SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6207797 | snp | A/C/T | 0.5 | 0 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61445840 | TGGAAGATCTTCCCA[A/C/T]CATGCATGTGAGCAG | 59009 |
rs6230650 | snp | C/G/T | 0.46875 | 0.121031 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61342194 | GCCAATGGTAAGCTT[C/G/T]NGTTCTGAGTCATTA | 59009 |
rs6230652 | snp | A/G | 0.5 | 0 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61342195 | CCAATGGTAAGCTTN[A/G]GTTCTGAGTCATTAC | 59009 |
rs6230711 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61342231 | TACCTATTTGGACTG[A/G]CTCTTACAGGCTGCA | 59009 |
rs6232275 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Sh3rf1 | Mm_Celera | 8:61342469 | TTAAATTTGTTTTAG[A/G]TTCTTAAACATGCGT | 59009 |
rs6262288 | snp | A/G | 0.5 | 0 | intron-variant | Sh3rf1, LOC102638389 | GRCm38.p3 | 8:61410142 | GATTCTAGGGGGCTG[A/G]TGATCTCTGTTAGCG | 59009 |
rs6262369 | snp | A/G | 0.375 | 0.216506 | intron-variant | Sh3rf1, LOC102638389 | GRCm38.p3 | 8:61410203 | CATGTGATGCTTTTT[A/G]AAAATGGTCCCTTTC | 59009 |
rs6262870 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Sh3rf1, LOC102638389 | Mm_Celera | 8:61410254 | TGACTGGAACTGCTT[A/G]TTTCTCCTCGNAGGA | 59009 |
rs6262894 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Sh3rf1, LOC102638389 | Mm_Celera | 8:61410265 | GCTTNTTTCTCCTCG[A/C]AGGAAAGATGGCTGT | 59009 |
rs6262923 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Sh3rf1, LOC102638389 | Mm_Celera | 8:61410282 | GGAAAGATGGCTGTC[C/T]TAGGAATTAGAACAT | 59009 |
rs6263466 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Sh3rf1, LOC102638389 | Mm_Celera | 8:61410370 | TCAAAGTGGACAAAT[G/T]TTGGAAGAGCGCAAC | 59009 |
rs6277479 | snp | C/G | 0.5 | 0 | intron-variant | Sh3rf1, LOC102638389 | Mm_Celera | 8:61410629 | ggcaggcagatctct[C/G]tgagtccaaagccag | 59009 |
rs6280700 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | Mm_Celera | 8:61312421 | TTTGTATTGTACATC[C/T]GGATTGAGGAGAGCT | 59009 |
rs6281116 | snp | A/C/T | 0.5 | 0.235702 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | GRCm38.p3 | 8:61312446 | AGAGCTCTTGTCTAC[A/C/T]GATAAACAAAGAGGT | 59009 |
rs6281182 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | GRCm38.p3 | 8:61312482 | TAGCTAGTCTCATAG[G/T]GGGGTGTCTGTGGGG | 59009 |
rs6281677 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | Mm_Celera | 8:61312555 | AGTATTTTCTGGACA[C/T]GCTGTCGGCGTCTGT | 59009 |
rs6294805 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | Mm_Celera | 8:61312707 | TCTCTCCCTACACGT[A/C]TCGGCTTTTGTCTAG | 59009 |
rs6295359 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | Mm_Celera | 8:61312780 | GAGTGTGTGTAAAGA[C/T]TCTCCATTTATAAGC | 59009 |
rs6295927 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Sh3rf1, LOC105244981 | Mm_Celera | 8:61312897 | TGTTTGTGTCTCCCA[A/G]GAGGTGGTGTGTGCA | 59009 |
rs6318489 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61346978 | CCATTAGTAAATCTC[C/T]AGCATCNAGCAGTTT | 59009 |
rs6318499 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61346985 | TAAATCTCNAGCATC[A/G]AGCAGTTTACTCTCC | 59009 |
rs6319638 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61347239 | GTTTTTGCCACCAAG[C/T]TTGATGACCTGTGTC | 59009 |
rs6366403 | snp | A/C | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61323690 | TGGTGCACATGCCCA[A/C]AGGAACTCAAACAAG | 59009 |
rs6366417 | snp | A/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61323700 | GCCCACAGGAACTCA[A/T]ACAAGATGCACACAT | 59009 |
rs6407298 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255708 | GAAAAGTTGCAAAGA[C/T]GCTGGGATAAGAGTT | 59009 |
rs6407910 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255846 | GAAGAGTGGAAGAGA[A/G]TCACTTNGCATTATA | 59009 |
rs6407912 | snp | A/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255853 | GGAAGAGANTCACTT[A/T]GCATTATAGTGTTGG | 59009 |
rs6408426 | snp | A/G | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255918 | GACTGAGAGTTTATA[A/G]ATTCTTNCAATCCNG | 59009 |
rs6408434 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255925 | AGTTTATANATTCTT[C/T]CAATCCNGGTCTCNA | 59009 |
rs6408451 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255932 | ANATTCTTNCAATCC[C/T]GGTCTCNAATACTCT | 59009 |
rs6408468 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255939 | TNCAATCCNGGTCTC[C/T]AATACTCTATAATGC | 59009 |
rs6408921 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Sh3rf1 | Mm_Celera | 8:61255982 | TGTGTCTGTGTGTAT[C/T]TGATTATCAGATTTA | 59009 |
rs6409063 | snp | C/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61256061 | AAAGGCAGTGTATCT[C/T]AGTGTTACAGTCAAC | 59009 |
rs6409583 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sh3rf1 | Mm_Celera | 8:61256127 | TTCTGCTTCTGGTGT[C/T]TTTTTCATTTGTTTG | 59009 |
rs13479791 | snp | A/G | 0.46875 | 0.121031 | synonymous-codon | Sh3rf1 | GRCm38.p3 | 8:61372559 | GTCTACTGCGGGTCA[A/G]GCAAGTCGCGGGGTG | 59009 |
rs31489335 | snp | A/C | 0.459184 | 0.136902 | intron-variant, nc-transcript-variant | Sh3rf1, 1700001D01Rik | GRCm38.p3 | 8:61288794 | CTCGTCCTGAGCACT[A/C]GGAACAGTAAGCTTT | 59009 |
rs31489338 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Sh3rf1, 1700001D01Rik | GRCm38.p3 | 8:61288805 | CACTCGGAACAGTAA[A/G]CTTTGGTGCACTTTG | 59009 |
rs31489341 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | GRCm38.p3 | 8:61289023 | GTTGTCATGAAAATG[C/T]CTTTTAGGTTTTAGA | 59009 |
rs31489834 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61289342 | GGCTGGCATTTGTTA[A/G]TTGCCAAGGCCAACT | 59009 |
rs31489837 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | GRCm38.p3 | 8:61289640 | TTCTTTCTTGCACAC[A/G]CTGAAGACAGCTGTG | 59009 |
rs31489840 | snp | G/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61289643 | TTTCTTGCACACGCT[G/T]AAGACAGCTGTGCTG | 59009 |
rs31489843 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290073 | ACAATAACATAAGTC[A/G]GTAAAAGGAGCACAG | 59009 |
rs31490486 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290211 | CATCTGGGAAGCTAC[C/T]GTTCAATTTCAGATC | 59009 |
rs31490489 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290342 | GTGTGAAAAGTGTTT[A/G]AAAACAGTAACGCTA | 59009 |
rs31490492 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290404 | TGTTTCCAATTTATC[C/T]GTGTTGCAGTGAGCA | 59009 |
rs31490655 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Sh3rf1 | Mm_Celera | 8:61296595 | ATCGTTTCTGCGAGC[A/G]GTTTTATTAAAAACA | 59009 |
rs31490658 | snp | A/T | 0.375 | 0.216506 | intron-variant | Sh3rf1 | Mm_Celera | 8:61296892 | AATAAATAAAACTAA[A/T]TTTTAAAATGTATCA | 59009 |
rs31490661 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297041 | GTCACTATAATAAAC[A/G]GTGTGCTGAGGGAGT | 59009 |
rs31490664 | snp | A/C | 0.32 | 0.24 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61302971 | GCAGCATTGGATCCC[A/C]TGAGGTTACAGACGT | 59009 |
rs31490667 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61303391 | AGGCTTAGGAGTTCG[C/T]TATCCTTGGCTCTCT | 59009 |
rs31490670 | snp | C/T | 0.32 | 0.24 | intron-variant | Sh3rf1 | Mm_Celera | 8:61303891 | ACTTAGGGAATATAG[C/T]TCTAGCAACCCTAAT | 59009 |
rs31490673 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sh3rf1 | Mm_Celera | 8:61304474 | AGTTCCGAACTCATA[C/T]AGTTTCATGACTTTG | 59009 |
rs31490676 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61292959 | ATACTGTTCAAGCTG[C/T]TCCACTTCACTTTCT | 59009 |
rs31490679 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61293019 | CTGTGGTGCTCCTTC[C/T]GCAGGCTGGCCACAC | 59009 |
rs31490682 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61293140 | AGGGCATGTCTGTGG[A/G]TAGCATGGCAGTTCA | 59009 |
rs31491055 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290420 | GTGTTGCAGTGAGCA[C/T]GGTTCCTGCCTACTG | 59009 |
rs31491058 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290603 | ATCTATTTTTGGAAA[C/T]CCATTGAGAATTTTG | 59009 |
rs31491061 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Sh3rf1, 1700001D01Rik | Mm_Celera | 8:61290738 | GGATTGCTGCAAGTT[C/T]ATGGCTAGCCTGGGG | 59009 |
rs31491404 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297074 | TATGTAAAAGTAGAT[A/T]AGATATAAACACAAA | 59009 |
rs31491407 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297098 | ACACAAAAAGAATTA[A/T]CGCATTAAAGACTAA | 59009 |
rs31491410 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297196 | TAAAATACAGTTGAA[A/G]TCTCAGGTGGTTAGA | 59009 |
rs31491413 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297215 | CAGGTGGTTAGACCT[A/G]AAATGGATCAGGTTT | 59009 |
rs31491415 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61293221 | CTAGATTTTTATGAG[C/T]TCTAAGCATAAGATA | 59009 |
rs31491418 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61293268 | CAGGCATCAAGCTAC[A/G]ATGAACAAAGGACTG | 59009 |
rs31491421 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61293287 | AACAAAGGACTGCCA[C/T]CTGCTCTACCTTTGA | 59009 |
rs31491456 | snp | A/G | 0.32 | 0.24 | intron-variant | Sh3rf1 | Mm_Celera | 8:61304556 | GCATGTATGTCTCTC[A/G]CCACGTATGTGCCAG | 59009 |
rs31491459 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Sh3rf1 | Mm_Celera | 8:61305052 | GAGGCTGGACTAGAG[A/T]CAAAGTTTTAAATGG | 59009 |
rs31491462 | snp | G/T | 0.375 | 0.216506 | intron-variant | Sh3rf1 | Mm_Celera | 8:61305216 | TAGGGACAAGAAGTT[G/T]TCAATCACCTTGGGA | 59009 |
rs31491874 | snp | A/T | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61290928 | TCCCTCGGTGTTTTT[A/T]ATTAAACTTTGCTAT | 59009 |
rs31491877 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Sh3rf1 | Mm_Celera | 8:61291090 | TGCTGCCACACCTGG[A/C]CTCCTAGAACTATGC | 59009 |
rs31491880 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Sh3rf1 | Mm_Celera | 8:61291133 | TAGTTTTCAGTTACA[A/C]TCTTAATCTTTCTCC | 59009 |
rs31491883 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Sh3rf1 | Mm_Celera | 8:61291629 | CTTGATGCTGGTACT[A/G]TCACCTTCTGCTCTC | 59009 |
rs31491994 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61293426 | AGTGCATTCCCATGT[A/G]ACTGGGACCCAGCCG | 59009 |
rs31491997 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61293473 | TGGTGTATGCCATTT[C/G]CTGGCAAGGCTCTTT | 59009 |
rs31492000 | snp | C/G | 0.375 | 0.216506 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294039 | GACCGGCTCTCCTGA[C/G]TGTGCCCTTCAGAAA | 59009 |
rs31492003 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61294104 | TGTCATCCTCTCACA[C/T]GGACCTTTCTCTCGG | 59009 |
rs31492316 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297247 | CCATTTCTGGTTTGT[A/T]GGTTTCATGGTGTTG | 59009 |
rs31492319 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297253 | CTGGTTTGTAGGTTT[C/T]ATGGTGTTGATACAT | 59009 |
rs31492322 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297265 | TTTCATGGTGTTGAT[A/G]CATAAACTTCATGTC | 59009 |
rs31492475 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Sh3rf1 | Mm_Celera | 8:61305480 | ATCTTGATCCACTCA[C/T]AGCAGAGAAAGAGTG | 59009 |
rs31492478 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | Mm_Celera | 8:61305690 | CGAGATTAAACACTA[C/T]ACGCACTTGGTTTGG | 59009 |
rs31492481 | snp | A/G | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | Mm_Celera | 8:61305715 | GTTTGGAGGGTTATC[A/G]TTCCTTCTGCCCTAT | 59009 |
rs31492516 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294133 | GGTCTTAACACTGGG[C/T]TGGCTTCTTTCCTTT | 59009 |
rs31492519 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294214 | TTCTTTTGAAGTCTA[G/T]CTGCATCCCATTGGT | 59009 |
rs31492522 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294369 | TGTATTAAAAGATAC[A/T]TTTGTAAAGATGTAC | 59009 |
rs31492706 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61291711 | AAGCTTTAGTAAGTG[C/T]TCCTAACTGCATTTG | 59009 |
rs31492709 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61291789 | TTCCTCCTCCTCTTC[C/T]GGTGACTTTAAAGTG | 59009 |
rs31492712 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61291898 | TTCCCTTGCACACTT[C/T]CTGTGACTCTGTAAG | 59009 |
rs31493065 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297279 | TACATAAACTTCATG[C/T]CTAAATGTAAGATGT | 59009 |
rs31493068 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61297385 | AAACAAGATTGAAGG[C/T]AAACATGCAGGTTCA | 59009 |
rs31493071 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Sh3rf1 | GRCm38.p3 | 8:61297405 | ATGCAGGTTCAATTC[G/T]GAGGCCCCAGTGACT | 59009 |
rs31493254 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | GRCm38.p3 | 8:61305769 | TTATTCATCACTTCA[C/T]ATTTGTGCTTTAGCC | 59009 |
rs31493257 | snp | A/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | Mm_Celera | 8:61306264 | ACCGTGCCTAAGTGT[A/G]GGACGTTAGAAATCT | 59009 |
rs31493260 | snp | A/T | 0.21875 | 0.248039 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | Mm_Celera | 8:61306382 | TGTTCTCTTTGGATC[A/T]GTTAAATCTGAATAG | 59009 |
rs31493263 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Sh3rf1, LOC105244981 | GRCm38.p3 | 8:61306575 | CCCATGGAACTAGCA[A/G]CAACTTAAATTTTGA | 59009 |
rs31493305 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294522 | AAAGGCTACACTCAC[A/T]ACTAAAAGTGTAAAA | 59009 |
rs31493308 | snp | G/T | 0.32 | 0.24 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294531 | ACTCACTACTAAAAG[G/T]GTAAAATTATACAAA | 59009 |
rs31493310 | snp | A/G | 0.5 | 0 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294626 | TACTTTGTGATGTGT[A/G]CAAAATGTACATTTT | 59009 |
rs31493313 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61294662 | AAAACACTGTGTGAG[C/T]GTAACCAGGCTTGTT | 59009 |
rs31493365 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Sh3rf1 | Mm_Celera | 8:61292278 | AAAACGTCTCCTCAC[A/G]GAAGTTGTAGCGTGT | 59009 |