SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3692334 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Grb2 | GRCm38.p3 | 11:115675907 | TTCTGTCCTGTCCTG[C/T]GGTCCTCAAGCATCT | 14784 |
rs3693512 | snp | C/T | 0.5 | 0 | intron-variant | Grb2 | GRCm38.p3 | 11:115676070 | TATAACCCCAGTACT[C/T]AGCAAGGGAAGTCAG | 14784 |
rs6219508 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699811 | CCTGTCAGAATCCAC[A/G]CAGGACTTGGGTCTC | 14784 |
rs6221522 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700141 | CACAAGAGCATGGCT[G/T]AAGTTCTCATTTATA | 14784 |
rs6221664 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700233 | gtagcctagaactcc[G/T]tataagtacaccaga | 14784 |
rs6297198 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710299 | AATGACAATATACCA[C/T]CCAAATACCAGAGTC | 14784 |
rs6298428 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710507 | aaagacccaggcttc[A/G]ttcccagcatcttca | 14784 |
rs6298883 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710540 | gcactaacgatcatc[C/T]ataactccagttcnt | 14784 |
rs6298898 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710554 | cnataactccagttc[C/T]tgggaatccaaggtc | 14784 |
rs13471888 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115644519 | CTTGTCTTCTGTGAG[C/T]TTTCCGTCCTCTGTA | 14784 |
rs13471889 | snp | A/C | | | utr-variant-5-prime | Grb2 | Mm_Celera | 11:115699239 | TGCTGAGCACTGAGC[A/C]GCGCTCAGAATGGAA | 14784 |
rs13471890 | snp | A/G | | | utr-variant-5-prime | Grb2 | GRCm38.p3 | 11:115708475 | GCGGGCGCCGCAGTC[A/G]GGGAGCAGCAGCGAG | 14784 |
rs13471891 | snp | A/G | | | missense | Grb2 | Mm_Celera | 11:115645907 | TGACCCCCAGGAGGA[A/G]GGCGAGCTGGGCTTT | 14784 |
rs27015950 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700927 | CTTAGTTAGTCTATG[C/T]GGTGCCACCTCTCAA | 14784 |
rs27015951 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700369 | ATACAGGCTGGTGCC[A/G]GACAGTCAGACCCCA | 14784 |
rs27015952 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Grb2 | Mm_Celera | 11:115698966 | AAGGCAGTTAAGGAC[A/G]ACACATCACAGCGAC | 14784 |
rs27015953 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Grb2 | Mm_Celera | 11:115698411 | AAGGAAACCGTCATC[C/T]GGAAGGGCGAGCTGC | 14784 |
rs27015954 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Grb2 | GRCm38.p3 | 11:115698163 | TCCATCACTTTGAGC[A/T]CTGAGGGCAAACGTT | 14784 |
rs27015955 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Grb2 | GRCm38.p3 | 11:115697813 | GGTTGAGTCCAGACC[C/T]GTTGCCTGGAAGAGG | 14784 |
rs27015956 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115696203 | CACACTCAGTGCAAA[A/G]GCGTGAAGCTTGCAG | 14784 |
rs27015957 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115695497 | CTTGCCACGACACTG[A/G]TTAAGCTGAGCTGGA | 14784 |
rs27015958 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115694061 | AAACCAGCACGGGCA[C/T]TCCTTTAAAAGCTAA | 14784 |
rs27015959 | snp | C/G/T | 0.297521 | 0.245442 | intron-variant | Grb2 | Mm_Celera | 11:115693210 | GCAGGAGGGCTTGCC[C/G/T]GAGTTTGAGGCCAGA | 14784 |
rs27015960 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Grb2 | Mm_Celera | 11:115692737 | GCTTTGCTCTTATTA[A/G]CGTGGCCTGCTCTCC | 14784 |
rs27015961 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Grb2 | Mm_Celera | 11:115692330 | GTCTATGGATGTCAG[C/T]CATTGCTTTGAGCAC | 14784 |
rs27015962 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115690935 | CAGAGCTATGAGGAT[A/G]AATAATCACCTTAAA | 14784 |
rs27015963 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115688030 | TACAGGCTCTGGGGT[A/G]CAGTCCATTTTCATC | 14784 |
rs27015964 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Grb2 | GRCm38.p3 | 11:115686933 | CGTCTGTAGCAGACC[A/T]CACTCAACACCAAAC | 14784 |
rs27015965 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115686923 | GAAGTTCAGTCGTCT[A/G]TAGCAGACCTCACTC | 14784 |
rs27015966 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115686584 | CACCAAATACACTTC[C/T]CCGAGACAATTTCAA | 14784 |
rs27015967 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Grb2 | Mm_Celera | 11:115684888 | CAGAATGGAAGTAAC[C/G]AGCTGTGGATGGACA | 14784 |
rs27015968 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115684704 | GAGGGCTAGGGACAA[C/T]GAGGCAGAAACAGAC | 14784 |
rs27015969 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115683897 | TCAGTGAAGTGCGTG[A/C]GACAAGCAGAAGGAC | 14784 |
rs27015970 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115683672 | GACACTTGGAAATGG[A/G]AAGACTGAGCAGTGG | 14784 |
rs27015971 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Grb2 | GRCm38.p3 | 11:115683604 | ACACACAGCATTTCA[A/C]GCCTAAATGCACAGC | 14784 |
rs27015972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grb2 | Mm_Celera | 11:115682819 | AATGTCCAAACCAGT[C/T]TTGAATAGGCCCCAG | 14784 |
rs27015973 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115682424 | AACTATAGTCACTCT[A/G]GGCGAGAATACGAAA | 14784 |
rs27015974 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Grb2 | GRCm38.p3 | 11:115682277 | GTACAGGCAAAAAGA[G/T]CAATATGGCTGAAGA | 14784 |
rs27015975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115680232 | CTCACTTAAAGCAGC[A/G]AGGTAAGCAACAGAG | 14784 |
rs27015976 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115680159 | CTGTCAACTAGCCTC[A/G]GCACTCTGGCAAGGC | 14784 |
rs27015977 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115680106 | AGAGGTCAAAGAGCA[C/G]CCGTGCAAATACAGG | 14784 |
rs27015978 | snp | C/T | 0.5 | 0 | intron-variant | Grb2 | GRCm38.p3 | 11:115680080 | GCACCACAGACCAAG[C/T]CACACCAGGAAGAGG | 14784 |
rs27015979 | snp | C/G/T | 0.391111 | 0.206368 | intron-variant | Grb2 | GRCm38.p3 | 11:115679991 | CCAAGACACAATGTA[C/G/T]GCTACCTGTCCTTTC | 14784 |
rs27015980 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grb2 | GRCm38.p3 | 11:115679967 | TCACTGAAGCTGCCC[C/T]GAGGCTGACCAAGAC | 14784 |
rs27015981 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115679872 | CAGTATCCTGTGGCC[C/T]GAAACCTGTCTGGGG | 14784 |
rs27015982 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115679635 | GGTCAAGGTCAGCCT[A/G]GCACCACAGACAGAG | 14784 |
rs27015983 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | GRCm38.p3 | 11:115679532 | AAAAAAGTACAACTC[A/G]AGGTTTCTTTGTATC | 14784 |
rs27015984 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Grb2 | GRCm38.p3 | 11:115679465 | GCACAGAATCTCAGC[A/G]TACATCAAGGCTAAG | 14784 |
rs27015985 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115679363 | GACCCATCTGAGAAG[A/T]GGTGATGCCATACCT | 14784 |
rs27015986 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115679102 | AAGCTAAAGCCTCAC[A/G]TGACACGAAATCTGT | 14784 |
rs27015987 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | GRCm38.p3 | 11:115678455 | AGAAGACATTTTGAA[C/T]CAGACAGCTTGGAGA | 14784 |
rs27015988 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Grb2 | Mm_Celera | 11:115677456 | TGTGCCGCGTGTGCA[C/T]CTGGGCATGTGCACA | 14784 |
rs27015989 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115677448 | CTTATGAGTGTGCCG[C/T]GTGTGCACCTGGGCA | 14784 |
rs27015990 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115673593 | GTCTATCGGCTCCCT[C/T]GCAACTAGAACTGCA | 14784 |
rs27015991 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Grb2 | GRCm38.p3 | 11:115673223 | AGATGATCCGAGTTC[C/G]GGACTGGTGAGATGA | 14784 |
rs27015992 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115673205 | CAAGCAATCTACCTA[A/C]AAAGATGATCCGAGT | 14784 |
rs27015993 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115671117 | TTTTTAGGAGCCTTC[G/T]TTCACTTTTCATCAT | 14784 |
rs27015994 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115671067 | TTTGTAATCCTTCCT[C/T]CACACAGAAGAGGGT | 14784 |
rs27015995 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115670782 | GAGAAGACAAGGATC[C/T]GAAACACTAATAACA | 14784 |
rs27015996 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115670535 | GTAAAGGCAGTCCTG[C/G]TAATTACCACATTTA | 14784 |
rs27015997 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115670386 | TGCAAGACCATGAGC[A/G]CATACCCTTTCATGA | 14784 |
rs27015998 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115670119 | GGAGGTCAAATAAGG[A/G]CAACAGAGCCTCTGG | 14784 |
rs27015999 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Grb2 | GRCm38.p3 | 11:115668005 | AAATGATCAATTGGT[A/G]ATGTCACTCCATTGC | 14784 |
rs27016000 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115667411 | CAGAGCAAGACAAGG[A/G]CAGAGCGGCCCAATG | 14784 |
rs27016001 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115667130 | TTAAGGGACTGCTAC[A/G]GTATGTTACAACTAC | 14784 |
rs27016002 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115667106 | TGGAAAGTGTAACCC[A/G]GCCGGCTATTAAGGG | 14784 |
rs27016003 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115666840 | CACTGTAGCTAAGCA[G/T]GGCGGCTCCTTGGGT | 14784 |
rs27016004 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115666757 | AAGCCATCCTCAGGC[C/T]TCATTCTCCTGAGCA | 14784 |
rs27016005 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115666345 | GTGCCCTGGGTCTAT[A/G]TGAACCACCAACAGG | 14784 |
rs27016006 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115665453 | GTGAGGTTAACATCT[C/G]GGCACTATAGTTACA | 14784 |
rs27016007 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Grb2 | GRCm38.p3 | 11:115665146 | CCACCCAGGAACCGG[A/G]ACCAAAGCTGTAAAT | 14784 |
rs27016008 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Grb2 | Mm_Celera | 11:115664491 | GCCTCACCAAGAAAG[C/T]CCATCCCAAACGTCA | 14784 |
rs27016009 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115664433 | TCTAGACTCCCATGC[C/T]GTCAGGTGTCCCAGG | 14784 |
rs27016010 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115664054 | AGCCCAAATGCTCAG[A/G]CACCACAGAACAGAC | 14784 |
rs27016011 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115663256 | GGAGAGCAGGCCCTG[C/T]CCAGAGTCCACTATC | 14784 |
rs27016012 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115662928 | ATGCAGAGATAAACG[C/T]GCTTCGGATACCCAA | 14784 |
rs27016013 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115662927 | GATGCAGAGATAAAC[A/G]CGCTTCGGATACCCA | 14784 |
rs27016014 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115662926 | TGATGCAGAGATAAA[C/T]GCGCTTCGGATACCC | 14784 |
rs27016015 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115662492 | CCATGTACCTCAAAG[C/T]GGGAAGGCGCAGAAT | 14784 |
rs27016016 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115660948 | CTGCTTCCTACACAC[A/G]CAAAGGTCGACACCT | 14784 |
rs27016017 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grb2 | GRCm38.p3 | 11:115660500 | GTTACACAGGAACGA[C/T]GGAGTGCTCACCAAG | 14784 |
rs27016018 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grb2 | Mm_Celera | 11:115659877 | CTCACTGTAACGGAA[A/G]TGTACCATCTTAGCT | 14784 |
rs27016019 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Grb2 | GRCm38.p3 | 11:115659128 | CTATCCTCAGGACCC[A/G]CACGGTAGAAAGAAA | 14784 |
rs27016020 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Grb2 | Mm_Celera | 11:115658989 | GAACTGGGTATGTTG[G/T]TTGTGGAAATTCAGT | 14784 |
rs27016021 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Grb2 | GRCm38.p3 | 11:115658675 | TAGCCTCTGTACTGC[G/T]TAGACTTATGACTCA | 14784 |
rs27016022 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115658537 | ACTGTCTCTCCTACC[C/G]TTTCTTTCTCTGCAG | 14784 |
rs27016023 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115658466 | AGAGAGCGCCCTGAA[C/T]GCTCACAGCCCTTAT | 14784 |
rs27016024 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Grb2 | GRCm38.p3 | 11:115658337 | TATAAAGTGAACATG[A/G]GTTTCAAGTATCGTG | 14784 |
rs27016025 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Grb2 | Mm_Celera | 11:115658019 | AGGGAGTTGTGGAGT[A/G]CAGTGGGTCAAACTG | 14784 |
rs27016026 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Grb2 | Mm_Celera | 11:115657995 | CGCATCTTCCAGAGC[C/T]GGAGTTACAGGGAGT | 14784 |
rs27016027 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Grb2 | Mm_Celera | 11:115657918 | AGTGCTCATCTTTTT[C/T]GATATGTGGGTATGT | 14784 |
rs27016028 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Grb2 | Mm_Celera | 11:115657793 | GTTCTAAGAGAGCCA[A/G]TGCTGCCTTCTAGAG | 14784 |
rs27016029 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115656917 | GACGGCAGGGAATAC[A/G]ATGCCTGGCGCCAAG | 14784 |
rs27016030 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115656889 | ACTTGGTGTATTATA[C/T]CTCTGTCGCCCAGAC | 14784 |
rs27016031 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115656833 | TCCCAGACCTGGAGA[C/T]GCTTTACAGCATGGT | 14784 |
rs27016032 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115656808 | TTAAAGCAGGAGGTA[C/T]CAAGGCAACTCCCAG | 14784 |
rs27016033 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115656768 | CAAGCTAGAGAAGCC[A/G]TGTCCCCTCAAAAGT | 14784 |
rs27016034 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115656733 | AGTCCCCAAAGCTGC[A/G]TGTTCTTACTGCCAA | 14784 |
rs27016035 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115655322 | GAGACAAGCAGGTGA[C/T]CTCTTTGCTTAGGGG | 14784 |
rs27016036 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Grb2 | Mm_Celera | 11:115654992 | TTTGTGTATCCTTGG[C/T]TGCCGCCAGAGCACT | 14784 |
rs27016037 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Grb2 | GRCm38.p3 | 11:115653394 | ATCAAGGAAGCCAAG[A/G]GTAGGAGATGTATTT | 14784 |
rs27016038 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115652812 | TTATGGGCATCAACC[C/T]GACATTTGTGTGAGC | 14784 |
rs27016039 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Grb2 | GRCm38.p3 | 11:115652217 | CTCTCCCTTCCCCGA[C/T]CACCAATCACATGCT | 14784 |
rs27016040 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grb2 | Mm_Celera | 11:115652171 | CTCCACACTCACCAG[A/G]GAAGGGCAAATGTTC | 14784 |
rs27016041 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115652126 | ATCTAGTCATGGCCA[C/T]AGGCTGATCCCCAGT | 14784 |
rs27016042 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Grb2 | GRCm38.p3 | 11:115651462 | GACAGCCTTTTGTGA[A/G]TTCCAGGGATGAAAT | 14784 |
rs27016043 | snp | A/G | 0.5 | 0 | intron-variant | Grb2 | Mm_Celera | 11:115651154 | GAGTCCTGGCTTTTC[A/G]CCCCAAGGACATGGG | 14784 |
rs27016044 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115650056 | TCCCTGGGGCTCTTA[C/T]CTGGCTCAGGGCCTT | 14784 |
rs27016045 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Grb2 | GRCm38.p3 | 11:115649973 | GCATGTAAATGAGAG[C/T]GCTCCTGTAGTGAGT | 14784 |
rs27016046 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Grb2 | Mm_Celera | 11:115649960 | GATGTACAACCTGGC[A/G]TGTAAATGAGAGCGC | 14784 |
rs27016047 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Grb2 | Mm_Celera | 11:115649424 | CATGTAATATCATGC[C/G]CAATTCCTAGTTGGA | 14784 |
rs27016048 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115648683 | TTCCTGCTGTCTTCA[C/T]TACATCACGGCCCAG | 14784 |
rs27016049 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grb2 | Mm_Celera | 11:115648559 | CCACTGAGCTGTGTT[A/G]TTAGCCTGGGTCTCA | 14784 |
rs27016050 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115646608 | TGAGTGCCAACTGCA[A/G]AGCCTCACTGCCATG | 14784 |
rs27016051 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115645678 | GCCAGGTGTTCTGCG[C/T]TCCCTCACAGGCTGT | 14784 |
rs27016052 | snp | A/G/T | 0.48 | 0.0979796 | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115645027 | CACAGGATAGGAGAC[A/G/T]AATCAACTGAAAAGC | 14784 |
rs27016053 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115644879 | GAGTCTGAGCTGAAG[C/T]GAGTGTTGCAGCTCA | 14784 |
rs27016054 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643570 | GTCACGGCTGTGTCA[C/T]GTAGCTGCCTCACCG | 14784 |
rs29385406 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115708180 | CCGGGTCTCTGCCCC[C/G]AGCGGGAGGAAGACC | 14784 |
rs29386602 | snp | A/T | 0.5 | 0 | intron-variant | Grb2 | GRCm38.p3 | 11:115680608 | GCGCTGAGCCATCTC[A/T]CCAGCCCCCAGACCC | 14784 |
rs29388062 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115649421 | AGGCATGTAATATCA[C/T]GCGCAATTCCTAGTT | 14784 |
rs29389250 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | Mm_Celera | 11:115704759 | TCACACACAACTACA[C/T]GAGGTTGAAACTAGC | 14784 |
rs29393520 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115647941 | GAGGACTGTGGCTCA[A/G]GCTCCAAAGGCCCAA | 14784 |
rs29393560 | snp | A/T | 0.5 | 0 | intron-variant | Grb2 | Mm_Celera | 11:115680440 | TTTTTTTTTTTTTTT[A/T]TAAACTTGTTTATTT | 14784 |
rs29397082 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709620 | TGTGCGATGCAAAGT[A/G]CATAGATAGGTTCCT | 14784 |
rs29402954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115688950 | GGCCAATGTGGGGGT[A/G]CCCCAGCTACCACCG | 14784 |
rs29403726 | snp | A/G | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115690488 | AGCTGGCCAGAGAGA[A/G]TGAGAGTCCTCCACA | 14784 |
rs29406776 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708629 | CGGCCCCGCCCCGCC[G/T]CGCCCCGCCCCCGCG | 14784 |
rs29407857 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115656452 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 14784 |
rs29407865 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115667698 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 14784 |
rs29409898 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115660816 | TGTCTGTGTCCTAGT[A/G]CTAGGATTACATTTT | 14784 |
rs29411251 | snp | G/T | 0.5 | 0 | intron-variant | Grb2 | GRCm38.p3 | 11:115680423 | AATTTTAGACCTTTG[G/T]TTTTTTTTTTTTTTT | 14784 |
rs29411296 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Grb2 | GRCm38.p3 | 11:115701211 | TCCTGGAAGAATTAA[C/T]GAGTGTTCTTAACCT | 14784 |
rs29411541 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | Mm_Celera | 11:115649942 | TTCCCCACAAAGAGA[C/T]GGGATGTACAACCTG | 14784 |
rs29412607 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115647401 | CTTTCTTTCTTTTTG[G/T]TTTTTTCGAGACAGG | 14784 |
rs29415005 | snp | A/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115695678 | CTTCTCAATCTTTGT[A/T]ACTTGACAGCCTTGG | 14784 |
rs29415280 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115651006 | TTATGCCATAGGTGT[A/G]TCCCACCATGCCTGG | 14784 |
rs29416815 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115666070 | AAAAAAACCAACCAA[A/C]CAAACAAACAAAAAA | 14784 |
rs29417401 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115664513 | CAAACGTCACTAAAC[C/G]GCATCTGCTCCTCTG | 14784 |
rs29421250 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115685674 | CTATTGGTATTTACT[G/T]TCTTTAGCAGAAAAA | 14784 |
rs29424422 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115665002 | TAACAGTTCATTCAG[C/T]TGAACTTGAGATCTT | 14784 |
rs29426797 | snp | C/T | 0.5 | 0 | intron-variant | Grb2 | GRCm38.p3 | 11:115693894 | AGCACTGTATACACA[C/T]GTGGTGCAGACACAC | 14784 |
rs29428781 | snp | A/T | 0.5 | 0 | intron-variant | Grb2 | Mm_Celera | 11:115680439 | TTTTTTTTTTTTTTT[A/T]TTAAACTTGTTTATT | 14784 |
rs29428842 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115648427 | ACTTCTCTAGATATG[C/T]GTGTGTGTGATGGGC | 14784 |
rs29440984 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115657125 | CCAAAAAGTAACTTT[C/T]TAGGCATGGAGAGAT | 14784 |
rs29441708 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708613 | CGAGAACTTCCCCAC[A/G]CGGCCCCGCCCCGCC | 14784 |
rs29442134 | snp | A/G | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115654217 | ACTTGTGGATGTCAG[A/G]GGACAACTTCTGAGA | 14784 |
rs29442158 | snp | A/T | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115661530 | GGGTGGGCTTTGAGG[A/T]TTCAAAGGCTAGAGC | 14784 |
rs29444626 | snp | A/C | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115650206 | AGCCAGTTTCTGAGG[A/C]CAAAGCCCTCCTGCC | 14784 |
rs29448016 | snp | A/T | 0.5 | 0 | intron-variant | Grb2 | Mm_Celera | 11:115680440 | TTTTTTTTTTTTTTT[A/T]AAACTTGTTTATTTA | 14784 |
rs29455369 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115707857 | CCAACAAGTATTTTT[C/T]CCCCCTCAAGTCCTT | 14784 |
rs29455599 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115661956 | AGCCTTCTCTCCCAG[C/T]TTTAGGTTCACAGTA | 14784 |
rs29456526 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115671759 | TCTATGTATCCCTGG[C/T]TGTCCTTGAACTCAG | 14784 |
rs29457760 | snp | A/G | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115673337 | GCCCTAAAGCTTTCT[A/G]ACTGCCATACATATC | 14784 |
rs29458058 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115664400 | AGGGGAACTAACAGA[A/G]GGACACCCTCCCAGG | 14784 |
rs29459263 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700720 | TATTATTCGTTTGTT[C/G]TAAAGTTAACATGTG | 14784 |
rs29461415 | snp | G/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115656414 | TGATATATAGAGACG[G/T]GTGTGTGTGTGTGTG | 14784 |
rs29462973 | snp | C/G | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115669387 | ATCTCAGGGCTGAGG[C/G]AGCTCAGAGGTGAAG | 14784 |
rs29463877 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115647923 | CAAGGGAGGTGCTTT[C/T]GAGAGGACTGTGGCT | 14784 |
rs29463964 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709654 | CGGGGCTGCCGGTTT[G/T]GGGGGAGTAGTAGAT | 14784 |
rs29464549 | snp | G/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115667506 | TTCACGCTGTGCTGG[G/T]CACCTACCATAAGAT | 14784 |
rs29464742 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115699553 | TCCAGCAGCCAATAG[A/C]ATCAGCTGCTTTACG | 14784 |
rs29466456 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115656458 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGCGTG | 14784 |
rs29467034 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Grb2 | Mm_Celera | 11:115681661 | CCCCAAATCTTCCAC[A/T]GAAAATTCAAGAGTT | 14784 |
rs29468359 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115664514 | AAACGTCACTAAACG[A/G]CATCTGCTCCTCTGC | 14784 |
rs29473184 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grb2 | GRCm38.p3 | 11:115654626 | TGCATGCTAGAGCAC[A/G]CTCTGCTCTGATGGA | 14784 |
rs29475154 | snp | C/G | 0.32 | 0.24 | intron-variant | Grb2 | Mm_Celera | 11:115650346 | AAGGCCTACAACTTC[C/G]CAGCTGTAGAAGGGT | 14784 |
rs29475249 | snp | A/T | 0.5 | 0 | intron-variant | Grb2 | Mm_Celera | 11:115650582 | GTATCTGAAAAAAAA[A/T]TTTTTTAAATTATTA | 14784 |
rs29478567 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grb2 | GRCm38.p3 | 11:115681181 | GGGCATCAGCTCTCA[C/T]ACAGTCACAGAGACA | 14784 |
rs29482339 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grb2 | Mm_Celera | 11:115656464 | GTGTGTGTGTGTGTG[C/T]GTGTGCGTGTGTGTG | 14784 |
rs29485736 | snp | C/T | 0.32 | 0.24 | intron-variant | Grb2 | GRCm38.p3 | 11:115661550 | AAGGCTAGAGCCAGG[C/T]CCAGTGTTGCTCGGT | 14784 |
rs45683411 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115686849 | TTAAGAATTCATCAA[A/C]ATGCTAGACTAGAAC | 14784 |
rs45770263 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687116 | AGTTAGTCAAAGAAA[C/T]GAGAGAATTTGAGAT | 14784 |
rs45974281 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659101 | CTGAAGCCAAGCCTT[C/T]TGACCTAAGTTCTAT | 14784 |
rs46252763 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115652290 | TCAGACACACCAGAA[A/G]AGGGAATTGGATACC | 14784 |
rs47030221 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702015 | AGTGATTGTCAGTGG[A/G]AAAGTGGTGCCCTAG | 14784 |
rs47086923 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115683754 | CTGAGTTCAAGACCA[A/G]CCTGGTCTACAAAGT | 14784 |
rs47111799 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115679938 | AAAGCACAGCATACG[C/T]TCCTCTGTGGCAGTC | 14784 |
rs47173334 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672644 | TATATGCAGGCAAAC[A/G]CCTACACACATAAAA | 14784 |
rs47266237 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115701950 | GAGGTGTTCTCACTG[A/G]GTACCGTTAGTGTGC | 14784 |
rs48498768 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672611 | TCTGGTTTCCTTGGG[C/T]ACAAGGCATGGCATG | 14784 |
rs49137735 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115683708 | GCACCTCTTTAATCC[A/C]AGCACTCAGGAGGCA | 14784 |
rs49778100 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115648320 | AGATCCTCTTGTTTC[A/G]TGGTAGTTACCAACC | 14784 |
rs50328142 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115651813 | CTGCAAAGTATTTTT[A/T]AAAAAAAATTCTGCC | 14784 |
rs50969738 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686874 | TAGAACACAAGTCTG[C/T]AAGAAGGAACAAGGT | 14784 |
rs51131050 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115670516 | ACCTCCTTTTACTGC[A/T]GAAGTAAAGGCAGTC | 14784 |
rs52177849 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658702 | CTCAACCTACACACA[C/T]ACACACACACACACA | 14784 |
rs52273768 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115687313 | ACAAAAAAAAAAAAA[A/C]AAAAGCAAAATAAAT | 14784 |
rs52322449 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658059 | TATATATATATATAT[A/G]TATGTATATACTCAC | 14784 |
rs52337349 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658073 | TGTATGTATATACTC[A/T]CTCTCACTCTCTCTC | 14784 |
rs52379684 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656470 | GTGTGTGTGTGTGTG[C/T]GTGTGTGCGCGCGCG | 14784 |
rs52384815 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658063 | TATATATATATGTAT[A/G]TATATACTCACTCTC | 14784 |
rs52530333 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658079 | TATATACTCACTCTC[A/T]CTCTCTCTCTCTCTC | 14784 |
rs52584457 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656420 | ATAGAGACGGGTGTG[G/T]GTGTGTGTGTGTGTG | 14784 |
rs108003362 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658723 | CACACACACACACAC[A/G]CACACGCACGCACAC | 14784 |
rs108236841 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115707262 | ACCACCCGCCCCCGC[C/G]CCCCTGGCTCCCAAG | 14784 |
rs211732118 | in-del | -/CATC | | | intron-variant | Grb2 | Mm_Celera | 11:115682016 | TACTATGCCAAAAGG[-/CATC]CATCCAACAAGGCTT | 14784 |
rs211784894 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661309 | TGGTGTTTCCCTCAC[A/G]ACAGTCAAGTTCCTA | 14784 |
rs211859329 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658517 | TCTGAGCTCTGAGAC[A/T]GAGAACTGTCTCTCC | 14784 |
rs211861807 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648271 | CAGCTCCACACGATC[C/T]CCCTCTCTAGCATCT | 14784 |
rs211907842 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115696167 | CATTCCAAGCCTCTG[C/T]ATGAGGATGGGAAAC | 14784 |
rs211941309 | snp | C/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709117 | TTAAATCGAGAGAAG[C/T]AGCAGAAGAGTAAAC | 14784 |
rs211983070 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707932 | TCCGGGTAACAATCA[C/T]TCTAAGTCACGGTGG | 14784 |
rs212040526 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675617 | GCATGGGCTGTGGTG[A/T]AGACGGAAAGGCAGG | 14784 |
rs212083624 | in-del | -/AAGA | | | intron-variant | Grb2 | Mm_Celera | 11:115693289 | TGTCTGAAAAAAAAG[-/AAGA]AAGAGAAAGAGCACA | 14784 |
rs212084815 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685976 | GAAATGTAGCTCATT[A/G]GCAAATCAAGCACTT | 14784 |
rs212087392 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705883 | CCTTCATCCCAACAC[C/T]TCAACAGAAAGCAGA | 14784 |
rs212119957 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692734 | GATGCTTTGCTCTTA[A/T]TAACGTGGCCTGCTC | 14784 |
rs212187086 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646603 | CCACCTGAGTGCCAA[C/G]TGCAGAGCCTCACTG | 14784 |
rs212237548 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115683694 | GAGCAGTGGTGGCTG[C/T]ACCTCTTTAATCCCA | 14784 |
rs212256758 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115697722 | CCCTCCCTGGCAAAG[A/T]AAGAAAAAGAAGCTC | 14784 |
rs212274352 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115693520 | AAGACAGCTACAGTG[A/C]ACTTACATATAATAA | 14784 |
rs212300897 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684568 | ACTCGGGAGGCAGAG[A/G]CAGGCAAATTTCTGA | 14784 |
rs212307297 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | Grb2 | GRCm38.p3 | 11:115657158 | CGCAGTGGCTATGGG[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 14784 |
rs212358135 | in-del | -/AACAATCTA | | | intron-variant | Grb2 | Mm_Celera | 11:115698296 | CAGCTGGCAAATCTC[-/AACAATCTA]GACTGAGGCTCAGAG | 14784 |
rs212388139 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115665716 | CCTGTCTCGAAAAAA[A/C]CAAAAAAGAAAAAAG | 14784 |
rs212399017 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655745 | GTGTTTTCTTAAGGC[A/G]GCTTCTCTAGCAGAC | 14784 |
rs212417686 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674228 | TTACAAGCCGAGTAA[A/G]TAAGTTGCTGGGTGG | 14784 |
rs212454355 | in-del | -/GGT | | | intron-variant | Grb2 | Mm_Celera | 11:115651424 | AAGACAACCCTGGGG[-/GGT]GGGGGGTGTCATTCT | 14784 |
rs212517862 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115688408 | ACACCACCCAATGCA[A/G]ACTGGGCTCAGTGCA | 14784 |
rs212537953 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115673229 | TCCGAGTTCCGGACT[A/G]GTGAGATGACTCACT | 14784 |
rs212600032 | in-del | -/AAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115707094 | AAACCATGATCTGTG[-/AAAA]AAAAAAAACACCAAA | 14784 |
rs212705211 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115679893 | CTGTCTGGGGAATCA[A/C]ACACAAGTTTAACCA | 14784 |
rs212707247 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668816 | GTTTAGGTCTGACAA[G/T]GAGGACAGAGAATTT | 14784 |
rs212724937 | snp | A/G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665217 | CTAATCAGTGCAGGC[A/G/T]TACGGTGATCACTCT | 14784 |
rs212755685 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650385 | CAAAAGCAAGAAGGG[A/G]GGCTTGCATTGTGAG | 14784 |
rs212804632 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661659 | CCTTGCTTCTCACCA[C/T]GATGATAATGAACCA | 14784 |
rs212817122 | snp | G/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700733 | TTCTAAAGTTAACAT[G/T]TGGGGCATTAATCAA | 14784 |
rs212869827 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669931 | AATGACCAGAATACA[C/T]CTCCATTCTTAGCAA | 14784 |
rs212925074 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676999 | TTCAGTAAAATCAAA[C/G]CAACTGTCCCACCAC | 14784 |
rs212941727 | in-del | -/TGA | | | intron-variant | Grb2 | Mm_Celera | 11:115681396 | TATATGGCCTAGAAT[-/TGA]TGATGACCTTGAGCT | 14784 |
rs212997994 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659607 | AAACCACCATTAAAA[C/T]TTTTAATCTATAAAA | 14784 |
rs213007317 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115680423 | AATTTTAGACCTTTG[-/G]TTTTTTTTTTTTTTA | 14784 |
rs213021930 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689421 | CCTGCAGTTAGCCTC[A/G]CCCAGGAAATCACTT | 14784 |
rs213032784 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667393 | AAATGAAGTAGCCAA[A/T]AGCAGAGCAAGACAA | 14784 |
rs213216517 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662549 | TGTCTCAGAGACAGG[A/G]AGGCTTCAGGATGGA | 14784 |
rs213261083 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651104 | TCATATTTACAATTT[C/T]TTATTTCAAGCTAGA | 14784 |
rs213318109 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672132 | CACCCGTAGTTTACA[A/G]TTATCCATGGCTCCA | 14784 |
rs213406988 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649217 | TGAAGGAAATATTTT[A/T]AAAAAAATTTTATAA | 14784 |
rs213443633 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668000 | CAAATAAATGATCAA[C/T]TGGTAATGTCACTCC | 14784 |
rs213473573 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665073 | AGTGAGAAACTCAAT[G/T]AGGAGGGTTTTAAAG | 14784 |
rs213491481 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646222 | AGCAGCAAACACTTT[-/G]GGGCTGTGTGTGCCA | 14784 |
rs213538202 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694575 | TATATACAAAATAAA[-/T]TTTTTTTTTCAGCCA | 14784 |
rs213556085 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115645976 | GAGAGAGCAGGGAAG[C/T]GGTGTTTCTCATGCT | 14784 |
rs213607011 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115707626 | ACCCAGTTTCTCTAG[A/C]CTCTTTCTGAGTGTC | 14784 |
rs213630319 | in-del | -/GA | | | intron-variant | Grb2 | Mm_Celera | 11:115702959 | GCCTGTATTTGTGTT[-/GA]GAGACAGCTTCTCTC | 14784 |
rs213639278 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646897 | AGGATGGGGAGAAAA[A/G]CCATGAAGCGGCCAC | 14784 |
rs213645805 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656742 | AGCTGCATGTTCTTA[C/T]TGCCAACTATCAAGC | 14784 |
rs213645915 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706073 | AAAAATTGAATAAAA[A/T]TTTTTAAAAAGAATT | 14784 |
rs213771734 | snp | A/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643937 | ACCCTGGTCTACAGA[A/G]TGAGTTCTGGGACAG | 14784 |
rs213920256 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655191 | GGAGGTAGAGGCAGG[C/T]AGGTTTCTATGAGGC | 14784 |
rs213933429 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664503 | AAGTCCATCCCAAAC[A/G]TCACTAAACGGCATC | 14784 |
rs213959129 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684382 | GGTCCATTCATTATA[-/G]CCAATGGGCTATATT | 14784 |
rs213993948 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682308 | CTAGAAATGTAAGAT[C/T]ACTTGATGAGCCAGG | 14784 |
rs214007036 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681186 | TCAGCTCTCATACAG[C/T]CACAGAGACAGACAA | 14784 |
rs214045101 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653800 | CTTCCTTCTGCAGAG[C/T]TTAGAGTGGGTGGGG | 14784 |
rs214054197 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709178 | GGTCAAAAACTGCTT[A/G]CTGCTCTTCCAGAGG | 14784 |
rs214055852 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115664684 | GTTTGTTTGTTATAT[-/A]TTTTTTGAAACAAAG | 14784 |
rs214058035 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702480 | AACCCAGGTCCCAGG[C/T]TTGGCAGCAGGCACT | 14784 |
rs214060756 | in-del | -/TG | | | intron-variant | Grb2 | Mm_Celera | 11:115663331 | GCTGGGGTTTGAATA[-/TG]TGGTCTTCATTTCAC | 14784 |
rs214157704 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693751 | GATGACAGGAACAAA[C/T]CCCAAATGGTCAATA | 14784 |
rs214209822 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710137 | TCCAGGACAGCCAGG[A/G]TGGCACAGAGAAACC | 14784 |
rs214214070 | in-del | -/AAAATAA | | | intron-variant | Grb2 | Mm_Celera | 11:115660016 | ATAATAATAAAATAT[-/AAAATAA]AAAATAAAAAATAGG | 14784 |
rs214302394 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692391 | GTGGCCCTAGGAAGG[C/T]AGGTATTGTTATTCA | 14784 |
rs214320308 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652867 | TAAGAATCAACACAA[A/T]TTTATTTTCAGCTTA | 14784 |
rs214324866 | in-del | -/AGAGAG | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659245 | TACACACACACACAC[-/AGAGAG]AGTAAAAATTTCAAC | 14784 |
rs214353965 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667495 | TAACACACACCTTCA[C/T]GCTGTGCTGGGCACC | 14784 |
rs214391883 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677042 | AAAATCTTCCTAGTG[C/T]TCCTTACCTAACTAC | 14784 |
rs214393011 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115703474 | CCTGCTTTTCAAAGA[A/C]AACAATATAACTCTA | 14784 |
rs214424540 | in-del | -/ATTTC | | | intron-variant | Grb2 | Mm_Celera | 11:115706912 | TCAAAGTTCTCTTCT[-/ATTTC]AAGCTATCTTACTTC | 14784 |
rs214441909 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649181 | GGAAACTAGGAAAGC[A/G]GATAGCATTTGAAAT | 14784 |
rs214467765 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691693 | TTTTACCCACATACA[C/T]GCACACACATGCATA | 14784 |
rs214489693 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115697775 | CTGTCAAGACAAGGC[A/G]CAAGGAAGAAGAGCT | 14784 |
rs214543866 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674271 | AACAGGAACAAAAAC[C/T]GCGTCTGCCTCTGTT | 14784 |
rs214564492 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686978 | CAAAGCAGGTCAGAC[C/T]GTATAAATCACAAAA | 14784 |
rs214697228 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665824 | GATCTCTGTGAGCTA[C/T]AAGCCAGGAAGAACT | 14784 |
rs214699105 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675470 | AAAGAGAGTGTAGGG[C/T]CCCTGGAACTAGTCA | 14784 |
rs214785232 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666487 | TTCTACCCCATTTCC[C/T]TGCCCAAGTCCCCAC | 14784 |
rs214793268 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694477 | GTTCACCACAGCACT[A/G]GCACAGCAGCTAAGC | 14784 |
rs214912244 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115696300 | GAACAAGAAAGGCGG[A/G]TGAATTTAAAACCAG | 14784 |
rs214966894 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684588 | CAAATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 14784 |
rs215088037 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677732 | TGTTTTTGAGGGTCA[C/T]AGGTGTGTGCACTGT | 14784 |
rs215093251 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662690 | GGGGGCTTCCTGAAC[A/T]GTGAAGATGCCATCT | 14784 |
rs215098929 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670712 | CTGAGCACCCACACA[C/T]GGGGAAGTGTAGAAA | 14784 |
rs215131214 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688021 | GGGCTGGCTTACAGG[C/T]TCTGGGGTACAGTCC | 14784 |
rs215178872 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663287 | ACCCAGAGTGATGAC[G/T]ACTGACGTCAAGACA | 14784 |
rs215244227 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679434 | AGTTCCATGTATCCA[C/T]TAGGACTGCAGCTCA | 14784 |
rs215300080 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668041 | CTCCTGCCTAGCAGA[C/T]AGACAGGCACCCACC | 14784 |
rs215318556 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671230 | GATTTCCAGTGGCCA[-/T]TTTTTCCCCCGGCCT | 14784 |
rs215320774 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661447 | AGGGAGTGGCAGCAC[C/T]TGAGAAGGATGGGGA | 14784 |
rs215320853 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115687796 | ATTACCACCACCTAG[-/A]AAAAAAAAAATAAGT | 14784 |
rs215360562 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668367 | ATGTGAGTGGACATA[C/T]GTGGCTCATAACTGT | 14784 |
rs215387395 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115680926 | ACTCTCATACATAAA[A/G]TAAATACATAAATAA | 14784 |
rs215545436 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702113 | GTACACATGTTTACC[C/T]TCAGATTCTTCCTTT | 14784 |
rs215571852 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700865 | GCAAAATCTCAAGAC[C/T]ATCATCCCCAAAACA | 14784 |
rs215650605 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665144 | TTCCACCCAGGAACC[A/G]GGACCAAAGCTGTAA | 14784 |
rs215675635 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658137 | CTCTCTCTCTGCTGC[C/T]GAGCCATTTCTCTAG | 14784 |
rs215711815 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690593 | CACAGATGGAACTTG[A/G]AAGCACATTTGCACT | 14784 |
rs215726451 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653092 | CTAAGTATACAGTCT[C/T]GAGTTTCCAGCAGTG | 14784 |
rs215733253 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656793 | AAAAGTATCCTTCTG[C/T]TAAAGCAGGAGGTAT | 14784 |
rs215733270 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665603 | ATGCACGCCTTTAAT[C/G]CCAGCACTCGGGAGG | 14784 |
rs215778830 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115707769 | GTGTTGCAGGAACCA[A/G]CGGGGCTCTCTCCCC | 14784 |
rs215894893 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115695990 | ACAGGGGTCTGTGGA[C/G]TTAAAACGACCCTTG | 14784 |
rs215934334 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694645 | TTCGAGGCTAGCCTG[G/T]TCTACAGAGTGAGTT | 14784 |
rs215952398 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703629 | GTGGTGGTTTGAAGA[C/T]GCTTGGCCCAGGGAG | 14784 |
rs215958504 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660870 | GTCACTTTGGAGCAT[C/G]AAGTGATAACGAACT | 14784 |
rs216051558 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115648291 | TCTAGCATCTGCCCT[-/G]TGGACCCTAACTCAG | 14784 |
rs216071696 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692446 | ATGCAAAATTGCTAA[A/G]CAAACTGACTAAGAT | 14784 |
rs216098329 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653870 | CCCAGTCTACCGTGC[C/T]GAGCTTCCTGCTTAG | 14784 |
rs216106973 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704602 | ATGGGGGCTGGAAAT[A/G]CTGCCCGGCTGGTGG | 14784 |
rs216132333 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115693461 | CCACATGGTGGCTCA[A/C]AACCATCTGTAATGG | 14784 |
rs216154893 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661860 | GGCAACGGCACCTCC[A/G]TTCTGTCTTGTGCTG | 14784 |
rs216161932 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689711 | AACCGTGGCGGCCAG[C/T]GTGTGAACAGCAATG | 14784 |
rs216226282 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657007 | AGAATGTAAGAACAG[C/T]TGGCTCTGCAGGGGG | 14784 |
rs216254065 | in-del | -/CACATGCA | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658739 | ACACGCACGCACACG[-/CACATGCA]CACACACACACACAC | 14784 |
rs216347914 | in-del | -/GTGT | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658350 | TGAGTTTCAAGTATC[-/GTGT]GTGTGTGTGTGTGTG | 14784 |
rs216356026 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698015 | CACATTCCTGTAACT[C/T]ACTCCAATAAAACCC | 14784 |
rs216426165 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650873 | GAGCAGTAAGTGCTC[C/T]TACCCACTGAGCCAT | 14784 |
rs216453139 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115690061 | AAACCCTGTCTCGAG[-/A]AAAAAAAAAAAGTAA | 14784 |
rs216470604 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115688097 | GCTGGAAGAGCTGAG[A/G]GTTCTACATTGTCAT | 14784 |
rs216502826 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698844 | ACATTTAGGATTTTT[A/T]AAAATCCCATGTTTG | 14784 |
rs216528341 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115689391 | AGGCCCAGCTGAAGA[A/C]TGACTGATGCATCTC | 14784 |
rs216574498 | in-del | -/CCCCC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115661251 | AGGAAGGTGGTATAA[-/CCCCC]CCCCCCCCCCCACTC | 14784 |
rs216766854 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645232 | GACCGGGGAGGACAG[C/T]GGGCCTCCTTCCCCT | 14784 |
rs216796627 | in-del | -/ATATATATAT | | | intron-variant | Grb2 | Mm_Celera | 11:115698694 | TCGGTGAGTTTGGGC[-/ATATATATAT]ATATATATATATATA | 14784 |
rs216834470 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666632 | TTATGGGGCAAGGGC[A/G]GTATTCAACTTCTAG | 14784 |
rs216846353 | in-del | -/AAAAAAG | | | intron-variant | Grb2 | Mm_Celera | 11:115693282 | GAAGCAGTGTCTGAA[-/AAAAAAG]AAGAAAGAGAAAGAG | 14784 |
rs216847874 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654721 | AGTTCATGGGATGGG[A/G]GGGGGGGTAAAGAAA | 14784 |
rs216849878 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647046 | GAATGCAGACCGTCC[C/T]AGGAGCCTCCCCTAA | 14784 |
rs216956194 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658832 | CAGTGAAGGGCTCGT[C/T]CCATTCCCCAGACAC | 14784 |
rs217032818 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659572 | TTAAAAAATCAAACC[A/T]ACCAAACAAACAAAA | 14784 |
rs217059644 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681005 | GTAAGAGCACTGACT[A/G]CTCTTCCGAAGGTCC | 14784 |
rs217115332 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115693545 | TAATAAATAAATCTT[-/AA]AAAAAAAAAAAAAGA | 14784 |
rs217122479 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684723 | GCAGAAACAGACAGA[G/T]AGGGGCCTCTGTGAA | 14784 |
rs217173359 | snp | A/C | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708892 | ACAAAGCAAAGAGGC[A/C]CCGAGGAGCGGGGAG | 14784 |
rs217250414 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673174 | AAGAATAAACTAATC[C/T]AAGTCTGCCATAAAC | 14784 |
rs217322932 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653997 | AGTGAAGGATCATAG[A/G]TTCGTGTACCCACCA | 14784 |
rs217325000 | snp | A/G | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644329 | GAAGGCCGCCTCCGA[A/G]CCTTAGGGGCGCCCT | 14784 |
rs217342092 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115683509 | CAACTCAATGCAAGC[C/T]AGGGAGTCCTTGACC | 14784 |
rs217344922 | snp | A/G | | | synonymous-codon | Grb2 | Mm_Celera | 11:115645943 | AAAGAGCGCCTGGAC[A/G]TAGGTTGGCTGCTGC | 14784 |
rs217405896 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654890 | GAACGATGCTATCTT[C/T]TAATGTCTATGGGCT | 14784 |
rs217412814 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652699 | TTAAAGTAGCCTAAA[C/T]GCACACTAAGGAAGA | 14784 |
rs217443523 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682358 | AGCATGTGCTGTGTA[C/T]TGCTGGACACACCAT | 14784 |
rs217452556 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652092 | GAAGCTTCGCTCACT[C/G]TATGGATGGTCCAGC | 14784 |
rs217557321 | snp | C/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710319 | ATACCAGAGTCACAG[C/T]AACTCCATAGGACAG | 14784 |
rs217583066 | in-del | -/TGGTGATC | | | intron-variant | Grb2 | Mm_Celera | 11:115647274 | CTGGTCTAGAACTCA[-/TGGTGATC]TGGTGATCCCTGCAT | 14784 |
rs217585579 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691427 | AGGTGGGCAGATCTC[G/T]GTGAGTTCAAGGCCA | 14784 |
rs217587215 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115680094 | GTCACACCAGGAAGA[C/G]GTCAAAGAGCACCCG | 14784 |
rs217610295 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115672323 | GTACTGGAGGCTCTT[A/C]TGTGGCCTCCACACT | 14784 |
rs217620607 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115690810 | TCTACATGCTTGAGG[C/T]CAAGTCAACCAGGTA | 14784 |
rs217705603 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115647129 | CCCACTAGGCTAACC[A/C]TCAGATGTCTATGAT | 14784 |
rs217734819 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701871 | TCTTTAAAAAAAAAA[-/C]AAAAACTATTTTCTT | 14784 |
rs217832622 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684912 | ATGGACAACTGTCCT[C/T]TAACCTCCCCACACA | 14784 |
rs217832690 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673855 | CCACAAGACAAGGTA[C/T]TATTATGTAGCTCTG | 14784 |
rs217863891 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683952 | TGGGTATGGCTGTGT[A/G]TGTCTGTGACCCTTG | 14784 |
rs217942211 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659295 | TAACAATCACCATAA[C/T]GGCACTTGTGTGTAT | 14784 |
rs217975532 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674689 | GGAAGTACAGCCACT[C/G]CTCCCCTTCAAAAGC | 14784 |
rs218006451 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668152 | CTGTTCCCAGGTGAT[A/G]ACACAGGGAAACAGG | 14784 |
rs218013162 | in-del | -/TAGT | | | intron-variant | Grb2 | Mm_Celera | 11:115687100 | ATGTTCCTCAATAAA[-/TAGT]TAGTCAAAGAAACGA | 14784 |
rs218063063 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668572 | TCCCCTTGCAAACCC[A/T]ATAGCTAGAGTGCTA | 14784 |
rs218063518 | in-del | -/GTGTGCGCGCGC | | | intron-variant | Grb2 | Mm_Celera | 11:115684958 | CTCCTGTGTGTGTGT[-/GTGTGCGCGCGC]ATGCGTGCGTGCGTA | 14784 |
rs218103955 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679260 | TATTATCTTTAGTAT[A/G]AGTTACACACCAAAG | 14784 |
rs218195260 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681463 | ACTTGAATTTTATTT[A/T]AAAAAAGTTAAGAGG | 14784 |
rs218224107 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662283 | ACTATGTGGCCCAGG[C/T]TGGCCCTAAACTCCA | 14784 |
rs218230565 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692200 | CTGAATCTGAGGCAA[C/G]AGCAGACCAGCACTT | 14784 |
rs218278990 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646374 | ATGGTTGTGAGCCAC[C/T]ATGTGGTTGCTGGGA | 14784 |
rs218291081 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655756 | AGGCGGCTTCTCTAG[C/T]AGACAGAGAAGCTGG | 14784 |
rs218301304 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675509 | AGTGAGCTGCCATGT[A/G]GGTACTGGTATCAAA | 14784 |
rs218301776 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115676351 | GACTCTCCCTCCAAC[G/T]GCCTTTCCCAATCTC | 14784 |
rs218343009 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682427 | TATAGTCACTCTGGG[C/T]GAGAATACGAAACTG | 14784 |
rs218346114 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115684060 | CCTGAGACCCTGTAT[-/A]AAAAAAACAAGTGGA | 14784 |
rs218504030 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667252 | AAGAAGAAAAGCCAA[A/T]CCTAGCTCTCAGAAG | 14784 |
rs218513419 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650023 | GAGCTCTTTACCTGC[A/G]GGTCTCCTGCCTAAG | 14784 |
rs218533251 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677135 | TGGTGGTGCACACTG[C/T]AATCCCAGCACTTAA | 14784 |
rs218627247 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652177 | ACTCACCAGGGAAGG[A/G]CAAATGTTCTCAGCA | 14784 |
rs218656704 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699784 | CCCTGAGAACCAAGA[-/T]TGCTCCCACTCCCTG | 14784 |
rs218694516 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115678459 | GACATTTTGAATCAG[A/T]CAGCTTGGAGAAGAG | 14784 |
rs218786171 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650139 | AATTCAAGGCAGCAA[C/T]ACAGGCCACTCTTCA | 14784 |
rs218805221 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663366 | CTACAGATTGGAGAG[A/G]GAGAAAAGTGGCAGT | 14784 |
rs219024509 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648604 | ACCCAGAACTTATAA[C/T]CCTACCTGATGCCCT | 14784 |
rs219048480 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664435 | TAGACTCCCATGCCG[C/T]CAGGTGTCCCAGGTA | 14784 |
rs219111284 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661341 | GCAGCCCACTTAGCT[-/G]GGTTCAGTCCAGCAA | 14784 |
rs219153362 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115673721 | CTGGACTGGGTTTTT[-/C]CTGTGTAGCCCTGCC | 14784 |
rs219187537 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687499 | CCTTGGTGTAGCATG[C/T]ACACACTGCTTTTGT | 14784 |
rs219240186 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705082 | TATTTATTTATTATA[C/T]GTAAGTACACTGTAG | 14784 |
rs219257090 | in-del | -/AGGAACGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115679613 | GAGGCTGAAACAAAA[-/AGGAACGTG]AGGCCAGGTCAAGGT | 14784 |
rs219281204 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115703939 | CTCTTTACAGCAATG[A/G]AAACCCTAAGACTTT | 14784 |
rs219283669 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115690740 | CAGAGTGAGCACTGG[-/T]TGGTGACACCTTCAG | 14784 |
rs219333916 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644747 | ATCTGCATGTAGGCC[C/T]ATAAGAGTGAAGGAT | 14784 |
rs219389941 | snp | C/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643690 | CTAAACCATTTTCCA[C/G]ATAATGAGCTACATC | 14784 |
rs219401637 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702347 | ACATGGAAGTATTTC[A/G]TTTTCTCACATTTAT | 14784 |
rs219511228 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679640 | AGGTCAGCCTGGCAC[C/T]ACAGACAGAGCATGG | 14784 |
rs219559862 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680222 | ACTCACCCATCTCAC[G/T]TAAAGCAGCGAGGTA | 14784 |
rs219569343 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681713 | GCTGGGGGAGGTGGG[A/G]TAAGGCCAGGTCTCT | 14784 |
rs219694653 | in-del | -/AAC | | | intron-variant | Grb2 | Mm_Celera | 11:115681508 | GCTAACCATGATATT[-/AAC]AACAACAACAACAAG | 14784 |
rs219701883 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115705254 | AACTCTATTTTTAAA[C/T]CAGTCCATTCAGGGA | 14784 |
rs219706212 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670367 | AAAACAGACACCTAA[A/G]GTTTGCAAGACCATG | 14784 |
rs219805147 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703306 | TTAGCAAACAGGGTA[A/T]GTACTAAGCCTCATC | 14784 |
rs219863612 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115674894 | TACCGTAATGTTCAG[A/C]CATACACATGTGATT | 14784 |
rs219889971 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706651 | CTTAAAACCAACTAT[C/T]GGGCCAGAGAGAAGA | 14784 |
rs219931649 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666211 | TACATAGTAAGTTCT[A/G]GGACAGCCAGGGCTA | 14784 |
rs219955948 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694820 | GCTCCCAGCACATTA[C/T]ATACACGCATAAGAA | 14784 |
rs220025603 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666961 | CCTGCTGGGAACTGA[A/G]CCCAAGACCTGGCAC | 14784 |
rs220112301 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695114 | ACCACCTAGCTTAAA[-/T]TTTTTTTTTTTTAAG | 14784 |
rs220128366 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663988 | ACAAAATAGGACAAT[C/T]GTTCACATTTCTGTG | 14784 |
rs220155180 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694115 | CTCAGCAAGTCGCTC[C/G]AGCTTGGTGGCCCAA | 14784 |
rs220185724 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115665242 | CACTCTACTAAACAA[-/AG]AGAGCTGCTGGGTAC | 14784 |
rs220294533 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115663965 | GGAAAGTTGCTCATG[A/C]TATTTTGACAAAATA | 14784 |
rs220349124 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666193 | TTCAAGGCCAGCCTG[A/G]TCTACATAGTAAGTT | 14784 |
rs220358550 | in-del | -/CCCC | | | intron-variant | Grb2 | Mm_Celera | 11:115661252 | AGGAAGGTGGTATAA[-/CCCC]CCCCCCCACTCCCAA | 14784 |
rs220361272 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671188 | TCTGGTTTGTAAAAT[C/T]GTGCTTCCATGGCCT | 14784 |
rs220445269 | in-del | -/AAAAC | | | intron-variant | Grb2 | Mm_Celera | 11:115687304 | AAACAAAAACAAAAA[-/AAAAC]AAAAAAAACAAAAGC | 14784 |
rs220449249 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665412 | GGAGGCTCATGAGCT[C/T]AGCATCCTCAAACAC | 14784 |
rs220460132 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664708 | AACAAAGTCTCTCTG[A/T]GTAGCCCTGACTGTC | 14784 |
rs220463241 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673418 | ACCAACACTCTCTTC[C/T]AGCTTATTGTATGGT | 14784 |
rs220626811 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671692 | TTGTTTGGTTTTTTT[-/G]GGGGGGTGGCTTTTA | 14784 |
rs220638636 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672529 | GGGCTGGAGACAGTT[C/T]TGGTTCCTAGCACCA | 14784 |
rs220669031 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707031 | CTCAATCTCCCTTAC[C/T]AACAGTGAGGGGAAA | 14784 |
rs220681481 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668199 | CAGGAGCGTGTCAAG[A/T]GCTGTAGAAGCAGTG | 14784 |
rs220739366 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664600 | TTCCTTAGTGAATAG[A/T]ATCAGACCTTCCTAA | 14784 |
rs220797796 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668187 | TAGATCAACAGCCAG[G/T]AGCGTGTCAAGTGCT | 14784 |
rs220800401 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709807 | CTGCTACAATAATGA[A/G]TCCACTAAAATAAGG | 14784 |
rs220816280 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661851 | CAATCTGTAGGCAAC[A/G]GCACCTCCGTTCTGT | 14784 |
rs220826505 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661279 | CTCCCAAATTCCTAT[C/T]GTTAAAACCATTTTT | 14784 |
rs220829635 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646641 | GTCGGCCTGAGCACA[C/T]AGGAAGTCGCTGTGG | 14784 |
rs220834351 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115669127 | ATATTTAGCAGTGGC[A/G]CTAAGCTGCATCCCT | 14784 |
rs220870847 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661136 | GTAACTTTGATAGTT[C/T]TTCTCCCAAACTATG | 14784 |
rs220877132 | in-del | -/TTT | | | intron-variant | Grb2 | Mm_Celera | 11:115656035 | AGTGGAAGGCTAGCC[-/TTT]TTTTTTTTTTAAAAG | 14784 |
rs220923217 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115664881 | ATCCGACACTAAGGT[-/AAA]AAAAGGTGAACAAAC | 14784 |
rs220974560 | snp | A/C | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699569 | ATCAGCTGCTTTACG[A/C]TATGCCAGAATACAC | 14784 |
rs221009091 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698278 | GTCACTCAGGGGTAG[C/T]AAACAGCTGGCAAAT | 14784 |
rs221038927 | snp | G/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701454 | TACTCAGTATAAGTG[G/T]TAACAGATAGAGTAT | 14784 |
rs221063881 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115672669 | ATAAAAATAAACATT[-/AAA]AAAAAAAAAAAGGAG | 14784 |
rs221145431 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666740 | CTTGAACTCCAAGAC[C/T]CAAGCCATCCTCAGG | 14784 |
rs221155488 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115704113 | AGCTCAAATGGGAAA[A/T]AAAGCTGACAGCACC | 14784 |
rs221204184 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660315 | CATTGGTTATGAACA[C/G]TGACTGCTCTTCTAG | 14784 |
rs221206573 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655605 | TAATTTCAACAGCCA[A/T]CATTATATGCTAAAC | 14784 |
rs221220029 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667586 | ATAATGTAACTGCCC[C/G]GCAATGGTGGCACAG | 14784 |
rs221299850 | in-del | -/AATGAATGAATGAATG | | | intron-variant | Grb2 | Mm_Celera | 11:115691511 | GCCCAAAAAACCAAA[-/AATGAATGAATGAATG]AATGAATGTATGAAT | 14784 |
rs221312023 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705157 | ATGGTTGTGAGCCAC[C/T]ATGTGGTTGCTGGGA | 14784 |
rs221346636 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115654573 | TATTTTTAAAAACTA[-/C]TTTTTCTTACGGTGC | 14784 |
rs221360569 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692938 | TGTCACGGAGGCAGG[C/T]TGGGGAGCCTCCAGG | 14784 |
rs221360594 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115706238 | CAGTGCTCTTAACCA[A/C]TGAGCCATCTCTCCG | 14784 |
rs221373975 | snp | G/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710550 | TCATCTATAACTCCA[G/T]TTCTTGGGAATCCAA | 14784 |
rs221429541 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664980 | TAGTTACCGACAACA[C/G]TAACAGTAACAGTTC | 14784 |
rs221446945 | in-del | -/TTGTT | | | intron-variant | Grb2 | Mm_Celera | 11:115663621 | GCCACCACACCTGGC[-/TTGTT]AAGCACTCTTGGGGA | 14784 |
rs221549002 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115670451 | CCTTCTTCAGAGTTT[A/C]TCAGGAGGAACTCTA | 14784 |
rs221592394 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698197 | TATTGATAGGTTCAC[A/T]TGAGTCTTTATACTT | 14784 |
rs221597815 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658315 | AATTAAATATACCAG[C/T]AAAGGCTATAAAGTG | 14784 |
rs221624958 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115706421 | ACTTGGCACAACTCA[-/G]GGGAAAATCAACTTT | 14784 |
rs221681428 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664558 | AAGGGCAAGGACAGA[C/T]CTCTTGGCCAAAGTT | 14784 |
rs221689833 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663770 | CCCTGTGGCCCTCCC[C/G]TTTGAGTTTTAGGAT | 14784 |
rs221755313 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115663810 | ATAAGCCTCCTAACC[-/AAA]AAAAAAAAAAAAAAA | 14784 |
rs221758460 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653380 | TCCTAAAAATAGCAA[G/T]CAAGGAAGCCAAGAG | 14784 |
rs221886609 | in-del | -/GGGA | | | intron-variant | Grb2 | Mm_Celera | 11:115656105 | GGTGGGGGTTGGGGG[-/GGGA]GGACGACAGACCTTG | 14784 |
rs221912154 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692293 | TCATATTAGTAAAAT[C/T]AACTACAGCTAGCCA | 14784 |
rs221924202 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115697119 | ACTATATAGTGAGTT[C/T]TGAGCAGTCCTGGGT | 14784 |
rs221937688 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659945 | CTGTTGCGTTGACCA[C/T]ACATAGCAATAGCAA | 14784 |
rs221954195 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702586 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCTG | 14784 |
rs221974251 | in-del | -/A | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645065 | TGTCTTTAACTTATT[-/A]AAAAAAAAAATGGTA | 14784 |
rs222074714 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115691913 | TAGTAATACTAAAAG[A/G]GTTTATACAGAATTT | 14784 |
rs222139608 | in-del | -/AC | | | intron-variant | Grb2 | Mm_Celera | 11:115666124 | AGCTGTGTACTGGTG[-/AC]ACACATCTTTCATTA | 14784 |
rs222180572 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115659068 | TGGGCCAGTAAGATA[-/G]GGCTCAGCGGGCAAA | 14784 |
rs222291860 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663637 | AAGCACTCTTGGGGA[C/T]AATGATTTCATATTA | 14784 |
rs222304901 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686339 | AGCATGGTCTAGAGA[C/T]GGACGTAGCCGTCCG | 14784 |
rs222348804 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115696795 | AACAGAATGTGAAAG[G/T]AAAACATGAATCTTC | 14784 |
rs222363989 | in-del | -/CC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691939 | ATTTGGAGTTTCCTA[-/CC]CCCCCCCCCAAAATA | 14784 |
rs222367308 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690024 | ACAGAGTGAGTTCCA[A/G]GACAGCCGGGGATAC | 14784 |
rs222368098 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654153 | CTTTTCTTTAATTTT[A/T]AAAAATTTATTATTG | 14784 |
rs222476870 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115651908 | AGTCTAAACACTCCC[-/AA]GTCTAGGTTTCAAAT | 14784 |
rs222539050 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682547 | AAAAACACAGTAATT[A/G]TGGTTTTGGAGAATT | 14784 |
rs222546288 | in-del | -/GT | | | intron-variant | Grb2 | Mm_Celera | 11:115707156 | TCCACTTGTGAACTG[-/GT]GTCACTATCACTTAC | 14784 |
rs222575293 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692738 | CTTTGCTCTTATTAA[C/T]GTGGCCTGCTCTCCC | 14784 |
rs222623407 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662872 | TTAACAGTCTGAAAG[A/T]CTTGGGAGCTTTAGT | 14784 |
rs222654978 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115693543 | ATAATAAATAAATCT[-/A]TAAAAAAAAAAAAAA | 14784 |
rs222679706 | in-del | -/TTTTT | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644129 | TAAGTACATAGTTGG[-/TTTTT]TTTTTTTTTTTTTTT | 14784 |
rs222733318 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690960 | CTTAAAAAACAGCAC[A/G]AAATAAAATGTGCCT | 14784 |
rs222750150 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694205 | TGACTTACACATGCA[G/T]GCTGTGACATGTTCA | 14784 |
rs222782454 | in-del | -/AA | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645128 | ACAAAGGCACTATTT[-/AA]AAAAAACAAACAAAC | 14784 |
rs222800624 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651334 | CATGGTTATTTGTTA[C/T]TACTGCCACCTAAAG | 14784 |
rs222852728 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658236 | GAACTCATCCACAGA[C/T]GAAGCTGGCCTCAAA | 14784 |
rs222862594 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657640 | AAGAATCTGTAACTC[C/T]GCTGGGCGTGGTGGC | 14784 |
rs222865906 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686114 | AAAAGAATGTATGAC[C/T]TGGCAGTGGTGGCGC | 14784 |
rs222897544 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115651810 | CCCTGCAAAGTATTT[-/A]TTAAAAAAAAATTCT | 14784 |
rs222927251 | snp | A/T | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699777 | GCTGCTGCCCTGAGA[A/T]CCAAGATTGCTCCCA | 14784 |
rs222948624 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115689774 | AAGTCCTAGAAACAT[A/C]GGCATTGGTGAGGTG | 14784 |
rs222991284 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689084 | GCAGATCTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 14784 |
rs222993609 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694967 | ACTTACTCTGTAGAC[C/G]CGGCTGGTCTAGAAC | 14784 |
rs223017678 | in-del | -/GAGGAATTA | | | intron-variant | Grb2 | Mm_Celera | 11:115650398 | GGAGGCTTGCATTGT[-/GAGGAATTA]GAGTCTAGGTTGTGG | 14784 |
rs223110459 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695368 | AACAGCCAAAACCTA[C/T]ATAGGTACTTAGCTC | 14784 |
rs223151290 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682152 | GTAGGCCACTGGGAG[C/G]GTGGTGGAGTTCAAA | 14784 |
rs223165160 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684999 | AATTAGATCTAATCA[A/G]AGAAACAAATCTATG | 14784 |
rs223189377 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115692359 | ACACTAATGAGTTAG[A/C]TCTTTTAAACTTAAT | 14784 |
rs223257293 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653288 | GGTTTCTTTCAATGA[A/T]GATAGTTATGTATGA | 14784 |
rs223269333 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652297 | CACCAGAAAAGGGAA[C/T]TGGATACCATTGCAG | 14784 |
rs223316178 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682879 | GGCATGGGGATTCAA[C/T]GTCCAAGGCAAGGAG | 14784 |
rs223345402 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655842 | CAGCAGCTTCTCTAC[A/G]GTCTCCCATCAAGCA | 14784 |
rs223415081 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648526 | taggtcacctggctg[G/T]acgacaagcaccttt | 14784 |
rs223458288 | snp | A/C | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644633 | GCACAACCCACTGCC[A/C]AGAGAGATGCGGCCG | 14784 |
rs223483460 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691154 | CGGCAACTGCCTAAA[G/T]CAAGTAACCATCAGC | 14784 |
rs223627009 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653552 | TTGGACCCAAGTGTA[C/T]CATTAGGGGGCTGGC | 14784 |
rs223688184 | snp | A/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643861 | TATAAAATAAAATCA[A/G]GACGGGCAGTGATCC | 14784 |
rs223689794 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654599 | GGTGCTGGGGCAGAA[C/T]CCAGGGCTTTGTGCA | 14784 |
rs223738839 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695242 | CCTACTTTCTATTTC[-/T]TTTATAACTTTTACT | 14784 |
rs223835419 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647373 | TTTTCTTTTCTCCTT[C/T]CTTCCTTCCTTCCTT | 14784 |
rs223859309 | snp | C/T | | | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115644931 | GAGACCTCCGGCCCA[C/T]TCAAGATGGGAAATA | 14784 |
rs223984280 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651617 | GCACCAATATGGCTG[C/T]CTCGGAATCCCACAC | 14784 |
rs224087434 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652236 | CAATCACATGCTTTA[C/T]TTATTTATTTCAGGT | 14784 |
rs224088466 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649693 | CCACAGGAAAAGATG[C/T]GTTAACATCTTCCCC | 14784 |
rs224182231 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650701 | TGCCCACCCCGGTTG[C/T]CCCCACTCACTCCAG | 14784 |
rs224226329 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115656683 | TCGAAAAAACCAAAA[A/C]ACAAACAACAACAAG | 14784 |
rs224317993 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649514 | CAGGAGTGGAGATGC[A/G]CACGTGGTCACCGTA | 14784 |
rs224332259 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659776 | GTTCACCCTCACATA[C/T]ACTCACACTCGCAGA | 14784 |
rs224431550 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687656 | TTTTAAAAGCTACGT[G/T]TTCCTGTGTAGCTCT | 14784 |
rs224482229 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115693766 | CCCCAAATGGTCAAT[-/A]AAAATATGAACAAAT | 14784 |
rs224593301 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677186 | TAAATTTGGGGAAAA[C/T]CTTGGCTACTCAATT | 14784 |
rs224648387 | in-del | -/ATATATAT | | | intron-variant | Grb2 | Mm_Celera | 11:115698695 | TCGGTGAGTTTGGGC[-/ATATATAT]ATATATATACTCCCA | 14784 |
rs224648689 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115678575 | GAAAAATTCTAGGCC[C/T]AGGTTAATAAACAGA | 14784 |
rs224693849 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115688935 | AAAGCCGGGCAGGGT[A/G]GCCAATGTGGGGGTG | 14784 |
rs224777067 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646271 | TTTTTTTTTTTTTTT[A/T]AAAAAAAAGATTTTA | 14784 |
rs224875210 | snp | A/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709929 | CAGTTTGCGATTTAG[A/T]TAGAGCTACTTAGTT | 14784 |
rs224904756 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686483 | GGCACTGAAGTATTT[C/T]TCAAAAACAAAAATA | 14784 |
rs225003134 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682696 | CATGGCACAGCCACC[C/T]GAGAAGAGGCAGCAC | 14784 |
rs225014778 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115647572 | CTGTTTTTCTTTCTG[A/C]TTCCTGTTCACTGCC | 14784 |
rs225057682 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690103 | CATTTGACCTTTAAT[A/G]TATTAAGATGCTGTA | 14784 |
rs225060547 | in-del | -/A | | | intron-variant | Grb2 | GRCm38.p3 | 11:115680438 | GTTTTTTTTTTTTTT[-/A]AAAAACTTGTTTATT | 14784 |
rs225137223 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681336 | ATCAGATGGCCTCAT[A/G]TAGCCCAGGCTGGCC | 14784 |
rs225160495 | in-del | -/GTTT | | | intron-variant | Grb2 | Mm_Celera | 11:115673477 | GGAGAGCACCTATAA[-/GTTT]GTTTGTTTTTTATAT | 14784 |
rs225200673 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685419 | TCCTCATATACCCAG[A/G]GGTCTGAAGTAGGAG | 14784 |
rs225215728 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672777 | AGCTGGCCAGAGAAC[A/T]TGACTTTGTTGGGTT | 14784 |
rs225237794 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684574 | GAGGCAGAGACAGGC[A/G]AATTTCTGAGTTCAA | 14784 |
rs225260737 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691111 | GTGCTGTTAGATCTG[C/T]TCTAGCTGAGAATTT | 14784 |
rs225322100 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115676144 | ACATTTACAATCACC[C/T]CTTATTGTCCACACT | 14784 |
rs225334119 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115677520 | AAGAAAGAAGGAAGG[A/G]AGAGAGGTTCTTTCA | 14784 |
rs225357973 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675292 | TGCGCCACCATGCCC[A/G]GCTTCAGGTAAACTC | 14784 |
rs225402304 | in-del | -/GAG | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643631 | CAGCTCGGAAGGGAA[-/GAG]GAGGAGCTTTCCAGC | 14784 |
rs225446192 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115680316 | CTTTCCCAAAGCCAT[A/G]GGCTGTATCTGGAAC | 14784 |
rs225468758 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701275 | TTTGATTTGCATTTC[-/T]TTTTTTTTTTAAACT | 14784 |
rs225477955 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668283 | GACTGGTTTGATACC[C/T]ACACCCATGGTGGAA | 14784 |
rs225523824 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678773 | GAGTTCAGGCCTCAC[A/G]CATGCCAGGCAAGCG | 14784 |
rs225530880 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115671538 | GGACAAATGTCTACA[A/C]GTAGTTTTTGTTTTA | 14784 |
rs225531081 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667031 | CCCAACACCTTGTTT[C/T]GTCTTACAAGAACAA | 14784 |
rs225558772 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115697101 | CTCACCTATAATCTT[-/A]AGACTATATAGTGAG | 14784 |
rs225567807 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676114 | TCAGACAGACAGACA[C/G]ACACACAGGCTCAGA | 14784 |
rs225601120 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680806 | AGCTGGGTGCTCTTC[C/T]TGAGGTCCAGAGTTC | 14784 |
rs225641039 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679905 | TCACACACAAGTTTA[A/T]CCACACACAAGGTTT | 14784 |
rs225647644 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654376 | CTCCTCTGCTCACTA[C/G]TGCACTGCCCTCCTC | 14784 |
rs225700945 | in-del | -/TTC | | | intron-variant | Grb2 | Mm_Celera | 11:115647392 | CCTTCCTTCCTTTCT[-/TTC]TTTTTGTTTTTTTCG | 14784 |
rs225729602 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671539 | GACAAATGTCTACAC[A/G]TAGTTTTTGTTTTAT | 14784 |
rs225768548 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670688 | CTGCTCTGTAGTCTA[C/T]AGCTCTCTCTGAGCA | 14784 |
rs225773027 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115673013 | TGCCTGGTTATCAGG[A/G]AGAACTGCTTCCCAT | 14784 |
rs225838811 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691675 | TTCAGCTACCTGGTG[-/T]TTTTTTACCCACATA | 14784 |
rs225861149 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651812 | CCTGCAAAGTATTTT[A/T]AAAAAAAAATTCTGC | 14784 |
rs225873194 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665588 | CTGCTGGGTGTGGTG[A/G]TGCACGCCTTTAATG | 14784 |
rs225899044 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674103 | CTCCAACTCACTCAC[A/T]GCCAACGTTACTCAG | 14784 |
rs225907962 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665075 | TGAGAAACTCAATGA[G/T]GAGGGTTTTAAAGGC | 14784 |
rs225925166 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115677096 | ATTTCTCTTGTGATA[A/C]AAAATAAAAATGTAT | 14784 |
rs225994181 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667537 | TATTTTTTGTTGCTA[C/T]TTTATAACTAAATTT | 14784 |
rs226017829 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115707679 | GAACGCGCTTCGGCT[A/C]CCCGGCAAACTGCAC | 14784 |
rs226051966 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687732 | AGAGATCTGCCTGCC[-/T]TTTGTCTCTTGAGTG | 14784 |
rs226052183 | snp | G/T | | | utr-variant-5-prime | Grb2 | Mm_Celera | 11:115708435 | CGGCCCGGCCCGCCC[G/T]GCGCTGCCGCCCGCA | 14784 |
rs226084207 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115687822 | TAAGTATTTTCTTAA[A/G]GAGAAAATGAAAACA | 14784 |
rs226092341 | in-del | -/TCTACC | | | intron-variant | Grb2 | Mm_Celera | 11:115676568 | TCCTTCCCTTCACAT[-/TCTACC]TTTAAAGACTCAGGT | 14784 |
rs226111579 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648528 | GGTCACCTGGCTGGA[C/T]GACAAGCACCTTTAC | 14784 |
rs226211662 | in-del | -/TAAC | | | intron-variant | Grb2 | Mm_Celera | 11:115706484 | TGGCCAATCAGCAGG[-/TAAC]TAACTACCTCTCAGT | 14784 |
rs226231364 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674371 | CATCAAACGTCTGAG[C/T]TCAGGAAGCAGCCAG | 14784 |
rs226255669 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670309 | CTGAATGCTCCACTT[A/T]AACTAATATACCCTA | 14784 |
rs226257493 | snp | C/T | | | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115645156 | AAACAAACAAAAAAA[C/T]GTCAAAACACCTGAA | 14784 |
rs226270638 | in-del | -/TTTTTTT | | | intron-variant | Grb2 | GRCm38.p3 | 11:115695113 | ACCACCTAGCTTAAA[-/TTTTTTT]TTTTTTTTTTTTTAA | 14784 |
rs226282806 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673028 | GAGAACTGCTTCCCA[A/T]GCAGGTCTAGGCTCA | 14784 |
rs226330937 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693358 | CTCAGAAGGCTACCA[-/T]TAAGAGGAAAACCTC | 14784 |
rs226393391 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646446 | CCGCTGAGCCATCTC[A/T]CCAGCCCCTCTTAAC | 14784 |
rs226423658 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658426 | AGACAGAGACAGAGA[C/G]AGACAGACATAGAGA | 14784 |
rs226444760 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662780 | AGGGCCGTACACAGG[C/T]TGGCCTGCCACTGTG | 14784 |
rs226540707 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653897 | TTAGCTACTTACCAA[-/G]GACCAGGAGGACCTG | 14784 |
rs226567094 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115659189 | CCACATACACACTGT[-/G]GTACTCAGATGCATG | 14784 |
rs226671059 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649292 | TAGGAAAGGATGATC[A/G]GTCAGACAGGGCAAA | 14784 |
rs226680567 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115655473 | GAAAAATAGTAAGAC[-/A]AAAAAAAAAATCAAT | 14784 |
rs226707228 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709579 | CAGAACAGAGAGATG[A/G]ATGGAGGCGTGAGAA | 14784 |
rs226728922 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115703702 | CTTGTTGAAGGAAGT[A/G]TGTCACCTAGGGGGT | 14784 |
rs226791951 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115680703 | TTTGGATCACTGTCT[-/A]AAAATAAAAATGGAT | 14784 |
rs226802950 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705413 | GGTGAGGGGTTGCTT[A/T]CAGGAGCAGAAATGA | 14784 |
rs226849585 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115704494 | TCTGCGCTAGCTTCA[C/T]TCCAGCATAGCACCA | 14784 |
rs226862209 | in-del | -/CTTC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663471 | CTTCTTCTTCTTCTT[-/CTTC]TTTTTTTTTTTCCTT | 14784 |
rs226888107 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115695744 | CTGCTGAATAGAGAG[A/G]GTAGTTTGTTTCTTC | 14784 |
rs226917412 | snp | A/C | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708798 | CGTTGTAACCCTCTA[A/C]GTGCCGGAGCAAGTG | 14784 |
rs226979651 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702649 | GGTGTGAGCCACCAC[A/G]CCCAGCATCAGCTGG | 14784 |
rs227006030 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115678679 | GAGAAACACTCTGGG[A/C]TCATCTCACTTCATC | 14784 |
rs227012986 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660463 | AAACATGTGCAGCAA[C/G]TTGCTTTCAGTTGCT | 14784 |
rs227027352 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115666272 | AATATGTGTAGATTT[-/A]AAAAAAAAAAGCAAA | 14784 |
rs227031018 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115697302 | GCACAATCACTTAGT[C/G]GCCAACGTTCCCTCT | 14784 |
rs227167811 | in-del | -/TATGTATGTATG | | | intron-variant | Grb2 | Mm_Celera | 11:115676253 | ATGTATACACGCATA[-/TATGTATGTATG]TATGTATGTACGTAC | 14784 |
rs227208860 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700370 | TACAGGCTGGTGCCG[A/G]ACAGTCAGACCCCAG | 14784 |
rs227215110 | in-del | -/TC | | | intron-variant | Grb2 | Mm_Celera | 11:115704742 | ATCAGAAATTCAAGG[-/TC]TCACACACAACTACA | 14784 |
rs227244082 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698638 | TATGATGTAGAATTC[C/T]AGTAGGTTTTTTTTC | 14784 |
rs227253355 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691423 | GCAAAGGTGGGCAGA[A/T]CTCTGTGAGTTCAAG | 14784 |
rs227276937 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660384 | ACAACCATCTGTAAT[-/G]GGGATCCAAAACTCT | 14784 |
rs227277108 | in-del | -/CGCACACACACACACACACACA | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709318 | GCGCGCGCGCGCGCG[-/CGCACACACACACACACACACA]CACACACACACACAC | 14784 |
rs227287262 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702852 | GTGCTACGATTACAG[A/G]TAATAAATCACAGTG | 14784 |
rs227352461 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115653364 | GGATTGGTGTGTGCT[A/G]TCCTAAAAATAGCAA | 14784 |
rs227401574 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692322 | CAATTACAGTCTATG[A/G]ATGTCAGTCATTGCT | 14784 |
rs227418869 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115671564 | TTTTATTTACAATTG[-/AAA]AAAAAAAATGGCTCC | 14784 |
rs227460130 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665028 | ATCTTCTTGATTCAA[A/G]GGACAAGCTGTAAAA | 14784 |
rs227478047 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659777 | TTCACCCTCACATAC[A/G]CTCACACTCGCAGAC | 14784 |
rs227519371 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115672969 | ACTCTACTAAACATC[A/C]CCGTGAGTCCTGCCA | 14784 |
rs227524986 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115671240 | GGCCATTTTTCCCCC[-/CT]GGCCTTATATTCTCA | 14784 |
rs227564545 | in-del | -/AAAAC | | | intron-variant | Grb2 | Mm_Celera | 11:115669075 | AACAAAACAAAACAA[-/AAAAC]AAAACAAAACAGAAG | 14784 |
rs227568648 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644858 | ACAGAGACTCTGATG[C/T]CCACTGAGTCTGAGC | 14784 |
rs227602702 | in-del | -/TATGAGAAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115679224 | TAAAGTCAACATTTT[-/TATGAGAAAA]TATGAGAAAATATCA | 14784 |
rs227612283 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668529 | ATAATCACAACTTCA[G/T]AGGCCAGAGAGAGCT | 14784 |
rs227620841 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669225 | GGAATTGGACCACAG[C/T]GCGCAGGCTTTAAAG | 14784 |
rs227648314 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675473 | GAGAGTGTAGGGTCC[C/T]TGGAACTAGTCACAG | 14784 |
rs227661680 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679475 | TCAGCATACATCAAG[A/G]CTAAGTCATTTAAAT | 14784 |
rs227697290 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670486 | AACATAAGTCCTGCC[G/T]GCAAGTTAAATTACA | 14784 |
rs227698583 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693198 | TAACAGGCTGAGGCA[A/G]GAGGGCTTGCCGGAG | 14784 |
rs227716384 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115662217 | CAAAAAACAAGAATC[A/C]CTTTTCTGGGAGCAG | 14784 |
rs227729074 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115667724 | CCTGTCTCGAAAAAA[A/C]CAAAGAAGAAAAGAA | 14784 |
rs227758104 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667242 | GGCAATGAGGAAGAA[C/G]AAAAGCCAATCCTAG | 14784 |
rs227761031 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669620 | GTGTTTTAAAGTCTC[C/T]ACAGCTAACATTAAA | 14784 |
rs227769047 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661503 | GGCCTTGTAGGAGGA[A/C]ATGTGTTACTGGGGT | 14784 |
rs227868060 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702119 | ATGTTTACCTTCAGA[G/T]TCTTCCTTTAATAAT | 14784 |
rs227943243 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663217 | AAGAGCCACTACCAT[C/T]ACTAGAAGATTCACG | 14784 |
rs227952543 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665644 | CAGATTTCTGAGTTC[C/G]AGGCCAGCCTGGTCT | 14784 |
rs228068876 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654722 | GTTCATGGGATGGGA[G/T]GGGGGGTAAAGAAAG | 14784 |
rs228069810 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664831 | CACAAGGTTTTTGTC[C/G]TATGTAAACCTCTCT | 14784 |
rs228092084 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657754 | CAGGACAGCCAGGGC[C/T]ACACCAAAGAGTCTG | 14784 |
rs228102994 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664402 | GGGAACTAACAGAAG[A/G]ACACCCTCCCAGGGC | 14784 |
rs228171341 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657952 | CAAGTTAAGTGGCAG[C/T]AGAAACCAGAAGATG | 14784 |
rs228194619 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665528 | GGGGAGTCTCAAAGG[A/G]GCATGAGGAAGTGGT | 14784 |
rs228200853 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659219 | GCACACACACAGACA[C/T]ACACACATACATACA | 14784 |
rs228207886 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662388 | TACATCCTAGAAAGA[A/G]GACAGATCCCCTAAA | 14784 |
rs228213656 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704379 | TCAAGATGTGAAGGT[A/G]TATGCCTATAATCTC | 14784 |
rs228304023 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115669766 | GCTGCTGAGGTGGAT[A/G]CTCAGCACTCTCCTC | 14784 |
rs228325175 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695992 | AGGGGTCTGTGGACT[G/T]AAAACGACCCTTGGA | 14784 |
rs228371000 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115685129 | ACTGAGGGGAAACTG[C/T]GTGGGACTGCTAAGT | 14784 |
rs228389744 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649556 | AACTGCAGTGAAGGC[A/G]GGGCGGGTGAGGAGT | 14784 |
rs228436368 | in-del | -/CACGCCCGCGCGCACG | | | intron-variant | Grb2 | Mm_Celera | 11:115706772 | ACACACACACACACA[-/CACGCCCGCGCGCACG]CGCAGGTAAATACAC | 14784 |
rs228446895 | in-del | -/AAA | | | intron-variant | Grb2 | GRCm38.p3 | 11:115679125 | AAATCTGTAAGTCTC[-/AAA]AAAAAAAAAAAAAAA | 14784 |
rs228488921 | in-del | -/AAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115655472 | GAAAAATAGTAAGAC[-/AAAA]AAAAAAAAAAATCAA | 14784 |
rs228535865 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Grb2 | GRCm38.p3 | 11:115701862 | AATAAATAAATCTTT[-/A]AAAAAAAAAAAAAAC | 14784 |
rs228569973 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656083 | GGTTAAACTGGAACC[C/T]TGTGGCTGGTGGGGG | 14784 |
rs228575836 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115697732 | CAAAGTAAGAAAAAG[A/C]AGCTCAACGTCTGCT | 14784 |
rs228580845 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115703322 | GTACTAAGCCTCATC[C/G]CGAGCCTGAATGTGG | 14784 |
rs228624341 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705831 | GGGGCTGAAGCAGAA[C/T]GGCTCAAAGCAAAAC | 14784 |
rs228746326 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694274 | CCGAGGAAGGAGACC[C/T]GACTTCATTCACAGT | 14784 |
rs228786887 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693467 | GGTGGCTCACAACCA[C/T]CTGTAATGGGTTCTG | 14784 |
rs228811119 | in-del | -/AAAAAAC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663831 | AAAAAAAAAAAAAAA[-/AAAAAAC]CCCACAAATCACAGT | 14784 |
rs228821993 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707500 | TGGCGCTACAGATGC[A/T]TTTCGTGTCCCTAGT | 14784 |
rs228909996 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651724 | ATGTCTGGTCAACAA[C/T]GGCCTACCAAGACCT | 14784 |
rs228921479 | in-del | -/GGTT | | | intron-variant | Grb2 | Mm_Celera | 11:115656174 | ATCACAAGCTGTTTG[-/GGTT]GGTTGGCTTTTGAGA | 14784 |
rs229008974 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115695723 | TAATGTGTTTTTCTT[-/G]CAGGGCTGCTGAATA | 14784 |
rs229063015 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694416 | TACATCATTCCTCTC[C/T]GATGTCCTTGAGACT | 14784 |
rs229102916 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115698817 | CTTTTACATAAAAAG[-/A]AAAAAAAAATCACAT | 14784 |
rs229136280 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689401 | GAAGAATGACTGATG[C/T]ATCTCCTGCAGTTAG | 14784 |
rs229175560 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115653261 | GACTGAGCTATACTC[-/A]AGAGCATGTCGGGTT | 14784 |
rs229251177 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698427 | GGAAGGGCGAGCTGC[C/T]CAGCCAGTTGAGTAA | 14784 |
rs229269850 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115691147 | GGCTCTCGGCAACTG[-/C]CCTAAATCAAGTAAC | 14784 |
rs229282621 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115666438 | CAGTGCCATCTCCTG[A/C]CGGTTATAGTCCCCT | 14784 |
rs229286348 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698394 | ACAATGCTCACCCTA[G/T]AAAGGAAACCGTCAT | 14784 |
rs229287654 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115686814 | ATTTAGACCTTGAAA[C/G]CTGGTCAAGGTAGGT | 14784 |
rs229308475 | in-del | -/TCT | | | intron-variant | Grb2 | Mm_Celera | 11:115663452 | TGAGCTGTCCTGCAC[-/TCT]TCTTCTTCTTCTTCT | 14784 |
rs229319433 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115697420 | TGTGTCAGCACAAAG[C/G]CTTCTACTCTGGGAG | 14784 |
rs229430739 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687783 | CACCTCTGACACAAT[C/T]ACCACCACCTAGAAA | 14784 |
rs229542138 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650901 | CATCTCGCCAGCCCT[G/T]GTATCTGAAAAATTT | 14784 |
rs229542214 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661379 | CAACACTCAGGCATC[A/G]TGGAGCAAGACTGAA | 14784 |
rs229578766 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115695530 | ACCAGGATCCACACA[A/C]CGGAAAGAGAGAAAA | 14784 |
rs229596704 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660771 | CTTGCTATGCACCAT[A/T]AAAAAGCTTTGAACT | 14784 |
rs229649793 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681048 | CCAGCAACCACATAG[C/T]TGCTCACAACCACCT | 14784 |
rs229656001 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702669 | GCATCAGCTGGCACT[C/T]TTACTTGCTGAGCTA | 14784 |
rs229739001 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654076 | AGGGAACCATGGCTT[C/G]TAGACTAAATGTACC | 14784 |
rs229758751 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691197 | CACAGGACAACACAG[C/T]ATCAACTGTCCCCTC | 14784 |
rs229773912 | in-del | -/AC | | | intron-variant | Grb2 | Mm_Celera | 11:115658695 | CTTATGACTCAACCT[-/AC]ACACACACACACACA | 14784 |
rs229779290 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702049 | AGCCACCAGACGGGG[G/T]GTGTGTGTGAGAGAG | 14784 |
rs229791041 | snp | A/G | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644699 | TGGGGAAATACGAGC[A/G]TGAAAAATGAAAGGC | 14784 |
rs229791414 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654925 | CAAATAAAACACATG[A/G]AGACACATACACAAT | 14784 |
rs229877102 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115645965 | GGCTGCTGCAAGAGA[A/G]AGCAGGGAAGCGGTG | 14784 |
rs229897598 | in-del | -/ATAAA | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643846 | AGTGAGACCCCATCT[-/ATAAA]ATAAAATAAAATCAG | 14784 |
rs229964280 | in-del | -/TTTAAC | | | intron-variant | Grb2 | Mm_Celera | 11:115648395 | TAACATCTTTAAATG[-/TTTAAC]TTTAAGAGGACACTT | 14784 |
rs229989143 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115690546 | GGAAATGCCCGTGCT[A/C]GAGAACGAGGAGGTT | 14784 |
rs230001029 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689156 | CTATGTAGGGTAGGG[C/G]TGGGGGAAGACTCCA | 14784 |
rs230188169 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652700 | TAAAGTAGCCTAAAT[A/G]CACACTAAGGAAGAA | 14784 |
rs230222520 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690892 | CACCAAATTCCTCTA[A/G]TATCATAATTACCTA | 14784 |
rs230278548 | in-del | -/GTCAGA | | | intron-variant | Grb2 | Mm_Celera | 11:115666372 | CAGGCTCCCCATGTT[-/GTCAGA]GTCAGTGTCTCCATC | 14784 |
rs230297775 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115687949 | TGCCTTAGGGTTTCC[A/G]CTGCTAAGAAAAGGT | 14784 |
rs230368660 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691444 | TGAGTTCAAGGCCAG[C/T]CTGGTCTACAGAGGA | 14784 |
rs230400384 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648308 | GGACCCTAACTCAGA[C/T]CCTCTTGTTTCGTGG | 14784 |
rs230485019 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652343 | CATGTGGTTGCTGGG[A/G]TTTGAACTCAGGACC | 14784 |
rs230500479 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662032 | TCATGTACCACTACT[C/T]TGTAATATATATTGG | 14784 |
rs230512523 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661422 | GCTCATACATTTACG[G/T]TTGCTCAGCAGGGAG | 14784 |
rs230522011 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649139 | TGGGGAGCAGGGAAG[C/G]GGGAGGGTATAGGGG | 14784 |
rs230583354 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115686040 | GTGACATACTAATGA[A/G]TAAGTAAATAAATAA | 14784 |
rs230640846 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683406 | GTCTCAACACACCCC[A/G]CTCCCCCTCCCCCCA | 14784 |
rs230647916 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682475 | TTGAACCTCACTCTA[A/G]ATGAGTCTACAGTAA | 14784 |
rs230680556 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651811 | CCCTGCAAAGTATTT[A/T]TAAAAAAAAATTCTG | 14784 |
rs230738881 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675642 | GGCAGGACCACTTGG[C/T]CATTGTTCTAGGAAC | 14784 |
rs230741894 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684102 | GGAAGACACACCTGA[C/T]GTTGACCTCTGTTTC | 14784 |
rs230756845 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115657891 | AATGAACAAATGGGG[A/G]GGGGCAGCAAGAGTG | 14784 |
rs230791098 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115676521 | AGTTTGTATTTTTTT[-/A]AAATGTGTATGTTAT | 14784 |
rs230879930 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647831 | TTACTTCTGGAACTT[C/T]CAGCTGGCTTGTGGT | 14784 |
rs230940135 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664219 | GGGAAGGGGAGCAAC[A/G]CACAAAGGAGACAGC | 14784 |
rs230948745 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674253 | GGGTGGGAAGACCAA[C/T]GGAACAGGAACAAAA | 14784 |
rs231081691 | in-del | -/TGCACATAAGTCATTA | | | intron-variant | Grb2 | Mm_Celera | 11:115660683 | GAAAAACACCCACAC[-/TGCACATAAGTCATTA]TGAACCTTTTCTATT | 14784 |
rs231134648 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648742 | CTGACTTGTCTCCCT[C/T]CCTGAGCTGTTTTAC | 14784 |
rs231150873 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658402 | TGTGAGAGAGAGACA[C/G]AGAGAGAGAGACAGA | 14784 |
rs231227706 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653828 | GGGATGGAGCCTACC[G/T]ACCATCCTTCAGCCA | 14784 |
rs231244455 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678469 | ATCAGACAGCTTGGA[C/G]AAGAGTTTGAGCCAG | 14784 |
rs231301537 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693312 | GAAAGAGCACAGTTC[A/G]CATCTAGGTACTTCA | 14784 |
rs231422116 | in-del | -/AAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115704807 | CTAATAGACAGAGCC[-/AAAA]AAAAAAAAAAAAAAT | 14784 |
rs231429309 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676949 | CCCATGACACCTACT[-/G]TCACTTCTCCTTTCC | 14784 |
rs231455917 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681411 | TGATGATGACCTTGA[A/G]CTCCTGATGTGGTTA | 14784 |
rs231456093 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115695851 | GACGGGCAGATGCTC[-/A]AAAAGCAGAAAGTAA | 14784 |
rs231474879 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692395 | CCCTAGGAAGGCAGG[A/T]ATTGTTATTCACATT | 14784 |
rs231479376 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679375 | AAGAGGTGATGCCAT[A/T]CCTGAGATCCCCATG | 14784 |
rs231486423 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667651 | ACGATTTCTGGGTTC[-/T]GAGGCTAGCCTGGTC | 14784 |
rs231487600 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677027 | CACAGTGCACCCCAG[A/T]AAATCTTCCTAGTGC | 14784 |
rs231514734 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669941 | ATACACCTCCATTCT[C/T]AGCAACCATTCACAT | 14784 |
rs231539850 | in-del | -/GTATGTGCACAAGC | | | intron-variant | Grb2 | Mm_Celera | 11:115687586 | ACTTCAAAGGTACCT[-/GTATGTGCACAAGC]GTATGTGCACAAGCG | 14784 |
rs231565300 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668501 | AAAAAAATAAACAAA[-/T]TTAAAAAAAAAGATA | 14784 |
rs231570315 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668932 | AGGTCCTGAGTTCAA[A/T]TCCCAGCAACCACAT | 14784 |
rs231810021 | in-del | -/GCGAGGGCAAAGACAGGCATATTTCAGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115683973 | GTGACCCTTGCTAGA[lengthTooLong]GCGAGCTGGCCATGC | 14784 |
rs231841277 | in-del | -/CGG | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643559 | AAAAGACCACTGTCA[-/CGG]CTGTGTCATGTAGCT | 14784 |
rs231850153 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672139 | AGTTTACAATTATCC[A/G]TGGCTCCAGCTCCTG | 14784 |
rs231850608 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685488 | AAAGAAACGGGAGGG[A/G]AGGAGGGGCACTATC | 14784 |
rs231862379 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663696 | CTCTCCCTTGTGAGT[A/G]CCTTTTGTGTTGCAT | 14784 |
rs231869321 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650833 | ACCATGTGGTTGTTG[A/G]GATTTGAACTCAGGA | 14784 |
rs231907895 | in-del | -/CAGA | | | intron-variant | Grb2 | Mm_Celera | 11:115688067 | GAAGCACAGCAGGTT[-/CAGA]CAGACAGGCATGGTG | 14784 |
rs231925427 | in-del | -/CTCCTCCTGG | | | intron-variant | Grb2 | Mm_Celera | 11:115663922 | TGTTGTCTCCTTCAA[-/CTCCTCCTGG]CTCCTCCTGTGTAAC | 14784 |
rs231955058 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650300 | GGCCTTTCAAAGCCA[G/T]TTCATAATAGGAGTG | 14784 |
rs232016552 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706088 | TTTTTTAAAAAGAAT[G/T]ATTTATTATATGTGT | 14784 |
rs232048378 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115705083 | ATTTATTTATTATAC[A/G]TAAGTACACTGTAGC | 14784 |
rs232158542 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689337 | AGGCTGTAACCGTAA[C/T]GGTAGCCCGAGGCCA | 14784 |
rs232232951 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671684 | GTTGTTGTTTGTTTG[G/T]TTTTTTTGGGGGGGT | 14784 |
rs232266578 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681919 | CTGACATAAAGATGG[C/T]GTCCACTCTCCATGC | 14784 |
rs232294536 | snp | A/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643951 | AGTGAGTTCTGGGAC[A/G]GCCAGGGCTACACAG | 14784 |
rs232414283 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676292 | CCTGTCTGACAAGCA[A/G]CTCAAGCTTAACCAT | 14784 |
rs232422055 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679789 | CAGGCCACTCCCTGA[C/T]AATGCACCCAAGCTC | 14784 |
rs232451196 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115686564 | GGTTCATCCACTTTC[A/C]TAACCACCAAATACA | 14784 |
rs232510345 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671077 | TTCCTTCACACAGAA[A/G]AGGGTTTTGTGTCAT | 14784 |
rs232585454 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115676980 | AGAACCCACATATAC[A/C]ACGTTCAGTAAAATC | 14784 |
rs232684567 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115666047 | TAAATAAATAAATAT[-/A]AAAAAAAAAAAAAAC | 14784 |
rs232720470 | snp | C/T | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643762 | TTAACATACTCTAAG[C/T]CTTTACTTTCAACAT | 14784 |
rs232730137 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653521 | CTGCAGCCGCTGCCA[C/T]CATAGTGGGTCTTCA | 14784 |
rs232796478 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115654583 | AAACTATttttctta[A/C]ggtgctggggcagaa | 14784 |
rs232827986 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674191 | AAGATGCTATAGATA[C/T]AAGTATTGAACACTT | 14784 |
rs232869721 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680951 | AAATAAATGATTTTT[A/T]AAAATCAAGAAGATG | 14784 |
rs232936335 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702552 | TGTGTAGCACTGGCT[A/G]TCCTGGAACTCATTC | 14784 |
rs232946655 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670721 | CACACACGGGGAAGT[A/G]TAGAAAACTAGCACT | 14784 |
rs232973653 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648985 | CTAACCAGTACCCCC[C/T]AGAGCTTGTGTCTTG | 14784 |
rs233000066 | snp | C/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708953 | GACCAGTTCTAGAAA[C/T]GTTTGGGGATCTGGT | 14784 |
rs233015112 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703486 | AGACAACAATATAAC[C/T]CTAGGTCTTCATCCA | 14784 |
rs233205556 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679223 | AATAAAGTCAACATT[A/T]TTATGAGAAAATATC | 14784 |
rs233281624 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646505 | CACTCGGGCTGTAAA[C/T]GAGGCAGTCCTAACC | 14784 |
rs233301382 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690695 | ATTCATTTGGTTCAA[A/G]GAAGAAAATGGAGAC | 14784 |
rs233312503 | in-del | -/GGG | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115710166 | CCTATCTAAAAAATA[-/GGG]GGGGGGGGGCTGTCA | 14784 |
rs233402519 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652564 | GGGATTAAAGGTGTG[C/T]GCCACCACGCCCGGC | 14784 |
rs233453640 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115696386 | ACAGGAAAAGAAGAG[A/C]GAGGACAAGTGTCTC | 14784 |
rs233462102 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710264 | CAACCTTAAAGCCTG[A/G]GAAGTAGATATCTGT | 14784 |
rs233510223 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684481 | AAAAACTAAACGTTT[A/G]AAGATAAAATTTCTC | 14784 |
rs233514981 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667523 | CCTACCATAAGATTA[-/T]TTTTTTGTTGCTATT | 14784 |
rs233519834 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709487 | AGAAGGTGATGTGGA[A/G]CTGAGTACTGGAGGG | 14784 |
rs233601174 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660881 | GCATCAAGTGATAAC[A/G]AACTTAGAAAAACTG | 14784 |
rs233646670 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115675258 | TGCCTCTGCCTCTGG[A/C]GTGCTGGGATTAAAG | 14784 |
rs233647183 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668053 | AGATAGACAGGCACC[C/T]ACCACAAGGGCACCA | 14784 |
rs233764191 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701585 | AGAGGGGAGAGGGAG[A/G]CAAAGAATGAGAATA | 14784 |
rs233814918 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700882 | TCATCCCCAAAACAC[C/T]ACACCATGGCTTGTT | 14784 |
rs233841563 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666377 | TCCCCATGTTGTCAG[A/T]GTCAGTGTCTCCATC | 14784 |
rs233847651 | snp | A/T | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699596 | ACACTTCCTCTTCCT[A/T]CCCGCAGGGTGTAAA | 14784 |
rs233871236 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652756 | CCCTGCCTTTCATCA[-/G]GAGTTGCTGGCTGCA | 14784 |
rs233871626 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689716 | TGGCGGCCAGCGTGT[A/G]AACAGCAATGAAGGC | 14784 |
rs233951082 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656801 | CCTTCTGTTAAAGCA[G/T]GAGGTATCAAGGCAA | 14784 |
rs233986248 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673430 | TTCTAGCTTATTGTA[G/T]GGTATTTTTCATCTT | 14784 |
rs233993297 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709894 | CCTTTCAGAGCAAAA[A/G]ATGAAGCCAATGACT | 14784 |
rs234008870 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655662 | TAGAAAGGGAAGGTC[A/G]GGCTTTTTTCTCAAT | 14784 |
rs234082274 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676642 | AAGGCAGAGGCACCA[A/G]GCTACAGTGAGACCT | 14784 |
rs234144072 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664133 | TTTGTTTTGGTTTTG[-/T]TTTTTACCTGAAAGG | 14784 |
rs234174394 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694736 | AAACAAAAAACGAAA[C/T]CATATACATACATAG | 14784 |
rs234190585 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694053 | CACTATGGAAACCAG[C/T]ACGGGCATTCCTTTA | 14784 |
rs234202976 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115674327 | GTCCTGAATTTAAAT[A/C]TTCTAAACTATGGGA | 14784 |
rs234212567 | in-del | -/TGCA | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709619 | CTGTGCGATGCAAAG[-/TGCA]TAGATAGGTTCCTGT | 14784 |
rs234214528 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666514 | CCACTCCCTAAGGTC[C/T]CTAGAGTAACCCTGT | 14784 |
rs234243352 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684795 | TTAAGTCCACCTATG[C/T]TCAGGGCCTGGCAAG | 14784 |
rs234262261 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668248 | TGAGCTCGGTGAGCA[C/T]GTGTGCTGTCAGGCC | 14784 |
rs234278632 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665841 | AGCCAGGAAGAACTA[C/T]ATAGTAAGCTTTCAA | 14784 |
rs234280784 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647501 | GTCTCTGCCTCCCGA[A/G]TGCTGGGATTAAAGG | 14784 |
rs234289749 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671011 | ATCAACTAAGATGTG[A/G]CTACTGTGTCCAGCT | 14784 |
rs234385050 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675316 | AAACTCTTAAACCAG[-/T]GGCCAAGGGGAAGTC | 14784 |
rs234395834 | in-del | -/GGTTGA | | | intron-variant | Grb2 | Mm_Celera | 11:115667077 | ATCAAGTTGGTAAGT[-/GGTTGA]GGGTACAAAGACTTG | 14784 |
rs234417797 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707135 | TAACACAAGCAAACA[G/T]GCAAAATCCACTTGT | 14784 |
rs234434128 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669134 | GCAGTGGCACTAAGC[G/T]GCATCCCTGGCCCTG | 14784 |
rs234497466 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663385 | AAAAGTGGCAGTGGT[A/G]TGTGTGTGTGTTTTA | 14784 |
rs234528866 | in-del | -/GAGAATGAACT | | | intron-variant | Grb2 | Mm_Celera | 11:115687441 | CATAAGGTAGAAAAA[-/GAGAATGAACT]CTAGCAAGGTGTGCT | 14784 |
rs234576614 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115698816 | CTTTTACATAAAAAG[-/AA]AAAAAAAAAATCACA | 14784 |
rs234608305 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704831 | AAAAAATGAGCATGG[A/G]CTTGAGGTGTATAGC | 14784 |
rs234608682 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663294 | GTGATGACGACTGAC[A/G]TCAAGACAGGCAGGA | 14784 |
rs234608772 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653165 | AGGCTAGTTACAAAC[C/T]TGATAAGCTTCTAAA | 14784 |
rs234616638 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667146 | TATGTTACAACTACA[-/T]TAGCCATCTCCTCTG | 14784 |
rs234668020 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662707 | TGAAGATGCCATCTT[C/T]TATGGGCATGTGTAA | 14784 |
rs234670953 | snp | C/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700440 | AGGAGAGTCCCACAC[C/G]GAGGAAGCAGTAGTG | 14784 |
rs234764420 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661563 | GGCCCAGTGTTGCTC[C/G]GTTTCTGCTTTCTTT | 14784 |
rs234775127 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664597 | AGGTTCCTTAGTGAA[C/T]AGAATCAGACCTTCC | 14784 |
rs234793297 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653929 | CCCCAGCCCCTCACC[A/G]AAGCCGCTTAAGTGC | 14784 |
rs234824886 | in-del | -/TTTTTTT | | | intron-variant | Grb2 | Mm_Celera | 11:115646254 | AGCTCTCTTAACAGG[-/TTTTTTT]TTTTTTTTTTAAAAA | 14784 |
rs234913057 | in-del | -/ACAA | | | intron-variant | Grb2 | Mm_Celera | 11:115671460 | CACACACACACAAAC[-/ACAA]ACACACACGGGCGGG | 14784 |
rs234954503 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115648246 | ATGGTAAGGCTGGGC[C/T]AGCTGGCTACAGCTC | 14784 |
rs234956531 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115670989 | TTACAAGGATCAGAC[-/AG]AGTGTGATCAACTAA | 14784 |
rs234965177 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702383 | TGTGTGTTTGTACAC[A/G]TATTCCCACCTACAC | 14784 |
rs235068700 | in-del | -/AAC | | | intron-variant | Grb2 | Mm_Celera | 11:115670851 | ATTCAGGGTCACAAG[-/AAC]AACAGCCTGATCTCA | 14784 |
rs235104022 | in-del | -/AAAG | | | intron-variant | Grb2 | Mm_Celera | 11:115670242 | TTTTGACACTGCTTT[-/AAAG]AAAGAAAAAAAAAGA | 14784 |
rs235139431 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651419 | GTTAGAAGACAACCC[-/T]GGGGGGTGGGGGGTG | 14784 |
rs235158145 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115708119 | GGCTGCTCCGGGCTC[C/T]CCAGCGTCCAGCCGG | 14784 |
rs235214091 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661007 | CAGCTGCTACAAGTC[A/C]ACAGCTCTGTGAGAA | 14784 |
rs235215687 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694829 | ACATTACATACACGC[A/G]TAAGAACAGCTTTCC | 14784 |
rs235262507 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667940 | AAGGGTTTGCATGCC[C/T]TTGGACAGCTGGCTG | 14784 |
rs235286570 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685686 | ACTTTCTTTAGCAGA[A/G]AAAACAGAGATGAGA | 14784 |
rs235302072 | in-del | -/TTGG | | | intron-variant | Grb2 | Mm_Celera | 11:115673483 | CACCTATAAGTTTGT[-/TTGG]TTTTTATATTTACTT | 14784 |
rs235420520 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115706263 | CTCCGGAGAGCCCAT[-/A]AAAATTTTTTTTAAT | 14784 |
rs235517953 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115677389 | GTTCAACAGGTGAAC[A/C]AACCTGGCCGCCAAC | 14784 |
rs235524935 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692735 | ATGCTTTGCTCTTAT[G/T]AACGTGGCCTGCTCT | 14784 |
rs235557313 | in-del | -/AGAG | | | intron-variant | Grb2 | Mm_Celera | 11:115678661 | GGCCTAAGCCTAGAT[-/AGAG]AGAAACACTCTGGGC | 14784 |
rs235597638 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691991 | AATGGGCTGGGTGTG[G/T]TGGCACAAGCCTCTA | 14784 |
rs235599107 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704609 | CTGGAAATGCTGCCC[A/G]GCTGGTGGAGTGCTT | 14784 |
rs235628348 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703650 | GCCCAGGGAGTGGCA[C/T]TATTAGGAGGTGTGG | 14784 |
rs235634891 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665221 | TCAGTGCAGGCTTAC[G/T]GTGATCACTCTACTA | 14784 |
rs235642433 | in-del | -/TA | | | intron-variant | Grb2 | Mm_Celera | 11:115662648 | AAGTGTGTTGGTGTC[-/TA]TAGAGTTCTAATGCC | 14784 |
rs235651948 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692454 | TTGCTAAGCAAACTG[A/T]CTAAGATCCCAAGTT | 14784 |
rs235674430 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689797 | TGAGGTGGGCGGGGC[-/T]TTTTATAAACTCTCA | 14784 |
rs235780224 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115679461 | TCAGCACAGAATCTC[-/A]AGCATACATCAAGGC | 14784 |
rs235784845 | in-del | -/TCTCTG | | | intron-variant | Grb2 | Mm_Celera | 11:115702533 | TTTCGAGACAGGGTT[-/TCTCTG]TGTAGCACTGGCTAT | 14784 |
rs235788312 | in-del | -/G | | | intron-variant, utr-variant-5-prime | Grb2 | Mm_Celera | 11:115699487 | TCCTCCTCCCTTCCA[-/G]GCAACAGCTCTCCTT | 14784 |
rs235843683 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656869 | ATCTACAGCACTGAA[C/T]TGTCACTTGGTGTAT | 14784 |
rs235864937 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689522 | CACAAACTCACCTGC[A/G]TGGGTACCTGATGTA | 14784 |
rs235869518 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670357 | TCACACCAAAAAAAC[A/G]GACACCTAAGGTTTG | 14784 |
rs235886867 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700750 | GGGGCATTAATCAAG[C/T]ATAACTGCAAATAGG | 14784 |
rs235910029 | in-del | -/GC | | | intron-variant | Grb2 | Mm_Celera | 11:115656450 | TGTGTGTGTGTGTGT[-/GC]GTGTGTGTGTGTGTG | 14784 |
rs235939207 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687807 | CTAGAAAAAAAAAAA[A/T]AAGTATTTTCTTAAA | 14784 |
rs235966524 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700957 | AGAGAAGAAACGAAG[-/A]AAAAAAATCCTAGCA | 14784 |
rs235968581 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664468 | GTGCTGCAGTAATGG[C/T]TGCCATAGCCTCACC | 14784 |
rs235977004 | in-del | -/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709654 | GGGGCTGCCGGTTTT[-/G]GGGGGAGTAGTAGAT | 14784 |
rs236001290 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689133 | ACAGCCAAGGCTACA[C/T]AGAGAAACTATGTAG | 14784 |
rs236049911 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115687196 | AACACTTGGGAGGCA[A/G]AGGCAGACGGATTTG | 14784 |
rs236073954 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115698151 | GTCACACAACACTCC[A/G]TCACTTTGAGCTCTG | 14784 |
rs236100649 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115657886 | AAGGAATGAACAAAT[-/G]GGGGAGGGGCAGCAA | 14784 |
rs236164578 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115689812 | CTTTTATAAACTCTC[A/C]AGTGAGGACTTGAGA | 14784 |
rs236166857 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678682 | AAACACTCTGGGCTC[A/G]TCTCACTTCATCTGA | 14784 |
rs236174317 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652886 | ATTTTCAGCTTAAAA[A/T]TTTAAAAATTTAATT | 14784 |
rs236196250 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688200 | TTCCTCCAGAAGACC[C/T]CACCCCTACTCCAAC | 14784 |
rs236234055 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662572 | AGGATGGATGTGTGA[C/G]TGCAGAAGGGACAAG | 14784 |
rs236246119 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679284 | ACCAAAGCGGGGACA[A/G]TTAGGGAAGGTTATT | 14784 |
rs236357318 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660832 | CTAGGATTACATTTT[C/T]AAGTCTAATTCACAA | 14784 |
rs236411394 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115683974 | TGACCCTTGCTAGAG[C/T]GAGGGCAAAGACAGG | 14784 |
rs236414982 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701034 | AATTTTCTGTAGTTA[C/T]TTTTGATAGCTATAA | 14784 |
rs236439994 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651139 | CAGCTCAGCACTTAC[A/G]AGTCCTGGCTTTTCG | 14784 |
rs236544838 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674781 | TAGGGGACAGGGATA[C/T]TTTGCAGGCATAAAG | 14784 |
rs236584085 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684915 | GACAACTGTCCTTTA[A/G]CCTCCCCACACATGC | 14784 |
rs236586113 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673900 | CAGATCTGCATGCTT[C/T]TACCTACTAACTGCT | 14784 |
rs236621271 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115659574 | AAAAAATCAAACCAA[A/C]CAAACAAACAAAAAA | 14784 |
rs236621423 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649301 | ATGATCGGTCAGACA[A/G]GGCAAAGCCATTCTT | 14784 |
rs236630056 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688659 | CACACACAAAAAAAA[-/T]TTTTTTTTAATTTTT | 14784 |
rs236682771 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115658846 | TTCCATTCCCCAGAC[A/C]CCCTTCCAGAGACTC | 14784 |
rs236749588 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646033 | CTGGCTCCCCCAGGG[A/T]GGGCAAGCATGTGGG | 14784 |
rs236828266 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115652304 | AAAGGGAATTGGATA[A/C]CATTGCAGATGGTTG | 14784 |
rs236828569 | in-del | -/GG | | | intron-variant | Grb2 | Mm_Celera | 11:115664200 | TTCAACTGCAGCAGT[-/GG]GGGGGGAAGGGGAGC | 14784 |
rs236908567 | snp | A/C | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709161 | GCTGGAGAGACCTCT[A/C]AGGTCAAAAACTGCT | 14784 |
rs236931536 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693810 | ACCAGCCATCAGAGA[A/G]ATGAAAATTAAAACT | 14784 |
rs236994776 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654600 | GTGCTGGGGCAGAAT[C/G]CAGGGCTTTGTGCAT | 14784 |
rs237017105 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653361 | ACTGGATTGGTGTGT[A/G]CTGTCCTAAAAATAG | 14784 |
rs237062650 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691172 | AGTAACCATCAGCCC[G/T]GCAGCAGACCACAGG | 14784 |
rs237063551 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647168 | ACAGCCCACTTGTGA[A/G]GCTACAGCTTTATCT | 14784 |
rs237126180 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646414 | AGGACCTTTGGAAGA[A/G]CAGTCAGTGCTCTTA | 14784 |
rs237221924 | in-del | -/CTT | | | intron-variant | Grb2 | Mm_Celera | 11:115691774 | GGAGTCAATCCTCTC[-/CTT]CTACCACGTTGATTC | 14784 |
rs237238964 | in-del | -/GGA | | | intron-variant | Grb2 | Mm_Celera | 11:115705003 | CTCCGAGGGGGCGGG[-/GGA]GGGGACGACGACGAC | 14784 |
rs237259909 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681231 | AAGCTTATTAAAAAA[A/T]TTTAATCTTACTATT | 14784 |
rs237278104 | in-del | -/AAGG | | | intron-variant | Grb2 | Mm_Celera | 11:115706568 | ACTCCATAATTCTCT[-/AAGG]AAGGGCTGCTGTACA | 14784 |
rs237300193 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691816 | ACCTCAGCTCATCAG[G/T]TTTGGCAGCAAGCAT | 14784 |
rs237312685 | in-del | -/AACAA | | | intron-variant | Grb2 | Mm_Celera | 11:115669050 | AATCTTTTAAAAAAC[-/AACAA]AACAAAACAAAACAA | 14784 |
rs237326364 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693606 | CTATACTGTGAGTTC[C/G]AGGCCAAGCTAGATC | 14784 |
rs237348786 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115705910 | CAGAGGCAGGAGAAT[C/G]TCTGTGAGTTTAAGG | 14784 |
rs237528424 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658004 | CAGAGCCGGAGTTAC[A/G]GGGAGTTGTGGAGTG | 14784 |
rs237578343 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115665717 | CTGTCTCGAAAAAAA[A/C]AAAAAAGAAAAAAGA | 14784 |
rs237611085 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115686128 | CTTGGCAGTGGTGGC[A/G]CATGCCTTTAATCCC | 14784 |
rs237673699 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688471 | GAAGAAGGTTGTGAA[A/T]TCAAGGCCAGCCTGA | 14784 |
rs237720325 | in-del | -/AC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684275 | CTACCACACACACAT[-/AC]ACACACACACACACA | 14784 |
rs237728749 | snp | C/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709688 | GCTTGGAGAAGTACC[C/T]CTCAGTTCCAAAAGC | 14784 |
rs237851488 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661778 | CTGACCAAGCCTCCC[A/G]TTTTACCCACTAACT | 14784 |
rs237903228 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115677765 | GACACATTATTTATC[A/G]ACTGTTCCGGCCCAA | 14784 |
rs237935274 | in-del | -/CACTGTACTCTGT | | | intron-variant | Grb2 | Mm_Celera | 11:115666823 | ATGTTAGGGGGAGTA[-/CACTGTACTCTGT]ACACTGTAGCTAAGC | 14784 |
rs237977145 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115683822 | GTCTCGAAAAATCAA[A/C]AACAACAACAACAAA | 14784 |
rs238097674 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652215 | TCCTCTCCCTTCCCC[A/G]ATCACCAATCACATG | 14784 |
rs238109967 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115697168 | AAAAAAAAACAAAAA[-/C]ACAAAAAAACCAAAT | 14784 |
rs238111670 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658141 | CTCTCTGCTGCTGAG[C/T]CATTTCTCTAGCCCC | 14784 |
rs238126362 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704001 | ATACTTTGGTATAAG[A/G]CTCAGAGTCAACTAT | 14784 |
rs238130100 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115670588 | GGCCAGAAGGCTTGG[-/A]AAGGAACAAAGTTCC | 14784 |
rs238156037 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681470 | TTTTATTTAAAAAAA[A/G]TTAAGAGGAAAAGTA | 14784 |
rs238171684 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702771 | GACATCTGCATTTTG[G/T]TTTTTAAGACAAACT | 14784 |
rs238281032 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672600 | CCACAGCCTCTTCTG[A/G]TTTCCTTGGGCACAA | 14784 |
rs238362063 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659707 | AACCAACCAATTAAG[C/T]AACCCCAACAGAGGA | 14784 |
rs238385646 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115659426 | CTGGCCTCACTCACA[C/G]ATCTGCCTGCCTCTG | 14784 |
rs238391642 | in-del | -/AAAAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115646270 | TTTTTTTTTTTTTTT[-/AAAAAA]AAAAAAAAAGATTTT | 14784 |
rs238441487 | in-del | -/AAAAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115707093 | AAACCATGATCTGTG[-/AAAAAA]AAAAAAAAAAAACAC | 14784 |
rs238500807 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679642 | GTCAGCCTGGCACCA[C/T]AGACAGAGCATGGAC | 14784 |
rs238501076 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115670152 | CTGGAGTTACAAACA[A/C]ATATGAGTGCTTGGA | 14784 |
rs238508903 | snp | C/G | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699540 | GGCGACTGACAGGTC[C/G]AGCAGCCAATAGCAT | 14784 |
rs238518442 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115667651 | GACGATTTCTGGGTT[A/C]GAGGCTAGCCTGGTC | 14784 |
rs238544616 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677146 | ACTGCAATCCCAGCA[C/T]TTAATAGACTATGAC | 14784 |
rs238557197 | in-del | -/CAACACATCACAG | | | intron-variant | Grb2 | Mm_Celera | 11:115698965 | AAAGGCAGTTAAGGA[-/CAACACATCACAG]CGACTCTCTTATGTC | 14784 |
rs238605090 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115670246 | GACACTGCTTTAAAG[-/A]AAAAAAAAAGATGCA | 14784 |
rs238640908 | snp | A/C | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644392 | GGGAGACTCTACCCG[A/C]AAGAGTCTAGCAGCC | 14784 |
rs238667355 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668190 | ATCAACAGCCAGGAG[C/T]GTGTCAAGTGCTGTA | 14784 |
rs238680395 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115669446 | AGCACCCACATGGTG[A/G]TTTACAACCCCGTGT | 14784 |
rs238824018 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651832 | AAAAATTCTGCCAGA[G/T]TAAAACTAAGATTCA | 14784 |
rs238898500 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646904 | GGAGAAAAACCATGA[A/T]GCGGCCACAGGGCTC | 14784 |
rs239092041 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691212 | ATCAACTGTCCCCTC[-/T]CCCCGGGAGAGTCAG | 14784 |
rs239094781 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666990 | ACAAAGCAAGAAGCA[C/T]TGTATCCTTGGGGTA | 14784 |
rs239106635 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666253 | ACAGCATCAAAAGAG[C/G]AAACAATATGTGTAG | 14784 |
rs239136266 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115691043 | GGTTATCATAGTCCC[A/G]TAACACACTGGCTAA | 14784 |
rs239216007 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706512 | CTCAGTGCTGCCTGT[C/T]GGGAGAGTGGCAGCT | 14784 |
rs239234768 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659131 | TCCTCAGGACCCGCA[C/T]GGTAGAAAGAAAGAG | 14784 |
rs239237715 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115676210 | CAACAAGTATGTATA[C/T]CTGCATATACATAAA | 14784 |
rs239337537 | snp | C/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643737 | CAGGGTCTGGAGATG[C/G]CGGCCAGAGTTAACA | 14784 |
rs239451667 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687053 | ACAGCCACAACAGTA[-/T]TTAAAAGAGAAGCAC | 14784 |
rs239494850 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682314 | ATGTAAGATCACTTG[A/G]TGAGCCAGGTAACTA | 14784 |
rs239532766 | snp | C/G | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644769 | GTGAAGGATGCCAGG[C/G]CTCCTCTGACCGTCT | 14784 |
rs239648729 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671610 | CATGTTTTCAACAGA[C/T]AGTCAATACTCACCT | 14784 |
rs239759616 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672441 | AGGCTCTGGGCTGAG[A/G]TAGGAACTTACATAA | 14784 |
rs239795865 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682381 | CACACCATTTCTGAA[C/T]TACTGACAAAGGTGT | 14784 |
rs239799671 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677058 | TCCTTACCTAACTAC[C/T]CACAGTTTAGATGAA | 14784 |
rs239841821 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115687012 | CTCCAATAATCTACA[C/G]AGACTAAAGCCATAC | 14784 |
rs239872425 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647081 | CTCCTGATTGCTGAT[C/G]ACTAGTTACAGGAGT | 14784 |
rs239958967 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698892 | CACAAGGTAAGCTTG[C/T]GACTCAAATCCCTTT | 14784 |
rs240045300 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684624 | GTGAGTTCTAGGACA[A/G]TCAAGGCTATACAGA | 14784 |
rs240093688 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694495 | ACAGCAGCTAAGCCA[C/T]GGAGCCAACATAGGC | 14784 |
rs240121993 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677117 | AAAAATGTATACTGG[G/T]TATGGTGGTGCACAC | 14784 |
rs240154646 | snp | A/C | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709820 | GAGTCCACTAAAATA[A/C]GGCAAGTGAATTGTT | 14784 |
rs240181282 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115698316 | GAGGCTCAGAGGGAG[A/G]ACAGCAAAACAGACA | 14784 |
rs240217676 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115697345 | TCTATGAAGCCAGCA[A/C]CAGCGACTGGTGCTC | 14784 |
rs240235439 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115695182 | GCCAACACTACCCAC[A/G]GGTAGTGGATTTCTC | 14784 |
rs240285254 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115655935 | AGGCAAGCAAATCCT[-/A]ACAACCCTGTGTTCA | 14784 |
rs240338207 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668628 | GATAACTGACTCACA[C/T]CCACACATCACCTCC | 14784 |
rs240379392 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666131 | TACTGGTGACACACA[C/T]CTTTCATTACCAGCA | 14784 |
rs240381781 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115669202 | AGGCAGTGAGGAGAC[-/AG]AGACAGGGAATTGGA | 14784 |
rs240416983 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674678 | TGTGCCCAGCAGGAA[A/G]TACAGCCACTCCTCC | 14784 |
rs240497521 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658800 | GATGAGATTGTAAAA[G/T]GAGGAAGAGCCAGTT | 14784 |
rs240525098 | in-del | -/GCTTC | | | intron-variant | Grb2 | Mm_Celera | 11:115650096 | TGGAGCTTTCAAACA[-/GCTTC]GCTTACTCCACACTC | 14784 |
rs240539986 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704175 | CTACCTGGTATCAAC[A/G]GTCCCTCTCCAACTC | 14784 |
rs240555517 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115647699 | caagtttgaaaccag[A/C]taccaaactccagat | 14784 |
rs240565906 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692959 | AGCCTCCAGGGGAGA[C/G]TGCGTGTCCTCAGTC | 14784 |
rs240586572 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664802 | TAAAGGCGTGCGCCA[C/T]CACGCCCGGCAAACA | 14784 |
rs240591288 | snp | A/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709580 | AGAACAGAGAGATGG[A/T]TGGAGGCGTGAGAAA | 14784 |
rs240610893 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679436 | TTCCATGTATCCATT[A/G]GGACTGCAGCTCAGC | 14784 |
rs240611704 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115667380 | ACATGCAGGAACAAA[A/C]TGAAGTAGCCAATAG | 14784 |
rs240615159 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672645 | ATATGCAGGCAAACG[C/T]CTACACACATAAAAA | 14784 |
rs240671267 | in-del | -/CA | | | intron-variant | Grb2 | Mm_Celera | 11:115664287 | GCCACAGAGCTCAGT[-/CA]CACAGACTGGCTGCC | 14784 |
rs240692221 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683938 | AACCATGGAAAAGCT[A/G]GGTATGGCTGTGTGT | 14784 |
rs240720376 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665433 | CCTCAAACACTGCTT[C/G]TGCTGTGAGGTTAAC | 14784 |
rs240727255 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682722 | AGCACTCTCAGGCCA[C/T]TCCAGGAGGACTGCA | 14784 |
rs240736104 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651319 | aaataataatGTTTT[C/T]ATGGTTATTTGTTAT | 14784 |
rs240830064 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661962 | CTCTCCCAGTTTTAG[G/T]TTCACAGTATTTAGT | 14784 |
rs240863514 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115708377 | CGCTCACTTCCCGCC[C/T]GCTCCCCTGCACTCA | 14784 |
rs240863545 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694217 | GCATGCTGTGACATG[C/T]TCACAATGTACCCCA | 14784 |
rs240899457 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707034 | AATCTCCCTTACTAA[C/T]AGTGAGGGGAAACAG | 14784 |
rs240976732 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661332 | AGTTCCTAAGCAGCC[C/T]ACTTAGCTGGGTTCA | 14784 |
rs241008341 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668207 | TGTCAAGTGCTGTAG[A/G]AGCAGTGAGCTCCGT | 14784 |
rs241053190 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702653 | TGAGCCACCACACCC[A/G]GCATCAGCTGGCACT | 14784 |
rs241073894 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653524 | CAGCCGCTGCCACCA[G/T]AGTGGGTCTTCATTG | 14784 |
rs241074151 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663890 | TCAAGAAACAGTTTA[A/G]TACTCAAAATATAAA | 14784 |
rs241129596 | in-del | -/GA | | | intron-variant | Grb2 | Mm_Celera | 11:115648903 | GGGCCCCCAATGGAG[-/GA]GAGCTAGAGAAAGTA | 14784 |
rs241146086 | snp | A/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701462 | ATAAGTGGTAACAGA[A/T]AGAGTATTTGAATGA | 14784 |
rs241178073 | in-del | -/AAT | | | intron-variant | Grb2 | Mm_Celera | 11:115705998 | CTGACCCTGCCTCAA[-/AAT]AAATCAATAGAGAAA | 14784 |
rs241190583 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654440 | CTCACTAGTGCACTG[C/T]CCTCCTCCTCTGCTC | 14784 |
rs241201737 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690215 | CCCCAAAAATAGGAT[A/G]AAGAAACCTCTGAAT | 14784 |
rs241218967 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702618 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 14784 |
rs241276574 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115699947 | CACCAGCTCCATTCA[C/T]GCCCAACTTGTCATC | 14784 |
rs241362294 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651253 | CCAATTCTGGCCTCT[A/G]AAGGCCTGTGACAAA | 14784 |
rs241399954 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649573 | GGCGGGTGAGGAGTG[A/G]GGCTAAGCCGCCTCG | 14784 |
rs241400314 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659958 | CATACATAGCAATAG[C/T]AATAATAATAAAATA | 14784 |
rs241467874 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659227 | ACAGACATACACACA[C/T]ACATACACACACACA | 14784 |
rs241524182 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651398 | CCACCGTGTATCCAC[A/G]TGGGGGTTAGAAGAC | 14784 |
rs241567869 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667854 | TGCTGCTCTGGTACA[C/T]AGCTGTCTGCCCACA | 14784 |
rs241573839 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115668503 | AAAAATAAACAAATT[-/AA]AAAAAAAAAGATAAT | 14784 |
rs241702735 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115669331 | AGGAAGCCCAGGTTA[C/G]TAAGCAAGCACTCAC | 14784 |
rs241711924 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115665063 | TTGATTTTCAGTGAG[-/A]AAACTCAATGAGGAG | 14784 |
rs241901833 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702992 | tctctctctctctct[C/T]tctctctctctctct | 14784 |
rs241973370 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707809 | TCCTTCCAGCATTCC[C/T]ATCCGCTGCTGCTGC | 14784 |
rs242041704 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665581 | ACAGAAACTGCTGGG[C/T]GTGGTGATGCACGCC | 14784 |
rs242086561 | in-del | -/TTG | | | intron-variant | Grb2 | Mm_Celera | 11:115671664 | TTTTGTTGTTTGGGT[-/TTG]TTGTTGTTGTTTGTT | 14784 |
rs242103905 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115691119 | AGATCTGCTCTAGCT[A/G]AGAATTTAGGGACGG | 14784 |
rs242226496 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659035 | GCTCTGTGTATTATA[C/T]CCTAATCAAAGTTAC | 14784 |
rs242246765 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671211 | CATGGCCTTCTGTGC[C/T]TTAAGATTTCCAGTG | 14784 |
rs242379213 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115676800 | AACCCGCACCGCCTG[A/C]ATGGTAAACTCCCTG | 14784 |
rs242436981 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115677417 | AACCCTGATGAGTTG[A/C]GTCTTGTGCCCTCCA | 14784 |
rs242473685 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686343 | TGGTCTAGAGATGGA[C/T]GTAGCCGTCCGACTT | 14784 |
rs242497229 | in-del | -/TT | | | intron-variant | Grb2 | Mm_Celera | 11:115698645 | TAGAATTCTAGTAGG[-/TT]TTTTTTCCCCCCAGA | 14784 |
rs242575391 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705287 | AATTTATTGTTGGGT[G/T]CCTACTTCTTGTGGA | 14784 |
rs242633635 | in-del | -/AT | | | intron-variant | Grb2 | Mm_Celera | 11:115693927 | GCAGGTAAAACACTC[-/AT]ACAGAAAACAAATTT | 14784 |
rs242670720 | in-del | -/TGC | | | intron-variant | Grb2 | Mm_Celera | 11:115664453 | GTGTCCCAGGTAGGG[-/TGC]TGCTGCAGTAATGGT | 14784 |
rs242755572 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683146 | TGGTGCCAGGAAGCC[A/G]GAAGAGGAAATATAA | 14784 |
rs242757631 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672055 | TTCAAGAGCTAAAGA[C/G]GTGGTTCCGAGGTTA | 14784 |
rs242796791 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657699 | GCAGAGGCAGGCAAA[A/T]TTCTGAGTTCGAGGC | 14784 |
rs242815089 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672988 | TGAGTCCTGCCAGTT[C/T]CTTACCAGCTGCCTG | 14784 |
rs242858227 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668160 | AGGTGATGACACAGG[C/G]AAACAGGGAAATAGA | 14784 |