SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4224803 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Fgr | GRCm38.p3 | 4:132999886 | CCCCCCCATTAACCT[C/T]CCTTCTCCCCAATAT | 14191 |
rs4224804 | snp | A/G | 0.477041 | 0.104654 | intron-variant | Fgr | Mm_Celera | 4:132999897 | ACCTTCCTTCTCCCC[A/G]ATATCTCCAGGAACC | 14191 |
rs4224805 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Fgr | Mm_Celera | 4:133000045 | CCCTACCCAGGTGAG[A/C]CGGGAGTTGGGGGTG | 14191 |
rs4224806 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Fgr | Mm_Celera | 4:133000047 | CTACCCAGGTGAGCC[G/T]GGAGTTGGGGGTGTG | 14191 |
rs4224807 | snp | C/T | 0.5 | 0 | synonymous-codon | Fgr | GRCm38.p3 | 4:133000202 | GTGCCCTCCAGGATG[C/T]CCTGCATCCCTGTAT | 14191 |
rs4224808 | snp | C/G | 0.375 | 0.216506 | synonymous-codon | Fgr | GRCm38.p3 | 4:133000235 | GGTCATGGAGCAGGC[C/G]TGGCGCCTGGATCCA | 14191 |
rs4224809 | snp | G/T | 0.277778 | 0.248452 | synonymous-codon | Fgr | Mm_Celera | 4:133000277 | CACCTTTGAGTACCT[G/T]CAGTCTTTCCTGGAA | 14191 |
rs27572342 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001787 | GCAGGACCCTGAGCA[A/C]ATAAAAATGAGTAAG | 14191 |
rs27572343 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001784 | TGAGCAGGACCCTGA[A/G]CAAATAAAAATGAGT | 14191 |
rs27572344 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001723 | GAGTTTGGAGTCACT[A/G]ATGCACTAGGCAATT | 14191 |
rs27572345 | snp | C/G | 0.408163 | 0.193609 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001605 | GTAGCTGACATGCCT[C/G]TTTGGAAACCAGGAG | 14191 |
rs27572346 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001504 | TGGAGATATTTTTAT[A/T]ATAGTGACTGGAAGC | 14191 |
rs27572347 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Fgr | GRCm38.p3 | 4:133001394 | CTCTCAGGCTCCCCA[A/G]AACACAGCAAGAGGA | 14191 |
rs27572348 | snp | A/C | 0.391111 | 0.206368 | utr-variant-3-prime | Fgr | GRCm38.p3 | 4:133001361 | GGCATGGAGAAGAAT[A/C]CAACAAACTCTCTAC | 14191 |
rs27572349 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Fgr | GRCm38.p3 | 4:133001317 | CCATCACAGGCACAC[C/T]GGCACAGTCTTAGGC | 14191 |
rs27572350 | snp | A/C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Fgr | GRCm38.p3 | 4:133001275 | TCGTACAGCTAATTC[A/C/T]TTACCTGATTTCAGC | 14191 |
rs27572351 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001265 | TTTTGAATCTTCGTA[C/T]AGCTAATTCTTTACC | 14191 |
rs27572352 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001211 | CACCATGAGTTGAGA[A/G]ACCCAGAAAGCAGGT | 14191 |
rs27572353 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133001145 | GCCAGATACCCAGCA[C/T]GTGGGGCTTCAGGGC | 14191 |
rs27572354 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133000954 | ACCCCTCTGAGGGAC[G/T]TGTATGTGTGTATTC | 14191 |
rs27572355 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Fgr | GRCm38.p3 | 4:133000924 | TCTGAGGGAGAGAGC[C/T]GTTGAATGCTCACCA | 14191 |
rs27572356 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133000642 | TCAGAGCTCCTCTCT[C/T]GAACACTCTGACCCC | 14191 |
rs27572357 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133000470 | GGATCAGAGAAGGTC[C/T]GACGCTCTGAAGCCA | 14191 |
rs27572358 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Fgr | Mm_Celera | 4:133000359 | CCTGACTGGGCATCA[C/T]TGACCCTCTGGGAGT | 14191 |
rs27572359 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:133000103 | CCTGCTCCCTTCTCC[C/T]TTCCTGTGGCTGACA | 14191 |
rs27572360 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fgr | Mm_Celera | 4:132999796 | CTGTGCACAGAGACC[A/T]CTATGCTTGGGGTTC | 14191 |
rs27572361 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fgr | GRCm38.p3 | 4:132999770 | CGTATAGAAAATAGC[A/G]GGTATTTCTGCTGTG | 14191 |
rs27572362 | snp | G/T | 0.5 | 0 | intron-variant | Fgr | Mm_Celera | 4:132999724 | TAAAGGCTAGAGACA[G/T]TCTAATATCTTATCT | 14191 |
rs27572363 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Fgr | Mm_Celera | 4:132999583 | TGACATAGTTCCTAA[A/C]ACAGTTCTGGGGCCT | 14191 |
rs27572364 | snp | A/G | 0.5 | 0 | intron-variant | Fgr | Mm_Celera | 4:132999570 | TTAATGTGTTAATTG[A/G]CATAGTTCCTAAAAC | 14191 |
rs27572365 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132999493 | GTTGTGCTGGCTGGG[A/C]AGAGAACTTATTTGC | 14191 |
rs27572366 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Fgr | GRCm38.p3 | 4:132999461 | CGCCAGAATGTCTAG[A/G]TCCTAGCCACTTGTT | 14191 |
rs27572367 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fgr | GRCm38.p3 | 4:132998620 | CACATGCAATTCTGA[A/G]TTCAAGTCTCCCCTC | 14191 |
rs27572368 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon | Fgr | Mm_Celera | 4:132998439 | CCTAATATGCAAGAT[A/C]GCTGACTTCGGGCTG | 14191 |
rs27572369 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fgr | GRCm38.p3 | 4:132998304 | TGAGCCCATGCTAGC[A/G]CCTGCCTCTCACTTC | 14191 |
rs27572370 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Fgr | GRCm38.p3 | 4:132997984 | TAGCTTGCTGGATTT[C/T]CTAAAGGATCGAGAA | 14191 |
rs27572371 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132997807 | GGGTCGTGTCCAGGG[A/G]TTCGGAGGTGGAGTC | 14191 |
rs27572372 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fgr | Mm_Celera | 4:132997792 | GAGAGGAGTCTAAGT[A/G]GGTCGTGTCCAGGGG | 14191 |
rs27572373 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132997781 | GAGCCGACCTGGAGA[A/G]GAGTCTAAGTGGGTC | 14191 |
rs27572374 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fgr | GRCm38.p3 | 4:132997770 | CTGGGAATGGAGAGC[C/T]GACCTGGAGAGGAGT | 14191 |
rs27572375 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fgr | GRCm38.p3 | 4:132997753 | AGCATACCAGGCAAG[C/T]TCTGGGAATGGAGAG | 14191 |
rs27572376 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Fgr | Mm_Celera | 4:132997212 | GGATGCCTGGGAGAT[C/T]GACCGGAACTCCATA | 14191 |
rs27572377 | snp | A/G | 0.152778 | 0.230321 | synonymous-codon | Fgr | Mm_Celera | 4:132997179 | CACCACTAAGCCCCA[A/G]ACTCTAGGCCTGGCC | 14191 |
rs27572378 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132996389 | TTTGTATACTTACTG[C/T]CCTTCCTTGGGCACA | 14191 |
rs27572379 | snp | A/C | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132996336 | TGGAGGCCACCTCCT[A/C]GGAAGACCCATAAAG | 14191 |
rs27572380 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132996268 | AGTTTCGCCTCAGAA[A/C]CTTACCTCTGTTTTT | 14191 |
rs27572381 | snp | C/T | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132996242 | TGCGGCAGGAACGGA[C/T]TCATGTCCACAGTTT | 14191 |
rs27572382 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132996230 | CAGGATGAGATCTGC[A/G]GCAGGAACGGACTCA | 14191 |
rs27572383 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132996190 | ACCTTCAGTGCCTCT[C/T]GTCCCCATCTTGACT | 14191 |
rs27572384 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132996142 | AAGCAGTTATGGTCC[A/G]TCCAGGAGTAAAACC | 14191 |
rs27572385 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Fgr | Mm_Celera | 4:132996025 | CCTTGGACAGCTGCG[C/G]TCATTTTCCATGTGG | 14191 |
rs27572386 | snp | C/T | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132995982 | TGTGTGCTACCTGGA[C/T]GTCGGGGACAAGGCT | 14191 |
rs27572387 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fgr | Mm_Celera | 4:132995972 | CTCTGGCTGTTGTGT[A/G]CTACCTGGACGTCGG | 14191 |
rs27572388 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fgr | Mm_Celera | 4:132995922 | GCTGCTCTAAGCAGT[A/G]GGTTGCAGAAGCTGA | 14191 |
rs27572389 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fgr | GRCm38.p3 | 4:132995211 | TGGAGTCTGAGCAGA[C/T]GGAGAGCAAGCAATG | 14191 |
rs27572390 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fgr | GRCm38.p3 | 4:132995165 | GGCTGGGCCACGTAC[A/G]TGCGTCCTTAGGCCA | 14191 |
rs27572391 | snp | A/G | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132995100 | ACTGACCGTGTTGTC[A/G]TGACGGGGAGACTGA | 14191 |
rs27572392 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Fgr | Mm_Celera | 4:132995051 | CTCCATACAGGACCT[A/G]GTGCGGCACTACATG | 14191 |
rs27572393 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fgr | Mm_Celera | 4:132994914 | AAGGACCCTTTCCAC[C/G]CAGGGGCCTACTCCC | 14191 |
rs27572394 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fgr | Mm_Celera | 4:132994894 | TCTGAGGGAGACGAG[A/G]ACTAAAGGACCCTTT | 14191 |
rs27572395 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fgr | Mm_Celera | 4:132994768 | GGGTTGGTACGGCAG[A/G]CATGCCACCAGACAA | 14191 |
rs27572396 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132994577 | AGACTTGGCTGTTGC[A/G]GTGACTTCCGGGGAA | 14191 |
rs27572397 | snp | A/G | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132993922 | TGAGAAGGGTCAAGG[A/G]CCCTGTGATACCTGA | 14191 |
rs27572398 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fgr | Mm_Celera | 4:132993870 | CCCTCTGAGACTTGA[A/G]TTCCTTGTCTGTAAA | 14191 |
rs27572399 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132993824 | GGAGAGAATCAGGGC[A/G]CGTGAGGACACTAAT | 14191 |
rs27572400 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fgr | Mm_Celera | 4:132993745 | TTGTCTCAGACAGCC[A/G]CAAGCAGGGAAAGAA | 14191 |
rs27572401 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993666 | AGAGTCTTCTACAGC[A/G]AGTGTGGTCACATCT | 14191 |
rs27572402 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993611 | GTTCTTTTCTATCAA[A/T]GCCCACAAGGCACAG | 14191 |
rs27572403 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Fgr | Mm_Celera | 4:132993602 | GAAAACTGTGTTCTT[G/T]TCTATCAATGCCCAC | 14191 |
rs27572404 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fgr | Mm_Celera | 4:132993578 | AGGTGTCCTCACCCG[C/T]CCTGATTTGAAAACT | 14191 |
rs27572405 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993556 | GACTGAGCGTGCCAG[C/T]GTTCCCAGGTGTCCT | 14191 |
rs27572406 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993551 | GTATGGACTGAGCGT[A/G]CCAGCGTTCCCAGGT | 14191 |
rs27572407 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fgr | Mm_Celera | 4:132993549 | AGGTATGGACTGAGC[A/G]TGCCAGCGTTCCCAG | 14191 |
rs27572408 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993529 | CCCAGATTTGCCTGG[G/T]GCTCAGGTATGGACT | 14191 |
rs27572409 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Fgr | Mm_Celera | 4:132993503 | ACGGTTAGCAGACAC[C/T]GCTTCTGTCTCCCAG | 14191 |
rs27572410 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fgr | Mm_Celera | 4:132993500 | CACACGGTTAGCAGA[C/G]ACCGCTTCTGTCTCC | 14191 |
rs27572411 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Fgr | Mm_Celera | 4:132993494 | CCCAGGCACACGGTT[A/T]GCAGACACCGCTTCT | 14191 |
rs27572412 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132993448 | AATGTGTATGGTATC[C/T]CTTCAACCCTTTCTC | 14191 |
rs27572413 | snp | C/T | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132993437 | AAACCTTTGACAATG[C/T]GTATGGTATCCCTTC | 14191 |
rs27572414 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fgr | Mm_Celera | 4:132993413 | GCTGGGGTTGAAGGA[G/T]GATCTTGAAAACCTT | 14191 |
rs27572415 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fgr | Mm_Celera | 4:132993250 | ACTTACTCTGCTGAT[C/T]CTTAAGGAAGTTTTT | 14191 |
rs27572416 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132993201 | ATGTAGCTCAGGCTA[C/T]CTCACTCTTAGAAGC | 14191 |
rs27572417 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132992599 | TTGTGGAGAGCGGCA[A/G]AAAGCATGGAGGATG | 14191 |
rs27572418 | snp | A/G | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132992595 | TGGATTGTGGAGAGC[A/G]GCAGAAAGCATGGAG | 14191 |
rs27572419 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132992427 | TTTAAAACACAGCAA[C/T]GTAGGACTCAGAACT | 14191 |
rs27572420 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991799 | TGCAGAACATCCAAG[G/T]CTGGAGGAGAAATTT | 14191 |
rs27572421 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Fgr | GRCm38.p3 | 4:132991788 | GCCCGGCCAAGTGCA[A/G]AACATCCAAGTCTGG | 14191 |
rs27572422 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991759 | AAGAGCCACTGGAGA[A/G]CGGAGAAAAGCAGGC | 14191 |
rs27572423 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Fgr | GRCm38.p3 | 4:132991747 | CTCTGGTGAAGAAAG[A/T]GCCACTGGAGAGCGG | 14191 |
rs27572424 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991683 | GCTGCCTAGTAGGAA[A/G]AAGGAGGAAGAGAGA | 14191 |
rs27572425 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991612 | CTCTGTCATTTGTTA[C/T]GGCACTCTGGTGCTG | 14191 |
rs27572426 | snp | C/T | 0.5 | 0 | intron-variant | Fgr | GRCm38.p3 | 4:132991590 | CTGTTCCTAATTGTC[C/T]CTGAGACTCTGTCAT | 14191 |
rs27572427 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991580 | GAAGGGGCTCCTGTT[C/T]CTAATTGTCTCTGAG | 14191 |
rs27572428 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fgr | GRCm38.p3 | 4:132991537 | GTGTATGAGAAGTGC[C/T]GGGCCATGCCACTTC | 14191 |
rs27572429 | snp | A/C/T | 0.497778 | 0.0332592 | intron-variant | Fgr | GRCm38.p3 | 4:132991519 | GCTAGACCAGGCTGC[A/C/T]CTGTGTATGAGAAGT | 14191 |
rs27572430 | snp | C/T | 0.32 | 0.24 | intron-variant | Fgr | Mm_Celera | 4:132991510 | TTACCAGAAGCTAGA[C/T]CAGGCTGCCCTGTGT | 14191 |
rs27572431 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132990626 | ACAGAGAGGAGCTGA[A/T]GTGTAGTTTAACATG | 14191 |
rs27572432 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fgr | Mm_Celera | 4:132990608 | GAGTTCATTTTGTTG[G/T]ACACAGAGAGGAGCT | 14191 |
rs27572433 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fgr | Mm_Celera | 4:132990577 | AAAAAAAAAGGCTTG[C/T]AAGGAACAGTCCTTA | 14191 |
rs27572434 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fgr | GRCm38.p3 | 4:132989567 | ATTACTACCTATGAG[C/T]GTTCAAGCCTATAAT | 14191 |