SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs242904444 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115678162 | GCGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 14784 |
rs242923635 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651605 | CTACAAGTCTGTGCA[C/T]CAATATGGCTGCCTC | 14784 |
rs242960573 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658266 | AAAGAGGCCCTCCTA[C/T]CATGCCCAGCTCCAA | 14784 |
rs242960673 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647531 | GCGTGCACCACCAAC[G/T]CCCCGGCTACCGAGG | 14784 |
rs242990834 | in-del | -/GTGGGGT | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644598 | TTGTGGGATGGAGGG[-/GTGGGGT]GGGGGGAGGGGCAGC | 14784 |
rs243014114 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695470 | GGTGACAGGGCTTCA[C/T]GTGTAAATGCACTTG | 14784 |
rs243017907 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661199 | CACTAAAATAGGTTA[A/G]TGATGCAATGCTATC | 14784 |
rs243037217 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648558 | CCCACTGAGCTGTGT[C/T]ATTAGCCTGGGTCTC | 14784 |
rs243072000 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115696834 | CTTCTTCATCATAAA[C/T]ACTCCCGGGAGAATA | 14784 |
rs243073381 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115685338 | AGGCACATTCCACCC[A/C]AACCACACCCACAGT | 14784 |
rs243127032 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675522 | GTGGGTACTGGTATC[A/G]AACTCTTGTCCTCTG | 14784 |
rs243232806 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651775 | ACAGGCAGAGCTCAC[A/G]GCTGGCTTAATAAAC | 14784 |
rs243268154 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653580 | GGCAGTCTAGGGTAG[A/G]ACTGCTCTCTTCCTC | 14784 |
rs243282287 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689402 | AAGAATGACTGATGC[A/G]TCTCCTGCAGTTAGC | 14784 |
rs243296267 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666633 | TATGGGGCAAGGGCG[A/G]TATTCAACTTCTAGA | 14784 |
rs243296936 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115658268 | AGAGGCCCTCCTACC[-/A]TGCCCAGCTCCAAGT | 14784 |
rs243349409 | snp | A/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643862 | ATAAAATAAAATCAG[A/G]ACGGGCAGTGATCCC | 14784 |
rs243404981 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679887 | CGAAACCTGTCTGGG[A/G]AATCACACACAAGTT | 14784 |
rs243440001 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115690529 | CCAGCCTCCACACTA[A/C]GGGAAATGCCCGTGC | 14784 |
rs243441367 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115679323 | ATCTGCCTGGTGTCC[A/C]CAGAAGACTCAGAGC | 14784 |
rs243466429 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698223 | TACTTCTTCCTCAAT[C/T]ATGTTTTTTTTCACT | 14784 |
rs243509403 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649142 | GGAGCAGGGAAGCGG[A/G]AGGGTATAGGGGACT | 14784 |
rs243549831 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687606 | GTGCACAAGCGTGCA[C/T]ACATGCACACACACA | 14784 |
rs243567772 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662832 | TTGTATTTTATAGCT[A/T]CCGTTCTCCCAGAAA | 14784 |
rs243693842 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701604 | AGAATGAGAATATGA[A/G]AAGTTAAACAAGAAT | 14784 |
rs243841225 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703805 | TCAGCACCTCCAGCA[C/T]CATGCCTGCCTGGAC | 14784 |
rs243880324 | in-del | -/AGACAGAC | | | intron-variant | Grb2 | Mm_Celera | 11:115658694 | CTTATGACTCAACCT[-/AGACAGAC]ACACACACACACACA | 14784 |
rs243921409 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692243 | GGCAGAGGCATAGGA[A/T]TCAGGAGTTCTCCAA | 14784 |
rs243950317 | in-del | -/C | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709958 | TTTCAAAGAGAAGAA[-/C]GCTGGCCCTAAGTAC | 14784 |
rs243964829 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681756 | GGCTGTCCTAGAATT[C/T]ACTATATAGACATGG | 14784 |
rs244012215 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692300 | AGTAAAATCAACTAC[A/T]GCTAGCCAATTACAG | 14784 |
rs244052575 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115705562 | GTCTTTTCAAAGTGA[-/CT]CTGGCCTAAGCCTCT | 14784 |
rs244125890 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664684 | TGTTTGTTTGTTATA[-/T]TTTTTTGAAACAAAG | 14784 |
rs244153069 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115698403 | ACCCTAGAAAGGAAA[A/C]CGTCATCCGGAAGGG | 14784 |
rs244211940 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690078 | AAAAAAAAAAGTAAA[A/G]TAGTAAAATCATTTG | 14784 |
rs244251577 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701338 | CTGACAAATACATAT[A/G]TGTGTGTGATATGCA | 14784 |
rs244285840 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646647 | CTGAGCACACAGGAA[A/G]TCGCTGTGGTGTCAC | 14784 |
rs244312763 | in-del | -/GCTGCT | | | intron-variant | Grb2 | Mm_Celera | 11:115667837 | ACCCCCAGGTTAAGA[-/GCTGCT]GCTCTGGTACATAGC | 14784 |
rs244319785 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702057 | GACGGGGGGTGTGTG[A/T]GAGAGAGAGACAGAG | 14784 |
rs244337769 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668262 | ATGTGTGCTGTCAGG[C/T]CTCAGGACTGGTTTG | 14784 |
rs244374457 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115669073 | AAAACAAAACAAAAC[-/AA]AAAACAAAACAAAAC | 14784 |
rs244386057 | in-del | -/CA | | | intron-variant | Grb2 | Mm_Celera | 11:115649363 | GGCTGGCCTGGAACT[-/CA]CAGAGATCCACCCGT | 14784 |
rs244472196 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649067 | CCCTTGGTCTTGAGA[A/T]GATTATATGCTGCAG | 14784 |
rs244534035 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661380 | AACACTCAGGCATCG[C/T]GGAGCAAGACTGAAC | 14784 |
rs244548523 | snp | A/C | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645136 | ACTATTTAAAAAAAA[A/C]AAACAAACAAACAAA | 14784 |
rs244560487 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115679596 | GAGCCCTAACTACTC[-/A]AAGAGGCTGAAACAA | 14784 |
rs244613388 | in-del | -/AC | | | intron-variant | Grb2 | Mm_Celera | 11:115671428 | ACTATCTCAGTACCA[-/AC]ACACACACACACACA | 14784 |
rs244617559 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694151 | ATCCCCAGGATTCAC[A/G]TGTCAGAAGGAGCAG | 14784 |
rs244623617 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668006 | AATGATCAATTGGTA[A/T]TGTCACTCCATTGCA | 14784 |
rs244623667 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678976 | ATTGCTATAATGAGA[A/G]TGTGCGAGCGTCACA | 14784 |
rs244633831 | in-del | -/CG | | | intron-variant | Grb2 | Mm_Celera | 11:115706785 | ACACGCCCGCGCGCA[-/CG]CGCGCAGGTAAATAC | 14784 |
rs244654052 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115677707 | ATCTGGCTGGTTTTT[A/G]TTAGTTTTATGTTTT | 14784 |
rs244667138 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662875 | ACAGTCTGAAAGTCT[C/T]GGGAGCTTTAGTCTT | 14784 |
rs244674396 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706882 | GGTAGGTAGGTAGGC[C/T]TTAATTCACAAATAT | 14784 |
rs244675107 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668322 | ACATTTCTGTGAGCT[C/G]TCCTCTGACCTGGAC | 14784 |
rs244719022 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667202 | TGTCTAACACACTGA[A/G]AAGGTTTGTTTAAGA | 14784 |
rs244771786 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710058 | TAATCCCAGCACTTG[A/G]GAGGCAAGGCAGGTG | 14784 |
rs244802008 | in-del | -/AGC | | | intron-variant | Grb2 | Mm_Celera | 11:115674288 | GTCTGCCTCTGTTTT[-/AGC]AGCCTGTCAGGTGCA | 14784 |
rs244807457 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671692 | TTGTTTGGTTTTTTT[G/T]GGGGGGTGGCTTTTA | 14784 |
rs244830653 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684154 | CATAACACGCCCCCA[C/T]CACACACACCACACT | 14784 |
rs244880614 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700793 | CCTGGGAATATTCAG[A/G]CAGGGTAGCAAGAGG | 14784 |
rs244959074 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665089 | AGGAGGGTTTTAAAG[G/T]CTAAACAGCAGACAG | 14784 |
rs244977466 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674151 | AAGCACTCCTGGAGA[G/T]ATTTTTAAGCATGTT | 14784 |
rs244997308 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668107 | GAGCTCACTTCAGAT[C/T]TGTCTCCACCATTCA | 14784 |
rs245012471 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673157 | TTCTGGGGCTCAGAA[C/T]CAAGAATAAACTAAT | 14784 |
rs245035739 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666200 | CCAGCCTGGTCTACA[C/T]AGTAAGTTCTAGGAC | 14784 |
rs245036579 | snp | C/G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665589 | TGCTGGGTGTGGTGA[C/G/T]GCACGCCTTTAATGC | 14784 |
rs245057015 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649225 | ATATTTTAAAAAAAA[-/T]TTTATAAAAAGAGAT | 14784 |
rs245085807 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647657 | CAGATGGCAGCACTG[A/G]ACTTCCAGTGCTTCT | 14784 |
rs245090985 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675928 | TCAAGCATCTCTTTA[C/T]CCTGTAAGTCCAGCC | 14784 |
rs245131229 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684587 | GCAAATTTCTGAGTT[C/T]AAGGCCAGCCTGGTC | 14784 |
rs245211260 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694562 | TGTGTCTGTGTGTGT[A/G]TATACAAAATAAATT | 14784 |
rs245228411 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708877 | GTCCTTTCTACCAAA[A/G]CAAAGCAAAGAGGCA | 14784 |
rs245244563 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707690 | GGCTACCCGGCAAAC[G/T]GCACTGCTATAGCTT | 14784 |
rs245254101 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675444 | ACCCATGCTCAGCAC[C/T]TTTGTATTCAAAAGA | 14784 |
rs245289252 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674269 | GGAACAGGAACAAAA[A/G]CCGCGTCTGCCTCTG | 14784 |
rs245306176 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655822 | AATTCCCAACCCCAG[A/G]CCTCCAGCAGCTTCT | 14784 |
rs245374730 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661854 | TCTGTAGGCAACGGC[A/G]CCTCCGTTCTGTCTT | 14784 |
rs245375888 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115664620 | GACCTTCCTAACTGA[A/C]GGAAAAAAACCCAAA | 14784 |
rs245535935 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655949 | CTACAACCCTGTGTT[C/G]AGGTCAGGCACTCCT | 14784 |
rs245618579 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670691 | CTCTGTAGTCTACAG[C/T]TCTCTCTGAGCACCC | 14784 |
rs245652151 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670007 | TCCACCATACACATA[C/T]TCCCCCTCCTCCTCT | 14784 |
rs245675996 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646473 | TAACAGGTTTGAACA[C/T]ACTCTCAGCATTCCC | 14784 |
rs245680914 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663286 | CACCCAGAGTGATGA[C/T]GACTGACGTCAAGAC | 14784 |
rs245736982 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660444 | GCACTCACATGCATG[A/G]AATAAACATGTGCAG | 14784 |
rs245844566 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650722 | CTCACTCCAGTCAAC[G/T]CCACTTGCTCAGTCC | 14784 |
rs245899568 | in-del | -/TTGTGCC | | | intron-variant | Grb2 | Mm_Celera | 11:115682499 | ACAGTAAGGGTAAAG[-/TTGTGCC]TTGCTTTTGTGAGAC | 14784 |
rs245908543 | in-del | -/TCTT | | | intron-variant | Grb2 | Mm_Celera | 11:115703016 | CTCTCTCTCTCTCTC[-/TCTT]TTTCTGAGACAGGGT | 14784 |
rs245930145 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115707460 | AGTAGATTTTTTTTT[-/A]AAAGGGGGCGGAGGG | 14784 |
rs246046587 | in-del | -/TCTGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115653048 | AAGCCATTTCACAGA[-/TCTGTG]TCTGTGTGTATGCTC | 14784 |
rs246094845 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115695819 | AAAATGTAACCCTGA[A/G]CCATACAAGCAGCAG | 14784 |
rs246192963 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115666289 | AAAAAAAAAGCAAAA[-/C]CTCTCTATTTCTACA | 14784 |
rs246194234 | in-del | -/AAT | | | intron-variant | Grb2 | Mm_Celera | 11:115651305 | CACCTATATACATAA[-/AAT]AATAATGTTTTCATG | 14784 |
rs246271155 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652242 | CATGCTTTATTTATT[C/T]ATTTCAGGTATATGA | 14784 |
rs246277169 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686526 | GTCTAAGATAAGACT[C/T]TTGGGTGTGCCGTGT | 14784 |
rs246319586 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115697163 | TGTTTCAAAAAAAAA[A/C]AAAAAACAAAAAAAC | 14784 |
rs246430837 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691424 | CAAAGGTGGGCAGAT[C/T]TCTGTGAGTTCAAGG | 14784 |
rs246454794 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650380 | TTCTGCAAAAGCAAG[A/G]AGGGAGGCTTGCATT | 14784 |
rs246460680 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654191 | ATACACATACTCACA[C/T]GACATGAAACACTTG | 14784 |
rs246515084 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661907 | TCCAGTTAGCTCTTG[-/C]CAGATGCATTTCAGA | 14784 |
rs246566895 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115664362 | TAGACAAGCTCTGCA[A/C]AATCCACTGTCACAC | 14784 |
rs246580141 | in-del | -/A | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643998 | AAAAAATAAATAAAT[-/A]AAAAAATAAACTGAA | 14784 |
rs246625546 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115658757 | ACACACACACACACA[-/AG]CGCTCAACAGAAGCA | 14784 |
rs246654359 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704548 | TAAGTCACCCCACCT[A/G]ACAGCCTTAATGCTA | 14784 |
rs246723637 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692776 | CAGAGCTTGATTCCC[A/T]GTACAGATGTTGGGT | 14784 |
rs246756573 | in-del | -/TG | | | intron-variant | Grb2 | Mm_Celera | 11:115658737 | ACACACGCACGCACA[-/TG]CGCACACACACACAC | 14784 |
rs246799516 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682637 | GCTGAAGACCACACC[A/T]CACAGGCCGTGGCAC | 14784 |
rs246815739 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115678606 | GGCTGGAAATTAAAA[C/T]CTTCAAGGTCATGGC | 14784 |
rs246816469 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115705672 | CTTAGTCTGACAGGC[A/G]GGGCCTAGTGAATCT | 14784 |
rs246823541 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662226 | AGAATCACTTTTCTG[A/G]GAGCAGGCGTGGATA | 14784 |
rs246888304 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115652017 | CCTACAGTGCCCAGG[A/G]AGCAGCCACACCAGG | 14784 |
rs246953087 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115652572 | AGGTGTGCGCCACCA[A/C]GCCCGGCTCAGTACA | 14784 |
rs246961785 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660480 | TGCTTTCAGTTGCTG[C/T]ACATGTTACACAGGA | 14784 |
rs246999895 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689317 | GCAAGGGGCTGCACT[C/G]ACACAGGCTGTAACC | 14784 |
rs247010719 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115656240 | CCCAATCCTCACCCT[-/C]CCAAATTCTAGGATT | 14784 |
rs247014158 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690698 | CATTTGGTTCAAAGA[A/G]GAAAATGGAGACAAA | 14784 |
rs247016255 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115703058 | GCCCTGGCTGGCCTG[A/G]AACTCACTTTGTAGA | 14784 |
rs247027135 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115698753 | ACCCACTAGGATCCT[A/G]CCACAAAATGCAGTC | 14784 |
rs247048161 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702337 | TATGCCACATACATG[A/G]AAGTATTTCGTTTTC | 14784 |
rs247058386 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115691949 | TTCCTACCCCCCCCC[-/A]AAATAATGTAGGATA | 14784 |
rs247129556 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657980 | ATGTTGGGGTCAGGT[C/T]GCATCTTCCAGAGCC | 14784 |
rs247132971 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689346 | CCGTAATGGTAGCCC[A/G]AGGCCAGGAAGCTCA | 14784 |
rs247165060 | snp | G/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700385 | GACAGTCAGACCCCA[G/T]CTGTATCCTGTTCCC | 14784 |
rs247165074 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688035 | GCTCTGGGGTACAGT[C/T]CATTTTCATCATGGC | 14784 |
rs247231936 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115682163 | GAGCGTGGTGGAGTT[-/C]CAAATGTGAGTGAAG | 14784 |
rs247255050 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658474 | CCCTGAACGCTCACA[A/G]CCCTTATAGATCAAG | 14784 |
rs247257027 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115648255 | CTGGGCTAGCTGGCT[A/C]CAGCTCCACACGATC | 14784 |
rs247263671 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672938 | TACAGTTGTAAGATG[A/T]TCATCTAGTTCCAAC | 14784 |
rs247336689 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649029 | CAGAGGATGGCCTAG[C/T]TGGCTATCAATGGGA | 14784 |
rs247381081 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685960 | AGCAGCTCCAGGACT[A/G]GAAATGTAGCTCATT | 14784 |
rs247410900 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115685058 | TAAGACATGTACTTA[C/T]CATGTGACAAGACTG | 14784 |
rs247419092 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115696135 | TGAGTTACAGCCCCA[A/G]TCTCTTCCTCAGGGC | 14784 |
rs247481907 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675028 | TACAGATGGTCGTGA[G/T]CCACCATGTGGTTGC | 14784 |
rs247511674 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667249 | AGGAAGAAGAAAAGC[C/T]AATCCTAGCTCTCAG | 14784 |
rs247524698 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680322 | CAAAGCCATGGGCTG[C/T]ATCTGGAACCACCCT | 14784 |
rs247550418 | in-del | -/GC | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710169 | ATCTAAAAAATAGGG[-/GC]GGGGGGCTGTCATTT | 14784 |
rs247552313 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666529 | TCTAGAGTAACCCTG[C/T]CTACACCTGGCAGTC | 14784 |
rs247577624 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659507 | TCAAGGCCAGCCTGG[C/T]CTACAGAGTGAGTTC | 14784 |
rs247589709 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115670454 | TCTTCAGAGTTTCTC[A/C]GGAGGAACTCTAGAC | 14784 |
rs247676597 | in-del | -/TAAT | | | intron-variant | Grb2 | Mm_Celera | 11:115686044 | ATACTAATGAATAAG[-/TAAT]TAAATAAATAAATAG | 14784 |
rs247887636 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663310 | TCAAGACAGGCAGGA[C/T]GGAGAAGCTGGGGTT | 14784 |
rs247928217 | in-del | -/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666045 | ATAAATAAATAAATA[-/T]TAAAAAAAAAAAAAA | 14784 |
rs248023049 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115654833 | TCAGTTCCCATCACC[A/C]ACATTGGTGGCTCAC | 14784 |
rs248051418 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675275 | TGCTGGGATTAAAGA[C/T]ATGCGCCACCATGCC | 14784 |
rs248124073 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651406 | TATCCACATGGGGGT[C/T]AGAAGACAACCCTGG | 14784 |
rs248208222 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667549 | CTATTTTATAACTAA[A/T]TTTTTGCTACTGATA | 14784 |
rs248288783 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115657096 | GGGAAACTGGACATC[A/G]GAATAATATTAACCC | 14784 |
rs248472145 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679513 | GCTAGAACAAGGAGT[-/G]GGAAAAAAAGTACAA | 14784 |
rs248479980 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115707300 | CCTGGCTGCCTGATG[A/G]ATACAGTGGACGTTA | 14784 |
rs248505151 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115666493 | CCATTTCCCTGCCCA[-/C]AGTCCCCACTCCCTA | 14784 |
rs248516315 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115678628 | GGTCATGGCTTGGAG[-/A]AGATTAAATTGTATG | 14784 |
rs248546504 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694017 | TTATATACTTCTGAT[-/G]GGAATATAAACAACT | 14784 |
rs248644564 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671046 | ACAACAGAACCACAC[G/T]CAGCCTTTGTAATCC | 14784 |
rs248691082 | in-del | -/AAAAACA | | | intron-variant | Grb2 | Mm_Celera | 11:115688691 | AATTAAAACAAAAAC[-/AAAAACA]AAAAAGGGTTGAGGA | 14784 |
rs248703091 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651680 | AGAGGAAGCCACCAA[A/G]GCTGGTGTCTGCTTT | 14784 |
rs248908412 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656257 | CAAATTCTAGGATTA[C/T]AGGTGTAGACCGCCA | 14784 |
rs248948056 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693472 | CTCACAACCATCTGT[A/G]ATGGGTTCTGATGCC | 14784 |
rs248961084 | snp | G/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700647 | AGATTATTTATAGTG[G/T]CACCTCTCTTGGATA | 14784 |
rs249050066 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115689923 | TAAACATTGTAAAAC[A/C]GCCGGGCGTGGTGGC | 14784 |
rs249050803 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684526 | TTGATTGAGCCGGGT[A/G]TGATGGCGCATGCCT | 14784 |
rs249065732 | in-del | -/CACG | | | intron-variant | Grb2 | Mm_Celera | 11:115706773 | ACACACACACACACA[-/CACG]CGCCCGCGCGCACGC | 14784 |
rs249079582 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115694340 | TCATTTACACACCAT[A/G]TAAACACACGAAGAC | 14784 |
rs249088816 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669902 | GAGCTTGTGTACCTG[C/T]CAGGGCCCACAGCAA | 14784 |
rs249225403 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649515 | AGGAGTGGAGATGCG[C/T]ACGTGGTCACCGTAA | 14784 |
rs249227064 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679621 | AAACAAAAAGGCCAG[G/T]TCAAGGTCAGCCTGG | 14784 |
rs249249633 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670364 | AAAAAAACAGACACC[C/T]AAGGTTTGCAAGACC | 14784 |
rs249257470 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115683234 | ACTCAAGTCCTCTGC[-/A]AAAAAAACACAACCA | 14784 |
rs249325743 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653558 | CCAAGTGTATCATTA[-/G]GGGGCTGGCAGTCTA | 14784 |
rs249328585 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687473 | AGGTGTGCTCTGACG[C/T]CCATCCATACCCTTG | 14784 |
rs249363703 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660793 | CTTTGAACTCAAGAT[C/T]CTGTTGTTGTCTGTG | 14784 |
rs249378790 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648319 | CAGATCCTCTTGTTT[C/T]GTGGTAGTTACCAAC | 14784 |
rs249381240 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667968 | CTGTGACTGCATCAA[A/G]CAGCCAACAGCTCTT | 14784 |
rs249386944 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677118 | AAAATGTATACTGGT[C/T]ATGGTGGTGCACACT | 14784 |
rs249387060 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688342 | TTAACACCCTAGACA[C/T]TCAGGGTGTTGCTGT | 14784 |
rs249472715 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677293 | TGTTAGGCTGTTCCA[C/T]CCTCAAGGCTCTGTG | 14784 |
rs249517986 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660888 | GTGATAACGAACTTA[A/G]AAAAACTGGCTAAGA | 14784 |
rs249519637 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687707 | TGTAGACCAAGCTGG[C/T]CCTGAATTTAAGAGA | 14784 |
rs249614947 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674884 | GGGCAAAGGGTACCG[C/T]AATGTTCAGCCATAC | 14784 |
rs249638839 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115677028 | ACAGTGCACCCCAGA[A/C]AATCTTCCTAGTGCT | 14784 |
rs249668476 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658303 | TTTTATCCAAAAAAT[G/T]AAATATACCAGCAAA | 14784 |
rs249675259 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675760 | GAGTTTGTCCTATGA[A/G]GAGTGTTGTGACGGG | 14784 |
rs249687866 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646356 | CATCAGATCTCATTA[C/T]AGATGGTTGTGAGCC | 14784 |
rs249736076 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705174 | TGTGGTTGCTGGGAA[C/T]TGAACTCAGGATCTC | 14784 |
rs249757838 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658973 | TTCCTCTACTGGTGC[C/T]GAACTGGGTATGTTG | 14784 |
rs249763795 | in-del | -/ATGT | | | intron-variant | Grb2 | Mm_Celera | 11:115679985 | GCTGACCAAGACACA[-/ATGT]ATGTACGCTACCTGT | 14784 |
rs249851765 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115706039 | CCAACTTGGACAATA[C/T]ATCAAGACCTTGTCT | 14784 |
rs249883177 | in-del | -/AAC | | | intron-variant | Grb2 | Mm_Celera | 11:115670631 | GCAGGGCCAGCGGAG[-/AAC]ACCACACTGTACTTG | 14784 |
rs249888541 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650135 | TCATAATTCAAGGCA[A/G]CAACACAGGCCACTC | 14784 |
rs249901995 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649304 | ATCGGTCAGACAGGG[C/T]AAAGCCATTCTTTTT | 14784 |
rs249940035 | in-del | -/ATCTTCAGTGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115689571 | TTCCAAAACTGACAA[-/ATCTTCAGTGTG]GTCTTCTCTGATAAC | 14784 |
rs250010710 | in-del | -/ATCTGCTGCAG | | | intron-variant | Grb2 | Mm_Celera | 11:115660600 | GCAGTCACCACCTCC[-/ATCTGCTGCAG]GTTTGCTCAGCAGAA | 14784 |
rs250049267 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647169 | CAGCCCACTTGTGAG[C/G]CTACAGCTTTATCTG | 14784 |
rs250082589 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662250 | TGGATAGGTGGAAGA[-/T]TTTTGAGACAGAGTC | 14784 |
rs250146358 | snp | A/G | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644391 | GGGGAGACTCTACCC[A/G]CAAGAGTCTAGCAGC | 14784 |
rs250182571 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673823 | CCCAAGTGATGGGAT[C/T]AACGCATGTGCCGCC | 14784 |
rs250212881 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703386 | TGTCTGTCTCAGGTT[C/T]TGATTGACATAAAAT | 14784 |
rs250277644 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115691461 | TGGTCTACAGAGGAA[A/G]TTCCAGCACAGCCAA | 14784 |
rs250300429 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115645972 | GCAAGAGAGAGCAGG[A/G]AAGCGGTGTTTCTCA | 14784 |
rs250307855 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679792 | GCCACTCCCTGACAA[A/T]GCACCCAAGCTCCAA | 14784 |
rs250309413 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644737 | CTTCAAGCCCATCTG[C/T]ATGTAGGCCTATAAG | 14784 |
rs250367626 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659331 | AACATTTTTGAAGCT[C/T]TTTTTGTTTGTTTTT | 14784 |
rs250513327 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649726 | AGCCTTACAATCCAG[C/T]CAAAGGCAGCAGCTT | 14784 |
rs250534726 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671134 | TCACTTTTCATCATT[A/G]AGTTTCTAGCCTACA | 14784 |
rs250589285 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667418 | AGACAAGGACAGAGC[A/G]GCCCAATGAGTGGAG | 14784 |
rs250653861 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115688007 | ACAACATTTAGCTGG[A/G]GCTGGCTTACAGGCT | 14784 |
rs250690344 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115698429 | AAGGGCGAGCTGCCC[A/G]GCCAGTTGAGTAAAT | 14784 |
rs250740128 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115676120 | AGACAGACACACACA[C/G]AGGCTCAGACATTTA | 14784 |
rs250754731 | in-del | -/GGGCGGGGAGTGGG | | | intron-variant | Grb2 | Mm_Celera | 11:115671472 | AACACAAACACACAC[-/GGGCGGGGAGTGGG]GGGAGACACTCCTAC | 14784 |
rs250827821 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115693717 | ATGGACCAATGAAAC[A/G]AGCAGATACCTCTCA | 14784 |
rs250852091 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695618 | AAATAAATATAAATG[C/T]CAAATTAACAATCTA | 14784 |
rs250884759 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115708144 | AGCCGGACGGCCGCC[A/G]CACCAGACCTCCCCG | 14784 |
rs250947554 | in-del | -/GCCCCCGC | | | intron-variant | Grb2 | Mm_Celera | 11:115707261 | ACCACCCGCCCCCGC[-/GCCCCCGC]CCCCCTGGCTCCCAA | 14784 |
rs251003635 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705126 | CACCAGAAGAGGGCA[G/T]CAGATTTCAGTACAG | 14784 |
rs251009954 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685420 | CCTCATATACCCAGG[A/G]GTCTGAAGTAGGAGG | 14784 |
rs251013056 | in-del | -/TTG | | | intron-variant | Grb2 | Mm_Celera | 11:115654953 | AATTTACTGTTTGTT[-/TTG]TTGTTTTCAACACAG | 14784 |
rs251033237 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709164 | GGAGAGACCTCTCAG[A/G]TCAAAAACTGCTTGC | 14784 |
rs251149593 | in-del | -/GAGTGAGTGAGT | | | intron-variant | Grb2 | Mm_Celera | 11:115672406 | CGCGGTACACCTGCA[-/GAGTGAGTGAGT]GAGTGAGTGAGTGGC | 14784 |
rs251149631 | in-del | -/TAAGA | | | intron-variant | Grb2 | Mm_Celera | 11:115686514 | GTATCACAATAAGTC[-/TAAGA]TAAGACTTTTGGGTG | 14784 |
rs251150663 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692786 | TTCCCTGTACAGATG[C/T]TGGGTGGTTCACAGC | 14784 |
rs251152547 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115706237 | TCAGTGCTCTTAACC[A/G]ATGAGCCATCTCTCC | 14784 |
rs251204303 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693836 | AAACTACAGAGCTCC[C/T]AGCTCACAGCTGTAG | 14784 |
rs251267595 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679937 | GAAAGCACAGCATAC[G/T]TTCCTCTGTGGCAGT | 14784 |
rs251302310 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690547 | GAAATGCCCGTGCTC[A/G]AGAACGAGGAGGTTT | 14784 |
rs251326605 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682530 | TGAGACAGTTCTGGG[A/G]TAAAAACACAGTAAT | 14784 |
rs251350110 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673413 | CAGCGACCAACACTC[A/T]CTTCTAGCTTATTGT | 14784 |
rs251384322 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683749 | GATCTCTGAGTTCAA[A/G]ACCAGCCTGGTCTAC | 14784 |
rs251470691 | in-del | -/CGTA | | | intron-variant | Grb2 | Mm_Celera | 11:115689021 | AGACTCCATGCCGGG[-/CGTA]CGTGGTGGCGCACGC | 14784 |
rs251475435 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650589 | AAAAAAAATTTTTTT[A/T]AATTATTATTTATTT | 14784 |
rs251481476 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665490 | GGCAGAGGACAGTAG[A/T]CGGAGGGGGCCGCAC | 14784 |
rs251522295 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663711 | GCCTTTTGTGTTGCA[A/T]CAGGCCAGCCCTGGG | 14784 |
rs251545276 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672183 | ACCATTCATATTTGT[C/T]ATATTTATCATATAT | 14784 |
rs251552369 | in-del | -/ACAC | | | intron-variant | Grb2 | Mm_Celera | 11:115672211 | TATGTGTGTGTCTAT[-/ACAC]ACACACATACATATA | 14784 |
rs251560645 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115706977 | CAATAGTTAACCTCA[C/G]TAAAACCTTAAAAAG | 14784 |
rs251577643 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115671112 | GTCTATTTTTAGGAG[A/C]CTTCGTTCACTTTTC | 14784 |
rs251627882 | in-del | -/ACAC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684274 | CTACCACACACACAT[-/ACAC]ACACACACACACACA | 14784 |
rs251675261 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115705340 | CAACCCAGCTAGGAG[-/C]CCACCAAAGTCCAAC | 14784 |
rs251729338 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115678492 | TGAGCCAGAACAGTT[G/T]AGTTGAACCAGCCAG | 14784 |
rs251758122 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668950 | CCAGCAACCACATGG[C/T]GGCTCACAACCATCT | 14784 |
rs251779576 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661438 | TTGCTCAGCAGGGAG[C/T]GGCAGCACTTGAGAA | 14784 |
rs251801892 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668191 | TCAACAGCCAGGAGC[A/G]TGTCAAGTGCTGTAG | 14784 |
rs251836540 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667511 | GCTGTGCTGGGCACC[A/T]ACCATAAGATTATTT | 14784 |
rs251887757 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668080 | ACCATCTGCAGGCCA[A/G]GCTGGATGAAGGAGC | 14784 |
rs251889305 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662687 | CTTGGGGGCTTCCTG[A/G]ACAGTGAAGATGCCA | 14784 |
rs252023811 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656784 | TGTCCCCTCAAAAGT[A/T]TCCTTCTGTTAAAGC | 14784 |
rs252271180 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648757 | CCCTGAGCTGTTTTA[C/T]TGCTACTTGGAGTAG | 14784 |
rs252333323 | snp | A/G | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644244 | AATCACATGGCCCAG[A/G]TGTGACTCCAGAGAT | 14784 |
rs252343509 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115653856 | CCAGCTTCAAATAGC[A/C]CAGTCTACCGTGCTG | 14784 |
rs252366963 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668742 | AGACCTAATCACACA[C/T]AAAGATGGGAGTCAA | 14784 |
rs252525937 | in-del | -/TTC | | | intron-variant | Grb2 | Mm_Celera | 11:115672833 | TTTTTTTTTTTTTTT[-/TTC]TTTTTGCTTTTTTGA | 14784 |
rs252532418 | in-del | -/ACACACACAC | | | intron-variant | Grb2 | Mm_Celera | 11:115706746 | GGGCACCAGGCATGT[-/ACACACACAC]ACACACACACACACA | 14784 |
rs252622710 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115656017 | CAAGCAACAGAGGGC[-/AG]AGAGTGGAAGGCTAG | 14784 |
rs252639664 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692418 | TTCACATTTTACAGA[A/T]GAGATAACCAAAATG | 14784 |
rs252687892 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660890 | GATAACGAACTTAGA[A/G]AAACTGGCTAAGAAA | 14784 |
rs252711314 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682324 | ACTTGATGAGCCAGG[C/T]AACTAAGCACTAACA | 14784 |
rs252737408 | snp | A/C | | | intron-variant, upstream-variant-2KB | Grb2 | Mm_Celera | 11:115699756 | CCTTCCCGTCCCTCG[A/C]CACCAGCTGCTGCCC | 14784 |
rs252798914 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650853 | TGAACTCAGGACCTT[C/T]AGAAGAGCAGTAAGT | 14784 |
rs252845755 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689066 | CTTGGGAGGCAGAGG[C/T]AGGCAGATCTCTGAG | 14784 |
rs252845832 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700917 | ACGGTCACCCCTTAG[C/T]TAGTCTATGCGGTGC | 14784 |
rs252861549 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667384 | GCAGGAACAAAATGA[A/T]GTAGCCAATAGCAGA | 14784 |
rs252888919 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689751 | CACGCTAAATGCGTT[G/T]TCCTGAAAAGTCCTA | 14784 |
rs252946735 | in-del | -/CGTGG | | | intron-variant | Grb2 | Mm_Celera | 11:115676878 | GGCCGTCTGCTGTGC[-/CGTGG]CGTCTCTGCCTAGAA | 14784 |
rs252952810 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646357 | ATCAGATCTCATTAC[A/G]GATGGTTGTGAGCCA | 14784 |
rs252962989 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702565 | CTATCCTGGAACTCA[C/T]TCGGTAGACCAGGCT | 14784 |
rs252978529 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115663049 | GCATTCAGGAGGCAG[-/A]AAAAGGTGGATCACT | 14784 |
rs253048303 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115703506 | GTCTTCATCCAGTTC[C/G]TGTAAACCAACACAA | 14784 |
rs253092643 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679224 | ATAAAGTCAACATTT[A/T]TATGAGAAAATATCA | 14784 |
rs253109482 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694813 | AAAATATGCTCCCAG[C/T]ACATTACATACACGC | 14784 |
rs253109507 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683939 | ACCATGGAAAAGCTG[C/G]GTATGGCTGTGTGTG | 14784 |
rs253129126 | in-del | -/GAGGGA | | | intron-variant | Grb2 | Mm_Celera | 11:115678356 | GAAAGAGGAAAGAGT[-/GAGGGA]GAGGGAGAGGGAGAG | 14784 |
rs253166691 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115684896 | AAGTAACGAGCTGTG[A/G]ATGGACAACTGTCCT | 14784 |
rs253169870 | in-del | -/TGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115667909 | TACACACAGTCTTGC[-/TGTG]TGTGATAGAGCCACT | 14784 |
rs253283934 | in-del | -/TC | | | intron-variant | Grb2 | Mm_Celera | 11:115689888 | TCACCTTCCTTACAT[-/TC]TCCAATTAAATTATC | 14784 |
rs253344260 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115696416 | CCCTATGTCAATCAA[A/G]GTTTAAGGATCCATG | 14784 |
rs253348087 | in-del | -/CGA | | | intron-variant | Grb2 | Mm_Celera | 11:115686585 | CCAAATACACTTCTC[-/CGA]CGAGACAATTTCAAG | 14784 |
rs253404094 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698013 | CCCACATTCCTGTAA[C/T]TCACTCCAATAAAAC | 14784 |
rs253450521 | in-del | -/ACTT | | | intron-variant | Grb2 | Mm_Celera | 11:115664086 | TTACAAAGCGTTTCC[-/ACTT]ACTTAAGTAACTGTC | 14784 |
rs253466144 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115676338 | ATGACATTGCAAAGA[A/C]TCTCCCTCCAACGGC | 14784 |
rs253494745 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655677 | AGGCTTTTTTCTCAA[C/T]ACCTAGAATTAAACC | 14784 |
rs253498733 | in-del | -/CCCATTA | | | intron-variant | Grb2 | Mm_Celera | 11:115650553 | CTCGAAAAACCAAAG[-/CCCATTA]CCTTATGGTATCTGA | 14784 |
rs253601187 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655723 | GAAGGAAGGCTGTAA[C/T]AGATCAGTGTTTTCT | 14784 |
rs253614706 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681002 | TGGGTAAGAGCACTG[A/G]CTGCTCTTCCGAAGG | 14784 |
rs253667873 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665438 | AACACTGCTTCTGCT[C/G]TGAGGTTAACATCTG | 14784 |
rs253678943 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670725 | CACGGGGAAGTGTAG[A/G]AAACTAGCACTTTGG | 14784 |
rs253749534 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665852 | ACTATATAGTAAGCT[G/T]TCAAAAAAAACCAAC | 14784 |
rs253773310 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650690 | TTTAGGACCTCTGCC[C/T]ACCCCGGTTGCCCCC | 14784 |
rs253823276 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649692 | TCCACAGGAAAAGAT[A/G]TGTTAACATCTTCCC | 14784 |
rs253839282 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115658811 | AAAAGGAGGAAGAGC[A/C]AGTTTCAGTGAAGGG | 14784 |
rs253871047 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658155 | GCCATTTCTCTAGCC[C/T]CACAAATTAACTTTT | 14784 |
rs253931711 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709500 | GAACTGAGTACTGGA[A/G]GGCGAGTAGGAGTTC | 14784 |
rs253949473 | in-del | -/AAAA | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643982 | AGAAACCCTGCCTTG[-/AAAA]AAATAAATAAATAAA | 14784 |
rs253969462 | snp | C/T | | | utr-variant-5-prime | Grb2 | Mm_Celera | 11:115708396 | CCCCTGCACTCACCG[C/T]GACGCGCCGTCCACT | 14784 |
rs253983323 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115704808 | CTAATAGACAGAGCC[-/AAA]AAAAAAAAAAATGAG | 14784 |
rs253998269 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668568 | GTCCTCCCCTTGCAA[A/G]CCCAATAGCTAGAGT | 14784 |
rs254028634 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665056 | AAAATCCATTGATTT[A/T]CAGTGAGAAACTCAA | 14784 |
rs254028955 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661880 | GTCTTGTGCTGTGGC[G/T]TCCTTGTTCTTATCC | 14784 |
rs254113473 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662718 | TCTTCTATGGGCATG[A/T]GTAAGCTGTGACCAG | 14784 |
rs254246307 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653947 | GCCGCTTAAGTGCTC[C/T]AGCACTGAGCTAACA | 14784 |
rs254272320 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653284 | GTCGGGTTTCTTTCA[A/G]TGATGATAGTTATGT | 14784 |
rs254297213 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663231 | TCACTAGAAGATTCA[C/T]GAGGAGAGTGGAGAG | 14784 |
rs254386482 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666425 | AGGTGTCTGTGTACA[A/G]TGCCATCTCCTGCCG | 14784 |
rs254401781 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115702640 | GGGATTAAAGGTGTG[A/C]GCCACCACACCCAGC | 14784 |
rs254579830 | in-del | -/AA | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645064 | TGTCTTTAACTTATT[-/AA]AAAAAAAAAAATGGT | 14784 |
rs254632735 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692372 | AGATCTTTTAAACTT[A/T]ATGGTGGCCCTAGGA | 14784 |
rs254658698 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115697623 | GAATGAAACATCCCA[C/T]CCAGCACAGAAGCTC | 14784 |
rs254661533 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687857 | AATGCACAATGTTTG[A/T]TACATGCTTGTAGTC | 14784 |
rs254687314 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704448 | ACAGCAAGTTTTAAT[A/G]AAGAGTGGTAAAGTA | 14784 |
rs254690694 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709922 | ACTCCAGCAGTTTGC[A/G]ATTTAGATAGAGCTA | 14784 |
rs254762045 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678730 | TTCCATTCACACCAC[C/G]GTGATGACTTGTTCA | 14784 |
rs254792821 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689155 | ACTATGTAGGGTAGG[A/G]GTGGGGGAAGACTCC | 14784 |
rs254817032 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704625 | GCTGGTGGAGTGCTT[A/G]CCTAGCATGCACAAA | 14784 |
rs254846816 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115658669 | GTTGTCTAGCCTCTG[C/T]ACTGCGTAGACTTAT | 14784 |
rs254967210 | in-del | -/AG | | | intron-variant | Grb2 | Mm_Celera | 11:115683635 | GTCCCAGCTTAGCCT[-/AG]AGAGTCAGAACCCAA | 14784 |
rs254971138 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115677917 | TCCAGCAACATGGCT[A/G]CTCTGGCAAGCGATG | 14784 |
rs255030060 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683182 | GGGAACTGGAGTTAC[A/G]GGCTGTTATGGGCCT | 14784 |
rs255131761 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115674054 | CAGATTTCACCCCTT[A/C]GTGGAGAAATCAACC | 14784 |
rs255160561 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115697741 | AAAAAGAAGCTCAAC[A/G]TCTGCTTCTCAGAGA | 14784 |
rs255166041 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115672989 | GAGTCCTGCCAGTTC[C/G]TTACCAGCTGCCTGG | 14784 |
rs255226128 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659603 | AAATAAACCACCATT[A/T]AAATTTTTAATCTAT | 14784 |
rs255279757 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665582 | CAGAAACTGCTGGGT[A/G]TGGTGATGCACGCCT | 14784 |
rs255302862 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653129 | ACAGCAGATAGCATC[C/T]GGTCGTCGATACTCT | 14784 |
rs255363398 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661058 | AGCTTCCCAGTCATG[A/G]CAGGCCTTTCATGAA | 14784 |
rs255373465 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666204 | CCTGGTCTACATAGT[A/G]AGTTCTAGGACAGCC | 14784 |
rs255383859 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692197 | ATCCTGAATCTGAGG[C/T]AAGAGCAGACCAGCA | 14784 |
rs255408703 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707607 | AAAAAACAACAACAA[C/T]AAAACCCAGTTTCTC | 14784 |
rs255412800 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668180 | AGGGAAATAGATCAA[C/T]AGCCAGGAGCGTGTC | 14784 |
rs255437210 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681432 | GATGTGGTTAATAAT[C/T]AATAATGGAAAGTAT | 14784 |
rs255438991 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692675 | AGTAAGCACAGACTA[C/T]GGTGTACTTTAGTCT | 14784 |
rs255487221 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694461 | GAGGTCTCTGATTAG[C/T]GTTCACCACAGCACT | 14784 |
rs255548937 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666723 | CTGTTCCTTAGGCTG[A/G]CCTTGAACTCCAAGA | 14784 |
rs255594311 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675553 | GGAGAGCAGCCAGTG[C/G]TCTTAAGGACCAAGC | 14784 |
rs255642917 | in-del | -/AGCTGAGGCTTCG | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644904 | AGCTCACAAAGTAAA[-/AGCTGAGGCTTCG]AGACCTCCGGCCCAT | 14784 |
rs255685707 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646445 | CCCGCTGAGCCATCT[C/T]TCCAGCCCCTCTTAA | 14784 |
rs255691880 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666470 | CATCTGTGGGCTGGA[A/T]ATTCTACCCCATTTC | 14784 |
rs255703129 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115694877 | AACAAAGACCGGTAC[-/A]AAAAAAAGGTCTGTT | 14784 |
rs255746331 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645092 | GGTACAAATACCATT[C/T]ATGAACACCCTTGAA | 14784 |
rs255768263 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115676129 | CACACACAGGCTCAG[A/C]CATTTACAATCACCC | 14784 |
rs255777412 | in-del | -/TTTG | | | intron-variant | Grb2 | Mm_Celera | 11:115694900 | GGTCTGTTTGTTTGT[-/TTTG]TTTGTTTGTTTGGGA | 14784 |
rs255863418 | in-del | -/TTTT | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644130 | TAAGTACATAGTTGG[-/TTTT]TTTTTTTTTTTTATT | 14784 |
rs255969146 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691212 | TATCAACTGTCCCCT[C/T]CCCCGGGAGAGTCAG | 14784 |
rs255991739 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662847 | ACCGTTCTCCCAGAA[A/T]CAGTCTCCATTAACA | 14784 |
rs256018801 | in-del | -/CGCCCCCG | | | intron-variant | Grb2 | GRCm38.p3 | 11:115707252 | ACCAACACCACCACC[-/CGCCCCCG]CGCCCCCGCCCCCCT | 14784 |
rs256086648 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647536 | CACCACCAACGCCCC[A/G]GCTACCGAGGAATTT | 14784 |
rs256106768 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703812 | CTCCAGCATCATGCC[C/T]GCCTGGACACTGCCA | 14784 |
rs256133706 | in-del | -/CAGCCAGGGCTACAC | | | intron-variant | Grb2 | Mm_Celera | 11:115678196 | GAGTGAGTTCCAGGA[-/CAGCCAGGGCTACAC]AAAGAAAAGAAAAGA | 14784 |
rs256141558 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657715 | TTCTGAGTTCGAGGC[C/T]AGCCTGGTCTACAGA | 14784 |
rs256162944 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648566 | GCTGTGTTATTAGCC[A/T]GGGTCTCATGTAGCC | 14784 |
rs256168083 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680807 | GCTGGGTGCTCTTCC[C/T]GAGGTCCAGAGTTCA | 14784 |
rs256185077 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694349 | CACCATGTAAACACA[C/T]GAAGACAACGAAAAA | 14784 |
rs256273469 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692249 | GGCATAGGAATCAGG[A/G]GTTCTCCAACACTGC | 14784 |
rs256339939 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115708781 | CGGCTCCGCCCCTGG[A/G]CCGTTGTAACCCTCT | 14784 |
rs256363879 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115675280 | GGATTAAAGACATGC[A/G]CCACCATGCCCGGCT | 14784 |
rs256365603 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115686378 | AGCTGGCACTTTCAC[A/G]TAGAGTCCTGTCCTA | 14784 |
rs256397756 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685367 | GTGCCACTAATCTCA[A/G]CTTTGAAAATAACTT | 14784 |
rs256457962 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660843 | TTTTTAAGTCTAATT[C/T]ACAACACTCTGGTCA | 14784 |
rs256476607 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701109 | TGCATCTGGGCACCA[C/T]GTGCATGCCTGGTGC | 14784 |
rs256506128 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652306 | AGGGAATTGGATACC[A/T]TTGCAGATGGTTGTG | 14784 |
rs256524521 | snp | C/T | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643651 | AGCTTTCCAGCCCAG[C/T]TCTGGGTTCTTCTGA | 14784 |
rs256535405 | snp | A/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709804 | CCTCTGCTACAATAA[A/T]GAGTCCACTAAAATA | 14784 |
rs256756950 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652382 | AGCAGTCGGTGCTCT[C/T]ACCTGCTGAGCCATT | 14784 |
rs256775242 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680681 | TAAAATAAAATGCTG[A/T]CACTATTTTGGATCA | 14784 |
rs256808158 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115702831 | CCCCTGGCCGTATCC[C/G]CTCAGGTGCTACGAT | 14784 |
rs256852495 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115696225 | AGCTTGCAGGAACAG[C/T]CCTTTCACTTAAAGC | 14784 |
rs256889975 | in-del | -/ACC | | | intron-variant | Grb2 | Mm_Celera | 11:115688264 | GCCAAGTATATACAA[-/ACC]ACCACCACCACAACA | 14784 |
rs256985247 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704099 | CAAATCCTAGCAACA[A/G]CTCAAATGGGAAAAA | 14784 |
rs256992573 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680423 | ATTTTAGACCTTTGG[-/T]TTTTTTTTTTTTTTA | 14784 |
rs257008483 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686064 | TAAATAAATAGCAGT[C/T]CCACCAAAGCATCTA | 14784 |
rs257067556 | in-del | -/TGCAATGCT | | | intron-variant | Grb2 | Mm_Celera | 11:115680077 | TGGCACCACAGACCA[-/TGCAATGCT]AGTCACACCAGGAAG | 14784 |
rs257082887 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115680190 | CGAGAAACATGGGGG[-/A]AAAAATCCTTCCCTT | 14784 |
rs257085143 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647877 | AAGCAAAACCAAGCA[C/T]CCAGCGACTTCATTG | 14784 |
rs257090272 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651794 | GGCTTAATAAACAAC[G/T]ACCCTGCAAAGTATT | 14784 |
rs257100986 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115657897 | CAAATGGGGAGGGGC[A/G]GCAAGAGTGCTCATC | 14784 |
rs257123860 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115680784 | GAGAGAAGGCTCAGC[-/G]GTTAAGAGCTGGGTG | 14784 |
rs257162046 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115660396 | AATGGGGATCCAAAA[-/CT]CTCTTCTGGTGTGTC | 14784 |
rs257207643 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664622 | CCTTCCTAACTGAAG[A/G]AAAAAAACCCAAAAC | 14784 |
rs257330570 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665798 | GTACTTGAGAGGCAG[C/T]AGAGTAAGTGGATCT | 14784 |
rs257331617 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654719 | TCAGTTCATGGGATG[A/G]GAGGGGGGGTAAAGA | 14784 |
rs257382346 | in-del | -/AAC | | | intron-variant | Grb2 | Mm_Celera | 11:115707596 | AAAACAAAACAAAAA[-/AAC]AACAACAACAAAACC | 14784 |
rs257385056 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669569 | AAATCCTAAAGTTTT[A/T]AAAATGAGAAATTGA | 14784 |
rs257387517 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115649374 | AACTCACAGAGATCC[-/A]CCCGTCTTTGTCTCT | 14784 |
rs257469021 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647738 | TTCCCCTATAGACAC[A/G]TATAGTCTGATAAAG | 14784 |
rs257515981 | snp | A/G | | | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115645221 | GACTCTCAGGAGACC[A/G]GGGAGGACAGTGGGC | 14784 |
rs257567681 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670430 | GAAAATTCAGACTGT[C/G]ACAACCCTTCTTCAG | 14784 |
rs257593642 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115662208 | ACTAGTTGACAAAAA[A/C]CAAGAATCACTTTTC | 14784 |
rs257602737 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683174 | TAAGCTCTGGGAACT[-/G]GAGTTACGGGCTGTT | 14784 |
rs257615972 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115702181 | AGCTACAGAGAGAAA[-/C]CCCGTCTCGAAAAAC | 14784 |
rs257647924 | in-del | -/CGCGCACACACACACA | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709316 | GCGCGCGCGCGCGCG[-/CGCGCACACACACACA]CACACACACACACAC | 14784 |
rs257663458 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115671373 | AGTTTCTAGAGGATC[A/G]CCACCCCAAGTTCAA | 14784 |
rs257684041 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115647090 | GCTGATGACTAGTTA[C/T]AGGAGTAACACAGTG | 14784 |
rs257692152 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115683468 | AGTACTAAGTTTGAG[A/G]CACTCATTGTTGCCT | 14784 |
rs257722652 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115663727 | AGGCCAGCCCTGGGC[-/CT]CTCTTTAACAGCTGG | 14784 |
rs257749878 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693411 | GTTAAGAGCACTGAT[C/T]CTTCTTCTGAAGTCC | 14784 |
rs257780155 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661807 | CTCTCCAAATGAACC[C/G]TTAGTTCAGGCAAAC | 14784 |
rs257857445 | in-del | -/TG | | | intron-variant | Grb2 | Mm_Celera | 11:115684947 | TGACATAAGCTCTCC[-/TG]TGTGTGTGTGTATGC | 14784 |
rs257912139 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115659734 | AGGAATACTTAGTAC[A/C]GTGCCATCTAGAGAT | 14784 |
rs257948791 | snp | C/G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659215 | GCATGCACACACACA[C/G/T]ACATACACACATACA | 14784 |
rs257958859 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115705291 | TATTGTTGGGTTCCT[A/G]CTTCTTGTGGAGAGA | 14784 |
rs258005633 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650308 | AAAGCCATTTCATAA[C/T]AGGAGTGCAGGGAAA | 14784 |
rs258013207 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666992 | AAAGCAAGAAGCACT[A/G]TATCCTTGGGGTATT | 14784 |
rs258013262 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658430 | AGAGACAGAGAGAGA[C/G]AGACATAGAGAAAGC | 14784 |
rs258074140 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677871 | TTTCTGCTTTCCTTT[C/T]CCCAGGAGTCACTGT | 14784 |
rs258139189 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667604 | AATGGTGGCACAGCC[-/T]TTTAATCCCAGCACT | 14784 |
rs258167010 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698494 | GGAGCAGGGCTCAAT[A/T]CGCTGCAACTGGGAC | 14784 |
rs258210036 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115688632 | ATAGTGAAACCCTCA[C/T]TGAAACAAACAACAC | 14784 |
rs258289776 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701447 | AAGGGCTTACTCAGT[A/G]TAAGTGGTAACAGAT | 14784 |
rs258317947 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115664534 | TGCTCCTCTGCCCAG[-/CT]GCCAAGCAAGGGCAA | 14784 |
rs258445742 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675506 | CACAGTGAGCTGCCA[C/T]GTGGGTACTGGTATC | 14784 |
rs258485561 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115685578 | AAAACAAAAGGACAT[C/T]CTGCTGGTGAAGGAA | 14784 |
rs258525570 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647042 | GAGAGAATGCAGACC[A/G]TCCCAGGAGCCTCCC | 14784 |
rs258678260 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677151 | AATCCCAGCACTTAA[A/T]AGACTATGACAGGAA | 14784 |
rs258680178 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667232 | AAGCTACAATGGCAA[A/T]GAGGAAGAAGAAAAG | 14784 |
rs258716969 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115676231 | TATACATAAACACAT[G/T]TGTTTGTATGTATAC | 14784 |
rs258779416 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680250 | GTAAGCAACAGAGAT[C/T]ACATGAGAACAGATT | 14784 |
rs258815634 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691071 | TAACTCTGAAATAAT[C/T]CCTTACTGTTATCCA | 14784 |
rs258856631 | in-del | -/AGCATTTTTCAGT | | | intron-variant | Grb2 | GRCm38.p3 | 11:115683430 | CCCCCCAAACAAGCA[-/AGCATTTTTCAGT]AGCATTTTTCAGTAC | 14784 |
rs258897767 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115681937 | CCACTCTCCATGCAT[A/G]CATGCTGAGAGGGTG | 14784 |
rs258916105 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115707875 | CCCTCAAGTCCTTCT[-/A]AAAAGAGAAGCGCCC | 14784 |
rs259039714 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115697350 | GAAGCCAGCAACAGC[A/G]ACTGGTGCTCTAAAG | 14784 |
rs259070199 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671640 | TCCAAACCATGGGAA[C/T]AGAGGTGTTTTTGTT | 14784 |
rs259123647 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115671688 | TTGTTTGTTTGGTTT[G/T]TTTGGGGGGGTGGCT | 14784 |
rs259154690 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115687019 | AATCTACACAGACTA[A/G]AGCCATACAAAATGT | 14784 |
rs259177061 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115687780 | GGCCACCTCTGACAC[A/C]ATTACCACCACCTAG | 14784 |
rs259243722 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686727 | TTAACTAAAAAAATC[C/T]GCCCAATGTCTTACA | 14784 |
rs259244724 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115698342 | AGACACAGGCAGCGC[C/T]CACTAAGTTTTTCTT | 14784 |
rs259256828 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669652 | ACACATATGCAGTGT[C/T]TAAAGAATCTAAATT | 14784 |
rs259343956 | in-del | -/CCACCACACACAGTTC | | | intron-variant | Grb2 | Mm_Celera | 11:115671887 | GTAATTTTAAACTCA[-/CCACCACACACAGTTC]TCACCACCTACACAG | 14784 |
rs259368241 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115677080 | TTAGATGAACGAGTT[C/G]ATTTCTCTTGTGATA | 14784 |
rs259391057 | in-del | -/CG | | | intron-variant | Grb2 | Mm_Celera | 11:115658751 | ACGCACACACACACA[-/CG]CACACACGCTCAACA | 14784 |
rs259440874 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115655343 | GCTTAGGGGAACCAT[-/A]AAAATCTGACTTACG | 14784 |
rs259492653 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115692358 | CACACTAATGAGTTA[A/G]ATCTTTTAAACTTAA | 14784 |
rs259528325 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674342 | CTTCTAAACTATGGG[A/T]GCCCTACGCACATCA | 14784 |
rs259565790 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684625 | TGAGTTCTAGGACAA[A/T]CAAGGCTATACAGAG | 14784 |
rs259619440 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115682852 | AAGAGGGGAGTAGTG[C/T]TGTGAGAGCAGGGCA | 14784 |
rs259653851 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682132 | AGCTGAAGGCAAGAA[A/G]TCCTGTAGGCCACTG | 14784 |
rs259654132 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115693048 | TGAAAGTTCATTCTC[A/C]GCACTGGGGTGGAAG | 14784 |
rs259693469 | snp | A/C | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643768 | TACTCTAAGCCTTTA[A/C]TTTCAACATTTGGGA | 14784 |
rs259792010 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665709 | GAGAAACCCTGTCTC[A/G]AAAAAAACAAAAAAG | 14784 |
rs259800677 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115649230 | TTAAAAAAAATTTTA[A/T]AAAAAGAGATGAATT | 14784 |
rs259886186 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663119 | CAAGGGCTACACAGA[-/G]GAAACCCTGTCTCTA | 14784 |
rs259924051 | in-del | -/GTTTTGTTTTG | | | intron-variant | Grb2 | Mm_Celera | 11:115652422 | CAGTACATACTTTTT[-/GTTTTGTTTTG]TTTTTGTTTTTTCAA | 14784 |
rs259967764 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669138 | TGGCACTAAGCTGCA[A/T]CCCTGGCCCTGCACA | 14784 |
rs260006377 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663088 | GGCCAGCCTGGTCTA[C/T]AGAATGAGTTTCAGG | 14784 |
rs260046491 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664821 | GCCCGGCAAACACAA[A/G]GTTTTTGTCCTATGT | 14784 |
rs260056004 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660197 | ACTCTTTTTAAAGGA[-/T]TTTTTTTTTAAACCT | 14784 |
rs260073202 | snp | A/G | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709019 | TAGTCTGTTCACGCA[A/G]TGAACCACATACCCA | 14784 |
rs260074862 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115657624 | CCACAAGGATGCTCA[C/T]AAGAATCTGTAACTC | 14784 |
rs260090819 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115705799 | CCCCTCCCAAGTGGC[A/G]GCAGAAGCACTGGGG | 14784 |
rs260133187 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115654556 | CCCTTTACAGTCTTT[A/C]TTTATTTTTAAAAAC | 14784 |
rs260141168 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115693079 | TGACACTCAGCTGAC[-/A]AAGTGAACGTCAGGG | 14784 |
rs260149870 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115707121 | CACCAAAATACAAGT[A/G]ACACAAGCAAACAGG | 14784 |
rs260192468 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115653537 | CATAGTGGGTCTTCA[G/T]TGGACCCAAGTGTAT | 14784 |
rs260194481 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663911 | AAAATATAAACTGTT[A/G]TCTCCTTCAACTCCT | 14784 |
rs260242924 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646537 | GAACTCCTGCTCATA[C/T]GTGAGGAGGACTGAG | 14784 |
rs260255999 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115676379 | CTCCCTTGACTCCTT[C/T]CAAGACTAATTCCTT | 14784 |
rs260272190 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115695358 | CCCAACTCCTAACAG[C/T]CAAAACCTACATAGG | 14784 |
rs260305945 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694226 | GACATGTTCACAATG[C/T]ACCCCACACACAAGT | 14784 |
rs260329510 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651313 | TACATAAAATAATAA[C/T]GTTTTCATGGTTATT | 14784 |
rs260357220 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651698 | TGGTGTCTGCTTTGA[A/G]TCAGGGTTTTATGTC | 14784 |
rs260359893 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115704109 | AACAGCTCAAATGGG[-/A]AAAAAAAGCTGACAG | 14784 |
rs260381438 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705874 | TGGCGCACACCTTCA[A/T]CCCAACACTTCAACA | 14784 |
rs260393102 | in-del | -/CGCGCGCA | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709314 | ATGCGCGCGCGCGCG[-/CGCGCGCA]CACACACACACACAC | 14784 |
rs260407339 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661366 | CAGCAAGGCCCACCA[A/C]CACTCAGGCATCGTG | 14784 |
rs260444139 | snp | A/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700409 | TGTTCCCCTCACACA[A/T]ATGCTTTCCTCAGTC | 14784 |
rs260480946 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115662051 | AATATATATTGGCTC[A/G]ACATCCAATGCTCAA | 14784 |
rs260488072 | snp | C/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701529 | CAACTTTAAGCTGCA[C/T]TGGTCTAATTCCATG | 14784 |
rs260513255 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115674220 | TTTTCGTTTTACAAG[C/T]CGAGTAAGTAAGTTG | 14784 |
rs260557866 | in-del | -/AAAAAAAAC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663829 | AAAAAAAAAAAAAAA[-/AAAAAAAAC]CCCACAAATCACAGT | 14784 |
rs260599040 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115691140 | TTAGGGACGGCTCTC[A/G]GCAACTGCCTAAATC | 14784 |
rs260617076 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115707830 | CTGCTGCTGCTGCTT[-/C]CCCCCCACCCCCCAA | 14784 |
rs260629691 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115690365 | AAAACAAAACAAAAC[A/C]CAAGCAAACAAAATG | 14784 |
rs260678893 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667582 | AGAAATAATGTAACT[A/G]CCCGGCAATGGTGGC | 14784 |
rs260686601 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115701286 | TTTCTTTTTTTTTTT[-/A]AACTTCCAGTTATAC | 14784 |
rs260780477 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687126 | agaaacgagagaatt[C/T]gagataagaataaaa | 14784 |
rs260843018 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115661641 | CATCATGTCTCCCTG[C/T]CACCTTGCTTCTCAC | 14784 |
rs260850223 | in-del | -/CCCA | | | intron-variant | Grb2 | Mm_Celera | 11:115674920 | TGATTTCAGGTAAAC[-/CCCA]CCTTTTTTTTTTAAA | 14784 |
rs260988452 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115666147 | CTTTCATTACCAGCA[A/G]TTAGGAGGCAGGGGC | 14784 |
rs260996139 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115671140 | TTCATCATTGAGTTT[A/C]TAGCCTACAGCACCA | 14784 |
rs261042776 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658410 | agagacacagagaga[C/G]agacagagacagaga | 14784 |
rs261154937 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665154 | GAACCGGGACCAAAG[C/T]TGTAAATCCCAGGCC | 14784 |
rs261213305 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115696836 | TCTTCATCATAAATA[C/G]TCCCGGGAGAATATC | 14784 |
rs261216658 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115656262 | TCTAGGATTATAGGT[A/G]TAGACCGCCATGCTT | 14784 |
rs261267368 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115663472 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTCCTTC | 14784 |
rs261293906 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115659283 | GTTGGTGAAACATAA[C/T]AATCACCATAACGGC | 14784 |
rs261332616 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667109 | AAAGTGTAACCCAGC[C/T]GGCTATTAAGGGACT | 14784 |
rs261340661 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115654096 | CTAAATGTACCCCAT[C/T]TTTTAATGTTCCACA | 14784 |
rs261543427 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115704964 | TACAAGCTTGACCAT[A/C]GTGAATAGGGTTCTA | 14784 |
rs261554674 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115665568 | AGAAAAGGCTTTACA[-/T]GAAACTGCTGGGTGT | 14784 |
rs261622680 | snp | A/G | | | utr-variant-5-prime | Grb2 | Mm_Celera | 11:115708521 | CCCGGCCGCAGCCCC[A/G]CTCGCTCTCGCCGCC | 14784 |
rs261651214 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702417 | GAGGTCAGAGGACAG[C/T]TTTTAGGAGTCAGTC | 14784 |
rs261710345 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646597 | ACTCAACCACCTGAG[C/T]GCCAACTGCAGAGCC | 14784 |
rs261826970 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115690541 | CTACGGGAAATGCCC[C/G]TGCTCGAGAACGAGG | 14784 |
rs261878440 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684940 | ACATGCTGTGACATA[A/T]GCTCTCCTGTGTGTG | 14784 |
rs261900323 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115694878 | AACAAAGACCGGTAC[A/C]AAAAAAGGTCTGTTT | 14784 |
rs261996379 | in-del | -/TG | | | intron-variant | Grb2 | Mm_Celera | 11:115692630 | CAGTCATCTGGGTTT[-/TG]TTTGTTTTTTAAGGT | 14784 |
rs262117353 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115668271 | GTCAGGCCTCAGGAC[A/T]GGTTTGATACCCACA | 14784 |
rs262159734 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661421 | GGCTCATACATTTAC[A/G]GTTGCTCAGCAGGGA | 14784 |
rs262178432 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115665228 | AGGCTTACGGTGATC[A/G]CTCTACTAAACAAAG | 14784 |
rs262185067 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694201 | CCTGTGACTTACACA[C/T]GCATGCTGTGACATG | 14784 |
rs262195043 | in-del | -/TAAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115706068 | TCAAAAAAATTGAAT[-/TAAAA]AAAATTTTTTAAAAA | 14784 |
rs262268601 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684030 | GCAGTTTAGTCAAAG[C/T]AGTAAGCTTCAGGTC | 14784 |
rs262296444 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115689677 | TTGTTTTCACGTCTG[C/T]ACTCTCAGAAAGCAC | 14784 |
rs262330777 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115679387 | CATACCTGAGATCCC[A/C]ATGTTACATGGACTT | 14784 |
rs262332860 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115658400 | TGTGTGAGAGAGAGA[C/G]ACAGAGAGAGAGACA | 14784 |
rs262416956 | in-del | -/ACATAC | | | intron-variant | Grb2 | Mm_Celera | 11:115659231 | CATACACACATACAT[-/ACATAC]ACACACACACACACA | 14784 |
rs262419653 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652890 | TCAGCTTAAAATTTT[A/T]AAAATTTAATTTTAG | 14784 |
rs262421234 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115663244 | CACGAGGAGAGTGGA[C/G]AGCAGGCCCTGCCCA | 14784 |
rs262499692 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115704449 | CAGCAAGTTTTAATG[A/G]AGAGTGGTAAAGTAT | 14784 |
rs262511465 | in-del | -/AAAAAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115686196 | AAAAACCAAAAAAAG[-/AAAAAAA]AAAAAAAAAAAAAGA | 14784 |
rs262535606 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115655832 | CCCAGACCTCCAGCA[C/G]CTTCTCTACGGTCTC | 14784 |
rs262581378 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115698270 | AGAAGAGTGTCACTC[A/G]GGGGTAGCAAACAGC | 14784 |
rs262607312 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115651153 | CGAGTCCTGGCTTTT[C/T]GCCCCAAGGACATGG | 14784 |
rs262640323 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115650830 | GCCACCATGTGGTTG[C/T]TGAGATTTGAACTCA | 14784 |
rs262643675 | in-del | -/TTTT | | | intron-variant | Grb2 | Mm_Celera | 11:115698226 | TCTTCCTCAATCATG[-/TTTT]TTTTTTTTCACTTTC | 14784 |
rs262665295 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115690163 | AGCCAAACATTCTGC[-/A]AAATGTGACATATAG | 14784 |
rs262672792 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115660459 | GAATAAACATGTGCA[A/G]CAACTTGCTTTCAGT | 14784 |
rs262702829 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115655579 | GGCTTATTTGAGAAT[C/T]AGAATTCTTTTAATT | 14784 |
rs262753957 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115646101 | CCCTCCGCTCTGACA[C/T]ACTCCTAAGTCCTAG | 14784 |
rs262754378 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115689333 | ACACAGGCTGTAACC[A/G]TAATGGTAGCCCGAG | 14784 |
rs262757469 | in-del | -/AGG | | | intron-variant | Grb2 | Mm_Celera | 11:115692486 | ACTTGGCTAGTTATT[-/AGG]AGAACTAAGATTCAG | 14784 |
rs262787967 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115698544 | ATTTTTTATGCAGTT[-/A]AGATTTTAATGTGCA | 14784 |
rs262831935 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115648716 | CTGCCCAAGGGTCCA[A/G]CCCCTACCTACTGAC | 14784 |
rs262850920 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115697170 | AAAAAAAACAAAAAA[A/C]AAAAAAACCAAATGA | 14784 |
rs262867806 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115683837 | AAACAACAACAACAA[A/C]AAAAGCAAGCAAGCA | 14784 |
rs262932265 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686536 | AGACTTTTGGGTGTG[C/T]CGTGTTATCAATGGT | 14784 |
rs262963771 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115694367 | AGACAACGAAAAATT[-/AAA]AACTAAAACTAAACA | 14784 |
rs262990413 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115691878 | ACTGCGCAGTGATAA[A/C]ACTTAGAAGACTTCT | 14784 |
rs263001500 | snp | A/C | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644835 | CAGACCATAACTGAG[A/C]CACGGAGACAGAGAC | 14784 |
rs263072132 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691383 | TTTTAGCCAGGCGCA[C/T]GCCCTTGGCACTGGT | 14784 |
rs263079808 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681237 | ATTAAAAAATTTTAA[C/T]CTTACTATTATTTAT | 14784 |
rs263146067 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672669 | ATAAAAATAAACATT[A/T]AAAAAAAAAAAAAGG | 14784 |
rs263167345 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115682682 | CACATTACACAGGCC[A/G]TGGCACAGCCACCTG | 14784 |
rs263220780 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115686131 | GGCAGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 14784 |
rs263236997 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679109 | AGCCTCACGTGACAC[A/G]AAATCTGTAAGTCTC | 14784 |
rs263303901 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115652560 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACGCC | 14784 |
rs263383974 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115707452 | AGAAGGGGAAGTAGA[-/T]TTTTTTTTAAAGGGG | 14784 |
rs263412827 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673518 | GTATGAGTGTTTTGT[C/T]TGCATGGATGTATGT | 14784 |
rs263428520 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115685075 | ATGTGACAAGACTGG[A/G]CATTCTTCCCAGCAG | 14784 |
rs263454654 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115675257 | CTGCCTCTGCCTCTG[G/T]AGTGCTGGGATTAAA | 14784 |
rs263461946 | in-del | -/AAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115650588 | AAAAAAAATTTTTTT[-/AAAA]AAATTATTATTTATT | 14784 |
rs263513923 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115648525 | ATAGGTCACCTGGCT[A/G]GACGACAAGCACCTT | 14784 |
rs263545463 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649516 | GGAGTGGAGATGCGC[A/G]CGTGGTCACCGTAAG | 14784 |
rs263553701 | snp | A/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709891 | ATGCCTTTCAGAGCA[A/T]AAGATGAAGCCAATG | 14784 |
rs263621979 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115670182 | AACCAAACCCAGGAC[C/T]CCTGCAAAAACAAGG | 14784 |
rs263722886 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115703654 | AGGGAGTGGCACTAT[A/T]AGGAGGTGTGGCCTT | 14784 |
rs263774575 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115647499 | CTGTCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 14784 |
rs263796199 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115650482 | TGATCTCTTTGGTTC[C/G]AGGTCAGCCTGGTCT | 14784 |
rs263991539 | in-del | -/AACCCT | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700542 | TAACCTCACCTTTGC[-/AACCCT]AAGGGAAAATGAAGC | 14784 |
rs263997196 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115679811 | CCCAAGCTCCAAGTT[C/T]ATCACAAAACATTTT | 14784 |
rs264099875 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115706625 | AAACCTCAGTAACAC[A/C]GCAAACGGTGCTTAA | 14784 |
rs264181561 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115677312 | CAAGGCTCTGTGAAG[C/T]GGGCAGTACCATCCT | 14784 |
rs264184889 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674686 | GCAGGAAGTACAGCC[A/G]CTCCTCCCCTTCAAA | 14784 |
rs264213180 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115667906 | AGGTTACACACAGTC[C/T]TGCTGTGATAGAGCC | 14784 |
rs264240656 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115705186 | GAACTGAACTCAGGA[C/T]CTCTGTAAGAGCAGT | 14784 |
rs264294957 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660581 | CACACTGAGTAAGAG[C/T]CTTGCAGTCACCACC | 14784 |
rs264361914 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664598 | GGTTCCTTAGTGAAT[A/G]GAATCAGACCTTCCT | 14784 |
rs264388620 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672449 | GGCTGAGGTAGGAAC[G/T]TACATAACCAGGCCA | 14784 |
rs264391424 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665500 | AGTAGTCGGAGGGGG[C/G]CGCACTTGAGAAGGG | 14784 |
rs264418129 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115673835 | GATCAACGCATGTGC[C/T]GCCACCACAAGACAA | 14784 |
rs264482909 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115669691 | TCCCCAACAACCCCT[A/C]CACACCCACCCCATG | 14784 |
rs264505801 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115666426 | GGTGTCTGTGTACAG[C/T]GCCATCTCCTGCCGG | 14784 |
rs264527150 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115667325 | GGAGTTACTGAATCT[-/G]AGCTGAACATGAATT | 14784 |
rs264551122 | snp | A/G | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643794 | TGGGAGCAGAGGCAG[A/G]AGAATCTCTGCGAAT | 14784 |
rs264589543 | snp | C/T | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115709925 | CCAGCAGTTTGCGAT[C/T]TAGATAGAGCTACTT | 14784 |
rs264630102 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115660253 | AAGTAAAAGTCTTTC[A/T]TGAGAGCTATTAAAA | 14784 |
rs264668230 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115650573 | ACCTTATGGTATCTG[-/A]AAAAAAAATTTTTTT | 14784 |
rs264706097 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115707476 | AAAGGGGGCGGAGGG[A/G]CCAATGACTGGCGCT | 14784 |
rs264802671 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115702662 | ACACCCAGCATCAGC[G/T]GGCACTCTTACTTGC | 14784 |
rs264819131 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115691194 | GACCACAGGACAACA[C/T]AGTATCAACTGTCCC | 14784 |
rs264869863 | snp | G/T | | | upstream-variant-2KB, intron-variant | Grb2 | Mm_Celera | 11:115700042 | GCACAAGATACCCAA[G/T]ATCTAGGGTCTGCCT | 14784 |
rs264939574 | in-del | -/GGAC | | | intron-variant | Grb2 | Mm_Celera | 11:115656106 | GTGGGGGTTGGGGGG[-/GGAC]GACGACAGACCTTGA | 14784 |
rs264947007 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115662018 | AAGTTTAGAATGTCT[C/T]ATGTACCACTACTCT | 14784 |
rs264961158 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115669336 | GCCCAGGTTACTAAG[C/T]AAGCACTCACGGCAG | 14784 |
rs265069305 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115657795 | TCTAAGAGAGCCAAT[A/G]CTGCCTTCTAGAGTC | 14784 |
rs265080101 | in-del | -/GGTGCTG | | | intron-variant | Grb2 | Mm_Celera | 11:115651030 | TGCCTGGTTTTATGT[-/GGTGCTG]GGTGCTGAACCTCAG | 14784 |
rs265105597 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115654619 | GGCTTTGTGCATGCT[A/G]GAGCACGCTCTGCTC | 14784 |
rs265122376 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664162 | GGCCTGTTACTGAGT[A/G]GATTGCTCTCACAAT | 14784 |
rs265170643 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115693215 | AGGGCTTGCCGGAGT[C/T]TGAGGCCAGACTGAC | 14784 |
rs265204770 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659401 | GTGCCCTGGAACTCT[G/T]TAGAGCAGGCTGGCC | 14784 |
rs265211592 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661214 | GTGATGCAATGCTAT[A/C]CAATAAAGAAAGAAG | 14784 |
rs265262378 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115651613 | CTGTGCACCAATATG[A/G]CTGCCTCGGAATCCC | 14784 |
rs265300204 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649471 | CCTCTAGGCTCCTGG[A/G]AAGCATGAGTTGGGT | 14784 |
rs265327794 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115685480 | ATTTAAAGAAAGAAA[A/C]GGGAGGGAAGGAGGG | 14784 |
rs265393129 | in-del | -/CT | | | intron-variant | Grb2 | Mm_Celera | 11:115651966 | CACACACCATGGAGA[-/CT]CACCTTCCTGTTGCT | 14784 |
rs265396354 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115687620 | ATACATGCACACACA[C/T]ACCATATTCAAAAAA | 14784 |
rs265427830 | snp | C/T | | | downstream-variant-500B | Grb2 | Mm_Celera | 11:115643738 | AGGGTCTGGAGATGC[C/T]GGCCAGAGTTAACAT | 14784 |
rs265437294 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115692314 | CAGCTAGCCAATTAC[A/T]GTCTATGGATGTCAG | 14784 |
rs265481111 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115681834 | TAAAGATGTGAGCCA[C/T]CACACCCCAAGAGTC | 14784 |
rs265534297 | snp | G/T | | | intron-variant | Grb2 | Mm_Celera | 11:115690098 | AAAATCATTTGACCT[G/T]TAATATATTAAGATG | 14784 |
rs265550295 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115679765 | GCACCATGTAGAGGT[A/G]TGCTAACACAGGCCA | 14784 |
rs265562247 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115706704 | GTAACTCCTGTTCAA[-/G]GGGTATTGGTCCTCC | 14784 |
rs265590150 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653484 | TATGTGTCATCTGCT[A/G]GGCACACAGCTCCCT | 14784 |
rs265607785 | in-del | -/AAACAA | | | cds-indel | Grb2 | Mm_Celera | 11:115645145 | AAAAAACAAACAAAC[-/AAACAA]AAAAACGTCAAAACA | 14784 |
rs265619949 | in-del | -/AT | | | intron-variant | Grb2 | Mm_Celera | 11:115659230 | GACATACACACATAC[-/AT]ACACACACACACACA | 14784 |
rs265640067 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674160 | TGGAGATATTTTTAA[A/G]CATGTTGGTTTGACC | 14784 |
rs265678006 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115648866 | CCTGGCAAATACAGA[A/T]GTGGAGGCTCACAGT | 14784 |
rs265730298 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115656046 | TAGCCTTTTTTTTTT[A/T]AAAGACAGTCTGTGT | 14784 |
rs265752403 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115646495 | AGCATTCCCTCACTC[A/G]GGCTGTAAACGAGGC | 14784 |
rs265785797 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115674126 | TTACTCAGAACACAC[-/G]GGAGTCAGGAAGCAC | 14784 |
rs265802390 | in-del | -/ACAACTGG | | | intron-variant | Grb2 | Mm_Celera | 11:115686786 | CTTCAGGAAGTTCTT[-/ACAACTGG]ACATTAAGTATTATT | 14784 |
rs265806507 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115684378 | ACAGTGGTCCATTCA[C/T]TATACCAATGGGCTA | 14784 |
rs265817534 | in-del | -/AAAA | | | intron-variant | Grb2 | Mm_Celera | 11:115679124 | AAATCTGTAAGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 14784 |
rs265823279 | in-del | -/CTC | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684168 | ACCACACACACCACA[-/CTC]CTCCACACCATCTCA | 14784 |
rs266014993 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115668220 | AGAAGCAGTGAGCTC[C/G]GTGAAGGAGCAGTGA | 14784 |
rs266025058 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115678645 | GATTAAATTGTATGG[A/G]GGCCTAAGCCTAGAT | 14784 |
rs266058817 | in-del | -/TG | | | intron-variant | Grb2 | Mm_Celera | 11:115680422 | AATTTTAGACCTTTG[-/TG]GTTTTTTTTTTTTTT | 14784 |
rs266103202 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115661833 | CAAACCAGTCAACTC[-/G]GGCAATCTGTAGGCA | 14784 |
rs266117091 | snp | C/T | | | intron-variant | Grb2 | Mm_Celera | 11:115672939 | ACAGTTGTAAGATGT[C/T]CATCTAGTTCCAACA | 14784 |
rs266171785 | snp | A/T | | | intron-variant | Grb2 | Mm_Celera | 11:115680438 | GTTTTTTTTTTTTTT[A/T]AAAAACTTGTTTATT | 14784 |
rs266188238 | in-del | -/TAAATGAAGC | | | intron-variant | Grb2 | Mm_Celera | 11:115672482 | CCCAACCTAAGTCTT[-/TAAATGAAGC]GCTAACAGGCTTCAT | 14784 |
rs266188923 | snp | C/G | | | intron-variant | Grb2 | Mm_Celera | 11:115670464 | TTCTCAGGAGGAACT[C/G]TAGACAAACATAAGT | 14784 |
rs266234595 | snp | C/T | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115644886 | AGCTGAAGCGAGTGT[C/T]GCAGCTCACAAAGTA | 14784 |
rs266242157 | snp | A/C | | | intron-variant | Grb2 | Mm_Celera | 11:115704264 | AACTCTTATGACAGA[A/C]ACATTAACAACCCTA | 14784 |
rs386837259 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659465 | GTGCTGGAATTAAAG[C/G]AGACAGAGGCAGGCA | 14784 |
rs386857633 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | Grb2 | Mm_Celera | 11:115658377 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTG]AGAGAGAGACACAGA | 14784 |
rs386860048 | in-del | -/GGGG | | | upstream-variant-2KB | Grb2 | Mm_Celera | 11:115710175 | AAAATAGGGGGGGGG[-/GGGG]CTGTCATTTGGTGGT | 14784 |
rs386876027 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650122 | TCCACACTCTAGATC[A/T]TAATTCAAGGCAGCA | 14784 |
rs386906225 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115707105 | GTGAAAAAAAAAAAA[-/A]CACCAAAATACAAGT | 14784 |
rs386918837 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650588 | GAAAAAAAATTTTTT[A/T]AAATTATTATTTATT | 14784 |
rs386919583 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115655483 | AAGACAAAAAAAAAA[-/A]TCAATCATTTACTCT | 14784 |
rs386941683 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656579 | CCCAGCACTCAGGAG[A/G]CAGAGGCAGGCGGAT | 14784 |
rs386968007 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115651687 | GCCACCAAGGCTGGT[A/G]TCTGCTTTGAATCAG | 14784 |
rs386997425 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663264 | GGCCCTGCCCAGAGT[C/T]CACTATCACCCAGAG | 14784 |
rs387017794 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115647076 | AGCCCCTCCTGATTG[C/T]TGATGACTAGTTACA | 14784 |
rs387038252 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659678 | ACATCAGAAGTTCAA[C/T]CTAGGTATTGACAAA | 14784 |
rs387040764 | in-del | -/AAA | | | intron-variant | Grb2 | Mm_Celera | 11:115679140 | AAAAAAAAAAAAAAA[-/AAA]TCAAACCTCAAAAGT | 14784 |
rs387057577 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115672588 | CAGTCTCAGGACCCA[C/T]AGCCTCTTCTGGTTT | 14784 |
rs387062329 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115668493 | CCATACACAAAAAAA[-/A]TAAACAAATTAAAAA | 14784 |
rs387082831 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702697 | CTATCTCTATAGCCT[C/T]TGCTTTGATTTTCTG | 14784 |
rs387110928 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115681143 | ACCCAGATCCAGGAG[C/T]TCTAATGCCTCTGGC | 14784 |
rs387124694 | snp | A/G | | | intron-variant | Grb2 | Mm_Celera | 11:115664775 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 14784 |
rs387131792 | in-del | -/CTTT | | | intron-variant | Grb2 | Mm_Celera | 11:115703017 | TCTCTCTCTCTCTCT[-/CTTT]TTCTGAGACAGGGTT | 14784 |
rs387168917 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666939 | CTCTCCGGCTCCCTT[A/G]CTGTTTCCTGCTGGG | 14784 |
rs387186027 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115648582 | GGTCTCATGTAGCCC[-/C]AGGCTGACCCAGAAC | 14784 |
rs387214245 | in-del | -/CA | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684296 | ACACACACACACACA[-/CA]AACACACCCTACCAC | 14784 |
rs387230591 | in-del | -/CAA | | | intron-variant | Grb2 | Mm_Celera | 11:115656695 | AAACACAAACAACAA[-/CAA]GACATCCACGGTATG | 14784 |
rs387237073 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115659070 | GGCCAGTAAGATAGG[-/G]CTCAGCGGGCAAAGA | 14784 |
rs387294659 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115670432 | AAATTCAGACTGTCA[C/T]AACCCTTCTTCAGAG | 14784 |
rs387304017 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115664138 | TTTGGTTTTGTTTTT[-/T]ACCTGAAAGGCCTGT | 14784 |
rs387327886 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650738 | CCACTTGCTCAGTCC[C/T]TGCTCCTGCTTATTA | 14784 |
rs387330660 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656734 | GTCCCCAAAGCTGCA[A/T]GTTCTTACTGCCAAC | 14784 |
rs387366519 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115672682 | TAAAAAAAAAAAAAA[-/A]GGAGAAAACAGACTA | 14784 |
rs387383307 | in-del | -/A | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645075 | TTATTAAAAAAAAAA[-/A]TGGTACAAATACCAT | 14784 |
rs387408390 | in-del | -/GAGAAAATAT | | | intron-variant | Grb2 | Mm_Celera | 11:115679237 | TTTATGAGAAAATAT[-/GAGAAAATAT]CAAGTTTTATTATCT | 14784 |
rs387412431 | in-del | -/CCTCTGGAGCT | | | intron-variant | Grb2 | Mm_Celera | 11:115670128 | TAAGGACAACAGAGC[-/CCTCTGGAGCT]GAGTTACAAACAAAT | 14784 |
rs387454769 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115654694 | CCAGAGTCTGACTTA[C/T]TATTCATATTCAGTT | 14784 |
rs387470073 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115705342 | ACCCAGCTAGGAGCC[-/C]ACCAAAGTCCAACTT | 14784 |
rs387475914 | in-del | -/TT | | | intron-variant | Grb2 | Mm_Celera | 11:115658095 | TCTCTCTCTCTCTCT[-/TT]CTCTCTCTCTCTCTC | 14784 |
rs387485218 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671851 | GGGAATCAGTTTTTA[A/C]ATATGTTTGGAACAA | 14784 |
rs387497287 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658713 | CACACACACACACAC[A/G]CACACACACACACAC | 14784 |
rs387516038 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656506 | ACGTGCACTCTCCCA[C/T]CTCCAATTCTAGAAA | 14784 |
rs387541802 | in-del | -/GCACACACACACACACACACAC | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709319 | CGCGCGCGCGCGCGC[-/GCACACACACACACACACACAC]ACACACACACACACA | 14784 |
rs387570775 | in-del | -/AA | | | intron-variant | Grb2 | Mm_Celera | 11:115693558 | TTAAAAAAAAAAAAA[-/AA]GAGGAAAACCTCAAG | 14784 |
rs387578339 | in-del | -/C | | | intron-variant | Grb2 | Mm_Celera | 11:115661262 | TATAACCCCCCCCCC[-/C]ACTCCCAAATTCCTA | 14784 |
rs387609517 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702375 | TATCTATTTGTGTGT[A/T]TGTACACATATTCCC | 14784 |
rs387624817 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678252 | AAAGAAAAGAAAAGA[A/G]AAGAGAAGAGAAGAG | 14784 |
rs387650338 | in-del | -/TGCACAGG | | | intron-variant | Grb2 | Mm_Celera | 11:115674300 | TTTTAGCCTGTCAGG[-/TGCACAGG]CTTTGTCCTGAATTT | 14784 |
rs387670902 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671785 | CTCAGAGATCCACCC[A/G]CCTCTGTCTCTGGGT | 14784 |
rs387680759 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115653898 | TAGCTACTTACCAAG[-/G]ACCAGGAGGACCTGA | 14784 |
rs387690747 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650401 | GGCTTGCATTGTGAG[A/G]AATTAGAGTCTAGGT | 14784 |
rs387702724 | in-del | -/G | | | intron-variant | Grb2 | Mm_Celera | 11:115649000 | CAGAGCTTGTGTCTT[-/G]TGTCTGCATGTAGCA | 14784 |
rs387705083 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115648343 | TACCAACCGAGCCAG[A/C]TACCTCTTATATTTT | 14784 |
rs387709966 | in-del | -/A | | | intron-variant | Grb2 | Mm_Celera | 11:115683841 | ACAACAACAAAAAAA[-/A]GCAAGCAAGCAATAA | 14784 |
rs387732331 | in-del | -/ATAT | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658040 | GTGGGTCAAACTGCA[-/ATAT]ATATATATATATATA | 14784 |
rs387760638 | in-del | -/A | | | utr-variant-3-prime | Grb2 | Mm_Celera | 11:115645135 | CACTATTTAAAAAAA[-/A]CAAACAAACAAACAA | 14784 |
rs387823118 | in-del | -/TTGAGG | | | intron-variant | Grb2 | Mm_Celera | 11:115667079 | CAAGTTGGTAAGTGG[-/TTGAGG]GTACAAAGACTTGGA | 14784 |
rs387823995 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115672218 | GTGTCTATACACACA[C/T]ACATACATATATATA | 14784 |
rs387838972 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115669106 | GAAGAGTCCCTGGAA[A/G]AAGGGATATTTAGCA | 14784 |
rs387842825 | in-del | -/AAGAAAAGAGAAGAGAAGAG | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678243 | AAGAAAAGAAAAGAA[-/AAGAAAAGAGAAGAGAAGAG]AAGAGAAGAGAAGAG | 14784 |
rs387858309 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658126 | TCTCTCTCTCTCTCT[C/G]TCTCTGCTGCTGAGC | 14784 |
rs387878936 | in-del | -/T | | | intron-variant | Grb2 | Mm_Celera | 11:115694584 | AATAAATTTTTTTTT[-/T]CAGCCAAAGAAGTGG | 14784 |
rs387882032 | in-del | -/AT | | | intron-variant | Grb2 | Mm_Celera | 11:115658732 | CACACACACACGCAC[-/AT]GCACACGCACACACA | 14784 |
rs578363099 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115652439 | TTTGTTTTGTTTTTG[G/T]TTTTTCAAGACAGGG | 14784 |
rs578372304 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115687275 | CTACACAGAGAAATT[C/T]TGTCTTGGGAAAAAA | 14784 |
rs578375560 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667144 | CGGTATGTTACAACT[A/G]CATAGCCATCTCCTC | 14784 |
rs578376797 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115662501 | TCAAAGCGGGAAGGC[A/G]CAGAATCACGTCACA | 14784 |
rs578404055 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115675099 | TCTTAACTGCTGAGC[A/C]ATCTCTCCAGCCCTC | 14784 |
rs578404924 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115646370 | ACAGATGGTTGTGAG[C/T]CACCATGTGGTTGCT | 14784 |
rs578419451 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678301 | AAAGAGGAAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs578430239 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658385 | GTGTGTGTGTGTGTG[A/T]GTGTGAGAGAGAGAC | 14784 |
rs578434322 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115670627 | TGGGGGCAGGGCCAG[C/T]GGAGACCACACTGTA | 14784 |
rs578442427 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115694889 | GTACAAAAAAAGGTC[A/T]GTTTGTTTGTTTTGT | 14784 |
rs578619303 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115648289 | CTCTCTAGCATCTGC[C/G]CTTGGACCCTAACTC | 14784 |
rs578619677 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664691 | TTGTTATATTTTTTT[A/G]AAACAAAGTCTCTCT | 14784 |
rs578801880 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115679590 | ATAAAGAGAGCCCTA[A/G]CTACTCAAGAGGCTG | 14784 |
rs578935382 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658350 | TGAGTTTCAAGTATC[A/G]TGTGTGTGTGTGTGT | 14784 |
rs578950881 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115694024 | CTTCTGATGGGAATA[C/T]AAACAACTCCAGCCA | 14784 |
rs578985232 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115649166 | GGGGACTTTCGGAGA[A/G]GAAACTAGGAAAGCA | 14784 |
rs578993803 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664794 | GCTGGGATTAAAGGC[A/G]TGCGCCATCACGCCC | 14784 |
rs579009618 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115676528 | ATTTTTTTAAAATGT[A/G]TATGTTATCATCCCT | 14784 |
rs579024728 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115653258 | CACTGACTGAGCTAT[A/G]CTCAGAGCATGTCGG | 14784 |
rs579036666 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667638 | GAGGCAGAGGCAGGA[C/G]GATTTCTGGGTTCGA | 14784 |
rs579042676 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689031 | GCCGGGCGTGGTGGC[A/G]CACGCCTTTAGTCCC | 14784 |
rs579062901 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115706781 | CACACACACGCCCGC[A/G]CGCACGCGCAGGTAA | 14784 |
rs579181010 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115661396 | GGAGCAAGACTGAAC[C/T]GGCCCCACAGGCTCA | 14784 |
rs579203113 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115675008 | AAGACGGCATTAGAT[C/G]ACATTACAGATGGTC | 14784 |
rs579328020 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667904 | CCAGGTTACACACAG[C/T]CTTGCTGTGATAGAG | 14784 |
rs579359277 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115703817 | GCATCATGCCTGCCT[A/G]GACACTGCCATGTTT | 14784 |
rs579376020 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115654412 | CTCACTAGTGCACTG[C/T]CCTCCTCCTCTGCTC | 14784 |
rs579390283 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689946 | GTGGTGGCGCACGCC[C/T]TTAGTCCCAGCACTT | 14784 |
rs579403053 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663584 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 14784 |
rs579407979 | snp | A/C | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709644 | GGTTCCTGTGCGGGG[A/C]TGCCGGTTTTGGGGG | 14784 |
rs579465405 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678242 | AAAGAAAAGAAAAGA[A/G]AAGAAAAGAGAAGAG | 14784 |
rs579561544 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663520 | TGTAGCCCTGGCTGT[C/T]CTGGAACTCACTCTG | 14784 |
rs579614174 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664871 | ACATGAAACCAATCC[G/T]ACACTAAGGTAAAAG | 14784 |
rs579617162 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658739 | CACACGCACGCACAC[A/G]CACACACACACACAC | 14784 |
rs579627646 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671887 | GTAATTTTAAACTCA[C/T]CACCACACACAGTTC | 14784 |
rs579641001 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115655953 | AACCCTGTGTTCAGG[G/T]CAGGCACTCCTGGAG | 14784 |
rs579642940 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668578 | TGCAAACCCAATAGC[C/T]AGAGTGCTATCCCCT | 14784 |
rs579924760 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658408 | AGAGAGACACAGAGA[C/G]AGAGACAGAGACAGA | 14784 |
rs579940955 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115682153 | TAGGCCACTGGGAGC[G/T]TGGTGGAGTTCAAAT | 14784 |
rs579955824 | snp | C/T | | | intron-variant, upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115699790 | GAACCAAGATTGCTC[C/T]CACTCCCTGTCAGAA | 14784 |
rs580030831 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671457 | ACACACACACACACA[A/C]ACACAAACACACACG | 14784 |
rs580040184 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115695719 | ACAGTAATGTGTTTT[C/T]CTTGCAGGGCTGCTG | 14784 |
rs580046087 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665560 | TCCCTTTCAAGAAAA[C/G]GCTTTACAGAAACTG | 14784 |
rs580131915 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656235 | AAAACTCCCAATCCT[C/T]ACCCTCCAAATTCTA | 14784 |
rs580279706 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668972 | CAACCATCTGTAATG[A/G]GATCCGATGCCCTCT | 14784 |
rs580286270 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115690725 | CAAACCACACACACA[C/G]AGAGTGAGCACTGGT | 14784 |
rs580487543 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668980 | TGTAATGGGATCCGA[C/T]GCCCTCTTCTGGTGT | 14784 |
rs580525341 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656462 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 14784 |
rs580542271 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691527 | ATGAATGAATGAATG[A/T]ATGAATGTATGAATG | 14784 |
rs580552209 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664521 | ACTAAACGGCATCTG[C/T]TCCTCTGCCCAGCTG | 14784 |
rs580565879 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663553 | GACCAGGCTAGCCTC[A/G]AACTCAGAAATCTGC | 14784 |
rs580569613 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115677698 | CATCAGGTCATCTGG[C/T]TGGTTTTTGTTAGTT | 14784 |
rs580579892 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115707860 | ACAAGTATTTTTTCC[C/T]CCTCAAGTCCTTCTA | 14784 |
rs580610065 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678308 | AAAGAGGAAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs580642555 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668993 | GATGCCCTCTTCTGG[A/T]GTGTTTGAAGACAGC | 14784 |
rs580650757 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115693063 | CGCACTGGGGTGGAA[A/G]CTGACACTCAGCTGA | 14784 |
rs580722324 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115651438 | GGGTGGGGGGTGTCA[C/T]TCTGTTCTGACAGCC | 14784 |
rs580787026 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666829 | AGGGGGAGTAACACT[A/G]TAGCTAAGCATGGCG | 14784 |
rs580941991 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115669030 | GTACTCACATACATA[A/G]AATAAATCTTTTAAA | 14784 |
rs581001636 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115693270 | CCACTACAAAATGAA[A/G]CAGTGTCTGAAAAAA | 14784 |
rs581111145 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115661326 | CAGTCAAGTTCCTAA[A/G]CAGCCCACTTAGCTG | 14784 |
rs581123230 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115703016 | TCTCTCTCTCTCTCT[C/T]TTTCTGAGACAGGGT | 14784 |
rs581191030 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702634 | AGTGCTGGGATTAAA[A/G]GTGTGAGCCACCACA | 14784 |
rs581191484 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115674273 | CAGGAACAAAAACCG[C/T]GTCTGCCTCTGTTTT | 14784 |
rs581194997 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115652524 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 14784 |
rs581195370 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667534 | GATTATTTTTTGTTG[C/T]TATTTTATAACTAAA | 14784 |
rs581201319 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689008 | TAAATGGTACATCAA[A/G]ACTCCATGCCGGGCG | 14784 |
rs581268637 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666295 | AAAGCAAAACCTCTC[C/T]ATTTCTACAAATAAG | 14784 |
rs581280845 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115684371 | GCAGTCAACAGTGGT[C/T]CATTCATTATACCAA | 14784 |
rs581294989 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678262 | AAAGAGAAGAGAAGA[A/G]AAGAGAAGAGAAGAG | 14784 |
rs581442050 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115687047 | TGTGAGACAGCCACA[A/G]CAGTATTTAAAAGAG | 14784 |
rs581477871 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663718 | GTGTTGCATCAGGCC[A/G]GCCCTGGGCCTCTTT | 14784 |
rs581662174 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115705012 | GGGCGGGGGGGACGA[C/T]GACGACAAACTAAAT | 14784 |
rs581815272 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115646269 | TTTTTTTTTTTTTTT[A/T]TAAAAAAAAAGATTT | 14784 |
rs581829896 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663919 | AACTGTTGTCTCCTT[C/T]AACTCCTCCTGGCTC | 14784 |
rs581840097 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678287 | GAAGAGGAAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs581896053 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658387 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGACAC | 14784 |
rs581908381 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115670982 | CTCCCAAATTACAAG[A/G]ATCAGACAGTGTGAT | 14784 |
rs581912815 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115695078 | GCCTCTGCCTCCAAA[A/G]TGTTGGGATTAAAGG | 14784 |
rs582038567 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115695727 | GTGTTTTTCTTGCAG[A/G]GCTGCTGAATAGAGA | 14784 |
rs582073048 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115675229 | CAGCCTGGCCTCAAA[A/C]TCAGAAATCCACCTG | 14784 |
rs582097986 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689950 | TGGCGCACGCCTTTA[A/G]TCCCAGCACTTGGGA | 14784 |
rs582163076 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671474 | CACAAACACACACGG[A/G]CGGGGAGTGGGGGGA | 14784 |
rs582204494 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115706192 | CCATATGGTTGCTGG[A/G]AACTGAACTCAGGAC | 14784 |
rs582207513 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664774 | CCTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA | 14784 |
rs582268953 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115706794 | GCGCGCACGCGCAGG[C/T]AAATACACTCAAGAA | 14784 |
rs582295849 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668965 | CGGCTCACAACCATC[C/T]GTAATGGGATCCGAT | 14784 |
rs582304078 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689979 | GAGGCAGAGGCAGGC[A/G]GATCTCTGAGTTCGA | 14784 |
rs582336091 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115662550 | GTCTCAGAGACAGGG[A/T]GGCTTCAGGATGGAT | 14784 |
rs582376470 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115653270 | TATACTCAGAGCATG[C/T]CGGGTTTCTTTCAAT | 14784 |
rs582407479 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115676577 | TTCACATTTTAAAGA[A/C]TCAGGTCCCAGCCAA | 14784 |
rs582456585 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667657 | TTCTGGGTTCGAGGC[C/T]AGCCTGGTCTACAAA | 14784 |
rs582458390 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689782 | GAAACATAGGCATTG[A/G]TGAGGTGGGCGGGGC | 14784 |
rs582741546 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668316 | AAAGGAACATTTCTG[C/T]GAGCTCTCCTCTGAC | 14784 |
rs582807225 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115661902 | TTCTTATCCAGTTAG[C/T]TCTTGCAGATGCATT | 14784 |
rs582807627 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115675009 | AGACGGCATTAGATG[A/T]CATTACAGATGGTCG | 14784 |
rs582855327 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664797 | GGGATTAAAGGCGTG[C/T]GCCATCACGCCCGGC | 14784 |
rs582866111 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115680431 | ACCTTTGGTTTTTTT[G/T]TTTTTTAAAAAACTT | 14784 |
rs582919230 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658358 | AAGTATCGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 14784 |
rs582927303 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115694029 | GATGGGAATATAAAC[A/G]ACTCCAGCCACTATG | 14784 |
rs582981069 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650560 | AACCAAAGCCCATTA[C/T]CTTATGGTATCTGAA | 14784 |
rs583004143 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115680528 | CATTACAGATGGTTG[C/T]GAGCCACCATGTGGT | 14784 |
rs583237379 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659076 | GTAAGATAGGCTCAG[C/T]GGGCAAAGACTGAAG | 14784 |
rs583247666 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702567 | ATCCTGGAACTCATT[C/T]GGTAGACCAGGCTGG | 14784 |
rs583402683 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663606 | GGGATTAAAGGCATG[C/T]GCCACCACACCTGGC | 14784 |
rs583403542 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668973 | AACCATCTGTAATGG[A/G]ATCCGATGCCCTCTT | 14784 |
rs583415029 | snp | A/G | | | upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115709650 | TGTGCGGGGCTGCCG[A/G]TTTTGGGGGAGTAGT | 14784 |
rs583415313 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115665584 | GAAACTGCTGGGTGT[A/G]GTGATGCACGCCTTT | 14784 |
rs583417484 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115683166 | AGGAAATATAAGCTC[C/T]GGGAACTGGAGTTAC | 14784 |
rs583444444 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656095 | ACCTTGTGGCTGGTG[A/G]GGGTTGGGGGGGACG | 14784 |
rs583590716 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656412 | CTTGATATATAGAGA[C/T]GGGTGTGGGTGTGTG | 14784 |
rs583739816 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656468 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGCGCGCG | 14784 |
rs583748082 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691783 | CCTCTCCTTCTACCA[C/T]GTTGATTCCAGGAAG | 14784 |
rs583816566 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115690736 | CACACAGAGTGAGCA[C/T]TGGTTGGTGACACCT | 14784 |
rs583822642 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663803 | CATTAAAATAAGCCT[A/C]CTAACCAAAAAAAAA | 14784 |
rs583827005 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678273 | AAGAGAAGAGAAGAG[A/G]AGAGGAAAGAGGAAA | 14784 |
rs583941673 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668983 | AATGGGATCCGATGC[C/T]CTCTTCTGGTGTGTT | 14784 |
rs583983555 | snp | C/T | | | intron-variant, upstream-variant-2KB | Grb2 | GRCm38.p3 | 11:115699791 | AACCAAGATTGCTCC[C/T]ACTCCCTGTCAGAAT | 14784 |
rs583990105 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666385 | TTGTCAGAGTCAGTG[C/T]CTCCATCTCCTGGCT | 14784 |
rs584012354 | snp | G/T | | | utr-variant-3-prime | Grb2 | GRCm38.p3 | 11:115644133 | GTACATAGTTGGTTT[G/T]TTTTTTTTTTTTATT | 14784 |
rs584022565 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663566 | TCAAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 14784 |
rs584026795 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678232 | AAAGAAAAGAAAAGA[A/G]AAGAAAAGAAAAGAA | 14784 |
rs584034974 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115707861 | CAAGTATTTTTTCCC[C/T]CTCAAGTCCTTCTAA | 14784 |
rs584070485 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658719 | CACACACACACACAC[A/G]CACACACACGCACGC | 14784 |
rs584080801 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115686575 | TTTCATAACCACCAA[A/G]TACACTTCTCCGAGA | 14784 |
rs584345034 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115687258 | TTCCAAGACAGCCAG[A/G]GCTACACAGAGAAAT | 14784 |
rs584373627 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115647389 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTTTGTTTT | 14784 |
rs584384003 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678315 | AAAGAGGAAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs584442579 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115662239 | TGGGAGCAGGCGTGG[A/G]TAGGTGGAAGATTTT | 14784 |
rs584444850 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115675026 | ATTACAGATGGTCGT[A/G]ATCCACCATGTGGTT | 14784 |
rs584454652 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115706188 | GTCACCATATGGTTG[C/T]TGGGAACTGAACTCA | 14784 |
rs584498127 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667587 | TAATGTAACTGCCCG[A/G]CAATGGTGGCACAGC | 14784 |
rs584510413 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689010 | AATGGTACATCAAGA[C/T]TCCATGCCGGGCGTG | 14784 |
rs584534248 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115674113 | CTCACTGCCAACGTT[A/C]CTCAGAACACACGGG | 14784 |
rs584594432 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664679 | TTTTTTGTTTGTTTG[C/T]TATATTTTTTTGAAA | 14784 |
rs584646935 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115652828 | GACATTTGTGTGAGC[C/T]CCAGTGCTTTCTCAT | 14784 |
rs584690491 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668998 | CCTCTTCTGGTGTGT[C/T]TGAAGACAGCGACAG | 14784 |
rs584691054 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115669086 | ACAAAAAACAAAACA[A/G]AACAGAAGAGTCCCT | 14784 |
rs584695024 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115693087 | CAGCTGACAAGTGAA[C/T]GTCAGGGTCAGGAAG | 14784 |
rs584757319 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115694358 | AACACACGAAGACAA[C/T]GAAAAATTAAAAACT | 14784 |
rs584936990 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689809 | GGGCTTTTATAAACT[C/T]TCAAGTGAGGACTTG | 14784 |
rs584946019 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115693536 | ACTTACATATAATAA[A/G]TAAATCTTAAAAAAA | 14784 |
rs585068045 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678294 | AAAGAGGAAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs585072129 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658362 | ATCGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 14784 |
rs585124496 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115646270 | TTTTTTTTTTTTTTT[A/T]AAAAAAAAAGATTTT | 14784 |
rs585199443 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115703030 | TCTTTCTGAGACAGG[A/G]TTTCTCTGTGTAGCC | 14784 |
rs585202390 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664280 | AGCTGGGGCCACAGA[A/G]CTCAGTCACACAGAC | 14784 |
rs585255157 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115661394 | GTGGAGCAAGACTGA[A/C]CTGGCCCCACAGGCT | 14784 |
rs585266284 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668323 | CATTTCTGTGAGCTC[C/T]CCTCTGACCTGGACA | 14784 |
rs585273631 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115674284 | ACCGCGTCTGCCTCT[A/G]TTTTAGCCTGTCAGG | 14784 |
rs585302249 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663116 | AGGACAAGGGCTACA[C/T]AGAGAAACCCTGTCT | 14784 |
rs585314616 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115706777 | CACACACACACACGC[A/C]CGCGCGCACGCGCAG | 14784 |
rs585485781 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115695709 | GCTGCTTAGTACAGT[A/G]ATGTGTTTTTCTTGC | 14784 |
rs585490502 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658717 | CACACACACACACAC[A/G]CACACACACACGCAC | 14784 |
rs585566575 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689978 | GGAGGCAGAGGCAGG[A/C]AGATCTCTGAGTTCG | 14784 |
rs585570602 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663567 | CAAACTCAGAAATCT[A/G]CCTGCCTCTGCCTCC | 14784 |
rs585607595 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115654966 | TTTTGTTGTTTTCAA[C/G]ACAGGGTTTGTTTGT | 14784 |
rs585608480 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115676513 | AAAATATAAGTTTGT[A/G]TTTTTTTAAAATGTG | 14784 |
rs585661461 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656226 | AGGCTGGTTAAAACT[C/G]CCAATCCTCACCCTC | 14784 |
rs585670780 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668970 | CACAACCATCTGTAA[C/T]GGGATCCGATGCCCT | 14784 |
rs585683603 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115689983 | CAGAGGCAGGCAGAT[C/T]TCTGAGTTCGAGGCC | 14784 |
rs585707309 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678237 | AAAGAAAAGAAAAGA[A/G]AAGAAAAGAAAAGAG | 14784 |
rs585824226 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671475 | ACAAACACACACGGG[C/T]GGGGAGTGGGGGGAG | 14784 |
rs585857696 | snp | A/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658389 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACACAG | 14784 |
rs585861700 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671224 | GCTTTAAGATTTCCA[A/G]TGGCCATTTTTCCCC | 14784 |
rs586032723 | snp | C/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115654404 | CTCCTCTGCTCACTA[C/G]TGCACTGTCCTCCTC | 14784 |
rs586088124 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663547 | TCTGTAGACCAGGCT[A/G]GCCTCAAACTCAGAA | 14784 |
rs586093451 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115676867 | TTGCCATCCATGGCC[A/G]TCTGCTGTGCCGTGG | 14784 |
rs586095828 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115707858 | CAACAAGTATTTTTT[C/T]CCCCTCAAGTCCTTC | 14784 |
rs586171902 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115698691 | CTCTTCGGTGAGTTT[A/G]GGCATATATATATAT | 14784 |
rs586206270 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115659203 | GTGTACTCAGATGCA[C/T]GCACACACACAGACA | 14784 |
rs586211532 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115680472 | TATATGTAAGTACAC[G/T]GTAGTTGGCTTCAGA | 14784 |
rs586259705 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115649161 | GTATAGGGGACTTTC[A/G]GAGAGGAAACTAGGA | 14784 |
rs586272366 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115664793 | TGCTGGGATTAAAGG[C/T]GTGCGCCATCACGCC | 14784 |
rs586274747 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115680183 | GCAAGGCCCGAGAAA[C/T]ATGGGGGAAAAATCC | 14784 |
rs586397005 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115667694 | TCCAGGACAGCCAGG[A/G]CTACACAGAGAAACC | 14784 |
rs586452739 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663615 | GGCATGTGCCACCAC[A/G]CCTGGCAAGCACTCT | 14784 |
rs586651871 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115692501 | AGGAGAACTAAGATT[A/C]AGAAGCTAGCCTGGA | 14784 |
rs586711321 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115672395 | TGTGTGGCCTGGCGC[A/G]GTACACCTGCAGAGT | 14784 |
rs586720151 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702568 | TCCTGGAACTCATTC[G/T]GTAGACCAGGCTGGC | 14784 |
rs586763373 | snp | C/G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668984 | ATGGGATCCGATGCC[C/G/T]TCTTCTGGTGTGTTT | 14784 |
rs586765298 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656456 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 14784 |
rs586776912 | snp | A/C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115691506 | ACCCTGCCCAAAAAA[A/C/T]CAAAAATGAATGAAT | 14784 |
rs586831640 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115674120 | CCAACGTTACTCAGA[A/G]CACACGGGAGTCAGG | 14784 |
rs586839278 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678257 | AAAGAAAAGAGAAGA[A/G]AAGAGAAGAGAAGAG | 14784 |
rs586909768 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656497 | CGCGCGCGCACGTGC[A/G]CTCTCCCACCTCCAA | 14784 |
rs586976017 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115656707 | CAACAAGACATCCAC[A/G]GTATGCCAAGAGTCC | 14784 |
rs586980169 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115669009 | GTGTTTGAAGACAGC[G/T]ACAGTGTACTCACAT | 14784 |
rs586984647 | snp | A/C | | | intron-variant | Grb2 | GRCm38.p3 | 11:115693090 | CTGACAAGTGAACGT[A/C]AGGGTCAGGAAGCTA | 14784 |
rs587012184 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115666496 | ATTTCCCTGCCCAAG[C/T]CCCCACTCCCTAAGG | 14784 |
rs587175700 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115663804 | ATTAAAATAAGCCTC[C/T]TAACCAAAAAAAAAA | 14784 |
rs587177404 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115668977 | ATCTGTAATGGGATC[C/T]GATGCCCTCTTCTGG | 14784 |
rs587178483 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115678280 | GAGAAGAGAAGAGGA[A/G]AGAGGAAAGAGGAAA | 14784 |
rs587217965 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115683167 | GGAAATATAAGCTCT[G/T]GGAACTGGAGTTACG | 14784 |
rs587247758 | snp | G/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115660379 | GGCTCACAACCATCT[G/T]TAATGGGGATCCAAA | 14784 |
rs587254279 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115702951 | AACTACCTCGCCTGT[A/G]TTTGTGTTGAGACAG | 14784 |
rs587391231 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115650829 | AGCCACCATGTGGTT[A/G]TTGAGATTTGAACTC | 14784 |
rs587396026 | snp | C/T | | | intron-variant | Grb2 | GRCm38.p3 | 11:115686595 | CTTCTCCGAGACAAT[C/T]TCAAGTGTTCTAGGA | 14784 |
rs587473988 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115658737 | CACACACGCACGCAC[A/G]CGCACACACACACAC | 14784 |
rs587482819 | snp | A/G | | | intron-variant | Grb2 | GRCm38.p3 | 11:115671882 | TCTTGGTAATTTTAA[A/G]CTCACCACCACACAC | 14784 |
rs587484383 | snp | A/G | | | upstream-variant-2KB, intron-variant | Grb2 | GRCm38.p3 | 11:115701668 | CCCTATCACTTCAAC[A/G]ATTAAAACTATTTTC | 14784 |