Mm_Celera | 19:45641668 | aagctctcagaccca[A/T]aacaatataaaaTAA | 30838 |
rs3156523 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Fbxw4 | GRCm38.p3 | 19:45640973 | TTGTGATTATGTCAC[C/T]GTCTCAGGAGGCAGT | 30838 |
rs3156524 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45640125 | GGAGTTACAGACAAT[C/T]GTGAGCCACCATGTG | 30838 |
rs3156525 | snp | G/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45639481 | tgagccacacctcca[G/T]tccTGTTTCTTTAAT | 30838 |
rs3156526 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45638042 | ACTAAACATTCTCAT[C/T]GGGGTCGTTCTCATT | 30838 |
rs3160336 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Fbxw4 | Mm_Celera | 19:45636319 | AGTCTTCTCTGGGCA[C/T]GATGAGGACGTCTGT | 30838 |
rs3160337 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45634077 | AGTTGCCAATAAATG[C/T]AGCACTAAGGTGCCC | 30838 |
rs3160338 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45633779 | GTCTCTGTTTACAGC[C/T]AGGAGCAGCAGCCTT | 30838 |
rs3160339 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632435 | AGCTACTAGAACACA[G/T]GTTTAGGCTGTCCTG | 30838 |
rs3160340 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Fbxw4 | Mm_Celera | 19:45632374 | ACCACACAAGCACGA[A/T]CCTGACTCTGAGGGA | 30838 |
rs3160341 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45632293 | ACCAGAAGGGCATCT[A/G]GTTATTACCAAAGGG | 30838 |
rs3160342 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Fbxw4 | Mm_Celera | 19:45631683 | AGTGCTGAGAGGCTC[C/G]GGAGTGTTGATTAGA | 30838 |
rs3160343 | snp | A/C/T | 0.46875 | 0.121031 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45631350 | CCTTGGTCTTCCCGC[A/C/T]GCTCTCTATGTGCCT | 30838 |
rs3160344 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45630460 | CCTTACAGGCTCTGG[G/T]TATCAGGAGAGGAGG | 30838 |
rs3160345 | snp | A/G | | | intron-variant | Fbxw4 | Mm_Celera | 19:45630116 | CTAAAACCAGAATCA[A/G]AATAAgtcttgctgt | 30838 |
rs3160346 | snp | A/G | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45630055 | cagcccagactggcc[A/G]tgagctagagcttcc | 30838 |
rs3160347 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45629310 | AGGCATCGCTCCAGC[C/T]CCTGTCTGGGCTATC | 30838 |
rs3160348 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45628256 | AGCGCTCTCTCTGTG[C/T]GGCCTTTCTTGGCTC | 30838 |
rs3160349 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45627735 | CTAAAAAAGCTTGTG[C/T]TGGACATTCTGACTT | 30838 |
rs3160350 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45627175 | CTTGGGCTTCCCCGG[G/T]CCTTCTGCCTCCCAG | 30838 |
rs3160351 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45622265 | TCCTAACTCTGGGTT[G/T]TGGCCGGAGGTTCAA | 30838 |
rs3160352 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Fbxw4 | GRCm38.p3 | 19:45621403 | CTAAATGTCACCTAT[A/G]CCTGTCCCAGGTAGC | 30838 |
rs3160353 | snp | G/T | | | intron-variant, downstream-variant-500B | Fbxw4 | GRCm38.p3 | 19:45619567 | GGAATCAGAGCAGTT[G/T]TGACAAGCAGGCCCC | 30838 |
rs3160354 | snp | C/T | 0.336735 | 0.234472 | intron-variant, downstream-variant-500B | Fbxw4 | GRCm38.p3 | 19:45619516 | TCCTGGTATTGTGGT[C/T]ACACATGTGTCACAG | 30838 |
rs3160355 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Fbxw4 | GRCm38.p3 | 19:45619506 | GTGGTTACACATGTG[C/T]CACAGTGCCTGGAAT | 30838 |
rs3160356 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45617980 | TTGGGACCGCACTGG[A/G]TGGAGATGCAACTCT | 30838 |
rs3160357 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw4 | GRCm38.p3 | 19:45617956 | CAACTCTTGGGTGAG[A/G]CTTTCAAGTAAAAGA | 30838 |
rs3160358 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Fbxw4 | Mm_Celera | 19:45617636 | GGTCTGAAATGCAGG[C/G]CAGAGGGCAACTTCA | 30838 |
rs3160359 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxw4 | Mm_Celera | 19:45617519 | GTCAGTCTAAAGAGT[C/G]AGATCTGAGCTGGTG | 30838 |
rs3160360 | snp | C/T | | | intron-variant | Fbxw4 | GRCm38.p3 | 19:45616207 | GATAGAGTGAGGGGT[C/T]CAGGGAGCGGTGTGC | 30838 |