SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3705751 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Crk | Mm_Celera | 11:75706848 | CTTTAGCATATGCAA[A/G]ATTAACAGCAAGGTG | 12928 |
rs3721353 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707036 | AGAGGCCCAGAGCGG[A/G]TGGTGGGAGCTGCAG | 12928 |
rs6330553 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Crk | Mm_Celera | 11:75677719 | GAATATGCCTTCCTG[G/T]GGGGGGGGGGCAAAG | 12928 |
rs13468390 | snp | G/T | 0.197531 | 0.244432 | utr-variant-3-prime | Crk | Mm_Celera | 11:75703733 | GTTTTAGGTGGTAGT[G/T]GCCGTGCCTGTATGA | 12928 |
rs13468391 | snp | C/G | 0.336735 | 0.234472 | utr-variant-3-prime | Crk | Mm_Celera | 11:75705207 | CAGTTAGCATAGATT[C/G]TGTAAATCCAAATGC | 12928 |
rs13468392 | snp | A/T | | | utr-variant-3-prime | Crk | Mm_Celera | 11:75705341 | gtctacagagctact[A/T]ccagaacagtcagga | 12928 |
rs26900983 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Crk | Mm_Celera | 11:75708339 | CTTGGATATTAACAC[A/G]GAGACCTGTTACTGA | 12928 |
rs26900984 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Crk | Mm_Celera | 11:75708315 | TCATGACTCTCAGAC[A/G]TGCCAGCTCTTGGAT | 12928 |
rs26900985 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Crk | Mm_Celera | 11:75708050 | ATGGTCCTTCATAGT[C/T]ACACAAAATGCTCTT | 12928 |
rs26900986 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707975 | AAGAGCACCTCAGCT[A/G]CTTCTCTAGTGTCCT | 12928 |
rs26900987 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707945 | TTCAAGCCACCACAG[A/G]TGTGCTGGAGATACA | 12928 |
rs26900988 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707382 | ATACCATTTTTGTGA[C/T]GGTTTAGCTCAACTA | 12928 |
rs26900989 | snp | C/T | 0.46281 | 0.131194 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707056 | GGGAGCTGCAGGAGC[C/T]ACCACGCATGCTATA | 12928 |
rs26900990 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Crk | Mm_Celera | 11:75706900 | ACAATAAAATAAACT[A/G]TCCACCGCTTTACTA | 12928 |
rs26900991 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Crk | Mm_Celera | 11:75706493 | CAGAGATGATGCGTT[C/T]CTGTGTGTCCATACC | 12928 |
rs26900992 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Crk | Mm_Celera | 11:75706374 | TCTGCAAACTTGAGA[C/T]TGCATTCTCTGTTGT | 12928 |
rs26900993 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime | Crk | Mm_Celera | 11:75706156 | TAAGGAATAGAAGGT[A/G]TGTGTCTCAGCTGTT | 12928 |
rs26900994 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime | Crk | Mm_Celera | 11:75705913 | TAATGGTTTGAAATG[G/T]GTGATAAGCAAACCA | 12928 |
rs26900995 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Crk | Mm_Celera | 11:75704984 | TGTATGGCCCAGGGA[C/T]GCCAGTTGGCATACA | 12928 |
rs26900996 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Crk | Mm_Celera | 11:75704439 | CCAAACTTTGCCCTC[G/T]GCATCATGTGCAAGT | 12928 |
rs26900997 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Crk | Mm_Celera | 11:75702907 | TGCTGTGGTCGCCTT[C/T]TGCTGAGCCAGCAGC | 12928 |
rs26900998 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Crk | Mm_Celera | 11:75702896 | TGCAGCATGCTTGCT[A/G]TGGTCGCCTTTTGCT | 12928 |
rs26900999 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75702877 | AGACACAGTAGGGTC[C/T]GAATGCAGCATGCTT | 12928 |
rs26901000 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Crk | Mm_Celera | 11:75702728 | TTCCCTTTGTCCCTA[A/G]TTGGGTAATAAATAT | 12928 |
rs26901001 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75702131 | TGAGTTTAAGTCGTA[A/C]GCTGGGTAAAGATCA | 12928 |
rs26901002 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Crk | Mm_Celera | 11:75702112 | TTTTGGTGTCAGGTA[A/G]TTCTGAGTTTAAGTC | 12928 |
rs26901003 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Crk | Mm_Celera | 11:75701975 | GATCAGACTGGTTCT[A/G]TAGATCATCCCTGGC | 12928 |
rs26901004 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Crk | Mm_Celera | 11:75701973 | GAGATCAGACTGGTT[C/G]TATAGATCATCCCTG | 12928 |
rs26901005 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Crk | Mm_Celera | 11:75701920 | TTTCCTTGGGGAAAT[C/T]ACAGACTGACCAGTA | 12928 |
rs26901006 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75701872 | TTTTCTGTTATCTAA[A/G]CCACCACATCAGTCC | 12928 |
rs26901007 | snp | A/C | 0.32 | 0.24 | intron-variant | Crk | Mm_Celera | 11:75701712 | TGGGTGCGGTGGTCG[A/C]CTAGATTCTGTGGGT | 12928 |
rs26901008 | snp | C/T | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Crk | Mm_Celera | 11:75701687 | GAGTGAATGCCAGAG[C/T]GTCCAGGCCTGGGTG | 12928 |
rs26901009 | snp | A/G | 0.408163 | 0.193609 | intron-variant, downstream-variant-500B | Crk | Mm_Celera | 11:75701525 | GGCCGTGTATATGCC[A/G]TGTGCATTCCATATC | 12928 |
rs26901010 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Crk | Mm_Celera | 11:75701518 | TGTCAAGGGCCGTGT[A/G]TATGCCATGTGCATT | 12928 |
rs26901011 | snp | C/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Crk | Mm_Celera | 11:75701452 | TGGGTATGATAATCA[C/G]GAAACTCAAGGTATT | 12928 |
rs26901012 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Crk | Mm_Celera | 11:75701251 | TGCTGTATGATGCAC[A/C]CAATTCTAGTAGCCT | 12928 |
rs26901013 | snp | A/C | 0.391111 | 0.206368 | intron-variant, stop-lost, missense | Crk | Mm_Celera | 11:75700559 | GCTCCTGATGGTTTG[A/C]TCTCTCTACTAAGGA | 12928 |
rs26901014 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Crk | Mm_Celera | 11:75700472 | TTATTTGCCCAGCTG[A/G]CTGCTTACATGTTCT | 12928 |
rs26901015 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75700273 | CCCCCAAACTGTTGG[A/G]AAACCTGTCTCGTGG | 12928 |
rs26901016 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Crk | Mm_Celera | 11:75700125 | ACGAAAGGAAGTGTT[A/G]AGTGTTGGACCTCCC | 12928 |
rs26901017 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Crk | Mm_Celera | 11:75700112 | GTCAGAAAGCTAGAC[A/G]AAAGGAAGTGTTGAG | 12928 |
rs26901018 | snp | A/T | 0.455 | 0.143091 | intron-variant | Crk | Mm_Celera | 11:75699798 | GGACCTCTGAGAATC[A/T]ATAGTGAGACAAACC | 12928 |
rs26901019 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Crk | Mm_Celera | 11:75698556 | AAGTTACACAGCAAG[A/G]CCCTGTTTCACTCCT | 12928 |
rs26901020 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Crk | Mm_Celera | 11:75698491 | AACAAACTGGTAAAA[A/G]GATGTTGGAGCTGTA | 12928 |
rs26901021 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Crk | Mm_Celera | 11:75698315 | GCTCATAGTTGACTT[C/T]GGTAGCAGTACAGAG | 12928 |
rs26901022 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75698301 | AATGTCTTCACTAGG[C/T]TCATAGTTGACTTCG | 12928 |
rs26901023 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Crk | Mm_Celera | 11:75698117 | CCTAGGAAAGCAGTC[A/C]CTGGGGCTATGCCCA | 12928 |
rs26901024 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75697253 | TTTGCTGATTGCTGC[C/T]GAAGAATGCTGTAGT | 12928 |
rs26901025 | snp | A/G | 0.18 | 0.24 | intron-variant | Crk | Mm_Celera | 11:75696555 | CAACTTCTTTCAAGT[A/G]TCTGTAGTGTATCCT | 12928 |
rs26901026 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Crk | Mm_Celera | 11:75696032 | CTAGCATTTGTATTT[C/G]TGAGTTACACACTCA | 12928 |
rs26901027 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Crk | Mm_Celera | 11:75695807 | GCTGAGATCACAAAC[C/T]TCTGTCACTATGCTT | 12928 |
rs26901028 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75695627 | TGAAGAGCAGGCTAA[A/G]TCAGGCTGATCTGGA | 12928 |
rs26901029 | snp | A/G | 0.32 | 0.24 | intron-variant | Crk | Mm_Celera | 11:75695334 | GAGACAGATAAGAGT[A/G]TGCTGCTGAGAGGCT | 12928 |
rs26901030 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75695284 | GCCTCCTAGGGCACC[A/G]TGCTCAGTGGGAACC | 12928 |
rs26901031 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Crk | Mm_Celera | 11:75695154 | GACTTGGATAGTTTC[C/G]TACTTGGAGACCTTT | 12928 |
rs26901032 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Crk | GRCm38.p3 | 11:75694513 | ACTGCTCTGTGCATT[A/G]TGGACGGGCTCTTAG | 12928 |
rs26901033 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Crk | Mm_Celera | 11:75693751 | CAGAGCCCGCCAACA[A/G]CCTGGCTTGAGTATA | 12928 |
rs26901034 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Crk | GRCm38.p3 | 11:75693582 | CCTCTGTGGAAGCCC[A/C/T]GTTGTTAGGACCTGG | 12928 |
rs26901035 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Crk | Mm_Celera | 11:75693363 | AAGCTGAATGCTAGC[C/T]TTCATCAGGCCTTGG | 12928 |
rs26901036 | snp | G/T | 0.32 | 0.24 | intron-variant | Crk | Mm_Celera | 11:75693012 | TAACTTGAAGTCATT[G/T]TTCTCATCTATATTC | 12928 |
rs26901037 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Crk | Mm_Celera | 11:75691141 | TTTGTGCTTAGAGTA[C/T]CTCTCAAACTTTTCT | 12928 |
rs26901038 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Crk | Mm_Celera | 11:75690230 | AGTGCTGAGCAGATT[A/G]CTTAGCTCACACTGA | 12928 |
rs26901039 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75689996 | CAAAACAGGAATGTA[C/T]GCTCCCCAACAAAAA | 12928 |
rs26901040 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Crk | Mm_Celera | 11:75687554 | TAGGTTCAGACTCTT[A/G]CTCAGGTTTGATGTA | 12928 |
rs26901041 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Crk | Mm_Celera | 11:75686187 | TTAGTCTGCAGAATC[C/T]CTCTTGGATGCAAGG | 12928 |
rs26901042 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Crk | Mm_Celera | 11:75684993 | TAGGTTTGTAACATG[C/G]ATGTGTTTGTGTGCC | 12928 |
rs26901043 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Crk | Mm_Celera | 11:75684457 | TACCTCATTTTGGAG[A/T]TGGTCAAGGTATCCC | 12928 |
rs29385448 | snp | A/G | 0.32 | 0.24 | intron-variant | Crk | Mm_Celera | 11:75695436 | ATAGGGGAGGGAGTT[A/G]AGGGAGTAGATCAGA | 12928 |
rs29389627 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Crk | Mm_Celera | 11:75678429 | TACAACTGAGAGTTT[A/T]AAAAAAAATCTGGCT | 12928 |
rs29394990 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Crk | Mm_Celera | 11:75708869 | GGGTGTGGTGGCACA[C/T]GCCTTTAATCCCAGC | 12928 |
rs29401144 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75697072 | ACAGCGGCAGAGTAG[A/G]ATGTTTATGAGTAGA | 12928 |
rs29404184 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Crk | Mm_Celera | 11:75705840 | ATTAATTTGTTGAAA[A/T]TGTTTATTAATAATG | 12928 |
rs29406906 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Crk | Mm_Celera | 11:75708857 | ATTCTCCCGGCCGGG[C/T]GTGGTGGCACACGCC | 12928 |
rs29412409 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75687641 | ACCAAGTATCTCCTT[C/T]CTTTCTCTTCCTTCT | 12928 |
rs29413251 | snp | C/G/T | 0.5 | 0 | downstream-variant-500B | Crk | GRCm38.p3 | 11:75708888 | TTTAATCCCAGCACT[C/G/T]GGGAGGCAGAGGCAG | 12928 |
rs29420881 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Crk | Mm_Celera | 11:75708866 | GCCGGGTGTGGTGGC[A/G]CACGCCTTTAATCCC | 12928 |
rs29423363 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Crk | GRCm38.p3 | 11:75690505 | TCTTTCTTTCTTTCT[A/T]TTTTTTTTTCTTTGT | 12928 |
rs29429341 | snp | A/G | 0.375 | 0.216506 | intron-variant | Crk | Mm_Celera | 11:75695092 | TGGTGTTTTCTTTAC[A/G]TGTAGTCTCCATTTT | 12928 |
rs29435015 | snp | A/C | 0.375 | 0.216506 | intron-variant | Crk | Mm_Celera | 11:75689464 | ATAACATGTAAGGCC[A/C]GTGAGATGGCTCAGT | 12928 |
rs29440757 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75690536 | TTTCTTTTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 12928 |
rs29441536 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Crk | Mm_Celera | 11:75703545 | TGGAACAATCTGTTT[C/T]CCCCCAATTGCCATC | 12928 |
rs29443194 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75688059 | TGCTTTGTGCCAGGC[A/G]AGGTAACCCATACCT | 12928 |
rs29448716 | snp | A/G | 0.375 | 0.216506 | intron-variant | Crk | Mm_Celera | 11:75681717 | GGTTGGCCTCAAAGA[A/G]GAGAAGATTGCCAGT | 12928 |
rs29473133 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Crk | Mm_Celera | 11:75696887 | TTGTTTTTGAGACAG[A/G]GTCTCACTGTATAGC | 12928 |
rs29480332 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Crk | Mm_Celera | 11:75707797 | ACTACTCCACTTCAG[A/C]TACCTTGAGAATCTG | 12928 |
rs29484993 | snp | C/T | 0.375 | 0.216506 | intron-variant | Crk | Mm_Celera | 11:75689698 | TCTGATCTCCACAGA[C/T]GTAAATAATAATAAT | 12928 |
rs47155126 | snp | A/G | | | intron-variant | Crk | Mm_Celera | 11:75683215 | CCCAGCTCAAACCCT[A/G]TTTGAACTTAACCAT | 12928 |
rs49982340 | snp | A/G | | | intron-variant | Crk | Mm_Celera | 11:75686505 | TGCAAATAGTAGTGA[A/G]GTGCCTACTTAAAAT | 12928 |
rs50163425 | snp | C/T | | | intron-variant | Crk | Mm_Celera | 11:75687349 | GCACGCCTTTAATCC[C/T]AGCACTTGGGAGGCA | 12928 |
rs51249377 | snp | A/G | | | intron-variant | Crk | Mm_Celera | 11:75682261 | TAAAGTATTTTCTTG[A/G]TGCAGGGGGAGAGGA | 12928 |
rs51980286 | snp | A/G | | | intron-variant | Crk | Mm_Celera | 11:75683794 | GTGCTAGGATTAAAG[A/G]TGTGGGGAATTATTT | 12928 |
rs52137739 | snp | A/G | | | downstream-variant-500B | Crk | Mm_Celera | 11:75708772 | AAAAGACAAAACAAA[A/G]CAAAACAACAACAAC | 12928 |
rs52264019 | snp | A/T | | | intron-variant | Crk | Mm_Celera | 11:75688751 | ATAAATAAATAAAAT[A/T]AAAATAAAAAATAAA | 12928 |
rs52314311 | snp | A/G | | | intron-variant | Crk | Mm_Celera | 11:75686996 | ATATGTAAGTACACT[A/G]TAGCTGTCTTCAGAC | 12928 |
rs52336861 | snp | A/T | | | intron-variant | Crk | Mm_Celera | 11:75686963 | TTTTTTTTTTTTTTT[A/T]AGATTTATTTATTTA | 12928 |
rs52366990 | snp | C/T | | | intron-variant | Crk | Mm_Celera | 11:75682907 | GTCCTGGAACTCACT[C/T]TGTAGACTAGGCTGG | 12928 |
rs52555859 | snp | C/T | | | intron-variant | Crk | Mm_Celera | 11:75686947 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 12928 |
rs211708024 | in-del | -/T | | | intron-variant | Crk | Mm_Celera | 11:75680387 | ATTAGTGGAGGAAGA[-/T]TTTTTTCCTTTAGAA | 12928 |
rs211867658 | snp | A/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | Crk | Mm_Celera | 11:75700871 | GAATTATATATATGT[A/T]TTTTTCTTTCTGAGA | 12928 |
rs211951645 | in-del | -/T | | | intron-variant | Crk | Mm_Celera | 11:75681842 | TTTTTGTTGTTGTTG[-/T]TTGTTTGTTTGTTTT | 12928 |